In the 1980s, scientists measured quantized jumps in the energy of ions for the first time. In the 2000s, it was photons’ turn. Now, thanks to a tour de force of device engineering and nanofabrication, researchers at Stanford University in the US are reporting that phonons – mechanical vibrations like those that carry sound – also display this quantum behaviour.

“We could see it by eye [in the data], which was very satisfying,” team leader Amir Safavi-Naeini tells Physics World. “I’ve been fascinated with the interface between the quantum world and the classical world and trying to move that interface closer to daily experience…and now we have mechanical objects.”

Laying the groundwork

The Stanford team’s recipe for observing quantum jumps in phonons begins with thin films of lithium niobate (LiNbO₃). Although bulk samples of this material had been available since the 1950s, the commercialization of thin-film LiNbO₃ a decade ago was a game changer for Safavi-Naeini and his colleagues once they worked out how to process the material.

Because LiNbO₃ is piezoelectric, placing it under stress – from a vibration, say – produces a voltage. This voltage allows vibrational quanta to couple to superconducting qubits, after which the qubit states can be “read out” to determine whether a phonon was present or not.

The problem was that initially, the phonons had lifetimes of only 800 nanoseconds – well short of the millisecond the team needed to observe them falling from an excited state to the ground state. Extending these phonon coherence times “took a lot of work by a number of graduate students in my group,” Safavi-Naeini says.

After probing various sources of dissipation, including material properties that cause quantum excitations to lose coherence, the researchers realized that surface defects were key offenders. They therefore switched from polymer processing, which left a residue, to shadow masks that superimpose one chip over the other and evaporate metal through it. “There were probably three generations of students that worked on getting that four to five orders of magnitude increase in the performance of the devices,” Safavi-Naeini says.

Once they’d extended their phonon lifetimes, the researchers had to find a way of combining their “very clean, long-lived” mechanical and superconducting systems without destroying either. For this, Safavi-Naeini credits past and present students Takuma Makihara and Erik Szakiel, who spent most of their PhDs tackling issues with the mechanical oscillators before finding a way to couple them to the superconducting systems. “That was the last piece,” Safavi-Naeini recalls. “Once we had that, we could do these experiments.”

Spot the missing phonon

Because the superconducting qubits detect whether an even or odd number of phonons is present in the LiNbO₃ (which at very low energies amounts to determining whether a phonon is there at all), they are effectively performing a parity measurement. That could make the Stanford team’s system useful for quantum error correction, where the goal is to find out whether an error has crept in without actually measuring the quantum states, since doing so would destroy their useful quantum characteristics.

One of the most common sources of error in superconducting qubits is the loss of an excitation, such as when a phonon decays. However, if data is encoded into phonons in pairs and the system detects an odd number of them, this loss becomes apparent without measuring all the states. This so-called “binomial” code has already been implemented for microwave photons, and Safavi-Naeini explains that it works best for long-lived particles – a further benefit of the team’s long-lived phonons.

Protein and gravity measurements

The Stanford researchers are now collaborating with Michael Roukes and colleagues at the California Institute of Technology (Caltech) to explore possible applications in high-precision measurements of single protein masses. They are also interested in fundamental science questions such as whether it’s possible to generate entanglement between mechanical systems through gravitational fields.

However, Safavi-Naeini cautions that their phonon lifetimes would need to be much longer – a factor of 10 for error correction and mass spectrometry, and for gravity perhaps as much as six orders of magnitude, with further modifications to the experimental set-up also required – before they can achieve these goals. “The hope is that by figuring out the fundamental sources of loss in these materials we can build our way up to those experiments in the coming decade,” he says. “Every time you improve, you hit some new source of noise, you understand it, then you can deal with it, and then you go to the next one. It’s a fun physics problem.”

The research is published in Science.

The post Sound waves come in quantum jumps appeared first on Physics World.

I have been involved in tribology for most of my working life, but even today it can feel like a well-kept secret. A highly interdisciplinary field with close ties to materials science, tribology is essentially the science and technology of friction, lubrication and wear between any moving surfaces. But tribology encompasses in part one age-old challenge.

I’m talking about the use of bearings, which dates back to at least 4600 BCE, when ancient Egyptians used wood log rollers to move large stone blocks during the construction of their pyramids. In 1500 Leonardo da Vinci used ball bearings in his conceptual helicopter design, while in 1740 the clock maker John Harrison invented caged roller bearings for his marine chronometer.

It was not until the mid-1960s that the word tribology was coined by the British engineer and entrepreneur Peter Jost after discussions with the then editor of the Oxford English Dictionary

The first patent on a ball bearing was granted to Philip Vaughan, an ironmaker from Carmarthen, Wales, bringing tribology firmly into the industrial world. But despite all the history, it was not until the mid-1960s that the word was coined by the British engineer and entrepreneur Peter Jost. After discussions with the then editor of the Oxford English Dictionary, the Greek word “tribos” – meaning rubbing – was suggested as a basis for describing the discipline.

This resonated with Jost, because the terms “tribo-chemistry” and “tribo-physics” were already in use. In an interview with the magazine Machinery Lubrication in 2005, Jost explained how “tribo science and tribo technology” then simply became shortened to tribology. “I felt that because it had a Greek basis, it could easily be adopted into a number of languages by most Western countries,” Jost recalled.

Wear’s the rub?

For the most part, the aim of tribology is to minimize friction and wear between components, which involves a knowledge of both materials and lubrication. Initially, the focus of the field was on moving parts in industrial or mechanical machines, such as bearings, gears, brakes and clutches. Indeed, one reason that the term came about was a conference in Cardiff in 1964 organized by the Iron and Steel Institute and the Institution of Mechanical Engineers (IMechE).

At the conference it became apparent that significant failures in plant machinery, which were being attributed to poor lubrication, were in fact due to a lack of fundamental design knowledge. These findings led to Jost chairing a UK government committee into lubrication education and research and the needs of industry. The resulting study – generally known as the “Jost report” – came out in 1964.

Now all this may seem like ancient history, which I suppose it is, but I was intrigued to discover that delegates to that 1964 conference visited the Llanwern steelworks at nearby Newport. As some of you may recall me describing, I also visited this site during my own student days, where I saw the steel rolling line in action. It was a truly impressive sight.

The total failure was remarkable, underlining just what can happen when moving parts fail without warning

From the viewing platform, I could see a massive volume of red-hot steel thunder along the rollers when, suddenly, there was a bang. Something failed and the steel landed in a crumpled mess all over the plant floor. We were safe but the total failure was remarkable to witness, underlining just what can happen when moving parts fail without warning.

The knock-on effect of this failure would have been costly and sustained. As well as a steel rolling line being out of action, new parts would have had to be sourced and old ones repaired. There’d have been quality concerns to address, safety reviews to be undertaken and the root cause of the problems to be worked out. Quite possibly all those jobs would have needed to be completed before production could restart.

What’s more, the failure of the machine’s moving parts, which depends on tribology, would have damaged the company’s reputation and led to customers annoyed with delays and late deliveries. It is this kind of event that those involved in tribology are trying to prevent, or at least minimize. By understanding tribology, in other words, engineers can design better machines and components.

What it says on the tin

This was made clear in the 1964 Jost report, which said that adopting good tribological practices could save the UK between 1% and 1.4% of its gross domestic product (GDP). In today’s money, that would amount to some £30bn, given that country’s GDP is a shade over £3 trillion. Put simply, designing and maintaining industrial equipment, based on a solid understanding of tribology, yields significant economic benefit.

More recently, a 2017 study by Kenneth Holmberg from the VTT Technical Research Centre of Finland and Ali Erdemir of the Argonne National Laboratory in the US (Friction (5 263) suggests that 20% of the world’s energy consumption originates in tribological contacts. And by the application of best practice, as much as 40% of this could be saved.

More than 60 years after the publication of the Jost report, the influence of tribology continues to grow. Alongside its impact on transportation and manufacturing, tribology is also relevant to extreme environments from aerospace, nuclear power, marine and subsea to space technology, high-voltage electrical systems and even the human body. There are also applications in nano-tribology, cosmetics, food, computational, digital, tribotronics, geotribology, hydrogen and green tribology.

Tribology will help to reduce our carbon footprint and counter climate change

As chair of the IMechE’s tribology group committee and a member of the tribology group committee of the Institute of Physics, naturally I am biased. Still, I feel privileged to be part of the tribology community and the amazing things it achieves. Whether it’s making products more energy efficient, creating green lubricants, or making plant-based protein more palatable to meat eaters, tribology will help to reduce our carbon footprint and counter climate change.

So next time you brush your teeth, comb your hair, switch on a light or ride on a bus, spare a thought for tribologists and their dedication to making the world run smoothly. It’s hard to think of anything that doesn’t involve tribology at all.

• The Institute of Physics is hosting the 5th Tribology and Net Zero seminar on 6 November in London co-organized with the Institution of Mechanical Engineers, the Royal Society of Chemistry, and the UK student chapter of the Society of Tribologists and Lubrication Engineers.

The post The secret world of tribology appeared first on Physics World.

Each year, approximately 5000 tonnes of dyes (about 50 times the weight of a blue whale) are discharged into industrial wastewater. These dyes block light from reaching aquatic plants and animals, cause unpleasant odours and pose risks to human health. Congo red, for instance, is notably persistent in the environment. Another dye, methyl orange, is difficult to remove using standard biological or chemical treatments and has been linked to cancer and DNA damage. Researchers in Egypt and the US are devising a new method to clean up such contamination.

One of the well-established routes for cleaning wastewater from dyes is using nanoparticles (of similar size to a small virus) with high surface area, which gives the dye molecules plenty of places to adsorb onto the nanoparticle surface. It’s especially useful if the nanoparticle has magnetic properties – then it’s possible to remove nanoparticles with adsorbed dyes from water using a magnet. The nanoparticles can then be washed and reused, for up to four cycles, enabling the same material to be used again and again instead of being thrown away.

Ideas for breakfast

Lead researcher Hebatullah Hassan Farghal from The American University in Cairo and her team have synthesized magnetite nanoparticles (particles made from a naturally magnetic form of iron oxide) directly in dye-polluted water. As the particles form, they pull the dye molecules out of the water and onto their own surfaces – meaning that the water is left with less dye in it. The researchers then used those same “dirty” nanoparticles to capture two entirely different dyes afterwards. This route, described in RSC Advances, skips the usual “make-wash-dry-treat” sequence. Instead, it offers a more efficient, simpler and greener way to create a working wastewater adsorbent.

Farghal’s previous research work had been on magnetic adsorbents. “The idea for this paper came exactly one or two days after my PhD defence,” she explains. “While I was having breakfast, I realized adsorbent synthesis requires time and cost…I then went to the lab and started my experiments to find that it was successful.”

Catch and catch again

First, Farghal loaded the nanoparticles with two dyes – congo red (CR) and bromocresol green (BCG) – as they formed in the wastewater. More than 90% of both dyes stuck to the particles and the loaded particles grew slightly larger (about 34 nm, compared with 26 nm for plain magnetite). Later, the same “dirty” particles went on to adsorb almost 80% of methylene blue (MB) from a single-dye system after about 3 h, dropping to just over 50% when a second dye, methyl orange (MO), was mixed in.

To reuse the particles after adsorption of MB, the researchers rinsed them in alcohol, which pulled the trapped blue dye molecules back off. They repeated this four times without any drop in performance, and none of the originally loaded dyes leaking out in the process. They note that MB removal worked best at high pH, where the nanoparticles become negatively charged (while MB molecules are positively charged). This electrostatic attraction gave the main mechanism an extra boost.

Simulations second the results

There are several different mechanisms that can happen when a dye molecule attaches to the surface of a nanoparticle. The two most common types are chemisorption, where the molecule forms new chemical bonds with the surface, and physisorption, a weaker attraction more like static cling – no permanent bond is formed, and the molecule can be pulled off relatively easily.

Several lab measurements, including infrared spectroscopy of the particle surface, already hinted that physisorption is the main mechanism responsible for binding CR, BCG and MB molecules to nanoparticles. This weak binding is also why the ethanol wash could strip the dye back off without damaging the particle.

To confirm this idea, the team also ran a computational method called density functional theory (DFT) on a single dye molecule sitting on a magnetite surface. All dyes bound with similar strength. The simulations also showed electrons flowing in opposite directions depending on the dye’s charge – from the negatively charged CR and BCG toward the surface, and from the surface toward the positively charged MB – the same charge attraction seen in the lab.

The researchers point out that DFT and experimental outcomes cannot be compared quantitatively, only qualitatively, since the first one examines a perfect molecule on an ideal surface and the second one concerns real-world conditions. They note that the DFT analysis was carried out by Ahmed A Abokifa and Mohamed S Mohamed from the University of Illinois Chicago, with Mayyada El-Sayed supervising the wider study.

Outside of the lab

In standard tap water or saline (3% NaCl), the story gets more complicated. The researchers increased the adsorbent dose by roughly 15 times – from 0.67 to 10 g/l – to try to compensate for real-world conditions. This worked in saline, but removal in tap water was only about half of what it was in distilled water, likely because calcium, magnesium and other substances naturally present in tap water compete with the dyes for space on the particle’s surface.

“Though the dose significantly increased in tap water and saline, this dose is still applied in the literature,” Farghal says, adding that her future investigation will try to close that gap and reduce costs.

Still, one thing works in the material’s favour: making the particles is cheap. Producing 1 kg costs around $3730 – roughly eight times cheaper than other nanomaterials sometimes used for the same purpose, such as cobalt ferrite (which costs roughly $30,100 per kilogram).

Farghal says her next research will involve “circular economy approaches that will be outside the box.” Circular economy is an approach in which waste from one process becomes a resource for the next – that waste doesn’t have to be wasted. This study is itself an example of that thinking: dye-polluted water became the raw material for a new, useful adsorbent.

The post Dirty magnetite nanoparticles keep cleaning up dyes appeared first on Physics World.

The performance of optoelectronic materials and devices relies on carrier transport, recombination, ion migration and phase segregation. They unfold on length scales from nanometers to micrometers and timescales from picoseconds to hours. Conventional characterization averages over this heterogeneity and rarely captures these events in operational devices.

Optical microscopy and spectroscopy can recover this hidden picture. They convert local material function directly into optical contrast, and that contrast can be resolved across the length and time scales where the function happens.

In this webinar, Dr Sudipta Seth will talk about advanced optical microscopy and spectroscopy that interrogate halide perovskite materials and corresponding optoelectronic devices under relevant in situ and operando conditions. This approach uncovers the local fields, transport bottlenecks, and defect chemistry that set solar cell performance. He will show how these local optical signatures translate into a mechanistic understanding of device operation, and how that understanding feeds back into the design of better probes, interfaces, defects and devices.

The talk is aimed equally at materials scientists curious about what happens inside their samples and at microscopists and spectroscopists looking for new problems suited to their tools.

Certificate of attendance will be awarded upon completion of the webinar.

Sudipta Seth is a research associate at KU Leuven, Belgium, where he conducts advanced research at the intersection of materials chemistry, optoelectronic devices and spectroscopy through the development of innovative microscopy methodologies. He leads the nanoscale device spectroscopy research line at Hofkens Laboratory. He completed his PhD at the University of Hyderabad and subsequently worked as a postdoctoral fellow at Lund University and as a visiting junior fellow at the Tokyo Institute of Technology. His work integrates single-particle spectroscopy, super-resolution and nanoscale microscopy and ultrafast spectroscopy to investigate fundamental photophysics in semiconductor materials and optoelectronic devices. He has received several academic fellowships, including INSPIRE-SHE (India), Wenner-Gren Postdoctoral Fellowship (Sweden), FWO Research Stay Abroad (Belgium), and Marie Sklodowska-Curie Postdoctoral Fellowship (European Commission).

The post In situ and operando optical microscopy and spectroscopy: investigating perovskite optoelectronic devices at work appeared first on Physics World.

By combining a band-structure engineered multi-quantum-well heterostructure with a nanostructure known as a metasurface, physicists in Austria and the US have created a device that can efficiently transform light into different frequencies – including those at technologically important near-infrared wavelengths. Their technique, which boosts nonlinear frequency conversion, could help in the development of smaller and more efficient components for telecommunications, quantum information transfer and other photonics technologies.

Nonlinear frequency conversion is an optical process in which a material is used to generate light of a different frequency to that incident on the material. It is now routinely employed in a wide range of photonics devices that rely on frequency mixing, ultrafast signal processing, broadband and pulsed light sources, and high-speed light modulation. It is also used to generate entangled photon pairs for quantum communication. One common type of frequency conversion, and the one used in this new study, is second-harmonic generation. Here, two input photons are combined to produce one photon with twice the energy.

Efficient nonlinear devices require light with high electric field strengths and materials that respond to these intense electromagnetic fields by producing a light polarization that is not directly proportional to the applied field. “Only a handful of such nonlinear crystals exist and these have complicated structures with weak nonlinearities, which means they require high optical powers to make photons interact with each other,” says Marcus Ossiander from the Institute of Experimental Physics at TU Graz in Austria, one of the authors of the new study published in Nature Nanotechnology. “While, new such crystals emerge from time to time, their structure is fixed, which dictates which light wavelengths they work at and how efficiently.”

Asymmetrically coupled multi-quantum wells

Recently, a group of researchers at the University of Texas at Austin in the US, led by Seth Bank, also an author of this latest study, succeeded in creating an optical nonlinearity not via a new crystal structure but by growing a semiconductor metamaterial made from nanoscale layers of gallium arsenide and aluminium gallium arsenide. These layers contain multiple quantum wells that are asymmetrically coupled to each other.

The quantum wells confine electrons in one dimension while allowing them to move freely in the other two dimensions, something that has the effect of restricting their energy levels into discrete, quantum states. Since they are asymmetrically coupled, the electrons end up mainly moving in one direction when exposed to light. This so-called “one-way street leads to increased nonlinear electron oscillations, allowing light waves to interact with each other extremely efficiently and exceed naturally occurring nonlinearities.

Ossiander and his colleagues, including Federico Capasso at the Harvard John A. Paulson School of Engineering and Applied Sciences (SEAS), have now added a second, two-dimensional metamaterial atop the first one. This metasurface, which consists of titanium dioxide pillars, each several hundred nanometres in size, precisely creates the particular light polarization required to deflect incoming light so that it scatters along the one-way street. This enhances the interactions between light waves even further and so increases the intensity of light in the structure.

An extra lap

Researchers have known for a while now that metasurfaces are extremely good at resonantly trapping light and increasing the interaction of light with matter. Usually, the process is straightforward, explains first author Pernille Undrum Fathi, who works in Capasso’s group: you implement a resonant metasurface, and it enhances, for example, the nonlinear effects that you are aiming for.

“The new material sent us for an extra lap, however, because, during our experiments, we discovered that the designable second-order nonlinear susceptibility tensor element (the required incident polarization) is different to that of conventional materials,” she says. “Therefore, when we shone light at exactly normal incidence, the metasurface–material combination generated light waves whose polarizations cancelled each other out completely, so annihilating any enhanced optical nonlinearity.”

However, the researchers found that tilting the sample by just 0.3° broke this symmetry and solved this challenge. Indeed, they were able to increase the effective nonlinear conversion of the light to three orders of magnitude higher than that for a non-patterned heterostructure. The effect is also higher than previously reported values for comparable devices at near‑infrared wavelengths.

“Nonlinear optics are ubiquitous in modern science and technology, with examples including the generation of light at new frequencies (where lasers might be unavailable), all-optical signal processing and the generation of entangled photon pairs for quantum communication,” Ossiander tells Physics World. “Enhancing the fundamental processes enabling this technology will allow for much more efficient, compact devices and enable new measurements that would previously be impossible.”

Metasurfaces offer an excellent route to control and enhance the interaction of light with matter, and the team was intrigued to find out what could be made possible when combining these materials with nanostructures, adds Fathi.

“Working with new materials of course comes with additional uncertainty, and we spent a lot of time learning about and understanding the mechanisms of these new structures and how the particular nonlinear tensor elements of this material interact with the resonant modes introduced by the metasurface,” she says.

“The material we studied is very interesting but also complex,” adds Ossiander, noting that the reseachers believe they can learn how to make even better use of the designer nonlinearity in it by further investigating its fundamental properties. “Indeed, there is a new publication in Optica by Bank’s group on how to improve the multi-quantum-well material even more.”

The post Metasurface optical device boosts nonlinear frequency conversion appeared first on Physics World.

For a few years in the early 1990s, a lot of New York streets sparkled. Picture a Manhattan avenue at dusk, wet from a passing shower, the streetlights and headlights catching something in the road surface itself. Not the usual dull black, but a faint, restless glitter, as if the asphalt had been dusted with something. That shimmer was crushed bottles. The city had figured out how to grind its glass waste into the road.

The material had a name that told you exactly what it was: glassphalt. It went from a curiosity nobody trusted, to something people demanded outside their own buildings, and then it quietly disappeared. And it’s a small case study in why good recycling ideas so often don’t stick.

The glittering street, and why the city made it

Asphalt is mostly sand and gravel held together by a black binder. Glassphalt is what you get when crushed glass replaces part of that sand and gravel.

The Federal Highway Administration, in its guidelines on waste glass in pavement, says road-surface mixes with roughly 10 to 15 percent crushed glass perform fine. From 1989, the city’s transportation department started putting the glass content of its mix at about 10 percent.

The FHWA called the New York program the “most aggressive” glass-recycling paving effort in the country. From 1990 through 1995 the city used roughly 225,000 metric tons, about 250,000 tons, of glass in resurfacing. By 1991, crews had already laid glassphalt on nearly 900 lane-miles of Manhattan and Brooklyn streets.

What made the idea clever, as far as we can tell, is the kind of glass it used. Bottle recyclers want clean glass sorted by color. They won’t buy the mixed-color material that piles up at the bottom of a recycling stream. Glassphalt didn’t care about color. It could swallow exactly the low-value waste glass that nobody else wanted and turn it into road. The city reported saving about $500,000 a year by using crushed glass in place of some sand and gravel, and keeping 38,000 tons of glass out of landfills in the process.

From public suspicion to actual demand

People did not warm to it right away. A road that shimmers looks, at first glance, like something is wrong with it. But the turnaround, if the accounts from the time are right, was fairly complete.

Harold Watson, the transportation department’s assistant commissioner for asphalt operations, had become something of an in-house champion for the material. Watson said in 1991: “Now, when we do a road, if we don’t have glass on it, people come in and start complaining.”

That’s a nice story about public mood, not a measured fact, and it comes from a fan of the material, so we’d hold it loosely. Watson was clearly frustrated by a quieter resistance too. In his telling, “There’s a lot of people who can’t find anything wrong with glassphalt but won’t say anything good about it.” Read that as one supporter’s view rather than a neutral account, but it captures the odd spot the material was in: hard to fault, hard to fully endorse.

The Plaza, and a request for more sparkle

The clearest sign that the public had come around involved one very visible stretch of Fifth Avenue. After the city resurfaced the section in front of the Plaza Hotel with glassphalt, the hotel’s owner, Donald Trump, wanted the surrounding streets given the same treatment. A recycled-glass road surface had become something worth lobbying for outside a luxury hotel.

There’s something funny in that. The exact same crushed bottles a bottle plant would reject as worthless were, when spread across Fifth Avenue and lit up after rain, a selling point. The sparkle did real marketing work that the engineering never asked for.

Why the biggest glass-paving program in the country faded

None of the appeal saved it. The program’s central weakness was that its raw material came from curbside recycling collection, and collection is expensive.

During a budget crisis, Mayor David Dinkins floated suspending the recycling operation to save about $65 million a year, which would have cut off the glass supply. Commissioner Lucius Riccio said at the time: “That would be a shame. We’re doing a record amount of paving and we could use all the glass they could give us.” That tension is the whole story in miniature. The paving side wanted all the glass it could get, and the collection side that fed it was the first thing on the chopping block when money got tight.

What we take from a road paved with bottles

New York didn’t invent glassphalt. Baltimore had paved at least 17 streets with it from the mid-1970s through the mid-1980s, chasing the same sparkle.

What New York proved was that the idea could run at real scale, absorb hundreds of thousands of tons of the exact glass nobody else wanted, and win over a skeptical public along the way.

The sparkle was arguably the least interesting thing about it. It got the headlines, it got Trump lobbying, it made a wet avenue look faintly enchanted. But the real achievement was much plainer: a workable use for low-value mixed glass that would otherwise cost money to bury.

The reason it faded had nothing to do with whether the roads glittered, and everything to do with the fragile system behind it, the collection network and the raw cost of glass against dirt-cheap gravel. A recycling idea can be sound as engineering and still lose to logistics. That, more than the shine, is what a road made of bottles has to teach.

The post Beginning in 1990, New York City repaved streets with asphalt containing crushed recycled glass. By 1995, crews had used 250,000 tons of glass in resurfacing applications across the city, including a section of Fifth Avenue in front of the Plaza Hotel. appeared first on Space Daily.

On Tuesday, two survivors of child sex abuse accused the Justice Department of failing to notify dozens of victims found in Jeffrey Epstein’s massive collection of child sex images.

In a proposed class action, survivors explained that Epstein apparently started collecting child sex images in the 1990s, many of which the DOJ recovered after his arrest. In 2025, the FBI started reviewing “tens of thousands of videos” containing illegal child sexual abuse material (CSAM) and issued a memo confirming that “a large volume of images” seized depicted likely minors.

Some of these victims may have had contact with Epstein, as the disgraced financier kept a "modelbook" of nude photos of young girls roped into his ring. However, the FBI also identified hundreds of CSAM images in cache, which include approximately 15–20 images of known CSAM dating back to the 1990s. And so far, the DOJ has largely ignored those victims, who likely never met Epstein and have no way of knowing if he possessed, transported, or traded their images, survivors alleged.

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My dentist, Dr Albora, told me I needed a new tooth. He made me bite down on a U-shaped tray filled with polyether, an elastomeric material that’s been used in dentistry for decades. I tried not to gag while the gooey stuff set. Albora then waggled it off and sent the imprint to a company on Long Island that makes false teeth. But as my tooth’s colouring was unusual, Dr Albora said I had to go there myself.

A week later I drove to Marotta Dental Studio, where Igor Binshteyn sat me in a chair, lifted my lip and inspected a tooth to the side of my upper jaw. He was helping to fabricate its replacement and needed to get the exact colour.

As Binshteyn finished, I remarked teasingly on the company’s car park, which was chock full. Do you need that many people to make false teeth? What could possibly be involved to make things smaller than the nail on my little finger?

Binshteyn laughed. “Follow me”.

He opened a door to a huge undivided warehouse-like space about 1200 square metres in size. Some 50 people were working at lines of tables where the steady hum of conversation was punctuated by the noise of ovens, lathes and grinding machines; imagine the sounds of a metalworking shop in a busy train station.

“Do you want a tour?” Binshteyn said.

Of course I did.

Open wide

My tour guide was Marotta’s vice-president, Steven Pigliacelli, who teaches prosthodontics at New York University. A prosthodontist is a dental specialist who has completed dental school and, in the US, has had at least three additional years of advanced training to focus on restoring and replacing missing or damaged teeth. As I learned, prosthodontists must practice materials science.

The lab has two paths for making teeth, Pigliacelli explained, each with different materials and methods. The first is known as “porcelain-fused-to-metal”, or PFM. It begins with technicians applying gypsum – hydrated calcium sulphate – to create stone replicas of the jaw and teeth from the impressions given to them by dentists such as Albora.

Gypsum has different coefficients of expansion for different dental purposes, and textbook formulas give the amounts of liquid for each kind. But Marotta employees found that tiny amounts of water must be added or subtracted to the gypsum to compensate for things like humidity and temperature before the gypsum is used. “It took us months,” Pigliacelli explained, “to realize that how it’s shipped, how it’s stored, what season it is – all these affect the material.”

I watched as a technician sectioned a stone jaw replica to cut out a tooth, turn it into a master model called a die, and test it in an articulator that mimics jaw movements. I saw another wax that die, use a lost wax technique to create a solid gypsum frame, and cast a silver-palladium alloy. That creates the metal inner core for the tooth, called a coping, which is shaped and finished before porcelain is applied. Porcelain is baked onto the coping in another area of the lab.

“The metal and porcelain need closely matched coefficients of thermal expansion or the porcelain can separate from the metal,” Pagliacelli told me. “Every once in a while a company tells us ‘We’ve got this really cool new alloy!’, but we need to match the coefficients of expansion in the ceramic material. We’re working with sensitive materials for sensitive applications, and we have to experiment with and adapt them. This stuff about materials you don’t learn in school but work out in the lab.”

Smile for the camera

The second path to making a tooth involves scanning the teeth rather than waxing a die. The electronic files are worked on in the computer, printed out, reworked and rescanned, and milled by a CAD machine using materials such as zirconia – nicknamed “ceramic steel” – and EMAX, a lithium disilicate glass-ceramic. Zirconia is extremely hard and used for teeth that endure heavy grinding forces, while EMAX is more aesthetically pleasing and often used for front teeth.

“So we have two parallel paths, PFM and digital scans”, Pigliacelli said. “It’s usually a personal choice of the dentist”. But external pressures are driving a move away from PFM, he said. Five years ago the price of palladium – a key component of the PFM alloy – soared as it was increasingly used in devices to reduce auto and other emissions. “That’s cut down on the PSM market.”

In another corner of the lab I ran into Binshteyn again, who was using different porcelains and ceramic stains to create colours. “Teeth are not a solid colour,” he said, “but vary in shade from reddish near the gum line to lighter colours toward the biting edge. They also vary in translucency.” (Check this out yourself.) Furthermore, the colour of a tooth must match not its neighbours but the corresponding tooth on the other side of the mouth. To make a natural-looking tooth, Igor picks out a base colour and then layers in shades of porcelain.

As my lab tour went on, Pigliacelli showed me different materials for different applications. One challenge is making teeth for a person with bulimia, whose acidic oral environment can corrode dental materials. Other challenges arise with people who have had failed implants, or temporomandibular joint – or TMJ – a disorder involving jaw joints and muscles.

On the way out I met Lenny Marotta, Pigliacelli’s brother-in-law, who had founded Marotta Studio in 1981. Marotta is fascinated by the history of dental materials, which include bone, ivory, wood, gold and silver. He showed me his collection of early prosthodontic instruments, including milling machines, furnaces, hammers and air compressors.

Later, Marotta also pointed out a strange-looking oven. “That’s for processing vulcanite, a hardened rubber material widely used for dentures before modern plastics.” But he’s been unable to find a museum interested in old prosthodontic stuff. “Nobody knows we exist,” he complained.

The critical point

I’d assumed that materials science was required to make prosthetic teeth biocompatible, corrosion resistant, and able to withstand mechanical motions such as crushing, biting and grinding. I also knew that teeth have to be made economically enough to be widely available, aesthetic enough to be desirable, and versatile enough to withstand a variety of oral environments.

But I had no idea how much materials science was required to bring all these properties together.

Back in his office, Dr Albora installed the tooth and handed me a mirror. I had to pull up my lip to see it way on the side of my mouth. “I’d have to smile before somebody notices it,” I complained. “Well,” he said, “that’s for just in case you do.”

The post Get your teeth into the cutting edge of materials science appeared first on Physics World.

A wind turbine blade is basically glass fibre set in hardened resin. The fibres give it strength, the resin holds them in place, and the two are bonded so tightly that a blade can survive wind, rain and stress.

That same toughness is the problem once the blade comes down. Thermoset epoxy does not melt back into a workable liquid, and its stable chemical bonds are difficult to break. So retired blades are typically cut into sections and sent to landfill.

That is the waste a group of researchers decided to work with. In a 2026 study published in ACS Applied Engineering Materials, a team at Xi’an Shiyou University, with collaborators at the Beijing Institute of Technology and Monash University, ground old blade material into powder and turned it into a lightweight, sponge-like insulation.

Here is what came out of the lab, and how it stacks up against the size of the problem.

It squashes to a fifth of its thickness and springs back

The most surprising thing about the material is how far you can crush it without wrecking it. The team reports it took a squeeze of over 80 percent and recovered, meaning you can press it down to roughly a fifth of its height and it bounces back. That matters because conventional silica aerogels are famously fragile. They insulate well but can be brittle. A material that can take a squeeze and spring back is far easier to handle and install.

The trick is in the structure. Instead of a solid block, the composite is a network full of tiny connected pores, with the blade powder stiffening a soft, springy scaffold. 

It combined low density with unusually high compressibility

Weight is where the main result sits. The material reached a density of 0.184 grams per cubic centimetre while sustaining more than 80 percent compressive strain. The authors say the composite showed “a superior combination of low bulk density (0.184 g cm–3) and high compressive strain (>80%), outperforming a wide range of reported silica-based or organic aerogels and composites.”

A caution is warranted: that line is the researchers describing their own work, not an outside verdict. “Outperforming” is their framing, and the comparison is against numbers from other published papers rather than a head-to-head test by a neutral lab. The figures themselves are measurable; whether the material performs as well in practice is the kind of thing other labs and larger-scale testing would need to settle.

It holds heat in about as well as ordinary insulation

Being light and squishy would not count for much if heat poured straight through it. It doesn’t. The composite measured a thermal conductivity of 0.068 watts per metre-kelvin, and lower is better here because it means less heat gets across. For comparison, ordinary glass wool building insulation sits around 0.04. So the blade composite is not a record-setting insulator, but it is in a sensible range for the job while remaining highly compressible.

It self-extinguishes instead of feeding a flame

Insulation lives inside walls and roofs, so how it behaves near fire matters. The team reports enhanced flame self-extinguishing capability, meaning it tended to stop burning once the flame source was removed rather than carrying the fire along. Again, this is one lab result on lab samples, though, and real fire-safety ratings require standardised testing. Read it as promising, not certified.

It turns a landfill problem into the raw material

The reason any of this is interesting is the sheer number of blades headed for the ground. Worldwide, the mass of blades expected to be discarded by 2050 may reach about 43 million tonnes. Right now, around 12,000 blades are retired across Europe and the US each year, and they are typically cut up and sent to landfill. A process that takes that same material and makes something useful flips the equation.

As the authors put it, reusing the blade waste “not only helps to reduce environmental burdens and resource waste but also opens up avenues for generating high-performing, useful materials.”

Where this actually sits

This is one study and one set of lab measurements. The chemistry is clever and the numbers look good, but the gap between a lab composite and a pallet of insulation shipped to a building site is wide. The paper doesn’t answer the questions that fill that gap: cost, batch-to-batch consistency, how the material holds up over years inside a wall, and whether grinding and processing old blades at scale actually makes economic sense.

That last question is the real hinge. Something has to make the recycled route cheaper or required before a lab result becomes a real supply chain.

None of that takes away from what the team built. This is a good answer to a narrow question, which is whether hard-to-recycle blade waste can be turned into a useful, light, tough insulating material at all. The evidence here says yes. The bigger question, whether it can be done by the tonne cheaply enough to matter, is still open.

The post In 2025, researchers ground retired wind turbine blades into powder, stirred it into a gel and set it into an insulation composite. The composite combined low density with much greater compressibility than many of the insulating aerogels and composites it was compared with, squashing to a fifth of its thickness without breaking apart. appeared first on Space Daily.

When evaluating new materials for optoelectronic applications – perhaps promising solar panel materials like halide perovskites or semiconductor compounds for microLED displays – optical characterization is almost always the materials scientists’ first port of call. And up to now steady-state photoluminescence (PL) has been the de facto workhorse for this task.

This non-destructive and highly sensitive technique involves optically exciting a sample and recording the integrated intensity and wavelength of re-emitted photons. Through this, researchers gain a quick understanding into a material’s electronic structure, optical transitions and emission characteristics.

However, these spectra alone can be misleading. Materials with substantially different microscopic properties can generate similar steady-state PL results, masking the fundamental physical dynamics that govern the material’s performance in the real world. To gain deeper understanding of a given material, a more comprehensive and correlated approach is needed.

Blinding average

The core issue lies in the fact that steady-state PL provides a time-integrated view of the emission and depending on the measurement geometry, may also average over spatial variations. Steady-state PL records a static equilibrium in which charge carrier generation balances recombination. This means that, on its own, it does not directly reveal how these excited charge-carriers evolve and ultimately dictate how a device manipulates energy and light.

For example, although two semiconductor thin films may show identical steady-state emission, they can perform very differently in a real device. One film might have long carrier lifetimes consistent with low non-radiative losses – useful in solar cells, for example – while the other could suffer from high defect densities that are masked by strong light absorption or intense excitation light.

Conversely, weak emission does not necessarily mean poor material quality. Again using a layered solar cell as an example, dim luminescence often signals fast, beneficial charge extraction across an interface rather than harmful defect recombination (where structural imperfections convert charge-carrier energy into wasted heat). Because steady-state measurements only show an overall average, they cannot separate these competing mechanisms.

Resolving in time, space and spectrum

Time-resolved PL (TRPL) is a key technique in illuminating these hidden dynamics. Unlike steady-state PL, which continuously bathes a sample with light, TRPL uses a short laser pulse and measures how the photoluminescence intensity evolves afterwards. This can reveal carrier dynamics over timescales ranging from picoseconds to microseconds.

TRPL is particularly important in materials where local variations strongly influence device behaviour. For instance, it can expose the difference between regions that exhibit long-lived emission consistent with efficient radiative recombination, and those that exhibit fast decay caused by, for example, defect recombination.

Of course, steady-state PL averages over time and space, and therefore TRPL only solves part of the problem. Spatially resolved TRPL addresses the missing spatial dimension. Combining a high-precision, motorized XY stage with TRPL’s precise timing, spatially resolved TRPL forms a 2D map that directly correlates localized structural features – such as grain boundaries and defects – with variations in carrier kinetics across the surface.

Complementary to these techniques is time-resolved emission spectroscopy (TRES), which combines spectral selection with time-resolved detection to measure how emission dynamics vary across the spectrum. By recording wavelength-dependent decay behaviour, TRES reveals how different spectral contributions evolve following excitation.

In short, where TRPL reveals kinetics over time and spatially resolved TRPL locates variations in space, TRES adds a spectral dimension, showing how the emission spectrum evolves after excitation. This allows researchers to track changes in the distribution of photon energies over time to understand carrier evolution and gain insight into the mechanisms underlying material behaviour.

A correlative approach

Though powerful in isolation, reconciling insights across these different instruments is slow and prone to errors. There can be microscopic differences between samples or even within positions in a single sample that dramatically alter emission spectra. Moreover, moving a sample between separate instruments is fraught with difficulty, potentially damaging the sample or causing delays that lead to sample degradation.

More comprehensive and reliable physical insight comes when temporal, spatial and spectral factors are recorded correlatively on the exact same sample region. This need for correlation is the motivation behind PicoQuant’s Solira, an integrated workflow platform for steady-state PL, TRPL, spatially resolved TRPL and TRES (the latter when combined with the complementary FlexLambda Kit), as well as additional imaging techniques, such as hyperspectral imaging, required for different scientific questions.

Bringing these techniques together within one configurable microscope system means a materials scientist can gain a more informed interpretation of material behaviour. For instance, they can identify the relevant emission bands at selected points of interest with steady-state PL. They can then wield TRPL to measure the associated decay kinetics, before perhaps applying TRES to resolve how those kinetics vary across the emission spectrum.

Bright demonstration

The power of this correlated approach was demonstrated recently by Professor Eva Unger’s group at Helmholtz-Zentrum Berlin, Germany, with measurements carried out by Maxim Simmonds. Investigating perovskite solar mini-modules, the team worked with PicoQuant and used Solira to locate precise laser-patterned lines – microscopic scribes used to interconnect individual cells in a solar module – before verifying emission from the active layer. Localized TRPL measurements then revealed significantly faster decay dynamics next to these laser cuts compared to the pristine bulk material, indicating altered carrier recombination or diffusion near structured features.

However, point measurements alone were not enough to discern whether the laser had fully removed the perovskite or merely modified it. Switching to spatially resolved TRPL imaging on Solira revealed that measurable photoluminescence persisted along the laser-patterned lines. This showed that laser structuring had altered local photophysical properties rather than eliminating the active layer – a conclusion only made possible by consistently mapping charge-carrier dynamics across temporal, spatial and spectral dimensions together on one setup.

As semiconductor materials and optoelectronic devices become more complex, optical characterization tools must keep pace. By unifying these tools within an integrated workflow platform such as Solira, materials scientists now have the means to paint a more complete picture of material characteristics and thereby unlock the next generation of innovative functional materials.

 

The post Above-average correlative materials characterization appeared first on Physics World.

Researchers used a specially designed cavity to strengthen quantum vacuum fluctuations and enhance superconductivity in a thin material. Empty space is not truly empty. Even a vacuum contains restless quantum fluctuations, and researchers have now shown for the first time that these normally subtle effects can be engineered to strengthen superconductivity. The work, led by [...]

A material once thought to be nonmagnetic may reveal a hidden magnetic side when made just a few atomic layers thick. A newly proposed class of magnetism known as altermagnetism could open new possibilities for making computer memory smaller and more efficient. Now, researchers have found evidence that ruthenium dioxide, a quantum material long debated [...]

Billions of people still suffer from hunger and food insecurity worldwide. Meanwhile, microbial contamination causes a third of global food waste annually, resulting in major economic losses and illnesses. Although antibiotics and pesticides help control contamination, their excessive use can promote bacterial resistance or leave toxic residues. 

One alternative uses materials that generate highly reactive forms of oxygen when exposed to light, called photocatalysts, to prolong food freshness. These molecules kill bacteria by damaging their cell components in a process called photodynamic inactivation or PDI. However, current PDI systems rely on energy-intensive lasers and long exposure times because the bacteria’s protective cell membranes block reactive oxygen molecules. As a result, the systems don’t kill bacteria effectively and risk overheating food, affecting its freshness and nutritional value.

Scientists at Zhejiang University in China thought that it would be possible to achieve a PDI system using accessible, free sunlight with the right photocatalyst. Moreover, they also wanted to integrate this photocatalyst into food packaging to combat microbes during storage. 

To make the photocatalyst, the researchers mixed water with a glue-like plant fiber that provides structural support, called pectin, and a chemical from plant seeds that supplies phosphorus, called phytic acid. Then they heated the mixture in a sealed reactor at 220ºC (428ºF) for 5 hours to form tiny structures composed of a carbon core surrounded by a phosphorus-rich shell called phosphorus-modified carbonized polymer dots or PCDs.

To incorporate the PCDs into film packaging, the researchers dissolved equal amounts of a plant fiber from konjac, called glucomannan, and another plant-derived molecule, called carboxymethylcellulose, in warm water to form a network of entangled molecular chains. Then, they added 1.5 milligrams of PCD per milliliter to this mixture, which linked the chains together like molecular fasteners. Finally, they added a moisture-binding chemical called glycerin to prevent brittleness. The researchers cast this mixture onto separate Petri dishes and dried them, forming thin, plastic-like PCD films.

To test the films, the researchers placed Escherichia coli bacteria between 2 sterilized film sheets and exposed the samples to either darkness or simulated sunlight for 20 minutes. They then transferred the microbes onto agar plates and incubated them for 15 hours, allowing surviving bacteria to form visible colonies. They compared the number of bacterial colonies with those of untreated samples to calculate the percentage of bacteria the films eliminated in each environment. 

Tests under darkness showed that the films eliminated about 60% of the bacteria. The researchers attributed this result to the positive electrical charge of PCDs, which attracts the bacteria’s negatively charged cell surfaces. The electrical attraction stresses their cell membranes, interfering with essential life processes. This result suggested that the films use a separate charge-based antibacterial mechanism apart from PDI, which requires light to work.

Under simulated sunlight, the films eliminated nearly 100% of the bacteria. The researchers identified 2 principal mechanisms causing this. First, the PCDs acted as tiny heaters that generated localized heat, which stretched holes in the bacterial membranes, allowing contents to leak out of their cells through a process called photoporation. Second, the PCDs generated reactive oxygen molecules that could then penetrate the bacteria. Once inside the cells, these molecules irreversibly damage the bacteria’s internal components and genetic material through PDI. 

The researchers also investigated whether PCD films could serve as food packaging by using them to wrap fresh strawberries. Compared with conventional nonbiodegradable polyethylene packaging where visible rotting occurred, the PCD films kept the strawberries fresh for more than 4 days by suppressing bacterial growth and regulating moisture levels. When the team tested whether the films were toxic, they found that the films are safe for humans and compatible for food applications. They also buried the films in soil for 24 days and found that they degraded by 78%, demonstrating biodegradability suitable for packaging fresh foods.

The team concluded that PCD films could be a biodegradable food packaging that combines plant-based materials with multiple antibacterial strategies. The films retained antibacterial activity in darkness and became more effective under sunlight through the combined effects of photoporation and PDI. These findings demonstrated that by combining multiple mechanisms into a single material, researchers can create multifunctional food packaging that remains effective across different storage conditions.

The post Harnessing sunlight to fight bacteria appeared first on Sciworthy.

Scientists have unveiled a computational design for a terahertz metasurface biosensor that combines five distinct materials—graphene, MXene, tungsten disulfide, gold, and copper—into a single multilayer architecture capable of detecting refractive-index changes associated with chikungunya virus infection. The study, published in Results in Optics by G. Arunachalam, A.R. Kalaiarasi, Giri.G. Hallur, and V. Parthasarathy, reports a numerically predicted sensitivity of 907 GHz per refractive-index unit, among the highest values reported for hybrid-material terahertz biosensors, and couples the electromagnetic design to an XGBoost machine-learning surrogate model that predicts sensor behavior with accuracies exceeding 99.8 percent.

Chikungunya virus is an enveloped, positive-sense single-stranded RNA alphavirus transmitted primarily by Aedes aegypti and Aedes albopictus mosquitoes. While mortality remains low, generally below 0.1 percent, the broader public health burden arises from severe polyarthralgia that can persist for months or even years in a substantial fraction of patients across tropical and subtropical regions. With no approved antiviral therapy or licensed vaccine currently available, diagnostic accuracy sits at the center of clinical management and transmission control. Yet existing diagnostic tools face significant practical constraints, particularly in point-of-care and field settings.

Serological methods such as enzyme-linked immunosorbent assay suffer from cross-reactivity with related alphaviruses, including Ross River and O’nyong-nyong viruses, reducing diagnostic specificity. Real-time reverse transcription polymerase chain reaction offers high sensitivity during the acute phase but depends on laboratory infrastructure, trained personnel, and controlled sample handling. Virus isolation in cell culture provides confirmatory results but requires biosafety level-3 facilities and extended processing time. These limitations have motivated the search for rapid, label-free sensing approaches capable of operating at clinically relevant concentrations in decentralized environments.

The new work turns to the terahertz band, spanning roughly 0.1 to 10 THz, which lies between microwave and infrared regions of the electromagnetic spectrum. Terahertz radiation is non-ionising, with photon energies in the millielectronvolt range, allowing interaction with biological samples without causing ionising damage. Crucially, terahertz waves couple to low-frequency vibrational and rotational modes of biomolecules such as proteins, nucleic acids, and polysaccharides, producing measurable spectral features that support label-free detection. Because biological media including blood plasma and viral suspensions exhibit refractive-index variations in this domain, differences on the order of 0.01 to 0.02 refractive-index units can shift resonance frequency and field distribution when coupled to resonant sensing structures.

The proposed sensor is built around a periodically repeated square unit cell containing two identical square resonators, 2000 nanometers on a side, coated with tungsten disulfide—a two-dimensional transition metal dichalcogenide with strong light–matter interaction, high carrier mobility, and excellent dielectric confinement. This layer localizes the electric field in the sensing region and increases the interaction volume between the resonant field and the surrounding analyte. A pair of concentric circular rings, 3200 and 3800 nanometers in diameter and functionalized with MXene, surrounds the resonators, enhancing electromagnetic coupling, promoting efficient charge transport, and strengthening plasmonic interactions between resonator elements. An outer gold ring, 6000 nanometers in diameter, serves as the main plasmonic resonator supporting strong localized surface plasmon resonances with low optical loss. The entire multi-resonant assembly is embedded within a monolayer graphene sheet measuring 14,000 by 14,000 nanometers, which acts as a broadband absorber and a high-mobility charge transport medium whose electrically tunable chemical potential allows dynamic, active control of the resonance characteristics. Copper elements woven into the architecture provide supplementary conductive pathways that reinforce current distribution and coupling among the hybrid resonators. The structure rests on a silicon dioxide substrate, chosen for its low dielectric loss and mechanical robustness, which preserves the resonance quality factor.

The authors stress that the multilayer design is compatible with established microfabrication techniques. Fabrication would begin with a cleaned silicon dioxide substrate, followed by polymer-assisted transfer of monolayer graphene and thermal annealing. Gold and copper resonators can be deposited through electron-beam evaporation or magnetron sputtering with lift-off patterning, MXene rings through solution-based deposition, and the tungsten disulfide layer through chemical vapor deposition or thin-film transfer. With a unit-cell dimension of approximately 14 micrometers, the required feature sizes fall comfortably within conventional photolithography capabilities, and because fabrication imperfections remain far smaller than the operating terahertz wavelength, moderate tolerances are expected to have only limited influence on the electromagnetic response. For biosensing, the graphene surface could subsequently be functionalized with chikungunya-specific antibodies or aptamers using EDC/NHS or pyrene-based linker chemistries.

The electromagnetic modeling, performed in COMSOL Multiphysics, reveals a pronounced resonance at 0.355 THz, where electric-field simulations show the strongest and most spatially extensive enhancement. Varying the graphene chemical potential from 0.1 to 0.9 electronvolts produced dramatic modulation of the transmission contrast, which increased roughly 36-fold at the highest bias, from less than one percentage point to more than 27 percentage points, while peak transmission remained essentially unchanged above 98.6 percent. This asymmetric response—stable maxima paired with strongly modulated minima—arises because increasing chemical potential enhances graphene’s intraband conductivity, deepening resonant absorption through stronger light–matter interaction. The sensor also demonstrated remarkable angular robustness, maintaining peak transmittance above 97.8 percent across incident angles from 0 to 80 degrees, an important tolerance for realistic deployment where normal incidence cannot always be guaranteed.

Geometric optimization identified an outer circular resonator radius of 2500 nanometers and a square resonator side length of 2500 nanometers as the dimensions that maximize resonance strength, driving minimum transmittance down to approximately 65 to 67 percent and signifying optimal electromagnetic confinement within the active sensing region. When evaluated across refractive indices from 1.33 to 1.39, a range encompassing reported values for healthy plasma (approximately 1.35 RIU), healthy platelets (1.39 RIU), chikungunya-infected plasma (1.33 RIU), and infected platelets (1.38 RIU), the optimized configuration achieved a maximum sensitivity of 907 GHz/RIU, a figure of merit of 18.519 RIU⁻¹, a minimum detection limit of 0.061 RIU, a sensor resolution of 55.178, and a refractive-index resolution of 0.001 RIU. In comparative benchmarks against recently reported graphene- and hybrid-material-based terahertz biosensors—including graphene/copper/aluminum, graphene/silicon dioxide, MXene–graphene–black phosphorus, and graphene-integrated copper–silver designs—the proposed architecture’s sensitivity exceeded most published values, reflecting the synergistic field confinement produced by the five-material stack.

The machine-learning component addresses one of the central bottlenecks in metasurface development: the computational cost of repeated full-wave finite-element simulations during structural optimization. The team trained an XGBoost regressor, an ensemble method based on gradient-boosted decision trees, on simulation data covering incidence-angle variation and circular-ring dimension variation, using stratified sampling with 80 percent of data for training and 20 percent held out for independent testing, alongside five-fold cross-validation and grid-search hyperparameter optimization. The model captured more than 99.7 percent of response variance on unseen data, with mean absolute percentage errors below 0.162 percent and prediction accuracies from 99.838 to 99.959 percent. Acting as a computational surrogate, the trained model enables rapid interpolation across the design space without sacrificing the fidelity of the underlying electromagnetic model.

The authors are careful to frame the work as a computational proof-of-concept rather than an experimentally validated diagnostic. The sensor detects changes in the local dielectric environment surrounding the resonators, not viral particles or nucleic acids directly, and refractive-index sensing alone cannot intrinsically distinguish chikungunya from other viruses with similar dielectric properties. Analytical specificity in practice will depend on surface biofunctionalization with chikungunya-specific recognition molecules immobilized on the graphene or gold sensing surface. Future work will focus on device fabrication, biofunctionalization, calibration with reference refractive-index standards, experimental validation with clinically relevant plasma and platelet samples, and systematic evaluation of selectivity against related arboviruses—steps that would transform this numerically validated platform into a practical tool for rapid, label-free infectious disease diagnostics in the field.

A single gram of crushed oyster shell pulled in up to around 1.5 grams of rare earth metal, more than the shell’s own weight, out of water spiked with the kind of contamination you would expect from severe industrial pollution. A throwaway material, the sort of thing you might crunch underfoot on a beach, holding more than its mass in metals that the electronics and clean-energy industries fight over.

That’s the finding a Trinity College Dublin team reported in early 2026. Below, we walk through what they actually did, why oysters won and mussels and cockles fell short, and how much of this holds up once you leave the lab bench.

What the researchers actually did

The setup was low-tech at the front end. As reported in The University Times, the team collected oyster, mussel and cockle shells from beaches around Dublin, cleaned them, dried them, and crushed them into small grains. Then they dropped those grains into solutions carrying three rare earth elements and watched what happened over time. The three metals were lanthanum, neodymium and dysprosium, at concentrations chosen to mimic badly polluted water.

The chemistry underneath is where it gets interesting. Shells are mostly calcium carbonate, and in the rare-earth-rich water that calcium carbonate dissolves and is replaced, more or less on the spot, by new solid minerals built around the rare earth metals. In the peer-reviewed paper, published in Science of the Total Environment, the crushed shells were reacted with the metal-rich solutions across a wide range of temperatures, 25 to 205 degrees Celsius for up to three months. What you end up with is not the original shell soaking up metal like a sponge, but the shell being rebuilt, mineral by mineral, into something new.

As principal investigator Juan Diego Rodriguez-Blanco put it, “the process is entirely mineral-driven – the shells naturally transform dissolved rare earth elements into new solid minerals, so this isn’t a process that is difficult to drive, or one that requires much financial outlay or technical equipment.” That last part is a lab-based expectation rather than a proven cost sheet, but the appeal is easy to see: no exotic reagents, no elaborate rig, just waste shell and time.

Why oysters won and the others didn’t

All three shells are made of the same basic stuff, so why did oysters run away with it? The answer is structure. Oyster shell has a porous, layered microstructure, and that lets the dissolve-and-replace reaction work its way right through the grain rather than stalling at the surface. That’s how oyster grains reached uptake of up to roughly 1.5 grams per gram.

Mussels and cockles behaved differently, and the reason is more physical than chemical. A crust of new mineral formed quickly on the outside and then sealed the grain off, so the reaction couldn’t reach the inside. In those shells, the study reports that more than half of the original shell was left unchanged once that crust became impermeable. Same starting material, very different outcome, decided by how the shell is put together.

Why pull rare earths out of water at all

Rare earth elements are the unglamorous ingredients in a lot of modern hardware, from the magnets in wind turbines and electric motors to phone components. Mining them is expensive and messy, and industrial processing can leave behind runoff carrying dissolved metals. Two problems are tangled together here: recovering a valuable resource, and cleaning up water that carries it.

The shell angle is attractive partly because the raw material is a nuisance to begin with. As first author Rémi Rateau described it, “every year, the global aquaculture industry generates millions of tonnes of shell waste, much of which is discarded or sent to landfill.”  Rateau also noted that “relatively small amounts of shell waste could remove substantial quantities of rare earth metals from contaminated water.” 

What this is, and what it isn’t

This is one study, and it is a lab result. The concentrations were high by design, the conditions were controlled, and real industrial wastewater is a far messier soup of competing ions, organics and pH swings than a prepared solution in a flask. The team is upfront that the work still needs pilot-scale testing under genuine conditions before anyone talks about a deployable cleanup system. A promising lead is not a finished product, and this sits firmly in the former category.

Our read lands roughly where the team’s does. The measured uptake is striking, the input material is cheap and otherwise wasted, and the driving chemistry looks simple. Rodriguez-Blanco frames the ambition plainly: “we can start designing” low-cost strategies to remove critical metals from contaminated waters while giving new value to a major waste product. Start designing is the honest verb. On the strength of these numbers, it’s a lead worth taking out of the beaker and testing against the real, dirty water it was built to handle.

The post Researchers picked oyster, mussel and cockle shells off Irish beaches, crushed the 3 kinds of shell into grains, and dropped them into water carrying rare earth metals at concentrations similar to badly polluted industrial runoff. The oyster grains took up as much as roughly 1.5 grams of metal for every gram of shell. appeared first on Space Daily.

Attractive interactions between particles do not necessarily lead to these particles aggregating. This is the new finding from researchers at the Tokyo University of Science in Japan who say this behaviour comes from non-reciprocal interactions amongst particles of different sizes that exert unequal forces on each other. These interactions could serve as a general design principle for creating active matter with a structure that continuously reorganizes rather than simply relaxing towards a static state.

Nature abounds with examples of active matter, with some well-known examples being flocks of birds, fish and insects, sheets of biological cells and swarms of bacteria. Researchers have been trying to copy this collective behaviour and make synthetic active materials – such as self-propelled colloids and dense phases of mechanically driven biopolymers – in the laboratory. Before such applications see the light of day, however, they need to first understand the fundamental physics of these systems.

In their new study, a team led by Yutaka Sumino and Kiwamu Yoshii of Tokyo University of Science’s department of applied physics, came across a system in which colloidal particles interact through electrohydrodynamic flow. “We found that mixing particles of two different sizes in such a system completely changed the collective behaviour of these particles,” explains Sumino. “Instead of forming increasingly large crystal-like aggregates, as is the case for particles with the same size, the system remained highly dynamic.”

The physicists’ experiment involved suspending polystyrene colloidal particles with radii of 1 and 1.5 µm in water and confining them between transparent indium tin oxide-coated electrodes. This set up allowed them track more than 10,000 particles and quantitatively analyse their dynamics for more than an hour, as opposed to just a few minutes in previous such studies.

Newton’s third law holds

When the researchers applied an alternating electric field to the system, they observed electrohydrodynamic flows around the particles, the strength of which increased strongly as the size of the particles became bigger. The electrohydrodynamic-mediated attractive interactions therefore became asymmetric, they explain, something that causes larger particles to attract smaller ones more strongly. This imbalance leads to non-reciprocal interactions, meaning that a larger particle pushes a smaller one, but a smaller one doesn’t push back.

While the effective interaction between the particles appears to break Newton’s third law, it doesn’t because there is no violation of momentum conservation, explains Sumino: momentum is transferred to the surrounding fluid through the induced flows and is ultimately dissipated through friction with the substrate.

The researchers also observed that particles of different sizes spontaneously pair together to form asymmetric structures with a distinct front and tail. These pairs behave as self-propelled units and move through the suspension – even though individual particles cannot propel themselves. As more self-propelled pairs form, they assemble into larger clusters, but these clusters do not continue growing into large aggregates and instead repeatedly fragment, rearrange themselves and reform. Importantly, they note: “the larger particle tends to be at the front of these moving pairs. This head-heavy size asymmetry, together with excluded-volume interactions, promotes the fragmentation of larger clusters and thereby prevents continuous coarsening”.

Sumino and Yoshii combined their experiments with numerical simulations, thereby identifying non-reciprocal pair motion as the microscopic origin of this behaviour.

The results, they say, suggest that non-reciprocal interactions can serve as a general design principle for creating active materials with structures that continuously reorganize rather than simply relaxing toward a static state. “An interesting aspect,” explains Sumino, “is that self-propulsion does not need to be built into each individual particle: it can emerge collectively from non-reciprocal interactions between particles that do not self-propel on their own.”

If such interactions can be controlled externally, they could provide a way to design microscopic systems that collectively gather, transport, fragment or mix materials, he tells Physics World. “Possible directions include programmable active materials and microrobotic systems, although these applications are still some way off.”

Reporting their findings in Physical Review Letters, the researchers say they would now like to understand how general this non-reciprocal mechanism is and whether the same principle – collective activity emerging from non-reciprocal interactions – can be transferred to other experimental systems. In the system studied in this work, the strength of the non-reciprocity depends on parameters such as particle size, composition and the applied electric field. By systematically tuning these parameters, they aim to explore what other types of collective states can be generated and whether transitions between them can be controlled.

“A more detailed hydrodynamic analysis of the system is also needed to develop a quantitative understanding of the interactions and ultimately predict the collective motion of the colloids,” says Sumino.

The post Non-reciprocal interactions keep particles in collective motion appeared first on Physics World.

Concrete is the second most-used substance on Earth after water, and the cement that holds it together is one of the biggest headaches in climate policy.

Making cement means heating limestone until it breaks down, a process that accounts for around 8 percent of global CO2 emissions. And we are not slowing down. Concrete production is projected to climb from roughly 14 billion cubic metres a year toward 20 billion by mid-century. So anything that lets you use less cement per wall, without the wall getting weaker, is worth a close look.

That is the claim in a new paper out of India, and it comes with an unusual ingredient: human waste. A team turned treated sewage sludge into a fine black powder, swapped it in for a tenth of the cement, and got concrete that ended up harder to crush, not softer.

It’s one study, and an early-access version still subject to edits, so treat what follows as a promising result, not a settled fact.

Why cement is the part worth fixing

The problem with concrete is not the gravel or the sand or the water. It is the cement paste that binds them together. Estimates of cement’s climate footprint vary a bit depending on how you count, landing somewhere between 5 and 8 percent of global human-caused CO2 emissions each year. Most of that comes from the chemistry of making cement, not the fuel in the furnace. That is why switching to cleaner energy alone will not fix it.

One line of research has spent years asking whether you can replace some of that cement with biochar. Biochar is a carbon-rich char made by heating organic matter with very little oxygen. The appeal is twofold: you use less cement, and the carbon in the char, which the original plant or waste pulled out of the air, gets locked inside the building instead of released. The open question has always been whether the concrete survives the swap.

What the Warangal team actually did

The material here started at a sewage-sludge treatment plant in Warangal, in the Indian state of Telangana, a facility set up as a public-private partnership to tackle the city’s sewage problem. Human solid waste that would otherwise be dumped or burned gets processed there.

V Srinivas Chary, whose institution is a partner on the project, praised the operation, saying that “From the toilet to the final conversion of the biochar, the process is scientific and comprehensive.” 

The research team, led by civil engineer Raghuvesh Tiwari of Manipal University Jaipur with colleagues at Louisiana Tech University, took that sludge, dried it, and heated it to between 350 and 450 degrees Celsius with very little oxygen. That heating step drives off gases and leaves char behind. They ground the char into a powder, then replaced 5, 10, and 15 percent of the cement in test concrete with it and ran the usual checks: how well it resisted crushing and bending, how much it shrank, how much water it soaked up, how many gaps it had inside.

Dumped waste versus a carbon sink in the wall

The study sets up a pointed contrast. Normally a city’s sewage sludge is a liability to be disposed of, and a builder’s cement is a material whose production loads the atmosphere. Both are problems flowing toward waste and emissions. The first is bigger than you might think: a single person produces up to around 400 grams of faeces a day, which across a city becomes a constant stream that has to go somewhere.

The idea here is to route that stream into the wall. The waste replaces some of the cement, and the carbon in the char stays put instead of being burned off. It is a tidy story on paper: two problems that might cancel out a slice of each other. The caveat is that this study did not actually measure the carbon side of that ledger, so the climate benefit is still an argument rather than a number the paper delivered.

Why it got stronger, not weaker

The surprise is that adding a char to concrete made it tougher. The study reports this clearly for the middle dose. As the authors put it, “After a 91-day curing period, concrete with a 10% biochar substitution demonstrated a 21% increase in compressive strength and a 42% increase in flexural strength.” The 5 percent mix was close behind, gaining about 20 percent in crushing strength and 36 percent in bending strength over the same period. Those gains are measured against this study’s own plain concrete, not a universal benchmark.

There is a limit, though, and the study found it. The 15 percent mix did worse. Past a certain point, the char stops helping and simply dilutes the cement, a useful reminder that the good result here depends on getting the dose right. The authors’ own summary is careful: the results indicate that biochar at the 5 and 10 percent levels “yields significant improvements in concrete properties.”

The catch, and what still has to be proven

A strong lab result is not a paving slab. Several things stand between this and a real building site, and the paper is upfront about the biggest one. Sewage sludge can carry heavy metals, and whether those slowly leak out of the finished concrete over time is an open question. That is not something you can wave away when the material might end up in a school foundation or a water channel.

How long it lasts is the other unknown. The tests ran to 91 days in controlled conditions. Real structures face decades of freezing and thawing, wetting and drying, weight and vibration, and nobody has shown yet how this concrete holds up over that span. The researchers say themselves that more work is needed to assess how it performs under real-world conditions such as freeze-thaw cycles and extreme temperatures. 

What the study earns, we think, is attention rather than adoption. The explanation is plausible, the numbers are real for the mix that was tested, and the idea that a waste stream and a carbon-heavy material might each solve part of the other’s problem is worth chasing. 

The post Researchers took biochar made from human waste at a treatment plant in Warangal, India, ground it into a fine black powder and mixed it into concrete in place of a tenth of the cement. After 91 days the concrete was 21 percent harder to crush. appeared first on Space Daily.

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