For centuries, civilizations have harnessed energy from water. However, hydropower often requires large bodies of water to move heavy machinery, confining its use to rivers. But what if the electricity needed to light up your house could be generated from raindrops hitting its roof? 

To achieve this, scientists rely on electrical charges created when materials come into contact and then separate, a phenomenon called the triboelectric effect. As an example, rubbing a balloon against your hair gives them opposite charges, causing your hair to stand up and stick to the balloon. Scientists apply the same principle to make droplet-based triboelectric nanogenerators, or D-TENGS, where raindrops slide across negatively charged surfaces. As the droplets move, their positive charges gather near the surface, freeing up their negative charges. When the droplets reach a metal strip called an electrode, these negative charges flow into a circuit, generating electricity. However, water often remains on D-TENG electrode surfaces, blocking subsequent droplets and corroding the device.

Researchers at the China Three Gorges University and the Chinese Academy of Sciences approached this problem by modifying the shape of the electrodes used in D-TENGs. They proposed that a needle rather than a strip would help droplets detach quickly, allowing charge to flow into a device that uses inexpensive components. They called this design a needle electrode droplet-based triboelectric nanogenerator, or NED-TENG.

To build the NED-TENG, the researchers prepared a plastic film using a water-repellent polymer called polytetrafluoroethylene as the negatively charged surface. They inserted a copper wire through the center of the plastic film, protruding 3 millimeters (0.1 inches) from the front side to form the needle-shaped electrode exposed to raindrops. Meanwhile, they attached copper foil to the plastic film’s backside as a second electrode, completing the circuit. The team connected both electrodes to an instrument that measures electrical performance and mounted the components on an acrylic sheet, sealing it with waterproof tape.

To simulate raindrops, the team inclined the NED-TENG at 50° from a table and dispensed tap water drop by drop from 30 centimeters (12 inches) above its plastic film. Like conventional D-TENGs, the device generated electricity as droplets slid across the film and contacted the needle electrode. However, because the water touched only a small area of the needle, it easily slid off the NED-TENG, preventing the water from building up like in D-TENGs.

The researchers then evaluated and optimized the device using 2 metrics: the force driving charges through its circuit, or voltage, and how fast its charges transfer, or current. First, they compared the NED-TENG with a conventional D-TENG. The NED-TENG generated about 564 Volts (V) and 5 milliamperes (mA) of current, nearly twice the voltage and 3 times the current of the D-TENG, and enough to power small electronics like indicator lights.

Next, they varied the droplets’ release height to maximize electricity production. They found that increasing the release height from 10 to 30 centimeters (4 to 12 inches) increased both voltage and current, peaking at about 543 V and 4 mA. At greater heights, droplets splashed hard on impact, scattering the water and disrupting the charging process they observed in sliding droplets. 

Similarly, the researchers tested different device inclination angles, ranging from 10° to 70°. Their tests revealed that the device’s electrical performance increased at steeper angles and peaked at 50°, reaching 521 V and 3 mA. At steeper angles, droplets spent less time in contact with the surface, reducing electrical output. They explained that because triboelectric materials are highly sensitive, results can vary slightly between experiments, leading to individual peak values that are lower than the highest overall outputs. 

The researchers then explored how the technology might perform in a simulated rooftop installation. To reduce power fluctuations during real-world applications, they connected multiple NED-TENGs. They observed that 10 connected devices could fill a small energy-storage component within 2 minutes and power 200 LED lights.

Overall, the NED-TENGs shed water efficiently and generated more electricity than D-TENGs, while remaining simple to build. The team noted that future upscaled studies should examine how rooftop systems can direct rainwater onto the devices at optimal heights, and how droplets interact with their surfaces to improve long-term performance. With further development, these low-cost systems could turn rooftops into practical generators powered by everyday rainfall. 

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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.

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What if your daily coffee routine could help power the world around you? 

Scientists are exploring ways to transform everyday waste, like spent coffee grounds, into materials for greener energy production. One promising method, called triboelectrification, uses electricity generated from motion. With this approach, materials that gain positive and negative charges are rubbed together to generate an electrical charge that can be harnessed by devices called triboelectric nanogenerators, or TENGs. TENGs are a greener alternative to fossil fuels because they generate electricity from everyday movement, such as pedestrian or vehicle motion. 

However, many negatively charged materials used in these devices are made from nonbiodegradable plastics, like PTFE, that persist as long-term waste in the environment. Over time, TENGs are also easily damaged by environmental conditions outside the laboratory. To create sustainable TENGs for real-world applications, scientists need to develop biodegradable and durable designs. 

To address this problem, researchers from Guangxi University in China developed a TENG that uses coffee grounds as its negatively charged material. Their design repurposes coffee waste to create a robust, low-cost device that can harvest energy.

To create the coffee-based material, the researchers mixed coffee grounds with a biodegradable glue-like plastic called polycaprolactone (PCL). They heated this mixture to 80°C (176°F) and molded it into cylindrical pellets. Then, they used a biodegradable plastic called polylactic acid (PLA) to 3D-print a fully enclosed box-like TENG containing vertical channels arranged like the parallel slots of a file organizer to house the pellets. 

Their TENG worked by shaking the coffee ground pellets within the channels, causing them to repeatedly rub against the PLA surfaces. Because coffee grounds strongly attract electrons, the pellets become negatively charged while the PLA surfaces become positively charged. This repeated pellet movement drove the electrons back and forth, generating electricity that was harvested through the TENG’s external circuit. 

To evaluate their TENG’s electrical performance, the researchers used an instrument that measures small amounts of electricity, called an electrometer. The electrometer measures electrical output based on how strongly the device pushes electrons through a circuit, called its voltage, how quickly electrons flow through it, called its current, and how many electrons flow through it, called its transferred charge.

The researchers verified that coffee ground pellets could serve as a viable TENG material by comparing their performance with commercial plastic pellets. The coffee ground pellet system produced a voltage of 0.6 Volts (V), a current of 18 nanoamperes (nA), and a charge transfer of 0.25 nanocoulombs (nC). This output was more than twice that of pure PCL pellets and over half that of nonbiodegradable PTFE. The researchers suggested that the negatively charged components of the coffee grounds altered the surface of the PCL to increase its charge generation and transfer. 

To optimize the TENG, the researchers experimented with different coffee grounds to PCL mass ratios, pellet lengths, and device vibrational frequencies. They found that their device achieved the best electrical performance at a 3:1 ratio of coffee grounds to PCL, with 8 millimeter long pellets, at a vibrational frequency of 2.6 Hertz. These conditions boosted the device’s electrical output to 4.7 V, 75 nA, and 1.3 nC, high enough to power tiny environmental sensors. 

The team also tested their device’s long-term durability by comparing its electrical performance before and after 6 months of storage. They observed only a 6% drop in voltage after storage, demonstrating that it could maintain stable long-term electrical performance for at least 6 months. 

Finally, to explore real-world applications, the researchers integrated 4 TENGs into a wind-energy harvesting system designed for remote island settings. The system used a wheel of rotating cups to capture wind energy and a sliding mechanism to convert it into repeated shaking of the TENGs. As the TENGs shook, the moving pellets inside generated enough electricity to power an LED light and a small weather-monitoring device. 

The researchers concluded that spent coffee grounds can function as biodegradable TENG materials while reducing dependence on fossil fuel-derived materials. By combining coffee waste with biodegradable plastics, the researchers created a TENG with good electrical performance, sustainability, and long-term stability. They suggested that with further development, the device could someday power road warning lights and provide sound-based alerts in remote areas.

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Over 20 million tons of polystyrene plastic are produced annually, yet only a small fraction is recycled worldwide. Current recycling methods consume large amounts of energy and often rely on harsh and toxic chemicals to break the strong molecular chains that make up polystyrene. One possible solution is the use of sulfur, which is an inexpensive byproduct formed when refining crude oil. Its unique chemical structure allows it to break up strong chemical chains in long plastic molecules. Despite its abundance, sulfur has very limited applications, and converting it into more usable forms tends to require a lot of heat, rendering it unused for long periods of time. 

Researchers at the Dalian Institute of Chemical Physics hypothesized that sulfur could help break down polystyrene waste to form more valuable chemicals. To power this reaction, they converted sunlight into heat energy through a process called photothermal conversion. They used this heat to transform polystyrene and sulfur into valuable chemicals like 2,4-diphenylthiophene, or chemical D, and 1,3,5-triphenylbenzene, or chemical T, which are used to make semiconductors and chemical sensors. 

To test this, the team mixed ground polystyrene and sulfur at a molar ratio of 1:0.5 in a glass test tube. They sealed the tube with a balloon and secured it onto an iron stand. Then, they focused sunlight onto the bottom of the tube using a curved mirror. As the mixture heated up, the yellow-white solids gradually melted and transformed into a reddish-black liquid after 2 minutes. After heating, the researchers removed the mirror and allowed the system to cool before collecting the gaseous products from the balloon and dissolving the remaining solids for further purification and analysis. 

The researchers then adjusted the reaction conditions to understand what factors influenced their results. They tested the reaction without sulfur, varied the sulfur ratios from 0.2 to 0.8, and replaced elemental sulfur with other sulfur-containing compounds. They also explored adding known photothermal agents, specifically metal oxide additives, to the mixture. 

To compare the difference between sunlight and artificial light, the researchers repeated the experiment indoors using a 100 Watt LED bulb and monitored temperature changes with a thermal camera. They also ran a control experiment using only polystyrene to check how sulfur affected the yield under LED light. They also tested exposure times from 1 to 6 minutes in 1-minute increments to determine how long it took to achieve the highest yields under LED. The researchers used these tests to identify which conditions were necessary for the reaction to occur and how different factors influenced its outcome.

They found that without sulfur or with alternative sulfur-containing compounds, the reaction did not produce chemical D or T under sunlight. In contrast, reactions that included sulfur successfully produced these target products, with the highest yields of 34% for D and 16% for T at a sulfur ratio of 0.5. When they added metal oxides, the chemical yields decreased to 22% and 12%, respectively, suggesting that these additives interfered with the desired reactions. In addition, when the researchers switched from sunlight to LED, the reaction yields dropped to 26% for D and 13% for T. 

Next, they examined how reaction time influenced product formation. They found that yields increased gradually before reaching the maximum at 4 minutes and leveling off. They also noted that mixtures containing sulfur heated up from room temperature to 320°C (608°F), while the control setup only showed a slight temperature increase. The researchers interpreted these results as confirmation of sulfur’s dual role as a reactant and a light-to-heat converter that enables the conversion of polystyrene to useful chemicals.

Taking it a step further, the researchers tested their method on real-world polystyrene wastes, including food packaging, cup lids, and foamed plastics. They successfully produced chemicals D and T from these materials, demonstrating that their process works beyond laboratory samples.

The team concluded that their study presents a simple, fast, and solvent-free approach to converting 2 abundant waste materials into valuable chemicals using sunlight. By combining polystyrene waste and excess sulfur, the researchers offer a new pathway for sustainable polymer upcycling that uses clean energy and is broadly applicable to everyday plastics.

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