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“Beyond Conventional Thinking: Unlocking the Potential of Single Atom Catalysts with Hydrogen Binding Energy”

Conventional thinking holds that the metal site in single atom catalysts (SACs) has been a limiting factor to the continued improvement of the design and, therefore, the continued improvement of the capability of these SACs. More specifically, the lack of outside-the-box thinking when it comes to the crucial hydrogen evolution reaction (HER), a half-reaction resulting in the splitting of water, has contributed to a lack of advancement in this field. New research emphasizes the importance of pushing the limits of the metal site design in SACs to optimize the HER and addressing the poisoning effects of HO* and O* that might affect the reaction. All of these improvements could lead to an improved performance of the reaction, which can make sustainable energy storage or hydrogen production more available.

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The world is shifting towards renewable energy sources, and hydrogen-based technologies are gaining attention. However, a new study suggests that the conventional thinking on single atom catalysts (SACs) might be limiting their potential. Researchers have found that the metal site in SACs can be improved by pushing the limits of design, optimizing the hydrogen evolution reaction (HER), and addressing the poisoning effects of HO* and O*. This breakthrough could lead to more efficient energy storage or hydrogen production.

Single atom catalysts are catalytically active metal sites distributed at the atomic level to enhance catalytic activity. However, hydroxyl radical (HO*) and oxygen radical (O*) poisoning can alter molecules and degrade performance. In contrast, sites where hydrogen molecules don’t readily accumulate can lead to an enhancing effect of the catalyst.

Researchers have discovered that HO* poisoning, realistic H* adsorption strengths at active metal sites, and the potential HER activity at coordinating N-sites are crucial factors to consider for accurate descriptor development. By effectively modifying these factors, more efficient catalysts can be developed to improve HER activity while not relying on conventional design of metal binding sites.

The study found that hydrogen binding energy (HBE) calculation under a realistic representation of accumulated molecules (adsorption) can serve as a good predictor of HER activity. Additionally, the combination of using HBE and Gibbs free energy as descriptors for SACs provides new guidelines for those working with this catalyst design.

This work addresses the long-lasting debate on HER descriptors and provides new methods to break out of conventional limitations put on by using just hydrogen binding energy as a solo descriptor. The researchers aim to further address the limitations of HO poisoning and develop novel single- and dual-atom catalysts for different pH conditions, especially in alkaline environments.

In conclusion, this study opens up new possibilities for SACs, highlighting the importance of pushing design limits, optimizing HER, and addressing poisoning effects. By doing so, researchers can unlock the full potential of SACs and contribute to more efficient energy storage or hydrogen production.

Alternative Fuels

“Breaking Down Barriers: Groundbreaking Recycling Technique Turns ‘Forever Chemicals’ into Renewable Resources”

A new technique that uses soundwaves to separate materials for recycling could help prevent potentially harmful chemicals leaching into the environment.

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Breaking Down Barriers: Groundbreaking Recycling Technique Turns ‘Forever Chemicals’ into Renewable Resources

In a major breakthrough, researchers at the University of Leicester have developed a revolutionary technique to efficiently separate valuable catalyst materials and fluorinated polymer membranes (PFAS) from catalyst-coated membranes (CCMs). This achievement has significant implications for preventing potentially harmful chemicals from contaminating our environment.

PFAS, often referred to as “forever chemicals,” are known to contaminate drinking water and have serious health implications. The Royal Society of Chemistry has urged government intervention to reduce PFAS levels in UK water supplies.

Fuel cells and water electrolysers, essential components of hydrogen-powered energy systems, rely on CCMs containing precious platinum group metals. However, the strong adhesion between catalyst layers and PFAS membranes has made recycling difficult.

The researchers’ innovative method uses organic solvent soaking and water ultrasonication to effectively separate these materials, revolutionizing the recycling process. Dr. Jake Yang from the University of Leicester School of Chemistry comments, “This method is simple and scalable. We can now separate PFAS membranes from precious metals without harsh chemicals – revolutionizing how we recycle fuel cells.”

Building on this success, a follow-up study introduced a continuous delamination process using high-frequency ultrasound to split the membranes, accelerating recycling. The innovative process creates bubbles that collapse when subjected to high pressure, allowing the precious catalysts to be separated in seconds at room temperature.

This groundbreaking research was carried out in collaboration with Johnson Matthey, a global leader in sustainable technologies. Industry-academia partnerships like this underscore the importance of collective efforts in driving technological progress.

Ross Gordon, Principal Research Scientist at Johnson Matthey, says, “The development of high-intensity ultrasound to separate catalyst-loaded membranes is a game-changer in how we approach fuel cell recycling. At Johnson Matthey, we are proud to collaborate on pioneering solutions that accelerate the adoption of hydrogen-powered energy while making it more sustainable and economically viable.”

As fuel cell demand continues to grow, this breakthrough contributes to the circular economy by enabling efficient recycling of essential clean energy components. The researchers’ efforts support a greener and more affordable future for fuel cell technology while addressing pressing environmental challenges.

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Breakthrough in Fuel Cell Lifespan: Paving the Way for Clean Long-Haul Trucking

Researchers have developed a new catalyst design capable of pushing the projected fuel cell catalyst lifespans to 200,000 hours. The research marks a significant step toward the widespread adoption of fuel cell technology in heavy-duty vehicles, such as long-haul tractor trailers. While platinum-alloy catalysts have historically delivered superior chemical reactions, the alloying elements leach out over time, diminishing catalytic performance. The degradation is further accelerated by the demanding voltage cycles required to power heavy-duty vehicles. To address this challenge, the team has engineered a durable catalyst architecture with a novel design that shields platinum from the degradation typically observed in alloy systems.

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With a significant breakthrough in extending the lifespan of hydrogen fuel cells, researchers at UCLA have made a major step towards making clean, long-haul trucking a reality. Led by Professor Yu Huang, the team has developed a new catalyst design that can push projected fuel cell lifespans to 200,000 hours – nearly seven times the US Department of Energy’s target for 2050.

Hydrogen fuel cells have been considered a promising alternative to batteries for long-haul trucks due to their ability to be refueled as quickly as traditional gasoline. However, one major challenge has been the durability of the catalysts used in these systems. The new design, which embeds ultrafine platinum nanoparticles within protective graphene pockets, addresses this issue by preventing the leaching of alloying elements and maintaining high catalytic activity over time.

The implications of this breakthrough are significant. Heavy-duty trucks account for nearly a quarter of greenhouse gas automobile emissions, making them an ideal entry point for polymer electrolyte membrane fuel cell technology. By using hydrogen fuel cells in these vehicles, it’s possible to deliver the same performance as conventional batteries while being significantly lighter and requiring less energy to move.

The researchers’ innovative catalyst design holds great promise for the adoption of hydrogen-powered heavy-duty vehicles, which would be a crucial step towards reducing emissions and improving fuel efficiency in a sector that accounts for a substantial share of transportation energy use. The team’s findings build on their earlier success in developing a fuel cell catalyst for light-duty vehicles, demonstrating a lifespan of 15,000 hours.

The new study, published in Nature Nanotechnology, was led by UCLA Ph.D. graduates Zeyan Liu and Bosi Peng, both advised by Huang, whose research group specializes in developing nanoscale building blocks for complex materials, such as fuel cell catalysts. Xiaofeng Duan, a professor of chemistry and biochemistry at UCLA, and Xiaoqing Pan, a professor of materials science and engineering at UC Irvine, are also authors on the paper.

UCLA’s Technology Development Group has filed a patent on the technology, which has significant implications for the development of clean energy solutions in the transportation sector.

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Affordable Hydrogen Fuel Production on the Horizon: Researchers Unveil Breakthrough Strategy

Researchers found a strategy to create catalysts that make the production of hydrogen for clean fuel more efficient and affordable.

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The world is on the cusp of a revolution in hydrogen fuel production. Researchers at Tohoku University have made a groundbreaking discovery that could finally bridge the gap between laboratory experiments and large-scale commercial production. The breakthrough involves a surface reconstruction strategy that utilizes non-noble metal-based cathodes to accelerate the hydrogen evolution reaction (HER).

The HER is a crucial process for creating clean hydrogen fuel, which has the potential to alleviate our climate change crisis. However, scaling up this reaction from lab to factory has been a daunting challenge due to its inefficiency and slowness. The researchers’ findings, published in Advanced Energy Materials on April 3, 2025, offer a promising solution.

By examining transition metal phosphides (TMPs), the research team discovered that adding fluorine (F) to the CoP lattice allows for P-vacancy sites to form on the surface. This leads to an increase in active sites, which speed up the HER reaction. The resulting F modified CoP cathode demonstrated exceptional performance, maintaining approximately 76 W for over 300 hours.

“This is a significant advancement in HER catalyst research,” says Heng Liu from the Advanced Institute for Materials Research (WPI-AIMR). “Our calculated cost of using this method is just $2.17 per kgH2-1 – mere cents over the current production target set for 2026.”

The researchers’ experiment extended beyond lab-scale testing, applying their findings to commercial-scale PEM electrolyzers. This breakthrough has far-reaching implications for the rational design of non-noble metal-based cathodes.

“We’re always thinking about the end goal, which is for research to make its way into everyday life,” says Liu. “This advancement brings us one step closer to designing more realistic options for commercial PEM application.”

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