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Unlocking Green Energy: Uncovering New Gene Clusters for Hydrogen Production in Marine Microbes

A genomic study of hydrogen-producing bacteria has revealed entirely new gene clusters capable of producing large volumes of hydrogen.

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A groundbreaking genomic study has unveiled novel gene clusters in marine bacteria that can produce substantial volumes of hydrogen, a game-changer for green energy solutions. Researchers led by Professor Tomoo Sawabe at Hokkaido University have used genome sequencing to investigate the biochemical mechanism behind this feat. Their findings were published in Current Microbiology.

The study focused on Vibrionaceae, a family of marine bacteria known for their bioluminescence and infamous member, the cholera pathogen. However, another unique feature of these microbes is their ability to generate large volumes of hydrogen gas through fermentation by breaking down formate into carbon dioxide and hydrogen. This remarkable trait has emerged as a potential solution for green energy production.

The researchers examined all 16 known species of Vibrionaceae, often found in symbiotic relationships with deep-sea animals. They focused on the sequence and structure of the Hyf-type formate hydrogenlyase (FHL) gene cluster, which catalyzes the breakdown of formate into hydrogen and carbon dioxide. This complex is also found in Escherichia coli, another bacteria that can generate hydrogen through fermentation, though in much smaller amounts than Vibrionaceae.

The team discovered two new types of FHL gene clusters among Vibrionaceae, bringing the total number of FHL gene clusters in these bacteria to six. They suggest that this diversity in the structure of the cluster is the result of speciation among the Vibrionaceae as they adapted and evolved to occupy a range of ecological niches.

The study also found differences in hydrogen fermentation and production associated with the different FHL gene clusters. Vibrio tritonius, a marine species, and Vibrio porteresiae, found in mangrove-dwelling wild rice, showed the highest levels of hydrogen production, while Vibrio aerogenes and Vibrio mangrovi showed the lowest.

There was a correlation between levels of hydrogen production and how well the bacteria were able to take up formate back into their cells. “These genotypes strengthen formate metabolism as a possible key factor in maintaining fermentative hydrogen production in specific groups of vibrios,” Sawabe concluded.

The findings support the researchers’ proposal that some species were driven to evolve higher hydrogen production because of their need to detoxify formate from the environment – what they call the formate detoxification hypothesis. The findings could also shed light on the evolution of hydrogen fermentation in other bacterial species, such as E. coli.

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A Breakthrough in Green Hydrogen Production: Cage Structured Material Transforms into High-Performance Catalyst

Clathrates are characterized by a complex cage structure that provides space for guest ions too. Now a team has investigated the suitability of clathrates as catalysts for electrolytic hydrogen production with impressive results: the clathrate sample was even more efficient and robust than currently used nickel-based catalysts. They also found a reason for this enhanced performance. Measurements at BESSY II showed that the clathrates undergo structural changes during the catalytic reaction: the three-dimensional cage structure decays into ultra-thin nanosheets that allow maximum contact with active catalytic centers.

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Scientists have made a groundbreaking discovery that could revolutionize the production of green hydrogen, a crucial component for a sustainable energy future. Researchers have found that a cage-structured material, previously unknown as an electrocatalyst, can outperform existing nickel-based catalysts in electrolytic hydrogen production. This breakthrough has significant implications for the chemical industry and our transition to renewable energy sources.

The study, published in Angewandte Chemie, investigates the suitability of clathrates – materials characterized by a complex three-dimensional cage structure – as catalysts for oxygen evolution reaction (OER) in electrolysis. Clathrates have shown promise in various applications, such as thermoelectrics and superconductors, but their potential as electrocatalysts has remained unexplored until now.

Dr. Prashanth Menezes and his team at the Technical University of Munich synthesized Ba₈Ni₆Ge₄₀ clathrates, which they then tested as OER catalysts in aqueous electrolytes. The results were astonishing: the clathrate sample exceeded the efficiency of nickel-based catalysts at a current density of 550 mA cm⁻², a value commonly used in industrial electrolysis. Moreover, its stability was remarkable, with activity remaining high even after 10 days of continuous operation.

To understand why this material performed so well, the researchers employed a combination of experiments, including in situ X-ray absorption spectroscopy (XAS) at BESSY II and basic structural characterization at the Freie and Technische Universität Berlin. Their analysis revealed that the clathrate particles undergo a structural transformation under an electric field: germanium and barium atoms dissolve out of the former three-dimensional framework, leaving behind highly porous, sponge-like nanolayers of nickel that offer maximum surface area.

“This transformation brings more and more catalytically active nickel centres into contact with the electrolyte,” says Dr. Niklas Hausmann from Menezes’ team. “We were actually surprised by how well these samples work as OER catalysts. We expect that we can observe similar results with other transition metal clathrates and that we have discovered a very interesting class of materials for electrocatalysts.”

This breakthrough has significant implications for the production of green hydrogen, which is seen as an essential building block for a sustainable energy future. With this new material, researchers may be able to develop more efficient and robust OER catalysts, enabling faster and more cost-effective production of green hydrogen.

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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.

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Harnessing Sunshine: Low-Cost Green Hydrogen Technology Yields Potable Water as Byproduct

Engineers have hit the trifecta of sustainability technology: A group has developed a low-cost method to produce carbon-free ‘green’ hydrogen via solar-powered electrolysis of seawater. A happy byproduct of the process? Potable water.

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The Cornell University-led collaboration has achieved a remarkable breakthrough in sustainable technology: developing a low-cost method to produce carbon-free “green” hydrogen through solar-powered electrolysis of seawater. This innovative approach not only produces green hydrogen but also yields potable water as a happy byproduct, addressing two critical global needs simultaneously.

Researchers from Cornell University, MIT, Johns Hopkins University, and Michigan State University have developed the hybrid solar distillation-water electrolysis (HSD-WE) device. Currently, this prototype device produces 200 milliliters of hydrogen per hour with an impressive 12.6% energy efficiency directly from seawater under natural sunlight.

The team estimates that within 15 years, the technology could reduce the cost of green hydrogen production to $1 per kilogram – a crucial step in achieving net-zero emissions by 2050.

According to Lenan Zhang, assistant professor and project lead, “Water and energy are both critically needed for our everyday life, but typically, if you want to produce more energy, you have to consume more water.” This paradox is reflected in the high cost of green hydrogen production, which can be roughly 10 times higher than that of regular hydrogen due to the massive amount of clean water required.

Zhang’s team devised a 10 centimeter by 10 centimeter prototype device that leverages one of the drawbacks of photovoltaics: their relatively low efficiency. By harnessing most of the waste heat generated by solar cells, the device warms the seawater until it evaporates. This process produces clean water, which is then passed through an electrolyzer to split the water molecules into hydrogen and oxygen.

The HSD-WE technology has significant potential for large-scale adoption, particularly in solar farms where it can be used to cool PV panels, improving their efficiency and prolonging their lifespan. As Zhang notes, “We want to avoid carbon emission, avoid pollution. But meanwhile, we also care about the cost, because the lower cost we have, the higher market potential for large-scale adoption.”

The research was supported by the National Science Foundation, and the team is optimistic about the future of this technology. With its potential to address two critical global needs – clean energy and clean water – while reducing costs and carbon emissions, the HSD-WE device represents a promising step towards a more sustainable future.

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