Electrolysis is a process that uses electricity to create hydrogen and oxygen molecules from water. The use of proton exchange membrane (PEM) and renewable energy for water electrolysis is widely regarded as a sustainable method for hydrogen production. However, a challenge in advancing PEM water electrolysis technology is the lack of efficient, low-cost, and stable catalysts for oxygen evolution reaction (OER) in acidic solutions during PEM water electrolysis. While iridium-based catalysts are a potential solution, metallic iridium is rare and expensive in nature. Alternately, oxides of ruthenium (RuO 2 ) offer a more affordable and reactive option, but they also suffer from stability issues. Therefore, researchers are exploring ways to improve the stability of the RuO 2 structure to develop promising OER catalysts for the successful implementation of the hydrogen production technology.
Now, in a recent study made available online on 22 September 2023 and to be published in Volume 88 of the Journal of Energy Chemistry in January 2024 , a group of researchers, led by Professor Haeseong Jang from the Department of Advanced Materials Engineering at Chung-Ang University, has developed a promising OER catalyst. Denoted as SA Zn-RuO 2 , the catalyst comprises of RuO 2 stabilized by single atoms of zinc. Elaborating about their study, Prof. Jang says, “We were motivated by the need to find efficient and cost-effective alternative electrocatalysts for OER in PEM water electrolysis. Based on our study, we propose a dual-engineering strategy, involving single atom Zn doping and the introduction of oxygen vacancies, to balance high catalytic activity with stability during acidic OER.”
The researchers synthesized SA Zn-RuO 2 by heating an organic framework with ruthenium (Ru) and zinc atoms, forming a structure with oxygen vacancies (missing oxygen atoms that positively alter the properties) and Zn-O-Ru linkages. These linkages stabilize the catalyst in two ways—one, by strengthening the Ru-O bonds, and second, by providing electrons from zinc atoms to protect ruthenium from overoxidation during the OER process. Furthermore, the improved electronic environment around the ruthenium atoms lowers the energies needed for molecules to stick to the surface, thus lowering the energy barrier for the reaction.
The resulting catalyst was more stable, with no apparent fall in reactivity, and significantly outperformed commercial RuO 2 . Moreover, it required less extra energy (low overpotential of 213 mV compared to 270 mV for commercial RuO 2 ) and remained functional for a longer period (43 hours compared to 7.4 hours for commercial RuO 2 ).
Due to its improved stability and features, the newly proposed SA Zn-RuO 2 catalyst has the potential to influence the development of cost-effective, active, and acid-resistant electrocatalysts for OER. This, in turn, could help in reducing costs and enhancing the production of green hydrogen, aiding in a shift toward cleaner energy sources and advancements in sustainable technologies.
“We believe that this shift can revolutionize industries, transportation, and energy infrastructure, and contribute to the efforts aimed at combating climate change and fostering a more resilient and environmentally conscious future. This is because accessible green hydrogen can have a transformative impact on societies by mitigating environmental impacts, creating jobs, and ensuring energy security through diversified and sustainable energy solutions,” envisions Prof. Jang.
In summary, the highly reactive and catalytically stable RuO 2 catalyst for the acidic OER has increased durability and favorable characteristics, and holds immense potential for guiding the design of robust and active non-iridium-based OER electrocatalysts for practical applications!
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Reference
DOI: https://doi.org/10.1016/j.jechem.2023.09.010
Authors: Qing Qin 1 , Tiantian Wang 1 , Zijian Li 2 , Guolin Zhang 1 , Haeseong Jang 3 , Liqiang Hou 1 , Yu Wang 1 , Min Gyu Kim 4 , Shangguo Liu 1 , and Xien Liu 1
Affiliations:
1 College of Chemical Engineering, Qingdao University of Science and Technology
2 Department of Chemistry, City University of Hong Kong
3 Department of Advanced Materials Engineering, Chung-Ang University
4 Beamline Research Division, Pohang Accelerator Laboratory (PAL)
About Chung-Ang University
Chung-Ang University is a private comprehensive research university located in Seoul, South Korea. It was started as a kindergarten in 1916 and attained university status in 1953. It is fully accredited by the Ministry of Education of Korea. Chung-Ang University conducts research activities under the slogan of “Justice and Truth.” Its new vision for completing 100 years is “The Global Creative Leader.” Chung-Ang University offers undergraduate, postgraduate, and doctoral programs, which encompass a law school, management program, and medical school; it has 16 undergraduate and graduate schools each. Chung-Ang University’s culture and arts programs are considered the best in Korea.
Website: https://neweng.cau.ac.kr/index.do
About Professor Haeseong Jang
Professor Haeseong Jang is currently a faculty member in the Department of Advanced Materials Engineering at Chung-Ang University in the Republic of Korea. His research primarily focuses on material characterization and electrochemical analysis within the field of energy storage, with a specific focus on processes such as oxygen reduction reactions, oxygen evolution reactions, and hydrogen evolution reactions. With over 80 publications to his credit, Prof. Jang has accumulated over 3200 citations. Additionally, he has also been serving as a reviewer for several journals, including Electrochimica Acta , Applied Surface Science , and the Journal of Energy Chemistry . Read more: https://scholarworks.bwise.kr/cau/researcher-profile?ep=1468
Journal of Energy Chemistry
Experimental study
Not applicable
Tuning electronic structure of RuO2 by single atom Zn and oxygen vacancies to boost oxygen evolution reaction in acidic medium
1-Jan-2024
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.