Journal
ADVANCED FUNCTIONAL MATERIALS
Volume 32, Issue 23, Pages -Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202201726
Keywords
acidic water electrolysis; high current density; intrinsic activity; long-term stability; oxygen evolution reaction; proton exchange membrane water electrolyzers
Categories
Funding
- National Science Fund for Distinguished Young Scholars [52125309]
- National Natural Science Foundation of China [52188101]
- Guangdong Innovative and Entrepreneurial Research Team Program [2017ZT07C341]
- Guangdong Basic and Applied Basic Research Foundation [2021A1515110829]
- Shenzhen Basic Research Project [JCYJ20200109144620815]
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The production of green hydrogen through water electrolysis is crucial for achieving carbon neutrality worldwide. Acidic water electrolysis has gained significant attention due to its higher current density operation and energy conversion efficiency compared to alkaline water electrolysis. However, the four-electron-transfer oxygen evolution reaction (OER) limits the overall efficiency of water electrolysis devices. Recent studies have focused on improving the intrinsic activity, high current density operation, and long-term stability of acidic OER catalysts through strategies such as surface chemistry engineering and constructing porous structures.
Production of green hydrogen (H-2) by water electrolysis is important for achieving the global mission of carbon neutrality. For this, acidic water electrolysis with a higher current density operation and energy conversion efficiency compared with alkaline water electrolysis has attracted much attention. The four-electron-transfer oxygen evolution reaction (OER) limits the overall efficiency of water electrolysis devices. In recent years, low-dimensional OER catalysts have been extensively explored to increase the overall efficiency of such devices, but most of them work well only at low current density and show unsatisfied long-term stability. In this review, recent progress in acidic OER is discussed and three aspects including intrinsic activity, high current density operation, and long-term stability are focused upon. Strategies to improve these aspects including surface chemistry engineering, constructing porous structure, and protecting the active sites' are comprehensively reviewed. Finally, prospects for developing high-performance catalysts with high current density operation and long-term stability for industrial applications are proposed.
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