Yin Li, Ding Yunxuan, Li Yingzheng, Liu Chang, Zhao Ziqi, Ning Hongxia, Zhang Peili, Li Fei, Sun Licheng, Li Fusheng
State Key Laboratory of Fine Chemicals, Frontier Science Center for Smart Materials, School of Chemical Engineering, Dalian University of Technology, Dalian, 116024, China.
Center of Artificial Photosynthesis for Solar Fuels and Department of Chemistry, School of Science and Research Center for Industries of the Future, Westlake University, Hangzhou, 310024, China.
ChemSusChem. 2025 Jan 2;18(1):e202400623. doi: 10.1002/cssc.202400623. Epub 2024 Sep 4.
The abundant, active, and acidic-stable catalysts for the oxygen evolution reaction (OER) are rare to proton exchange membrane-based water electrolysis. Mn-based materials show promise as electrocatalysts for OER in acid electrolytes. However, the relationship between the stability, activity and structure of Mn-based catalysts in acidic environments remains unclear. In this study, phase-pure MnSbO was successfully prepared and investigated as a catalyst for OER in a sulfuric acid solution (pH of 2.0). A comprehensive mechanistic comparison between MnSbO and MnO revealed that the rate-determining step for OER on MnSbO is the direct formation of Mn=O from Mn-HO by the 2H/2e process. This process avoids the rearrangement of adjacent Mn intermediates, leading to outstanding stability and activity.
用于析氧反应(OER)的丰富、活性且耐酸性的催化剂在基于质子交换膜的水电解中很少见。锰基材料有望成为酸性电解质中OER的电催化剂。然而,锰基催化剂在酸性环境中的稳定性、活性和结构之间的关系仍不清楚。在本研究中,成功制备了纯相的MnSbO,并将其作为硫酸溶液(pH为2.0)中OER的催化剂进行了研究。MnSbO和MnO之间的综合机理比较表明,MnSbO上OER的速率决定步骤是通过2H/2e过程由Mn-HO直接形成Mn=O。该过程避免了相邻锰中间体的重排,从而导致出色的稳定性和活性。