Xu Qiucheng, Jiang Hao, Duan Xuezhi, Jiang Zheng, Hu Yanjie, Boettcher Shannon W, Zhang Weiyu, Guo Shaojun, Li Chunzhong
Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China.
Shanghai Engineering Research Center of Hierarchical Nanomaterials, School of Chemical Engineering, East China University of Science and Technology, Shanghai 200237, China.
Nano Lett. 2021 Jan 13;21(1):492-499. doi: 10.1021/acs.nanolett.0c03950. Epub 2020 Dec 1.
Developing low-cost and efficient electrocatalysts to accelerate oxygen evolution reaction (OER) kinetics is vital for water and carbon-dioxide electrolyzers. The fastest-known water oxidation catalyst, Ni(Fe)OH, usually produced through an electrochemical reconstruction of precatalysts under alkaline condition, has received substantial attention. However, the reconstruction in the reported catalysts usually leads to a limited active layer and poorly controlled Fe-activated sites. Here, we demonstrate a new electrochemistry-driven F-enabled surface-reconstruction strategy for converting the ultrathin NiFeOF nanosheets into an Fe-enriched Ni(Fe)OH phase. The activated electrocatalyst shows a low OER overpotential of 218 ± 5 mV at 10 mA cm and a low Tafel slope of 31 ± 4 mV dec, which is among the best for NiFe-based OER electrocatalysts. Such superior performance is caused by the effective formation of the Fe-enriched Ni(Fe)OH active-phase that is identified by Raman spectroscopy and the substantially improved surface wettability and gas-bubble-releasing behavior.
开发低成本且高效的电催化剂以加速析氧反应(OER)动力学对于水和二氧化碳电解槽至关重要。目前已知最快的水氧化催化剂Ni(Fe)OH通常是在碱性条件下通过预催化剂的电化学重构制备的,已受到广泛关注。然而,报道的催化剂中的重构通常会导致活性层有限且铁活化位点控制不佳。在此,我们展示了一种新的电化学驱动的氟促进表面重构策略,用于将超薄NiFeOF纳米片转化为富铁的Ni(Fe)OH相。活化后的电催化剂在10 mA cm时表现出218±5 mV的低OER过电位和31±4 mV dec的低塔菲尔斜率,这在基于镍铁的OER电催化剂中是最佳之一。这种优异的性能是由通过拉曼光谱鉴定的富铁Ni(Fe)OH活性相的有效形成以及显著改善的表面润湿性和气泡释放行为所导致的。