过电位
催化作用
析氧
电子转移
铱
氧化物
材料科学
钙钛矿(结构)
无机化学
吸附
化学
物理化学
电化学
结晶学
电极
生物化学
冶金
作者
Jianyi Li,Lirong Zheng,Bolong Huang,Yang Hu,Li An,Yaxiong Yao,Min Lu,Jing Jin,Nan Zhang,Pinxian Xi,Chun‐Hua Yan
出处
期刊:Small
[Wiley]
日期:2022-10-31
卷期号:18 (50)
被引量:21
标识
DOI:10.1002/smll.202204723
摘要
Tuning the structure of the active center of catalysts to atomic level provides the most efficient utilization of the active component, which plays an especially important role for precious metals. In this study, the liquid phase ion exchange method is used to introduce atomic Ir into LaNiO3 perovskite oxide, which shows excellent catalytic performance in the oxygen evolution reaction (OER). The catalyst, LaNi0.96 Ir0.04 O3 , with the optimal concentration of Ir, displays an overpotential of just 280 mV at 10 mA cm-2 . The introduced Ir enriches the surface electron density significantly, which not only improves site-to-site electron transfer between O and Ni sites but also allows stable adsorption of the intermediates. The results of cyclic voltammetry tests reveal the superior overpotential and remarkable efficiency of the OER process because of the strong interactions in Ni-O-Ir. Moreover, the Ir atom inhibits the participation of a lattice oxygen oxidation mechanism (LOM) in LaNiO3 that guarantees the stability of the catalyst in alkaline conditions. It is anticipated that this work will be instrumental for the preparation and study of a broad range of atomic metal-doped perovskite oxides for water splitting.
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