催化作用
钙钛矿(结构)
氧气
吸附
塔菲尔方程
析氧
化学
化学工程
动力学
纳米
氧化还原
无机化学
材料科学
物理化学
结晶学
有机化学
电化学
工程类
物理
量子力学
电极
作者
J. W. Zhao,Chengfei Li,Zixiao Shi,Jielun Guan,Gao‐Ren Li
出处
期刊:Research
[AAAS00]
日期:2020-01-01
卷期号:2020
被引量:135
标识
DOI:10.34133/2020/6961578
摘要
In the process of oxygen evolution reaction (OER) on perovskite, it is of great significance to accelerate the hindered lattice oxygen oxidation process to promote the slow kinetics of water oxidation. In this paper, a facile surface modification strategy of nanometer-scale iron oxyhydroxide (FeOOH) clusters depositing on the surface of LaNiO3 (LNO) perovskite is reported, and it can obviously promote hydroxyl adsorption and weaken Ni-O bond of LNO. The above relevant evidences are well demonstrated by the experimental results and DFT calculations. The excellent hydroxyl adsorption ability of FeOOH-LaNiO3 (Fe-LNO) can obviously optimize OH- filling barriers to promote lattice oxygen-participated OER (LOER), and the weakened Ni-O bond of LNO perovskite can obviously reduce the reaction barrier of the lattice oxygen participation mechanism (LOM). Based on the above synergistic catalysis effect, the Fe-LNO catalyst exhibits a maximum factor of 5 catalytic activity increases for OER relative to the pristine perovskite and demonstrates the fast reaction kinetics (low Tafel slope of 42 mV dec-1) and superior intrinsic activity (TOFs of ~40 O2 S-1 at 1.60 V vs. RHE).
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