过电位
纳米片
析氧
催化作用
正交晶系
热稳定性
镍
腐蚀
材料科学
化学
化学工程
纳米技术
电化学
冶金
有机化学
物理化学
晶体结构
电极
工程类
作者
Xiong Liu,Kun Ni,Bo Wen,Ruiting Guo,Chaojiang Niu,Jiashen Meng,Qi Li,Peijie Wu,Yanwu Zhu,Xiaojun Wu,Liqiang Mai
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2019-09-27
卷期号:4 (11): 2585-2592
被引量:170
标识
DOI:10.1021/acsenergylett.9b01922
摘要
Oxygen evolution reaction (OER)-induced reconstruction on precatalysts generally results in surface-reconstructed catalysts with less active species and thus low mass activity. Herein, the deeply reconstructed (DR) catalyst is proposed and derived from a sub-10 nm precatalyst to achieve high-mass-activity catalysis. As a proof-of-concept, the DR-NiOOH with a multilevel nanosheet structure interconnected by sub-5 nm nanoparticles was obtained via a lithiation-induced deep reconstruction strategy. The robust DR-NiOOH with abundant active species enables its significantly enhanced mass activity (170 mV decrease in OER overpotential to achieve 5 mA mg–1) and better durability (>10 days) than that of incompletely reconstructed Ni@NiOOH. Its strong corrosion resistance (30 wt % KOH, 72 h) and high thermal stability (52.8 °C, >40 h) were also confirmed. Theoretical analyses support that the unsaturated OH coverages on orthorhombic NiOOH endow its good OER-active property. This work highlights the merits of high-utilization DR catalysts toward potential catalytic applications under realistic conditions.
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