Fe(Co)OOH Dynamically Stable Interface Based on Self-Sacrificial Reconstruction for Long-Term Electrochemical Water Oxidation

被引:40
作者
Yang, Min [1 ]
Xie, Jing-Yi [1 ]
Yu, Wen-Li [1 ]
Cao, Yu-Ning [1 ]
Dong, Bin [1 ]
Zhou, Ya-Nan [1 ]
Wang, Fu-Li [1 ]
Li, Qing-Zong [2 ]
Zhou, Yu-Lu [1 ]
Chai, Yong-Ming [1 ]
机构
[1] China Univ Petr East China, Coll Sci, State Key Lab Heavy Oil Proc, Qingdao 266580, Peoples R China
[2] Yantai Univ, Sch Chem & Chem Engn, Lab Theoret & Computat Chem, Yantai 264005, Peoples R China
关键词
CoMoO4; self-sacrificial reconstruction; FeOOH; dynamically stable interface; water oxidation; METAL-ORGANIC FRAMEWORKS; OXYGEN-EVOLUTION ELECTROCATALYSTS; EFFICIENT ELECTROCATALYST; INTRINSIC ACTIVITY; CARBON; OXIDE; OXYHYDROXIDE; STABILITY; ELECTRODE; TRENDS;
D O I
10.1021/acsami.0c22620
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
FeOOH on the real catalytic interface for the oxygen evolution reaction (OER) is chemically unstable to dissolve in alkaline media. Herein, based on the perspective of the dynamically stable interface, we purposely design the well-dispersed nanorod arrays of CoMoO4 as a host on activated iron foam (IF) to realize the optimal redeposition of FeOOH, constructing a self-sacrificial template rich in the FeOOH surface. Notably, at long-time oxidation potential, the precatalyst FeOOH-CoMoO4 can realize MoO42- dissolution and redeposition of Co oxyhydroxides on FeOOH host simultaneously, constructing a dynamically stable Fe(Co)OOH interface. The introduction of CoOOH improves conductivity and provides synergistic effect with FeOOH to lower the energy barrier for OER and maintain long-time stability, eventually exhibiting a low overpotential of 298 mV to reach the current density of 100 mA cm(-2) and high stability over 60 h. This work demonstrates the feasibility of manipulating metal dissolution-redeposition process for a dynamically stable interface.
引用
收藏
页码:17450 / 17458
页数:9
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