Metal -organic framework -derived heterostructured ZnCo 2 O 4 @FeOOH hollow polyhedrons for oxygen evolution reaction

被引:18
作者
Yu, Zhou [1 ,2 ]
Bai, Yu [1 ]
Zhang, Naiqing [3 ]
Yang, Weiwei [1 ]
Ma, Jiahuan [1 ]
Wang, Zhenhua [1 ,4 ]
Sun, Wang [1 ]
Qiao, Jinshuo [1 ]
Sun, Kening [1 ,4 ]
机构
[1] Beijing Inst Technol, Beijing Key Lab Chem Power Source & Green Catalys, Beijing 100081, Peoples R China
[2] Shenyang Normal Univ, Coll Chem & Chem Engn, Shenyang 110034, Peoples R China
[3] Harbin Inst Technol, Sch Chem & Chem Engn, Harbin 150090, Peoples R China
[4] Collaborat Innovat Ctr Elect Vehicles, 5 Zhongguancun South Ave, Beijing 100081, Peoples R China
关键词
ENHANCED ELECTROCATALYTIC ACTIVITY; HIGH-PERFORMANCE; HIGHLY EFFICIENT; COFE2O4; NANOPARTICLES; REACTION CATALYST; POROUS ZNCO2O4; OXIDE; COBALT; OXIDATION; ARRAYS;
D O I
10.1016/j.jallcom.2020.155067
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Exploration of non-noble metal electrocatalysts for efficient and durable oxygen evolution reaction (OER) is highly desirable but still remains a great challenge. Herein, we report the rational design and synthesis of heterostructured ZnCo2O4/FeOOH hollow polyhedrons (ZnCo2O4/FeOOH HPs) as a high-efficient electrocatalyst for OER in alkaline condition. ZnCo2O4 hollow polyhedrons (ZnCo2O4 HPs), which derived from the bimetallic Zn, Co-zeolitic imidazolate frameworks (ZnCo-ZIFs), are employed as the substrate for the growth of FeOOH nanowires. Benefiting from the hollow structure as well as the synergistic effect between ZnCo2O4 HPs and FeOOH nanowires, the ZnCo2O4/FeOOH HPs show enhanced OER activity with a low overpotential of 299 mV at the current density of 10 mA cm−2 and excellent durability. This work offers a promising strategy to develop high-efficient and robust non-noble metal electrocatalysts for large-scale electrochemical applications. © 2020 Elsevier B.V.
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页数:7
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