Layered Metal-Organic Framework-Derived Metal Oxide/Carbon Nanosheet Arrays for Catalyzing the Oxygen Evolution Reaction

被引:175
|
作者
Zhou, Jian [1 ]
Dou, Yibo [1 ]
Zhou, Awu [1 ]
Shu, Lun [1 ]
Chen, Ya [1 ]
Li, Jian-Rong [1 ]
机构
[1] Beijing Univ Technol, Coll Environm & Energy Engn, Beijing Key Lab Green Catalysis & Separat, Beijing 100124, Peoples R China
来源
ACS ENERGY LETTERS | 2018年 / 3卷 / 07期
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
GRAPHENE; CARBON; ELECTROCATALYSTS; REDUCTION; SHEETS; CO3O4; CATALYSTS; SPINELS; MOFS; FE;
D O I
10.1021/acsenergylett.8b00809
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
The oxygen evolution reaction (OER) in water splitting plays a critical role in some clean energy production systems. Transition-metal oxides as one of the most common OER electrocatalysts have been widely explored; however, their activity is limited by low electrical conductivity, slow mass transfer, and inadequate active sites. Herein, we develop a feasible strategy in which layered two-dimensional metal-organic frameworks (2D MOFs) act as templates to construct metal oxide/carbon (MOx/C, M = Co, Ni, and Cu) nanosheet arrays for the OER. Because of improved conductivity and more exposed active sites afforded by their 2D structures with rich hierarchical pores and the incorporation with porous carbon, these 2D MOF-derived MOx/C arrays present high electrocatalytic activities and good durability. Particularly, Co3O4/CBDc, NiO/CBDc, and Cu2O/S-C-TDC exhibit low overpotentials of 208, 285, and 313 mV at the current density of 10 mA cm(-2), respectively, outperforming all previously reported corresponding metal oxide-based catalysts.
引用
收藏
页码:1655 / 1661
页数:13
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