Modulating the Electronic Structure of Porous Nanocubes Derived from Trimetallic Metal-Organic Frameworks to Boost Oxygen Evolution Reaction Performance

被引:9
|
作者
Lu, Mengting [1 ]
Yang, Xigaogang [1 ]
Li, Yuwen [1 ]
Zhu, Zhenwang [1 ]
Wu, Yuhang [1 ]
Xu, Hui [2 ]
Gao, Junkuo [1 ]
Yao, Juming [1 ]
机构
[1] Zhejiang Sci Tech Univ, Inst Fiber Based New Energy Mat, Key Lab Adv Text Mat & Mfg Techol, Minist Educ,Sch Mat Sci & Engn, Hangzhou 310018, Zhejiang, Peoples R China
[2] China Jiliang Univ, Coll Mat Sci & Engn, Hangzhou 310018, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
electrocatalysis; metal-organic frameworks; nanostructures; oxygen evolution reaction; trimetallic catalyst; ELECTROCATALYSTS; REDUCTION; CATALYSTS; NI; NANOPARTICLES; STORAGE; DESIGN; OXIDES;
D O I
10.1002/asia.201900871
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The preparation of noble metal-free catalysts for water splitting is the key to low-cost, sustainable hydrogen generation. Herein, through a pyrolysis-oxidation process, we prepared a series of Co-Fe-Ni trimetallic oxidized carbon nanocubes (Co1-XFeXNi-OCNC) with a continuously changeable Co/Fe ratio (X=0, 0.1, 0.2, 0.5, 0.8, 0.9, 1). The Co1-XFeXNi-OCNC shows a volcano-type oxygen evolution reaction (OER) activity. The optimized Co0.1Fe0.9Ni-OCNC achieves a low overpotential of 268 mV at 10 mA cm(-2) with a very low Tafel slope of 48 mV dec(-1) in 1 m KOH. At the same time, the stability of the Co0.1Fe0.9Ni-OCNC is also outstanding; after 1000 CV cycles, the LSV plot is almost coincident. Moreover, the potential remains almost of the same value at 10 mA cm(-2) after 12 h in comparison to the initial value. The excellent electrocatalytic properties can be attributed to the synergistic cooperation between each component. Therefore, the Co0.1Fe0.9Ni-OCNC is a promising candidate instead of precious metal-based electrocatalysts for OER.
引用
收藏
页码:3357 / 3362
页数:6
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