Ultrafast Formation of Amorphous Bimetallic Hydroxide Films on 3D Conductive Sulfide Nanoarrays for Large-Current-Density Oxygen Evolution Electrocatalysis

被引:538
作者
Zou, Xu [1 ]
Liu, Yipu [1 ]
Li, Guo-Dong [1 ]
Wu, Yuanyuan [1 ]
Liu, Da-Peng [2 ]
Li, Wang
Li, Hai-Wen [3 ]
Wang, Dejun [1 ,4 ]
Zhang, Yu [2 ]
Zou, Xiaoxin [1 ]
机构
[1] Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China
[2] Beihang Univ, Sch Chem & Environm, Key Lab Bioinspired Smart Interfacial Sci & Techn, Minist Educ, Beijing 100191, Peoples R China
[3] Kyushu Univ, Int Res Ctr Hydrogen Energy, Fukuoka 8190395, Japan
[4] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
关键词
WATER OXIDATION; METAL-OXIDE; RATIONAL DESIGN; NI; CATALYSTS; COBALT; ARRAYS; IRON; NANOSHEETS;
D O I
10.1002/adma.201700404
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Developing nonprecious oxygen evolution electrocatalysts that can work well at large current densities is of primary importance in a viable water-splitting technology. Herein, a facile ultrafast (5 s) synthetic approach is reported that produces a novel, efficient, non-noble metal oxygen-evolution nano-electrocatalyst that is composed of amorphous Ni-Fe bimetallic hydroxide film-coated, nickel foam (NF)-supported, Ni3S2 nanosheet arrays. The composite nanomaterial (denoted as Ni-Fe-OH@Ni3S2/NF) shows highly efficient electrocatalytic activity toward oxygen evolution reaction (OER) at large current densities, even in the order of 1000 mA cm(-2). Ni-Fe-OH@Ni3S2/NF also gives an excellent catalytic stability toward OER both in 1 m KOH solution and in 30 wt% KOH solution. Further experimental results indicate that the effective integration of high catalytic reactivity, high structural stability, and high electronic conductivity into a single material system makes Ni-Fe-OH@Ni3S2/NF a remarkable catalytic ability for OER at large current densities.
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页数:7
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