Interface Engineering of MoS2/Ni3S2 Heterostructures for Highly Enhanced Electrochemical Overall-Water-Splitting Activity

被引:1397
|
作者
Zhang, Jian [1 ,2 ]
Wang, Tao [3 ]
Pohl, Darius [4 ]
Rellinghaus, Bernd [4 ]
Dong, Renhao [1 ,2 ]
Liu, Shaohua [1 ,2 ]
Zhuang, Xiaodong [1 ,2 ]
Feng, Xinliang [1 ,2 ]
机构
[1] Tech Univ Dresden, Cfaed, D-01062 Dresden, Germany
[2] Tech Univ Dresden, Dept Chem & Food Chem, D-01062 Dresden, Germany
[3] Univ Rostock, Leibniz Inst Katalyse eV, D-18059 Rostock, Germany
[4] IFW Dresden, Inst Metall Mat, D-01171 Dresden, Germany
关键词
electrocatalysts; interface engineering; molybdenum disulfide; nickel sulfide; water splitting; HYDROGEN EVOLUTION REACTION; OXYGEN EVOLUTION; CARBON NANOTUBES; EFFICIENT; ELECTROCATALYSTS; OXIDATION; CATALYSTS; HYDROXIDES; CONVERSION; FRAMEWORKS;
D O I
10.1002/anie.201602237
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
To achieve sustainable production of H-2 fuel through water splitting, low-cost electrocatalysts for the hydrogen-evolution reaction (HER) and the oxygen-evolution reaction (OER) are required to replace Pt and IrO2 catalysts. Herein, for the first time, we present the interface engineering of novel MoS2/Ni3S2 heterostructures, in which abundant interfaces are formed. For OER, such MoS2/Ni3S2 heterostructures show an extremely low overpotential of ca. 218 mV at 10 mAcm(-2), which is superior to that of the state-of-the-art OER electrocatalysts. Using MoS2/Ni3S2 heterostructures as bifunctional electrocatalysts, an alkali electrolyzer delivers a current density of 10 mAcm(-2) at a very low cell voltage of ca. 1.56 V. In combination with DFT calculations, this study demonstrates that the constructed interfaces synergistically favor the chemisorption of hydrogen and oxygen-containing intermediates, thus accelerating the overall electrochemical water splitting.
引用
收藏
页码:6702 / 6707
页数:6
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