TY - JOUR
T1 - Interface Engineering of MoS2/Ni3S2Heterostructures for Highly Enhanced Electrochemical Overall-Water-Splitting Activity
AU - Zhang, Jian
AU - Wang, Tao
AU - Pohl, Darius
AU - Rellinghaus, Bernd
AU - Dong, Renhao
AU - Liu, Shaohua
AU - Zhuang, Xiaodong
AU - Feng, Xinliang
N1 - Publisher Copyright:
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
PY - 2016/6/1
Y1 - 2016/6/1
N2 - To achieve sustainable production of H2fuel through water splitting, low-cost electrocatalysts for the hydrogen-evolution reaction (HER) and the oxygen-evolution reaction (OER) are required to replace Pt and IrO2catalysts. Herein, for the first time, we present the interface engineering of novel MoS2/Ni3S2heterostructures, in which abundant interfaces are formed. For OER, such MoS2/Ni3S2heterostructures show an extremely low overpotential of ca. 218 mV at 10 mA cm-2, which is superior to that of the state-of-the-art OER electrocatalysts. Using MoS2/Ni3S2heterostructures as bifunctional electrocatalysts, an alkali electrolyzer delivers a current density of 10 mA cm-2at 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.
AB - To achieve sustainable production of H2fuel through water splitting, low-cost electrocatalysts for the hydrogen-evolution reaction (HER) and the oxygen-evolution reaction (OER) are required to replace Pt and IrO2catalysts. Herein, for the first time, we present the interface engineering of novel MoS2/Ni3S2heterostructures, in which abundant interfaces are formed. For OER, such MoS2/Ni3S2heterostructures show an extremely low overpotential of ca. 218 mV at 10 mA cm-2, which is superior to that of the state-of-the-art OER electrocatalysts. Using MoS2/Ni3S2heterostructures as bifunctional electrocatalysts, an alkali electrolyzer delivers a current density of 10 mA cm-2at 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.
KW - electrocatalysts
KW - interface engineering
KW - molybdenum disulfide
KW - nickel sulfide
KW - water splitting
UR - http://www.scopus.com/inward/record.url?scp=84992297638&partnerID=8YFLogxK
U2 - 10.1002/anie.201602237
DO - 10.1002/anie.201602237
M3 - 文章
AN - SCOPUS:84992297638
SN - 1433-7851
VL - 55
SP - 6702
EP - 6707
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 23
ER -