4.7 Article

Facilitating active species by decorating CeO2 on Ni3S2 nanosheets for efficient water oxidation electrocatalysis

Journal

CHINESE JOURNAL OF CATALYSIS
Volume 42, Issue 3, Pages 482-489

Publisher

SCIENCE PRESS
DOI: 10.1016/S1872-2067(20)63663-4

Keywords

Ni3S2-CeO2 nanosheet; Oxygen evolution reaction; Alkaline conditions; Density functional theory calculations

Funding

  1. National Natural Science Foundation of China [21801127, 21802104]
  2. Science and Technology Development Plan of Weifang City [2019GX002]
  3. Science and Technology Huimin Plan of Weifang High-tech Zone [2019KJHM10]

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In this study, a Ni3S2-CeO2 hybrid nanostructure was successfully developed via electrodeposition method, showing strong interfacial interaction and significantly enhanced water oxidation activity for Ni3S2 nanosheets. The electrocatalyst exhibited excellent electrochemical performance in 1.0 M KOH and demonstrated superior stability.
In the pursuit of stable, high performance Ni-based oxygen evolution reaction (OER) electrocatalysts, modifying the local chemical compositions or fabricating hybrid nanostructures to generate abundant interfaces for improving the water oxidation activity of electrocatalysts has emerged as an effective strategy. Herein, we report the facile development of a Ni3S2-CeO2 hybrid nanostructure via an electrodeposition method. Benefiting from the strong interfacial interaction between Ni3S2 and CeO2, the electron transfer is notably improved and the water oxidation activity of Ni3S2 nanosheets is significantly enhanced. In 1.0 M KOH, the Ni3S2-CeO2 electrocatalyst achieves a current density of 20 mA cm(-2) at a low overpotential of 264 mV, which is 92 mV lower than that of Ni3S2. Moreover, Ni3S2-CeO2 exhibits superior electrochemical stability. Density functional theory calculations demonstrate that the enhanced OER electrocatalytic performance of Ni3S2-CeO2 can be ascribed to an increase in the binding strength of the reaction intermediates at the Ni3S2-CeO2 interface. (C) 2021, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.

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