FeS2 crystal lattice promotes the nanostructure and enhances the electrocatalytic performance of WS2 nanosheets for the oxygen evolution reaction

The control of surface elements and nanostructures is one of the effective ways to design and synthesize high performance catalysts. Herein, we, for the first time, prepare FeS2 crystal lattices on WS2 nanosheets (FeS2 CL@WS2 NS) by solvothermal methods for the oxygen evolution reaction (OER). The F...

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Published in:Dalton transactions : an international journal of inorganic chemistry 2020-07, Vol.49 (28), p.9804-9810
Main Authors: Zhang, Guoteng, Hao, Zaitao, Yin, Jie, Wang, Chen, Zhang, Jinghao, Zhao, Zhiyu, Denghu Wei, Zhou, Huawei, Li, Zhongcheng
Format: Article
Language:English
Subjects:
Catalytic activity
Charge transport
Chemical synthesis
Crystal lattices
Diffraction patterns
Durability
Electrocatalysts
Electron diffraction
Metal foams
Nanosheets
Nanostructure
Noble metals
Oxidation
Oxygen evolution reactions
Pyrite
Surface defects
Tungsten disulfide
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Summary:The control of surface elements and nanostructures is one of the effective ways to design and synthesize high performance catalysts. Herein, we, for the first time, prepare FeS2 crystal lattices on WS2 nanosheets (FeS2 CL@WS2 NS) by solvothermal methods for the oxygen evolution reaction (OER). The FeS2 CLs effectively prevent the oxidation and aggregation of WS2 nanosheets and increase the electrochemically active surface area. The abundant surface defect in the FeS2 CL@WS2 NS electrocatalyst reduces the stress between the crystal lattices of FeS2 and that of WS2. The overpotential (260 mV) of the FeS2 CL@WS2 NS electrocatalyst for the OER at a current density of 10 mA cm−2 is superior to those of WS2 NS/Ni foam (310 mV) and IrO2/Ni foam (300 mV) in 1.0 M KOH solution. An electrochemical–kinetic study shows that the Tafel slope of 54 mV per decade for the FeS2 CL@WS2 NS electrocatalyst is lower than those of WS2 NS (102 mV per decade) and IrO2/Ni foam (77 mV per decade). In addition, the charge transport resistor (2.3 Ω) of the FeS2 CL@WS2 NS electrocatalyst for the OER is smaller than that of WS2 NS. These faster kinetic properties, in turn, explain the high catalytic activity of the FeS2 CL@WS2 NS electrocatalyst for the OER. The XPS and HRTEM results of the post stability sample confirm that Fe2+ and W4+ are oxidized after durability measurement. Thus, we think that the FeS2 CL@WS2 NS electrocatalyst is a promising candidate for efficient, low-cost, and stable non-noble-metal-based OER electrocatalysts.
ISSN:1477-9226
1477-9234
DOI:10.1039/d0dt01660h