Defect engineered 2D mesoporous Mo-Co-O nanosheets with crystalline-amorphous composite structure for efficient oxygen evolution

Two-dimensional (2D) mesoporous metal-oxide (hydroxide) nanomaterials with defects are promising towards the realization of efficient electrocatalysis. Herein, we report a facile and effective one-pot solvothermal route to synthesize mesoporous Mo x -Co-O hybrid nanosheets (NSs) which is composed of...

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Veröffentlicht in:Science China materials 2022-12, Vol.65 (12), p.3470-3478
Hauptverfasser: He, Chuansheng, Hu, Xiaochen, Wang, Jia, Bu, Lingzheng, Zhan, Changhong, Xu, Bingyan, Li, Leigang, Li, Yunchao, Huang, Xiaoqing
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Sprache:eng
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Zusammenfassung:Two-dimensional (2D) mesoporous metal-oxide (hydroxide) nanomaterials with defects are promising towards the realization of efficient electrocatalysis. Herein, we report a facile and effective one-pot solvothermal route to synthesize mesoporous Mo x -Co-O hybrid nanosheets (NSs) which is composed of crystalline Mo 4 O 11 and amorphous cobalt hydroxide. Due to the corrosion of 1-octylamine at high temperatures, abundant mesoporous holes are created in situ over the Mo x -Co-O hybrid NSs during the solvothermal process, which is beneficial to increasing the electrochemical surface area. The dimension of the Mo x -Co-O NSs, size of mesoporous and the concentration of defects can be easily modulated by controlling the molar ratio of Mo/Co. Electrochemical measurements reveal that the 2D mesoporous Mo x -Co-O NSs show an excellent activity for the oxygen evolution reaction with the highest catalytic activity of η 10 = 276 mV at 10 mA cm −2 in 1 mol L −1 KOH. Enhanced adsorption of intermediates and abundant oxygen vacancies achieved by appropriate Mo doping are the two main factors that contribute to the excellent catalytic activity of Mo 0.2 -Co-O NSs. This work, with the construction of 2D metal-oxide (hydroxide) crystalline-amorphous nanomaterials possessing abundant holes, oxygen vacancies and enhanced adsorption of intermediates, provides important insight on the design of more efficient catalysts.
ISSN:2095-8226
2199-4501
DOI:10.1007/s40843-022-2098-x