NH2-MoS2@BP的制备及其电催化析氢性能研究

余泓1, 郭军1,2*, 张丹2

化工新型材料 ›› 2023, Vol. 51 ›› Issue (3) : 209 -214.

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化工新型材料 ›› 2023, Vol. 51 ›› Issue (3) : 209-214. DOI: 10.19817/j.cnki.issn1006-3536.2023.03.037
科学研究

NH2-MoS2@BP的制备及其电催化析氢性能研究

    余泓1, 郭军1,2*, 张丹2
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Preparation of NH2-MoS2@BP and its electrocatalytic hydrogen evolution performance

  • Yu Hong1, Guo Jun1,2, Zhang Dan2
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摘要

采用液相剥离法制备二维黑磷烯纳米片(BP),将其与改性的MoS2通过水热法合成得到NH2-MoS2@BP,利用XRD、SEM、TEM对材料的形貌结构进行表征,并通过三电极体系测试析氢性能。结果表明,NH2-MoS2@BP形貌呈片层结构,BP在催化剂中颗粒很小且均匀的分布在其表面。在0.5mol/L H2SO4溶液中,当电流密度为10mA/cm2时,氨基的加入使催化剂的析氢过电位降低了20mV,BP的加入使催化剂的析氢过电位降低了90mV,塔菲尔斜率为95mV/dec,表明BP有利于改善改性MoS2的催化性能。此外,连续的循环伏安测试表明NH2-MoS2@BP具有较好的电催化稳定性。

Abstract

Two-dimensional black phosphorous nanosheets (BP) were prepared by liquid phase stripping method,and were further reacted with modified MoS2 to synthesize NH2-MoS2@BP by hydrothermal method.The morphology and structure of the materials were characterized by XRD,SEM and TEM,and the hydrogen evolution performance was tested by three-electrode system.The results showed that the morphology of NH2-MoS2@BP presented a lamellar structure,and the particles of BP in the catalyst were very small and evenly distributed on the surface.In 0.5mol/L H2SO4 solution,when the current density was 10 mA·cm-2,the addition of amino group reduced the hydrogen evolution overpotential of the catalyst by 20mV.The addition of BP reduced the hydrogen evolution overpotential of the catalyst by 90mV,and the Tafel slope was 95mV·dec-1,indicating that BP was beneficial to improve the catalytic performance of the modified MoS2.In addition,continuous cyclic voltammetry test exhibited that NH2-MoS2@BP had good electrocatalytic stability.

关键词

改性二硫化钼 / 黑磷烯 / 电催化剂 / 析氢

Key words

modified molybdenum disulfide / black phosphorous / electrocatalyst / hydrogen evolution

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NH2-MoS2@BP的制备及其电催化析氢性能研究[J]. 化工新型材料, 2023, 51(3): 209-214 DOI:10.19817/j.cnki.issn1006-3536.2023.03.037

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基金资助

国家自然科学基金(21862005);贵州省科技厅计划(黔科合LH字、黔合基础、黔科合支撑、黔科合平台人才,[2017]7336、[2019]1457、[2019]2835、[2018]5769);贵州省教育厅青年科技人才成长(黔科合KY字[2018]126);中低品位磷矿及其共伴生资源高效利用国家重点实验室开发课题(WFKF2017-03)

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