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Electrocatalytic hydrogen evolution reaction on sulfur-deficient MoS_2 nanostructures

机译:缺硫MoS_2纳米结构上的电催化析氢反应

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摘要

Molybdenum disulfide (MoS2) is a 2D layered structured material with a Mo:S of 1:2 and is a great attention seeker for hydrogen production through water-splitting. In the present work, we prepared nanostructured MoSx with different sulfur molar concentrations (x = 2, 1, 0.5) through a one-step hydrothermal method. The decrease in sulfur concentration resulted in a new phase that is MoO3 with a Mo:S of 1:0.5. The structural, morphological, and optical properties of all the samples were studied through X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Fourier Transform Infrared spectroscopy (FTIR), and Ultraviolet-Visible (UV-Vis) spectroscopy, respectively. Moreover, the electrochemical behavior was studied using cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), linear sweep voltammetry (LSV), and Tafel slope. Optimum properties were observed for Mo:S (1:1) with an onset potential of 96 mV, an overpotential of 130 mV for hydrogen evolution reaction (HER) coupled with a specific capacitance of 889 F/g and low charge transfer resistance of 43 U. Further, it was noted that the electrocatalytic activity of MoS1 was better than that of the composite and bare MoO3. It is proposed that the excellent electrochemical activity arises from sulfur vacancies which provide active sites for HER and a free path for ions to flow through the material. (c) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:二硫化钼(MoS2)是一种二维层状结构材料,Mo:S为1:2,是水分解制氢的热门产品。本工作采用一步水热法制备了不同硫摩尔浓度(x = 2, 1, 0.5)的纳米结构MoSx。硫浓度的降低导致了MoO3的新相,Mo:S为1:0.5。分别采用X射线衍射(XRD)、扫描电子显微镜(SEM)、傅里叶变换红外光谱(FTIR)和紫外-可见(UV-Vis)光谱研究了样品的结构、形貌和光学性质。此外,采用循环伏安法(CV)、电化学阻抗谱法(EIS)、线性扫描伏安法(LSV)和塔菲尔斜率研究了其电化学行为。Mo:S (1:1) 的起始电位为 96 mV,析氢反应 (HER) 的过电位为 130 mV,比电容为 889 F/g,电荷转移电阻低至 43 U,观察到最佳性能。此外,注意到MoS1的电催化活性优于复合和裸MoO3。有人提出,优异的电化学活性来自硫空位,硫空位为HER提供了活性位点,并为离子流过材料提供了自由路径。(c) 2021 Hydrogen Energy Publications LLC.,由爱思唯尔有限公司出版。保留所有权利。

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