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石墨基底上原位生长纳米MoS作为析氢反应催化剂

In Situ Growth of Nano-MoS on Graphite Substrates as Catalysts for Hydrogen Evolution Reaction.

作者信息

Zhao Yifan, Zhang Mingyang, Zhao Huimin, Zeng Zhiqiang, Xia Chaoqun, Yang Tai

机构信息

School of Materials Science and Engineering, Hebei University of Technology, Tianjin 300130, China.

Tianjin Key Laboratory of Laminating Fabrication and Interface Control Technology for Advanced Materials, Hebei University of Technology, Tianjin 300130, China.

出版信息

Materials (Basel). 2023 Jun 27;16(13):4627. doi: 10.3390/ma16134627.

Abstract

In order to synthesize a high-efficiency catalytic electrode for hydrogen evolution reactions, nano-MoS was deposited in situ on the surface of graphite substrates via a one-step hydrothermal method. The effects of the reactant concentration on the microstructure and the electrocatalytic characteristics of the nano-MoS catalyst layers were investigated in detail. The study results showed that nano-MoS sheets with a thickness of about 10 nm were successfully deposited on the surface of the graphite substrates. The reactant concentration had an important effect on uniform distribution of the catalyst layers. A higher or lower reactant concentration was disadvantageous for the electrochemical performance of the nano-MoS catalyst layers. The prepared electrode had the best electrocatalytic activity when the thiourea concentration was 0.10 mol·L. The minimum hydrogen evolution reaction overpotential was 196 mV ( = 10 mV·cm) and the corresponding Tafel slope was calculated to be 54.1 mV·dec. Moreover, the prepared electrode had an excellent cycling stability, and the microstructure and the electrocatalytic properties of the electrode had almost no change after 2000 cycles. The results of the present study are helpful for developing low-cost and efficient electrode material for hydrogen evolution reactions.

摘要

为了合成用于析氢反应的高效催化电极,通过一步水热法将纳米MoS原位沉积在石墨基底表面。详细研究了反应物浓度对纳米MoS催化剂层微观结构和电催化特性的影响。研究结果表明,成功地在石墨基底表面沉积了厚度约为10 nm的纳米MoS片。反应物浓度对催化剂层的均匀分布有重要影响。反应物浓度过高或过低都不利于纳米MoS催化剂层的电化学性能。当硫脲浓度为0.10 mol·L时,制备的电极具有最佳的电催化活性。析氢反应的最小过电位为196 mV(j = 10 mV·cm-2),计算得到的相应塔菲尔斜率为54.1 mV·dec-1。此外,制备的电极具有优异的循环稳定性,经过2000次循环后,电极的微观结构和电催化性能几乎没有变化。本研究结果有助于开发用于析氢反应的低成本高效电极材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0800/10342737/9f39f2fa1e14/materials-16-04627-g001.jpg

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