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增强的析氢反应调节二维CoO纳米片与CC基底之间的吸附性。

Enhanced hydrogen evolution reaction regulating the adsorbability between 2D CoO nanosheets and CC substrate.

作者信息

Wang Zhijun, Xiong Ying, Liu Limin, Xia Lili, Wang Yinfeng, Liu Xuexia

机构信息

College of Chemistry and Chemical Engineering, Jinggangshan University, Ji'an, Jiangxi 343009, PR China.

School of Forensic Medicine, Wannan Medical College, Wuhu 241002, Anhui, PR China.

出版信息

Phys Chem Chem Phys. 2023 Oct 4;25(38):26196-26202. doi: 10.1039/d3cp02122j.

Abstract

In recent years, bifunctional electrocatalysts, nanomaterials directly grown on the substrate for application towards the hydrogen evolution reaction (HER), have become of interest for sustainable and clean energy technologies. However, the influence of interfacial interactions between the electrode materials and substrate on device performance remains unclear and is rarely investigated. Herein, we report two-dimensional (2D) CoO nanosheets grown on carbon cloth (CC) (2D CoO/CC) to construct a hybrid electrocatalyst with a seamlessly conductive network. By a series of structure analyses, we recommend that the CoO nanosheets and CC are connected adsorption. The 2D CoO/CC nanosheets show superior HER performance to the commercial Pt/C and CoO(aq.)/CC nanosheets, including onset potentials of 2 mV, low overpotential of 22 mV at 10 mA cm and Tafel slope of 37 mV dec. The results of density functional theory (DFT) calculations reveal that the adsorbability plays an important role in determining the performance of the electrocatalysts for the HER. This work provides a new insight into the interfacial interactions between the electrode material and the substrate in electrochemical devices, and paves the way for the rational design and construction of high-performance electrochemical devices for practical energy applications.

摘要

近年来,作为用于析氢反应(HER)的直接生长在基底上的双功能电催化剂的纳米材料,已成为可持续和清洁能源技术的研究热点。然而,电极材料与基底之间的界面相互作用对器件性能的影响仍不明确,且鲜有研究。在此,我们报道了生长在碳布(CC)上的二维(2D)CoO纳米片(2D CoO/CC),以构建具有无缝导电网络的混合电催化剂。通过一系列结构分析,我们认为CoO纳米片和CC通过吸附相连。2D CoO/CC纳米片对析氢反应表现出优于商业Pt/C和CoO(水溶液)/CC纳米片的性能,包括2 mV的起始电位、在10 mA cm时22 mV的低过电位以及37 mV dec的塔菲尔斜率。密度泛函理论(DFT)计算结果表明,吸附性在决定析氢反应电催化剂的性能方面起着重要作用。这项工作为电化学器件中电极材料与基底之间的界面相互作用提供了新的见解,并为实际能源应用中高性能电化学器件的合理设计和构建铺平了道路。

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