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用于析氢的磷掺杂碳@MoP电催化剂的电化学表面重构

Electrochemical Surface Restructuring of Phosphorus-Doped Carbon@MoP Electrocatalysts for Hydrogen Evolution.

作者信息

Jiang Huimin, Yan Liting, Zhang Shuo, Zhao Yanchao, Yang Xue, Wang Yameng, Shen Jianxing, Zhao Xuebo, Wang Lianzhou

机构信息

School of Materials Science and Engineering, Qilu University of Technology (Shandong Academy of Sciences), No. 3501, Daxue Road, Changqing District, Jinan, 250353, People's Republic of China.

College of Chemical Engineering, China University of Petroleum (East China), Huangdao District, No. 66, West Changjiang Road, Qingdao, 266580, People's Republic of China.

出版信息

Nanomicro Lett. 2021 Oct 21;13(1):215. doi: 10.1007/s40820-021-00737-w.

Abstract

The hydrogen evolution reaction (HER) through electrocatalysis is promising for the production of clean hydrogen fuel. However, designing the structure of catalysts, controlling their electronic properties, and manipulating their catalytic sites are a significant challenge in this field. Here, we propose an electrochemical surface restructuring strategy to design synergistically interactive phosphorus-doped carbon@MoP electrocatalysts for the HER. A simple electrochemical cycling method is developed to tune the thickness of the carbon layers that cover on MoP core, which significantly influences HER performance. Experimental investigations and theoretical calculations indicate that the inactive surface carbon layers can be removed through electrochemical cycling, leading to a close bond between the MoP and a few layers of coated graphene. The electrons donated by the MoP core enhance the adhesion and electronegativity of the carbon layers; the negatively charged carbon layers act as an active surface. The electrochemically induced optimization of the surface/interface electronic structures in the electrocatalysts significantly promotes the HER. Using this strategy endows the catalyst with excellent activity in terms of the HER in both acidic and alkaline environments (current density of 10 mA cm at low overpotentials, of 68 mV in 0.5 M HSO and 67 mV in 1.0 M KOH).

摘要

通过电催化的析氢反应(HER)对于清洁氢燃料的生产具有广阔前景。然而,在该领域中,设计催化剂结构、控制其电子性质以及操纵其催化位点是一项重大挑战。在此,我们提出一种电化学表面重构策略,以协同设计用于HER的磷掺杂碳@MoP电催化剂。开发了一种简单的电化学循环方法来调节覆盖在MoP核上的碳层厚度,这对HER性能有显著影响。实验研究和理论计算表明,通过电化学循环可以去除无活性的表面碳层,从而使MoP与几层包覆的石墨烯紧密结合。MoP核提供的电子增强了碳层的附着力和电负性;带负电荷的碳层作为活性表面。电催化剂中表面/界面电子结构的电化学诱导优化显著促进了HER。使用该策略使催化剂在酸性和碱性环境中的HER方面均具有优异活性(在低过电位下,电流密度为10 mA cm,在0.5 M HSO中为68 mV,在1.0 M KOH中为67 mV)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f5a/8531175/d98e4182cbd4/40820_2021_737_Fig1_HTML.jpg

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