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通过镀铂策略在铂/富电子位点上诱导协同效应:在析氢反应中产生超高电流密度

Inducing a Synergistic Effect on Pt/Electron-Rich Sites via a Platinization Strategy: Generating Hyper-High Current Density in Hydrogen Evolution Reaction.

作者信息

Wang Shanshan, Zhao Qin, Ma Quanlei, Gan Rong, Ran Yiling, Fang Weizhen, Wang Cuijuan, Fang Ling, Feng Qingguo, Zhang Yan, Wang Dingsheng, Li Yadong

机构信息

School of Chemistry, Southwest Jiaotong University, Chengdu 610031, China.

Analytical and Testing Center of Southwest Jiaotong University, Chengdu 610031, China.

出版信息

Nano Lett. 2024 Sep 11;24(36):11286-11294. doi: 10.1021/acs.nanolett.4c03031. Epub 2024 Aug 30.

Abstract

Herein, we propose a platinization strategy for the preparation of Pt/X catalysts with low Pt content on substrates possessing electron-rich sites (Pt/X: X = CoO, NiO, CeO, Covalent Organic Framework (COF), etc.). In examples with inorganic and organic substrates, respectively, Pt/CoO possesses remarkable catalytic ability toward HER, achieving a current density at an overpotential of 500 mV that is 3.22 times higher than that of commercial Pt/C. It was also confirmed by using Raman spectroscopy that the enhancement of catalytic activity was achieved after platinization of the COF, with a reduction of overpotential from 231 to 23 mV at 10 mA cm. Density functional theory (DFT) reveals that the improved catalytic activity of Pt/CoO and Pt/COF originated from the re-modulation of Pt on the electronic structure and the synergistic effect of the interfacial Pt/electron-rich sites. This work provides a rapid synthesis strategy for the synthesis of low-content Pt catalysts for electrocatalytic hydrogen production.

摘要

在此,我们提出了一种铂化策略,用于在具有富电子位点的基底上制备低铂含量的Pt/X催化剂(Pt/X:X = CoO、NiO、CeO、共价有机框架(COF)等)。在分别以无机和有机基底为例的实验中,Pt/CoO对析氢反应具有显著的催化能力,在过电位为500 mV时的电流密度比商业Pt/C高3.22倍。通过拉曼光谱也证实,COF铂化后催化活性增强,在10 mA cm时过电位从231 mV降低到23 mV。密度泛函理论(DFT)表明,Pt/CoO和Pt/COF催化活性的提高源于Pt对电子结构的重新调制以及界面Pt/富电子位点的协同效应。这项工作为合成用于电催化制氢的低含量铂催化剂提供了一种快速合成策略。

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