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通过引入无序非晶相打破高度有序的PtPbBi金属间化合物以促进电催化析氢和醇氧化反应

Breaking Highly Ordered PtPbBi Intermetallic with Disordered Amorphous Phase for Boosting Electrocatalytic Hydrogen Evolution and Alcohol Oxidation.

作者信息

Feng Fukai, Ma Chaoqun, Han Sumei, Ma Xiao, He Caihong, Zhang Huaifang, Cao Wenbin, Meng Xiangmin, Xia Jing, Zhu Lijie, Tian Yahui, Wang Qi, Yun Qinbai, Lu Qipeng

机构信息

State Key Laboratory of Nuclear Power Safety Technology and Equipment, University of Science and Technology Beijing, Beijing, 100083, China.

School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing, 100083, China.

出版信息

Angew Chem Int Ed Engl. 2024 Jun 17;63(25):e202405173. doi: 10.1002/anie.202405173. Epub 2024 May 14.

DOI:10.1002/anie.202405173
PMID:38622784
Abstract

Constructing amorphous/intermetallic (A/IMC) heterophase structures by breaking the highly ordered IMC phase with disordered amorphous phase is an effective way to improve the electrocatalytic performance of noble metal-based IMC electrocatalysts because of the optimized electronic structure and abundant heterophase boundaries as active sites. In this study, we report the synthesis of ultrathin A/IMC PtPbBi nanosheets (NSs) for boosting hydrogen evolution reaction (HER) and alcohol oxidation reactions. The resulting A/IMC PtPbBi NSs exhibit a remarkably low overpotential of only 25 mV at 10 mA cm for the HER in an acidic electrolyte, together with outstanding stability for 100 h. In addition, the PtPbBi NSs show high mass activities for methanol oxidation reaction (MOR) and ethanol oxidation reaction (EOR), which are 13.2 and 14.5 times higher than those of commercial Pt/C, respectively. Density functional theory calculations demonstrate that the synergistic effect of amorphous/intermetallic components and multimetallic composition facilitate the electron transfer from the catalyst to key intermediates, thus improving the catalytic activity of MOR. This work establishes a novel pathway for the synthesis of heterophase two-dimensional nanomaterials with high electrocatalytic performance across a wide range of electrochemical applications.

摘要

通过用无序的非晶相破坏高度有序的金属间化合物相来构建非晶态/金属间化合物(A/IMC)异相结构,是提高贵金属基金属间化合物电催化剂电催化性能的有效方法,因为其具有优化的电子结构和丰富的异相边界作为活性位点。在本研究中,我们报道了用于促进析氢反应(HER)和醇氧化反应的超薄A/IMC PtPbBi纳米片(NSs)的合成。所得的A/IMC PtPbBi NSs在酸性电解质中对HER在10 mA cm时仅表现出25 mV的极低过电位,并且具有100小时的出色稳定性。此外,PtPbBi NSs对甲醇氧化反应(MOR)和乙醇氧化反应(EOR)表现出高的质量活性,分别比商业Pt/C高13.2倍和14.5倍。密度泛函理论计算表明,非晶态/金属间化合物组分和多金属组成的协同效应促进了电子从催化剂向关键中间体的转移,从而提高了MOR的催化活性。这项工作为合成具有高电催化性能的异相二维纳米材料建立了一条新途径,可广泛应用于各种电化学领域。

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