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甲酸氧化和脱氢中 AgPd 纳米合金的原子应变和催化性能。

Atomic strain and catalytic properties of formate oxidation and dehydrogenation in AgPd nanoalloys.

机构信息

State Key Laboratory of Solidification Processing, Northwestern Polytechnical University, Xi'an, 710072, China.

School of Materials Science and Engineering, Northwestern Polytechnical University, Xi'an, 710072, China.

出版信息

Nanoscale. 2023 Jul 6;15(26):11131-11140. doi: 10.1039/d3nr01221b.

Abstract

Formate is a promising hydrogen carrier for safe storage and transport and a fuel for direct formate fuel cells. However, the sluggish kinetics of catalysts for formate dehydrogenation (FDH) and oxidation reactions (FORs) significantly limit the potential applications of formate. Strain effects can effectively modulate catalytic properties by altering the electronic structure. Nevertheless, the lack of theoretical principles to quantify atomic strain and its effects on FDH and FOR catalytic activity has made experimental efforts laborious. In this work, we establish a database of atomic strain distributions for AgPd nanoalloys, reveals that the presence of compressive strain at the edges and corners and compressive strain exerted on the surface of Ag@Pd nanoalloys, particularly the one with an icosahedral shape, boost the FDH and FOR catalytic activity by shifting down the d-band center, thus weakening the adsorption of key intermediate H. This study provides a theoretical perspective on the development and use of formate as a hydrogen carrier and fuel.

摘要

甲酸盐作为一种有前途的储氢和输氢载体,以及直接甲酸盐燃料电池的燃料,受到了广泛的关注。然而,甲酸盐脱氢(FDH)和氧化反应(FOR)催化剂的缓慢动力学限制了其潜在应用。应变效应对催化剂的电子结构进行有效的调节,从而改变其催化性能。然而,缺乏定量原子应变及其对 FDH 和 FOR 催化活性影响的理论原理,使得实验工作变得非常困难。在这项工作中,我们建立了一个 AgPd 纳米合金原子应变分布数据库,揭示了在边缘和角落处存在压缩应变以及在 Ag@Pd 纳米合金表面存在压缩应变,特别是在具有二十面体形状的纳米合金中,通过向下移动 d 带中心,削弱了关键中间体 H 的吸附,从而提高了 FDH 和 FOR 的催化活性。本研究为甲酸作为储氢和燃料载体的开发和应用提供了理论视角。

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