甲醇
电催化剂
接口(物质)
金属
材料科学
化学
化学工程
无机化学
电化学
冶金
电极
有机化学
物理化学
工程类
分子
吉布斯等温线
作者
Bartłomiej M. Szyja,Joanna Zasada
标识
DOI:10.1021/acs.cgd.3c01466
摘要
In this work, we present a theoretical investigation of the SrTiO3 perovskite-supported Pd catalyst in the methanol electro-oxidation reaction. In order to determine the metal-support interactions, we designed a system consisting of a Pd (100) double layer supported on one of the two possible terminations of the (100) perovskite surface. These terminations are characterized by different reducibilities of the layers directly interacting with the Pd bilayer and result in the difference in the stability of the surface-bound intermediates. Despite the fact that the Pd surface is identical in terms of geometry, we observed significant differences in the overpotential required for the reaction; in the case of TiO2 termination, the overpotential has been determined to be 0.68 V, while in the case of SrO termination, it amounts to as much as 1.35 V. We further investigate the charge transfers within the components of the system and the geometries of the intermediates to unravel the role of the electron structure on the overall efficiency of the process.
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