催化作用
格式化
离解(化学)
合金
材料科学
X射线吸收精细结构
扫描透射电子显微镜
纳米颗粒
介孔材料
X射线光电子能谱
密度泛函理论
吸附
无机化学
化学工程
结晶学
物理化学
光谱学
透射电子显微镜
化学
纳米技术
有机化学
计算化学
冶金
工程类
物理
量子力学
作者
Guoxiang Yang,Yasutaka Kuwahara,Kohsuke Mori,Catherine Louis,Hiromi Yamashita
标识
DOI:10.1021/acs.jpcc.0c10962
摘要
It is intriguing yet challenging to synthesize high-performance heterogeneous catalysts for carbon dioxide (CO2) hydrogenation reactions. The excellent catalytic performance of heterogeneous catalysts has attracted widespread attention recently. Herein, a series of Pd–Cu alloy nanoparticles confined within mesoporous hollow carbon spheres (MHCS) were prepared and tested as catalysts for CO2 hydrogenation to formate. The optimized Pd2Cu14–N@MHCS catalyst, which was obtained with about 1 wt % Pd loading and a Pd/Cu molar ratio of 2:14 by the coreduction method, exhibited high activity for CO2 hydrogenation to formate, showing a high turnover number (TON) of 1432 at 100 °C after 24 h. Scanning transmission electron microscopy (HAADF-STEM) and X-ray absorption fine structure spectroscopy (XAFS) analyses revealed that when the Pd/Cu molar ratio was 2:14, the Pd atoms were well isolated by the Cu atoms via a Pd–Cu alloy. Density functional theory (DFT) calculations demonstrated that the PdCu2(111) surface enhanced not only the dissociation of H2 but also the attack of the C atoms of the adsorbed HCO3– on Cu atoms by the dissociated H atoms on Pd atoms. This was attributed to an electron transfer from Cu to Pd in the alloy.
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