镧系元素
铂金
甲醇
配体(生物化学)
材料科学
电子结构
组合化学
化学
化学工程
无机化学
催化作用
计算化学
有机化学
离子
受体
生物化学
工程类
作者
Shuai Zhang,Leilei Yin,Qian Liu,Guangtong Hai,Yaping Du
出处
期刊:ACS Nano
[American Chemical Society]
日期:2024-08-05
标识
DOI:10.1021/acsnano.4c08156
摘要
The ligand effect in alloy catalysts is one of the decisive parameters of the catalytic performance. However, the strong interrelation between the ligand effect and the geometric effect of the active atom and its neighbors as well as the systematic alteration of the microenvironment of the active site makes the active mechanism unclear. Herein, Pt3Tm, Pt3Yb, and Pt3Lu with a cubic crystal system (Pm-3m) were selected. With the difference of Pt−Pt interatomic distance within 0.02 Å, we minimize the geometric effect to realize the disentanglement of the system. Through precise characterization, due to the low electronegativity of Ln (Ln = Tm, Yb, and Lu) and the ligand effect in the alloy, the electronic structure of Pt is continuously optimized, which improves the electrochemical methanol oxidation reaction (MOR) performance. The Ln electronegativity has a linear relationship with the MOR performance, and Pt3Yb/C achieves a high mass activity of up to 11.61 A mgPt−1, which is the highest value reported so far in Pt-based electrocatalysts. The results obtained in this study provide fundamental insights into the mechanism of ligand effects on the enhancement of electrochemical activity in rare-earth nanoalloys.
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