催化作用
羟甲基
金属
化学
滴定法
多相催化
电子转移
呋喃
动力学
化学工程
吸附
光化学
材料科学
物理化学
有机化学
物理
工程类
量子力学
作者
Enhui Du,Jie Yang,Liyuan Huai,Panpan Hao,Mingxin Lv,Zhilin Chen,Yuxiang Chen,Jian Zhang
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2024-12-13
卷期号:15 (1): 54-62
被引量:6
标识
DOI:10.1021/acscatal.4c05341
摘要
Strong metal–support interactions (SMSI) typically induce the migration of a coverage layer to the metal surface accompanied by electron transfer, forming a unique metal–support interface. This dual modification in geometric and electronic structures reconstructs the active surface, adjusting the activity and stability of the catalyst. However, identifying and quantifying such newly formed interfacial sites remains a challenge. Herein, by varying the reduction temperature to control the TiO2–x coverage on Au nanoparticles, the catalytic activity of Au/TiO2 in 2,5-bis(hydroxymethyl)furan (BHMF) oxidation shows a volcano-shaped trend. Combined thiol titration and poisoning kinetics analysis to quantify the ratio of interfacial to surface sites and normalize it to intrinsic activity, revealing that Au-TiO2–x interfacial sites positively contribute to catalytic performance. This study offers valuable insights into the active sites in heterogeneous catalytic systems with SMSI effects.
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