Quantifying Interface-Dependent Active Sites Induced by Strong Metal–Support Interactions on Au/TiO<sub>2</sub> in 2,5-Bis(hydroxymethyl)furan Oxidation

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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Publication Details

Journal
ACS Catalysis
Published
2024-12-13
DOI
https://doi.org/10.1021/acscatal.4c05341
Citations
9
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
1.05

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article

Quantifying Interface-Dependent Active Sites Induced by Strong Metal–Support Interactions on Au/TiO2 in 2,5-Bis(hydroxymethyl)furan Oxidation

Liyuan Huai, Zhilin Chen, Panpan Hao, Mingxin Lv et al.
9 citations
ACS Catalysis
Catalytic Processes in Materials Science
1.05
article

Quantifying Interface-Dependent Active Sites Induced by Strong Metal–Support Interactions on Au/TiO2 in 2,5-Bis(hydroxymethyl)furan Oxidation

Liyuan Huai, Zhilin Chen, Panpan Hao, Mingxin Lv, Enhui Du, Yuxiang Chen, Jian Zhang, Jie Yang
article en
9 citations

Abstract

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.

ACS CatalysisVol. 15(1)
Chinese Academy of Sciences (CN), University of Chinese Academy of Sciences (CN), Ningbo Institute of Industrial Technology (CN)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, Ningbo Municipal Bureau of Science and Technology
Openalex Percentile: Top 20%
Catalytic Processes in Materials Science
1.05
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Quantifying Interface-Dependent Active Sites Induced by Strong Metal–Support Interactions on Au/TiO<sub>2</sub> in 2,5-Bis(hydroxymethyl)furan Oxidation — Liyuan Huai, Zhilin Chen, et al. · ACS Catalysis (2024) | TGRS Research Map | TGRS