Metal–Sulfur Interfaces as the Primary Active Sites for Catalytic Hydrogenations

• Published in: Journal of the American Chemical Society 2024-04, Vol.146 (16), p.11542-11552
• Main Authors: Chen, Weiming, Che, Yixuan, Xia, Jing, Zheng, Lirong, Lv, Haifeng, Zhang, Jie, Liang, Hai-Wei, Meng, Xiangmin, Ma, Ding, Song, Weiguo, Wu, Xiaojun, Cao, Changyan
• Format: Article
• Language: English
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/jacs.4c02692

The determination of catalytically active sites is crucial for understanding the catalytic mechanism and providing guidelines for the design of more efficient catalysts. However, the complex structure of supported metal nanocatalysts (e.g., support, metal surface, and metal–support interface) still presents a big challenge. In particular, many studies have demonstrated that metal–support interfaces could also act as the primary active sites in catalytic reactions, which is well elucidated in oxide-supported metal nanocatalysts but is rarely reported in carbon-supported metal nanocatalysts. Here, we fill the above gap and demonstrate that metal–sulfur interfaces in sulfur-doped carbon-supported metal nanocatalysts are the primary active sites for several catalytic hydrogenation reactions. A series of metal nanocatalysts with similar sizes but different amounts of metal–sulfur interfaces were first constructed and characterized. Taking Ir for quinoline hydrogenation as an example, it was found that their catalytic activities were proportional to the amount of the Ir–S interface. Further experiments and density functional theory (DFT) calculations suggested that the adsorption and activation of quinoline occurred on the Ir atoms at the Ir–S interface. Similar phenomena were found in p-chloronitrobenzene hydrogenation over the Pt–S interface and benzoic acid hydrogenation over the Ru–S interface. All of these findings verify the predominant activity of metal–sulfur interfaces for catalytic hydrogenation reactions and contribute to the comprehensive understanding of metal–support interfaces in supported nanocatalysts.