文献类型：期刊文献

英文题名：Dual Pt atoms stabilized by an optimized coordination environment for propane dehydrogenation

作者：Hu, Ping[1];Chang, Qing-Yu[1];Zhang, Wei[1];Yang, Ming-Lei[1];Lei, Ming[1];Chen, De[2];Zhou, Xing-Gui[1];Sui, Zhi-Jun[1];Zhu, Yi-An[1]

机构：[1]East China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, UNILAB, Shanghai 200237, Peoples R China;[2]Norwegian Univ Sci & Technol, Dept Chem Engn, N-9491 Trondheim, Norway

年份：2024

卷号：429

外文期刊名：JOURNAL OF CATALYSIS

收录：;WOS:【SCI-EXPANDED(收录号:WOS:001339310300001)】；

基金：This work is supported by the National Natural Science Foundation of China (91645122, 22073027, and 22278130) . The computational time provided by the Notur project is highly acknowledged.

语种：英文

外文关键词：Coordination environments; Dual Pt atoms; Single Pt atom; Reduced TiO2; DFT; Propane dehydrogenation

摘要：Tailoring atomically dispersed catalysts by various methods has been the subject of intense current research in heterogeneous catalysis. In this work, the structural stability and propane dehydrogenation performance of PtTiO2 catalysts with single, dual, and triple Pt atoms doped on the reduced TiO2 surface have been examined. Experimental results indicate the atomically dispersed Pt is thermally very stable and shows exceptionally high activity (TOFpropane = 4.93 s(-1)) and selectivity (similar to 98.5 %) for the dehydrogenation reaction. The recently developed machine-learning-based SSW-NN method is then employed to explore the global potential energy surface of the atomically dispersed Pt atom-doped TiO2, which suggests that the single and dual Pt atoms can be tightly held by the vacancies created on the reduced transition-metal oxide, as confirmed by DFT + U calculated energetics. After that, advanced characterization techniques are used in conjunction with microkinetic analysis to establish the quantitative structure-activity relationships. It is found that the dual-Pt-atom structure with two Pt atoms embedded in adjacent Ti and O vacancies is the only active ensemble that dramatically promotes the C-H bond activation and hydrogen recombination, as compared to single Pt atoms accommodated by either Ti or O vacancies. These results provide new and direct evidence in support of the idea that specific function can be imparted to specific active sites by tuning their coordination environments, which makes it possible to tailor the catalytic properties of metal oxides to a particular reaction such as propane dehydrogenation.