Atomically Precise Single Metal Oxide Cluster Catalyst with Oxygen‐Controlled Activity

纳米团簇 材料科学 催化作用 星团(航天器) 脱氢 氧化物 石墨烯 金属 纳米技术 价(化学) 费米能级 密度泛函理论 光化学 无机化学 计算化学 化学 有机化学 物理 量子力学 计算机科学 电子 程序设计语言 冶金
作者
Xinzhe Li,Na Guo,Zhongxin Chen,Xin Zhou,Xiaoxu Zhao,Yonghua Du,Lu Ma,Yiyun Fang,Haomin Xu,Huimin Yang,Wei Yu,Shangchen Lu,Mingjiao Tian,Qian He,Kian Ping Loh,Shibo Xi,Chun Zhang,Jiong Lu
出处
期刊:Advanced Functional Materials [Wiley]
卷期号:32 (25) 被引量:21
标识
DOI:10.1002/adfm.202200933
摘要

Abstract Single cluster catalysts (SCCs) consisting of atomically precise metal nanoclusters dispersed on supports represent a new frontier of heterogeneous catalysis. However, the ability to synthesize SCCs with high loading and to precisely introduce non‐metal atoms to further tune their catalytic activity and reaction scope of SCCs have been longstanding challenges. Here, a new interface confinement strategy is developed for the synthesis of a high density of atomically precise Ru oxide nanoclusters (Ru 3 O 2 ) on reduced graphene oxide (rGO), attributed to the suppression of diffusion‐induced metal cluster aggregation. Ru 3 O 2 /rGO exhibits a significantly enhanced activity for oxidative dehydrogenation of 1,2,3,4‐tetrahydroquinoline (THQ) to quinoline with a high yield ( ≈ 86%) and selectivity ( ≈ 99%), superior to Ru and RuO 2 nanoparticles, and homogeneous single/multiple‐site Ru catalysts. In addition, Ru 3 O 2 /rGO is also capable of efficiently catalyzing more complex oxidative reactions involving three reactants. The theoretical calculations reveal that the presence of two oxygen atoms in the Ru 3 O 2 motif not only leads to a weak hydrogen bonding interaction between the THQ reactant and the active site, but also dramatically depletes the density of states near the Fermi level, which is attributed to the increased positive valence state of Ru and the enhanced oxidative activity of the Ru 3 O 2 cluster for hydrogen abstraction.
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