丙烯
脱氢
丙烷
催化作用
选择性
化学
无机化学
金属
多相催化
烷烃
光化学
氧气
材料科学
乙烯
石油化工
氧原子
钴
碳氢化合物
化学工程
有机化学
作者
Q Zhang,Yuming Li,Xinxin Tian,Vita A. Kondratenko,Elizaveta A. Fedorova,Tong Yang,Xiangnong Ding,Dmitry E. Doronkin,Dan Zhao,Chun Deng,Huihui Chen,Shutao Xu,Anna Zanina,Stephan Bartling,Tatiana Otroshchenko,Yajun Wang,Zhen Zhao,Chunming Xu,G. C. Jiang,Haijun Jiao
出处
期刊:Nature Catalysis
[Nature Portfolio]
日期:2026-02-23
卷期号:9 (3): 269-280
被引量:8
标识
DOI:10.1038/s41929-026-01488-w
摘要
Abstract Understanding the nature of active sites in heterogeneous catalysts and how to create them purposefully opens up the possibility of tailored catalyst design. Here we report mixed-valence subnanometre CoO x clusters, consisting of a few metallic Co 0 atoms on top of Co 2+ , bound to a silicalite-1 support through lattice oxygen atoms as active species for non-oxidative propane dehydrogenation (PDH) to propene. Compared with commercial-like PtSn/Al 2 O 3 and K-CrO x /Al 2 O 3 catalysts also tested in the present study, as well as other state-of-the-art Pt- or Co-containing PDH catalysts, this system showed high on-stream stability, propene productivity and selectivity at close-to-equilibrium propane conversion. Moreover, it showed durability in a series of PDH/regeneration cycles between 500 and 550 °C. The performance of this catalyst system is industrially attractive in terms of propene production costs, as suggested by our initial techno-economic assessment.
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