脱氢
纳米片
催化作用
硅醇
铂金
材料科学
烧结
化学工程
乙烯
路易斯酸
沸石
钛
焦炭
无机化学
化学
纳米技术
有机化学
冶金
工程类
作者
Ying Pan,Antara Bhowmick,Wei Wu,Yuan Zhang,Yuxia Diao,Aiguo Zheng,Chen Zhang,Rongxuan Xie,Zixiao Liu,Jianqiang Meng,Dongxia Liu
标识
DOI:10.1021/acscatal.1c02676
摘要
Studies of stable catalysts for non-oxidative dehydrogenation of ethane (NDE) have been challenged by coke deposition from side reactions and thermal sintering of active species. Herein, we report a catalyst mechanism that overcomes both challenges to enable highly stable, active, and selective NDE. The catalyst is made of subnanometric platinum (Pt) species (i.e., single atoms and clusters) habituated on a two-dimensional (2D) multilamellar titanium silicalite-1 (M-TS-1) zeolite nanosheet support (i.e., Pt/M-TS-1). The ultrathin (∼3 nm) M-TS-1 nanosheets provide high external surface areas, high terminal silanol/titanol (−OH) groups, and weak Lewis acid sites. The first two characteristics enhance molecular transport and Pt dispersion in the catalyst support. The third characteristic prohibits side reactions to avoid coking and create strong Pt–support interaction, leading to well-dispersed Pt species against thermal sintering. The M-TS-1 nanosheet-supported Pt catalyst exhibited durable catalytic activity and high ethylene selectivity in the NDE.
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