脱氢
催化作用
氧气
化学
选择性
密度泛函理论
晶界
光化学
化学物理
材料科学
结晶学
计算化学
微观结构
有机化学
作者
Bowen Liu,Chao Wan,Qinyang Zhao,Junjie Zhou,Jinyao Wang,Xiaoling Liu,Mingben Chong,Dang‐guo Cheng,Fengqiu Chen
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-08-15
卷期号:15 (17): 15050-15059
标识
DOI:10.1021/acscatal.5c03123
摘要
The mechanistic understanding of the simultaneous activation of molecular oxygen (O2) and surface lattice oxygen (O2–) at grain boundaries (GBs) remains elusive. Herein, we report that GB-rich Bi2WO6 catalysts, engineered via controlled GB modulation, enable the dual activation of both the O2 and lattice oxygen species. Specifically, GBs facilitate the formation of oxygen vacancies and enhance the electron-donating ability of the Bi and W centers, thereby promoting O2 activation. Simultaneously, GB-induced lattice strain activates surface lattice oxygen, with the density of GBs positively correlating with its reactivity. However, an excessively high GB density can adversely affect catalytic performance, underscoring the need for an optimal GB configuration. Notably, the synergistic action between peroxo-like species (O22–) and surface lattice oxygen (O2–) at the GBs enables highly efficient oxidative dehydrogenation (ODH) of 1-butene to 1,3-butadiene. Compared with the GB-deficient counterpart, the GB-rich Bi2WO6 catalyst exhibits markedly enhanced activity and selectivity. This work provides critical insights into GB-mediated dual oxygen activation and advances the understanding of structure–activity relationships in oxidative heterogeneous catalysis.
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