富晶界Bi2WO6催化剂使1-丁烯氧化脱氢的分子氧和点阵氧协同活化

IF 13.1 1区 化学 Q1 CHEMISTRY, PHYSICAL
Bowen Liu, Chao Wan, Qinyang Zhao, Junjie Zhou, Jinyao Wang, Xiaoling Liu, Mingben Chong, Dang-guo Cheng* and Fengqiu Chen, 
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引用次数: 0

摘要

分子氧(O2)和表面晶格氧(O2 -)在晶界(GBs)同时活化的机理尚不清楚。在此,我们报告了富GB的Bi2WO6催化剂,通过可控的GB调制,实现了O2和晶格氧的双重活化。具体来说,GBs促进了氧空位的形成,增强了Bi和W中心的给电子能力,从而促进了O2的活化。同时,gb诱导的晶格应变激活了表面晶格氧,其密度与其反应活性呈正相关。然而,过高的GB密度会对催化性能产生不利影响,这强调了对最佳GB配置的需求。值得注意的是,过氧类物质(O22 -)和表面晶格氧(O2 -)在GBs上的协同作用使1-丁烯高效氧化脱氢(ODH)成为1,3-丁二烯。与缺乏gb的Bi2WO6催化剂相比,富gb的Bi2WO6催化剂的活性和选择性明显增强。这项工作为gb介导的双氧活化提供了重要的见解,并推进了对氧化非均相催化中结构-活性关系的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Grain Boundary-Rich Bi2WO6 Catalysts Enable Synergistic Activation of Molecular and Lattice Oxygen for Oxidative Dehydrogenation of 1-Butene

Grain Boundary-Rich Bi2WO6 Catalysts Enable Synergistic Activation of Molecular and Lattice Oxygen for Oxidative Dehydrogenation of 1-Butene

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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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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