{"title":"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","authors":"Bowen Liu, Chao Wan, Qinyang Zhao, Junjie Zhou, Jinyao Wang, Xiaoling Liu, Mingben Chong, Dang-guo Cheng* and Fengqiu Chen, ","doi":"10.1021/acscatal.5c03123","DOIUrl":null,"url":null,"abstract":"<p >The mechanistic understanding of the simultaneous activation of molecular oxygen (O<sub>2</sub>) and surface lattice oxygen (O<sup>2–</sup>) at grain boundaries (GBs) remains elusive. Herein, we report that GB-rich Bi<sub>2</sub>WO<sub>6</sub> catalysts, engineered via controlled GB modulation, enable the dual activation of both the O<sub>2</sub> 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 O<sub>2</sub> 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 (O<sub>2</sub><sup>2–</sup>) and surface lattice oxygen (O<sup>2–</sup>) 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 Bi<sub>2</sub>WO<sub>6</sub> 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.</p>","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":"15 17","pages":"15050–15059"},"PeriodicalIF":13.1000,"publicationDate":"2025-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Grain Boundary-Rich Bi2WO6 Catalysts Enable Synergistic Activation of Molecular and Lattice Oxygen for Oxidative Dehydrogenation of 1-Butene\",\"authors\":\"Bowen Liu, Chao Wan, Qinyang Zhao, Junjie Zhou, Jinyao Wang, Xiaoling Liu, Mingben Chong, Dang-guo Cheng* and Fengqiu Chen, \",\"doi\":\"10.1021/acscatal.5c03123\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The mechanistic understanding of the simultaneous activation of molecular oxygen (O<sub>2</sub>) and surface lattice oxygen (O<sup>2–</sup>) at grain boundaries (GBs) remains elusive. Herein, we report that GB-rich Bi<sub>2</sub>WO<sub>6</sub> catalysts, engineered via controlled GB modulation, enable the dual activation of both the O<sub>2</sub> 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 O<sub>2</sub> 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 (O<sub>2</sub><sup>2–</sup>) and surface lattice oxygen (O<sup>2–</sup>) 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 Bi<sub>2</sub>WO<sub>6</sub> 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.</p>\",\"PeriodicalId\":9,\"journal\":{\"name\":\"ACS Catalysis \",\"volume\":\"15 17\",\"pages\":\"15050–15059\"},\"PeriodicalIF\":13.1000,\"publicationDate\":\"2025-08-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Catalysis \",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acscatal.5c03123\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acscatal.5c03123","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
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.
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.