{"title":"Periodic Frustrated Lewis Pairs on Bimetallic Oxide Semiconductors for CO2 Adsorption and Photocatalytic Conversion","authors":"Linqun Yu, Qiushi Wang, Chunqiang Zhuang, Jin-Dou Huang, Yongan Zhu, Xuedong Jing, Yuhang Guo, Ye-Xiang Tong, Zhenyi Zhang","doi":"10.1021/acsnano.4c17231","DOIUrl":null,"url":null,"abstract":"Lewis acids (LAs) or Lewis bases (LBs) have been recognized as crucial catalytically active sites for enhancing the adsorption and conversion of inert CO<sub>2</sub>. However, engineering of periodic frustrated Lewis pairs (PFLPs) on the surfaces of semiconductor photocatalysts presents significant challenges, and the synergistic mechanism of PFLPs in CO<sub>2</sub> photoreduction remains unclear. In this study, we propose a strategy that utilizes periodic oxygen vacancies to engineer dual-metallic PFLPs on bimetallic oxide semiconductor surfaces. We employ SrNb<sub>2</sub>O<sub>6–<i>x</i></sub> as a model photocatalyst to elucidate the synergistic effect of PFLPs on CO<sub>2</sub> photoreduction. Within each FLP unit, the LA (Sr<sup>2+</sup>) captures an O atom from CO<sub>2</sub> while the LB (Nb<sup>4+</sup>) engages in an interaction with the C atom and concurrently facilitates transfer of photoinduced electrons from SrNb<sub>2</sub>O<sub>6–<i>x</i></sub> to adsorbed CO<sub>2</sub>. Thus, SrNb<sub>2</sub>O<sub>6–<i>x</i></sub> with the PFLPs-enriched surface exhibits ultrahigh CO<sub>2</sub> adsorption and a low energy barrier for CO desorption. Under focused sunlight irradiation, SrNb<sub>2</sub>O<sub>6–<i>x</i></sub> demonstrates nearly 100% selectivity in converting CO<sub>2</sub> to CO at a rate of 25.5 μmol g<sup>–1</sup> h<sup>–1</sup>. This study presents a method for designing metal PFLPs on inorganic photocatalyst surfaces, which could contribute to the practical implementation of CO<sub>2</sub> photoreduction.","PeriodicalId":21,"journal":{"name":"ACS Nano","volume":"49 1","pages":""},"PeriodicalIF":15.8000,"publicationDate":"2025-02-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Nano","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acsnano.4c17231","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Lewis acids (LAs) or Lewis bases (LBs) have been recognized as crucial catalytically active sites for enhancing the adsorption and conversion of inert CO2. However, engineering of periodic frustrated Lewis pairs (PFLPs) on the surfaces of semiconductor photocatalysts presents significant challenges, and the synergistic mechanism of PFLPs in CO2 photoreduction remains unclear. In this study, we propose a strategy that utilizes periodic oxygen vacancies to engineer dual-metallic PFLPs on bimetallic oxide semiconductor surfaces. We employ SrNb2O6–x as a model photocatalyst to elucidate the synergistic effect of PFLPs on CO2 photoreduction. Within each FLP unit, the LA (Sr2+) captures an O atom from CO2 while the LB (Nb4+) engages in an interaction with the C atom and concurrently facilitates transfer of photoinduced electrons from SrNb2O6–x to adsorbed CO2. Thus, SrNb2O6–x with the PFLPs-enriched surface exhibits ultrahigh CO2 adsorption and a low energy barrier for CO desorption. Under focused sunlight irradiation, SrNb2O6–x demonstrates nearly 100% selectivity in converting CO2 to CO at a rate of 25.5 μmol g–1 h–1. This study presents a method for designing metal PFLPs on inorganic photocatalyst surfaces, which could contribute to the practical implementation of CO2 photoreduction.
期刊介绍:
ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.