Chao An, Yu Nie, Jian-Hua Mei, Xin Tan, Zhuofeng Hu*, Jinhua Ye and Tao Yu*,
{"title":"调节电子分布加速CO2光催化还原为C2H4","authors":"Chao An, Yu Nie, Jian-Hua Mei, Xin Tan, Zhuofeng Hu*, Jinhua Ye and Tao Yu*, ","doi":"10.1021/acsnano.5c0154810.1021/acsnano.5c01548","DOIUrl":null,"url":null,"abstract":"<p >How to promote the efficiency of C–C coupling is a bottleneck problem in the process of the photocatalytic reduction of CO<sub>2</sub> to C<sub>2</sub>H<sub>4</sub>. Herein, a highly efficient photocatalyst for converting CO<sub>2</sub> into C<sub>2</sub>H<sub>4</sub> (with a yield of ∼12.45 μmol h<sup>–1</sup> and a selectivity of ∼94.5%) was synthesized by implanting Ga atoms in CoS<sub>2</sub>. Ga promotes the formation of neighboring sulfur vacancies on pristine CoS<sub>2</sub>, which induces a highly asymmetric distribution of electrons around Co atoms due to the delocalization of electrons around sulfur vacancies. Theoretical calculations prove that the asymmetric electron distribution enhances the attraction between adjacent atoms, leading to a shortened distance between adjacent Co<sup>δ+</sup> (δ = 2, 3) atoms from 3.91 to 2.49 Å. The coexistence of adjacent Co<sup>δ+</sup> makes the <i>d</i>-band center closer to the Fermi level, which is conducive to the strong adsorption of *CO and subsequent *COCO dimerization. The asymmetric electronic structure between adjacent Co<sup>δ+</sup> atoms on Ga-CoS<sub>2</sub> provides a lower activation barrier for C–C coupling, thereby significantly promoting C<sub>2</sub>H<sub>4</sub> formation. This study proposes a strategy to modulate the selectivity of the photocatalytic reduction of CO<sub>2</sub> to C<sub>2</sub>H<sub>4</sub>.</p>","PeriodicalId":21,"journal":{"name":"ACS Nano","volume":"19 16","pages":"15912–15923 15912–15923"},"PeriodicalIF":16.0000,"publicationDate":"2025-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Regulating the Electron Distribution to Accelerate the Photocatalytic Reduction of CO2 to C2H4\",\"authors\":\"Chao An, Yu Nie, Jian-Hua Mei, Xin Tan, Zhuofeng Hu*, Jinhua Ye and Tao Yu*, \",\"doi\":\"10.1021/acsnano.5c0154810.1021/acsnano.5c01548\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >How to promote the efficiency of C–C coupling is a bottleneck problem in the process of the photocatalytic reduction of CO<sub>2</sub> to C<sub>2</sub>H<sub>4</sub>. Herein, a highly efficient photocatalyst for converting CO<sub>2</sub> into C<sub>2</sub>H<sub>4</sub> (with a yield of ∼12.45 μmol h<sup>–1</sup> and a selectivity of ∼94.5%) was synthesized by implanting Ga atoms in CoS<sub>2</sub>. Ga promotes the formation of neighboring sulfur vacancies on pristine CoS<sub>2</sub>, which induces a highly asymmetric distribution of electrons around Co atoms due to the delocalization of electrons around sulfur vacancies. Theoretical calculations prove that the asymmetric electron distribution enhances the attraction between adjacent atoms, leading to a shortened distance between adjacent Co<sup>δ+</sup> (δ = 2, 3) atoms from 3.91 to 2.49 Å. The coexistence of adjacent Co<sup>δ+</sup> makes the <i>d</i>-band center closer to the Fermi level, which is conducive to the strong adsorption of *CO and subsequent *COCO dimerization. The asymmetric electronic structure between adjacent Co<sup>δ+</sup> atoms on Ga-CoS<sub>2</sub> provides a lower activation barrier for C–C coupling, thereby significantly promoting C<sub>2</sub>H<sub>4</sub> formation. This study proposes a strategy to modulate the selectivity of the photocatalytic reduction of CO<sub>2</sub> to C<sub>2</sub>H<sub>4</sub>.</p>\",\"PeriodicalId\":21,\"journal\":{\"name\":\"ACS Nano\",\"volume\":\"19 16\",\"pages\":\"15912–15923 15912–15923\"},\"PeriodicalIF\":16.0000,\"publicationDate\":\"2025-04-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Nano\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsnano.5c01548\",\"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}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Nano","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsnano.5c01548","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}
Regulating the Electron Distribution to Accelerate the Photocatalytic Reduction of CO2 to C2H4
How to promote the efficiency of C–C coupling is a bottleneck problem in the process of the photocatalytic reduction of CO2 to C2H4. Herein, a highly efficient photocatalyst for converting CO2 into C2H4 (with a yield of ∼12.45 μmol h–1 and a selectivity of ∼94.5%) was synthesized by implanting Ga atoms in CoS2. Ga promotes the formation of neighboring sulfur vacancies on pristine CoS2, which induces a highly asymmetric distribution of electrons around Co atoms due to the delocalization of electrons around sulfur vacancies. Theoretical calculations prove that the asymmetric electron distribution enhances the attraction between adjacent atoms, leading to a shortened distance between adjacent Coδ+ (δ = 2, 3) atoms from 3.91 to 2.49 Å. The coexistence of adjacent Coδ+ makes the d-band center closer to the Fermi level, which is conducive to the strong adsorption of *CO and subsequent *COCO dimerization. The asymmetric electronic structure between adjacent Coδ+ atoms on Ga-CoS2 provides a lower activation barrier for C–C coupling, thereby significantly promoting C2H4 formation. This study proposes a strategy to modulate the selectivity of the photocatalytic reduction of CO2 to C2H4.
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.