Facilitating photocatalytic CO2 methanation via synergetic feed of photon-induced carriers and reactants over S-scheme BiVO4@TiO2 nanograss/needle arrays
{"title":"Facilitating photocatalytic CO2 methanation via synergetic feed of photon-induced carriers and reactants over S-scheme BiVO4@TiO2 nanograss/needle arrays","authors":"Dawei Zhao, Yimin Xuan, Chen Sun, Longzhen Zhang, Qibin Zhu, Xianglei Liu","doi":"10.1016/j.jcat.2024.115760","DOIUrl":null,"url":null,"abstract":"<div><p>Herein, a unique structure BiVO<sub>4</sub>@TiO<sub>2</sub> nanograss/needle arrays S-scheme heterojunction photocatalyst for CO<sub>2</sub> photoreduction reaction was created. The photocatalyst can drive electrons to the reactive spots spontaneously and continuously, which effectively tackles the problem of severe recombination and disordered migration of photogenerated carriers. Theoretical calculations and experimental results demonstrate that adding BMIM-BF<sub>4</sub> ionic liquid to generate BMIM-*CO<sub>2</sub> intermediate promotes CO<sub>2</sub> activation and enrichment of reactants concentration around the catalytic sites. Benefiting from the sufficient electron supply of catalytic sites and reinforced reactants supply in the interfacial microenvironment, the BiVO<sub>4</sub>@TiO<sub>2</sub> photocatalyst shows high selectivity and activity of CO<sub>2</sub>-to-CH<sub>4</sub> conversion. The CH<sub>4</sub> selectivity increased to 57.3 % (132.7 μmol m<sup>-2</sup>h<sup>−1</sup>) and the methanation activity was increased by 8.6 times in the 5.0 % BMIM-BF<sub>4</sub> aqueous solution. Significantly, the BiVO<sub>4</sub>@TiO<sub>2</sub> NNAs catalyst obtains a solar-to-fuels energy efficiency of ∼ 0.46 ‰ under ultraviolet-enhanced light sources without any sacrificial agent or co-catalyst. This work displays the relationship between reaction process factors (electron supply, CO<sub>2</sub> molecule, and proton supply) and CO<sub>2</sub> photoreduction activity and selectivity, giving new insight into achieving efficient CO<sub>2</sub> photoreduction conversion.</p></div>","PeriodicalId":346,"journal":{"name":"Journal of Catalysis","volume":"439 ","pages":"Article 115760"},"PeriodicalIF":6.5000,"publicationDate":"2024-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Catalysis","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0021951724004731","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Herein, a unique structure BiVO4@TiO2 nanograss/needle arrays S-scheme heterojunction photocatalyst for CO2 photoreduction reaction was created. The photocatalyst can drive electrons to the reactive spots spontaneously and continuously, which effectively tackles the problem of severe recombination and disordered migration of photogenerated carriers. Theoretical calculations and experimental results demonstrate that adding BMIM-BF4 ionic liquid to generate BMIM-*CO2 intermediate promotes CO2 activation and enrichment of reactants concentration around the catalytic sites. Benefiting from the sufficient electron supply of catalytic sites and reinforced reactants supply in the interfacial microenvironment, the BiVO4@TiO2 photocatalyst shows high selectivity and activity of CO2-to-CH4 conversion. The CH4 selectivity increased to 57.3 % (132.7 μmol m-2h−1) and the methanation activity was increased by 8.6 times in the 5.0 % BMIM-BF4 aqueous solution. Significantly, the BiVO4@TiO2 NNAs catalyst obtains a solar-to-fuels energy efficiency of ∼ 0.46 ‰ under ultraviolet-enhanced light sources without any sacrificial agent or co-catalyst. This work displays the relationship between reaction process factors (electron supply, CO2 molecule, and proton supply) and CO2 photoreduction activity and selectivity, giving new insight into achieving efficient CO2 photoreduction conversion.
期刊介绍:
The Journal of Catalysis publishes scholarly articles on both heterogeneous and homogeneous catalysis, covering a wide range of chemical transformations. These include various types of catalysis, such as those mediated by photons, plasmons, and electrons. The focus of the studies is to understand the relationship between catalytic function and the underlying chemical properties of surfaces and metal complexes.
The articles in the journal offer innovative concepts and explore the synthesis and kinetics of inorganic solids and homogeneous complexes. Furthermore, they discuss spectroscopic techniques for characterizing catalysts, investigate the interaction of probes and reacting species with catalysts, and employ theoretical methods.
The research presented in the journal should have direct relevance to the field of catalytic processes, addressing either fundamental aspects or applications of catalysis.