{"title":"MXene-Induced Construction of SnS<sub>2</sub> Nano-Arrays with Sulfur Vacancies for High-Efficiency Photocatalytic CO<sub>2</sub> Reduction.","authors":"Wei Wang, Jingyi Wu, Xudan Chen, Xuhang Shen, Xiaoyong Jin, Yuxia Sun, Changzeng Yan, Yuehui Li, Peng Zhang","doi":"10.1002/asia.202500086","DOIUrl":null,"url":null,"abstract":"<p><p>Solar-driven CO<sub>2</sub> reduction has gained significant attention as a sustainable approach for CO<sub>2</sub> utilization, enabling the selective production of fuels and chemicals. SnS<sub>2</sub>, a non-precious metal sulfide semiconductor, has great potential in photocatalytic CO<sub>2</sub> reduction due to its unique physicochemical properties. However, low electrical conductivity and susceptibility to aggregation of pure SnS<sub>2</sub> lead to a high charge recombination rate and hinder the photocatalytic efficiency. In this study, we report that single/few-layered MXene induces ordered growth of SnS<sub>2</sub> through electrostatic interactions and in situ solvothermal heating. Interconnected SnS<sub>2</sub> nano-array with abundant sulfur vacancies was successfully prepared on MXene surface (Vs-SnS<sub>2</sub>/MXene). This unique structure promotes the separation and migration of photogenerated charges and effectively inhibits electron-hole recombination. Compared with pure SnS<sub>2</sub>, the average lifetime of photogenerated charges in Vs-SnS<sub>2</sub>/MXene increased by 45.6 %. Meanwhile, its CO production rate reached 47.6 μmol⋅g<sup>-1</sup>⋅h<sup>-1</sup>, which was 2.6-fold higher than that of pure SnS<sub>2</sub> (18.3 μmol⋅g<sup>-1</sup>⋅h<sup>-1</sup>), and showed excellent photocatalytic CO<sub>2</sub> reduction performance in gas-solid-phase reaction mode. In addition, Vs-SnS<sub>2</sub>/MXene also showed excellent stability. The results showcased the transformative potential of integration strategies for designing high-performance photocatalytic systems.</p>","PeriodicalId":145,"journal":{"name":"Chemistry - An Asian Journal","volume":" ","pages":"e202500086"},"PeriodicalIF":3.5000,"publicationDate":"2025-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry - An Asian Journal","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1002/asia.202500086","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Solar-driven CO2 reduction has gained significant attention as a sustainable approach for CO2 utilization, enabling the selective production of fuels and chemicals. SnS2, a non-precious metal sulfide semiconductor, has great potential in photocatalytic CO2 reduction due to its unique physicochemical properties. However, low electrical conductivity and susceptibility to aggregation of pure SnS2 lead to a high charge recombination rate and hinder the photocatalytic efficiency. In this study, we report that single/few-layered MXene induces ordered growth of SnS2 through electrostatic interactions and in situ solvothermal heating. Interconnected SnS2 nano-array with abundant sulfur vacancies was successfully prepared on MXene surface (Vs-SnS2/MXene). This unique structure promotes the separation and migration of photogenerated charges and effectively inhibits electron-hole recombination. Compared with pure SnS2, the average lifetime of photogenerated charges in Vs-SnS2/MXene increased by 45.6 %. Meanwhile, its CO production rate reached 47.6 μmol⋅g-1⋅h-1, which was 2.6-fold higher than that of pure SnS2 (18.3 μmol⋅g-1⋅h-1), and showed excellent photocatalytic CO2 reduction performance in gas-solid-phase reaction mode. In addition, Vs-SnS2/MXene also showed excellent stability. The results showcased the transformative potential of integration strategies for designing high-performance photocatalytic systems.
期刊介绍:
Chemistry—An Asian Journal is an international high-impact journal for chemistry in its broadest sense. The journal covers all aspects of chemistry from biochemistry through organic and inorganic chemistry to physical chemistry, including interdisciplinary topics.
Chemistry—An Asian Journal publishes Full Papers, Communications, and Focus Reviews.
A professional editorial team headed by Dr. Theresa Kueckmann and an Editorial Board (headed by Professor Susumu Kitagawa) ensure the highest quality of the peer-review process, the contents and the production of the journal.
Chemistry—An Asian Journal is published on behalf of the Asian Chemical Editorial Society (ACES), an association of numerous Asian chemical societies, and supported by the Gesellschaft Deutscher Chemiker (GDCh, German Chemical Society), ChemPubSoc Europe, and the Federation of Asian Chemical Societies (FACS).