4.6 Article

In situ growth of Ag2S quantum dots on SnS2 nanosheets with enhanced charge separation efficiency and CO2 reduction performance

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 10, Issue 13, Pages 7291-7299

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ta10463b

Keywords

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Funding

  1. National Research Foundation of Korea (NRF) - Korean government [2020R1A4A1017737]
  2. National Research Foundation of Korea [2020R1A4A1017737] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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SnS2 nanosheets with excellent light-driven CO production rate were obtained through a facile hydrothermal method. After modification with Ag2S quantum dots, the nanocomposites exhibited significantly higher CO/CH4 production rate than pristine SnS2. The study provides new opportunities for exploring efficient photocatalytic CO2 reduction systems.
Photocatalytic CO2 reduction to carbon fuels is a desirable solution to replace conventional fossil fuels. Herein, SnS2 nanosheets (NSs) were fabricated via a facile hydrothermal method, and they transformed to thinner and more homogeneous dispersions with gradually increasing hydrothermal temperature to 200 degrees C because of the hydrothermal self-exfoliation effect. The obtained SnS2-200 NSs displayed optimum photoelectrochemical properties with an excellent light-driven CO production rate. After modification with Ag2S quantum dots (QDs) by an in situ cation-exchange reaction, the SnS2/Ag2S-50 nanocomposites bridged with Sn-S-Ag bonds exhibited 7-fold higher CO/CH4 (48.7/3.18 mu mol g(-1) h(-1)) production than pristine SnS2-200. The intimate contact between SnS2-200 NSs and Ag2S through co-shared S atom layers facilitates the photoelectron transfer to the SnS2-200 surface and then to Ag2S QDs for CO2 reduction. This study presents a novel example for heterostructure design and offers new opportunities for exploring efficient photocatalytic CO2 reduction systems for solar-to-chemical energy conversion.

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