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MXene‐Induced Construction of SnS 2 Nano‐Arrays with Sulfur Vacancies for High‐Efficiency Photocatalytic CO 2 Reduction
Author(s) -
Wang Wei,
Wu Jingyi,
Chen Xudan,
Shen Xuhang,
Jin Xiaoyong,
Sun Yuxia,
Yan Changzeng,
Li Yuehui,
Zhang Peng
Publication year - 2025
Publication title -
chemistry – an asian journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.18
H-Index - 106
eISSN - 1861-471X
pISSN - 1861-4728
DOI - 10.1002/asia.202500086
Subject(s) - photocatalysis , materials science , sulfur , semiconductor , sulfide , chemical engineering , phase (matter) , nanotechnology , redox , metal , catalysis , optoelectronics , chemistry , metallurgy , biochemistry , organic chemistry , engineering
Abstract Solar‐driven CO 2 reduction has gained significant attention as a sustainable approach for CO 2 utilization, enabling the selective production of fuels and chemicals. SnS 2 , a non‐precious metal sulfide semiconductor, has great potential in photocatalytic CO 2 reduction due to its unique physicochemical properties. However, low electrical conductivity and susceptibility to aggregation of pure SnS 2 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 2 through electrostatic interactions and in situ solvothermal heating. Interconnected SnS 2 nano‐array with abundant sulfur vacancies was successfully prepared on MXene surface (Vs‐SnS 2 /MXene). This unique structure promotes the separation and migration of photogenerated charges and effectively inhibits electron‐hole recombination. Compared with pure SnS 2 , the average lifetime of photogenerated charges in Vs‐SnS 2 /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 SnS 2 (18.3 μmol⋅g −1 ⋅h −1 ), and showed excellent photocatalytic CO 2 reduction performance in gas‐solid‐phase reaction mode. In addition, Vs‐SnS 2 /MXene also showed excellent stability. The results showcased the transformative potential of integration strategies for designing high‐performance photocatalytic systems.

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