异质结
光催化
材料科学
罗丹明B
量子点
可见光谱
光化学
化学工程
半导体
纳米技术
光电子学
催化作用
化学
有机化学
工程类
作者
Xiaorui Zhang,Gui‐Peng Yang,Chuang Han,Jian Yang,Zikang Zeng,Zhuoran Xiong,Jin Jia,Ke Sa,Hanlin Ye,Yujun Liang
标识
DOI:10.1016/j.colsurfa.2023.131184
摘要
Fabricating zero-dimensional/two-dimensional (0D/2D) heterojunctions is considered to be an efficient approach to boost the transfer/separation of photo-induced charges. Herein, a novel visible-light-driven 0D/2D CdZnS/SnIn4S8 heterostructures were successfully prepared by in situ growth of 0D CdZnS quantum dots on the surface of 2D SnIn4S8 nanosheets. Such unique dimensional coupling structure with large specific surface area and appropriate pore size of CdZnS/SnIn4S8 expedited the mass transfer rate of interfacial catalytic reaction. Under visible light irradiation, the as-prepared heterojunctions not only showed excellent photocatalytic oxidation activity towards the degradation of tetracycline and rhodamine B, but also exhibited outstanding performance of reducing H2O to hydrogen. The significantly enhanced photocatalytic capability could be attributed to the strong light absorption, highly effective separation and migration of charges, and abundant reactive sites, which encouraged by the uniformly and intimately contacted interface between CdZnS quantum dots and SnIn4S8 nanosheets. Moreover, the possible degradation pathway and ecological toxicity during rhodamine B degradation were also investigated and discussed in detail. This study will provide valuable information for the development of transition metal sulfide-based photocatalytic heterostructures for solving environmental pollution and energy shortage.
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