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Insight into l-cysteine-assisted growth of Cu2S nanoparticles on exfoliated MoS2 nanosheets for effective photoreduction removal of Cr(VI)

Journal 2020 · IF 6.182 · 发表于 2020 年 3 月 28 日
作者: Yiming Zhang,Xiaoyan Yang,Yonglin Wang,Peng Zhang,Dan Liu,Yongwei Li,Zhouzheng Jin,Bhekie B. Mamba,Alex T. Kuvarega,Jianzhou Gui
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摘要

For obtaining ultra-fine Cu 2 S nanoparticles with reduced recombination of their photogenerated electron/hole pairs, in-situ growth of Cu 2 S nanoparticles on exfoliated MoS 2 nanosheets was achieved in this study. We have exhaustively studied l -cysteine in-situ conjugation with sulfur defects on the surface of MoS 2 nanosheets, which makes particle-level superlattice structured Cu 2 S nanoparticles (average 6.2 nm) well disperse on MoS 2 nanosheets. Further, XPS and Raman analysis confirm that the intense interfacial effects are formed between Cu 2 S and MoS 2 for the 2-Cu 2 S-MoS 2 composite, which significantly promote separation of photogenerated electron-hole pairs and prolong their lifetime, as shown by PL and TRPL. As a result, 2-Cu 2 S-MoS 2 exhibits the fastest photoreduction rate of Cr(VI) (0.0058 min −1 ) under visible light irradiations, which are almost 8.3 times and 2.9 times higher than that of MoS 2 nanosheets (0.0007 min −1 ) and pure Cu 2 S (0.002 min −1 ), respectively. Meanwhile, 2-Cu 2 S-MoS 2 also possesses an optimal composite proportion between Cu 2 S and MoS 2 , which presents outstanding photocatalytic activity among series of x-Cu 2 S-MoS 2 composites. The photoreduction mechanism of Cr(VI) is investigated in detail. As a matter of fact, l -cysteinecoupled with sulfur defects on MoS 2 nanosheets could produce the coordination inner heterojunction interface of 2-Cu 2 S-MoS 2 samples, which greatly improves migration efficiency of photoinduced carriers and ultimately endows it outstanding photoreduction activities. Furthermore, the strategy was extended to fabricate CdS-MoS 2 and ZnS-MoS 2 heterojunctions, implying that this strategy is of promising potentials for designing more active metal sulfides heterojunction photocatalysts.

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