期刊
JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 576, 期 -, 页码 264-279出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2020.05.025
关键词
MgIn2S4/CdS composite; 2D/1D heterostructure; Density functional theory; Wastewater treatment; H-2 production
资金
- Pearl River S&T Nova Program of Guangzhou [201710010134]
- Key R&D project in Hunan [2018SK2048]
- National Natural Science Foundation of China (NSFC) [51541801, 51521006]
A novel visible-light-driven 2D/1D MgIn2S4/CdS catalyst with heterostructure was fabricated for sewage treatment and energy conversion. In this study, MIS/CdS-0.3 heterostructure catalyst displayed the remarkable photocatalytic performance, which could reduce about 100% of Cr(VI) within 30 min and decompose approximately 95.98% of oxytetracycline (OTC) after 60 min. Meanwhile, the degradation details and possible decomposition pathways for OTC solution were further verified by 3D EEM and LC-MS. Moreover, the as-obtained 2D/1D MgIn2S4/CdS hybrid composites signally promoted the hydrogen evolved in the light illumination at 420 nm. Meanwhile, some consequences based on various characterization technologies confirmed that the significant photo-induced charge separation rate is a crucial factor in the enhancement of photocatalytic capacity. The intimate contact and the formation of heterostructure between 2D MgIn2S4 nanosheets and 1D CdS nanorods with matched band gaps were beneficial for charge migration. Moreover, the band structures and the density of states (DOS) of MgIn2S4 and CdS were obtained based on density functional theory (DFT). In addition, the results of cycling experiments, XRD spectra and PL showed that the composition and performance of the composite are well-maintained, suggesting the great recyclability and stability. This work indicated that developing a 2D/1D heterostructure photocatalyst offers a cracking approach to enhance the photocatalytic property of semiconductor-based catalysts for pollutant removal and the generation of clean energy. (C) 2020 Elsevier Inc. All rights reserved.
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