光催化
光降解
罗丹明B
材料科学
降级(电信)
催化作用
氧化物
二硫化钼
化学工程
光化学
复合材料
化学
计算机科学
有机化学
冶金
电信
工程类
作者
Yuanzhi Hong,Lan Yang,Yuwen Tian,Xue Lin,Enli Liu,Wei Sun,Yanan Liu,Chengzhang Zhu,Xiangyu Li,Junyou Shi
标识
DOI:10.1016/j.jtice.2023.104862
摘要
Currently, the solar-driven photocatalytic H2 evolution coupled with pollutants photodegradation is a promising strategy for the developing sustainable solar energy and environmental processes. Thus, development of the high-efficiency, robust, and low-cost photocatalysts for photocatalytic H2 production combined with pollutants photodegradation in a one-pot system is urgently needed. In this study, the two-dimension (2D) thin-layered molybdenum disulfide (MoS2) was decorated on the surface of three-dimension (3D) cube-like indium oxide (In2O3) to forming the new 2D/3D MoS2/In2O3 composites by a hydrothermal method. The photoreactivities of as-obtained MoS2/In2O3 composites were carefully studied by the photocatalytic H2 generation coupled with dye (Rhodamine B, RhB) degradation. The photocatalysis results suggested that all of the as-formed composites could greatly boost photocatalytic H2 production simultaneous with RhB degradation performance with respect to pristine In2O3. Moreover, it was found that the 10 wt% MoS2 content of sample (10-MoS2/In2O3) showed the optimum activities both in H2 generation and RhB photodegradation under simulated sunlight irradiation. The H2 evolved rate of 10-MoS2/In2O3 was 15.5 μmol/g/h, which was 77.5 times higher than that of pure In2O3. Meanwhile, The RhB photodegraded efficiency of 10-MoS2/In2O3 could achieve nearly 100%, and the total organic carbon (TOC) removal rate was 12.1-folds greater than that of single In2O3. Eventually, the charge carrier's transferring from In2O3 photocatalyst to MoS2 co-catalyst was evidenced by density functional theory (DFT) calculations, and further a dramatical improvement of photocatalytic mechanism was proposed.
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