Precisely engineered type II ZnO-CuS based heterostructure: A visible light driven photocatalyst for efficient mineralization of organic dyes

光催化 可见光谱 异质结 亚甲蓝 纳米复合材料 降级(电信) 材料科学 矿化(土壤科学) 兴奋剂 化学工程 载流子 纳米颗粒 光化学 催化作用 纳米技术 化学 光电子学 有机化学 计算机科学 氮气 工程类 电信
作者
Bhawna Kaushik,Sneha Yadav,Pooja Rana,Pooja Rana,Kanika Solanki,Deepti Rawat,Ritika Sharma
出处
期刊:Applied Surface Science [Elsevier]
卷期号:590: 153053-153053 被引量:31
标识
DOI:10.1016/j.apsusc.2022.153053
摘要

• Construction of sustainable type-II Fe 3 O 4 @SiO 2 @ZnO-CuS heterojunction via simple chemical route. • Synergism of CuS nanoplates and magnetic ZnO in visible light mediated degradation process. • Magnetic ZnO-CuS degrades cationic dyes within 18 min under energy efficient LEDs. • GC–MS analysis was conducted to deduce the degradation pathway of methylene blue. • High photodegradation ability of nanocomposites retained even after five recycles. Herein, type-II band alignment of magnetic ZnO/CuS has been achieved by assembling p-type CuS nanoparticles on n-type ZnO heterostructures to accomplish the photocatalytic degradation of two colored cationic dyes, namely, methylene blue (MB) and toluidine blue (TB). The material exhibited excellent photocatalytic efficiency towards MB and TB with 93% and 87.5% degradation in just 16 and 18 min respectively. The efficacy of doped photocatalyst (FSZCS) was found to be 6 times higher than the undoped material (Fe 3 O 4 @SiO 2 @ZnO; FSZ) whereas pristine CuS degraded only 50% of the dye sample under identical conditions. Therefore, the dramatic enhancement of the photocatalytic degradation performance could be attributed to the synergetic effect created by doping CuS over magnetic ZnO nanocomposites which extended the photoresponse of ZnO by driving the entire degradation process under visible light irradiation and also reducing the charge recombination rate. The plausible mechanistic pathway and identification of degradation products was discussed in detail on the basis of scavenger studies as well as GC–MS analysis. Furthermore, the designed catalyst could be recycled and reused up to 5 runs without any significant decrease in its photocatalytic activity. The reported procedure exhibited multiple advances as it proceeded by utilizing renewable household LEDs as power source at room temperature without the use of any additional oxidant under neutral pH conditions thus, paving a strong path towards sustainable, green and responsible chemistry.
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