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首页> 外文期刊>Applied Surface Science >The direct Z-scheme Cd_xZn_(1-x)S nanorods-Fe_2O_3 quantum dots heterojunction/reduced graphene oxide nanocomposites for photocatalytic degradation and photocatalytic hydrogen evolution
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The direct Z-scheme Cd_xZn_(1-x)S nanorods-Fe_2O_3 quantum dots heterojunction/reduced graphene oxide nanocomposites for photocatalytic degradation and photocatalytic hydrogen evolution

机译:直接Z-SchemeD CD_XZN_(1-X)S纳米棒-2O_3量子点异质结/杂交氧化物纳米复合材料,用于光催化降解和光催化氢气进化

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摘要

In this paper, we reported a simple hydrothermal strategy to prepare the direct Z-scheme CdxZn1-xS nanorods-Fe2O3 quantum dots heterojunction/reduced graphene oxide (CdxZn1-xS-FG) nanocomposites as the multifunctional photocatalysts for photocatalytic degradation of organic dyes and photocatalytic hydrogen evolution. By adjusting the molar mass ratio of Cd2+ and Zn2+ ions from 9:1 to 1:9, the bandgap of the CdxZn1-xS-FG nano composites can be turned from 2.23 to 3.49 eV. The Cd0.3Zn0.7S-FG nanocomposites exhibited the highest H-2 evolution rate of 26.8 mmol h(-1) g(-1) and the highest degradation efficiency of 97.32% towards MB in 120 min under the visible light irradiation. The excellent photocatalytic activity can be attributed to the high-efficiency transportation and separation of the photogenerated electron-hole pairs, more catalytic active sites and large specific surface area. The mechanism of the photocatalytic hydrogen evolution and photocatalytic degradation had been investigated by ultraviolet photoelectron spectroscopy, scavenging experiment, and UV-Vis absorption spectra. Considering the unique structure, morphology, and excellent photocatalytic performances of the CdxZn1-xS-FG nanocomposites, it will become a burning star in the field of photocatalysis.
机译:在本文中,我们报道了一种简单的水热策略,制备直接Z-SchemeDXZN1-XS纳米棒-FE2O3量子点异质结/还原的氧化物(CDXZN1-XS-FG)纳米复合材料作为有机染料和光催化的光催化降解的多功能光催化剂氢气进化。通过将CD2 +和Zn2 +离子的摩尔质量比调节为9:1至1:9,CDXZN1-XS-FG纳米复合材料的带隙可以从2.23到3.49eV转动。 CD0.3ZN0.7S-FG纳米复合材料显示出最高的H-2进化速率为26.8mmol H(-1)g(-1),并且在可见光照射下120分钟的MB朝MB的最高降解效率为97.32%。优异的光催化活性可以归因于光静效应的电子 - 空穴对,更催化的活性位点和大的比表面积的高效运输和分离。通过紫外光电子光谱,清除实验和UV-Vis吸收光谱研究了光催化氢进化和光催化降解的机理。考虑到CDXZN1-XS-FG纳米复合材料的独特结构,形态和优异的光催化性能,它将成为光催化领域的燃烧星。

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