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Photocatalytic hydrogen evolution and antibiotic degradation by S-scheme ZnCo_2S_4/TiO_2

机译:S型ZnCo_2S_4/TiO_2光催化析氢和抗生素降解

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摘要

In this study, ZnCo_2S_4 (ZCS) nanoparticles were coupled on the surface of TiO_2 by simple solvothermal method to form S-scheme heterojunction. Compared with ZCS and TiO_2, the photocatalytic performance of ZCS/TiO_2 under simulated sunlight is significantly improved, and its hydrogen evolution efficiency reaches 5580 μmol·g~(-1)·h~(-1) with the apparent quantum efficiency (AQY) up to 11.5 at 420 nm, which is 88.3 times and 54.3 times that of TiO_2 and ZCS, respectively. Moreover, ZCS/TiO_2 also has excellent performance in the photocatalytic degradation of tetracycline (TC). The enhancement of photocatalytic performance of ZCS/TiO_2 is mainly due to S-scheme heterojunction. On the one hand, the S-scheme electron transfer path not only improves the electron-hole separation efficiency, but also improves the charge transfer efficiency. On the other hand, ZCS significantly enhances the visible light absorption of ZCS/TiO_2. The photocatalytic mechanism and S-scheme heterojunction structure is confirmed by XPS, EPR, ultraviolet photoelectron spectroscopy (UPS) and energy band structure. This work provides a new idea for designing and constructing S-scheme heterojunction to improve the performance of photocatalytic hydrogen evolution and TC degradation.
机译:本研究采用简单的溶剂热法将ZnCo_2S_4(ZCS)纳米颗粒耦合在TiO_2表面,形成S型异质结。与ZCS和TiO_2相比,ZCS/TiO_2在模拟太阳光下的光催化性能显著提高,在420 nm处析氢效率达到5580 μmol·g~(-1)·h~(-1),表观量子效率(AQY)高达11.5%,是TiO_2和ZCS的88.3倍和54.3倍, 分别。此外,ZCS/TiO_2在光催化降解四环素(TC)方面也具有优异的性能。ZCS/TiO_2光催化性能的增强主要得益于S型异质结。一方面,S型电子转移路径不仅提高了电子-空穴分离效率,而且提高了电荷转移效率。另一方面,ZCS显著增强了ZCS/TiO_2的可见光吸收。通过XPS、EPR、紫外光电子能谱(UPS)和能带结构证实了光催化机理和S型异质结结构。本工作为设计和构建S型异质结以提高光催化析氢和TC降解性能提供了新的思路。

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