Qihong Lu, Ning Yang, Lei Zuo, Wenjian Fang, Jing Dong, Xianghua Zeng
{"title":"Photostability and visible-light-driven photoactivity enhancement of hierarchical C@ZnCdS/ZnS/MoS2","authors":"Qihong Lu, Ning Yang, Lei Zuo, Wenjian Fang, Jing Dong, Xianghua Zeng","doi":"10.1088/2632-959x/ad2fd2","DOIUrl":null,"url":null,"abstract":"Zinc cadmium sulfide solid (Zn<sub>\n<italic toggle=\"yes\">x</italic>\n</sub>Cd<sub>1−<italic toggle=\"yes\">x</italic>\n</sub>S) related composites received great attention in photocatalytic hydrogen production because of their tunable bandgap and strong visible light absorption range. But sulfide-based metal materials commonly suffer from photo-corrosion issues. It is very important to construct the photocatalysts with high efficient activity and photostability for H<sub>2</sub> production. Herein, we successively prepared ZnCdS/ZnS (ZCS/ZS) heterostructures, ZnCdS/ZnS/MoS<sub>2</sub> (ZCS/ZS/M) heterostructures decorated ZCS/ZS with MoS<sub>2</sub> quantum dots, then we obtained <italic toggle=\"yes\">x</italic>-C@ZCS/ZS and <italic toggle=\"yes\">x</italic>-C@ZCS/ZS/M heterostructures encapsulated ZCS/ZS and ZCS/ZS/M with carbon layer. The performance of the photocatalytic hydrogen production showed that sample 0.05-C@ZCS/ZS/M has a remarkable photocatalytic H<sub>2</sub> evolution rate of 15.231 mmol·h<sup>−1</sup>·g<sup>−1</sup> with noble metal-free co-catalysts. This rate was approximately 21 times higher than that of the pristine ZCS/ZS photocatalyst. The optimized sample reveals an excellent stability, without activity losses after 10 h. The improved photocatalytic activity can be attributed to the unique heterojunction structure formed by ZCS/ZS and MoS<sub>2</sub>. Additionally, the carbon films played a crucial role in providing excellent stability by spatially separating the sites for redox reactions, thereby inhibiting the recombination of photo-generated electron–hole pairs.","PeriodicalId":501827,"journal":{"name":"Nano Express","volume":"13 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nano Express","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1088/2632-959x/ad2fd2","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Zinc cadmium sulfide solid (ZnxCd1−xS) related composites received great attention in photocatalytic hydrogen production because of their tunable bandgap and strong visible light absorption range. But sulfide-based metal materials commonly suffer from photo-corrosion issues. It is very important to construct the photocatalysts with high efficient activity and photostability for H2 production. Herein, we successively prepared ZnCdS/ZnS (ZCS/ZS) heterostructures, ZnCdS/ZnS/MoS2 (ZCS/ZS/M) heterostructures decorated ZCS/ZS with MoS2 quantum dots, then we obtained x-C@ZCS/ZS and x-C@ZCS/ZS/M heterostructures encapsulated ZCS/ZS and ZCS/ZS/M with carbon layer. The performance of the photocatalytic hydrogen production showed that sample 0.05-C@ZCS/ZS/M has a remarkable photocatalytic H2 evolution rate of 15.231 mmol·h−1·g−1 with noble metal-free co-catalysts. This rate was approximately 21 times higher than that of the pristine ZCS/ZS photocatalyst. The optimized sample reveals an excellent stability, without activity losses after 10 h. The improved photocatalytic activity can be attributed to the unique heterojunction structure formed by ZCS/ZS and MoS2. Additionally, the carbon films played a crucial role in providing excellent stability by spatially separating the sites for redox reactions, thereby inhibiting the recombination of photo-generated electron–hole pairs.