Air-condition process for scalable fabrication of CdS/ZnS 1D/2D heterojunctions toward efficient and stable photocatalytic hydrogen production
作者机构:College of Materials Science and EngineeringHunan UniversityChangshaPeople's Republic of China Institute of Micro/Nano Materials and DevicesNingbo University of TechnologyNingboZhejiangPeople's Republic of China Department of Mechanical EngineeringUniversity of BathBathUK
出 版 物:《Carbon Energy》 (碳能源(英文))
年 卷 期:2023年第5卷第7期
页 面:1-14页
核心收录:
学科分类:081705[工学-工业催化] 08[工学] 0817[工学-化学工程与技术]
基 金:Hunan Provincial Innovation Foundation for Postgraduate,Grant/Award Number:CX20200454 National Natural Science Foundation of China,Grant/Award Number:51972178
主 题:air condition CdS heterojunctions photocatalytic hydrogen production ZnS
摘 要:We report the scalable fabrication of CdS/ZnS 1D/2D heterojunctions under ambient air conditions(i.e.,room temperature and atmospheric pressure)in which ZnS nanoparticles are anchored on the surface of CdS *** as-formed heterojunctions exhibit a significantly enhanced photocatalytic H_(2) evolution rate of 14.02 mmol h^(-1) g^(-1) when irradiated with visible light,which is~10 and 85 times higher than those of pristine CdS nanosheets and CdS nanoparticles,respectively,and superior to most of the CdS-based photocatalysts reported to ***,they provide robust photocatalytic performance with demonstratable stability over 58 h,indicating their potential for practical *** formation of 1D/2D heterojunctions not only provides improved exposed active sites that respond to illumination but also provides a rapid pathway to generate photogenerated carriers for efficient separation and transfer through the matrix of single-crystalline CdS *** addition,first-principles simulations demonstrate that the existence of rich Zn vacancies increases the energy level of the ZnS valence band maximum to construct type-II and Z-scheme mixed heterojunctions,which plays a critical role in suppressing the recombination of carriers with limited photocorrosion of CdS to enhance photocatalytic behavior.