光催化
异质结
X射线光电子能谱
材料科学
制氢
电子顺磁共振
分解水
催化作用
氧化还原
光化学
可见光谱
光电子学
化学工程
化学
物理
核磁共振
工程类
生物化学
冶金
作者
Ziyu Xie,Linjun Xie,Q. Fang,Haizhen Liu,Lingyi Meng,Jiangli Wang,Yiming Xie,Zheng Jiang,Can‐Zhong Lu
标识
DOI:10.1016/j.jcis.2023.07.032
摘要
ZnIn2S4/ZnO heterostructures have been achieved by a simple in-situ growth solvothermal method. Under full spectrum irradiation, the optimal photocatalyst 2ZnIn2S4/ZnO exhibits H2 evolution rate of 13,638 (water/ethanol = 1:1) and 3036 (water) μmol·g-1h-1, which is respectively 4 and 5 times higher than that of pure ZnIn2S4. In situ illumination X-ray photoelectron spectroscopy (ISI-XPS) analysis and density functional theory (DFT) calculations show that the electrons of ZnIn2S4 are removed to ZnO through hybridization and form an internal electric field between ZnIn2S4 and ZnO. The optical properties of the catalyst and the effect of internal electric field (IEF) can increase photo-generated electrons (e-)-holes (h+) transport rate and enhance light collection, resulting in profitable photocatalytic properties. The photoelectrochemical and EPR results show that a stepped (S-scheme) heterojunction is formed in the ZnIn2S4/ZnO redox center, which greatly promotes separation of e--h+ pairs and efficient H2 evolution. This research offers an effective method for constructing an efficient S-Scheme photocatalytic system for H2 evolution.
科研通智能强力驱动
Strongly Powered by AbleSci AI