同质结
纳米晶
锌黄锡矿
材料科学
硫化铜
硫系化合物
捷克先令
纤锌矿晶体结构
铜
化学工程
纳米技术
光电子学
兴奋剂
薄膜
冶金
工程类
锌
作者
Liang Wu,Qian Wang,Tao‐Tao Zhuang,Guozhen Zhang,Yang Li,Hui Li,Fengjia Fan,Shu‐Hong Yu
标识
DOI:10.1038/s41467-022-33065-7
摘要
Abstract Designing polytypic homojunction is an efficient way to regulate photogenerated electrons and holes, thereafter bringing desired physical and chemical properties and being attractive photocatalysts for solar-to-hydrogen conversion. However, the high-yield and controllable synthesis of well-defined polytypes especially for multinary chalcogenide - the fundamental factor favoring highly efficient solar-to-hydrogen conversion - has yet to be achieved. Here, we report a general colloidal method to construct a library of polytypic copper-based quaternary sulfide nanocrystals, including Cu 2 ZnSnS 4 , Cu 2 CdSnS 4 , Cu 2 CoSnS 4 , Cu 2 MnSnS 4 , Cu 2 FeSnS 4 , Cu 3 InSnS 5 and Cu 3 GaSnS 5 , which can be synthesized by selective epitaxial growth of kesterite phase on wurtzite structure. Besides, this colloidal method allows the precise controlling of the homojunction number corresponding to the photocatalytic performance. The single-homojunction and double-homojunction polytypic Cu 2 ZnSnS 4 nanocrystal photocatalysts show 2.8-fold and 3.9-fold improvement in photocatalytic hydrogen evolution rates relative to the kesterite nanocrystals, respectively. This homojunction existed in the polytypic structure opens another way to engineer photocatalysts.
科研通智能强力驱动
Strongly Powered by AbleSci AI