光电流
化学
位阻效应
金属有机骨架
蚀刻(微加工)
纳米技术
配位复合体
金属
化学工程
光电子学
立体化学
有机化学
材料科学
工程类
吸附
图层(电子)
作者
Hong‐Ye Bai,Lihao Yu,Jinfu Xu,Xuliang Pang,Yajie Bai,Jianguo Cui,Weiqiang Fan
标识
DOI:10.1016/j.cjsc.2023.100096
摘要
Decoration of metal-organic framework (MOF) has been considered as an effective route to improve the photoelectrochemical (PEC) performance of TiO2, but there is still a lack of understanding of the regulatory structure. Herein, Ni-MOF was rationally introduced by in-situ etching method, which helps for artificially regulating the coordination state of Ni sites. The photocurrent density (0.81 mA/cm2) and IPCE value (33.1%) of TiO2-MOF-2 are about twice higher than that of pristine TiO2 due to the rich unsaturated sites of Ni-MOF. Meanwhile, the saturated coordination has caused the decline of PEC performance because of the obvious steric hindrance. Therefore, this work presents an insight for the effect of coordination state on PEC activity especially in MOF system.
科研通智能强力驱动
Strongly Powered by AbleSci AI