光催化
金属
光化学
电子转移
辐照
载流子
材料科学
氧化还原
化学
催化作用
电子
离子
氧化物
无机化学
光电子学
冶金
有机化学
物理
核物理学
量子力学
作者
Xiaolang Chen,Yong Cai,Rui Liang,Ying Tao,Wenchao Wang,Jingjing Zhao,Xiaofeng Chen,Hexing Li,Dieqing Zhang
标识
DOI:10.1016/j.apcatb.2020.118687
摘要
MOFs-based photocatalysts always suffer from poor performance owing to its slow charge transfer. Herein, transient metal Cu (CuI/II) species were introduced to NH2-UiO-66(Zr) (Cu-NU0) via in-situ partial reduction of CuII ions to CuI. A ligand to linker metal charge transfer (LLMCT) pathway in MOFs was constructed for accelerating the photogenerated electrons transfer from organic linkers to Cu species, greatly enhanced increasing both the carrier density value and the separation efficiency of photogenerated carriers. A longer photogenerated charge lifetime (78.2 ps) was obtained and about 4 times higher than that of Cu-NU0. More photogenerated electrons in the Cu coordinated MOFs (Cu-NU7) were transferred to the outside surface of the MOFs, producing O2− for the photocatalytic oxidation of low-concentration (550 ppb) of NO indoor flow gas. An 88 % removal rate of NO under visible-light irradiation (λ > 420 nm) was obtained and well maintained up to 24 h with excellent durability.
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