NH2-UiO-66(Zr) with fast electron transfer routes for breaking down nitric oxide via photocatalysis

被引:123
作者
Chen, Xiaolang [1 ]
Cai, Yong [1 ]
Liang, Rui [1 ]
Tao, Ying [1 ]
Wang, Wenchao [1 ]
Zhao, Jingjing [1 ]
Chen, Xiaofeng [1 ]
Li, Hexing [1 ]
Zhang, Dieqing [1 ]
机构
[1] Shanghai Normal Univ, Coll Chem & Mat Sci, Shanghai Key Lab Rare Earth Funct Mat, Educ Minist Key Lab Resource Chem, Shanghai 200234, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal organic frameworks; Cu-I/II; Photocatalysis; Electron transfer; NO oxidation; METAL-ORGANIC FRAMEWORKS; SELECTIVE CATALYTIC-REDUCTION; TIO2 NANOTUBE ARRAYS; HIGHLY EFFICIENT; AMBIENT PM2.5; NOX; OXIDATION; REMOVAL; G-C3N4; HYDROGENATION;
D O I
10.1016/j.apcatb.2020.118687
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
MOFs-based photocatalysts always suffer from poor performance owing to its slow charge transfer. Herein, transient metal Cu (Cu-I/II) species were introduced to NH2 -UiO-66(Zr) (Cu-NUO) via in-situ partial reduction of Cu-II ions to Cu-I. 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-NUO. More photogenerated electrons in the Cu coordinated MOFs (Cu-N137) were transferred to the outside surface of the MOFs, producing center dot O-2(-) for the photocatalytic oxidation of low-concentration (550 ppb) of NO indoor flow gas. An 88 % removal rate of NO under visible-light irradiation (lambda > 420 nm) was obtained and well maintained up to 24 h with excellent durability.
引用
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页数:8
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