From molecular metal complex to metal-organic framework: The CO2 reduction photocatalysts with clear and tunable structure

被引：239

作者：

Luo, Yu-Hui ^{[1
,2
]}

Dong, Long-Zhang ^{[1
]}

Liu, Jiang ^{[1
]}

Li, Shun-Li ^{[1
]}

Lan, Ya-Qian ^{[1
]}

机构：

[1] Nanjing Normal Univ, Sch Chem & Mat Sci, Nanjing 210023, Jiangsu, Peoples R China

[2] Huaihai Inst Technol, Dept Chem Engn, Lianyungang 222000, Jiangsu, Peoples R China

来源：

COORDINATION CHEMISTRY REVIEWS | 2019年 / 390卷

基金：

中国博士后科学基金; 中国国家自然科学基金;

关键词：

Molecular metal complexes (MMCs); Metal-organic frameworks (MOFs); Crystal engineering; Photocatalysis; CO2 reduction reaction (CO2RR); CARBON-DIOXIDE REDUCTION; SELECTIVE PHOTOCHEMICAL REDUCTION; SEMICONDUCTOR HYBRID PHOTOCATALYSTS; TERPHENYL-CATALYZED PHOTOREDUCTION; VISIBLE-LIGHT PHOTOREDUCTION; HIGH TURNOVER FREQUENCY; HIGHLY EFFICIENT; ELECTRON-TRANSFER; EXCITED-STATE; SUPRAMOLECULAR PHOTOCATALYSTS;

D O I：

10.1016/j.ccr.2019.03.019

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

Photocatalytic reduction of CO2 to high value-added productions is considered as a green and sustainable approach to reducing excessive CO2 emissions. Molecular metal complexes (MMCs) and metal-organic frameworks (MOFs) are wildly studied as potential photocatalysts for CO2 reduction reaction (CO2RR) due to their clear and tunable structures. In this review, we summarize the photochemical CO2RR based on both homogeneous MMCs and heterogeneous MOFs and discuss molecular engineering approaches and key advances in this field. Discussing the photocatalytic CO2RR properties of MMCs and MOFs is beneficial to elucidating the structure-activity relationship and reaction mechanism in the photocatalytic process. These discussions will provide scientific and technical guidance for the rational design and development of more creative systems for photocatalytic CO2RR. In addition, challenges and prospects for future research of photocatalytic CO2RR based on these coordination compounds are proposed. (C) 2019 Elsevier B.V. All rights reserved.

引用

页码：86 / 126

页数：41

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