Recent Advances in MOF-based Nanocatalysts for Photo-Promoted CO2 Reduction Applications

被引:27
|
作者
Liu, Chang [1 ]
Wang, Wenzhi [2 ]
Liu, Bin [2 ]
Qiao, Jing [1 ]
Lv, Longfei [1 ]
Gao, Xueping [1 ]
Zhang, Xue [1 ]
Xu, Dongmei [3 ]
Liu, Wei [3 ]
Liu, Jiurong [1 ]
Jiang, Yanyan [1 ]
Wang, Zhou [1 ]
Wu, Lili [1 ]
Wang, Fenglong [1 ]
机构
[1] Shandong Univ, Sch Mat Sci & Engn, Jinan 250061, Shandong, Peoples R China
[2] Univ Jinan, Sch Mat Sci & Engn, Jinan 250022, Shandong, Peoples R China
[3] Shandong Univ, State Key Lab Crystal Mat, Jinan 250061, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal-organic frameworks (MOFs); photocatalysis; carbon dioxide reduction; renewable energy; METAL-ORGANIC FRAMEWORK; CARBON-DIOXIDE REDUCTION; VISIBLE-LIGHT; PHOTOCATALYTIC REDUCTION; ARTIFICIAL PHOTOSYNTHESIS; EFFICIENT; CONVERSION; PHOTOREDUCTION; NANOCOMPOSITES; SOLAR;
D O I
10.3390/catal9080658
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
The conversion of CO2 to valuable substances (methane, methanol, formic acid, etc.) by photocatalytic reduction has important significance for both the sustainable energy supply and clean environment technologies. This review systematically summarized recent progress in this field and pointed out the current challenges of photocatalytic CO2 reduction while using metal-organic frameworks (MOFs)-based materials. Firstly, we described the unique advantages of MOFs based materials for photocatalytic reduction of CO2 and its capacity to solve the existing problems. Subsequently, the latest research progress in photocatalytic CO2 reduction has been documented in detail. The catalytic reaction process, conversion efficiency, as well as the product selectivity of photocatalytic CO2 reduction while using MOFs based materials are thoroughly discussed. Specifically, in this review paper, we provide the catalytic mechanism of CO2 reduction with the aid of electronic structure investigations. Finally, the future development trend and prospect of photocatalytic CO2 reduction are anticipated.
引用
收藏
页数:16
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