Co-porphyrin/carbon nitride hybrids for improved photocatalytic CO2 reduction under visible light

被引:215
作者
Zhao, Guixia [1 ]
Pang, Hong [1 ,2 ]
Liu, Guigao [1 ,2 ]
Li, Peng [1 ]
Liu, Huimin [1 ]
Zhang, Huabin [1 ]
Shi, Li [1 ,2 ]
Ye, Jinhua [1 ,2 ,3 ,4 ]
机构
[1] Natl Inst Mat Sci, Int Ctr Mat Nanoarchitecton WPI MANA, 1-1 Namiki, Tsukuba, Ibaraki 3050044, Japan
[2] Hokkaido Univ, Grad Sch Chem Sci & Engn, Sapporo, Hokkaido 0600814, Japan
[3] Tianjin Univ, Sch Mat Sci & Engn, TU NIMS Joint Res Ctr, Tianjin 300072, Peoples R China
[4] Collaborat Innovat Ctr Chem Sci & Engn, Tianjin 300072, Peoples R China
基金
日本学术振兴会;
关键词
Photocatalysis; CO2; reduction; Carbon nitride; Co-porphyrin; Covalent hybrids; GRAPHITIC CARBON NITRIDE; CATALYZED ELECTROCHEMICAL REDUCTION; SOLID-STATE NMR; PHOTOCHEMICAL REDUCTION; WATER OXIDATION; COBALT; DIOXIDE; CONVERSION; COMPLEXES; POLYMER;
D O I
10.1016/j.apcatb.2016.06.074
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
A covalently linked reaction center/antenna hybrid composed of Co-porphyrin and low-molecular weight carbon nitride was developed for the reduction of CO2 into CO under visible light for the first time. The hybrids possessed thirteen-fold higher photocatalytic activity (17 mu mol/g/h) compared with bulk carbon nitride, and it is more than twice what it was in the Co-porphyrin loaded C3N4 heterojunction system. The efficient electron transfer and trapping by the Co active sites as well as the affinity of Co-porphyrin for CO2 are considered to account for the enhanced activity. Our findings may open a promising route to modify carbon nitride and provide a feasible approach to immobilize the active site into the light-harvest antenna for efficient electron-hole separation, electron transferring and the following redox reaction in photocatalytic process, which reforms the conventional semiconductor-cocatalyst heterojunction system. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:141 / 149
页数:9
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