Nature-Inspired, Highly Durable CO2 Reduction System Consisting of a Binuclear Ruthenium(II) Complex and an Organic Semiconductor Using Visible Light

被引:413
作者
Kuriki, Ryo [1 ]
Matsunaga, Hironori [2 ]
Nakashima, Takuya [1 ]
Wada, Keisuke [1 ]
Yamakata, Akira [2 ,3 ]
Ishitani, Osamu [1 ]
Maeda, Kazuhiko [1 ]
机构
[1] Tokyo Inst Technol, Sch Sci, Dept Chem, Meguro Ku, 2-12-1-NE-2 Ookayama, Tokyo 1528550, Japan
[2] Toyota Technol Inst, Grad Sch Engn, Tempaku Ku, 2-12-1 Hisakata, Nagoya, Aichi 4688511, Japan
[3] Japan Sci & Technol Agcy, PRESTO, 4-1-8 Honcho, Kawaguchi, Saitama 3220012, Japan
关键词
ULTRAFAST ELECTRON-TRANSFER; EFFICIENT WATER OXIDATION; CARBON-DIOXIDE REDUCTION; PHOTOGENERATED ELECTRONS; PHOTOCATALYTIC SYSTEM; HYDROGEN-PRODUCTION; SINGLE-CRYSTALLINE; RECENT PROGRESS; METAL-COMPLEX; NITRIDE;
D O I
10.1021/jacs.6b01997
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A metal-free organic semiconductor of mesoporous graphitic carbon nitride (C3N4) coupled with a Ru(II) binuclear complex (RuRu') containing photosensitizer and catalytic units selectively reduced CO2 into HCOOH under visible light (lambda > 400 nm) in the presence of a suitable electron donor with high durability, even in aqueous solution. Modification of C3N4 with Ag nano particles resulted in a RuRu'/Ag/C3N4 photocatalyst that exhibited a very high turnover number (>33000 with respect to the amount of RuRu'), while maintaining high selectivity for HCOOH production (87-99%). This turnover number was 30 times greater than that reported previously using C3N4 modified with a mononuclear Ru(II) complex, and by far the highest among the metal-complex/semiconductor hybrid systems reported to date. The results of photocatalytic reactions, emission decay measurements, and time-resolved infrared spectroscopy indicated that Ag nanoparticles on C3N4 milliseconds from the conduction band of C3N4, which were transferred to photocatalytic CO2 reduction driven by two-step photoexcitation of C3N4 and Ag/C3N4 hybrid photocatalyst worked efficiently in water containing a proper nature of C3N4 and low solubility of CO2 in an aqueous environment. collected electrons having lifetimes of several the excited state of RuRu', thereby promoting RuRu'. This study also revealed that the RuRu'/electron donor, despite the intrinsic hydrophobic nature of C3N4 and low solubility of CO2 in an aqueous environment.
引用
收藏
页码:5159 / 5170
页数:12
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