Solar driven CO2 reduction with a molecularly engineered periodic mesoporous organosilica containing cobalt phthalocyanine

被引:8
|
作者
Navarro, M. Angeles [1 ,2 ]
Sain, Sunanda [2 ]
Wuenschek, Maximilian [3 ]
Pichler, Christian M. M. [3 ,4 ]
Romero-Salguero, Francisco J. J. [1 ]
Esquivel, Dolores [1 ]
Roy, Souvik [2 ]
机构
[1] Univ Cordoba, Fac Ciencias, Dept Quim Organ, Inst Quim Energia & Medioambiente IQUEMA, Campus Rabanales, Cordoba 14071, Spain
[2] Univ Lincoln, Sch Chem, Green Lane, Lincoln LN6 7TS, England
[3] TU Vienna, Inst Appl Phys, Wiedner Hauptstr 8-10, A-1040 Vienna, Austria
[4] Ctr Electrochem & surface technol, Viktor Kaplan Str 2, A-2700 Wiener Neustadt, Austria
关键词
PHOTOCHEMICAL REDUCTION; HIGHLY EFFICIENT; COMPLEX; WATER; ELECTROCATALYSTS; PHOTOREDUCTION; PHOTOCATALYST; CONVERSION; CATALYST; BEARING;
D O I
10.1039/d2nr06026d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A molecular cobalt phthalocyanine (CoPc) catalyst has been integrated in an ethylene-bridged periodic mesoporous organosilica (PMO) to fabricate a hybrid material, CoPc-PMO, that catalyses CO2 reduction to CO in a photocatalytic system using [Ru(bpy)(3)](2+) (bpy = 2,2 '-bipyridine) as a photosensitizer and 1,3-dimethyl-2-phenyl-2,3-dihydro-1H-benzo[d]imidazole (BIH) as an electron donor. CoPc-PMO displays a Co-based turnover number (TONCO) of >6000 for CO evolution with >70% CO-selectivity after 4 h irradiation with UV-filtered simulated solar light, and a quantum yield of 1.95% at 467 nm towards CO. This system demonstrates a benchmark TONCO for immobilised CoPc-based catalysts towards visible light-driven CO2 reduction.
引用
收藏
页码:2114 / 2121
页数:8
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