Light-Driven Electron Transfer between a Photosensitizer and a Proton-Reducing Catalyst Co-adsorbed to NiO

被引:85
作者
Gardner, James M. [1 ]
Beyler, Maryline [1 ]
Karnahl, Michael [1 ]
Tschierlei, Stefanie [1 ]
Ott, Sascha [1 ]
Hammarstrom, Leif [1 ]
机构
[1] Uppsala Univ, Angstrom Lab, Dept Chem, S-75120 Uppsala, Sweden
基金
瑞典研究理事会;
关键词
SENSITIZED SOLAR-CELLS; SELF-EXCHANGE REACTIONS; NANOSTRUCTURED NIO; MOLECULAR CATALYST; HOLE TRANSFER; FILMS; SPECTROSCOPY; PORPHYRIN; OXIDATION; ENERGY;
D O I
10.1021/ja3082268
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
While intermolecular hole-hopping along the surface of semiconductors is known, there are no previous examples of electron-hopping between molecules on a surface. Herein, we present the first evidence of electron transfer from the photoreduced sensitizer, Coumarin-343 (C343) to complex 1, both bound on the surface of NiO. In solution, 1 has been shown to be a mononuclear Fe-based proton-reducing catalyst. The reduction of 1 is reversible and occurs within 50 ns after excitation of C343. Interfacial recombination between the reduced 1((-)) and NiO hole occurs on a 100 mu s time scale by non-exponential kinetics. The observed process is the first essential step in the photosensitized generation of Hz from a molecular catalyst in the absence of a sacrificial donor reagent.
引用
收藏
页码:19322 / 19325
页数:4
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