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Photoinduced hydrogen evolution by a Zwitterionic diquat electron acceptor. The functions of SiO/sub 2/ colloid in controlling the electron-transfer process

Journal Article · · J. Am. Chem. Soc.; (United States)
DOI:https://doi.org/10.1021/ja00358a006· OSTI ID:5514080
Photosensitized hydrogen evolution from a basic aqueous silicon dioxide (SiO/sub 2/) colloid (pH 9 to 10) is accomplished with N,N'-bis-(3-sulfonatopropyl)-2,2'-bipyridinium (DQS/sup 0/) and colloidal platinum as mediating catalysts. In this system Ru(bpy)/sub 3//sup 2 +/ (ruthenium (bipyridium)/sub 3//sup 2 +/) acts as a photosensitizer and triethanolamine (TEOA) as ultimate electron donor. No hydrogen formation is observed in a homogeneous aqueous solution under similar conditions. The SiO/sub 2/ colloid affects the formation and stabilization of the intermediate photoproducts, Ru(bpy)/sub 3//sup 3 +/ and DQS/sup -/., by means of electrostatic interactions. The electric potential of the particles assists the separation of the products from the initial encounter cage complex and results in the repulsion of the reduced product, DQS/sup -/., from the colloidal interface. Consequently, the recombination rate of DQS/sup -/. with the oxidized product Ru(bpy)/sub 3//sup 3 +/ is retarded. The electrostatic functions of the colloid are confirmed by alteration of the ionic strength and pH of the colloid solution. The structure of DQS/sup 0/ was determined by X-ray crystallography. The compound crystallizes in space group P2/sub 1//n with unit cell dimensions of a = 10.392 (1) A, b = 22.390 (3) A, c = 8.235 (1) A, ..beta.. = 95.07 (2)/sup 0/, V = 1909 (1) A/sup 3/, and Z = 4. 4 figures, 4 tables.
Research Organization:
Hebrew Univ. of Jerusalem, Israel
OSTI ID:
5514080
Journal Information:
J. Am. Chem. Soc.; (United States), Journal Name: J. Am. Chem. Soc.; (United States) Vol. 105:20; ISSN JACSA
Country of Publication:
United States
Language:
English

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