化学
水溶液
光电化学
制氢
无机化学
生产(经济)
电化学
氢
光催化
化学工程
催化作用
电极
有机化学
物理化学
宏观经济学
经济
工程类
作者
Stefano Caramori,Vito Cristino,Roberto Argazzi,L. Meda,Carlo Alberto Bignozzi
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2010-03-08
卷期号:49 (7): 3320-3328
被引量:50
摘要
The use of TiO(2) photoanodes sensitized with ruthenium(II) polypyridine complexes bearing phosphonic acid anchoring groups has been investigated in the context of photoinduced hydrogen generation. The photoanodes sustained 240 h of irradiation without undergoing appreciable hydrolysis and decomposition in an aqueous environment at pH 3. While the use of organic sacrificial donors, like ascorbic acid, considerably enhanced the photoanodic response, the exploitation of iodide was more problematic because the adsorption of photogenerated I(3)(-) from aqueous media favored charge recombination with conduction band electrons, thus limiting the efficiency of the photoelectrosynthetic device. However, experiments performed in a three-compartment cell, where the photolectrode was in contact with an organic solvent, showed a remarkable photocurrent, with an electrolysis yield close to 87%.
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