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Photochemical conversion of solar energy. First quarter progress report, January 1, 1974--March 31, 1974. [Iron--thionine]

Technical Report ·
OSTI ID:5385235
Work was continued on the iron-thionine photogalvanic cell. Thin layer wholly illuminated photogalvanic cells were constructed using NESA and platinum electrodes. In some of these cells, the electrolyte consisted of iron-thionine solution absorbed on a polyelectrolyte membrane. Power at the level of microwatts was obtained with single thin layer, wholly illuminated cells. Evaluation of the performance of cells using aqueous-organic mixtures as solvents was pursued. Performance superior to that obtained in pure aqueous solutions was observed with aqueous N-methylpropionamide or aqueous acetonitrile and platinum electrodes. A number of kinetic parameters were evaluated employing solutions in solvents composed of various proportions of water and dimethylacetamide (DMA). Using the technique of pulsed laser photolysis-kinetic spectrometry, it was found that in aqueous solution semithionine appears to be generated in part by reaction of discreet molecules of triplet thionine with Fe(II) and in part by electron transfer within excited complexes of thionine and Fe(II). In solvents ranging in composition from 18 mole percent DMA to 90 mole percent DMA, the lifetime of semithionine increases with increasing proportion of DMA. In 18 mole percent DMA, the specific rate of oxidation of leucothionine by Fe(III) is approximately 40 times as great as it is in pure water.
Research Organization:
Boston Univ., Mass. (USA). Dept. of Chemistry
OSTI ID:
5385235
Report Number(s):
NSF/RANN/SE/GI-38103/PR/74/1
Country of Publication:
United States
Language:
English