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Photochemical conversion of solar energy. Third quarter progress report, July 1, 1975--September 30, 1975. [Iron--thionine]

Technical Report ·
OSTI ID:5253047
Quantum yield for current conversion of the totally illuminated thin layer (TI-TL) photogalvanic cell with SnO/sub 2/ anode and platinum cathode filled with an approximately saturated solution of thionine (TH/sup +/) in 50 v/v percent aq. CH/sub 3/CN is 7 percent with 80 ..mu.. electrode spacing and 15 percent with 25 ..mu.. spacing. I/sub sc/ varies linearly with light intensity up to 65 mW cm/sup -2/. Electrical output of the methylene blue element of a two element stacked TI-TL SnO/sub 2//InSnO/sub 2/ cell (80 ..mu.. spacing) with approximately saturated TH/sup +/ (in 50 v/v percent aq. CH/sub 3/CN) in the element exposed directly to light and saturated methylene blue (MB/sup +/) in the second element is the same as the output of the separated MB/sup +/ element. Deaerated TH/sup +/ and MB/sup +/ cell solutions in 50 v/v percent aq. CH/sub 3/CN degrade upon exposure to sunlight for several days. The addition of approximately 10 v/v percent of benzyl alcohol to 50 v/v percent aq. CH/sub 3/CN approximately doubles the solubility of TH/sup +/ sulfate without changing electrical output. Output from 80..mu.. TI-TL SnO/sub 2//Pt cells is unchanged when TH/sup +/ is replaced by thionine-1-sulfonic acid (TS) if the solvent is water but is reduced by approximately 95 percent with 50 v/v percent aq. CH/sub 3/CN as solvent. Lauryl sulfate in concentrations greater than 10/sup -2/ M solubilizes TH/sup +/ sulfate in water and suppresses dimerization. Such solutions produce very low electrical output. Additional kinetic characteristics of triplet excited states of TH/sup +/ and MB/sup +/ have been determined in solution in water and in 50 v/v percent aq. CH/sub 3/CN. The specific rates of oxidation of leucomethylene blue (MBH/sub 2//sup +/) and leucothionine (TH/sub 3//sup +/) by ferric sulfate are similar in these solvents. The oxidation of TH/sub 3//sup +/ by Fe(III) has been shown to proceed via a reversibly formed complex.
Research Organization:
Boston Univ., Mass. (USA). Dept. of Chemistry
OSTI ID:
5253047
Report Number(s):
NSF/RANN/SE/AER-72-03597/A03/75/3
Country of Publication:
United States
Language:
English