Y. Kureishi et al., Self-aggregates of synthetic zinc chlorins as the photosensitizer on carbon paste electrodes for a novel solar cell, J ELEC CHEM, 496(1-2), 2001, pp. 13-20
To investigate a dye-based solar cell, a naturally occurring chlorophyll an
alogue (chlorin 1) modified electrode was prepared. Synthetic zinc chlorin
1 easily self-aggregated to form supramolecules (1)(n) in non-polar organic
solvents as well as in the thin film. The photocurrent of the electrode mo
dified with self-aggregated chlorin (1)(n) (CE1) was measured in the range
from - 300 to 300 mV (vs. Ag \ Ag+) by irradiation with > 510 nm light. Bel
ow 100 mV of the bias potential, cathodic photocurrents of CE1 were observe
d in an aqueous solution of 0.1 M 2-(N-morpholino)ethanesulfonic acid + 0.1
M Na2SO4 at pH 6.7. The photocurrent action spectrum of CE1 was similar to
the visible absorption spectrum of (1), on a Pyrex plate, indicating that
the photoexcited slate of zinc chlorin aggregates (1)(n)* played a role as
a photosensitizer on CE1 with a wide band of longer wavelength light. An ox
ygen molecule dissolved in an aqueous solution was an electron acceptor; el
ectron transfer from (1)(n)* to O-2 at the interface between the carbon pas
te electrode and the aqueous solution yielded the cathodic photocurrent. Th
e quantum yield for CE1 was estimated to be 0.09% (730 nm). The value was l
arger than the quantum yield for the carbon paste electrode modified with m
onomeric zinc chlorin 3 (CE3), 0.01% (660 nm). These results indicate that
self-aggregation of zinc chlorin (1)(n) made an efficient photosensitizer o
f solar cells and utilized up to 800 nm light. (C) 2001 Elsevier Science B.
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