부산대학교 도서관

A time-correlated single photon counting technique, coupled with a red sensitive photomultiplier tube, was used to determine the singlet-state lifetimes and energy transfer mechanisms of Chl a·H2O, (Chl a·H2O)2, and (Chl a·2H2O)n. The use of low concentrations and low incident light fluxes permitted measurements in a regime where nonlinear quenching effects are absent. The lifetimes exhibit a pronounced dependence on aggregate size. The results are examined in terms of exciton interactions in the excited singlet state of the Chl a aggregate. It is shown that in the absence of exciton annihilation effects, the rate of singlet-state decay via radiative coupling and intersystem crossing of a Chl a aggregate containing n equivalent monomeric units is equal to n times that of monomeric Chl a. [ABSTRACT FROM AUTHOR]