Abstract
Solvated electrons in glycerol were generated via a resonant one-photon photodetachment of the charge-transfer-to-solvent (CTTS) band of I- in glycerol (Gl) after irradiation with a 248 nm excimer laser. Optical absorption spectra of solvated electrons (esolv-) in Gl were recorded as a function of temperature (381<or=T<or=505 K). The observed redshift of the absorption maximum, homegamax, yields a temperature coefficient d(homegamax)/dT=-(2.67+/-0.07)x10(-3) eV K-1. For solutions with a concentration c(I-) approximately 10(-3)M, the absorbance of esolv- at homegamax increases by a factor of about 65 when the temperature is raised from 329 to 536 K. This effect can be partially explained by a temperature-dependent redshift of the CTTS spectrum of I- in Gl with respect to the laser wavelength. The main contribution to the increasing yield of esolv- is determined by diffusion controlled escape dynamics of the electron in the contact pair (I:e-)solv which is formed very fast during the detachment process. At room temperature no absorption of esolv- (absorbance<1.0x10(-3)) could be observed which is probably a result of an extremely small self-diffusion coefficient of Gl (a factor of 1250 lower than that of water at 298 K). The results are compared with a previous study of I- in ethylene glycol.
Published Version
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