Exchange interactions, charge delocalization, and spin relaxation in a mixed-valence di-iron complex studied by Mössbauer spectroscopy.

Autor: Ding, X.-Q., Bill, E., Trautwein, A. X., Winkler, H., Kostikas, A., Papaefthymiou, V., Simopoulos, A., Beardwood, P., Gibson, J. F.
Předmět:
Zdroj: Journal of Chemical Physics; 11/1/1993, Vol. 99 Issue 9, p6421, 8p
Abstrakt: Exchange interactions and charge transfer in the Fe2+Fe3+ pair of the mixed valence [Fe2S2(dimethylmethanebisbenzimidazolate)2]3- trianion have been studied by analysis of Mössbauer spectra in the temperature range of 1.5–180 K and in applied fields of 10 mT, 0.35 T, and 6.2 T. The low-temperature spectra reveal a ground state with total spin St=1/2 and hyperfine parameters intermediate between values for a Fe2+Fe3+ localized mixed-valence pair and a fully delocalized system where the two iron atoms are equivalent. A consistent set of hyperfine parameters has been derived by fitting the spectra with a stochastic relaxation model taking into account spin relaxation in the St=1/2 state and electron hopping between the iron ions. An interpretation of the values of the hyperfine parameters has been given by solving a spin Hamiltonian, which includes antiferromagnetic and double exchange in an asymmetric Fe2+Fe3+ pair and which allows partial electron delocalization. Using the value a2=0.8 for the delocalization coefficient and an estimate of Δ=105 cm-1 for the difference between the St=1/2 and the first excited St=3/2 state we have derived limits for the exchange-coupling constant J, the double-exchange parameter B, and the energy difference EA-EB arising from the two possible configurations FeA2+FeB3+ and FeA3+FeB2+, i.e., 70 cm-1≲=J≲=300 cm-1, 0<|B|≲=395 cm-1, and 0<|EA-EB|≲=590 cm-1. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index