TY - JOUR

T1 - Relaxation and nonradiative decay in disordered systems. II. Two-fracton inelastic scattering

AU - Alexander, S.

AU - Entin-Wohlman, Ora

AU - Orbach, R.

PY - 1986/1/1

Y1 - 1986/1/1

N2 - The two localized-vibrational quanta (Raman) relaxation process is calculated for a localized electronic state. The calculation is expected to be relevant to relaxation at elevated temperatures where the principal vibrational excitations are of high energy (and hence of short length scale). Localization of the vibrational eigenstates is most likely for this regime. Vibrational localization can be geometrical in origin (as on a fractal network, with the quantized vibrational states fractons), or as a consequence of scattering (analogous to Anderson localization, with the quantized vibrational states localized phonons). The relaxation rate is characterized by a probability density which is calculated for both classes of localization under the assumption that the electronic and vibrational energy widths are larger than the maximum electronic relaxation rate. The time profile of the initial elec- tronic state population is calculated. The long-time behavior begins as t[1/2(a-1)]exp[-c1(t)1/(a-1)], where a=4q+2d̄̄ and 4q+2d̄̄-2 for Kramers and non-Kramers transitions, respectively. Here, d̄̄ is the fracton dimensionality and q=d̄̄dφ/D. The fractal dimensionality is D, and dφ is defined by the range dependence of the fracton wave &). The long-time behavior thus begins as a stretched exponential. After a crossover time, the long-time behavior varies as (lnt)η-1/2t-c1(ln t)2η where c1 is a constant and η=D/dφ. This portion of the time decay is faster than any power law but slower than exponential or stretched exponential. In the presence of rapid electronic cross relaxation, the time profile is exponential, with a low-temperature relaxation time 1/T1ave proportional to T2d̄̄[1+2(dφ/D)]-1 and T2d̄̄[1+2(dφ/D)]-3 for Kramers and non-Kramers transitions, respectively. These results may explain recent fractional temperature exponents found for electronic spin-lattice relaxation in macromolecules and nuclear spin-lattice relaxation in glasses.

AB - The two localized-vibrational quanta (Raman) relaxation process is calculated for a localized electronic state. The calculation is expected to be relevant to relaxation at elevated temperatures where the principal vibrational excitations are of high energy (and hence of short length scale). Localization of the vibrational eigenstates is most likely for this regime. Vibrational localization can be geometrical in origin (as on a fractal network, with the quantized vibrational states fractons), or as a consequence of scattering (analogous to Anderson localization, with the quantized vibrational states localized phonons). The relaxation rate is characterized by a probability density which is calculated for both classes of localization under the assumption that the electronic and vibrational energy widths are larger than the maximum electronic relaxation rate. The time profile of the initial elec- tronic state population is calculated. The long-time behavior begins as t[1/2(a-1)]exp[-c1(t)1/(a-1)], where a=4q+2d̄̄ and 4q+2d̄̄-2 for Kramers and non-Kramers transitions, respectively. Here, d̄̄ is the fracton dimensionality and q=d̄̄dφ/D. The fractal dimensionality is D, and dφ is defined by the range dependence of the fracton wave &). The long-time behavior thus begins as a stretched exponential. After a crossover time, the long-time behavior varies as (lnt)η-1/2t-c1(ln t)2η where c1 is a constant and η=D/dφ. This portion of the time decay is faster than any power law but slower than exponential or stretched exponential. In the presence of rapid electronic cross relaxation, the time profile is exponential, with a low-temperature relaxation time 1/T1ave proportional to T2d̄̄[1+2(dφ/D)]-1 and T2d̄̄[1+2(dφ/D)]-3 for Kramers and non-Kramers transitions, respectively. These results may explain recent fractional temperature exponents found for electronic spin-lattice relaxation in macromolecules and nuclear spin-lattice relaxation in glasses.

UR - http://www.scopus.com/inward/record.url?scp=5544252162&partnerID=8YFLogxK

U2 - 10.1103/PhysRevB.33.3935

DO - 10.1103/PhysRevB.33.3935

M3 - Article

AN - SCOPUS:5544252162

VL - 33

SP - 3935

EP - 3946

JO - Physical Review B

JF - Physical Review B

SN - 2469-9950

IS - 6

ER -