Energy and temperature dependence of relaxation time and Wiedemann-Franz law on PbTe

Recent revival of interest in high-temperature $(T)$ thermoelectrics has made it necessary to understand in detail the T dependence of different transport coefficients, and different processes contributing to this temperature dependence. Since PbTe is a well-studied prototypical high-temperature thermoelectric, we have carried out theoretical studies to analyze how different physical sources contribute to electronic transport coefficients in this system over a wide T and concentration $(n)$ range; 300 K<T<900 K and 1<n/nₒ<10, where nₒ=10¹⁹ cm^-3, extending earlier works on this problem. We have used Boltzmann equation within energy-dependent relaxation time approximations. Although the T dependence of the electrical conductivity σ comes from several sources (band structure parameters, chemical potential μ, relaxation time τ), we find that the T dependence of τ dominates. We fit the T and the energy (ε) dependence of the total relaxation time τₜₒₜ by a simple function τ~aT^-p/(b+cεʳ), where a, b, c, p, and r are T and ε independent parameters but depend on n. Using this function, we find that for concentration range of interest, changing r which governs the energy dependence of scattering does not appreciably affect the T dependence of σ. Electronic thermal conductivities both at constant current J and constant electric field E were calculated using this τ to reexamine the validity of Wiedemann-Franz (WF) law in PbTe, extending the earlier work of Bhandari and Rowe to higher temperatures. We find that using standard WF law to obtain the electronic contribution of the thermal conductivity (κₑₗ) usually overestimates this contribution by more than 0.5 WK^-1 m^-1. Therefore the value of the lattice thermal conductivity obtained by subtracting this κₑₗ from the total thermal conductivity is underestimated roughly by the same amount.