Search arXivSearch

arXiv · 2410.00141

Simplified approach to estimate Lorenz number using experimental Seebeck coefficient for non parabolic band

Abstract

Reduction of lattice thermal conductivity ($κ_L$) is one of the most effective ways of improving thermoelectric properties. However extraction of $κ_L$ from the total measured thermal conductivity can be misleading if Lorenz ($L$) number is not estimated correctly. The $κ_L$ is obtained using Wiedemann-Franz law which estimates electronic part of thermal conductivity $κ_e$ = $L$$σ$T where, $σ$ and T are electrical conductivity and temperature. The $κ_L$ is then estimated as $κ_L$ = $κ_T$ - $L$$σ$T. For the metallic system the Lorenz number has universal value of 2.44 $\times$ 10$^{-8}$ W$Ω$K$^{-2}$ (degenerate limit), but for no-degenerate semiconductors, the value can deviate significantly for acoustic phonon scattering, the most common scattering mechanism for thermoelectric above room temperatures. Up till now, $L$ is estimated by solving a series of equation derived form Boltzmann transport equations. For the single parabolic band (SPB) an equation was proposed to estimate $L$ directly from the experimental Seebeck coefficient. However using SPB model will lead to overestimation of $L$ in case of low band gap semiconductors which result in underestimation of $κ_L$ sometimes even negative $κ_L$. In this letter we propose a simpler equation to estimate $L$ for a non parabolic band. Experimental Seebeck coefficient, band gap($E_g$), and Temperature ($T$) are the main inputs in the equation which nearly eliminates the need of solving multiple Fermi integrals besides giving accurate values of $L$.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Ankit Kumar. 2025-07-24. Simplified approach to estimate Lorenz number using experimental Seebeck coefficient for non parabolic band. https://doi.org/10.1063/5.0229780

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Incommensurate structural and magnetic modulations in potassium-rich cryptomelane, K$_x$Mn$_8$O$_{16}$ ($x\approx1.45$)

Cryptomelane is a hollandite-like material consisting of K$^+$ cations in an $α$-MnO$_2$ tunnel-like crystallographic motif. Cryptomelane with stoichiometry K$_x$Mn$_8$O$_{16}$ ($x\approx1.45$) has been synthesized and its magnetic properties investigated using variable-temperature magnetic susceptibility, heat capacity, and neutron powder diffraction. Three distinct transitions at $T_1=184$\,K, $T_2=54.5$\,K, and $T_3=24$\,K are observed. At $T_1$ there is a subtle tetragonal$\rightarrow$monoclinic transition associated with emergence of a set of non-magnetic superstructure peaks indexable to a $\vec{k}_\mathrm{struc}\approx0.74\vec{c^*}$ incommensurate modulation parallel to the $α$-MnO$_2$ tunnels. Our findings are consistent with a relation previously reported in titanate hollandites, that $x\approx2|\vec{k}_\mathrm{struc}|$. Magnetic Bragg peaks emerge below $T_2=54.5$\,K, and their positions indicate an incommensurate modulated magnetic structure. The model consistent with the data is a dual-$\vec{k}_\mathrm{mag}$ structure with a ferromagnetic $|\vec{k}_\mathrm{mag}|=0$ component and an incommensurate $\vec{k}_\mathrm{mag}\approx0.37\vec{c^*}$, with the latter most likely to be helical. The period of oscillation of the incommensurate magnetic component is in line with predictions based on a Heisenberg spin Hamiltonian [Mandal \textit{et al}. Phys. Rev. B 90, 104420 (2014)]. Below $T_3=24$\,K, there is a magnetic transition, which gives rise to a different set of magnetic Bragg peaks indicative of a highly complex magnetic structure.

cond-mat.mtrl-sci

An anisotropic functional for two-dimensional material systems

Density function theory is the workhorse of modern electronic structure theory. However, its accuracy in practical calculations is limited by the choice of the exchange-correlation potential. In this respect, two-dimensional materials pose a special challenge, as all these materials and their heterostructures have a crucial similarity. The underlying atomic structures are strongly spatially inhomogeneous, implying that current exchange-correlation functionals, that in almost all cases are isotropic, are ill-prepared for an accurate description. We present an anisotropic screened-exchange potential, that remedies this problem and reproduces the band-gap of 2D materials as well as the piecewise linearity of the total energy with fractional occupation number.

cond-mat.mtrl-sci

Thermally-driven reorientation of the Néel vector in altermagnetic MnTe

Altermagnets are novel magnetic systems that possess a spin-polarized electronic band structure without a net magnetic moment, making them promising for device applications. Hexagonal MnTe, a prototypical altermagnet, arguably exhibits the most properties consistent with theoretical predictions, including an anomalous Hall effect despite a vanishing net magnetization, and altermagnetinduced electronic band splitting. However, fundamental questions remain, including why some effects only appear significantly below the magnetic ordering temperature. Here, we resolve this discrepancy by revealing a reorientation of the Néel vector in single-crystalline MnTe. The Néel vector points 30° from the a-axis at low $T$, before aligning directly with the a-axis around $T\simeq 260$ K. We attribute this to single-ion anisotropy, which depends on temperature-dependent lattice parameters. We obtained these results using muon-spin spectroscopy, magnetization measurements, and X-ray diffraction; we show that the findings are consistent with neutron diffraction. Manipulating this effect, for example through strain, could unlock sensitive electronic detection schemes for external stimuli, paving the way for functional altermagnetic devices.

cond-mat.mtrl-sci