Search arXivSearch

arXiv · 2403.04332

A new metric for the comparison of permittivity models in terahertz time-domain spectroscopy

Abstract

We present a robust method, as well as a new metric, for the comparison of permittivity models in terahertz timedomain spectroscopy (THz-TDS). In this work, we perform an extensive noise analysis of a THz-TDS system, we remove and model the unwanted deterministic noises and implement them into our fitting process. This is done using our open-source software, Fit@TDS, available at : https://github.com/THzbiophotonics/Fit-TDS. This work is the first step towards the derivation of uncertainties, and therefore the use of error bars. We hope that this will lead to performing analytical analysis with THz-TDS, as results obtained from different setups will be comparable. Finally, we apply this protocol to the study of a $α$-lactose monohydrate pellet in order to give more insight on the molecular dynamics behind the absorption peaks. The comparison with simulation results is made easier thanks to the probabilities derived from the metric.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Romain Peretti, Mélanie Lavancier, Nabil Vindas-Yassine, Juliette Vlieghe, Theo Hannotte, Jean-Francois Lampin, François Orieux. 2024-05-24. A new metric for the comparison of permittivity models in terahertz time-domain spectroscopy. https://arxiv.org/abs/2403.04332

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

KEEP EXPLORING

Related papers

Janus Dipoles: Fundamentals, Realizations, and Emerging Applications

The Janus dipole - featuring orthogonally oriented electric and magnetic dipoles with a 90-degree phase difference - has emerged as a powerful paradigm for wave manipulation. Unlike traditional Huygens dipoles used for directional control, this unique configuration exhibits strongly asymmetric, face-selective near-field behavior while maintaining a quasi-isotropic far-field radiation pattern. These remarkable properties make the Janus dipole an essential platform for directional wave shaping, with wide-ranging applications in on-chip photonics, quantum interactions, and wireless power transfer. This review systematically traces the rapid development of the Janus dipole from its foundational theoretical inception to its diverse implementation platforms across optical, microwave, and acoustic frequencies. In this paper, we explore the governing principles, classify realization strategies into passive Janus dipoles, active Janus dipoles, and advanced near-field coupling control, and highlight emerging frontiers. By bridging foundational electrodynamics with advanced device engineering, this paper serves as an essential reference and roadmap for researchers designing next-generation, highly integrated, and compact wave-manipulation systems.

physics.app-ph

Evaluation of effective wave velocities in polycrystalline materials using the ultrasonic reflection matrix

In-depth characterization of heterogeneous materials has long been a challenge in non-destructive testing. Here, a method is proposed to determine the elastic constants of metallic polycrystalline materials using back-scattered ultrasound. The waves scattered by the microstructure are analyzed to image the effective bulk velocities. To this end, a reflection matrix is acquired with an array of transducers. The projection of this matrix onto a focused basis is used to estimate an average point spread function. Optimizing this function with respect to the propagation model leads to an estimation of the longitudinal velocity. Additional treatments are developed to adapt the method to map the shear wave velocity. The local Poisson's ratio is then deduced from the ratio between those two velocities. Young's modulus and shear modulus can also be obtained assuming known densities. This matrix approach is experimentally validated on different polycrystalline materials. A sample displaying heterogeneous mechanical properties is then simulated to assess the accuracy and the resolution of the method. Its strengths and limitations are discussed, demonstrating its potential for quantitative non-destructive material characterization.

physics.app-ph

A Green's-function method for vertical thermal boundary conductance in anisotropic multilayers

Vertical thermal interfaces occur in both engineered and natural materials. Their vertical thermal boundary conductance can differ from the horizontal counterpart, requiring dedicated characterization. Yet current thermal metrology resolves vertical thermal boundary conductance only in restricted geometries such as two bulk media, for lack of an efficient forward solution that admits anisotropy, multilayers, and depth-dependent vertical thermal boundary conductance together. We present a Green's-function boundary integral equation (GBIE) method that couples transfer-matrix Green's functions to an interface-only integral equation for depth-dependent $G_v(z)$, supporting dissimilar orthotropic multilayers ($k_x\neq k_y\neq k_z$) on either side and horizontal conductance $G_h$. For anisotropic film-on-substrate multilayers with films from $1~μ\mathrm{m}$ to $100~\mathrm{nm}$, the GBIE agrees with three-dimensional finite element method (FEM) predictions to within one percent mean normalized phase and amplitude error, while running $29\text{--}210\times$ faster and reducing peak memory by factors of $120\text{--}450$ in single-core tests; a JIT-compiled JAX implementation reaches up to $4100\times$ on a matched 16-core comparison. The GBIE further reproduces a continuous film over a buried interface, representative of a thermoreflectance measurement, and a finite-depth interface with depth-dependent $G_v(z)$. The GBIE accommodates lateral-to-film-thickness ratios above $10^{5}$, where volumetric FEM can become computationally prohibitive. These results establish an efficient forward solution for vertical-interface heat transport in systems ranging from microelectronic device sidewalls to grain boundaries in polycrystalline solids.

physics.app-ph