arXiv subjects

H. T. M. Nghiem

Publications and source records attributed to H. T. M. Nghiem.

9 recordsLinked to original sources

arXiv2026

Work distribution for strongly coupled many-body open quantum systems

The non-equilibrium quantum thermodynamics of many-body open systems is notoriously rich, especially in the strong-coupling regime where strong system-bath correlations develop and interactions produce non-perturbative effects. Such systems can be described by `quantum impurity models' where the system and bath are treated on an equal footing as a single composite. Paradigmatic examples are the spin-boson and Anderson impurity models, in which system degrees of freedom interact with either bosonic or fermionic gapless baths. Here we study the quantum work distribution function (WDF) of such systems following a quench. Capturing the full continuum of many-body excitations in the WDF requires a non-perturbative solution of the underlying non-equilibrium quantum impurity problem. For this purpose, we extend the time-dependent numerical renormalization group (TDNRG) approach to the calculation of the WDF, which applies directly in the thermodynamic limit, can be used for arbitrary quench amplitudes at zero or finite temperature, and provides exponentially fine low-energy resolution. Our numerically-exact solution reveals power-law threshold behavior due to the Anderson orthogonality catastrophe when the work approaches its minimum value, with universal scaling collapse of the distribution below an emergent low-energy scale induced by system-bath correlations.

quant-ph↗

arXiv2025

Absorption and scattering properties of nanoparticles in an absorbing medium: modeling with experimental validation

Absorption and scattering properties of nanoparticles immersed in an absorbing medium are essential in understanding the overall properties of composites and in designing materials with expected functionalities. In this paper, we establish a model based on both Kubelka-Munk theory and Mie theory that links the absorption and scattering properties of individual particles with the reflectance and transmittance spectra of its thin-film composite, supported by detailed experiments. Thin films consisting of TiO$_2$ nanoparticles embedded in PMMA are fabricated on glass substrates using spin-coating and then peeled off to form standalone samples for spectroscopy measurements. By using the Kubelka-Munk theory in combination with the Saunderson correction, the absorption $K$ and scattering $S$ coefficients of multiple nanoparticles are extracted from the measured transmittance and reflectance. On the other hand, the absorption $K$ and scattering $S$ coefficients are the sum of absorption and scattering cross-sections of individual particles, which are calculated from the Mie theory specified for particles in an absorbing medium, with the scattering $S$ coefficient further modulated by the anisotropy factor $g$. The effect of the particulate medium is incorporated through an effective refractive index. The overall model is validated by matching well between the $K-S$ coefficients extracted from experimental data and theoretical calculations. This agreement provides deep insight into the significant attenuating effect of absorption and scattering on each particle due to the surrounding medium. The validated model of nanoparticles immersed in an absorbing medium can be used to obtain preliminary results for materials designed in a number of applications, such as radiative cooling.

physics.optics↗

arXiv2023

Complex refractive index measurements of Poly(methyl methacrylate) (PMMA) over the UV-VIS-NIR region

Poly(methyl methacrylate), PMMA, is a popular polymer for optical applications due to its superior transmission and reflection. However, its optical properties in the ultraviolet regime still need to be thoroughly studied. Using the reflection-transmission method, we determine its complex refractive index by numerically analyzing the measured data from thin films. The PMMA standalone film is fabricated by peeling off its substrate after spin-coating. Its transmittance and reflectance are then measured in a spectrophotometer using an integrated sphere. The complex refractive index $n+ik$ is extracted theoretically from the measured transmittance $T$ and reflectance $R$. The uncertainties of measured $n$ and $k$ are discussed in the two limits of strong absorption and weak absorption of the materials to illustrate the advantage and disadvantages of the approach.

physics.optics↗

arXiv2021

Self-energy method for time-dependent spectral functions of the Anderson impurity model within the time-dependent numerical renormalization group approach

The self-energy method for quantum impurity models expresses the correlation part of the self-energy in terms of the ratio of two Green's functions and allows for a more accurate calculation of equilibrium spectral functions than is possible directly from the one-particle Green's function [Bulla et al., J. Phys.: Condens. Matter 10, 8365 (1998)], for example, within the numerical renormalization group method. In addition, the self-energy itself is a central quantity required in the dynamical mean field theory of strongly correlated lattice models. Here, we show how to generalize the self-energy method to the time-dependent situation for the prototype model of strong correlations, the Anderson impurity model. We use the equation of motion method to obtain closed expressions for the local Green's function in terms of a time-dependent correlation self-energy, with the latter being given as a ratio of a one-particle time-dependent Green's function and a higher-order correlation function. We benchmark this self-energy approach to time-dependent spectral functions against the direct approach within the time-dependent numerical renormalization group method. The self-energy approach improves the accuracy of time-dependent spectral function calculations, and the closed-form expressions for the Green's function allow for a clear picture of the time-evolution of spectral features at the different characteristic time-scales. The self-energy approach is of potential interest also for other quantum impurity solvers for real-time evolution, including time-dependent density matrix renormalization group and continuous-time quantum Monte Carlo techniques.

cond-mat.str-el↗

arXiv2020

Time-dependent spectral functions of the Anderson impurity model in response to a quench with application to time-resolved photoemission spectroscopy

We investigate several definitions of the time-dependent spectral function $A(ω,t)$ of the Anderson impurity model following a quench and within the time-dependent numerical renormalization group method. In terms of the two-time retarded Green function $G^r(t_1,t_2)$, the definitions differ in the choice of the time variable $t$ with respect to $t_1$ and/or $t_2$. In a previous study [Nghiem {\it et al.} Phys. Rev. Lett. 119, 156601 (2017)], we investigated the spectral function, obtained from the Fourier transform of ${\rm Im}[G^r(t_1,t_2)]$ w.r.t. the time difference $t'=t_1-t_2$, with $t=t_2$. Here, we derivie expressions for the retarded Green function for the choices $t=t_1$ and the average time $t=(t_1+t_2)/2$, within the TDNRG approach. We compare and contrast the resulting $A(ω,t)$ for the different choices of time reference. Expressions for the lesser, greater and advanced Green functions are also derived within TDNRG for all choices of time reference. The average time lesser Green function $G^<(ω,t)$ is particularly interesting, as it determines the time-dependent occupied density of states $N(ω,t)=G^<(ω,t)/(2πi)$, a quantity that determines the photoemission current in time-resolved pump-probe photoemission spectroscopy. We present calculations for $N(ω,t)$ for the Anderson model following a quench, and discuss the resulting time evolution of the spectral features, such as the Kondo resonance and high-energy peaks. We also discuss the issue of thermalization at long times for $N(ω,t)$. Finally, we use the results for $N(ω,t)$ to calculate the time-resolved photoemission current for the Anderson model following a quench (acting as the pump) and study the different behaviors that can be observed for different resolution times of a Gaussian probe pulse.

cond-mat.str-el↗

arXiv2018

Time-dependent numerical renormalization group method for multiple quenches: towards exact results for the long time limit of thermodynamic observables and spectral functions

We develop an alternative time-dependent numerical renormalization group (TDNRG) formalism for multiple quenches and implement it to study the response of a quantum impurity system to a general pulse. Within this approach, we reduce the contribution of the NRG approximation to numerical errors in the time evolution of observables by a formulation that avoids the use of the generalized overlap matrix elements in our previous multiple-quench TDNRG formalism [Nghiem {\em et al.,} Phys. Rev. B {\bf 89}, 075118 (2014); Phys. Rev. B {\bf 90}, 035129 (2014)]. We demonstrate that the formalism yields a smaller cumulative error in the trace of the projected density matrix as a function of time and a smaller discontinuity of local observables between quenches than in our previous approach. Moreover, by increasing the switch-on time, the time between the first and last quench of the discretized pulse, the long-time limit of observables systematically converges to its expected value in the final state, i.e., the more adiabatic the switching, the more accurately is the long-time limit recovered. The present formalism can be straightforwardly extended to infinite switch-on times. We show that this yields highly accurate results for the long-time limit of both thermodynamic observables and spectral functions, and overcomes the significant errors within the single quench formalism [Anders {\em et al.}, Phys. Rev. Lett. {\bf 95}, 196801 (2005); Nghiem {\em et al.}, Phys. Rev. Lett. {\bf 119}, 156601 (2017)]. This improvement provides a first step towards an accurate description of nonequilibrium steady states of quantum impurity systems, e.g., within the scattering states NRG approach [Anders, Phys. Rev. Lett. {\bf 101}, 066804 (2008)].

cond-mat.str-el↗

arXiv2017

Time evolution of the Kondo resonance in response to a quench

We investigate the time evolution of the Kondo resonance in response to a quench by applying the time-dependent numerical renormalization group (TDNRG) approach to the Anderson impurity model in the strong correlation limit. For this purpose, we derive within TDNRG a numerically tractable expression for the retarded two-time nonequilibrium Green function $G(t+t',t)$, and its associated time-dependent spectral function, $A(ω,t)$, for times $t$ both before and after the quench. Quenches from both mixed valence and Kondo correlated initial states to Kondo correlated final states are considered. For both cases, we find that the Kondo resonance in the zero temperature spectral function, a preformed version of which is evident at very short times $t\to 0^{+}$, only fully develops at very long times $t\gtrsim 1/T_{\rm K}$, where $T_{\rm K}$ is the Kondo temperature of the final state. In contrast, the final state satellite peaks develop on a fast time scale $1/Γ$ during the time interval $-1/Γ\lesssim t \lesssim +1/Γ$, where $Γ$ is the hybridization strength. Initial and final state spectral functions are recovered in the limits $t\rightarrow -\infty$ and $t\rightarrow +\infty$, respectively. Our formulation of two-time nonequilibrium Green functions within TDNRG provides a first step towards using this method as an impurity solver within nonequilibrium dynamical mean field theory.

cond-mat.str-el↗

arXiv2016

The Ohmic two-state system from the perspective of the interacting resonant level model: Thermodynamics and transient dynamics

We investigate the thermodynamics and transient dynamics of the (unbiased) Ohmic two-state system by exploiting the equivalence of this model to the interacting resonant level model. For the thermodynamics, we show, by using the numerical renormalization group (NRG) method, how the universal specific heat and susceptibility curves evolve with increasing dissipation strength, $α$, from those of an isolated two-level system at vanishingly small dissipation strength, with the characteristic activated-like behavior in this limit, to those of the isotropic Kondo model in the limit $α\to 1^{-}$. For the transient dynamics of the two-level system, $P(t)=\langle σ_{z}(t)\rangle$, with initial-state preparation $P(t\leq0)=+1$, we apply the time-dependent extension of the NRG (TDNRG) to the interacting resonant level model, and compare the results obtained with those from the noninteracting-blip approximation (NIBA), the functional renormalization group (FRG), and the time-dependent density matrix renormalization group (TD-DMRG). We demonstrate excellent agreement on short to intermediate time scales between TDNRG and TD-DMRG for $0\lesssimα\lesssim 0.9$ for $P(t)$, and between TDNRG and FRG in the vicinity of $α=1/2$. Furthermore, we quantify the error in the NIBA for a range of $α$, finding significant errors in the latter even for $0.1\leq α\leq 0.4$. We also briefly discuss why the long-time errors in the present formulation of the TDNRG prevents an investigation of the crossover between coherent and incoherent dynamics. Our results for $P(t)$ at short to intermediate times could act as useful benchmarks for the development of new techniques to simulate the transient dynamics of spin-boson problems.

cond-mat.str-el↗

arXiv2014

Time-Dependent Numerical Renormalization Group Method for Multiple Quenches: Application to General Pulses and Periodic Driving

The time-dependent numerical renormalization group method (TDNRG) [Anders et al., Phys. Rev. Lett. {\bf 95}, 196801 (2005)] was recently generalized to multiple quenches and arbitrary finite temperatures [Nghiem et al., Phys. Rev. B {\bf 89}, 075118 (2014)] by using the full density matrix approach [Weichselbaum et al., Phys. Rev. Lett. {\bf 99}, 076402 (2007)]. In this paper, we numerically implement this formalism to study the response of a quantum impurity system to a general pulse and periodic driving which are approximated by a sufficient number of quenches. We show how the NRG approximation affects the trace of the projected density matrices and the continuity of the time-evolution of a local observable. For the general pulse case, the local observable in the long-time limit exhibits a dependence on the switch-on time, the time interval between the first and last quenches, as well as on the pulse shape. In particular, the long-time limit is improved for longer switch-on times and smoother pulses. This lends support to our earlier suggestion that the long-time limit of observables can be improved by replacing a sudden large quench by a sequence of smaller ones acting over a finite time-interval: longer switch-on times and smoother pulses, i.e., increased adiabaticity, favor relaxation of the system to its correct thermodynamic long-time limit. For the case of periodic driving, we compare the TDNRG results to exact analytic ones for the non-interacting resonant level model, finding better agreement at short to intermediate time scales in the case of smoother driving. Finally, we demonstrate the validity of the multiple-quench TDNRG formalism for arbitrary temperatures by studying the time-evolution of the occupation number in the Anderson impurity model in response to a periodic switching of the local level from the mixed valence to the Kondo regime at finite temperatures.

cond-mat.str-el↗