Our direct atomic simulations reveal that a thermally activated phonon mode involves a large population of elastic wavepackets. These excitations are characterized by a wide distribution of lifetimes and coherence times expressing particle- and wave-like natures. In agreement with direct simulations, our theoretical derivation yields a generalized law for the decay of the phonon number taking into account coherent effects. Before the conventional exponential decay due to phonon-phonon scattering, this law introduces a delay proportional to the square of the coherence time. This additional regime leads to a moderate increase in relaxation times and thermal conductivity. This work opens new horizons in the understanding of the origin and the treatment of thermal phonons.
By means of first-principles calculations and modeling analysis, we have predicted that the traditional 2D-graphene hosts the topological phononic Weyl-like points (PWs) and phononic nodal line (PNL) in its phonon spectrum. The phonon dispersion of graphene hosts three type-I PWs (both PW1 and PW2 at the BZ corners emph{K} and emph{K}, and PW3 locating along the $Gamma$-emph{K} line), one type-II PW4 locating along the $Gamma$-emph{M} line, and one PNL surrounding the centered $Gamma$ point in the $q_{x,y}$ plane. The calculations further reveal that Berry curvatures are vanishingly zero throughout the whole BZ, except for the positions of these four pairs of Weyl-like phonons, at which the non-zero singular Berry curvatures appear with the Berry phase of $pi$ or -$pi$, confirming its topological non-trivial nature. The topologically protected non-trivial phononic edge states have been also evidenced along both the zigzag-edged and armchair-edged boundaries. These results would pave the ways for further studies of topological phononic properties of graphene, such as phononic destructive interference with a suppression of backscattering and intrinsic phononic quantum Hall-like effects.
The design of graphene-based composite with high thermal conductivity requires a comprehensive understanding of phonon coupling in graphene. We extended the two-temperature model to coupled groups of phonon. The study give new physical quantities, the phonon-phonon coupling factor and length, to characterize the couplings quantitatively. Besides, our proposed coupling length has an obvious dependence on system size. Our studies can not only observe the nonequilibrium between different groups of phonon, but explain theoretically the thermal resistance inside graphene.
We introduce a procedure to generate scattering states which display trajectory-like wave function patterns in wave transport through complex scatterers. These deterministic scattering states feature the dual property of being eigenstates to the Wigner-Smith time-delay matrix and to the transmission matrix with classical (noiseless) transmission eigenvalues close to 0 or 1. Our procedure to create such beam-like states is based solely on the scattering matrix and successfully tested numerically for regular, chaotic and disordered cavities. These results pave the way for the experimental realization of highly collimated wave fronts in transport through complex media with possible applications like secure and low-power communication.
Self-synchronization is a ubiquitous phenomenon in nature, in which oscillators are collectively locked in frequency and phase through mutual interactions. While self-synchronization requires the forced excitation of at least one of the oscillators, we demonstrate that this mechanism spontaneously appears due to the activation from thermal fluctuations. By performing molecular dynamic simulations, we demonstrate the self-synchronization of thermal phonons in a platform supporting doped silicon resonators. We find that thermal phonons are spontaneously converging to the same frequency and phase. In addition, the dependencies to intrinsic frequency difference and coupling strength agree well with the Kuramoto model predictions. More interestingly, we find that a balance between energy dissipation resulting from phonon-phonon scattering and potential energy between oscillators is required to maintain synchronization. Finally, a wavelet transform approach corroborates the generation of coherent thermal phonons in the collective state of oscillators. Our study provides a new perspective on self-synchronization and on the relationship between fluctuations and coherence.
Comprehensive understanding of thermal transport in nanostructured materials needs large scale simulations bridging length scales dictated by different physics related to the wave versus particle nature of phonons. Yet, available computational approaches implicitly treat phonons as either just waves or as particles. In this work, using a full wave-based Non-Equilibrium Greens Function (NEGF) method, and a particle-based ray-tracing Monte Carlo (MC) approach, we investigate the qualitative differences in the wave and particle-based phonon transport at the vicinity of nanoscale features. For the simple example of a nanoporous geometry, we show that phonon transmission agrees very well for both methods with an error margin of approximately 15%, across phonon wavelengths even for features with sizes down to 3-4 nm. For cases where phonons need to squeeze in smaller regions to propagate, we find that MC underestimates the transmission of long wavelength phonons whereas wave treatment within NEGF indicates that those long wavelength phonons can propagate more easily. We also find that particle-based simulation methods are somewhat more sensitive to structural variations compared to the wave-based NEGF method. The insight extracted from comparing wave and particle methods can be used to provide a better and more complete understanding of phonon transport in nanomaterials.