Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userAbsence of Casimir regime in two-dimensional nanoribbon phonon conduction
78
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
In stark contrast with three-dimensional (3D) nanostructures, we show that boundary scattering in two-dimensional (2D) nanoribbons alone does not lead to a finite phonon mean free path. If combined with an intrinsic scattering mechanism, 2D boundary scattering does reduce the overall mean free path, however the latter does not scale proportionally to the ribbon width, unlike the well known Casimir regime occurring in 3D nanowires. We show that boundary scattering can be accounted for by a simple Mathiessen type approach for many different 3D nanowire cross sectional shapes, however this is not possible in the 2D nanoribbon case, where a complete solution of the Boltzmann transport equation is required. These facts have strong implications for the thermal conductivity of suspended nanostructures.
rate research
Read More
We investigated theoretically the phonon thermal conductivity of single layer graphene. The phonon dispersion for all polarizations and crystallographic directions in graphene lattice was obtained using the valence-force field method. The three-phonon Umklapp processes were treated exactly using an accurate phonon dispersion and Brillouin zone, and accouting for all phonon relaxation channels allowed by the momentum and energy conservation laws. The uniqueness of graphene was reflected in the two-dimensional phonon density of states and restrictions on the phonon Umklapp scattering phase-space. The phonon scattering on defects and graphene edges has been also included in the model. The calculations were performed for the Gruneisen parameter, which was determined from the ab initio theory as a function of the phonon wave vector and polarization branch, and for a range of values from experiments. It was found that the near room-temperature thermal conductivity of single layer graphene, calculated with a realistic Gruneisen parameter, is in the range ~ 2000 - 5000 W/mK depending on the defect concentration and roughness of the edges. Owing to the long phonon mean free path the graphene edges produce strong effect on thermal conductivity even at room temperature. The obtained results are in good agreement with the recent measurements of the thermal conductivity of suspended graphene.
In the hydrodynamic regime, phonons drift with a nonzero collective velocity under a temperature gradient, reminiscent of viscous gas and fluid flow. The study of hydrodynamic phonon transport has spanned over half a century but has been mostly limited to cryogenic temperatures (~1 K) and more recently to low-dimensional materials. Here, we identify graphite as a three-dimensional material that supports phonon hydrodynamics at significantly higher temperatures (~100 K) based on first-principles calculations. In particular, by solving the Boltzmann equation for phonon transport in graphite ribbons, we predict that phonon Poiseuille flow and Knudsen minimum can be experimentally observed above liquid nitrogen temperature. Further, we reveal the microscopic origin of these intriguing phenomena in terms of the dependence of the effective boundary scattering rate on momentum-conserving phonon-phonon scattering processes and the collective motion of phonons. The significant hydrodynamic nature of phonon transport in graphite is attributed to its strong intralayer sp2 hybrid bonding and weak van der Waals interlayer interactions. As a boundary-sensitive transport regime, phonon hydrodynamics opens up new possibilities for thermal management and energy conversion.
Thermal transport in solids changes its nature from phonon propagation that suffers from perturbative scattering to thermally activated hops between localized vibrational modes as the level of disorder increases. Models have been proposed to understand these two distinct extremes that predict opposite temperature dependence of the thermal conductivity, but not for the transition or the intermediate regime. Here we explore thermal transport in two-dimensional crystalline and amorphous silica with varying levels of disorder, {alpha}, by performing atomistic simulations as well as analysis based on the kinetic and Allen-Feldman theories. We demonstrate the crossover between the crystalline and amorphous regimes at {alpha} ~ 0.3, which can be identified by a turnover of the temperature dependence in thermal conductivity, and explained by the dominance of thermal hopping processes. The determination of this critical disorder level is also validated by the analysis of the participation ratio of localized vibrational modes, and the spatial localization of heat flux. These factors can serve as key indicators in characterizing the transition in heat transport mechanisms.
We measure the temperature-dependent carrier density and resistivity of the topological surface state of thin exfoliated Bi2Se3 in the absence of bulk conduction. When the gate-tuned chemical potential is near or below the Dirac point the carrier density is strongly temperature dependent reflecting thermal activation from the nearby bulk valence band, while above the Dirac point, unipolar n-type surface conduction is observed with negligible thermal activation of bulk carriers. In this regime linear resistivity vs. temperature reflects intrinsic electron-acoustic phonon scattering. Quantitative comparison with a theoretical transport calculation including both phonon and disorder effects gives the ratio of deformation potential to Fermi velocity D/hbarvF = 4.7 {AA}-1. This strong phonon scattering in the Bi2Se3 surface state gives intrinsic limits for the conductivity and charge carrier mobility at room temperature of ~550 {mu}S per surface and ~10,000 cm2/Vs.
We report on the exciton formation and relaxation dynamics following photocarrier injection in a single-layer two-dimensional lead-iodide perovskite. We probe the time evolution of four distinct exciton resonances by means of time-resolved photoluminescence and transient absorption spectroscopies, and find that at 5,K a subset of excitons form on a $lesssim$ 1-ps timescale, and that these relax subsequently to lower-energy excitons on $sim$ 5--10,ps with a marked temperature dependence over $<$ 100,K. We implement a mode projection analysis that determines the relative contribution of all observed phonons with frequency $leq$50,cm$^{-1}$ to inter-exciton nonadiabatic coupling, which in turn determines the rate of exciton relaxation. This analysis ranks the relative contribution of the phonons that participate in polaronic lattice distortions to the exciton inter-conversion dynamics and thus establishes their role in the nonadiabatic mixing of exciton states, and this in the exciton relaxation rate.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
