No Arabic abstract
We present an approach to describing fluctuational electrodynamic (FED) interactions, particularly van der Waals (vdW) interactions as well as radiative heat transfer (RHT), between material bodies of vastly different length scales, allowing for going between atomistic and continuum treatments of the response of each of these bodies as desired. Any local continuum description of electromagnetic (EM) response is compatible with our approach, while atomistic descriptions in our approach are based on effective electronic and nuclear oscillator degrees of freedom, encapsulating dissipation, short-range electronic correlations, and collective nuclear vibrations (phonons). While our previous works using this approach have focused on presenting novel results, this work focuses on the derivations underlying these methods. First, we show how the distinction between atomic and macroscopic bodies is ultimately somewhat arbitrary, as formulas for vdW free energies and RHT look very similar regardless of how the distinction is drawn. Next, we demonstrate that the atomistic description of material response in our approach yields EM interaction matrix elements which are expressed in terms of analytical formulas for compact bodies or semianalytical formulas based on Ewald summation for periodic media; we use this to compute vdW interaction free energies as well as RHT powers among small biological molecules in the presence of a metallic plate as well as between parallel graphene sheets in vacuum, showing strong deviations from conventional macroscopic theories due to the confluence of geometry, phonons, and EM retardation effects. Finally, we propose formulas for efficient computation of FED interactions among material bodies in which those that are treated atomistically as well as those treated through continuum methods may have arbitrary shapes, extending previous surface-integral techniques.
A rigourous theory for the determination of the van der Waals interactions in colloidal systems is presented. The method is based on fluctuational electrodynamics and a multiple-scattering method which provides the electromagnetic Greens tensor. In particular, expressions for the Greens tensor are presented for arbitrary, finite, collections of colloidal particles, for infinitely periodic or defected crystals as well as for finite slabs of crystals. The presented formalism allows for {it ab initio} calculations of the vdW interactions is colloidal systems since it takes fully into account retardation, many-body, multipolar and near-fields effects.
Phonons (collective atomic vibrations in solids) are more effective in transporting heat than photons. This is the reason why the conduction mode of heat transport in nonmetals (mediated by phonons) is dominant compared to the radiation mode of heat transport (mediated by photons). However, since phonons are unable to traverse a vacuum gap (unlike photons) it is commonly believed that two bodies separated by a gap cannot exchange heat via phonons. Recently, a mechanism was proposed by which phonons can transport heat across a vacuum gap - through Van der Waals interaction between two bodies with gap less than wavelength of light. Such heat transfer mechanisms are highly relevant for heating (and cooling) of nanostructures; the heating of the flying heads in magnetic storage disks is a case in point. Here, the theoretical derivation for modeling phonon transmission is revisited and extended to the case of two bodies made of different materials separated by a vacuum gap. Magnitudes of phonon transmission, and hence the heat transfer, for commonly used materials in the micro and nano-electromechanical industry are calculated and compared with the calculation of conduction heat transfer through air for small gaps.
Quantum corrections to charge transport can give rise to an oscillatory magnetoconductance, typically observed in mesoscopic samples with a length shorter than or comparable with the phase coherence length. Here, we report the observation of magnetoconductance oscillations periodic in magnetic field with an amplitude of the order of $e^2/h$ in macroscopic samples of Highly Oriented Pyrolytic Graphite (HOPG). The observed effect emerges when all carriers are confined to their lowest Landau levels. We argue that this quantum interference phenomenon can be explained by invoking moire superlattices with a discrete distribution in periodicity. According to our results, when the magnetic length $ell_B$, the Fermi wave length $lambda_F$ and the length scale of fluctuations in local chemical potential are comparable in a layered conductor, quantum corrections can be detected over centimetric length scales.
The van der Waals interactions between two parallel graphitic nanowiggles (GNWs) are calculated using the coupled dipole method (CDM). The CDM is an efficient and accurate approach to determine such interactions explicitly by taking into account the discrete atomic structure. Our findings show that the van der Waals forces vary from attraction to repulsion as nanoribbons move along their lengths with respect to each other. This feature leads to a number of stable and unstable positions of the system during the movement process. These positions can be tuned by changing the length of GNW. Moreover, the influence of the thermal effect on the van der Waals interactions is also extensively investigated. This work would give good direction for both future theoretical and experimental studies.
Van der Waals heterostructures have emerged as promising building blocks that offer access to new physics, novel device functionalities, and superior electrical and optoelectronic properties. Applications such as thermal management, photodetection, light emission, data communication, high-speed electronics and light harvesting require a thorough understanding of (nanoscale) heat flow. Here, using time-resolved photocurrent measurements we identify an efficient out-of-plane energy transfer channel, where charge carriers in graphene couple to hyperbolic phonon polaritons in the encapsulating layered material. This hyperbolic cooling is particularly efficient, giving picosecond cooling times, for hexagonal BN, where the high-momentum hyperbolic phonon polaritons enable efficient near-field energy transfer. We study this heat transfer mechanism through distinct control knobs to vary carrier density and lattice temperature, and find excellent agreement with theory without any adjustable parameters. These insights may lead to the ability to control heat flow in van der Waals heterostructures.