Search

Emitted photons stemming from the radiative recombination of electron-hole pairs carry chemical potential in radiative energy converters. This luminescent effect can substantially alter the local net photogeneration in near-field thermophotovoltaic cells. Several assumptions involving the luminescent effect are commonly made in modeling photovoltaic devices; in particular, the photon chemical potential is assumed to be zero or a constant prescribed by the bias voltage. The significance of photon chemical potential depends upon the emitter temperature, the semiconductor properties, and the injection level. Hence, these assumptions are questionable in thermophotovoltaic devices operating in the near-field regime. In the present work, an iterative solver that combines fluctuational electrodynamics with the drift-diffusion model is developed to tackle the coupled photon and charge transport problem, enabling the determination of the spatial profile of photon chemical potential beyond the detailed balance approach. The difference between the results obtained by allowing the photon chemical potential to vary spatially and by assuming a constant value demonstrates the limitations of the conventional approaches. This study is critically important for performance evaluation of near-field thermophotovoltaic systems., Comment: 40 pages, 11 figures

Accurate modeling of charge transport and both thermal and luminescent radiation is crucial to the understanding and design of radiative thermal energy converters. Charge carrier dynamics in semiconductors are well-described by the Poisson-drift-diffusion equations, and thermal radiation in emitter/absorber structures can be computed using multilayer fluctuational electrodynamics. These two types of energy flows interact through radiation absorption/luminescence and charge carrier generation/recombination. However, past research has typically only assumed limited interaction, with thermal radiation absorption as an input for charge carrier models to predict device performance. To examine this assumption, we develop a fully-coupled iterative model of charge and radiation transport in semiconductor devices, and we use our model to analyze near-field and far-field GaSb thermophotovoltaic and thermoradiative systems. By comparing our results to past methods that do not consider cross-influences between charge and radiation transport, we find that a fully-coupled approach is necessary to accurately model photon recycling and near-field enhancement of external luminescence. Because these effects can substantially alter device performance, our modeling approach can aid in the design of efficient thermophotovoltaic and thermoradiative systems., Comment: 21 pages, 8 figures

Systems of many nanoparticles or volume-discretized bodies exhibit collective radiative properties that could be used for enhanced, guided, or tunable thermal radiation. These are commonly treated as assemblies of point dipoles with interactions described by Maxwell's equations and thermal fluctuations correlated by the fluctuation-dissipation theorem. Here, we unify different theoretical descriptions of these systems and provide a complete derivation of many-dipole thermal radiation, showing that the correct use of the fluctuation-dissipation theorem depends on the definitions of fluctuating and induced dipole moments. We formulate a method to calculate the diffusive radiative thermal conductivity of arbitrary collections of nanoparticles; this allows the comparison of thermal radiation to other heat transfer modes and across different material systems. We calculate the radiative thermal conductivity of ordered and disordered arrays of SiC and SiO2 nanoparticles and show that thermal radiation can significantly contribute to thermal transport in these systems. We validate our calculations by comparison to the exact solution for a one-dimensional particle chain, and we demonstrate that the dipolar approximation significantly underpredicts the exact results at separation distances less than the particle radius., Comment: 20 pages, 6 figures

Photons typically do not contribute to thermal transport within a solid due to their low energy density and tendency to be quickly absorbed. We propose a practical material system - infrared plasmonic resonators embedded in a semiconductor nanowire - that leverages near-field electromagnetic coupling to achieve photonic thermal transport comparable to the electronic and phononic contributions. We analytically show photonic thermal conductivities up to about 1 W m-1 K-1 for 10 nm diameter Si and InAs nanowires containing repeated resonators at 500 K. The nanowire system outperforms plasmonic particles in isotropic environments and presents a pathway for photonic thermal transport to exceed that of phonons and electrons., Comment: 10 pages, 4 figures, plus supplementary information

In chains of closely-spaced nanoparticles supporting surface polaritons, near-field electromagnetic coupling leads to collective effects and super-Planckian thermal radiation exchange. Researchers have primarily used two analytical approaches to calculate radiative heat transfer in these systems: fluctuational electrodynamics, which directly incorporates fluctuating thermal currents into Maxwell's equations, and a kinetic approach where the dispersion relation provides modes and propagation lengths for the Boltzmann transport equation. Here, we compare results from the two approaches in order to identify regimes in which kinetic theory is valid and to explain differing results in the literature on its validity. Using both methods, we calculate the diffusive radiative thermal conductivity of nanoparticle chains. We show that kinetic theory is valid and matches predictions by fluctuational electrodynamics when the propagation lengths are greater than the particle spacing., Comment: 10 pages, 6 figures, preprint accepted for the 9th International Symposium on Radiative Transfer