We comparatively study the onset of photo-induced non-radiative intrinsic Auger recombination processes for red, yellow and green light emitting InGaNsingle bondGaN hetero-structures grown along the polar orientation. We find a dramatic reduction of the photo excitation densities triggering the domination of Auger effect with increasing emission wavelength; that is to say in concert with the enhancement of the internal electric field in the structure. In long wavelength emitters, the internal electric field is stronger, and hence reducing the impact of the internal electric field is more critical.

A promising route towards nanodevice applications relies on the association of graphene and transition metal dichalcogenides with hexagonal boron nitride (h-BN). Due to its insulating nature, h-BN has emerged as a natural substrate and gate dielectric for graphene-based electronic devices. However, some fundamental properties of bulk h-BN remain obscure. For example, the band structure and the position of the Fermi level have not been experimentally resolved. Here, we report a direct observation of parabolic dispersions of h-BN crystals using high-resolution angle-resolved photoemission spectroscopy (ARPES). We find that h-BN exfoliation on epitaxial graphene enables overcoming the technical difficulties of using ARPES with insulating materials. We show trigonal warping of the intensity maps at constant energy. The valence-band maxima are located around the K points, 2.5 eV below the Fermi level, thus confirming the residual p-type character of typical h-BN.

We calculate the radiative heat transfer between two identical metallic one-dimensional lamellar gratings. To this aim we present and exploit a modification to the widely used Fourier modal method, known as adaptive spatial resolution, based on a stretch of the coordinate associated with the periodicity of the grating. We first show that this technique dramatically improves the rate of convergence when calculating the heat flux, allowing us to explore smaller separations. We then present a study of heat flux as a function of the grating height, highlighting a remarkable amplification of the exchanged energy, ascribed to the appearance of spoof-plasmon modes, whose behavior is also spectrally investigated. Differently from previous works, our method allows us to explore a range of grating heights extending over several orders of magnitude. By comparing our results to recent studies we find a consistent quantitative disagreement with some previously obtained results going up to 50%. In some cases, this disagreement is explained in terms of an incorrect connection between the reflection operators of the two gratings.

We address the intrinsic optical properties of hexagonal boron nitride in the deep ultraviolet. Weshow that the fine structure of the phonon replicas arises from overtones involving up to six low-energy interlayer shear modes. These lattice vibrations are specific to layered compounds since theycorrespond to the shear rigid motion between adjacent layers, with a characteristic energy of about6-7 meV. We obtain a quantitative interpretation of the multiplet observed in each phonon replicaunder the assumption of a cumulative Gaussian broadening as a function of the overtone index,and with a phenomenological line-broadening taken identical for all phonon types. We show fromour quantitative interpretation of the full emission spectrum above 5.7 eV that the energy of theinvolved phonon mode is 6.8±0.5 meV, in excellent agreement with temperature-dependent Ramanmeasurements of the low-energy interlayer shear mode in hexagonal boron nitride. We highlightthe unusual properties of this material where the optical response is tailored by the phonon groupvelocities in the middle of the Brillouin zone.

Two dimensional materials like graphene, transition metal dichalcogenides, and hexagonal boron nitride (h-BN) have attracted a keen interest over the past few years due to their possible integration in the next generation of nano-components. Here, we used high resolution X-ray photoemission spectroscopy and near-edge X-ray absorption fine structure (NEXAFS) to perform a complete study of stacking configuration and identify sp3 crystal deformations of a single domain h-BN crystal. The AA′ stacking was found to best reproduce features in the experimental B and N K-edges. The NEXAFS also shows that the splitting of the 1s to π* peak in the B K-edge, recently predicted by density functional theory, may be accounted for by the presence of AB′ stacking faults. The presence of this stacking fault has, as a result, the introduction of point defects in the crystal such as boron atoms in a pyramidal or sp3 configuration. Interstitial nitrogen defects are also present in the crystal forming a N-N pair as expected for a p-type h-BN crystal.

Heat radiation and near-field radiative heat transfer can be strongly manipulated by adjusting geometrical shapes, optical properties, or the relative positions of the objects involved. Typically, these objects are considered as embedded in vacuum. By applying the methods of fluctuational electrodynamics, we derive general closed-form expressions for heat radiation and heat transfer in a system of N arbitrary objects embedded in a passive nonabsorbing background medium. Taking into account the principle of reciprocity, we explicitly prove the symmetry and positivity of transfer in any such system. Regarding applications, we find that the heat radiation of a sphere as well as the heat transfer between two parallel plates is strongly enhanced by the presence of a background medium. Regarding near- and far-field transfer through a gas like air, we show that a microscopic model (based on gas particles) and a macroscopic model (using a dielectric contrast) yield identical results. We also compare the radiative transfer through a medium like air and the energy transfer found from kinetic gas theory.

We investigate the transport of energy in a linear chain of two-level quantum emitters (atoms) weakly coupled to a blackbody radiation bath. We show that simply by displacing one or more atoms from their regular-chain positions, the efficiency of the energy transport can be considerably amplified of at least one order of magnitude. In addition, in configurations providing an efficiency greater than 100%, the distance between the last two atoms of the chain can be up to 20 times larger than the one in the regular chain, thus achieving a much longer-range energy transport. By performing both a stationary and time-dependent analysis, we ascribe this effect to an elementary block of three atoms, playing the role of excitation injector from the blackbody bath to the extraction site. By considering chains with up to seven atoms, we also show that the amplification is robust and can be further enhanced up to 1400%.