Phonon polaritons, hybrid light-matter quasiparticles resulting from strong coupling of the electromagnetic field with the lattice vibrations of polar crystals are a promising platform for mid-infrared photonics but for the moment there has been no proposal allowing for their electrical pumping. Electrical currents in fact mainly generate longitudinal optical phonons, while only transverse ones participate in the creation of phonon polaritons. We demonstrate how to exploit long-cell polytypes of silicon carbide to achieve strong coupling between transverse phonon polaritons and zone-folded longitudinal optical phonons. We develop a microscopic theory predicting the existence of the resulting hybrid longitudinal-transverse excitations. We then provide an experimental observation by tuning the resonance of a nanopillar array through the folded longitudinal optical mode, obtaining a clear spectral anti-crossing. The hybridisation of phonon polaritons with longitudinal phonons could represent an important step toward the development of phonon polariton-based electrically pumped mid-infrared emitters.
Piezoluminescence (PZL), also referred to as mechanoluminescence (ML), is a promising energy conversion mechanism for realizing mechanically driven photon sources including hand-held displays, lighting, bioimaging and sensing applications.
In this study, detailed temperature dependent simulations for absorption and photogenerated recombination of hot electrons are compared with experimental data for an InAs/AlAsSb multi-quantum well. The simulations describe the actual photoluminescence (PL) observations accurately; in particular, the room temperature e1-hh1 simulated transition energy of 805 meV closely matches the 798 meV transition energy of the experimental PL spectra, a difference of only 7 meV. Likewise, the expected energy separations between local maxima (p1-p2) in the simulated/experimental spectra have a difference of just 2 meV: a simulated energy separation of 31 meV compared to the experimental value of 33 meV. Utilizing a non equilibrium generalized Planck relation, a full spectrum fit enables individual carrier temperatures for both holes and electrons. This results in two very different carrier temperatures for holes and electrons: where the hole temperature, T h , is nearly equal to the lattice temperature, T L ; while, the electron temperature, T e , is 'hot' (i.e., T e > T L ). Also, by fitting the experimental spectra via three different methods a 'hot' carrier temperature is associated with electrons only; all three methods yield similar 'hot' carrier temperatures.
Oxide thermoelectric materials are nontoxic, chemically and thermally stable in oxidizing environments, cost-effective, and comparatively simpler to synthesize. However, thermoelectric oxides exhibit comparatively lower figure of merit ( ZT ) than that of metallic alloy counterparts. In this study, nanoscale texturing and interface engineering were utilized for enhancing the thermoelectric performance of oxide polycrystalline Ca 3 Co 4 O 9 materials, which were synthesized using conventional sintering and spark plasma sintering (SPS) techniques. Results demonstrated that nanoscale platelets (having layered structure with nanoscale spacing) and metallic inclusions provide effective scattering of phonons, resulting in lower thermal conductivity and higher ZT . Thermoelectric measurement direction was found to have a significant effect on the magnitude of ZT because of the strong anisotropy in the transport properties induced by the layered nanostructure. The peak ZT value for the Ca 2.85 Lu 0.15 Co 3.95 Ga 0.05 O 9 specimen measured along both perpendicular and parallel directions with respect to the SPS pressure axis is found be 0.16 at 630 °C and 0.04 at 580 °C, respectively. The peak ZT of 0.25 at 670 °C was observed for the spark plasma-sintered Ca 2.95 Ag 0.05 Co 4 O 9 sample. The estimated output power of 2.15 W was obtained for the full size model, showing high-temperature thermoelectric applicability of this nanostructured material without significant oxidation.
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