This content will become publicly available on May 2, 2025
- Award ID(s):
- 1952210
- PAR ID:
- 10521038
- Publisher / Repository:
- Nature
- Date Published:
- Journal Name:
- Nature
- Volume:
- 629
- Issue:
- 8010
- ISSN:
- 0028-0836
- Page Range / eLocation ID:
- 67 to 73
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
Silicon carbide (SiC) supports surface phonons in the infrared region of the electromagnetic spectrum where these modes can be thermally emitted. Additionally, the magnitude, spectrum, and direction of thermal radiation from SiC can be controlled by engineering this material at the sub-wavelength scale. For these reasons, SiC nanopillars are of high interest for thermal-radiation tuning. So far, theoretical and experimental studies of thermal emission from SiC nanopillars have been limited to long-pitch arrays with a microscale interpillar spacing. It is not clear how far-field thermal emission from SiC nanopillars is affected when the interparticle spacing reduces to the nanometer scale, where the near-field interaction between adjacent nanopillars arises and the array becomes zero order. In this Letter, we study physical mechanisms of far-field thermal radiation from zero-order arrays of silicon-carbide nanopillars with a nanoscale interpillar spacing. We show that the increased volume of thermal emitters and thermal radiation of the hybrid waveguide-surface-phonon-polariton mode from zero-order arrays increase the spectral emissivity of silicon carbide to values as large as 1 for a wide range of angles. The enhanced, dispersion-less thermal emission from a zero-order SiC array of nano-frustums with an optimized interspacing of 300 nm is experimentally demonstrated. Our study provides insight into thermal radiation from dense nanostructures and has significant implications for thermal management of electronic devices and energy harvesting applications.more » « less
-
Abstract Recent theoretical studies have suggested that transition metal perovskite oxide membranes can enable surface phonon polaritons in the infrared range with low loss and much stronger subwavelength confinement than bulk crystals. Such modes, however, have not been experimentally observed so far. Here, using a combination of far-field Fourier-transform infrared (FTIR) spectroscopy and near-field synchrotron infrared nanospectroscopy (SINS) imaging, we study the phonon polaritons in a 100 nm thick freestanding crystalline membrane of SrTiO3transferred on metallic and dielectric substrates. We observe a symmetric-antisymmetric mode splitting giving rise to epsilon-near-zero and Berreman modes as well as highly confined (by a factor of 10) propagating phonon polaritons, both of which result from the deep-subwavelength thickness of the membranes. Theoretical modeling based on the analytical finite-dipole model and numerical finite-difference methods fully corroborate the experimental results. Our work reveals the potential of oxide membranes as a promising platform for infrared photonics and polaritonics.
-
Abstract Hyperbolic phonon polaritons (HPhPs) are stimulated by coupling infrared (IR) photons with the polar lattice vibrations. Such HPhPs offer low‐loss, highly confined light propagation at subwavelength scales with out‐of‐plane or in‐plane hyperbolic wavefronts. For HPhPs, while a hyperbolic dispersion implies multiple propagating modes with a distribution of wavevectors at a given frequency, so far it has been challenging to experimentally launch and probe the higher‐order modes that offer stronger wavelength compression, especially for in‐plane HPhPs. In this work, the experimental observation of higher‐order in‐plane HPhP modes stimulated on a 3C‐SiC nanowire (NW)/α‐MoO3heterostructure is reported where leveraging both the low‐dimensionality and low‐loss nature of the polar NWs, higher‐order HPhPs modes within 2D α‐MoO3crystal are launched by the 1D 3C‐SiC NW. The launching mechanism is further studied and the requirements for efficiently launching of such higher‐order modes are determined. In addition, by altering the geometric orientation between the 3C‐SiC NW and α‐MoO3crystal, the manipulation of higher‐order HPhP dispersions as a method of tuning is demonstrated. This work illustrates an extremely anisotropic low dimensional heterostructure platform to confine and configure electromagnetic waves at the deep‐subwavelength scales for a range of IR applications including sensing, nano‐imaging, and on‐chip photonics.
-
Ultra-wide band gap semiconductor devices based on β-phase gallium oxide (Ga2O3) offer the potential to achieve higher switching performance and efficiency and lower manufacturing cost than that of today’s wide band gap power electronics. However, the most critical challenge to the commercialization of Ga2O3 electronics is overheating, which impacts the device performance and reliability. We fabricated a Ga2O3/4H–SiC composite wafer using a fusion-bonding method. A low-temperature (≤600 °C) epitaxy and device processing scheme was developed to fabricate MOSFETs on the composite wafer. The low-temperature-grown epitaxial Ga2O3 devices deliver high thermal performance (56% reduction in channel temperature) and a power figure of merit of (∼300 MW/cm2), which is the highest among heterogeneously integrated Ga2O3 devices reported to date. Simulations calibrated based on thermal characterization results of the Ga2O3-on-SiC MOSFET reveal that a Ga2O3/diamond composite wafer with a reduced Ga2O3 thickness (∼1 μm) and a thinner bonding interlayer (<10 nm) can reduce the device thermal impedance to a level lower than that of today’s GaN-on-SiC power switches.more » « less
-
Abstract The structure and properties of segmented block copolymer films of aromatic polyimide (PI) and poly(ethylene glycol) (PEG) doped with an ionic liquid are studied for potential polymer electrolyte membrane applications for fuel cells. Poly(amic acid) precursors of PI‐PEG copolymers of 4,4′‐(hexafluoroisopropylidene) diphthalic anhydride, 4,4′‐(1,3‐phenylenedioxy) dianiline, and bis(3‐aminopropyl) terminated PEG (
M n≈ 1500) are synthesized and then thermally imidized in membrane films, followed by swelling in ethylammonium nitrate (EAN) ionic liquid. The small‐angle X‐ray scattering results from the EAN‐doped PI‐PEG copolymer films show disordered bicontinuous phase‐separated nanostructures described by Teubner–Strey theory, with the interface fractal dimension determined from the Porod equation. Thermal annealing of the EAN‐doped membranes at 100–140 °C results in increased correlation lengths and smoother interfaces of the bicontinuous nanostructures. Such improved nanostructures lead to the increased ionic conductivity by two to five times with the maximum conductivity of 210 mS cm−1at 60 °C and 70% RH, much greater (nearly fivefold) than that of Nafion films, while maintaining the mechanical stability possibly up to 140 °C. Moreover, the investigation of the disordered bicontinuous phase‐separated nanostructure of EAN‐doped PI‐PEG copolymer membranes is highly relevant to understanding the nanostructures of hydrated Nafion membranes and segmented block copolymers in general.