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William A. Smith

Publications and source records attributed to William A. Smith.

2 recordsLinked to original sources

Exceptional Optical Phonon Coherence in Enriched Cubic Boron Arsenide via Suppression of Three-Phonon Scattering

Cubic boron arsenide (BAs) is a promising semiconductor for next-generation electronics due to its outstanding ambipolar mobility and thermal conductivity, the latter of which is attributed to the suppression of three-phonon scattering. However, precisely accounting for different high-order anharmonic scattering processes is challenging from both theory and experiment, so that questions remain open regarding the ultimate limit of phonon lifetime and thermal conductivity in BAs. Here we show that this gap nearly eliminates three-phonon scattering for zone-center optical phonons in a wide temperature range, leading to a record-high, isotope purity-limited phonon coherence with a quality factor above $3.7\times 10^3$ for >98% enriched $^{11}$BAs below 100 K. We discriminate three decoherence mechanisms by their temperature-dependent contribution to the damping rate using high-resolution Raman and Fourier transform infrared spectroscopy. For the as-synthesized crystals, we find that defect scattering has negligible contributions to the linewidth of optical phonons in comparison to isotope scattering. These results provide critical insights into the intrinsic and extrinsic scattering mechanisms of optical phonons in BAs, motivating further studies to quantify anharmonic effects and realize superior phonon transport.

cond-mat.mtrl-sci

Unconventional Temperature Dependence of Exciton Diamagnetism in 2D Ruddlesden-Popper Lead Halide Perovskites

Layered hybrid perovskites containing larger organic cations have demonstrated superior environmental stability, but the presence of these insulating spacers also strengthens the exciton binding energy, which contributes to reduced carrier separation. The consequences of increased binding energy on device efficiency are still not fully documented, and binding energy measurements are often conducted at cryogenic temperatures where linewidths are decreased and a series of hydrogen-like bound states can be identified, but not under ambient conditions where devices are expected to operate. In contrast to the quenching observed in 3D perovskites such as methylammonium lead iodide, where exciton binding energies are thought to decrease at higher temperatures, we present evidence for a smaller excitonic radius at higher temperatures in the $n=5$ member of butylammonium-spaced methylammonium lead iodide, (BA)$_2$(MA)$_{n-1}$Pb$_n$I$_{3n+1}$. We measured the temperature-dependent diamagnetic shift coefficient in magnetic fields up to 40\,T, which is one-third as large at room temperature as those at cryogenic temperatures. In both the ideal 2D and 3D hydrogen models, this trend would indicate that the exciton binding energy more than triples at room temperature.

cond-mat.mtrl-sci