arXiv subjects

Huarui Sun

Publications and source records attributed to Huarui Sun.

6 recordsLinked to original sources

arXiv2026

Monolithic integration of diverse crystalline thin films on diamond for near-junction thermal management

The pursuit of extreme miniaturization and high power in 6G RF front-ends has cast thermal dissipation as the central challenge. Here, we have demonstrated the monolithic integration of functionally distinct single-crystal thin films, including \b{eta}-Ga2O3, Si, GaN, and LiTaO3, onto a single diamond substrate using a multi-step transfer printing technique. Focusing on the critical \b{eta}-Ga2O3/diamond interface, we achieve an exceptional interfacial thermal conductance (ITC) of 149 MW m-2 K-1 through ultra-high vacuum (UHV) annealing, creating an atomically sharp interface featuring covalent bonding. Vibrational electron energy-loss spectroscopy (EELS) analysis combining with molecular dynamics (MD) simulations reveal that distinctive interfacial phonon modes at the \b{eta}-Ga2O3/diamond heterointerface dominate ultrahigh ITC. We experimentally demonstrate that by improving the ITC, the thermal resistance (Rth) of a diamond-based \b{eta}-Ga2O3 MOSFET is driven to a record-low value of 1.58 K mm W-1, underscoring the critical role of interface engineering in near-junction thermal management for diamond-integrated devices. This work demonstrates a scalable, diamond-based monolithic integration platform designed to solve the near-junction thermal challenges in high-power RF front-ends.

cond-mat.mtrl-sci↗

arXiv2025

Interface phonon modes governing the ideal limit of thermal transport across diamond/cubic boron nitride interfaces

Understanding the ideal limit of interfacial thermal conductance (ITC) across semiconductor heterointerfaces is crucial for optimizing heat dissipation in practical applications. By employing a highly accurate and efficient machine-learned potential trained herein, we perform extensive non-equilibrium molecular dynamics simulations to investigate the ITC of diamond/cubic boron nitride ($c$BN) interfaces. The ideal diamond/$c$BN interface exhibits an unprecedented ITC of 11.0 $\pm$ 0.1 GW m$^{-2}$ K$^{-1}$, setting a new upper bound for heterostructure interfaces. This exceptional conductance originates from extended phonon modes due to acoustic matching and localized C-atom modes that propagate through B-C bonds. However, atomic diffusion across the ideal interface creates mixing layers that disrupt these characteristic phonon modes, substantially suppressing the thermal transport from its ideal limit. Our findings reveal how interface phonon modes govern thermal transport across diamond/$c$BN interfaces, providing insights for thermal management in semiconductor devices.

cond-mat.mtrl-sci↗

arXiv2023

Dissimilar thermal transport properties in $\kappa$-Ga$_2$O$_3$ and $\beta$-Ga$_2$O$_3$ revealed by machine-learning homogeneous nonequilibrium molecular dynamics simulations

The lattice thermal conductivity (LTC) of Ga$_2$O$_3$ is an important property due to the challenge in the thermal management of high-power devices. We develop machine-learned neuroevolution potentials for single-crystalline $\beta$-Ga$_2$O$_3$ and $\kappa$-Ga$_2$O$_3$, and apply them to perform homogeneous nonequilibrium molecular dynamics simulations to predict their LTCs. The LTC of $\beta$-Ga$_2$O$_3$ was determined to be 10.3 $\pm$ 0.2 W/(m K), 19.9 $\pm$ 0.2 W/(m K), and 12.6 $\pm$ 0.2 W/(m K) along [100], [010], and [001], respectively, aligning with previous experimental measurements. For the first time, we predict the LTC of $\kappa$-Ga$_2$O$_3$ along [100], [010], and [001] to be 4.5 $\pm$ 0.0 W/(m K), 3.9 $\pm$ 0.0 W/(m K), and 4.0 $\pm$ 0.1 W/(m K), respectively, showing a nearly isotropic thermal transport property. The reduced LTC of $\kappa$-Ga$_2$O$_3$ versus $\beta$-Ga$_2$O$_3$ stems from its restricted low-frequency phonons up to 5 THz. Furthermore, we find that the $\beta$ phase exhibits a typical temperature dependence slightly stronger than $\sim T^{-1}$, whereas the $\kappa$ phase shows a weaker temperature dependence, ranging from $\sim T^{-0.5}$ to $\sim T^{-0.7}$.

cond-mat.mtrl-sci↗

arXiv2023

Hidden phase uncovered by ultrafast carrier dynamics in thin Bi2O2Se

Bi2O2Se has attracted intensive attention due to its potential in electronics, optoelectronics, as well as ferroelectric applications. Despite that, there have only been a handful of experimental studies based on ultrafast spectroscopy to elucidate the carrier dynamics in Bi2O2Se thin films, Different groups have reported various ultrafast timescales and associated mechanisms across films of different thicknesses. A comprehensive understanding in relation to thickness and fluence is still lacking. In this work, we have systematically explored the thickness-dependent Raman spectroscopy and ultrafast carrier dynamics in chemical vapor deposition (CVD)-grown Bi2O2Se thin films on mica substrate with thicknesses varying from 22.44 nm down to 4.62 nm at both low and high pump fluence regions. Combining the thickness dependence and fluence dependence of the slow decay time, we demonstrate a ferroelectric transition in the thinner (< 8 nm) Bi2O2Se films, influenced by substrate-induced compressive strain and non-equilibrium states. Moreover, this transition can be manifested under highly non-equilibrium states. Our results deepen the understanding of the interplay between the ferroelectric phase and semiconducting characteristics of Bi2O2Se thin films, providing a new route to manipulate the ferroelectric transition.

cond-mat.mtrl-sci↗

arXiv2022

Reliable and Broad-range Layer Identification of Au-assisted Exfoliated Large Area MoS$_2$ and WS$_2$ Using Reflection Spectroscopic Fingerprints

The emerging Au-assisted exfoliation technique provides a wealth of large-area and high-quality ultrathin two-dimensional (2D) materials compared with traditional tape-based exfoliation. Fast, damage-free, and reliable determination of the layer number of such 2D films is essential to study layer-dependent physics and promote device applications. Here, an optical method has been developed for simple, high throughput, and accurate determination of the layer number for Au-assisted exfoliated MoS$_2$ and WS$_2$ films in a broad thickness range. The method is based on quantitative analysis of layer-dependent white light reflection spectra, revealing that the reflection peak intensity can be used as a clear indicator for determining the layer number. The simple yet robust method will facilitate the fundamental study on layer-dependent optical, electrical, and thermal properties and device applications of 2D materials. The technique can also be readily combined with photoluminescence and Raman spectroscopies to study other layer-dependent physical properties of 2D materials.

cond-mat.mtrl-sci↗

arXiv2018

Excitation Wavelength Dependent Reversible Photoluminescence Peak in Iodide Perovskites

Halide perovskites have indisputably exceptional optical and electronic properties, which are attractive for next-generation optoelectronic device technologies. We report on a reversible photoluminescence (PL) peak in iodide-based organic-inorganic lead halide perovskite materials under a two-photon absorption (TPA) process, while tuning the excitation wavelength. This phenomenon occurs when the incoming femtosecond (fs) laser photon energy is higher than a threshold energy. Intriguingly, this phenomenon also occurs in other kinds of iodide perovskite materials. Moreover, two more shorter wavelength peaks exhibit and become prominent when the excitation photon energy is being tuned in the high energy wavelength spectrum, while laser power is remained constant. However, the spectral PL energy window between the original material peak and the first high energy peak can vary based on the optoelectronic properties of the prepared films. The same phenomenon of reversible PL peak is also observed in various iodide based organic-inorganic halides as well as all-inorganic perovskite single crystals and polycrystals. We attribute to the reversible PL peak to the photoinduced structural deformation and the associated change in optical bandgap of iodide perovskites under the femtosecond laser excitation. Our findings will introduce a new degree of freedom in future research as well as adding new functionalities to optoelectronic applications in these emerging perovskite materials.

physics.optics↗