arXiv subjects

Junhan Huang

Publications and source records attributed to Junhan Huang.

5 recordsLinked to original sources

arXiv2026

Coherent seeding and control of dynamical ferroelectricity by phonon anharmonicity

Optical control of quantum materials has progressed along two separate directions: creating non-equilibrium states inaccessible at equilibrium, and coherently controlling ultrafast dynamics with multi-pulse protocols. Ferroelectricity is especially attractive in this context because its order parameter, macroscopic polarization, directly links inversion-symmetry breaking to functional response. Yet light-induced ferroelectricity has so far been confined to quantum paraelectrics near the ferroelectric instability, where critical fluctuations obscure the formation of a homogeneous ferroelectric state and complicate its deterministic coherent control. Unifying these capabilities -- preparing a symmetry-broken state and then coherently steering its functionality -- remains a central challenge. Here we show that intense terahertz excitation of a soft phonon mode induces a ferroelectric state in centrosymmetric PbTe, a thermoelectric material with strong lattice anharmonicity but no ferroelectric transition at finite temperature. The light-induced symmetry-broken state can be realized up to about 100 K, without relying on local dipolar fluctuations. Experiment and theory together reveal that terahertz-driven anharmonic coupling between degenerate transverse optical phonons underlies this ferroelectric induction. Furthermore, we demonstrate coherent amplification and suppression of the induced polarization via a double-pulse-excitation protocol. These results establish terahertz-driven anharmonic mode coupling as a general strategy for controlling mode-mediated functionalities in quantum materials, opening a route to ultrafast information processing.

cond-mat.mtrl-sci↗

arXiv2026

Efficient high-harmonic generation in van der Waals ferroelectric NbOI$_2$ crystals

Layered NbOX$_2$ ($X=\mathrm{Cl,\,Br,\,I}$), a member of the van der Waals ferroelectric family, exhibits intrinsic ferroelectricity and pronounced nonlinear optical responses, making it a promising candidate for integrated nanophotonics applications. While previous studies have emphasized the material's strong second-order nonlinear responses, higher-order nonlinear responses are still mostly unexplored. This work systematically investigates NbOI$_2$ using high harmonic generation (HHG) spectroscopy. Driven by an intense mid-infrared laser field centered at $\sim4~\mu\mathrm{m}$ wavelength, highly anisotropic odd- and even-order harmonics up to the 16th order are generated at a low peak intensity of $0.4~\mathrm{TW\,cm^{-2}}$, extending beyond the material's bandgap. Both bulk and flake forms of NbOI$_2$ display pronounced harmonic emission from the near-infrared to the deep-ultraviolet spectral region, with a notably high overall conversion efficiency compared to other known materials. Polarization-resolved measurements reveal that even-order harmonics remain aligned with the crystal polar axis regardless of the driving-field orientation, whereas odd-order harmonics are dynamically affected. First-principles calculations suggest that the flat valence band associated with Peierls dimerization enhances HHG efficiency through electron correlation. These findings provide fresh perspectives on HHG in van der Waals ferroelectric materials and facilitate the development of compact and tunable quantum light sources.

cond-mat.mtrl-sci↗

arXiv2025

Ultrafast giant enhancement of second harmonic generation in a strongly correlated cobaltite

In quantum materials, nonlinear optical responses are highly sensitive to electronic structure and many-body interactions. Probing and manipulating such nonlinear processes is a complex and subtle endeavor, yet it offers deep insights into emerging physics and functionalities. Here, we report an anomalous ultrafast enhancement of second harmonic generation (SHG) in a strongly correlated cobaltite YbBaCo$_4$O$_7$. Above-bandgap femtosecond pumping increases SHG intensity by up to 60 % within 200 fs, with the enhancement persisting for tens of picoseconds. The enhancement is strongly anisotropic, with substantial amplification of in-plane susceptibility tensors, whereas the out-of-plane counterpart shows negligible change. We attribute these anomalies to ultrafast photodoping-induced modulation of the on-site Coulomb repulsion, which dynamically renormalizes the band structure and selectively amplifies specific $\chi^{(2)}$ components. These nonlinear dynamics encode rich information about the orbital symmetries and energies of the states involved, opening new avenues for all-optical probing of electronic structure in strongly correlated materials.

cond-mat.str-el↗

arXiv2025

Ultrafast Orbital-Selective Photodoping Melts Charge Order in Overdoped Bi-based Cuprates

High-temperature superconductivity in cuprates remains one of the enduring puzzles of condensed matter physics, with charge order (CO) playing a central yet elusive role, particularly in the overdoped regime. Here, we employ time-resolved X-ray absorption spectroscopy and resonant X-ray scattering at a free-electron laser to probe the transient electronic density of states and ultrafast CO dynamics in overdoped (Bi,Pb)$_{2.12}$Sr$_{1.88}$CuO$_{6+\delta}$. We reveal a striking pump laser wavelength dependence - the 800 nm light fails to suppress CO, whereas the 400 nm light effectively melts it. This behavior originates from the fact that 400 nm photons can promote electrons from the Zhang-Rice singlet band to the upper Hubbard band or apical oxygen states, while 800 nm photons lack the energy to excite electrons across the charge-transfer gap. The CO recovery time ($\sim$3 ps) matches that of the underdoped cuprates, indicating universal electronic instability in the phase diagram. Additionally, melting overdoped CO requires an order-of-magnitude higher fluence highlighting the role of lattice interactions. Our findings demonstrate orbital-selective photodoping and provide a route to ultrafast control of emergent quantum phases in correlated materials.

cond-mat.supr-con↗

arXiv2025

Stabilization and Destabilization of Multimode Solitons in Nonlinear Degenerate Multi-Pass Cavities

Optical solitons in multimode nonlinear optical systems offer a unique platform for exploring the interplay of nonlinearity, dispersion, and spatial mode coupling, offering insights into complex nonlinear wave phenomena. Multi-pass cavities (MPCs) incorporating nonlinear Kerr media serve as prototypical systems, enabling high-efficiency supercontinuum generation and pulse compression. However, stabilizing femtosecond laser pulses in solid-medium-based MPCs (solid MPCs) under strong Kerr nonlinearity remains a significant challenge due to multimode coupling, which disrupts beam stability. In this work, we address this challenge by investigating the stability of laser pulses in MPCs using Floquet and perturbation model. We identify novel mode-coupling-suppression (MCS) medium lengths, where destructive interference among multimode wave components suppresses coupling and facilitates soliton stabilization. Under MCS conditions, our simulations demonstrate stable beam propagation in solid MPCs with nonlinear phases up to 1.5{\pi} per pass, achieving >13-fold pulse compression with excellent spatio-spectral homogeneity. Our findings offer valuable guidance for designing advanced MPCs with tailored Kerr media.

physics.optics↗