Search arXiv⌕ Search

arXiv · 2610.29109

Coherent dynamics and ultrafast evolution of optical nonlinearity of self-hybridized exciton-polaritons in WSe2

Abstract

Exciton-polaritons (EPs) are valuable for investigating macroscopic quantum coherent phenomena. However, overcoming the rapid decoherence of EPs under ambient conditions is challenging, even using delicately fabricated optical cavities. Here, we show pronounced coherent dynamics in thin flakes of WSe2 supporting self-hybridized EPs. Ultrafast two-dimensional electronic spectroscopy (2DES) resolves two types of quantum beating: Rabi oscillation with a period of ~ 24 fs and a slower, ~ 50 fs period oscillation, revealing coherent coupling not only between excitons and cavity, but also between polaritons and dark states. Rapid evolution of 2DES line shape indicates a change of dominant optical nonlinearities from Rabi contraction of polaritons to many-body interactions of excitons in the first 100 fs, marking the transition from coherent to incoherent polariton excitations. The results are rationalized by a three-coupled oscillator model considering the inhomogeneous cavity field distribution. We also demonstrate coherent quantum beating between A exciton and its excited Rydberg state A* under ambient conditions. Our results shed light on the coherent control in readily accessible semiconductor thin flakes.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Niu Xu, Jin Yang, Kaizhen Liu, Jianghao Shen, Weiming Song, Abbas Chimeh, Daniel Timmer, Jinhui Zhong. 2026-10-21. Coherent dynamics and ultrafast evolution of optical nonlinearity of self-hybridized exciton-polaritons in WSe2. https://arxiv.org/abs/2610.29109

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Global approximations to the error function of real argument for vectorized computation

The error function of real argument can be approximated to a given uniform relative accuracy by a single closed-form expression for the whole variable range either in terms of addition, multiplication, division, and square root operations only, or also using the exponential function. Approximations to the complementary error function have also been found, including those where either only additions, multiplications, and one division, or also the exponential, are used to reach either a uniform absolute, or a uniform relative, accuracy. The coefficients have been tabulated for up to 128-bit precision. Tests of a computer code implementation using the standard single- and double-precision floating-point arithmetic show good performance and vectorizability.

physics.chem-ph↗

Accelerating Periodic Coupled Cluster and Algebraic Diagrammatic Construction Theories With Frozen Natural Orbitals

We present a unified frozen natural orbital (FNO) framework for periodic Gaussian-orbital post-Hartree-Fock calculations with explicit k-point sampling. The approach includes conventional ground-state FNOs together with state-specific (SS-FNO) and state-averaged (SA-FNO) variants constructed from perturbative one-particle density matrices. We implement these approximations for periodic Moller-Plesset perturbation theory, algebraic diagrammatic construction, and equation-of-motion coupled cluster methods in the PySCF software package and benchmark them for correlation energies, equations of state, fundamental band gaps, and quasiparticle band structures of semiconductors and insulators. FNO truncation reproduces canonical results with small errors while substantially reducing computational cost. SS-FNO enables accurate large-basis band-gap calculations, including quadruple-zeta results, whereas SA-FNO efficiently compresses the virtual space for multi-state band-structure calculations. Combined with basis-set and thermodynamic-limit extrapolations, the framework provides a practical route to high-accuracy correlated calculations in periodic systems.

physics.chem-ph↗

SU(2)-Equivariant Spinor Message Passing for Molecular Magnetism

Predicting molecular magnetism often requires electronic-structure calculations with spin-orbit coupling (SOC), which are costly to repeat across many molecules. The underlying electronic states can transform as spinors, yet equivariant surrogates typically use only integer-rank features. Inspired by the spinor nature of these electronic states, we develop eSpinor, an SU(2)-equivariant graph neural network that propagates spinor features. We initialize spinor features from eigenvectors of an approximate SOC Hamiltonian and use gauge-covariant message passing with a gauge-invariant readout to make predictions independent of the arbitrary eigenbasis choice. On cobalt single-molecule magnet candidates, eSpinor improves zero-field-splitting predictions relative to NequIP, including for unseen ligands. For a dysprosium magnetic resonance imaging probe, eSpinor improves real electron-spin correlations over a Hamiltonian-informed baseline despite similar static crystal-field errors and fewer parameters, while accurately predicting low-field nuclear relaxation in water and after transfer to methanol without retraining. Overall, these results demonstrate that SU(2)-equivariant spinor message passing is a useful inductive bias for molecular magnetism. We also find that similar static tensor errors can yield different dynamical errors, motivating model selection based on accuracy for the intended physical observables.

physics.chem-ph↗