Related Experiment Video
Updated: Aug 17, 2026

Resonance Fluorescence of an InGaAs Quantum Dot in a Planar Cavity Using Orthogonal Excitation and Detection
Published on: October 13, 2017
Dynamically Tunable Exciton-Photon Coupling via Multi-Physics Field in Transition Metal Dichalcogenide Microcavities
Jingwen Zhang1,2, Wenqi Qian1,2, Haiyi Liu1,2
1Institute of Modern Optics, Tianjin Key Laboratory of Micro-Scale Optical Information Science and Technology, Nankai University, Tianjin, China.
None:
Atomically thin transition-metal dichalcogenides (TMDs) host tightly bound excitons with large oscillator strengths, making them ideal for studying light-matter interactions and polaritonic devices. When integrated with optical microcavities, TMD monolayers and van der Waals heterostructures enable engineering of the local density of optical states (LDOS), giving rise to Purcell-enhanced emission in the weak coupling regime and exciton-polaritons in the strong coupling regime. Practical polariton devices require dynamic, reversible control of exciton-photon detuning and coupling strength, as these parameters determine Hopfield coefficients, dispersion, linewidth, relaxation dynamics, and nonlinear response. Unlike static microcavities, dynamic control enables exciton-polaritons to adapt to diverse operating conditions, allowing real-time functional switching and precise performance optimization. This strategy overcomes the inherent limitations of static control, such as limited functionality and adaptability. Recent advances have established several effective tuning strategies, including piezoelectric, electrical, thermal, and all-optical approaches, enabling control over polariton states and functions including energy tuning, polarization/valley-selective responses, and ultrafast optical modulation. This review summarizes these dynamic control strategies in microcavities and discusses key challenges and future directions toward scalable, stable, on-chip integrated polariton platforms.
Related Concept Videos
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
Colors and Magnetism
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human eye.

