Understanding how charge and energy evolve on ultrafast time and nanoscale length scales is a central challenge in modern physics and nanoscience. In this regime, electronic and vibrational degrees of freedom are strongly coupled, and quantum effects govern how excitations are created, redistributed, and dissipated through complex relaxation pathways.
Our research focuses on directly resolving these non-equilibrium dynamics in quantum materials, molecular systems, and biological complexes. To achieve this, we develop and apply ultrafast and multidimensional optical spectroscopy that accesses electronic dynamics on femtosecond timescales with microscope resolution, enabling real-time observation of energy flow.
By combining advanced spectroscopy with nanoscale material design, we investigate how interfacial structure and dimensionality control energy transport in low-dimensional systems. This approach allows us to establish microscopic mechanisms of light–matter interaction and connect them to emergent functionality in optoelectronic, sensing, and quantum materials.
We are interested in how quantum coherence and nonequilibrium dynamics evolve in low-dimensional systems, where reduced dimensionality and strong light–matter interactions fundamentally reshape energy and charge flow. A central goal of our work is to understand what determines the lifetime and controllability of quantum states in nanoscale materials, and whether optical excitation can be used to actively manipulate these states on ultrafast timescales. We approach these questions by developing time-resolved optical spectroscopy and microscopy capable of probing dynamics under controlled environments.
We are interested in how symmetry, dimensionality, and local structure in quantum materials determine their emergent optical and electronic properties. In particular, we study how engineered symmetry breaking in low-dimensional systems gives rise to new excitonic behavior, modified optical selection rules, and nonlinear optical responses that do not exist in the bulk or isolated building blocks. These effects can be tuned through stacking, strain, and geometric distortions, providing pathways to control exciton localization and collective optical responses.
We are interested in how interactions at molecular–material interfaces reshape electronic structure and give rise to emergent optical responses that are not present in either component alone. At these interfaces, charge redistribution and coupling between molecular excitations and solid-state excitons lead to complex, often hidden, pathways for energy transfer and optical modulation. Our work aims to reveal these interactions by combining ultrafast optical spectroscopy, modeling, and data-driven analysis methods. By uncovering how interfacial coupling governs spectral response and dynamics, we seek to establish general principles for designing highly sensitive and adaptive optical sensing platforms.