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Abstract
Ultrafast Raman spectroscopy with attosecond pulses in the extreme ultraviolet and X-ray regime has been proposed theoretically for tracking the non-adiabatic dynamics of molecules in great detail. The large bandwidth of these pulses, which span several electronvolts within a couple of femtoseconds, provides a unique tool for tracking non-adiabatic phenomena. However, spectroscopy with classical light is limited by the time-bandwidth product of the probe laser pulse. In this work, we theoretically investigate an ultrafast Raman spectroscopy scheme that utilizes pairs of entangled photons. Our model simulations demonstrate that the dynamics in the vicinity of a conical intersection can be resolved with unprecedented resolution in the time and frequency domain. © 2024 The Authors. Published by American Chemical Society.
| Original language | English |
|---|---|
| Pages (from-to) | 2023-2030 |
| Journal | Journal of Physical Chemistry Letters |
| Volume | 15 |
| Issue number | 7 |
| Online published | 13 Feb 2024 |
| DOIs | |
| Publication status | Published - 22 Feb 2024 |
Funding
M.K. acknowledges support from the Swedish Research Council (Grant VR 2022-05005). Z.Z. is thankful for the support of the Early Career Scheme from Hong Kong Research Grants Council (21302721), the National Science Foundation of China (12104380), and the National Science Foundation of China/RGC Collaborative Research Scheme (CRS-CUHK401/22).
Publisher's Copyright Statement
- This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/
RGC Funding Information
- RGC-funded
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ECS: Theory of Novel Quantum Nonlinear Spectroscopy for Molecular Relaxation and Radiative Processes in Nanoscale
ZHANG, Z. (Principal Investigator / Project Coordinator)
1/01/22 → …
Project: Research