TY - JOUR
T1 - Femtosecond Photophysics of Molecular Polaritons
AU - Fassioli, Francesca
AU - Park, Kyu Hyung
AU - Bard, Sarah E.
AU - Scholes, Gregory D.
N1 - Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/11/25
Y1 - 2021/11/25
N2 - Molecular polaritons are hybrid states of photonic and molecular character that form when molecules strongly interact with light. Strong coupling tunes energy levels and, importantly, can modify molecular properties (e.g., photoreaction rates), opening an avenue for novel polariton chemistry. In this Perspective, we focus on the collective aspects of strongly coupled molecular systems and how this pertains to the dynamical response of such systems, which, though of key importance for attaining modified function under polariton formation, is still not well-understood. We discuss how the ultrafast time and spectral resolution make pump-probe spectroscopy an ideal tool to reveal the energy-transfer pathways from polariton states to other molecular states of functional interest. Finally, we illustrate how analyzing the free (rather than electronic) energy structure in molecular polariton systems may provide new clues into how energy flows and thus how strong coupling may be exploited.
AB - Molecular polaritons are hybrid states of photonic and molecular character that form when molecules strongly interact with light. Strong coupling tunes energy levels and, importantly, can modify molecular properties (e.g., photoreaction rates), opening an avenue for novel polariton chemistry. In this Perspective, we focus on the collective aspects of strongly coupled molecular systems and how this pertains to the dynamical response of such systems, which, though of key importance for attaining modified function under polariton formation, is still not well-understood. We discuss how the ultrafast time and spectral resolution make pump-probe spectroscopy an ideal tool to reveal the energy-transfer pathways from polariton states to other molecular states of functional interest. Finally, we illustrate how analyzing the free (rather than electronic) energy structure in molecular polariton systems may provide new clues into how energy flows and thus how strong coupling may be exploited.
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U2 - 10.1021/acs.jpclett.1c03183
DO - 10.1021/acs.jpclett.1c03183
M3 - Article
C2 - 34792371
AN - SCOPUS:85119954122
SN - 1948-7185
VL - 12
SP - 11444
EP - 11459
JO - Journal of Physical Chemistry Letters
JF - Journal of Physical Chemistry Letters
IS - 46
ER -