TY - JOUR
T1 - Picosecond Charge-Transfer-State Dynamics in Wide Band Gap Polymer-Non-Fullerene Small-Molecule Blend Films Investigated via Transient Infrared Spectroscopy
AU - Nuber, Matthias
AU - Spanier, Lukas V.
AU - Roth, Sebastian
AU - Vayssilov, Georgi N.
AU - Kienberger, Reinhard
AU - Müller-Buschbaum, Peter
AU - Iglev, Hristo
N1 - Publisher Copyright:
© 2022 American Chemical Society. All rights reserved.
PY - 2022/11/10
Y1 - 2022/11/10
N2 - Organic solar cells based on wide band gap polymers and nonfullerene small-molecule acceptors have demonstrated remarkably good device performances. Nevertheless, a thorough understanding of the charge-transfer process in these materials has not been achieved yet. In this study, we use Fano resonance signals caused by the interaction of broad electronic charge carrier absorption and the molecular vibrations of the electron acceptor molecule to monitor the charge-transfer state dynamics. In our time-resolved infrared spectroscopy experiments, we find that in the small-molecule acceptor, they have additional dynamics on the order of a few picoseconds. A change in the solvent used in thin film deposition, leading to different morphologies, influences this time further. We interpret our findings as the dynamics of the charge-transfer state at the interface of the electron donor and the electron- acceptor. The additional mid-infrared transient signal is generated in this state, as both electron and hole polarons can interact with small-molecule acceptor vibrational modes.
AB - Organic solar cells based on wide band gap polymers and nonfullerene small-molecule acceptors have demonstrated remarkably good device performances. Nevertheless, a thorough understanding of the charge-transfer process in these materials has not been achieved yet. In this study, we use Fano resonance signals caused by the interaction of broad electronic charge carrier absorption and the molecular vibrations of the electron acceptor molecule to monitor the charge-transfer state dynamics. In our time-resolved infrared spectroscopy experiments, we find that in the small-molecule acceptor, they have additional dynamics on the order of a few picoseconds. A change in the solvent used in thin film deposition, leading to different morphologies, influences this time further. We interpret our findings as the dynamics of the charge-transfer state at the interface of the electron donor and the electron- acceptor. The additional mid-infrared transient signal is generated in this state, as both electron and hole polarons can interact with small-molecule acceptor vibrational modes.
UR - http://www.scopus.com/inward/record.url?scp=85141578664&partnerID=8YFLogxK
U2 - 10.1021/acs.jpclett.2c02864
DO - 10.1021/acs.jpclett.2c02864
M3 - Article
C2 - 36326207
AN - SCOPUS:85141578664
SN - 1948-7185
VL - 13
SP - 10418
EP - 10423
JO - Journal of Physical Chemistry Letters
JF - Journal of Physical Chemistry Letters
IS - 44
ER -