Charge generation dynamics in polymer/polymer solar cells studied by transient absorption spectroscopy

  • Ohkita H
18Citations
Citations of this article
36Readers
Mendeley users who have this article in their library.

Abstract

Currently, polymer/fullerene solar cells have significantly higher power conversion efficiency than polymer/polymer solar cells. In order to address the origin of this wide gap, we measured the transient absorption spectra of polymer/polymer blend films based on poly(3-hexylthiophene) (P3HT) and poly(9,9-dioctylfluorene-alt-benzothiadiazole) (F8BT), and analyzed the charge generation dynamics in comparison with that of a polymer/fullerene blend film based on P3HT and [6,6]-phenyl-C-61 butyric acid methyl ether (PCBM). In P3HT/PCBM blend films, half of the polarons are generated immediately after pulsed laser excitation at the P3HT absorption band and the other half are generated with a rise constant of similar to 10 ps. The prompt polaron formation is assigned to the charge generation from P3HT singlet excitons located near the P3HT/PCBM interface and the delayed polaron formation to the charge generation after the exciton migration to the P3HT/PCBM interface. In P3HT/F8BT, on the other hand, F8BT singlet excitons observed immediately after the laser excitation decayed in a picosecond and P3HT singlet excitons increased on the same time constant, suggesting efficient energy transfer from F8BT to P3HT. Polymer polarons were generated on a time scale of similar to 40 ps, some of which were observed on a microsecond timescale but the yield was much smaller than that in P3HT/PCBM. We discuss the difference in charge generation dynamics in terms of kinetics and interfacial structures. (C) 2011 Society of Photo-Optical Instrumentation Engineers (SPIE). [DOI: 10.1117/1.3569105]

Cite

CITATION STYLE

APA

Ohkita, H. (2011). Charge generation dynamics in polymer/polymer solar cells studied by transient absorption spectroscopy. Journal of Photonics for Energy, 1(1), 011118. https://doi.org/10.1117/1.3569105

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free