Issue 5, 2019

Hole delocalization as a driving force for charge pair dissociation in organic photovoltaics

Abstract

Charge carrier photogeneration is studied in photovoltaic blends of the conjugated polymer PTB7 with the electron acceptor PC71BM at low excitation densities using broadband transient absorption spectroscopy. In the optimized blend we observe a rise of hole polaron absorption on a 500 ps time scale which implies an increase of hole delocalization when photo-generated charge pairs dissociate into free charges. This concept is supported by the observed saturation of polaron absorption with electrochemical oxidation of polymer films, and the significant differences in transient absorption spectra observed in an inefficient blend due to bound charge transfer (CT) states. Our results suggest that hole polaron delocalization on polymer chains and entropy provide driving force for charge separation by lowering the free energy of the spatially separated charge pair. A potential barrier to the reformation of CT states appears as a result of carrier delocalization which also helps to reduce non-geminate carrier recombination.

Graphical abstract: Hole delocalization as a driving force for charge pair dissociation in organic photovoltaics

Supplementary files

Article information

Article type
Communication
Submitted
25 Sep 2018
Accepted
15 Jan 2019
First published
27 Feb 2019
This article is Open Access
Creative Commons BY license

Mater. Horiz., 2019,6, 1050-1056

Hole delocalization as a driving force for charge pair dissociation in organic photovoltaics

A. B. Matheson, A. Ruseckas, S. J. Pearson and I. D. W. Samuel, Mater. Horiz., 2019, 6, 1050 DOI: 10.1039/C8MH01204K

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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