Geminate Charge Recombination in Polymer/Fullerene Bulk Heterojunction Films and Implications for Solar Cell Function
Artikel i vetenskaplig tidskrift, 2010

We have studied the influence of three different fullerene derivatives on the charge generation and recombination dynamics of polymer/fullerene bulk heterojunction (BHJ) solar cell blends. Charge generation in APFO3/[70]PCBM and APFO3/[60]PCBM is very similar and somewhat slower than charge generation in APFO3/[70]BTPF. This difference qualitatively matches the trend in free energy change of electron transfer estimated from the LUMO energies of the polymer and fullerene derivatives. The first order (geminate) charge recombination rate is significantly different for the three fullerene derivatives studied and increases in the order APFO3/[70]PCBM < APFO3/[60]PCBM < APFO3/[70]BTPF. The variation in electron transfer rate cannot be explained from the LUMO energies of the fullerene derivatives and single-step electron transfer in the Marcus inverted region and simple considerations of expected trends for the reorganization energy and free energy change. Instead we suggest that geminate charge recombination occurs from a state where electrons and holes have separated to different distances in the various materials because of an initially high charge mobility, different for different materials. In a BHJ thin film this charge separation distance is not sufficient to overcome the electrostatic attraction between electrons and holes and geminate recombination occurs on the nanosecond to hundreds of nanoseconds time scale. In a BHJ solar cell, we suggest that the internal electric field in combination with polarization effects and the dynamic nature of polarons are key features to overcome electron hole interactions to form free extractable charges.

conjugated polymers

open-circuit voltage

photovoltaic cells

transfer

polymer

photoinduced electron-transfer

morphology

polyfluorene copolymer/fullerene blends

excitons

efficient

transient

absorption-spectroscopy

devices

Författare

S. K. Pal

Lunds universitet

Bowling Green State University

T. Kesti

Oulun Yliopisto

M. Maiti

Lunds universitet

Fengling Zhang

Linköpings universitet

Olle Inganäs

Linköpings universitet

Stefan Hellström

Chalmers, Kemi- och bioteknik, Polymerteknologi

Mats Andersson

Chalmers, Kemi- och bioteknik, Polymerteknologi

F. Oswald

Universidad de Castilla-La Mancha

F. Langa

Universidad de Castilla-La Mancha

T. Osterman

Lunds universitet

Torbjoern Pascher

Lunds universitet

A. Yartsev

Lunds universitet

V. Sundstrom

Lunds universitet

Journal of the American Chemical Society

0002-7863 (ISSN) 1520-5126 (eISSN)

Vol. 132 12440-12451

Ämneskategorier

Kemi

DOI

10.1021/ja104786x