TY - JOUR
T1 - The role of spin in the kinetic control of recombination in organic photovoltaics
AU - Rao, Akshay
AU - Chow, Philip C. Y.
AU - Gélinas, Simon
AU - Schlenker, Cody W.
AU - Li, Chang-Zhi
AU - Yip, Hin-Lap
AU - Jen, Alex K.-Y.
AU - Ginger, David S.
AU - Friend, Richard H.
PY - 2013/8/22
Y1 - 2013/8/22
N2 - In biological complexes, cascade structures promote the spatial separation of photogenerated electrons and holes, preventing their recombination. In contrast, the photogenerated excitons in organic photovoltaic cells are dissociated at a single donor-acceptor heterojunction formed within a de-mixed blend of the donor and acceptor semiconductors. The nanoscale morphology and high charge densities give a high rate of electron-hole encounters, which should in principle result in the formation of spin-triplet excitons, as in organic light-emitting diodes. Although organic photovoltaic cells would have poor quantum efficiencies if every encounter led to recombination, state-of-the-art examples nevertheless demonstrate near-unity quantum efficiency. Here we show that this suppression of recombination arises through the interplay between spin, energetics and delocalization of electronic excitations in organic semiconductors. We use time-resolved spectroscopy to study a series of model high-efficiency polymer-fullerene systems in which the lowest-energy molecular triplet exciton (T 1) for the polymer is lower in energy than the intermolecular charge transfer state. We observe the formation of T 1 states following bimolecular recombination, indicating that encounters of spin-uncorrelated electrons and holes generate charge transfer states with both spin-singlet (1 CT) and spin-triplet (3 CT) characters. We show that the formation of triplet excitons can be the main loss mechanism in organic photovoltaic cells. But we also find that, even when energetically favoured, the relaxation of 3 CT states to T 1 states can be strongly suppressed by wavefunction delocalization, allowing for the dissociation of 3 CT states back to free charges, thereby reducing recombination and enhancing device performance. Our results point towards new design rules both for photoconversion systems, enabling the suppression of electron-hole recombination, and for organic light-emitting diodes, avoiding the formation of triplet excitons and enhancing fluorescence efficiency. © 2013 Macmillan Publishers Limited. All rights reserved.
AB - In biological complexes, cascade structures promote the spatial separation of photogenerated electrons and holes, preventing their recombination. In contrast, the photogenerated excitons in organic photovoltaic cells are dissociated at a single donor-acceptor heterojunction formed within a de-mixed blend of the donor and acceptor semiconductors. The nanoscale morphology and high charge densities give a high rate of electron-hole encounters, which should in principle result in the formation of spin-triplet excitons, as in organic light-emitting diodes. Although organic photovoltaic cells would have poor quantum efficiencies if every encounter led to recombination, state-of-the-art examples nevertheless demonstrate near-unity quantum efficiency. Here we show that this suppression of recombination arises through the interplay between spin, energetics and delocalization of electronic excitations in organic semiconductors. We use time-resolved spectroscopy to study a series of model high-efficiency polymer-fullerene systems in which the lowest-energy molecular triplet exciton (T 1) for the polymer is lower in energy than the intermolecular charge transfer state. We observe the formation of T 1 states following bimolecular recombination, indicating that encounters of spin-uncorrelated electrons and holes generate charge transfer states with both spin-singlet (1 CT) and spin-triplet (3 CT) characters. We show that the formation of triplet excitons can be the main loss mechanism in organic photovoltaic cells. But we also find that, even when energetically favoured, the relaxation of 3 CT states to T 1 states can be strongly suppressed by wavefunction delocalization, allowing for the dissociation of 3 CT states back to free charges, thereby reducing recombination and enhancing device performance. Our results point towards new design rules both for photoconversion systems, enabling the suppression of electron-hole recombination, and for organic light-emitting diodes, avoiding the formation of triplet excitons and enhancing fluorescence efficiency. © 2013 Macmillan Publishers Limited. All rights reserved.
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U2 - 10.1038/nature12339
DO - 10.1038/nature12339
M3 - RGC 21 - Publication in refereed journal
SN - 0028-0836
VL - 500
SP - 435
EP - 439
JO - Nature
JF - Nature
IS - 7463
ER -