Ultrafast Charge and Triplet State Formation in Diketopyrrolopyrrole Low Band Gap Polymer/Fullerene Blends: Influence of Nanoscale Morphology of Organic Photovoltaic Materials on Charge Recombination to the Triplet State

Femtosecond transient absorption spectroscopy of thin films of two types of morphologies of diketopyrrolopyrrole low band gap polymer/fullerene-adduct blends is presented and indicates triplet state formation by charge recombination, an important loss channel in organic photovoltaic materials. At lo...

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Main Authors: René M. Williams, Hung-Cheng Chen, Daniele Di Nuzzo, Stephan C. J. Meskers, René A. J. Janssen
Format: Article
Language:English
Published: Wiley 2017-01-01
Series:Journal of Spectroscopy
Online Access:http://dx.doi.org/10.1155/2017/6867507
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author René M. Williams
Hung-Cheng Chen
Daniele Di Nuzzo
Stephan C. J. Meskers
René A. J. Janssen
author_facet René M. Williams
Hung-Cheng Chen
Daniele Di Nuzzo
Stephan C. J. Meskers
René A. J. Janssen
author_sort René M. Williams
collection DOAJ
description Femtosecond transient absorption spectroscopy of thin films of two types of morphologies of diketopyrrolopyrrole low band gap polymer/fullerene-adduct blends is presented and indicates triplet state formation by charge recombination, an important loss channel in organic photovoltaic materials. At low laser fluence (approaching solar intensity) charge formation characterized by a 1350 nm band (in ~250 fs) dominates in the two PDPP-PCBM blends with different nanoscale morphologies and these charges recombine to form a local polymer-based triplet state on the sub-ns timescale (in ~300 and ~900 ps) indicated by an 1100 nm absorption band. The rate of triplet state formation is influenced by the morphology. The slower rate of charge recombination to the triplet state (in ~900 ps) belongs to a morphology that results in a higher power conversion efficiency in the corresponding device. Nanoscale morphology not only influences interfacial area and conduction of holes and electrons but also influences the mechanism of intersystem crossing (ISC). We present a model that correlates morphology to the exchange integral and fast and slow mechanisms for ISC (SOCT-ISC and H-HFI-ISC). For the pristine polymer, a flat and unstructured singlet-singlet absorption spectrum (between 900 and 1400 nm) and a very minor triplet state formation (5%) are observed at low laser fluence.
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institution Kabale University
issn 2314-4920
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spelling doaj-art-1503aac3aa0c41b6ba86e6547ce3cd482025-02-03T01:11:25ZengWileyJournal of Spectroscopy2314-49202314-49392017-01-01201710.1155/2017/68675076867507Ultrafast Charge and Triplet State Formation in Diketopyrrolopyrrole Low Band Gap Polymer/Fullerene Blends: Influence of Nanoscale Morphology of Organic Photovoltaic Materials on Charge Recombination to the Triplet StateRené M. Williams0Hung-Cheng Chen1Daniele Di Nuzzo2Stephan C. J. Meskers3René A. J. Janssen4Molecular Photonics Group, Van’t Hoff Institute for Molecular Sciences (HIMS), Universiteit van Amsterdam, Science Park 904, 1098 XH Amsterdam, NetherlandsMolecular Photonics Group, Van’t Hoff Institute for Molecular Sciences (HIMS), Universiteit van Amsterdam, Science Park 904, 1098 XH Amsterdam, NetherlandsMolecular Materials and Nanosystems, Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven, NetherlandsMolecular Materials and Nanosystems, Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven, NetherlandsMolecular Materials and Nanosystems, Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven, NetherlandsFemtosecond transient absorption spectroscopy of thin films of two types of morphologies of diketopyrrolopyrrole low band gap polymer/fullerene-adduct blends is presented and indicates triplet state formation by charge recombination, an important loss channel in organic photovoltaic materials. At low laser fluence (approaching solar intensity) charge formation characterized by a 1350 nm band (in ~250 fs) dominates in the two PDPP-PCBM blends with different nanoscale morphologies and these charges recombine to form a local polymer-based triplet state on the sub-ns timescale (in ~300 and ~900 ps) indicated by an 1100 nm absorption band. The rate of triplet state formation is influenced by the morphology. The slower rate of charge recombination to the triplet state (in ~900 ps) belongs to a morphology that results in a higher power conversion efficiency in the corresponding device. Nanoscale morphology not only influences interfacial area and conduction of holes and electrons but also influences the mechanism of intersystem crossing (ISC). We present a model that correlates morphology to the exchange integral and fast and slow mechanisms for ISC (SOCT-ISC and H-HFI-ISC). For the pristine polymer, a flat and unstructured singlet-singlet absorption spectrum (between 900 and 1400 nm) and a very minor triplet state formation (5%) are observed at low laser fluence.http://dx.doi.org/10.1155/2017/6867507
spellingShingle René M. Williams
Hung-Cheng Chen
Daniele Di Nuzzo
Stephan C. J. Meskers
René A. J. Janssen
Ultrafast Charge and Triplet State Formation in Diketopyrrolopyrrole Low Band Gap Polymer/Fullerene Blends: Influence of Nanoscale Morphology of Organic Photovoltaic Materials on Charge Recombination to the Triplet State
Journal of Spectroscopy
title Ultrafast Charge and Triplet State Formation in Diketopyrrolopyrrole Low Band Gap Polymer/Fullerene Blends: Influence of Nanoscale Morphology of Organic Photovoltaic Materials on Charge Recombination to the Triplet State
title_full Ultrafast Charge and Triplet State Formation in Diketopyrrolopyrrole Low Band Gap Polymer/Fullerene Blends: Influence of Nanoscale Morphology of Organic Photovoltaic Materials on Charge Recombination to the Triplet State
title_fullStr Ultrafast Charge and Triplet State Formation in Diketopyrrolopyrrole Low Band Gap Polymer/Fullerene Blends: Influence of Nanoscale Morphology of Organic Photovoltaic Materials on Charge Recombination to the Triplet State
title_full_unstemmed Ultrafast Charge and Triplet State Formation in Diketopyrrolopyrrole Low Band Gap Polymer/Fullerene Blends: Influence of Nanoscale Morphology of Organic Photovoltaic Materials on Charge Recombination to the Triplet State
title_short Ultrafast Charge and Triplet State Formation in Diketopyrrolopyrrole Low Band Gap Polymer/Fullerene Blends: Influence of Nanoscale Morphology of Organic Photovoltaic Materials on Charge Recombination to the Triplet State
title_sort ultrafast charge and triplet state formation in diketopyrrolopyrrole low band gap polymer fullerene blends influence of nanoscale morphology of organic photovoltaic materials on charge recombination to the triplet state
url http://dx.doi.org/10.1155/2017/6867507
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