Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/18244
Title: Dependence of charge separation efficiency on film microstructure in Poly(3-hexylthiophene-2,5-diyl): [6,6]-phenyl-C61 butyric acid methyl ester blend films
Authors: Keivanidis, Panagiotis E. 
Clarke, Tracey M. 
Lilliu, Samuele 
Agostinelli, Tiziano 
MacDonald, J. Emyr 
Durrant, James R. 
Bradley, Donal D.C. 
Nelson, Jenny 
Major Field of Science: Engineering and Technology
Field Category: Electrical Engineering - Electronic Engineering - Information Engineering
Keywords: Kinetics;Spectroscopy
Issue Date: 18-Feb-2010
Source: The Journal of Physical Chemistry Letters, 2010, vol. 1, iss. 4, pp. 734-738
Volume: 1
Issue: 4
Start page: 734
End page: 738
Journal: The Journal of Physical Chemistry Letters 
Abstract: Herein we address the factors controlling photocurrent generation in P3HT:PCBM blend films as a function of blend composition and annealing treatment. Absorption, photoluminescence, and transient absorption spectroscopy are used to distinguish the role of exciton dissociation, charge pair separation, and charge collection. Variations in blend film microstructure with composition and annealing treatment are studied using X-ray diffraction. While the trend in photocurrent generation with composition and annealing [Muller, et al., Adv. Mater. 2008, 20, 3510] does not follow the trend in exciton dissociation, it closely follows the trend in charge pair generation. Moreover, charge pair generation efficiency is positively correlated to the degree of polymer crystallization and the appearance of large domains of both polymer and fullerene phases. We argue that larger domains assist charge pair separation by increasing the probability of escape from the P3HT:PCBM interface, thus reducing geminate charge recombination. © 2010 American Chemical Society.
ISSN: 19487185
DOI: 10.1021/jz900296f
Rights: © American Chemical Society
Type: Article
Affiliation : Imperial College London 
Cardiff University 
Publication Type: Peer Reviewed
Appears in Collections:Άρθρα/Articles

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