Please use this identifier to cite or link to this item: https://ktisis.cut.ac.cy/handle/10488/14102
Title: Impact of Polymer Side Chain Modification on OPV Morphology and Performance
Authors: Neophytou, Marios 
Liu, Shengjian 
Gu, Xiaodan 
Savikhin, Victoria 
Babics, Maxime 
Beaujuge, Pierre M. 
Oosterhout, Stefan D. 
Yan, Hongping 
Toney, Michael F. 
Keywords: conformal deposition;large area;nickel oxide;p-i-n perovskite device configuration;perovskite solar cells;room-temperature processing;sputtering
Issue Date: 13-Nov-2018
Source: ACS Applied Energy Materials, Volume 1, Issue 11, 26 November 2018, Pages 6227-6233
Journal: Chemistry of Materials
Abstract: © 2018 American Chemical Society. Efficiencies of organic photovoltaic (OPV) devices have been steadily climbing, but there is still a prominent gap in understanding the relationship between fabrication and performance. Side chain substitution is one processing parameter that can change OPV device efficiency considerably, primarily because of variations in morphology. In this work, we explain the morphological link between side chain selection and device performance in one polymer to aid in the development of design rules more broadly. We study the morphology of an OPV active layer using a PBDTTPD-backbone polymer with four different side chain configurations, which are shown to change device efficiency by up to 4 times. The optimal device has the smallest domain sizes, the highest degree of crystallinity, and the most face-on character. This is achieved with two branched 2-ethylhexyl (2EH) side chains placed symmetrically on the BDT unit and a linear octyl (C8) side chain on the TPD unit. Substituting either side chain (C14 on BDT and/or 2EH on TPD) makes the orientation less face-on, while the TPD side chain primarily affects domain size. For all side chains, the addition of fullerene increases polymer crystallization compared to the neat film, but the degree of mixing between polymer and fullerene varies with side chain. Interestingly, the optimal device has a negligible amount of mixed phase. The domain sizes present in the optimal system are remarkably unchanged with a changing fullerene ratio between 10 and 90%, hinting that the polymer preferentially self-assembles into 10-20 nm crystallites regardless of concentration. The formation of this crystallite may be the key factor inhibiting mixed phase.
URI: https://ktisis.cut.ac.cy/handle/10488/14102
ISSN: 25740962
DOI: 10.1021/acs.chemmater.8b03455
Type: Article
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