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Side-chain sequence enabled regioisomeric acceptors, bearing different side-chain sequences on the same conjugated backbone, are herein reported. Two regioregular polymers PTBI-1 and PTBI-2 and one regiorandom polymer PTBI-3 were synthesized from these two regioisomeric acceptors for a comparative study. UV–vis–NIR absorption spectroscopy and electrochemical study confirmed similar frontier molecular orbital levels of the three polymers in their solid state. More intriguingly, absorption profiles suggest that the sequence of side chains greatly governs the aggregation behaviors. Furthermore, the PTBI-2 film shows larger ordered domains than PTBI-1 and PTBI-3 films, as supported by AFM and GIWAXS measurements. As a result, PTBI-2-based FET devices achieved an average hole mobility of 1.37 cm2 V–1 s–1, much higher than the two polymers with other side-chain sequences. The regiorandom PTBI-3 exhibited the lowest average hole mobility of 0.27 cm2 V–1 s–1. This study highlights the significant impact of side-chain sequence regioisomerism on aggregation behaviors, morphologies, and subsequently charge transport properties of donor–acceptor type conjugated polymers.
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Carbon nanoonion-ferrocene conjugates as acceptors in organic photovoltaic devices
Many macromolecular systems, including carbon nanostructures (CNs), have been synthesized and investigated as acceptors in photovoltaic devices. Some CNs have shown interesting electrochemical, photophysical and electrocatalytic properties and have been used in energy and sustainability applications. This study focuses on the covalent functionalization of carbon nanoonion (CNO) surfaces with ferrocene moieties to obtain donor–acceptor systems involving CNOs as acceptors. The systems were synthesized and characterized by infrared, Raman, UV-vis and fluorescence spectroscopies, thermogravimetric analysis, scanning electron microscopy, nitrogen adsorption and electrochemical measurements. The HOMO–LUMO levels were calculated to evaluate the possibility of using these systems in photoactive devices. In this study, for the first time, the CNO-based derivatives were applied as acceptors in the active layer of photovoltaic devices. This study is the first to use large CNO-based derivatives as acceptors in organic photovoltaic devices, and a power conversion efficiency as high as 1.89% was achieved.
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- Award ID(s):
- 1801317
- PAR ID:
- 10172700
- Date Published:
- Journal Name:
- Nanoscale Advances
- Volume:
- 1
- Issue:
- 8
- ISSN:
- 2516-0230
- Page Range / eLocation ID:
- 3164 to 3176
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1039/c9na00135b
