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Cited 11 time in webofscience Cited 11 time in scopus
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Outer sidechain engineering of selenophene and thiophene-based Y-series acceptors to produce efficient indoor organic solar cells

Authors
Kim, S.Hong, K.-P.Saeed, M.A.Kim, T.H.Ahn, H.Lee, W.Shim, J.W.Kim, Y.-H.
Issue Date
Jun-2023
Publisher
Elsevier BV
Keywords
Indoor organic photovoltaics; Molecular engineering; Non-fullerene acceptor; Side-chain modification; Y-series acceptor
Citation
Applied Surface Science, v.623
Indexed
SCIE
SCOPUS
Journal Title
Applied Surface Science
Volume
623
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/30844
DOI
10.1016/j.apsusc.2023.157140
ISSN
0169-4332
1873-5584
Abstract
In recent years, efficient indoor organic photovoltaics (OPVs) have emerged as promising energy harvesters to drive Internet of Nanothings (IoNT) applications. The diverse design strategies developed for non-fullerene acceptor (NFA) materials have dramatically increased the power conversion efficiency (PCE) of indoor OPVs to 31%, and progress tends to continue. In this context, the current study investigated the indoor performance of NFA-OPVs by modifying the chalcogen-containing heterocycle of the acceptor molecule to thiophene (ThTh) and selenophene (ThSe), and changing the length of the external side chain using n-hexyl (C6) and n-nonyl (C9) components. Compared with the ThSe systems, the ThTh-containing OPVs exhibited enhanced current densities (JSC) and open-circuit voltages (VOC) owing to their enhanced crystallinity and reduced degree of bimolecular recombination. Similarly, the introduction of a short side chain (i.e., C6) led to relatively reduced monomolecular recombination and a moderated planarity compared to the system modified with the long side chain (i.e., C9). Ultimately, this resulted in an enhanced JSC and improved charge transport properties. Finally, the optimized OPV exhibited a PCE of 24.6% under a 1000 lx light-emitting diode lamp. © 2023 Elsevier B.V.
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