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S,N-Heteropentacene based small molecules with A-D-A structure for solution processed organic bulk heterojunction solar cells

Authors
Jo, HyeonjunPark, SojinChoi, HyejuLee, SubokSong, KihyungBiswas, S.Sharma, AbhishekSharma, Ganesh. D.Ko, Jaejung
Issue Date
2015
Publisher
ROYAL SOC CHEMISTRY
Citation
RSC ADVANCES, v.5, no.123, pp.102115 - 102125
Indexed
SCIE
SCOPUS
Journal Title
RSC ADVANCES
Volume
5
Number
123
Start Page
102115
End Page
102125
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/96279
DOI
10.1039/c5ra21657e
ISSN
2046-2069
Abstract
Two small molecules with acceptor-donor-acceptor (A-D-A) structures, i.e. SN(BTTh2)(2) and SN(BTAOTh(2))(2), denoted as J and K, respectively, containing an electron rich planar S, N-heteropentacene as the central core flanked with alkoxy substituted and un-substituted benzothiadiazole (BT) and end capped with hexyl-substituted bi-thiophene units, were designed and synthesized. Optical and electrochemical investigation of these two small molecules reveals that these compounds possess low optical bandgaps and broader absorption profiles to harvest solar photons, as well as suitable electrochemical molecular energy levels for application as donors in bulk heterojunction organic solar cells. The photovoltaic properties of these two small molecules as donors and PC71BM as the acceptor in solution processed bulk heterojunction cells were investigated. Devices based on cast J : PC71BM and K : PC71BM active layers showed power conversion efficiencies (PCE) of 1.96% and 1.57%, respectively; these efficiencies improved to 6.02% and 5.06% when the active layers were subjected to two steps annealing (TSA), i.e. combined thermal annealing followed by solvent vapor annealing. The increase in PCE was due to the enhancement of both the short circuit current (Jsc) and fill factor (FF) due to the enhancement of the light harvesting ability of the active layer, better phase separation between the small molecules and PC71BM, and more balanced charge transport induced by the TSA treatment.
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