TY - JOUR
T1 - Side Group Engineering of Small Molecular Acceptors for High-Performance Fullerene-Free Polymer Solar Cells
T2 - Thiophene Being Superior to Selenophene
AU - Gao, Wei
AU - An, Qiaoshi
AU - Ming, Ruijie
AU - Xie, Dongjun
AU - Wu, Kailong
AU - Luo, Zhenghui
AU - Zou, Yang
AU - Zhang, Fujun
AU - Yang, Chuluo
N1 - Publisher Copyright:
© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2017/9/13
Y1 - 2017/9/13
N2 - Side group of ITIC-like small molecular acceptor (SMA) plays a critical role in crystallization property. In this article, two new SMAs with n-hexylthienyl and n-hexylselenophenyl as side chain, namely ITCPTC-Th and ITCPTC-Se, are designed and synthesized by employing newly developed thiophene-fused ending group (CPTCN). And thiophene and selenophene side group substituted effects of SMA-based fullerene-free polymer solar cells (PSCs) are investigated. A stronger σ-inductive effect between selenophene side group and electron-donating backbone endows ITCPTC-Se with better optical absorption and higher LUMO level, ITCPTC-Th-based PSCs deliver a higher power conversion efficiency of 10.61%. Charge transport and collection, recombination loss mechanism, and morphology of blend films are intensively studied. These results confirm that side group substituted effects of SMAs are multiple and thiophene is a superior option to selenophene as aromatic side group of ITIC-like SMAs.
AB - Side group of ITIC-like small molecular acceptor (SMA) plays a critical role in crystallization property. In this article, two new SMAs with n-hexylthienyl and n-hexylselenophenyl as side chain, namely ITCPTC-Th and ITCPTC-Se, are designed and synthesized by employing newly developed thiophene-fused ending group (CPTCN). And thiophene and selenophene side group substituted effects of SMA-based fullerene-free polymer solar cells (PSCs) are investigated. A stronger σ-inductive effect between selenophene side group and electron-donating backbone endows ITCPTC-Se with better optical absorption and higher LUMO level, ITCPTC-Th-based PSCs deliver a higher power conversion efficiency of 10.61%. Charge transport and collection, recombination loss mechanism, and morphology of blend films are intensively studied. These results confirm that side group substituted effects of SMAs are multiple and thiophene is a superior option to selenophene as aromatic side group of ITIC-like SMAs.
KW - fullerene-free polymer solar cells
KW - selenophene
KW - side groups
KW - small molecular acceptors
KW - thiophene
UR - http://www.scopus.com/inward/record.url?scp=85025081341&partnerID=8YFLogxK
U2 - 10.1002/adfm.201702194
DO - 10.1002/adfm.201702194
M3 - Article
AN - SCOPUS:85025081341
SN - 1616-301X
VL - 27
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 34
M1 - 1702194
ER -