TY - JOUR
T1 - Thieno[3,4-c]pyrrole-4,6(5H)-dione Polymers with Optimized Energy Level Alignments for Fused-Ring Electron Acceptor Based Polymer Solar Cells
AU - Lin, Fengyuan
AU - Huang, Wei
AU - Sun, Haitao
AU - Xin, Jingming
AU - Zeng, Hao
AU - Yang, Tingbin
AU - Li, Meilin
AU - Zhang, Xing
AU - Ma, Wei
AU - Liang, Yongye
N1 - Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/7/11
Y1 - 2017/7/11
N2 - Rapid advances have been recently demonstrated in polymer solar cells (PSCs) with fused-ring electron acceptors (FREAs), which have low bandgap and high electron mobility. Semiconducting polymer donors with medium bandgap to complement the absorption and proper energy level alignments to minimize energy loss are preferred in this system, but there are few studies on them. Here, we explore thieno[3,4-c]pyrrole-4,6(5H)-dione (TPD) based polymers for high performance PSCs with FREAs. A new TPD polymer, PMOT16, is developed with 4-methoxyl thiophene as conjugated side chains on the benzo[1,2-b:4,5-b′]dithiophene unit. PMOT16 exhibits lower energy levels and enhanced interactions compared to the thiophene counterpart, PBDTT-6ttTPD. However, in PSCs with ITIC as the acceptor, PMOT16 shows inferior performance to PBDTT-6ttTPD on short circuit current (JSC) and fill factor. When IDIC with lower energy levels is employed as acceptor, PMOT16 PSCs show decent power conversion efficiencies (PCEs) of around 10% with low energy loss, which surpasses that of PBDTT-6ttTPD due to increase of open circuit voltage. It is found that the lower JSC and inferior PCE in PMOT16:ITIC are ascribed to the approaching of energy levels between PMOT16 and ITIC. Our studies highlight the potential of TPD based polymers for high performance FREA-PSCs and the necessity for tuning energy level alignments.
AB - Rapid advances have been recently demonstrated in polymer solar cells (PSCs) with fused-ring electron acceptors (FREAs), which have low bandgap and high electron mobility. Semiconducting polymer donors with medium bandgap to complement the absorption and proper energy level alignments to minimize energy loss are preferred in this system, but there are few studies on them. Here, we explore thieno[3,4-c]pyrrole-4,6(5H)-dione (TPD) based polymers for high performance PSCs with FREAs. A new TPD polymer, PMOT16, is developed with 4-methoxyl thiophene as conjugated side chains on the benzo[1,2-b:4,5-b′]dithiophene unit. PMOT16 exhibits lower energy levels and enhanced interactions compared to the thiophene counterpart, PBDTT-6ttTPD. However, in PSCs with ITIC as the acceptor, PMOT16 shows inferior performance to PBDTT-6ttTPD on short circuit current (JSC) and fill factor. When IDIC with lower energy levels is employed as acceptor, PMOT16 PSCs show decent power conversion efficiencies (PCEs) of around 10% with low energy loss, which surpasses that of PBDTT-6ttTPD due to increase of open circuit voltage. It is found that the lower JSC and inferior PCE in PMOT16:ITIC are ascribed to the approaching of energy levels between PMOT16 and ITIC. Our studies highlight the potential of TPD based polymers for high performance FREA-PSCs and the necessity for tuning energy level alignments.
UR - https://www.scopus.com/pages/publications/85022346999
U2 - 10.1021/acs.chemmater.7b01335
DO - 10.1021/acs.chemmater.7b01335
M3 - 文章
AN - SCOPUS:85022346999
SN - 0897-4756
VL - 29
SP - 5636
EP - 5645
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 13
ER -