TY - JOUR
T1 - Methyl Thioether Functionalization of a Polymeric Donor for Efficient Solar Cells Processed from Non-Halogenated Solvents
AU - Zhang, Chun Hui
AU - Wang, Wei
AU - Huang, Wei
AU - Wang, Jiang
AU - Hu, Zhubin
AU - Lin, Zhichao
AU - Yang, Tingbin
AU - Lin, Fengyuan
AU - Xing, Yun
AU - Bai, Junxian
AU - Sun, Haitao
AU - Liang, Yongye
N1 - Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/4/23
Y1 - 2019/4/23
N2 - Polymer solar cells (PSCs) processed from non-halogenated solvents are favorable for large scale production. However, the photovoltaic performance of devices from non-halogenated solvents is generally inferior to that of the counterparts from halogenated solvents. Herein, we report the utilization of 5-alkyl-4-(methylthio)thiophene (MTT) as a conjugated side chain of the polymeric donor to achieve efficient PSCs processed from toluene. The derived polymer PMTT56 exhibits lower energy levels than the 5-alkyl-4-methoxythiophene (MOT) counterpart (PMOT39) and 5-(alkylthio)thiophene counterpart (PEHTT). PMTT56 is superior to PMOT39 with an enhanced interchain interaction and hole mobility, and also shows better solubility than PEHTT in toluene. In toluene-processed PSCs, the PMTT56 devices deliver a power conversion efficiency (PCE) of up to 12.6% with IT-2F as the acceptor. By introducing [6,6]-phenyl C 71 -butyric acid methyl ester (PC 71 BM) as the second acceptor, a remarkable PCE of 13.2% is further achieved in the ternary devices, which is among the best for PSCs processed from toluene. Our study presents a fine-tuning approach to develop efficient organic photovoltaic materials processed from non-halogenated solvents.
AB - Polymer solar cells (PSCs) processed from non-halogenated solvents are favorable for large scale production. However, the photovoltaic performance of devices from non-halogenated solvents is generally inferior to that of the counterparts from halogenated solvents. Herein, we report the utilization of 5-alkyl-4-(methylthio)thiophene (MTT) as a conjugated side chain of the polymeric donor to achieve efficient PSCs processed from toluene. The derived polymer PMTT56 exhibits lower energy levels than the 5-alkyl-4-methoxythiophene (MOT) counterpart (PMOT39) and 5-(alkylthio)thiophene counterpart (PEHTT). PMTT56 is superior to PMOT39 with an enhanced interchain interaction and hole mobility, and also shows better solubility than PEHTT in toluene. In toluene-processed PSCs, the PMTT56 devices deliver a power conversion efficiency (PCE) of up to 12.6% with IT-2F as the acceptor. By introducing [6,6]-phenyl C 71 -butyric acid methyl ester (PC 71 BM) as the second acceptor, a remarkable PCE of 13.2% is further achieved in the ternary devices, which is among the best for PSCs processed from toluene. Our study presents a fine-tuning approach to develop efficient organic photovoltaic materials processed from non-halogenated solvents.
UR - https://www.scopus.com/pages/publications/85064803983
U2 - 10.1021/acs.chemmater.9b00926
DO - 10.1021/acs.chemmater.9b00926
M3 - 文章
AN - SCOPUS:85064803983
SN - 0897-4756
VL - 31
SP - 3025
EP - 3033
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 8
ER -