TY - JOUR
T1 - Designing simple non-fused terthiophene-based electron acceptors for efficient organic solar cells
AU - Li, Jiayu
AU - Li, Kun
AU - Mei, Zhe
AU - Chen, Yu
AU - Xie, Qian
AU - Yu, Chenxu
AU - Liu, Xuefeng
AU - Wang, Yanqi
AU - Wu, Yishi
AU - Liao, Qing
AU - An, Cunbin
AU - Fu, Hongbing
N1 - Publisher Copyright:
© 2024
PY - 2024/9
Y1 - 2024/9
N2 - Low-cost photovoltaic materials are essential for realizing large-scale commercial applications of organic solar cells (OSCs). However, highly efficient OSCs based on low-cost photovoltaic materials are scarce due to a deficiency in understanding the structure-property relationship. Herein, we investigated two low-cost terthiophene-based electron acceptors, namely, 3TC8 and 3TEH, with 3,4-bis(octan-3-yloxy)thiophene, differing only in the alkylated thiophene-bridges. Both acceptors exhibit low optical gaps (∼1.43 eV) and possess deep highest occupied molecular orbital (HOMO) levels (∼−5.8 eV). Notably, the single-crystal structure of 3TEH demonstrates highly planar conjugated backbone and strong π-π stacking between intermolecular terminal groups, attributed to the presence of the bulky alkylated noncovalently conformational locks. Upon utilizing both acceptors to fabricate OSCs, the 3TC8-based device exhibited a power conversion efficiency (PCE) of 11.1%, while the 3TEH-based OSC demonstrated an excellent PCE of 14.4%. This PCE is the highest among OSCs based on terthiophene-containing electron acceptors. These results offer a new strategy for designing low-cost electron acceptors for highly efficient OSCs.
AB - Low-cost photovoltaic materials are essential for realizing large-scale commercial applications of organic solar cells (OSCs). However, highly efficient OSCs based on low-cost photovoltaic materials are scarce due to a deficiency in understanding the structure-property relationship. Herein, we investigated two low-cost terthiophene-based electron acceptors, namely, 3TC8 and 3TEH, with 3,4-bis(octan-3-yloxy)thiophene, differing only in the alkylated thiophene-bridges. Both acceptors exhibit low optical gaps (∼1.43 eV) and possess deep highest occupied molecular orbital (HOMO) levels (∼−5.8 eV). Notably, the single-crystal structure of 3TEH demonstrates highly planar conjugated backbone and strong π-π stacking between intermolecular terminal groups, attributed to the presence of the bulky alkylated noncovalently conformational locks. Upon utilizing both acceptors to fabricate OSCs, the 3TC8-based device exhibited a power conversion efficiency (PCE) of 11.1%, while the 3TEH-based OSC demonstrated an excellent PCE of 14.4%. This PCE is the highest among OSCs based on terthiophene-containing electron acceptors. These results offer a new strategy for designing low-cost electron acceptors for highly efficient OSCs.
KW - Low cost
KW - Non-fused electron acceptor
KW - Organic solar cells
KW - Terthiophene
UR - http://www.scopus.com/inward/record.url?scp=85193906977&partnerID=8YFLogxK
U2 - 10.1016/j.jechem.2024.04.050
DO - 10.1016/j.jechem.2024.04.050
M3 - Article
AN - SCOPUS:85193906977
SN - 2095-4956
VL - 96
SP - 501
EP - 508
JO - Journal of Energy Chemistry
JF - Journal of Energy Chemistry
ER -