TY - JOUR
T1 - Controlling Molecular Packing and Orientation via Constructing a Ladder-Type Electron Acceptor with Asymmetric Substituents for Thick-Film Nonfullerene Solar Cells
AU - Feng, Shiyu
AU - Zhang, Cai'E
AU - Bi, Zhaozhao
AU - Liu, Yahui
AU - Jiang, Pengcheng
AU - Ming, Shouli
AU - Xu, Xinjun
AU - Ma, Wei
AU - Bo, Zhishan
N1 - Publisher Copyright:
© 2018 American Chemical Society.
PY - 2019/1/23
Y1 - 2019/1/23
N2 - A nonfullerene acceptor, IDTT-OB, employing indacenodithieno[3,2-b]thiophene (IDTT) decorated with asymmetric substituents as the core, is designedly prepared. In comparison with the analogue IDT-OB, extending the five-heterocyclic indacenodithiophene (IDT) core to seven-heterocyclic fused ring endows IDTT-OB with more broad absorption and elevated highest occupied molecular orbital energy level. In addition, IDTT-OB shows a more intense molecular packing and a higher crystalline behavior with a strong face-on orientation in the neat film and the PBDB-T:IDTT-OB blend film. Furthermore, an ideal nanomorphology with a domain size of 19 nm can be obtained, which is in favor of exciton diffusion and charge separation. Accordingly, PBDB-T:IDTT-OB-based polymer solar cells demonstrate a maximum power conversion efficiency (PCE max ) of 11.19% with an impressive fill factor of 0.74, comparable to the state-of-the-art acceptors with similar molecular backbones. More importantly, IDTT-OB-based devices show good tolerance to the film thickness, which maintain a high PCE of 10.20% with a 250 nm thick active layer, demonstrating that the asymmetric acceptor is profound for fabricating high-efficiency thick-film nonfullerene solar cells.
AB - A nonfullerene acceptor, IDTT-OB, employing indacenodithieno[3,2-b]thiophene (IDTT) decorated with asymmetric substituents as the core, is designedly prepared. In comparison with the analogue IDT-OB, extending the five-heterocyclic indacenodithiophene (IDT) core to seven-heterocyclic fused ring endows IDTT-OB with more broad absorption and elevated highest occupied molecular orbital energy level. In addition, IDTT-OB shows a more intense molecular packing and a higher crystalline behavior with a strong face-on orientation in the neat film and the PBDB-T:IDTT-OB blend film. Furthermore, an ideal nanomorphology with a domain size of 19 nm can be obtained, which is in favor of exciton diffusion and charge separation. Accordingly, PBDB-T:IDTT-OB-based polymer solar cells demonstrate a maximum power conversion efficiency (PCE max ) of 11.19% with an impressive fill factor of 0.74, comparable to the state-of-the-art acceptors with similar molecular backbones. More importantly, IDTT-OB-based devices show good tolerance to the film thickness, which maintain a high PCE of 10.20% with a 250 nm thick active layer, demonstrating that the asymmetric acceptor is profound for fabricating high-efficiency thick-film nonfullerene solar cells.
KW - asymmetric side chains
KW - face-on orientation
KW - non-fullerene acceptor
KW - solar cells
KW - thick film
UR - https://www.scopus.com/pages/publications/85060062511
U2 - 10.1021/acsami.8b19596
DO - 10.1021/acsami.8b19596
M3 - 文章
C2 - 30585714
AN - SCOPUS:85060062511
SN - 1944-8244
VL - 11
SP - 3098
EP - 3106
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 3
ER -