TY - JOUR
T1 - A Highly Crystalline Fused-Ring n-Type Small Molecule for Non-Fullerene Acceptor Based Organic Solar Cells and Field-Effect Transistors
AU - Song, Xin
AU - Gasparini, Nicola
AU - Nahid, Masrur Morshed
AU - Chen, Hu
AU - Macphee, Sky Marie
AU - Zhang, Weimin
AU - Norman, Victoria
AU - Zhu, Chenhui
AU - Bryant, Daniel
AU - Ade, Harald
AU - McCulloch, Iain
AU - Baran, Derya
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: D.B. acknowledges KAUST Solar Center Competitive Fund (CCF) for financial support. GIWAXS/R-SoXS measurements and analysis by M. M. Nahid and H. Ade were supported by ONR grant N00141512322 and KAUST's Center Partnership Fund (No. 3321). X-ray data were acquired at beamlines 7.3.3 and 11.0.1.2 at the Advanced Light Source (ALS) in Berkeley National Lab, which was supported by the U.S. Department of Energy (DE-AC02-05CH11231). Z.P., S.S., and I.A. assisted with part of the R-SoXS data acquisition. C.W., C.Z., A.L.D.K., and E.S. are acknowledged for the beamline support.
PY - 2018/7/13
Y1 - 2018/7/13
N2 - N-type organic small molecules (SMs) are attracting attention in the organic electronics field, due to their easy purification procedures with high yield. However, only a few reports show SMs that perform well in both organic field-effect transistors (OFETs) and organic solar cells (OSCs). Here, the synthesis and characterization of an n-type small molecule with an indacenodithieno[3,2-b]thiophene (IDTT) core unit and linear alkylated side chain (C16) (IDTTIC) are reported. Compared to the state-of-the-art n-type molecule IDTIC, IDTTIC exhibits smaller optical bandgap and higher absorption coefficient, which is due to the enhanced intramolecular effect. After mixing with the polymer donor PBDB-T, IDTIC-based solar cells deliver a power conversion efficiency of only 5.67%. In stark contrast, the OSC performance of IDTTIC improves significantly to 11.2%. It is found that the superior photovoltaic properties of PBDB-T:IDTTIC blends are mainly due to reduced trap-assisted recombination and enhanced molecular packing coherence length and higher domain purity when compared to IDTIC. Moreover, a significantly higher electron mobility of 0.50 cm2 V−1 s−1 for IDTTIC in OFET devices than for IDTIC (0.15 cm2 V−1 s−1) is obtained. These superior performances in OSCs and OFETs demonstrate that SMs with extended π-conjugation of the backbone possess a great potential for application in organic electronic devices.
AB - N-type organic small molecules (SMs) are attracting attention in the organic electronics field, due to their easy purification procedures with high yield. However, only a few reports show SMs that perform well in both organic field-effect transistors (OFETs) and organic solar cells (OSCs). Here, the synthesis and characterization of an n-type small molecule with an indacenodithieno[3,2-b]thiophene (IDTT) core unit and linear alkylated side chain (C16) (IDTTIC) are reported. Compared to the state-of-the-art n-type molecule IDTIC, IDTTIC exhibits smaller optical bandgap and higher absorption coefficient, which is due to the enhanced intramolecular effect. After mixing with the polymer donor PBDB-T, IDTIC-based solar cells deliver a power conversion efficiency of only 5.67%. In stark contrast, the OSC performance of IDTTIC improves significantly to 11.2%. It is found that the superior photovoltaic properties of PBDB-T:IDTTIC blends are mainly due to reduced trap-assisted recombination and enhanced molecular packing coherence length and higher domain purity when compared to IDTIC. Moreover, a significantly higher electron mobility of 0.50 cm2 V−1 s−1 for IDTTIC in OFET devices than for IDTIC (0.15 cm2 V−1 s−1) is obtained. These superior performances in OSCs and OFETs demonstrate that SMs with extended π-conjugation of the backbone possess a great potential for application in organic electronic devices.
UR - http://hdl.handle.net/10754/630744
UR - https://doi.org/10.1002/adfm.201802895
UR - http://www.scopus.com/inward/record.url?scp=85050371947&partnerID=8YFLogxK
U2 - 10.1002/adfm.201802895
DO - 10.1002/adfm.201802895
M3 - Article
SN - 1616-301X
VL - 28
SP - 1802895
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 35
ER -