TY - JOUR
T1 - A fully fused non-fullerene acceptor containing angular-shaped
T2 - S, N -heteroacene and perylene diimide for additive-free organic solar cells
AU - Li, Zhaoning
AU - Wang, Jungan
AU - Huang, Hongyan
AU - Liu, You
AU - Yun, Yikai
AU - Cheng, Zhengchun
AU - Liu, Shuli
AU - Ding, Zhucheng
AU - Zhao, Baomin
AU - Huang, Wei
N1 - Publisher Copyright:
This journal is © 2019 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.
PY - 2019
Y1 - 2019
N2 - Constructing fused perylene diimide (PDI) dimers with heteroaromatic bridges toward non-fullerene acceptors (NFAs) has become an efficient strategy to achieve high performance organic solar cells (OSCs). Here, FDTC-PDI containing fully fused two PDIs with one central unit of angular-shaped S,N-heteroacene was developed and explored as a novel NFA for OSCs. The molecular geometry, optical spectra, energy levels, charge carrier mobilities and the morphology discrepancies as well as the corresponding photovoltaic performance of FDTC-PDI and its non-fused precursor, DTC-PDI, were investigated and compared. Theoretical calculations reveal that FDTC-PDI has a better planar molecular conformation and more effective conjugated length than DTC-PDI. As a consequence, by blending FDTC-PDI with PTB7-Th as the electron acceptor and the electron donor material, respectively, the inverted solar cells exhibited an encouraging PCE of 4.78% along with a Jsc of 11.72 mA cm-2, a Voc of 0.96 V and a FF of 42.5%, which were superior to those of its counterpart DTC-PDI (2.68%). These results are associated with the higher molar extinction coefficient, more balanced carrier mobility and better morphology of FDTC-PDI as well as its high-lying LUMO energy level. Note that no solvent additive was used in the process of device optimizations, thus simplifying the device fabrication, and improving the stability and reproducibility of the photovoltaic devices. We also prospect much broader application of the angular-shaped S,N-heteroacene with rigidity and planarity as a promising building block for fully fused electron acceptors for accomplishing the challenges in organic solar cells.
AB - Constructing fused perylene diimide (PDI) dimers with heteroaromatic bridges toward non-fullerene acceptors (NFAs) has become an efficient strategy to achieve high performance organic solar cells (OSCs). Here, FDTC-PDI containing fully fused two PDIs with one central unit of angular-shaped S,N-heteroacene was developed and explored as a novel NFA for OSCs. The molecular geometry, optical spectra, energy levels, charge carrier mobilities and the morphology discrepancies as well as the corresponding photovoltaic performance of FDTC-PDI and its non-fused precursor, DTC-PDI, were investigated and compared. Theoretical calculations reveal that FDTC-PDI has a better planar molecular conformation and more effective conjugated length than DTC-PDI. As a consequence, by blending FDTC-PDI with PTB7-Th as the electron acceptor and the electron donor material, respectively, the inverted solar cells exhibited an encouraging PCE of 4.78% along with a Jsc of 11.72 mA cm-2, a Voc of 0.96 V and a FF of 42.5%, which were superior to those of its counterpart DTC-PDI (2.68%). These results are associated with the higher molar extinction coefficient, more balanced carrier mobility and better morphology of FDTC-PDI as well as its high-lying LUMO energy level. Note that no solvent additive was used in the process of device optimizations, thus simplifying the device fabrication, and improving the stability and reproducibility of the photovoltaic devices. We also prospect much broader application of the angular-shaped S,N-heteroacene with rigidity and planarity as a promising building block for fully fused electron acceptors for accomplishing the challenges in organic solar cells.
UR - http://www.scopus.com/inward/record.url?scp=85072115525&partnerID=8YFLogxK
U2 - 10.1039/c9nj02918d
DO - 10.1039/c9nj02918d
M3 - 文章
AN - SCOPUS:85072115525
SN - 1144-0546
VL - 43
SP - 13775
EP - 13782
JO - New Journal of Chemistry
JF - New Journal of Chemistry
IS - 35
ER -