TY - JOUR
T1 - Investigation of low-bandgap nonfullerene acceptor-based polymer solar cells with very low photovoltage loss
AU - Zhang, Ying
AU - Liu, Delong
AU - Fong, Patrick W.K.
AU - Li, Gang
N1 - Funding Information:
G.L. thanks funding support from Shenzhen Science and Technology Innovation Commission (Project No. JCYJ20170413154602102), the Research Grants Council of Hong Kong (GRF grant 15218517), the Project of Strategic Importance provided by the Hong Kong Polytechnic University (ProjectCode: 1-ZE29), and the State Key Laboratory of Luminescent Materials and Devices, South China University of Technology.
Publisher Copyright:
© 2019 Society of Photo-Optical Instrumentation Engineers (SPIE).
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2019/10/1
Y1 - 2019/10/1
N2 - Polymer solar cells (PSCs) have seen great progress in recent years, with power conversion efficiencies of over 15%. However, PSCs suffer from larger energy losses than inorganic and perovskite solar cells, leading to lower open-circuit voltage (VOC). The main factors that hinder the VOC improvements include (i) relatively large nonradiative recombination losses and thus low electroluminescence quantum efficiency (EQEEL) in PSCs and (ii) the existence of a charge transfer state at the interface of donor and acceptor. For efficient charge separation in state-of-the-art PSCs, empirically, the driving force for exciton dissociation is considered to be at least 0.3 eV. The large driving force could lead to large voltage losses and thus hinder the PSC performance. In this study, we report using wide bandgap material PB3T as electron donor and low bandgap material IEICO-4F as electron acceptor for nonfullerene PSCs with very small driving forces, which, however, show a decent maximum external quantum efficiency (EQE) of nearly 40%. Moreover, we demonstrate a nonfullerene PSC with high EQEEL up to 5.1 × 10- 4, corresponding to very low nonradiative recombination losses of 0.20 eV and overall photovoltage energy losses of 0.46 to 0.52 eV, derived from different bandgap (Egap) determination methods, which can now be comparable to those in perovskite solar cells and inorganic solar cells.
AB - Polymer solar cells (PSCs) have seen great progress in recent years, with power conversion efficiencies of over 15%. However, PSCs suffer from larger energy losses than inorganic and perovskite solar cells, leading to lower open-circuit voltage (VOC). The main factors that hinder the VOC improvements include (i) relatively large nonradiative recombination losses and thus low electroluminescence quantum efficiency (EQEEL) in PSCs and (ii) the existence of a charge transfer state at the interface of donor and acceptor. For efficient charge separation in state-of-the-art PSCs, empirically, the driving force for exciton dissociation is considered to be at least 0.3 eV. The large driving force could lead to large voltage losses and thus hinder the PSC performance. In this study, we report using wide bandgap material PB3T as electron donor and low bandgap material IEICO-4F as electron acceptor for nonfullerene PSCs with very small driving forces, which, however, show a decent maximum external quantum efficiency (EQE) of nearly 40%. Moreover, we demonstrate a nonfullerene PSC with high EQEEL up to 5.1 × 10- 4, corresponding to very low nonradiative recombination losses of 0.20 eV and overall photovoltage energy losses of 0.46 to 0.52 eV, derived from different bandgap (Egap) determination methods, which can now be comparable to those in perovskite solar cells and inorganic solar cells.
KW - low bandgap acceptor
KW - low photovoltage loss
KW - nonradiative recombination loss
KW - polymer solar cells
UR - http://www.scopus.com/inward/record.url?scp=85077794236&partnerID=8YFLogxK
U2 - 10.1117/1.JPE.9.045502
DO - 10.1117/1.JPE.9.045502
M3 - Journal article
AN - SCOPUS:85077794236
SN - 1947-7988
VL - 9
JO - Journal of Photonics for Energy
JF - Journal of Photonics for Energy
IS - 4
M1 - 045502
ER -