Reducing the efficiency–stability–cost gap of organic photovoltaics with highly efficient and stable small molecule acceptor ternary solar cells
Hanifi, David A.
Röhr, Jason A.
Emmott, Christopher J. M.
Brabec, Christoph J.
Durrant, James R.
KAUST DepartmentChemical Science Program
KAUST Solar Center (KSC)
Material Science and Engineering Program
Organic Electronics and Photovoltaics Group
Physical Science and Engineering (PSE) Division
Online Publication Date2016-11-21
Print Publication Date2017-03
Permanent link to this recordhttp://hdl.handle.net/10754/622456
MetadataShow full item record
AbstractTechnological deployment of organic photovoltaic modules requires improvements in device light-conversion efficiency and stability while keeping material costs low. Here we demonstrate highly efficient and stable solar cells using a ternary approach, wherein two non-fullerene acceptors are combined with both a scalable and affordable donor polymer, poly(3-hexylthiophene) (P3HT), and a high-efficiency, low-bandgap polymer in a single-layer bulk-heterojunction device. The addition of a strongly absorbing small molecule acceptor into a P3HT-based non-fullerene blend increases the device efficiency up to 7.7 ± 0.1% without any solvent additives. The improvement is assigned to changes in microstructure that reduce charge recombination and increase the photovoltage, and to improved light harvesting across the visible region. The stability of P3HT-based devices in ambient conditions is also significantly improved relative to polymer:fullerene devices. Combined with a low-bandgap donor polymer (PBDTTT-EFT, also known as PCE10), the two mixed acceptors also lead to solar cells with 11.0 ± 0.4% efficiency and a high open-circuit voltage of 1.03 ± 0.01 V.
CitationBaran D, Ashraf RS, Hanifi DA, Abdelsamie M, Gasparini N, et al. (2016) Reducing the efficiency–stability–cost gap of organic photovoltaics with highly efficient and stable small molecule acceptor ternary solar cells. Nature Materials. Available: http://dx.doi.org/10.1038/nmat4797.
SponsorsD.B. thanks Helmholtz Association for a Helmholtz Postdoc Fellowship. S.H. thanks BASF for financial support. The authors acknowledge EC FP7 Project SC2 (610115), EC FP7 Project ArtESun (604397), and EPSRC Project EP/G037515/1 and EP/K030671/1, EC FP7 Project POLYMED (612538) and Project Synthetic carbon allotropes project SFB 953.