TY - JOUR
T1 - Elucidating How Low Energy Offset Matters to Performance of Nonfullerene Acceptor-Based Solar Cells
AU - Tokmoldin, Nurlan
AU - Sun, Bowen
AU - Moruzzi, Floriana
AU - Patterson, Acacia
AU - Alqahtani, Obaid
AU - Wang, Rong
AU - Collins, Brian A.
AU - McCulloch, Iain
AU - Lüer, Larry
AU - Brabec, Christoph J.
AU - Neher, Dieter
AU - Shoaee, Safa
N1 - Generated from Scopus record by KAUST IRTS on 2023-09-21
PY - 2023/6/9
Y1 - 2023/6/9
N2 - The energetic offset between the highest occupied molecular orbitals of the donor and acceptor components of organic photovoltaic blends is well-known to affect the device efficiency. It is well-established that a decreasing offset increases the open-circuit voltage but reduces the short-circuit current, which has been explained by insufficient exciton dissociation. However, the impact of the offset on the fill factor and underlying processes is less clear. Here, we study free charge generation and recombination in three different nonfullerene acceptors, Y6, ITIC, and o-IDBTR, blended with the same donor polymer PM6. We demonstrate that a diminishing offset results in field-dependent charge generation related to field-assisted exciton dissociation. On the other hand, reformation of excitons from free charges is identified as an additional channel for charge recombination, which goes along with a substantial rise in the bimolecular recombination coefficient. In combination of these two effects, the fill factor drops considerably with a decreasing energy offset. Using the comparison between PM6:ITIC and PM6:o-IDBTR, we show that bulk properties such as morphology and carrier mobilities can not fully explain the observed difference in performance, highlighting the importance of interfacial kinetics and thermodynamics in controlling the device efficiency, both through generation and recombination of charge carriers.
AB - The energetic offset between the highest occupied molecular orbitals of the donor and acceptor components of organic photovoltaic blends is well-known to affect the device efficiency. It is well-established that a decreasing offset increases the open-circuit voltage but reduces the short-circuit current, which has been explained by insufficient exciton dissociation. However, the impact of the offset on the fill factor and underlying processes is less clear. Here, we study free charge generation and recombination in three different nonfullerene acceptors, Y6, ITIC, and o-IDBTR, blended with the same donor polymer PM6. We demonstrate that a diminishing offset results in field-dependent charge generation related to field-assisted exciton dissociation. On the other hand, reformation of excitons from free charges is identified as an additional channel for charge recombination, which goes along with a substantial rise in the bimolecular recombination coefficient. In combination of these two effects, the fill factor drops considerably with a decreasing energy offset. Using the comparison between PM6:ITIC and PM6:o-IDBTR, we show that bulk properties such as morphology and carrier mobilities can not fully explain the observed difference in performance, highlighting the importance of interfacial kinetics and thermodynamics in controlling the device efficiency, both through generation and recombination of charge carriers.
UR - https://pubs.acs.org/doi/10.1021/acsenergylett.3c00572
UR - http://www.scopus.com/inward/record.url?scp=85160954308&partnerID=8YFLogxK
U2 - 10.1021/acsenergylett.3c00572
DO - 10.1021/acsenergylett.3c00572
M3 - Article
SN - 2380-8195
VL - 8
SP - 2552
EP - 2560
JO - ACS Energy Letters
JF - ACS Energy Letters
IS - 6
ER -