2021
DOI: 10.1002/adfm.202104552
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Stability Of Non‐Fullerene Electron Acceptors and Their Photovoltaic Devices

Abstract: Non-fullerene electron acceptors (NFAs) are recognized as "rising star" in recent years in the organic solar cells (OSCs) community. In contrast to the traditional fullerene electron acceptors, NFAs promise superior feasibility in molecular design with tunable optoelectronic properties, experiencing unprecedented development in the last 5 years with maximum achievable power conversion efficiencies over 18% are acquired in NFA based OSCs. Nevertheless, the stability of NFAs and their OSCs is still problematic a… Show more

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Cited by 59 publications
(55 citation statements)
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“…Similarly, molecular stacking and aggregation also occurs in non-fullerene acceptor systems under thermal conditions, affecting the stability of OPV devices. 90,91 Therefore, it is extremely crucial to enhance the stability of the photoactive layer morphology.…”
Section: Long-term Stabilitymentioning
confidence: 99%
“…Similarly, molecular stacking and aggregation also occurs in non-fullerene acceptor systems under thermal conditions, affecting the stability of OPV devices. 90,91 Therefore, it is extremely crucial to enhance the stability of the photoactive layer morphology.…”
Section: Long-term Stabilitymentioning
confidence: 99%
“…In addition to the photovoltaic performance of devices, the thermal stability of OSCs has been received extensive attention recently. [44,45] Therefore, we further explored the thermal stability of PTFS additive processed devices comparing with the non-additive and the PS treated devices. The changing photovoltaic parameters of the corresponding devices were shown in Figure 8.…”
Section: Thermal Stability and Universality Characterizationmentioning
confidence: 99%
“…46 Furthermore, most emerging NFAs containing 2-(3-oxo-2,3-dihydroinden-1-ylidene)malononitrile (IC)-type terminals are synthesized by the Knoevenagel condensation reaction, which would make them prone to decompose under persistent light irritation. 47–53 It has been demonstrated that the photodegradation products of typical NFAs such as ITIC with IC end groups contain fused-ring isomers via a 6-e electrocyclic reaction between the dicyanomethylene unit and the thiophene ring. 50 A promising and efficient method is employing robust carbon–carbon bonds instead of the vulnerable exocyclic double bonds to link the donor unit and the acceptor unit of NFAs, which can not only lead to intrinsically stable acceptors but also successfully adjust the optoelectronic properties of NFAs.…”
Section: Introductionmentioning
confidence: 99%