Long-lived and disorder-free charge transfer states enable endothermic charge separation in efficient non-fullerene organic solar cells.

Long-lived and disorder-free charge transfer states enable endothermic charge separation in efficient non-fullerene organic solar cells.
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DOI:
10.1038/s41467-020-19332-5
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发表时间:
2020-11-05
影响因子:
16.6
通讯作者:
Chow PCY
Chow PCY
中科院分区:
综合性期刊1区
文献类型:
--
作者:
Hinrichsen TF;Chan CCS;Ma C;Paleček D;Gillett A;Chen S;Zou X;Zhang G;Yip HL;Wong KS;Friend RH;Yan H;Rao A;Chow PCY

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Organic solar cells based on non-fullerene acceptors can show high charge generation yields despite near-zero donor–acceptor energy offsets to drive charge separation and overcome the mutual Coulomb attraction between electron and hole. Here, we use time-resolved optical spectroscopy to show that free charges in these systems are generated by thermally activated dissociation of interfacial charge-transfer states that occurs over hundreds of picoseconds at room temperature, three orders of magnitude slower than comparable fullerene-based systems. Upon free electron–hole encounters at later times, both charge-transfer states and emissive excitons are regenerated, thus setting up an equilibrium between excitons, charge-transfer states and free charges. Our results suggest that the formation of long-lived and disorder-free charge-transfer states in these systems enables them to operate closely to quasi-thermodynamic conditions with no requirement for energy offsets to drive interfacial charge separation and achieve suppressed non-radiative recombination. Designing efficient organic solar cells is limited by the energy required to overcome the mutual Coulomb attraction between electron and hole. Here, the authors reveal long-lived and disorder-free charge-transfer states enable efficient endothermic charge separation in non-fullerene systems with marginal energy offset.
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