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Impact of intentional photo-oxidation of a donor polymer and PC <sub/>70</sub> BM on solar cell performance

DOI:10.1039/C9CP04384E 期刊:Physical Chemistry Chemical Physics 出版年份:2019 更新时间:2025-09-19 17:13:59
摘要: Impact of intentional photo-oxidation of a donor polymer and PC70BM on solar cell performance. A short lifetime is the main factor hindering the wider implementation of low-cost organic photovoltaics through non-ideal encapsulation layers is a known cause of degradation for polymer/fullerene based solar cells. To better understand the origin of this performance degradation, we study the effect of intentional exposure of the photo-active layer to simulated sunlight (AM1.5) in air both on the solar cell performance and on the molecular semiconductor materials. Cathode-free thin films of a blend of the electron donor polymer poly[2,3-bis-(3-octyloxyphenyl)quinoxaline-5,8-diyl-alt-thiophene-2,5-diyl] (TQ1) and the electron acceptor fullerene derivative [6,6]-phenyl-C70-butyric acid methyl ester (PC70BM) were exposed to simulated sunlight in air. Fourier-transform infrared spectra demonstrate the formation of carbonyl photo-oxidation products in the blend films, as well as in the pristine polymer and fullerene films. Solar cells prepared with photo-oxidized active layers show increasingly degraded electrical performance (lower short circuit current, open circuit voltage and fill factor) with increasing exposure time. The increased diode ideality factor indicates that trap-assisted recombination hinders device operation after exposure. The external quantum efficiency decreases drastically with increasing exposure time over the whole photon energy range, while the UV-vis absorption spectra of the blend films only show a mild photo-induced bleaching. This demonstrates that not only the photo-induced degradation of the solar cell performance is not predominantly caused by the loss in light absorption, but charge transport and collection are also hampered. This is explained by the fact that photo-oxidation of PC70BM causes bonds in its conjugated cage to break, as evidenced by the decreased p* intensity in C1s-NEXAFS spectra of PC70BM films. This degradation of unoccupied states of PC70BM will hinder the transport of photo-generated electrons to the electrode. Surface photovoltage spectroscopy gives direct evidence for gap states at the surface of a PC70BM film, formed after 2 hours of exposure and resulting in upward band bending at the PC70BM/air surface. These observations indicate that the photo-oxidation of PC70BM is likely to be the main cause of the performance degradation observed when the photoactive layer of a TQ1:PC70BM solar cell is intentionally exposed to light in air.
作者: Vanja Blazinic,Andreas Opitz,Leif K. E. Ericsson,Ellen Moons,Igal Levine,Rickard Hansson
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To better understand the origin of performance degradation in polymer/fullerene based solar cells when exposed to simulated sunlight and ambient air.

The photo-oxidation of PC70BM is identified as the main cause of performance degradation in TQ1:PC70BM solar cells when exposed to light in air. The degradation leads to the formation of trap states that hinder charge transport and collection, significantly affecting the solar cell's electrical performance. The study suggests that replacing fullerenes with more stable non-fullerene acceptors could improve device lifetime.

The study focuses on the degradation mechanisms in TQ1:PC70BM solar cells under specific conditions of simulated sunlight and ambient air exposure. The findings may not be directly applicable to other polymer/fullerene systems or under different environmental conditions. The study also does not explore the long-term stability of devices under operational conditions.

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