Issue 8, 2018

Passivation against oxygen and light induced degradation by the PCBM electron transport layer in planar perovskite solar cells

Abstract

Herein, we investigate the causes of a 20 fold improved stability of inverted, planar structure devices (ITO/PTAA/CH3NH3PbI3/PCBM/BCP/Cu) compared to conventional structure devices (FTO/compact-TiO2/meso-TiO2/CH3NH3PbI3/spiro-OMeTAD/Au) under oxygen and light stress. The PCBM layer is shown to function as an oxygen diffusion barrier and passivation layer against superoxide mediated degradation. The passivation properties of the PCBM layer are shown to depend on the electron affinity of the fullerene acceptor, attributed to the low LUMO level of PCBM energetically inhibiting superoxide generation. We also find that planar structure devices show slower lateral oxygen diffusion rates than mesoporous scaffold devices, with these slower diffusion rates (days per 100 μm) also being a key factor in enhancing stability. Faster degradation is observed under voltage cycling, attributed to oxygen diffusion kinetics being ion motion dependent. We conclude by discussing the implications of these results for the design of perovskite solar cells with improved resistance to oxygen and light induced degradation.

Graphical abstract: Passivation against oxygen and light induced degradation by the PCBM electron transport layer in planar perovskite solar cells

Supplementary files

Article information

Article type
Communication
Submitted
27 Feb 2018
Accepted
23 Mac 2018
First published
21 Jun 2018
This article is Open Access
Creative Commons BY license

Sustainable Energy Fuels, 2018,2, 1686-1692

Passivation against oxygen and light induced degradation by the PCBM electron transport layer in planar perovskite solar cells

C. Lin, S. Pont, J. Kim, T. Du, S. Xu, X. Li, D. Bryant, M. A. Mclachlan and J. R. Durrant, Sustainable Energy Fuels, 2018, 2, 1686 DOI: 10.1039/C8SE00095F

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