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Main Authors: Jiang, Fangyuan, Koizumi, Haruka, Contreras, Hannah, Giridharagopal, Rajiv, Dasgupta, Akash, Huang, Zixu, DeCrescent, Ryan A., Fremouw, Kell, McGehee, Michael D., Armstrong, Neal R., Ginger, David S.
Format: Preprint
Published: 2026
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Online Access:https://arxiv.org/abs/2603.20516
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author Jiang, Fangyuan
Koizumi, Haruka
Contreras, Hannah
Giridharagopal, Rajiv
Dasgupta, Akash
Huang, Zixu
DeCrescent, Ryan A.
Fremouw, Kell
McGehee, Michael D.
Armstrong, Neal R.
Ginger, David S.
author_facet Jiang, Fangyuan
Koizumi, Haruka
Contreras, Hannah
Giridharagopal, Rajiv
Dasgupta, Akash
Huang, Zixu
DeCrescent, Ryan A.
Fremouw, Kell
McGehee, Michael D.
Armstrong, Neal R.
Ginger, David S.
contents Previous studies of reverse-bias stability in perovskite solar cells have focused primarily on voltage controlled reverse-bias tests. Here we instead present an investigation of perovskite solar cell degradation under well-defined, constant reverse-current stress. We show that the choice of hole-transport layer dictates the dominant degradation pathway: cells using thick poly(triphenylamine) (PTAA) layers with better indium-doped tin oxide (ITO) coverage can tolerate high reverse bias but quickly undergo catastrophic breakdown under fixed reverse current near their one-sun maximum power-point. In contrast, cells modified with the phosphonic-acid interface layer MeO-2PACz, with poorer ITO coverage compared to PTAA, exhibit soft, gradual, and largely recoverable degradation, regardless of the shading conditions. For MeO-2PACz devices, degradation increases with both current magnitude and duration. Importantly, when normalized by injected charge (current times duration), lower currents applied over longer times cause more severe degradation than higher currents over shorter periods. Combining electrical measurements with spatially resolved photoluminescence imaging, we argue against shunt formation and instead support an ion- and charge-mediated interfacial electrochemical degradation mode.
format Preprint
id arxiv_https___arxiv_org_abs_2603_20516
institution arXiv
publishDate 2026
record_format arxiv
spellingShingle Degradation Dynamics of Perovskite Solar Cells Under Fixed Reverse Current Injection
Jiang, Fangyuan
Koizumi, Haruka
Contreras, Hannah
Giridharagopal, Rajiv
Dasgupta, Akash
Huang, Zixu
DeCrescent, Ryan A.
Fremouw, Kell
McGehee, Michael D.
Armstrong, Neal R.
Ginger, David S.
Applied Physics
Materials Science
Previous studies of reverse-bias stability in perovskite solar cells have focused primarily on voltage controlled reverse-bias tests. Here we instead present an investigation of perovskite solar cell degradation under well-defined, constant reverse-current stress. We show that the choice of hole-transport layer dictates the dominant degradation pathway: cells using thick poly(triphenylamine) (PTAA) layers with better indium-doped tin oxide (ITO) coverage can tolerate high reverse bias but quickly undergo catastrophic breakdown under fixed reverse current near their one-sun maximum power-point. In contrast, cells modified with the phosphonic-acid interface layer MeO-2PACz, with poorer ITO coverage compared to PTAA, exhibit soft, gradual, and largely recoverable degradation, regardless of the shading conditions. For MeO-2PACz devices, degradation increases with both current magnitude and duration. Importantly, when normalized by injected charge (current times duration), lower currents applied over longer times cause more severe degradation than higher currents over shorter periods. Combining electrical measurements with spatially resolved photoluminescence imaging, we argue against shunt formation and instead support an ion- and charge-mediated interfacial electrochemical degradation mode.
title Degradation Dynamics of Perovskite Solar Cells Under Fixed Reverse Current Injection
topic Applied Physics
Materials Science
url https://arxiv.org/abs/2603.20516