Beyond the Gold Standard: Towards Industrially Viable Electrodes for Durable Perovskite Solar Cells
Tino Lukas a b i, Manuel Kober-Czerny a, Ali Reza Nazari Pour c, James McGettrick d, Georgios Loukeris b e f, Clemens Baretzky b f, Shuaifeng Hu a, Junke Wang a, Chia-Yu Chang g, Sam Teale a, Bowei Li h, Trystan M. Watson d, Robert L.Z. Hoye g, Philippe Holzhey a, Lukas Wagner c, Markus Kohlstädt b f, Henry J. Snaith a
a Department of Physics, University of Oxford, Clarendon Laboratory, Parks Road, Oxford, OX1 3PU, United Kingdom
b Fraunhofer Institute for Solar Energy Systems ISE, Freiburg, 79110, Germany
c Philipps-Universität Marburg, Department of Physics, Group Physics of Solar Energy Conversion, Marburg, Germany
d SPECIFIC, Faculty of Science and Engineering, Swansea University, Swansea, SA1 8EN, UK.
e Institute of Physics, University of Freiburg, Herman-Herder-Straße 3, 79104 Freiburg, Germany
f Freiburg Materials Research Center FMF, University of Freiburg, Stefan-Meier-Str. 21, 79104 Freiburg, Germany
g Inorganic Chemistry Department, University of Oxford, South Parks Road, Oxford
h Advanced Technology Institute, Department of Electrical and Electronic Engineering, University of Surrey, Guildford, Surrey GU2 7XH, UK
i Shun Hing Institute of Advanced Engineering Chinese University of Hong Kong Sha Tin, Hong Kong, China
Proceedings of International Conference on Hybrid and Organic Photovoltaics (HOPV26)
Uppsala, Sweden, 2026 May 18th - 20th
Organizers: Gerrit Boschloo, Ellen Moons, Feng Gao and Anders Hagfeldt
Oral, Tino Lukas, presentation 035
Publication date: 11th March 2026

While perovskite solar cells (PSC) have reached efficiencies near the practical limit, sustaining high energy yields through long-term operation remains challenging. For thin-film PSCs, evaporated Au electrodes are commonly used as the most stable metallic contact. Au is, however, unsuitable for industrial applications because of its high cost. Devices with cheaper metals are often observed to lead to unstable PSCs. To overcome this challenge, we assess the impact of a 5 nm chrome (Cr) interlayer, often used in semiconductor devices to inhibit metal interdiffusion, beneath Cu, Ag and Al electrodes. We find comparable stability for devices with Cr/Al electrodes and Au-based devices, while being 100,000 times more cost-effective in terms of raw materials price. On the opposite side of the PSC, transparent conducting oxides (TCOs) are usually used as the “window” electrode. We reveal a large difference in stability between indium tin oxide (ITO) and fluorine-doped tin oxide (FTO) electrodes, with FTO-based PSCs being more stable across different temperatures under simulated solar irradiance. We show that significant amounts of In³⁺ ions throughout the perovskite layers are deleterious to stability. Combining the most stable electrodes, devices on FTO substrates with Cr/Al bilayers, were stable across laboratories, with champion devices retaining over 66% of their initial efficiency after 1037 hours at 75 °C under simulated sunlight. Our findings highlight the importance of substrate and electrode selection for durable, scalable perovskite solar cells and offer a sustainable solution. This also has broader implications for stable and cost-effective electrode materials for other optoelectronic devices composed of perovskites and other PV technologies.

 

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