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Charge Extraction Multilayers Enable Positive-Intrinsic-Negative Perovskite Solar Cells with Carbon Electrodes

Tino Lukas Orcid Logo, Seongrok Seo Orcid Logo, Philippe Holzhey Orcid Logo, Katherine Stewart, Charlie Henderson Orcid Logo, Lukas Wagner Orcid Logo, David Beynon Orcid Logo, Trystan Watson Orcid Logo, Ji-Seon Kim Orcid Logo, Markus Kohlstädt Orcid Logo, Henry J. Snaith Orcid Logo

ACS Energy Letters, Volume: 10, Issue: 6, Pages: 2736 - 2742

Swansea University Authors: David Beynon Orcid Logo, Trystan Watson Orcid Logo

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Abstract

Perovskite solar cells achieve high power conversion efficiencies but usually rely on vacuum-deposited metallic contacts, leading to high material costs for noble metals and stability issues for more reactive metals. Carbon-based materials offer a cost-effective and potentially more stable alternati...

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Published in: ACS Energy Letters
ISSN: 2380-8195 2380-8195
Published: American Chemical Society 2025
Online Access: Check full text

URI: https://cronfa.swan.ac.uk/Record/cronfa69746
Abstract: Perovskite solar cells achieve high power conversion efficiencies but usually rely on vacuum-deposited metallic contacts, leading to high material costs for noble metals and stability issues for more reactive metals. Carbon-based materials offer a cost-effective and potentially more stable alternative. The vast majority of carbon-electrode PSCs use the negative-intrinsic-positive (n-i-p) or “hole-transport-layer-free” architectures. Here, we present a systematic study to assess the compatibility of “inverted”, p-i-n configuration PSC contact layers with carbon top electrodes. We identify incompatibilities between common electron transport layers and the carbon electrode deposition process and previously unobserved semiconducting properties in carbon electrodes with unique implications for charge extraction and electronic behavior. To overcome these issues, we introduce a double-layer atomic layer deposited tin oxide (SnO2) and Poly­(2,3-dihydrothieno-1,4-dioxin)-poly­(styrenesulfonate) (PEDOT:PSS), yielding up to 16.1% PCE and a retained 94% performance after 500 h of outdoor aging. The study is a crucial step forward for printable, metal-electrode-free, and evaporation-free perovskite PV technologies.
Item Description: Letter
College: Faculty of Science and Engineering
Funders: This work was part funded by the EPSRC Programme Grant ATIP (Application Targeted and Integrated Photovoltaics) (EP/T028513/1) and the Perovskite solar cells with graphite electrodes: Advanced interfaces for highest performance and stability (PeroGAIN) project by Deutsche Forschungsgemeinschaft (DFG, SPP2196). We acknowledge the EPSRC National Thin Film Facility for Advanced Functional Materials (NTCF), hosted by the Department of Physics at the University of Oxford, and Dr Jin Yao, the facility engineer, for his support. The NTCF was funded by ESPRC (EP/M022900/1), the Wolfson Foundation and the University of Oxford.
Issue: 6
Start Page: 2736
End Page: 2742