Solvent selection for highly reproducible carbon-based mixed-cation hybrid lead halide perovskite solar cells via adduct approach

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Date

2020

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Elsevier Ltd

Abstract

The major problem identified in carbon-based mixed cation perovskite solar cells (PSCs) is the selection of a suitable solvent for single-step solution-processed perovskite deposition in order to promote their scalable production. Herein we report a detailed study on the selection of appropriate solvent for the one-step deposition of cesium-formamidinium lead iodide (Cs<inf>0.1</inf>FA<inf>0.9</inf>PbI<inf>3</inf>) perovskite via Lewis acid-base adduct approach for fully printable mesoporous PSCs with mesoporous TiO<inf>2</inf>/ZrO<inf>2</inf>/C architecture. Highly reproducible Cs<inf>0.1</inf>FA<inf>0.9</inf>PbI<inf>3</inf> solar cells were fabricated via adducts of PbI<inf>2</inf> with eco-friendly dimethyl sulfoxide (DMSO). The best cells fabricated with the above approach yielded a photoconversion efficiency (PCE) of 12.33% for a small area device (active area: 0.09 cm2) and 10.1% for a large area device (active area 0.7cm2). The average power conversion efficiency for 62 PSCs was found to be 10.5% under an AM 1.5G illumination. Finally, the mixed cation perovskite in carbon architecture using the Lewis acid-base adduct approach is remarkably stable, with less than 1% change from the initial PCE after 1800h of storage under dark ambient conditions (25 °C, 60–70% RH). © 2020 International Solar Energy Society

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Keywords

Carbon, Cesium iodide, Deposition, Dimethyl sulfoxide, Efficiency, Iodine compounds, Layered semiconductors, Organic solvents, Perovskite, Perovskite solar cells, Positive ions, Titanium dioxide, Zirconium compounds, Ambient conditions, Dimethyl sulfoxide (DMSO), Large area devices, Lewis acid-base, Photoconversion efficiency, Scalable production, Solution-processed, Solvent selection, Lead compounds, cation, cesium isotope, halide, iodide, lead, photochemistry, solar power, solvent, storage structure

Citation

Solar Energy, 2020, 199, , pp. 761-771

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