Ionic accumulation as a diagnostic tool in perovskite solar cells: characterising band alignment with rapid voltage pulses

Hill, N. et al. (2023) Ionic accumulation as a diagnostic tool in perovskite solar cells: characterising band alignment with rapid voltage pulses. Advanced Materials, 35(32), 2302146. (doi: 10.1002/adma.202302146) (PMID:37145114)

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Abstract

Despite record-breaking devices, interfaces in perovskite solar cells are still poorly understood, inhibiting further progress. The mixed ionic-electronic nature of lead-halide perovskites results in compositional variations at the interfaces, depending on the history of externally applied biases. This makes it difficult to measure critical parameters accurately, for example, the band energy alignment of charge extraction layers. As a result, the field often resorts to a lengthy trial-and-error process to optimise these interfaces. While techniques to measure interfacial energy level alignment exist, they are typically carried out in a vacuum and on incomplete cells, hence values may not reflect those found in complete device stacks. To address this, w e have developed a pulsed measurement technique that can characterise the electrostatic potential energy drop across the perovskite layer in a functioning device. O ur method reconstructs the JV curve for a range of stabilisation biases which hold the ion distribution “static” during subsequent rapid voltage pulses. W e observe two different regimes: at low applied biases, the reconstructed JV curve is “s-shaped”, whereas, at high applied biases, typical diode-shaped curves are returned. Using drift-diffusion simulations, w e demonstrate that the intersection of the two regimes changes based on the band offsets at the transport layer interfaces. This approach effectively allows measurements of interfacial energy level alignment in a complete device under illumination and without the need for expensive vacuum equipment.

Item Type:Articles
Additional Information:N.H. and M.V.C. contributed equally to this work. N.H. was supported by the EPSRC-UKRI DTP and would like to thank Abigail Seddon for help with the interpretation of the dipole moments of benzoic acid groups. M.V.C. was supported by the EPSRC Centre for Doctoral Training in Sustainable Chemical Technologies EP/L016354/1. M.H.F. was supported by the EPSRC Centre for Doctoral Training in Renewable Energy Northeast Universities (ReNU) EP/SO23836/1. M.H.F. thanks Julien Eng for help with visualizing the dipole moments. This research made use of the Rocket High Performance Computing service at Newcastle University. P.D. acknowledges funding from the EPSRC under grant agreement EP/T010568/1. N.G. acknowledges funding from the Australian Government through the Australian Centre for Advanced Photovoltaics (ACAP) and the Australian Research Council through the Centre of Excellence in Exciton Science (CE170100026). Y.H. acknowledges funding from the Federal Ministry of Education and Research (BMBF) under project ID 03SF0514A/B. A.B.W. would like to thank the EPSRC for funding from grant EP/SO00763/1 (Supergen Supersolar+ Network+).
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Docampo, Dr Pablo
Authors: Hill, N., Cowley, M. V., Gluck, N., Fsadni, M. H., Clarke, W., Hu, Y., Wolf, M., Healy, N., Freitag, M., Penfold, T. J., Richardson, G., Walker, A., Cameron, P., and Docampo, P.
College/School:College of Science and Engineering > School of Chemistry
Journal Name:Advanced Materials
Publisher:Wiley
ISSN:0935-9648
ISSN (Online):1521-4095
Published Online:05 May 2023
Copyright Holders:Copyright © 2023 The Authors
First Published:First published in Advanced Materials 35(32):2302146
Publisher Policy:Reproduced under a Creative Commons license

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Project CodeAward NoProject NamePrincipal InvestigatorFunder's NameFunder RefLead Dept
310679Hybrid Perovskite Heterojunctions (AoE ENG Materials & Manufacturing)Pablo DocampoEngineering and Physical Sciences Research Council (EPSRC)EP/T010568/1Chemistry