Affiliation:
1. Department of Physics University of Oxford, Clarendon Laboratory Oxford OX1 3PU UK
2. Department of Materials University of Oxford Oxford OX1 3PH UK
3. The Faraday Institution Quad One Harwell Science and Innovation Campus Didcot OX11 0RA UK
4. Department of Physics and Astronomy University of Sheffield Hicks Building, Hounsfield Road Sheffield S3 7RH UK
Abstract
AbstractMixed lead‐tin (Pb:Sn) halide perovskites are promising absorbers with narrow‐bandgaps (1.25–1.4 eV) suitable for high‐efficiency all‐perovskite tandem solar cells. However, solution processing of optimally thick Pb:Sn perovskite films is notoriously difficult in comparison with their neat‐Pb counterparts. This is partly due to the rapid crystallization of Sn‐based perovskites, resulting in films that have a high degree of roughness. Rougher films are harder to coat conformally with subsequent layers using solution‐based processing techniques leading to contact between the absorber and the top metal electrode in completed devices, resulting in a loss of VOC, fill factor, efficiency, and stability. Herein, this study employs a non‐continuous layer of alumina nanoparticles distributed on the surface of rough Pb:Sn perovskite films. Using this approach, the conformality of the subsequent electron‐transport layer, which is only tens of nanometres in thickness is improved. The overall maximum‐power‐point‐tracked efficiency improves by 65% and the steady‐state VOC improves by 28%. Application of the alumina nanoparticles as an interfacial buffer layer also results in highly reproducible Pb:Sn solar cell devices while simultaneously improving device stability at 65 °C under full spectrum simulated solar irradiance. Aged devices show a six‐fold improvement in stability over pristine Pb:Sn devices, increasing their lifetime to 120 h.
Funder
Engineering and Physical Sciences Research Council
Subject
Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials
Cited by
9 articles.
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