TY - JOUR
T1 - Single-Source Vapor-Deposition of MA1–xFAxPbI3 Perovskite Absorbers for Solar Cells
AU - Soto-Montero, Tatiana
AU - Kralj, Suzana
AU - Soltanpoor, Wiria
AU - Solomon, Junia S.
AU - Gómez, Jennifer S.
AU - Zanoni, Kassio P.S.
AU - Paliwal, Abhyuday
AU - Bolink, Henk J.
AU - Baeumer, Christoph
AU - Kentgens, Arno P.M.
AU - Morales-Masis, Monica
N1 - Funding Information:
This project was financed by the European Research Council (ERC) under the European Union's Horizon 2020 Research and Innovation Program (CREATE, Grant Agreement No. 852722). The authors would like to thank D.M Cunha, Y. Smirnov, Y. A. Birkhölzer, P‐A Repecaud, M. Huijben, G. Rijnders, and G. Koster for fruitful discussions; N. Rodkey, A. Peñaherrera, and TSST Demcon for their experimental support; D. Post for his technical assistance; M. Smithers, M. Goodwin, and M. Tsvetanova for SEM and STEM imaging. K.P.S.Z acknowledges support from the Spanish Ministry of Science and Innovation via a Juan de la Cierva scholarship (IJC2020‐045130‐I). A.P. acknowledges a Grisolia scholarship from Generalitat Valenciana (GRISOLIAP/2020/134). J. S. G. and A. P. N. K. thank the Dutch Research Council (NWO) for the support of the “Solid‐State NMR Facility for Advanced Materials Science,” which is part of the uNMR‐NL ROADMAP facility (grant nr. 184.035.002). The NMR facilities technicians Gerrit Janssen, Hans Janssen, and Ruud Aspers are thanked for their support.
Publisher Copyright:
© 2023 The Authors. Advanced Functional Materials published by Wiley-VCH GmbH.
PY - 2023/3/16
Y1 - 2023/3/16
N2 - Vapor deposition of halide perovskites presents high potential for scalability and industrial processing of perovskite solar cells. It prevents the use of toxic solvents, allows thickness control, and yields conformal and uniform coating over large areas. However, the distinct volatility of the perovskite organic and inorganic components currently requires the use of multiple thermal sources or two-step deposition to achieve the perovskite phase. In this work, single-source, single-step MA1–xFAxPbI3 thin film deposition with tunable stoichiometry by pulsed laser deposition is demostrated. By controlling the laser ablation of a solid target containing adjustable MAI:FAI:PbI2 ratios, the room temperature formation of cubic α-phase MA1–xFAxPbI3 thin films is demonstrated. The target-to-film transfer of the ablated species, including the integrity of the organic molecules and the desired MA+:FA+ ratio, is confirmed by x-ray photoelectron spectroscopy and solid-state NMR. Photoluminescence analysis further confirms the shift of the bandgap with varying the MA+:FA+ ratio. Finally, proof-of-concept n-i-p solar cells with 14% efficiency are demonstrated with as-deposited non-passivated pulsed laser deposition (PLD)-MA1–xFAxPbI3. This study opens the path for future developments in industry-compatible vapor-deposition methods for perovskite solar cells.
AB - Vapor deposition of halide perovskites presents high potential for scalability and industrial processing of perovskite solar cells. It prevents the use of toxic solvents, allows thickness control, and yields conformal and uniform coating over large areas. However, the distinct volatility of the perovskite organic and inorganic components currently requires the use of multiple thermal sources or two-step deposition to achieve the perovskite phase. In this work, single-source, single-step MA1–xFAxPbI3 thin film deposition with tunable stoichiometry by pulsed laser deposition is demostrated. By controlling the laser ablation of a solid target containing adjustable MAI:FAI:PbI2 ratios, the room temperature formation of cubic α-phase MA1–xFAxPbI3 thin films is demonstrated. The target-to-film transfer of the ablated species, including the integrity of the organic molecules and the desired MA+:FA+ ratio, is confirmed by x-ray photoelectron spectroscopy and solid-state NMR. Photoluminescence analysis further confirms the shift of the bandgap with varying the MA+:FA+ ratio. Finally, proof-of-concept n-i-p solar cells with 14% efficiency are demonstrated with as-deposited non-passivated pulsed laser deposition (PLD)-MA1–xFAxPbI3. This study opens the path for future developments in industry-compatible vapor-deposition methods for perovskite solar cells.
KW - mixed-organic-cation halide perovskites
KW - physical vapor deposition
KW - pulsed laser deposition
KW - solvent-free methods
KW - stoichiometry control
KW - vacuum-processed perovskite solar cells
KW - UT-Hybrid-D
UR - http://www.scopus.com/inward/record.url?scp=85150826100&partnerID=8YFLogxK
U2 - 10.1002/adfm.202300588
DO - 10.1002/adfm.202300588
M3 - Article
AN - SCOPUS:85150826100
SN - 1616-301X
JO - Advanced functional materials
JF - Advanced functional materials
ER -