Affiliation:
1. MESA+ Institute for Nanotechnology University of Twente Enschede 7500 AE The Netherlands
2. Institute for Molecules and Materials Radboud University Nijmegen 6525 AJ The Netherlands
3. Instituto de Ciencia Molecular Universidad de Valencia C/Catedrático J. Beltrán 2 Paterna 46980 Spain
Abstract
AbstractVapor 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.
Funder
European Research Council
Subject
Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials
Cited by
16 articles.
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