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      Low Damage Scalable Pulsed Laser Deposition of SnO 2 for p– i–n Perovskite Solar Cells

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          Abstract

          Pulsed laser deposition (PLD) has already been adopted as a low damage deposition technique of transparent conducting oxides on top of sensitive organic charge transport layers in optoelectronic devices. Herein, SnO 2 deposition is demonstrated as buffer layer in p– i–n perovskite solar cells (PSCs) via wafer‐scale (4 inch) PLD at room temperature. The PLD SnO 2 properties, its interface with perovskite/C 60, and device performance are compared to atomic layer deposited (ALD) SnO 2, i.e., state‐of‐the‐art buffer layer in perovskite‐based single junction and tandem photovoltaics. The PLD SnO 2‐based solar cells exhibit on par efficiencies (17.8%) with that of SnO 2 fabricated using ALD. The solvent‐free room temperature processing and wafer‐scale approach of PLD open up possibilities for buffer layer formation with increased deposition rates while mitigating potential thermal or physical damage to the top organic layers. This is a promising outlook for fully physical vapor‐processed halide PSCs and optoelectronic devices requiring low thermal budget.

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          Photoluminescence‐Based Characterization of Halide Perovskites for Photovoltaics

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            Effective Carrier-Concentration Tuning of SnO2 Quantum Dot Electron-Selective Layers for High-Performance Planar Perovskite Solar Cells.

            The carrier concentration of the electron-selective layer (ESL) and hole-selective layer can significantly affect the performance of organic-inorganic lead halide perovskite solar cells (PSCs). Herein, a facile yet effective two-step method, i.e., room-temperature colloidal synthesis and low-temperature removal of additive (thiourea), to control the carrier concentration of SnO2 quantum dot (QD) ESLs to achieve high-performance PSCs is developed. By optimizing the electron density of SnO2 QD ESLs, a champion stabilized power output of 20.32% for the planar PSCs using triple cation perovskite absorber and 19.73% for those using CH3 NH3 PbI3 absorber is achieved. The superior uniformity of low-temperature processed SnO2 QD ESLs also enables the fabrication of ≈19% efficiency PSCs with an aperture area of 1.0 cm2 and 16.97% efficiency flexible device. The results demonstrate the promise of carrier-concentration-controlled SnO2 QD ESLs for fabricating stable, efficient, reproducible, large-scale, and flexible planar PSCs.
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              Suppressed decomposition of organometal halide perovskites by impermeable electron-extraction layers in inverted solar cells

              The area of thin-film photovoltaics has been overwhelmed by organometal halide perovskites. Unfortunately, serious stability concerns arise with perovskite solar cells. For example, methyl-ammonium lead iodide is known to decompose in the presence of water and, more severely, even under inert conditions at elevated temperatures. Here, we demonstrate inverted perovskite solar cells, in which the decomposition of the perovskite is significantly mitigated even at elevated temperatures. Specifically, we introduce a bilayered electron-extraction interlayer consisting of aluminium-doped zinc oxide and tin oxide. We evidence tin oxide grown by atomic layer deposition does form an outstandingly dense gas permeation barrier that effectively hinders the ingress of moisture towards the perovskite and—more importantly—it prevents the egress of decomposition products of the perovskite. Thereby, the overall decomposition of the perovskite is significantly suppressed, leading to an outstanding device stability.
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                Author and article information

                Contributors
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                Journal
                Solar RRL
                Solar RRL
                Wiley
                2367-198X
                2367-198X
                December 2023
                October 15 2023
                December 2023
                : 7
                : 23
                Affiliations
                [1 ] MESA+ Institute for Nanotechnology University of Twente 7500 AE Enschede The Netherlands
                [2 ] Department of Applied Physics and Science of Education Eindhoven University of Technology 5600 MB Eindhoven The Netherlands
                [3 ] Instituto de Ciencia Molecular Universidad de Valencia 46980 Paterna Spain
                [4 ] Eindhoven Institute for Renewable Energy Systems (EIRES) Eindhoven University of Technology 5600 MB Eindhoven The Netherlands
                Article
                10.1002/solr.202300616
                83c23696-1bfb-4b0a-9025-0b9de62a44cc
                © 2023

                http://creativecommons.org/licenses/by/4.0/

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