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Coevaporation Stabilizes Tin-Based Perovskites in a Single Sn-Oxidation State
[Image: see text] Chemically processed methylammonium tin-triiodide (CH(3)NH(3)SnI(3)) films include Sn in different oxidation states, leading to poor stability and low power conversion efficiency of the resulting solar cells (PSCs). The development of absorbers with Sn [2+] only has been identified...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9479155/ https://www.ncbi.nlm.nih.gov/pubmed/35998901 http://dx.doi.org/10.1021/acs.nanolett.2c02204 |
Sumario: | [Image: see text] Chemically processed methylammonium tin-triiodide (CH(3)NH(3)SnI(3)) films include Sn in different oxidation states, leading to poor stability and low power conversion efficiency of the resulting solar cells (PSCs). The development of absorbers with Sn [2+] only has been identified as one of the critical steps to develop all Sn-based devices. Here, we report on coevaporation of CH(3)NH(3)I and SnI(2) to obtain absorbers with Sn being only in the preferred oxidation state [+2] as confirmed by X-ray photoelectron spectroscopy. The Sn [4+]-free absorbers exhibit smooth highly crystalline surfaces and photoluminescence measurements corroborating their excellent optoelectronic properties. The films show very good stability under heat and light. Photoluminescence quantum yields up to 4 × 10(–3) translate in a quasi Fermi-level splittings exceeding 850 meV under one sun equivalent conditions showing high promise in developing lead-free, high efficiency, and stable PSCs. |
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