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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...

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Detalles Bibliográficos
Autores principales: Singh, Ajay, Hieulle, Jeremy, Machado, Joana Ferreira, Gharabeiki, Sevan, Zuo, Weiwei, Farooq, Muhammad Uzair, Phirke, Himanshu, Saliba, Michael, Redinger, Alex
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
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
Descripción
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.