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Thermal Stability of Chalcogenide Perovskites.
Bystrický, Roman; Tiwari, Sameer Kumar; Hutár, Peter; Sýkora, Milan.
Afiliação
  • Bystrický R; Laboratory for Advanced Materials, Faculty of Natural Sciences, Comenius University, Ilkovicova 6, 842 15 Bratislava, Slovakia.
  • Tiwari SK; Center for Advanced Materials Applications, Slovak Academy of Sciences, Dúbravská cesta 9, 845 11 Bratislava, Slovakia.
  • Hutár P; Laboratory for Advanced Materials, Faculty of Natural Sciences, Comenius University, Ilkovicova 6, 842 15 Bratislava, Slovakia.
  • Sýkora M; Laboratory for Advanced Materials, Faculty of Natural Sciences, Comenius University, Ilkovicova 6, 842 15 Bratislava, Slovakia.
Inorg Chem ; 63(28): 12826-12838, 2024 Jul 15.
Article em En | MEDLINE | ID: mdl-38951510
ABSTRACT
Chalcogenide perovskites (CPs) have recently attracted interest as a class of materials with practical potential in optoelectronics and have been suggested as a more thermally stable alternative to intensely studied halide perovskites (HPs). Here we report a comparative study of the thermal stability of representative HPs, MAPbI3 (MA = CH3NH3+, methylammonium) and CsPbI3, and a series of CPs with compositions BaZrS3, ß-SrZrS3, BaHfS3, SrHfS3. Changes in the crystal structure, chemical composition, and optical properties upon heating in air up to 800 °C were studied using thermogravimetric analysis, temperature-dependent X-ray diffraction, energy-dispersive X-ray spectroscopy, and diffuse reflectance spectroscopy. While HPs undergo phase transitions and thermally decompose at temperatures below 300 °C, the CPs show no changes in crystal phase or composition when heated up to at least 450 °C. At 500 °C CPs oxidize on time scales of several hours, forming oxides and sulfates. The structural origins of the higher thermal and phase stability of the CPs are discussed.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article