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Lead-Free Double Perovskite Cs2 AgInCl6.
Liu, Ying; Nag, Angshuman; Manna, Liberato; Xia, Zhiguo.
Afiliação
  • Liu Y; The Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing, 100083, P. R. China.
  • Nag A; Department of Chemistry, Indian Institute of Science Education and Research (IISER), Pune, 411008, India.
  • Manna L; Nanochemistry Department, Istituto Italiano di Tecnologia, Via Morego 30, 16163, Genova, Italy.
  • Xia Z; The Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing, 100083, P. R. China.
Angew Chem Int Ed Engl ; 60(21): 11592-11603, 2021 May 17.
Article em En | MEDLINE | ID: mdl-33084115
Lead-free halide perovskites have drawn wide attention as alternatives to their toxic and poorly stable lead-based counterparts. Among them, double perovskites with Cs2 AgInCl6 composition, often doped with various elements, have been in the spotlight owing to their intriguing optical properties, namely, self-trapped exciton (STEs) emission and dopant-induced photoluminescence. This interest has sparked different synthesis approaches towards both crystals and nanocrystals, and the exploration of many alloy compositions with mono- and trivalent cations other than Ag+ and In3+ . In this Minireview we describe the recent developments on Cs2 AgInCl6 bulk crystals and nanocrystals, their synthesis strategies, intrinsic optical properties, and tunable photoluminescence originating from different alloying and doping effects. We also discuss progress on computational studies aimed at understanding the thermodynamic stability, the role of defects, and the origin of photoluminescence in relation to the STEs and the direct band gap character.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article