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Universal insertion of molecules in ionic compounds under pressure.
Peng, Feng; Ma, Yanming; Pickard, Chris J; Liu, Hanyu; Miao, Maosheng.
Afiliação
  • Peng F; College of Physics and Electronic Information, Luoyang Normal University, Luoyang 471022, China.
  • Ma Y; Department of Chemistry and Biochemistry, California State University Northridge, Northridge 91330, USA.
  • Pickard CJ; State Key Laboratory of Superhard Materials & Key Laboratory of Material Simulation Methods and Software of Ministry of Education, College of Physics, Jilin University, Changchun 130012, China.
  • Liu H; International Center of Future Science, Jilin University, Changchun 130012, China.
  • Miao M; Department of Materials Science & Metallurgy, University of Cambridge, Cambridge CB3 0FS, UK.
Natl Sci Rev ; 11(1): nwae016, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38343648
ABSTRACT
Using first-principles calculations and crystal structure search methods, we found that many covalently bonded molecules such as H2, N2, CO2, NH3, H2O and CH4 may react with NaCl, a prototype ionic solid, and form stable compounds under pressure while retaining their molecular structure. These molecules, despite whether they are homonuclear or heteronuclear, polar or non-polar, small or large, do not show strong chemical interactions with surrounding Na and Cl ions. In contrast, the most stable molecule among all examples, N2, is found to transform into cyclo-N5- anions while reacting with NaCl under high pressures. It provides a new route to synthesize pentazolates, which are promising green energy materials with high energy density. Our work demonstrates a unique and universal hybridization propensity of covalently bonded molecules and solid compounds under pressure. This surprising miscibility suggests possible mixing regions between the molecular and rock layers in the interiors of large planets.
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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