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Polymorphism and Temperature-Induced Phase Transitions of Na2CoP2O7.
Avdeev, Maxim; Wang, Chin-Wei; Barpanda, Prabeer; Fujii, Kotaro; Yashima, Masatomo.
Afiliação
  • Avdeev M; Australian Nuclear Science and Technology Organisation , New Illawarra Road , Lucas Heights , NSW 2234 , Australia.
  • Wang CW; School of Chemistry , The University of Sydney , Sydney 2006 , Australia.
  • Barpanda P; Department of Chemistry, School of Science , Tokyo Institute of Technology , 2-12-1-W4-17, Ookayama, Meguro-ku, Tokyo 152-8551 , Japan.
  • Fujii K; National Synchrotron Radiation Research Center , Hsinchu 30076 , Taiwan.
  • Yashima M; Faraday Materials Laboratory, Materials Research Center , Indian Institute of Science , C.V. Raman Avenue , Bangalore 560012 , India.
Inorg Chem ; 58(24): 16823-16830, 2019 Dec 16.
Article em En | MEDLINE | ID: mdl-31799837
Polymorphism and temperature-induced phase transitions of Na2CoP2O7 were studied by in situ neutron powder diffraction and complemented by ab initio calculations to reconcile previous reports of its three polymorphs. We show that the "blue" form prepared at 873 K exists at room temperature in the orthorhombic Pna21 (= P21cn) phase, which transforms via a first-order transition to the tetragonal form at the temperature close to room temperature (∼335 K). Just above the transition, the tetragonal form is likely incommensurately modulated with the modulation vanishing at ∼423 K. Above that temperature the phase remains in the unmodulated tetragonal state (P42/mnm) until melting at ∼900 K. Upon cooling after melting, Na2CoP2O7 crystallizes into the "rose" triclinic P1 form which persists while it cools to room temperature, apparently stabilized by the barrier of the reconstructive "rose"-"blue" transition. We also discuss the relationship between the tetragonal and orthorhombic structures, the driving forces of the orthorhombic distortion, and similarity to Na2ZnP2O7 and the melilite-type structural family.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Inorg Chem Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Inorg Chem Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Austrália