Synthesis and crystal structure study of Y 2 O 3  high‐pressure polymorph | Zendy

Skrikanth V. | Zendy; Sato A. | Zendy; Yoshimoto J. | Zendy; Kim J. H. | Zendy; Ikegami T. | Zendy

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Synthesis and crystal structure study of Y 2 O 3 high‐pressure polymorph

Author(s) -

Skrikanth V.,

Sato A.,

Yoshimoto J.,

Kim J. H.,

Ikegami T.

Publication year - 1994

Publication title -

crystal research and technology

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.377

H-Index - 64

eISSN - 1521-4079

pISSN - 0232-1300

DOI - 10.1002/crat.2170290712

Subject(s) - monoclinic crystal system , crystal structure , crystallography , materials science , high pressure , yttria stabilized zirconia , crystal structure prediction , lattice (music) , ambient pressure , polymorphism (computer science) , phase (matter) , crystal (programming language) , single crystal , mineralogy , chemistry , thermodynamics , cubic zirconia , metallurgy , ceramic , organic chemistry , physics , acoustics , programming language , computer science , biochemistry , gene , genotype

Single crystal high pressure polymorph of yttria was synthesized for the first time using a link–type cubic anvil apparatus. Crystal structure was refined from single crystal data. High pressure polymorph was confirmed as a monoclinic phase. Lattice parameters of the high pressure polymorph at room temperature and ambient pressure were determined as follows: a = 13.8714 Å, b = 3.4487 Å, c = 8.5862 Å, β = 100.12°.

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