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The X-ray powder diffraction data for CeCo3Ni2

Published online by Cambridge University Press:  28 May 2014

Degui Li
Affiliation:
Department of Physics and Communication Engineering, Baise University, Baise, Guangxi 533000, China
Ming Qin*
Affiliation:
Department of Physics and Communication Engineering, Baise University, Baise, Guangxi 533000, China
Liuqing Liang
Affiliation:
Department of Physics and Communication Engineering, Baise University, Baise, Guangxi 533000, China
Zhao Lu
Affiliation:
Department of Physics and Communication Engineering, Baise University, Baise, Guangxi 533000, China
Shuhui Liu
Affiliation:
Department of Physics and Communication Engineering, Baise University, Baise, Guangxi 533000, China
Caimin Huang
Affiliation:
Department of Physics and Communication Engineering, Baise University, Baise, Guangxi 533000, China
Bing He
Affiliation:
Department of Physics and Communication Engineering, Baise University, Baise, Guangxi 533000, China
Lingmin Zeng
Affiliation:
College of Materials Science and Engineering, Guangxi University, Nanning, Guangxi 530004, China
*
a) Author to whom correspondence should be addressed. Electronic mail: [email protected]

Abstract

The CeCo3Ni2 compound was synthesized by arc melting under argon atmosphere. High-quality powder X-ray diffraction (XRD) data of CeCo3Ni2 have been collected using a Rigaku SmartLab X-ray powder diffractometer. The refinement of the XRD pattern for the CeCo3Ni2 compound shows that the CeCo3Ni2 is a hexagonal structure, space group P6/mmm (No.191) with a = b = 4.9081(2) Å, c = 4.0034(2) Å, V = 83.52 Å3, Z = 1, and ρ x  = 8.6347 g cm−3. The Smith–Snyder FOM F 30 = 112.7(0.0089, 30) and the intensity ratio RIR = 0.48.

Type
New Diffraction Data
Copyright
Copyright © International Centre for Diffraction Data 2014 

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