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Study of the mechanism for controlled crystallization of BaF2 under two kinds of monolayers

Published online by Cambridge University Press:  31 January 2011

L. Lu
Affiliation:
Laboratory of Rare Earth Chemistry and Physics, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China
H. Cui
Affiliation:
Laboratory of Rare Earth Chemistry and Physics, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China
W. Li
Affiliation:
Laboratory of Rare Earth Chemistry and Physics, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China
H. Zhang
Affiliation:
Laboratory of Rare Earth Chemistry and Physics, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China
S. Xi*
Affiliation:
Laboratory of Rare Earth Chemistry and Physics, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, China
*
a)Address all correspondence to this author.xisq@public.cc.jl.cn
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Abstract

Controlled crystallization of BaF2 under two different kinds of monolayers, octadecylamine [CH3(CH2)17NH2] and hexadecanol [CH3(CH2)14CH2OH], has been studied by using x-ray diffraction (XRD) and scanning electron microscope. It was found that the monolayer headgroup, the degree of ionization of the headgroup, etc., had a complicated effect on the selectivity of monolayers for crystal and on the morphology and orientation of crystals grown under the compressed monolayers. At pH = 7.0, XRD analysis showed that (100)-oriented BaF2 crystals were formed under the octadecylamine monolayer, while several kinds of crystals were found under the hexadecanol monolayer. In comparison, at pH = 8.5, both (100)-oriented BaF2 and (111)-oriented Ba(NO3)2 crystals were obtained under the monolayer of octadecylamine. However, crystals formed under hexadecanol monolayer consist of BaF2, Ba(NO3)2, etc. The detailed mechanism for crystallization was discussed in terms of the specific interaction and lattice matching between the monolayer headgroup and the nucleating species.

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Articles
Copyright
Copyright © Materials Research Society 2001

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References

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