Anisotropic growth of La2NiO4+δ: Influential pre-treatment in molten-flux synthesis

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OriginalspracheEnglisch
Aufsatznummer125135
FachzeitschriftJournal of Crystal Growth
Jahrgang523
Frühes Online-Datum24 Juni 2019
PublikationsstatusVeröffentlicht - 1 Okt. 2019

Abstract

Molten-flux synthesis was applied to the mixed ionic-electronic conducting oxide La2NiO4+δ. Melt of NaOH was used to dissolve precursors, which were either coarse mixtures of the oxides La2O3 and NiO from a classical solid-state route or ultrafine mixtures of La2CO5 and NiO from a sol-gel process. To estimate optimum synthesis temperature for the sol-gel process, reaction sequence was monitored by in-situ X-ray diffraction. The molten-flux synthesis in ambient air was conducted at 400 °C for up to 14 h with variation of additional water content and the precursor stoichiometry. Purity and composition of products were investigated by ex-situ X-ray diffraction and wavelength dispersive X-ray spectroscopy. A maximum length of plate-like crystals of ca. 30 μm in the a,b-plane was observed at a thickness of ca. 2 μm in the c-axis (i.e. aspect ratio of 15). By varying several parameters of the molten-flux synthesis, both size and aspect ratio of La2NiO4+δ plate-like crystals could be varied over a wide range.

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Anisotropic growth of La2NiO4+δ: Influential pre-treatment in molten-flux synthesis. / Hinterding, Richard; Zhao, Zhijun; Zhang, Chao et al.
in: Journal of Crystal Growth, Jahrgang 523, 125135, 01.10.2019.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Hinterding R, Zhao Z, Zhang C, Feldhoff A. Anisotropic growth of La2NiO4+δ: Influential pre-treatment in molten-flux synthesis. Journal of Crystal Growth. 2019 Okt 1;523:125135. Epub 2019 Jun 24. doi: 10.1016/j.jcrysgro.2019.06.021
Hinterding, Richard ; Zhao, Zhijun ; Zhang, Chao et al. / Anisotropic growth of La2NiO4+δ : Influential pre-treatment in molten-flux synthesis. in: Journal of Crystal Growth. 2019 ; Jahrgang 523.
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abstract = "Molten-flux synthesis was applied to the mixed ionic-electronic conducting oxide La2NiO4+δ. Melt of NaOH was used to dissolve precursors, which were either coarse mixtures of the oxides La2O3 and NiO from a classical solid-state route or ultrafine mixtures of La2CO5 and NiO from a sol-gel process. To estimate optimum synthesis temperature for the sol-gel process, reaction sequence was monitored by in-situ X-ray diffraction. The molten-flux synthesis in ambient air was conducted at 400 °C for up to 14 h with variation of additional water content and the precursor stoichiometry. Purity and composition of products were investigated by ex-situ X-ray diffraction and wavelength dispersive X-ray spectroscopy. A maximum length of plate-like crystals of ca. 30 μm in the a,b-plane was observed at a thickness of ca. 2 μm in the c-axis (i.e. aspect ratio of 15). By varying several parameters of the molten-flux synthesis, both size and aspect ratio of La2NiO4+δ plate-like crystals could be varied over a wide range.",
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note = "Funding Information: This work was supported by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) – FE 928/15-1 . Z. Zhao acknowledges financial support by the Graduate Academy of the Leibniz University Hannover. Authors gratefully appreciate technical assistance by F. Steinbach. ",
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T1 - Anisotropic growth of La2NiO4+δ

T2 - Influential pre-treatment in molten-flux synthesis

AU - Hinterding, Richard

AU - Zhao, Zhijun

AU - Zhang, Chao

AU - Feldhoff, A.

N1 - Funding Information: This work was supported by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) – FE 928/15-1 . Z. Zhao acknowledges financial support by the Graduate Academy of the Leibniz University Hannover. Authors gratefully appreciate technical assistance by F. Steinbach.

PY - 2019/10/1

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N2 - Molten-flux synthesis was applied to the mixed ionic-electronic conducting oxide La2NiO4+δ. Melt of NaOH was used to dissolve precursors, which were either coarse mixtures of the oxides La2O3 and NiO from a classical solid-state route or ultrafine mixtures of La2CO5 and NiO from a sol-gel process. To estimate optimum synthesis temperature for the sol-gel process, reaction sequence was monitored by in-situ X-ray diffraction. The molten-flux synthesis in ambient air was conducted at 400 °C for up to 14 h with variation of additional water content and the precursor stoichiometry. Purity and composition of products were investigated by ex-situ X-ray diffraction and wavelength dispersive X-ray spectroscopy. A maximum length of plate-like crystals of ca. 30 μm in the a,b-plane was observed at a thickness of ca. 2 μm in the c-axis (i.e. aspect ratio of 15). By varying several parameters of the molten-flux synthesis, both size and aspect ratio of La2NiO4+δ plate-like crystals could be varied over a wide range.

AB - Molten-flux synthesis was applied to the mixed ionic-electronic conducting oxide La2NiO4+δ. Melt of NaOH was used to dissolve precursors, which were either coarse mixtures of the oxides La2O3 and NiO from a classical solid-state route or ultrafine mixtures of La2CO5 and NiO from a sol-gel process. To estimate optimum synthesis temperature for the sol-gel process, reaction sequence was monitored by in-situ X-ray diffraction. The molten-flux synthesis in ambient air was conducted at 400 °C for up to 14 h with variation of additional water content and the precursor stoichiometry. Purity and composition of products were investigated by ex-situ X-ray diffraction and wavelength dispersive X-ray spectroscopy. A maximum length of plate-like crystals of ca. 30 μm in the a,b-plane was observed at a thickness of ca. 2 μm in the c-axis (i.e. aspect ratio of 15). By varying several parameters of the molten-flux synthesis, both size and aspect ratio of La2NiO4+δ plate-like crystals could be varied over a wide range.

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KW - A2. Solid-state synthesis

KW - B1. LaNiO

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