Features of the Synthesis of InGaMgO4 from Nitrate-Organic Precursors and the Study of Its’ Physical Properties

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This work reports on the possibility of producing the InGaMgO4 oxide by two-stage heat treatment of glycine-, starch- and PVA-nitrate precursors. The products formed as a result of their heating at low temperatures (≈ 90°С) were studied by powder X-ray diffraction. It was found that the powder formed from the glycine-nitrate precursor contains nanocrystalline In2O3, and drying of the polymer-nitrate compositions leads to the production of a thermally stable X-ray amorphous product. Its' annealing at temperatures above 800°C allows synthesizing InGaMgO4 powder free of impurity phases. High-temperature treatment of the powder formed from the glycine-nitrate precursor also leads to the production of InGaMgO4, but does not remove the In2O3 impurity. Using scanning electron microscopy, it was found that single-phase InGaMgO4 powders synthesized from polymer-nitrate precursors have a similar grain structure but differ in grain size distribution. Presumably, this difference is due to the structural features of starch and PVA macromolecules used for the preparation of precursors. The InGaMgO4 oxide was characterized using differential scanning calorimetry, Raman and diffuse reflectance spectroscopy. The value of its' band gap energy Eg was determined using the Tauc method.

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作者简介

M. Smirnova

Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences

编辑信件的主要联系方式.
Email: smirnova_macha1989@mail.ru
俄罗斯联邦, Moscow

O. Kondratyeva

Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences

Email: smirnova_macha1989@mail.ru
俄罗斯联邦, Moscow

G. Nikiforova

Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences

Email: smirnova_macha1989@mail.ru
俄罗斯联邦, Moscow

A. Yapryntsev

Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences

Email: smirnova_macha1989@mail.ru
俄罗斯联邦, Moscow

A. Averin

Frumkin Institute of Physical Chemistry and Electrochemistry of the Russian Academy of Sciences

Email: smirnova_macha1989@mail.ru
俄罗斯联邦, Moscow

A. Khoroshilov

Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences

Email: smirnova_macha1989@mail.ru
俄罗斯联邦, Moscow

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2. Fig. 1. Digital photographs of products formed at the heating stage of the NOP: HNP (a), KNP (b) and PNP (c). The inserts show photos of the final powders

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3. Fig. 2. Temperature dependence of the InGaMgO4 heat capacity: 1 — DSC data; 2 — calculated curve (equation (5))

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4. Fig. 3. X-ray images of HNP evaporation products before and after their annealing in air at 1300°C

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5. Fig. 4. X-ray images of the products of evaporation of CNP (a) and PNP (b) before and after their annealing in air at temperatures from 400 to 1200°C

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6. Fig. 5. SEM images of InGaMgO4 powder annealed in air at 1200°C for 4 hours: a — CNG; b — PNP

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7. Fig. 6. Raman spectrum of InGaMgO4 measured at room temperature

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8. Fig. 7. The spectrum of diffuse reflection of InGaMgO4 in the UV and visible regions. The box shows a graph of the dependence (F(R) hv)2 of hv, used to evaluate Eg

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