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Article

Molten Salt Synthesis of Micro-Sized Hexagonally Shaped REMnO3 (RE = Y, Er, Tm, Yb)

by
Dovydas Karoblis
,
Aleksej Zarkov
*,
Tomas Murauskas
and
Aivaras Kareiva
Institute of Chemistry, Vilnius University, Naugarduko 24, LT-03225 Vilnius, Lithuania
*
Author to whom correspondence should be addressed.
Inorganics 2023, 11(5), 178; https://doi.org/10.3390/inorganics11050178
Submission received: 24 February 2023 / Revised: 10 April 2023 / Accepted: 18 April 2023 / Published: 23 April 2023
(This article belongs to the Special Issue Mixed Metal Oxides II)
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Abstract

:
Yttrium manganite (YMnO3) is a compound belonging to the hexagonal rare earth manganites family, which demonstrates multiferroic properties. This material can be prepared by several synthetic approaches, with the most common one being the solid-state synthesis. In this work, we show a possibility of preparing this material via molten salt synthesis using the NaCl-KCl mixture as the reaction medium and yttrium and manganese nitrates as the starting materials. We demonstrate that, by varying the reaction temperature and the nitrates-to-chlorides ratio, it is feasible to synthesize hexagonally shaped particles of microscopic dimensions. A similar synthesis procedure can be successfully applied for the preparation of other hexagonal manganites—ErMnO3, TmMnO3, and YbMnO3.

Graphical Abstract

1. Introduction

Hexagonal rare earth manganites REMnO3 (RE = rare earth element) have attracted a lot of scientific attention due to the possibility of obtaining two ferroic orders in the same phase [1]. The trimer structural distortion observed in these materials leads to the appearance of polarization, as well as bulk magnetization and the linear magnetoelectric effect [2]. Rare earth manganites with hexagonal structure have antiferromagnetic ordering at lower temperatures (TN varies in 57–130 K range) [3] and are ferroelectrics at high temperatures (TC–620–1000 K) [4]. This type of multiferroics could be applied in energy-efficient devices [5], relying upon electric-field control of magnetism, biomedicine [6], photocatalysis [7], solid oxide fuel cells [8], gas sensors [9], etc.
Out of all the rare earth manganites with hexagonal crystal structures, YMnO3 is one of the most studied. This material has a low Néel temperature (TN~80 K) and a high Curie temperature (TC~910 K) [10] Moreover, it displays mutual coupling between structural translation and the antiferromagnetic and ferroelectric domains walls [11]. This multiferroic vortex have been extensively investigated due to its fascinating physics and possible application in data storage devices [12]. The ferroelectric hexagonal YMnO3 has a P63 cm space group and the structure of this compound consists of non-connected MnO5 trigonal bipyramid layers with Y3+ layers in between [13]. In addition to demonstrating multiferroic properties, this manganite has shown photocatalytic activity towards methyl red degradation [14], a high near-infrared reflectance [15], various gas sensing abilities [16], and excellent photodetection performance [17].
Various synthetic approaches can be used for the synthesis of YMnO3 in the form of nanoparticles, bulk material, or thin films [18,19,20,21]. While it has some drawbacks, solid-state synthesis is the most used method. This synthetic route usually involves several annealing stages, a long mixing of the starting materials and sintering times (more than 10 h), and high temperatures (higher than 1100 °C) [22,23]. On the other hand, different salts can be used as the reaction medium to increase the rate of diffusion for solid-state reactions. The preparation technique where metal oxides are synthesized in inorganic melt, with temperatures slightly beyond the melting point, is known as molten salt synthesis [24]. This approach is cheap, easy to upscale, clean, does not require sophisticated equipment, and offers the possibility of obtaining uniformly shaped particles at lower temperatures and shorter reaction times [25].
Few different studies dealing with the preparation of YMnO3 by molten salt synthesis have been already reported [26,27,28]. In all cases, either NaCl or the eutectic mixture of NaCl and KCl were used as the reaction medium. When sodium oleate was added to the reaction mixture, the formation of nanoplates transpired [28], while the use of sodium and potassium chlorides resulted in short, prism-like particles [26]. Furthermore, it was demonstrated that the reaction temperature plays a significant role in the formation of YMnO3 with an orthorhombic or hexagonal structure [27]. While some work was already conducted by preparing YMnO3 via molten salt synthesis, there are many different parameters, including starting materials, the use of new salts as the reaction medium, temperature, the ratio between salts and precursors, reaction time, etc., which could influence the physical properties or shape of the finals products. Moreover, there are three distinctive phases where the Y and Mn molar ratio is 1:1, such as Y2Mn2O7 pyrochlore and orthorhombic YMnO3 (which are metastable ones), as well as thermodynamically stable hexagonal YMnO3 potential changes in reaction conditions could lead to the selective phase synthesis.
In our work, we present a novel way to conduct molten salt synthesis, where metal nitrates are used as the starting materials instead of oxides. We demonstrate that the temperature and precursors-to-chlorides ratio influence the formation of phase-pure hexagonal YMnO3 consisting of hexagonally shaped particles without any sodium or potassium doping. We also show that this synthetic approach can be applied to prepare different hexagonal rare earth manganites, in particular ErMnO3, TmMnO3, and YbMnO3. To the best of our knowledge, thulium and ytterbium manganites were synthesized by the molten salt method for the first time.

2. Results and Discussion

Typically, in the molten salt synthesis, metal oxides are used as the starting materials, while for the reaction medium different salts can be exploited. Since in previously reported works [26,27] yttrium and manganese (IV) oxides were used for the preparation of YMnO3 by the molten salt method, we applied similar experimental conditions for comparison. The XRD patterns of the synthesis products are represented in Figure S1. As can be seen, depending on the synthesis temperature, two different phases of YMnO3 can form. When annealing was performed at a lower temperature (700 °C), the main phase was YMnO3 with an orthorhombic structure (o-YMnO3), while a higher temperature resulted in the formation of hexagonal YMnO3 (h-YMnO3). In both cases, the diffraction peaks associated with the starting Y2O3 can be seen in the XRD profiles. Interestingly, the amount of this impurity did not change with the increase in the reaction temperature. According to Rietveld refinement, the ratio between o-YMnO3 and Y2O3 was 94% to 6%, while the ratio between h-YMnO3 and Y2O3 was calculated as 93% to 7%.
Since the synthesis from metal oxides did not lead to the formation of single-phase YMnO3, we prepared YMnO3 from the yttrium and manganese nitrates, with an expectation of the in situ formation of more reactive oxides. Firstly, we analyzed the thermal decomposition of the starting mixture consisting of nitrates and chlorides by thermogravimetric analysis; the results are demonstrated in Figure 1.
The DTG curve clearly reveals that the degradation of starting materials occurs in several steps. The first peak can be seen at 49 °C and could be related to the melting of manganese nitrate, where a small endotherm in the DSC curve confirms this process. Moreover, a significant weight loss can be distinguished in the 70–260 °C range with two peaks in the DTG curve, which are centered around 88 °C and 143 °C. The removal of adsorbed as well as structural water and the decomposition of manganese nitrate are the processes which may take place during this stage. According to Jian et al. [29], the degradation of manganese nitrate to manganese oxide transpires at 250 °C, which matches well with our study. The most significant weight loss (around 24% of initial mass is lost) occurs in the 300–450 °C region and could be associated with the degradation of yttrium nitrate to yttrium oxide and nitrogen oxide. In addition, a small endotherm at 648 °C in the DSC curve could be related to the melting of the eutectic NaCl-KCl mixture. Prior to the eutectic point, this salt mixture is known to be stable [30]. It is noteworthy that NaCl could potentially react with the formed MnO2, but only in acidic conditions, which is not the case in our system. The mass is constantly decreasing from 500 °C to 850 °C and this could be explained by two processes. First of all, the complete degradation of yttrium nitrate happens at around 640 °C [31], while the latter mass decrease could be explained by the generation of oxygen gas during the reaction between the in situ formed yttrium and manganese oxides.
While it is known that the formation of o-YMnO3 can transpire at lower temperatures, higher temperatures are usually used for the preparation of h-YMnO3. In our case, we performed synthesis at 900 °C and 1100 °C, with the molar ratio between starting materials and chlorides being 1:2; the XRD patterns of the obtained products are given in Figure 2.
It is clearly seen that, regardless of the temperature, h-YMnO3 formed as the main crystal phase. It is worth noting that Y2O3 was not detected in the synthesis products. Rietveld refinement was performed for both samples and the results are presented in Table 1. The cell parameters match well with those of the h-YMnO3 synthesized by the conventional solid-state method [32]. One of the advantages of the molten salt method is shorter reaction times in comparison with a solid-state reaction. For this reason, we tried to synthesize materials, varying the reaction time at 900 °C; the results are shown in Figure S2. Shorter or prolonged reaction times did not lead to the formation of monophasic h-YMnO3. When the reaction time was 1 h, few different impurity phases could be witnessed, like o-YMnO3, Y2O3 and MnO2, while for longer reaction times, small amounts of yttrium and manganese oxides as the neighboring phases were present.
FT-IR spectroscopy was applied in order to investigate the structure of one of the specimens, specifically the one prepared at 1100 °C; the results are presented in Figure 3.
The FT-IR can be applied to distinguish the differences between an orthorhombic and a hexagonal structure [33] for similar compounds. Compounds with an orthorhombic structure have two distinguishable peaks centered at 530 and 490 cm−1 associated with O-Mn-O bending and Re-O vibrations, respectively, while these absorption bands are missing in the samples with hexagonal structures. For our sample, three absorption bands can be observed. The first and broad one, which is centered around 662 cm−1, can be associated with the stretching Mn-O bond vibration. The sharp and more intense peak at 594 cm−1 corresponds to the Mn-O bond vibration in MnO5 [34]. Lastly, the sharp peak at 419 cm−1 was previously observed for the Y-O bond vibration [35]. It should be noted that our sample did not contain any peaks which could be attributed to the MnO2 phase [36], as well as peaks in the 4000–800 cm−1 range which usually correspond to organic groups, such as carbonates, etc.
The morphology of the specimens synthesized at 900 °C and 1100 °C with reaction times of 10 h was further investigated; the SEM images are displayed in Figure 4.
The synthesis temperature influenced not only the particle size, but also the shape. For the sample prepared at 900 °C (Figure 4a), several particles with regular hexagonal and convex hexagonal shapes could be observed. The side length of these hexagons varies in the 0.5–1.5 µm range. This sample also contained smaller particles varying in nanoscale and microscale dimensions. The sample obtained at 1100 °C (Figure 4b) showed agglomerated micro-sized particles without distinctive shapes. According to the previous studies [32,37,38], h-YMnO3 prepared by conventional solid-state synthesis route at similar temperatures consisted of larger agglomerates and clusters without particular shapes.
Taking into account that our proposed molten salt synthetic approach can lead to the formation of particles with well-defined hexagonal shapes, we tried to dilute the starting nitrates mixture by increasing the amount of NaCl-KCl by five times. The XRD patterns of specimens prepared at 900 °C, 1000 °C, and 1100 °C are represented in Figure 5.
The dilution of the starting nitrates mixture with chlorides resulted in the emergence of different YMnO3 structures depending on the reaction temperature. When the ratio between the starting nitrates and chlorides was 1:2, at 900 °C only hexagonal YMnO3 was present, whereas with the ratio of 1:10 the mixture of orthorhombic and hexagonal structures was observed. According to the results of Rietveld refinement, the ratio between the 2 phases was 23% to 77%, with a dominant orthorhombic phase. The increased synthesis temperature prompted the formation of h-YMnO3. Both XRD profiles of the samples prepared at 1000 °C and 1100 °C had more intense [004] diffraction peaks in comparison to the previously described compounds, suggesting a textured structure. The unit cell parameters of these compounds are summarized in Table 1 and match well with the other samples prepared using a different precursors-to-chlorides ratio.
While metal halides are considered to be inert systems for molten salt synthesis, the use of nitrate salts, which have oxidizing properties, could potentially lead to several oxidative states for manganese ions in YMnO3 or other samples. Another problem associated with molten salt synthesis is the possibility of doping of the final product with crucible material or salt medium cations, such as Na+ or K+ in our case. XPS analysis was performed in order to investigate the oxidation states of manganese ions, as well as to determine if any yttrium or manganese ions were potentially substituted with potassium or sodium ions. The results for YMnO3 prepared at 1100 °C for 10 h with a nitrates-to-chlorides molar ratio of 1:10 are presented in Figure 6.
XPS can detect all elements except hydrogen and helium, probes the surface of the sample to a depth of 5–7 nanometers, and has detection limits ranging from 0.1 to 0.5 atomic percent depending on the element. In the XPS spectra of YMnO3 (Figure 6), four different elements can be identified: Y, Mn, O, which constitutes the compound, and C, which gives additional signal unrelated with final sample. The additional high-resolution XPS spectra of Na 1s, K 2p, and K 2s were recorded and no subsidiary signals were detected, indicating no adventitious doping from the alkali salt medium. The analysis of Mn with different states is quite complicated due to the fact that the oxidation states are characterized by similar binding energies. For the determination of the manganese oxidation states, Mn 3s and Mn 2p3/2 spectra were recorded. The spin-orbit splitting ensuing in Mn 2p3/2 and Mn 2p1/2, as well as multiplet splitting, can be seen in the Mn +2, +3, and +4 spectra. The Mn2+ 2p3/2 spectrum revealed a distinctive satellite peak with a higher binding energy [39], which was not observed in our case, indicating the presence of the +2 oxidative state as highly improbable. Therefore, the YMnO3 spectra was fitted with the Mn3+/4+ model, which revealed that the main oxidation state in this compound was +3 (87 to 13% in comparison with 4+ state). The small percentage of Mn4+ could be related to the formation of manganite on the surface. Moreover, the oxidation states could also be determined by comparing the energy differences in the Mn 2s spectra. The smallest difference could be observed for MnO2 (around 4.7 eV) and largest for the MnO compound (ΔE~5.9 eV) [40]. In our sample, the measured ΔE value was around 5.5 eV, indicating that the majority of manganese ions were in the +3 oxidation state. This correlates well with the results of the structural and Rietveld analysis.
The morphology was analyzed for both samples prepared at 1000 and 1100 °C with the reaction time of 10 h and the ratio between nitrates and chlorides as 1:10; SEM micrographs are shown in Figure 7.
Notwithstanding synthesis temperature, both compounds demonstrated some particles with hexagonal shapes. In the case of the sample prepared at a lower reaction temperature (Figure 7a), larger hexagons were obtained in comparison with the specimen obtained at higher temperature (Figure 7b). The side length of hexagons in the first sample (Figure 7a) varied in the 1.5–4 µm range, while the other sample contained hexagons with 0.7–3 µm side lengths. Whereas the sample prepared at 1000 °C contained mostly hexagonal plates, the sample obtained at 1100 °C also consisted of hexagonal rods. Moreover, the sample (Figure 7a) prepared at 1000 °C also contained smaller particles in the nanometer range, while higher temperatures resulted in the formation of polyhedral particles with regular shapes only in the micrometer range. Not only the solid-state method could not be used to obtain hexagonally shaped particles, but other synthesis techniques, such as sol-gel [41] or sol-gel auto-combustion [42], did not produce hexagonal particles as well. Using these synthetic approaches, only spherical particles of nanoscale dimensions could be prepared. This indicates that our synthesis method could be applied to prepare particles with distinctive shapes.
It is known that smaller lanthanides can also form manganites (LnMnO3) with hexagonal crystal structures. In order to investigate if our proposed synthetic approach was applicable for the preparation of other hexagonal manganites, additionally, we tried to synthesize Er, Tm, and Yb manganites using identical synthesis conditions (900 °C, the ratio between nitrates and chlorides as 1:2). The XRD patterns for these specimens are presented in Figure 8.
In all cases, identical synthesis resulted in the formation of REMnO3 with a hexagonal crystal structure; however, all samples additionally contained small amounts of lanthanide and manganese oxides as the neighboring phases. Additionally, TmMnO3 demonstrated high-intensity (002) and (004) diffraction peaks, leading us to believe that this mixed oxide has a specific texture, which similarly was the case for the YMnO3 samples with higher amounts of chlorides. More intense (002) diffraction peaks can also be seen for ErMnO3, as well as YbMnO3.
SEM analysis was executed to determine if the hexagonally shaped particles formed when yttrium changed with the other lanthanides; the results are presented in Figure 9.
Regardless of the chemical composition, all lanthanide manganites demonstrated the presence of hexagonally shaped plate-like particles. The size of these hexagons was slightly dependent on the lanthanide element. The side lengths of these hexagons for ErMnO3 (Figure 9a) and YbMnO3 (Figure 9c) were very similar and varied in the 0.5–2 µm range, while TmMnO3 (Figure 9b) contained smaller hexagons—up to 1 µm in length. Additionally, all samples had smaller particles in the nanometer range without distinctive shapes.

3. Materials and Methods

3.1. Synthesis

For the preparation of REMnO3 (RE = Y, Er, Tm, Yb), yttrium(III) oxide (Y2O3, 99.99%, Sigma-Aldrich, St. Louis, MO, USA), manganese(IV) oxide (MnO2, Sigma-Aldrich, ≥99%), yttrium(III) nitrate hexahydrate (Y(NO3)3∙6H2O, Sigma-Aldrich, 99.9%), erbium(III) nitrate hexahydrate (Er(NO3)3∙6H2O, Sigma-Aldrich, 99.9%), thulium(III) nitrate pentahydrate (Tm(NO3)3∙5H2O, Sigma-Aldrich, 99.9%), ytterbium(III) nitrate pentahydrate (Yb(NO3)3∙5H2O, Sigma-Aldrich, 99.9%), and manganese(II) nitrate tetrahydrate (Mn(NO3)2∙4H2O, 99.9%, Alfa Aesar, Haverhill, MA, USA) were used as the starting materials. Sodium chloride (NaCl, ≥99.5%, Carl Roth, Karlsruhe, Germany) and potassium chloride (KCl, Carl Roth, ≥99.5%) were used as the synthesis medium.
For the synthesis of YMnO3, yttrium and manganese nitrates (the molar ratio between starting materials was 1:1) were taken and mixed with sodium and potassium chlorides in an agate mortar. The molar ratio between the sum of yttrium and manganese ions and chlorides was 1:2 or 1:10 (later, this ratio will be referred in the text as the nitrates to chlorides ratio), while the molar ratio between NaCl and KCl was 1:1. The mixture obtained after grinding was transferred to the corundum crucible and annealed at different temperatures (900 and 1100 °C) for different periods of time (1, 10, and 20 h). In all cases, the heating rate was set as 5 °C/min. The obtained products were taken out of the furnace and washed with a hot distilled water to dissolve the residual alkali metal chlorides. The obtained powders were filtered using a Büchner funnel and the presence of residual chloride ions was determined using a silver nitrate solution. This washing procedure was repeated 3 times for the complete separation of chlorides and the final product. All collected powders were then dried in an oven at 80 °C for 1 h and ground in an agate mortar. For comparison, a similar synthesis procedure was conducted using yttrium and manganese oxides, with the main difference being that samples were annealed at 700 and 1100 °C for 10 h. The detailed procedure for the synthesis of YMnO3 using oxides as the starting materials is reported elsewhere [27]. For the preparation of Er, Tm, and Yb manganites, an identical synthetic approach was applied, and specimens were prepared at 900 °C with the molar ratio between the nitrates and chlorides as 1:2.

3.2. Characterization

The thermal decomposition of nitrates in a mixture of chlorides was investigated by thermogravimetric and differential scanning calorimetric (TG/DTG/DSC) analysis using PerkinElmer STA 6000 Simultaneous Thermal Analyzer. About 5–10 mg of the sample was heated from 30 °C to 850 °C at 10 °C/min heating rate in a dry flowing air (20 mL/min). Powder X-ray diffraction (XRD) analysis was performed using Rigaku MiniFlex II diffractometer (Cu Kα, λ = 1.5419 Å) working in Bragg-Brentano (θ/2θ) geometry. The data were collected within the 10–70° 2θ range with a step of 0.02° and scanning speed of 1°/min. The obtained diffraction data were refined by the Rietveld method using the Fullprof suite. The Fourier transform infrared spectra (FTIR) were obtained in the range of 4000–400 cm−1 with a Bruker ALPHA-FTIR spectrometer with 4 cm−1 resolution. The morphology of the synthesized powders was analyzed by scanning electron microscopy (SEM) using Hitachi SU-70 microscope. The particle size was estimated from the SEM micrographs using ImageJ software (LOCI, Madison, WI, USA). The X-ray photoelectron spectroscopy (XPS) analyses were carried out with a Kratos Axis Supra spectrometer using a monochromatic Al-Kα source (25 mA, 15 kV). The instrument work function was calibrated to give a binding energy (BE) of 83.96 eV for the Au 4f7/2 line for metallic gold and the spectrometer dispersion was adjusted to give a BE of 932.62 eV for the Cu 2p3/2 line of metallic copper. The Kratos charge neutralizer system was used on all specimens. Survey (wide) scan analyses were carried out with an analysis area of 300 × 700 microns and a pass energy of 160 eV. High-resolution analyses were carried out with an analysis area of 300 × 700 microns and a pass energy of 20 eV. The spectra have been charge corrected to the main line of the carbon 1 s spectrum (adventitious carbon) set to 284.8 eV. The spectra were analyzed using CasaXPS software (version 2.3.23rev1.1R).

4. Conclusions

Hexagonal yttrium manganite (YMnO3) was prepared with the simple, cheap, and non-sophisticated equipment required for the molten salt synthesis method. The in situ formation of oxides from the starting nitrates resulted in the formation of phase pure YMnO3 in comparison to the synthesis, where oxides were used as the starting materials. By varying the synthesis temperature and the nitrates-to-chlorides ratio, a hexagonally shaped particles could be obtained. XPS analysis revealed that neither K+ or Na+ were doped into the YMnO3 structure and the main manganese oxidation state was +3. By applying identical synthesis procedures, hexagonally shaped erbium, thulium, and ytterbium manganites can also be acquired. This synthetic approach where nitrates were used instead of oxides could potentially be applied for the preparation of similar oxide systems, as well as monocrystal growth.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/inorganics11050178/s1, Figure S1: XRD patterns of YMnO3 prepared by using oxides as starting material; Figure S2: XRD patterns of YMnO3 prepared at 900 °C with different reaction times.

Author Contributions

Conceptualization, D.K. and A.Z.; methodology, D.K.; formal analysis, D.K.; investigation, D.K., T.M. and A.Z.; resources, A.K.; data curation, D.K.; writing—original draft preparation, D.K. and T.M.; writing—review and editing, A.K.; supervision, A.Z. and A.K.; funding acquisition, A.K. and A.Z. All authors have read and agreed to the published version of the manuscript.

Funding

The work has been performed in frame of the TransFerr project. It has received funding from the European Union’s Horizon 2020 research and innovation program under the Marie Skłodowska-Curie grant agreement No. 778070.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

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Inorganics 11 00178 g001 550
Figure 1. TG/DTG/DSC curves of starting reaction mixture of metal nitrates and alkali metal chlorides.
Figure 1. TG/DTG/DSC curves of starting reaction mixture of metal nitrates and alkali metal chlorides.
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Figure 2. XRD patterns of YMnO3, prepared at 900 °C and 1100 °C with the molar ratio between nitrates and chlorides as 1:2 with reaction time of 10 h.
Figure 2. XRD patterns of YMnO3, prepared at 900 °C and 1100 °C with the molar ratio between nitrates and chlorides as 1:2 with reaction time of 10 h.
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Figure 3. FT-IR spectrum of YMnO3 sample synthesized at 1100 °C.
Figure 3. FT-IR spectrum of YMnO3 sample synthesized at 1100 °C.
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Figure 4. SEM micrographs of YMnO3, prepared at 900 (a) and 1100 (b), with the ratio between nitrates and chlorides of 1:2.
Figure 4. SEM micrographs of YMnO3, prepared at 900 (a) and 1100 (b), with the ratio between nitrates and chlorides of 1:2.
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Figure 5. XRD patterns of YMnO3 prepared at different temperatures with the molar ratio between precursors and chlorides 1:10. * represents the peaks belonging to the h-YMnO3.
Figure 5. XRD patterns of YMnO3 prepared at different temperatures with the molar ratio between precursors and chlorides 1:10. * represents the peaks belonging to the h-YMnO3.
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Figure 6. XPS spectra of YMnO3 prepared at 1100 °C for 10 h with precursors-to-chlorides molar ratio of 1:10.
Figure 6. XPS spectra of YMnO3 prepared at 1100 °C for 10 h with precursors-to-chlorides molar ratio of 1:10.
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Figure 7. SEM micrographs of YMnO3 prepared at 1000 °C (a) and 1100 °C (b) with the molar ratio between nitrates and chlorides as 1:10.
Figure 7. SEM micrographs of YMnO3 prepared at 1000 °C (a) and 1100 °C (b) with the molar ratio between nitrates and chlorides as 1:10.
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Figure 8. XRD patterns of ErMnO3, TmMnO3, and YbMnO3. ^ represents respective lanthanide oxide phase, while * represents MnO2.
Figure 8. XRD patterns of ErMnO3, TmMnO3, and YbMnO3. ^ represents respective lanthanide oxide phase, while * represents MnO2.
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Figure 9. SEM micrographs of ErMnO3 (a), TmMnO3 (b), and YbMnO3 (c) prepared at 900 °C with the molar ratio between nitrates and chlorides as 1:2.
Figure 9. SEM micrographs of ErMnO3 (a), TmMnO3 (b), and YbMnO3 (c) prepared at 900 °C with the molar ratio between nitrates and chlorides as 1:2.
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Table
Table 1. Cell parameters of YMnO3 samples with hexagonal structure.
Table 1. Cell parameters of YMnO3 samples with hexagonal structure.
Synthesis Conditionsa, Åb, Åc, ÅV, Å3
Temperature, °CMolar Ratio between Precursors and Chlorides
9001:26.1490 (6)6.1490 (6)11.4065 (7)373.51 (0)
11001:26.1359 (4)6.1359 (4)11.3902 (5)371.38 (6)
10001:106.1432 (5)6.1432 (5)11.4039 (0)372.71 (8)
11001:106.1376 (1)6.1376 (1)11.3907 (3)371.60 (4)
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Karoblis, D.; Zarkov, A.; Murauskas, T.; Kareiva, A. Molten Salt Synthesis of Micro-Sized Hexagonally Shaped REMnO3 (RE = Y, Er, Tm, Yb). Inorganics 2023, 11, 178. https://doi.org/10.3390/inorganics11050178

AMA Style

Karoblis D, Zarkov A, Murauskas T, Kareiva A. Molten Salt Synthesis of Micro-Sized Hexagonally Shaped REMnO3 (RE = Y, Er, Tm, Yb). Inorganics. 2023; 11(5):178. https://doi.org/10.3390/inorganics11050178

Chicago/Turabian Style

Karoblis, Dovydas, Aleksej Zarkov, Tomas Murauskas, and Aivaras Kareiva. 2023. "Molten Salt Synthesis of Micro-Sized Hexagonally Shaped REMnO3 (RE = Y, Er, Tm, Yb)" Inorganics 11, no. 5: 178. https://doi.org/10.3390/inorganics11050178

APA Style

Karoblis, D., Zarkov, A., Murauskas, T., & Kareiva, A. (2023). Molten Salt Synthesis of Micro-Sized Hexagonally Shaped REMnO3 (RE = Y, Er, Tm, Yb). Inorganics, 11(5), 178. https://doi.org/10.3390/inorganics11050178

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