Molten-Salt Synthesis of Complex Metal Oxide Nanoparticles

Jose P. Zuniga; Maya Abdou; Santosh K. Gupta; Yuanbing Mao

doi:10.3791/58482

JoVE Journal > Chemistry

화학

Molten-Salt Synthesis of Complex Metal Oxide Nanoparticles

Published: October 27, 2018

doi:

10.3791/58482

Jose P. Zuniga¹, Maya Abdou¹, Santosh K. Gupta^1,2, Yuanbing Mao^1,3

¹Department of Chemistry,University of Texas Rio Grande Valley, ²Radiochemistry Division,Bhabha Atomic Research Centre, ³School of Earth, Environmental, and Marine Sciences,University of Texas Rio Grande Valley

Summary

Here, we demonstrate a unique, relatively low-temperature, molten-salt synthesis method for preparing uniform complex metal oxide lanthanum hafnate nanoparticles.

Abstract

The development of feasible synthesis methods is critical for the successful exploration of novel properties and potential applications of nanomaterials. Here, we introduce the molten-salt synthesis (MSS) method for making metal oxide nanomaterials. Advantages over other methods include its simplicity, greenness, reliability, scalability, and generalizability. Using pyrochlore lanthanum hafnium oxide (La₂Hf₂O₇) as a representative, we describe the MSS protocol for the successful synthesis of complex metal oxide nanoparticles (NPs). Furthermore, this method has the unique ability to produce NPs with different material features by changing various synthesis parameters such as pH, temperature, duration, and post-annealing. By fine-tuning these parameters, we are able to synthesize highly uniform, non-agglomerated, and highly crystalline NPs. As a specific example, we vary the particle size of the La₂Hf₂O₇ NPs by changing the concentration of the ammonium hydroxide solution used in the MSS process, which allows us to further explore the effect of particle size on various properties. It is expected that the MSS method will become a more popular synthesis method for nanomaterials and more widely employed in the nanoscience and nanotechnology community in the upcoming years.

Introduction

Molten-salt synthesis (MSS) involves the use of a molten salt as the reaction medium for preparing nanomaterials from their constituent precursors. The molten salt acts as the solvent and facilitates the enhanced reaction rate by increasing the contact area between reactants and their mobility. The choice of molten salts is of paramount importance for the success of the MSS method. The salt must meet some important quality requirements such as low melting point, compatibility with reacting species, and optimum aqueous solubility. Molten salt has been used previously to enhance the rate of solid-state reactions; however, in a flux system, only a small amount of molten salt is used (unlike in MSS, in which a large quantity is added to form a soluble medium for the reaction and control the properties of the synthesized nanomaterials, such as particle size, shape, and crystallinity, etc.). In this sense, MSS is a modification of the powder metallurgical method and different from the flux method¹^,²^,³. The employment of molten salt can (1) increase reaction kinetic rate⁴ while decreasing synthesis temperature⁵, (2) increase the degree of reactant homogeneity⁶, (3) control crystalline size and morphology⁷, and (4) reduce the level of agglomeration.

Nanomaterials have been in high demand in scientific research and novel industrial applications because of their superior electrical, chemical, magnetic, optical, electronic, and thermal properties. Their properties are highly dependent on the particle size, shape, and crystallinity. Compared with other synthesis methods for nanomaterials, MSS has several obvious advantages; although, it is not yet as well-known as other synthesis methods in the nanoscience and nanotechnology community. As described below, these advantages include its simplicity, reliability, scalability, generalizability, environmental friendliness, cost effectiveness, relative low synthesis temperature, and free agglomeration of NPs with clean surface⁸.

Simplicity: The MSS process can be easily carried out in a simple laboratory with basic facilities. No sophisticated instrumentation is needed. Precursors and molten salts are air stable with no need for glove box handling.

Reliability: Once all initial synthesis parameters such as concentration, pH, processing time, and annealing temperature are optimized, high-quality and pure products are assured when using the MSS method. If all synthesis steps are carried out properly, the final products may attain all basic criteria needed for good-quality NPs. A novice to the MSS method will not change the synthesis outcome, as long as all synthesis parameters are properly and carefully followed.

Scalability: The MSS method's ability to produce large quantities of size- and shape-controlled particles is crucial. This critical factor is important because it allows for the determination of industrial usefulness and efficiency. Compared to other synthesis techniques, MSS can easily generate a sufficient amount of products by adjusting stoichiometric amounts during the process. This is an important feature of the method because it allows for convenience at the industrial level, making it a more desired approach due to this scalability⁹^,¹⁰.

Generalizability: The MSS method is also a generalizable technique to produce nanoparticles with various compositions. Other than simple metal oxides and some fluorides, nanomaterials of complex metal oxides that have been successfully synthesized by the MSS method include perovskites (ABO₃)¹⁰^,¹¹^,¹²^,¹³^,¹⁴, spinel (AB₂O₄)¹⁵^,¹⁶, pyrochlore (A₂B₂O₇)⁴^,¹⁷^,¹⁸^,¹⁹, and orthorhombic structures (A₂B₄O₉)²^,³^,²⁰. More specifically, these nanomaterials include ferrites, titanates, niobates, mullite, aluminium borate, wollastonite, and carbonated apatite⁷^,⁹^,²¹. The MSS method has also been used to produce nanomaterials of various morphologies such as nanospheres⁴, ceramics powder bodies²², nanoflakes²³, nanoplates⁷, nanorods²⁴, and core-shell nanoparticles (NPs)²⁵, depending on synthesis conditions and crystal structure of the products.

Environmental friendliness: Several traditional methods for making nanomaterials involve the use of large amounts of organic solvents and toxic agents that generate environmental issues. The partial or total elimination of the use of them and the generation of waste by sustainable processes is in demand of green chemistry nowadays⁸. The MSS method is an environmentally friendly approach to synthesize nanomaterials by employing nontoxic chemical and renewable materials and minimizing waste, byproducts, and energy.

Relative low synthesis temperature: The processing temperature of the MSS method is relatively low compared to that required in a conventional solid-state reaction²⁶ or a sol-gel combustion reaction²⁷. This lower temperature saves energy while producing high-quality NPs.

Cost effectiveness: The MSS method does not require any harsh or costly reactants or solvents nor any specialized instrumentation. Water is the main solvent used for washing away the used molten salts, which are also cheap. Moreover, experimental setup needed includes only simple glassware and a furnace without specialized instrumentation, while nanomaterials with complex composition and refractory nature can be produced.

Agglomeration free with clean surface: During the MSS process, the formed nanoparticles are well-dispersed in the molten salt medium due to its large quantity, used along with its high ionic strength and viscosity¹^,⁶^,⁸. Unlike colloidal synthesis and most hydrothermal/solvothermal processes, no protective surface layer is necessary to prevent the continuous growth and agglomeration of the formed NPs.

Exemplary synthesis of complex metal oxide NPs by the MSS method: The MSS method as a universal and cost-effective approach to rationally and large-scale synthesize nanomaterials for a sufficiently wide spectrum of material may be highly welcomed by scientists working in nanoscience and nanotechnology. Here, lanthanum hafnate (La₂Hf₂O₇) was selected because of its multifunctional applications in the areas of X-ray imaging, high k-dielectric, luminescence, thermographic phosphor, thermal barrier coating, and nuclear waste host. La₂Hf₂O₇ is also a good host for doped scintillators due to its high density, large effective atomic number, and the possibility of its crystal structure to be engineered along with an order-disorder phase transition. It belongs to the A₂B₂O₇ family of compounds, in which "A" is a rare-earth element with a +3 oxidation state, and "B" represents a transition metallic element with a +4 oxidation state. However, due to the refractory nature and complex chemical composition, there has been a lack of proper low-temperature and large-scale synthesis methods for La₂Hf₂O₇ NPs.

For fundamental scientific investigation and advanced technological applications, it is a prerequisite to make monodisperse, high-quality, and uniform A₂B₂O₇ NPs. Here we use the synthesis of highly crystalline La₂Hf₂O₇ NPs as an example to demonstrate the advantages of the MSS method. As schematically shown in Figure 1, La₂Hf₂O₇ NPs were prepared by the MSS method with a two-step process following our previous reports. First, a single-source complex precursor of La(OH)₃·HfO(OH)₂·nH₂O was prepared via a coprecipitation route. In the second step, size-controllable La₂Hf₂O₇ NPs were synthesized through the facile MSS process using the single-source complex precursor and nitrate mixture (NaNO₃:KNO₃ = 1:1, molar ratio) at 650 °C for 6 h.

Figure 1: Schematic of the synthesis steps for La₂Hf₂O₇ NPs via the MSS method. Please click here to view a larger version of this figure.

Protocol

1. Preparation of Single-Source Complex Precursor via a Coprecipitation Route

Preparation of lanthanum and hafnium precursor solution
1. Measure 200 mL of distilled water in a 500 mL beaker and start stirring at 300 rpm.
2. Dissolve lanthanum and hafnium precursors in the stirring water [i.e., 2.165 g of lanthanum nitrate hexahydrate (La(NO₃)₃•6H₂O) and 2.0476 g of hafnium dichloride oxide octahydrate (HfOCl₂•8H₂O)].
3. Let the solution stir for 30 min before starting the titration.
Preparation of diluted ammonia solution
1. Prepare 200 mL of diluted ammonia solution with different concentrations, including 0.75%, 1.5%, 3.0%, 6.0%, and 7.5%. For example, add 20 mL of concentrated ammonia solution (NH₄OH (aq), 28-30%) to 180 mL of distilled water in a separate beaker to make 3.0% diluted ammonia solution.
Titration and washing the single source complex precursor
1. Add the diluted ammonia solution prepared in the previous step into a burette and ensure that the burette is covered at all times, since ammonia solution tends to evaporate which decreases its concentration.
2. Add the diluted ammonia solution in the burette into the stirring solution of lanthanum nitrate and hafnium dichloride oxide dropwise.
3. Adjust the dropping speed of the ammonia solution accordingly so that it will be added over a period of 2 h.
4. After several mL of ammonia solution have been delivered, ensure that the solution becomes cloudy. This is a simple sign that the precipitate of the single-source complex precursor of La(OH)₃·HfO(OH)₂·nH₂O is forming.
5. After 2 h, remove the stirring bar and allow the precipitate to age overnight.
6. Check the pH of the coprecipitated solution before washing. Wash the precipitate with distilled water until the supernatant reaches a neutral pH, which normally takes 5-8 washes.
Vacuum filtration and drying of precursor
1. Vacuum filter the coprecipitated solution using a filter paper with a coarse porosity (40-60 µm; see Table of Materials) to separate the solid precipitate from the supernatant.
2. Ensure that all complex precursor remnants are washed from the walls of the beaker.
3. Air dry the resulting single-source complex precursor La(OH)₃·HfO(OH)₂·nH₂O at room temperature overnight.

2. Molten-Salt Synthesis of Lanthanum Hafnate NPs

Preparation of salt and precursor mixture
1. Measure 30 mmol (3.033 g) of potassium nitrate (KNO₃) and 30 mmol (2.549 g) of sodium nitrate (NaNO₃).
2. Combine the measured salts with 0.35 g of the as-prepared single-source complex precursor La(OH)₃·HfO(OH)₂·nH₂O.
3. If necessary, add 1-5 mL of acetone or ethanol to the mixture to facilitate the grinding. Ensure that all the solvent is evaporated before placing the mixture into a crucible.
4. Grind the mixed salts and precursor as fine as possible for about 30 min using a mortar and pestle.
Molten-salt processing
1. Place the resulting mixture in a corundum crucible, then place it in a muffle furnace.
2. Set the furnace at 650 °C for 6 h with a ramp rate of 10 °C/min.
3. After the sample and furnace have cooled to room temperature, take out the crucible and soak the sample in a beaker filled with distilled water overnight.
Washing and drying the La₂Hf₂O₇ NPs
1. Empty the sample from the crucible into a 1 L beaker.
2. Wash the sample with distilled water 5-8 times until the supernatant is clear of salts and not cloudy anymore.
3. Purify the product by centrifugation or vacuum filtration to remove any residual impurity.
4. Dry the product in the oven at 90 °C overnight.

Representative Results

The as-synthesized La₂Hf₂O₇ NPs may exist in the ordered pyrochlore phase. However, chemical doping, pressure, and temperature could modify the phase to defect fluorite. It is possible for our material to have multiple phases; however, here we focus only on the pyrochlore phase for simplicity. X-ray diffraction (XRD) and Raman spectroscopy have been used to systematically characterize their phase purity, structure, and phase. The crystalline size can be calculated using Debye-Scherrer's formula. On the other hand, Raman spectroscopy is used as a secondary structural characterization technique due to it high sensitivity to M-O vibrational modes²⁸. It identifies the exact crystallographic phase of the La₂Hf₂O₇ NPs²⁹.

Compared to other synthetic techniques such as solid-state reactions, MSS has a high reaction constant, meaning that the reaction is more likely to go in the forward direction³⁰. The production of pyrochlore La₂Hf₂O₇ is achieved by increasing the contact interfacial area and mobility of the reactant species inside the molten salt system. Figure 2 illustrates the XRD patterns of the synthesized La₂Hf₂O₇NPs made by the MSS method from the single-source complex precursors using different concentrations of ammonia solution. XRD results shows the formation of pure La₂Hf₂O₇ with high crystallinity. The peak position and Miller indices may be indexed based on the Joint Committee on Powder Diffraction Standard (JCPDS) pattern #78-1292. No visible impurity phases such as La₂O₃, Eu₂O₃, or HfO₂ were detected. There is no change in XRD pattern as a function of the used ammonia concentration except for the increase of particle size. Table 1 shows the corresponding calculated crystal parameter and particle size of the La₂Hf₂O₇ NPs.

Figure 2: X-ray diffraction patterns of the La₂Hf₂O₇NPs prepared by adjusting the used ammonia solution concentration then indexed based on the defect fluorite pattern. Please click here to view a larger version of this figure.

Concentration of NH₄OH(aq) used	XRD data of the synthesized La₂Hf₂O₇ NPs
Concentration of NH₄OH(aq) used	2θ (°)	FWHM (β)	Lattice parameters (Å)	Particle size (nm)
[0.75%]	28.57	0.4	10.81	19.00
[1.5%]	28.64	0.39	10.79	20.00
[3.0%]	28.67	0.37	10.78	21.00
[6.0%]	28.69	0.31	10.77	26.00
[7.5%]	28.74	0.27	10.75	29.00

Table 1: Crystallographic parameter and particle size of the La₂Hf₂O₇NPs prepared by adjusting the used ammonia solution concentration showing a continuous particle size growth. FWHM = full-width at half-maximum.

There are two common phases of the A₂B₂O₇ compounds: the disordered fluorite phase and ordered pyrochlore phase. The disordered fluorite phase exists in the Fm3̅m space group, wherein all the cationic ions (A³⁺ and B⁴⁺) are randomly distributed, allowing for one active mode. On the other hand, ordered pyrochlore phase exists in Fd3̅m space group. Therefore, it exhibits close structural resemblance to fluorite phase except that there are two cationic sites, three anionic sites [48f(O_I), 8a(O_II), and 8b(O_III)], and 1/8^th of the oxygen ions (O_III) at 8b site absent in the pyrochlore structure, allowing for 6 active modes¹⁹^,²⁸^,²⁹. Based on the group theory, the defect fluorite structure has one vibrational mode due to T₂_g, while a pyrochlore phase has six vibrational modes in the range of 200-1000 cm^-1. This information is vital for the correct phase identification of the La₂Hf₂O₇ NPs (Figure 3). In this case, the prepared La₂Hf₂O₇ NPs are in pure pyrochlore form.

Figure 3: Raman spectra of the La₂Hf₂O₇NPs prepared by adjusting the used ammonia solution concentration, with six active modes pertaining to the pyrochlore phase. Please click here to view a larger version of this figure.

Discussion

The chart in Figure 4 provides several reliable controlling factors of the MSS method and accounts for alternative pathways to fine-tune the features of synthesized nanomaterials. In addition, it helps identify critical steps in the MSS process.

Figure 4: Flowchart of the critical steps of MSS indicating the controlling factors of the synthetic procedure for NPs with potential pathways to fine-tune their characteristics. Please click here to view a larger version of this figure.

First, the identity of precursors is critical, especially for the synthesis of complex metal oxide NPs. When producing A₂B₂O₇ NPs, it is important to first generate a single-source complex precursor that contains the main elements making up the final product [i.e., A and B, at an atomic level with the formula of A(OH)₃·BO(OH)₂·nH₂O]. In this experiment, the particle size of the final La₂Hf₂O₇ NPs could be controlled during this step by adjusting the concentration of the titrant ammonia solution, where a higher ammonia solution concentration generated bigger La₂Hf₂O₇ NPs. Other trials have also been performed to make A₂B₂O₇NPs using different precursors, such as commercially available nitrates or oxides containing the main elements of A₂B₂O₇; however, none have worked⁴. The advantages of this amorphous single-source complex precursor are that the composing elements of A₂B₂O₇ are mixed at an atomic level and are homogeneously distributed in the same order as the final A₂B₂O₇ product, decreasing the space or range over which the reactants need to be transported.

Second, the selection of proper molten salt has major importance in obtaining nanomaterials with desirable morphology and characteristics. The melting point of the selected salt should be appropriate for the synthesis of the required phase of nanomaterials. The formation of nanomaterials is ultimately governed by the melting point of salts used as molten solvents, such as alkali chloride, sulfate, carbonate, or hydroxide¹^,⁶^,³¹^,³². It has been reported that the use of different molten salts can modify the formation temperature, thereby altering the particle size and morphology¹⁸.

In addition, the ramp rate tends to affect the synthesis of the NPs. A fast ramp rate tends to generate agglomerated NPs³³, which affects their properties. In the case of luminescent and scintillation materials, high agglomeration is not desirable, as it can scatter excited and emitted light¹⁷^,¹⁹. A slow ramp rate is thus more suitable and allows enough time to reach the actual temperature inside the crucible. A slower cooling process usually allows for NPs with a spherical shape to form³⁴.

Another important criterion for the selection of the salt is that it should have sufficient aqueous solubility. With simple washing by water, the used molten salt should be easily washed away after the MSS.

Finally, the addition of a volatile liquid such as acetone and ethanol during the mixing of the salts used and single-source complex precursor helps ease the grinding process but is not essential. The addition of a liquid is helpful to make a homogenous mixture in a shorter time and requires less effort, which is important in generating pure products. The added volatile liquid does not affect the characteristics of the resultant NPs since it fully evaporates by the end of the grinding process. Due to its high volatility, the amount added may range anywhere from 1 to 5 mL.

The MSS method is a straightforward and simple way to synthesize NPs at any university and industrial location. However, modifications of the protocol can be made. For example, in case a vacuum filter system is not available, the single-source complex precursor obtained from the coprecipitation step can be centrifuged. Different eutectic salt mixtures can be used to engineer NPs with desired characteristics.

Even though the MSS method is generally easy to be employed, limitations include (1) the possibility of the product formation being limited by the contact area of the dissimilar reactants in the reaction¹. Additionally, (2) not every nanostructured product can be formed within selected molten salts. These cases are rare but can certainly happen³⁵. It is desirable that the selected salts act only as pure solvents and do not react with the reactants or products. Furthermore, common mistakes that may hinder the quality of the final nanoparticle products include the following: (1) First, if the burette is not covered during the titration, this may change the concentration of the ammonium hydroxide and eventually change the size of obtained nanoparticles. Another common mistake is (2) not giving the coprecipitation a period of two hours to form. Adding the ammonia titrant too fast affects the coprecipitation kinetics, which might render inhomogeneous complex precursor. The third pitfall is (3) not grinding the salt(s) and precursor(s) as fine as possible, which generates impure products or inhomogeneous particles.

The MSS method is simple, effective, fast, low-temperature, and cost-efficient as proven with previously reported results, compared to conventional solid-state and sol-gel/combustion synthesis methods²⁷. It is also scalable, reliable, and generalizable in regards to making agglomeration-free NPs without a surface protective layer, unlike colloidal and hydrothermal/solvothermal synthesis methods.

Application of the MSS method has widely spread in the last couple of decades, from ferroelectric and ferromagnetic materials to materials for Li-ion batteries³⁶, semiconductors¹⁷^,³⁷, phosphors¹⁷^,¹⁹, and electro-catalysts³⁸^,³⁹, mainly for nanosized materials, especially those with complex compositions. In conclusion, the MSS method provides a suitable pathway in the synthesis of simple and complex metal oxide NPs. It is expected that the MSS method will become an even more popular synthesis method for nanomaterials and more widely employed in the nanoscience and nanotechnology community in the upcoming years.

Disclosures

The authors have nothing to disclose.

Acknowledgements

The authors thank the financial support provided by the National Science Foundation under CHE (award #1710160) and the USDA National Institute of Food and Agriculture (award #2015-38422-24059). The Department of Chemistry at the University of Texas Rio Grande Valley is grateful for the generous support provided by a Departmental Grant from the Robert A. Welch Foundation (Grant No. BX-0048). S.K.G. would like to thank the United States-India Education Foundation (USIEF) and the Institute of International Education (IIE) for his Fulbright Nehru Postdoctoral Fellowship (award #2268/FNPDR/2017).

Materials

Acetone, ACS, 99.5+%	Alfa Aesar	67-64-1	Dried over 4A sieves
Hafnium dichloride oxide octahydrate, 98+% (metals basis excluding Zr), Zr <1.5%	Alfa Aesar	14456-34-9	Hygroscopic
Lanthanum(III) nitrate hexahydrate	Aldrich	10277-43-7	Hygroscopic
Potassium nitrate, ReagentPlus R, ≥99.0%	Sigma-Aldrich	7757-79-1	Hygroscopic
Sodium nitrate, ReagentPlus R, ≥99.0%	Sigma-Aldrich	7631-99-4
Ammonium hydroxide, 28% NH3, NH4OH	Alfa Aesar	1336-21-6
Filter paper, P8 grade	Fisherbrand

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Zuniga, J. P., Abdou, M., Gupta, S. K., Mao, Y. Molten-Salt Synthesis of Complex Metal Oxide Nanoparticles. J. Vis. Exp. (140), e58482, doi:10.3791/58482 (2018).