New Precursors towards the Hypergolic Synthesis of Inorganic Materials with Peculiar Morphologies

Article Information

Athanasios B Bourlinos*

Physics Department, University of Ioannina, 45110 Ioannina, Greece

*Corresponding author: Athanasios B Bourlinos, Physics Department, University of Ioannina, 45110 Ioannina, Greece.

Received: 18 July 2022; Accepted: 25 July 2022; Published: 29 July 2022

Citation: Athanasios B Bourlinos. New Precursors towards the Hypergolic Synthesis of Inorganic Materials with Peculiar Morphologies. Journal of Nanotechnology Research 4 (2022): 111-122

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Abstract

Hypergolic reactions have been recently introduced from our group as a radically new preparative tool in materials science, namely hypergolic materials synthesis, allowing the fast and spontaneous synthesis of several nanomaterials at ambient conditions in an energy-liberating manner. Although the majority of the examples given from our group in this context have been mainly referred to carbon, hypergolic materials synthesis can be, in principle, extended to the synthesis of inorganic materials as well. For instance, in previous works we have illustrated that metallocenes and metallocene dichlorides in combination with fuming nitric acid HNO3 are versatile organometallic reagents towards the hypergolic synthesis of a wide range of inorganic material. In our search for additionally new precursors towards the hypergolic synthesis of inorganic materials, here we take another step-forward to show the great potential of metal (IV) dimethylamides with fuming nitric acid HNO3 or of low melting point, hydrated transition metal salts (chlorides or nitrates) with sodium hydride NaH, in the synthesis of inorganic materials with peculiar morphologies through the corresponding hypergolic reactions. In particular, we show that titania TiO2 nanoparticles with twin structure can be derived by ignition of titanium (IV) dimethylamide with fuming nitric acid HNO3, whereas thin maghemite γ-Fe2O3 nanosheets by ignition of molten iron (III) chloride hexahydrate FeCl3•6H2O with sodium hydride NaH. The method can be equally applied to other metal (IV) dimethylamides or low melting point, hydrated transition metal salts with fuming nitric acid HNO3 or sodium hydride NaH, respectively, thus emphasizing the generality and simplicity of this new type of precursors in the hypergolic synthesis of inorganic materials.

Keywords

Fuming nitric acid; Hypergolic materials synthesis; Inorganic materials; Hydrated transition metal chlorides or nitrates; Metal(IV) dimethylamides; Sodium hydride

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Article Details

1. Introduction

Recently our group has introduced hypergolic materials synthesis as a radically new preparative technique in materials science that allows a wide range of carbon or inorganic solids with useful properties to be obtained [1-11]. Driven by simple hypergolic reactions, the new technique not only allows the fast and spontaneous synthesis of several nano-materials at ambient conditions, but also releases sizable amount of energy in the process. Despite the fact that most of the examples provided from our group involved the synthesis of carbon materials (nanosheets, nanodiscs, fluorescent carbon dots, hollow spheres, carbon nitride, graphite/graphene and fullerols), hypergolic materials synthesis can be extended beyond carbon to include inorganic materials as well. Characteristically, in previous works we have shown the synthesis of several inorganic materials (γ-Fe2O3, Cr2O3, Co, Ni, alloy CoNi, TiO2, ZrO2, HfO2, MoO2) by the hypergolic ignition of metallocene or metallocene dichloride organometallic precursors with fuming nitric acid HNO3 [1, 7, 11]. However, the exploration of even more chemical options in the direction of inorganic materials synthesis through hypergolic reactions still remains a challenge in order to further expand the method’s portfolio of materials processing capabilities. To address this challenge, herein we exploit for the first time metal (IV) dimethylamides and low melting point, hydrated transition metal salts (chlorides or nitrates) as potentially new precursors towards the hypergolic synthesis of inorganic materials with scarce morphologies. Metal (IV) dimethylamides are an important class of metalorganic compounds used extensively in chemical vapor deposition to produce thin films on various substrates. On the other hand, hydrated transition metal salts are economic and diverse starting reagents for inorganic synthesis. Indicatively here, we show that hypergolic ignition of titanium (IV) dimethylamide Ti[N(CH3)2]4 by fuming nitric acid HNO3 results in titania TiO2 nanoparticles of twin morphology, while that of molten iron(III) chloride hexahydrate FeCl3·6H2O by sodium hydride NaH in thin maghemite γ-Fe2O3 nanosheets. The structure and morphology of the samples were verified by means of X-ray diffraction and atomic force microscopy, along with additionally 57Fe Mössbauer spectroscopy and magnetic measurements in the case of maghemite γ-Fe2O3. Tin (IV) dimethylamide Sn[N(CH3)2]4 with fuming nitric acid HNO3, as well as, low melting point cobalt(II) chloride hexahydrate CoCl2·6H2O and copper(II) nitrate hexahydrate Cu(NO3)2·6H2O with sodium hydride NaH, are also complementary mentioned in this work in order to highlight the general use of this type of precursors in the hypergolic synthesis of inorganic materials.

2. Materials and Methods

All experiments were conducted with great care in a fume hood with ceramic tile bench using small quantities of reagents. Titanium(IV) dimethylamide Ti[N(CH3)2]4 (99.999 %), tin(IV) dimethylamide Sn[N(CH3)2]4 (99.9 %), iron(III) chloride hexahydrate FeCl3·6H2O (> 99 %), cobalt(II) chloride hexahydrate CoCl2·6H2O (> 99 %), copper(II) nitrate hexahydrate Cu(NO3)2·6H2O (> 99 %), fuming nitric acid HNO3 (100 %) and sodium hydride NaH (dry, 90 %) were all purchased from Sigma-Aldrich. In the case of titanium(IV) dimethylamide Ti[N(CH3)2]4, a glass test tube was charged with 0.5 mL of the liquid reagent followed by the slow, dropwise addition of 1 mL fuming nitric acid HNO3. Addition of the acid triggered ignition of the metalorganic precursor (Figure 1) towards the formation of titania TiO2. The residue was successively washed with deionized water until neutral pH (e.g., fuming nitric acid HNO3 is strongly acidic) and acetone prior to drying at 100 °C. Because the sample also contained 15 % w/w residual carbon from the metalorganic precursor, this had to be removed by calcination at 600 oC for 1 h under air. In this way, an off-white titania TiO2 powder was obtained with N2 BET specific surface area of 16 m2 g-1.

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Figure 1: Hypergolic ignition of titanium (IV) dimethylamide Ti[N(CH3)2]4 by fuming nitric acid HNO3.

In the case of iron (III) chloride hexahydrate FeCl3·6H2O (melting point: 37 °C), 1.5 g of the transition metal salt were first melted at 100 oC inside a glass test tube. Then a total of 0.5 g of solid sodium hydride NaH were slowly added to the molten salt at small portions, causing ignition of the mixture (Figure 2) towards the formation of maghemite γ-Fe2O3 as the major phase. The obtained solid was successively washed with deionized water until neutral pH (e.g., sodium hydride NaH is strongly alkaline) and acetone prior to drying at 100 °C, finally affording a strongly magnetic brown powder of maghemite γ-Fe2O3 with N2 BET specific surface area of 129 m2 g-1.

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Figure 2: Hypergolic ignition of molten iron (III) chloride hexahydrate FeCl3·6H2O by sodium hydride NaH.

X-ray Diffraction (XRD) was conducted on background-free holders using Co Kα radiation from X’Pert PRO diffractometer (Malvern Panalytical) operating in Bragg-Brentano geometry. Atomic force microscopy (AFM) images were obtained in tapping mode with a Bruker Multimode 3D Nanoscope (Ted Pella Inc.) using a microfabricated silicon cantilever type TAP-300G, with a tip radius of < 10 nm and a force constant of approximately 20-75 N m-1. 57Fe Mössbauer Spectra (MS) were collected at room temperature (RT or 300 K) and 77 K using constant-acceleration spectrometers equipped with 57Co(Rh) sources kept at RT, in combination with a liquid nitrogen N2 bath cryostat (Oxford Instruments Variox 760). Metallic iron α-Fe at RT was used for the velocity calibration of the spectrometers and all isomer shift (IS) values are given relative to this standard. The recorded MS were fitted using the IMSG code [12]. The magnetic properties were investigated by isothermal magnetization (M) versus applied magnetic field (H) measurements conducted at RT on a vibrating sample magnetometer (VSM) (LakeShore 7300).

3. Results and Discussion

The hypergolic reaction between titanium (IV) dimethylamide Ti[N(CH3)2]4 and fuming nitric acid HNO3 towards the formation of titania TiO2 can be overall described as following:

Ti [N(CH3)2]4 + 12 HNO3 → TiO2 + 8 N2 + 18 H2O + 8 CO2   (1)

The XRD pattern of the as-derived titania TiO2 displays characteristic diffraction peaks of the anatase and rutile phases in a ratio 70/30, based on Rietveld analysis (Figure 3). Stable anatase and metastable rutile are the two main polymorphs usually co-existing in photocatalytic titania TiO2 [11]. The average particle size in the sample was estimated to be 10 nm by applying the Scherrer equation for the largest intensity diffraction peak of anatase. AFM microscopy was used in order to study the morphology of the sample (Figure 4). Accordingly, this majorly consisted of nanoparticles with twin structure and sizes in the range of 4-10 nm. These sizes are comparable to that calculated above from X-rays and the Scherrer equation. In general, nanotwinned materials have attracted great attention in recent years due to their distinctive structure [13]. At this point it is worth mentioning that the analogous liquid reagent tin (IV) dimethylamide Sn[N(CH3)2]4 also reacts hypergolically with fuming nitric acid HNO3 to afford instead conductive stannic oxide SnO2 (conductivity was checked by a two-point multimeter directly on the solid deposit over the glass surface of the test tube), thus overall making metal (IV) dimethylamides an important class of metalorganic precursors in the hypergolic synthesis of inorganic materials.

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Figure 3: XRD pattern of the as-derived titania TiO2 along with Rietveld analysis of the anatase and rutile phases.

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Figure 4: AFM images and corresponding height profiles of titania TiO2 nanoparticles with twin morphology.

On the other hand, the hypergolic reaction between molten iron(III) chloride hexahydrate FeCl3·6H2O and sodium hydride NaH towards the formation of maghemite γ-Fe2O3 can be represented from the following set of reactions:

2 FeCl3 + 6 NaH → 2 Fe + 6 NaCl + 3 H2   (2)

3 Fe + 4 H2O → Fe3O4 + 4 H2   (3)

4 Fe3O4 + O2 → 6 γ-Fe2O3   (4)

Where iron(III) chloride FeCl3 is first reduced to metallic iron Fe by the hydride (equation 2), then the metallic iron Fe is hydrothermally converted to magnetite Fe3O4 (equation 3), and lastly, magnetite Fe3O4 is oxidized to maghemite γ-Fe2O3 (equation 4). The XRD pattern of the magnetic sample predominantly shows characteristic diffraction peaks from the maghemite γ-Fe2O3 phase (61 %), as well as from metallic iron α-Fe (13 %), hematite α-Fe2O3 (15 %) and goethite α-FeOOH (11 %) to a less extend (Figure 5). Metallic iron α-Fe is expected on account of equation (2), while hematite α-Fe2O3 and goethite α-FeOOH must be rather the byproducts of complex side reactions. Interestingly, AFM study showed mostly the presence of micron-sized thin nanosheets with thickness of 4-10 nm (Figure 6), i.e., close to the average thickness of the sheets calculated by applying the Scherrer equation for the largest intensity diffraction peak of maghemite γ-Fe2O3 (6 nm). The two-dimensional morphology of the sample is an intriguing result taking into consideration that the synthesis of thin maghemite γ-Fe2O3 nanosheets is scarce in the literature, similarly involving hydride reduction of iron(III) chloride FeCl3 [14]. In addition, the formation of nanosheets also explains the relatively high specific surface area of the sample (129 m2 g-1) [14]. Besides molten iron(III) chloride hexahydrate FeCl3·6H2O, molten cobalt(II) chloride hexahydrate CoCl2·6H2O (melting point: 86 °C) and copper(II) nitrate hexahydrate Cu(NO3)2·6H2O (melting point: 27 °C) react as well hypergolically with sodium hydride to afford metallic cobalt Co and copper(II) oxide CuO, respectively, thereby suggesting that low melting point, hydrated transition metal salts are also an important source of inorganic materials through hypergolic reactions.

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Figure 5: XRD pattern of the as-derived magnetic solid along with the Rietveld analysis of the maghemite γ-Fe2O3, metallic iron α-Fe, hematite α-Fe2O3 and goethite α-FeOOH phases.

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Figure 6: AFM images and corresponding height profiles of thin maghemite γ-Fe2O3 nanosheets.

The presence of the above-mentioned phases in the magnetic sample was further confirmed by 57Fe Mössbauer spectroscopy at 300 K (RT) and 77 K (liquid nitrogen) (Figure 7). The spectrum at 300 K contains contributions from a main central quadrupole split component, as well as several magnetically split components, presenting both relatively narrow as well as broad resonant lines. There are clearly two magnetically split contributions with relatively narrow resonant lines, one of which contributes its outermost lines at the highest (in absolute values) velocity scale of the absorption part of the spectrum, denoting thus a high hyperfine magnetic field (Bhf) value, and a second with lower Bhf value, but higher in absorption intensity relative to the former. We used a set of seven components to fit this spectrum, and for the broad resonant line components a spreading of Bhf values (ΔBhf), either symmetric or asymmetric around a central BhfC value, was allowed in order to describe this broadening. The Mössbauer parameters (MPs) resulting from the best fit of this spectrum are listed in Table 1, where the greatest contribution comes from the maghemite γ-Fe2O3 phase.

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Figure 7: 57Fe Mössbauer spectra of the magnetic sample recorded at 300 and 77 K. The points correspond to the experimental data and the continuous lines to the components used to fit these spectra.

The MPs values of the two narrow resonant line components correspond to hematite α-Fe2O3 (cyan) and metallic iron α-Fe (blue) phases, while contributions from other iron oxide and oxyhydroxide phases with clearly magnetically resolved resonant lines such as maghemite γ-Fe2O3 (brown) and goethite α-FeOOH (green) are also evident [15], in line with the XRD findings. The most broadened magnetically split components acquire MPs that are characteristic of Fe3+ high spin states in oxygen first neighbor environment. These iron oxide phases are experiencing superparamagnetic (SPM) relaxation resulting from the thermal agitation of their magnetization due to their nanosizes. The broadening of the Mössbauer resonant lines of the components corresponding to these phases comes as an effect of this relaxation, which causes the gradual collapse (COL) of their Bhf values [16]. Consequently, the broad resonant line components (magenta and orange) are assigned to nanomaghemite γ-Fe2O3 experiencing SPM relaxation. Considering a size distribution for the derived nanostructures, we can assign the part of the smaller particles in this distribution to ultrafine sized nanomaghemite γ-Fe2O3 for which the SPM relaxation is so fast at 300 K that their Bhf values collapse completely (Bhf = 0). This group of nanostructures is represented by the quadrupole split component in the RT spectrum, which acquires also MPs characteristic of Fe3+ high spin states in oxygen first neighbor environment. At 77 K the thermal agitation of the magnetization for the smaller maghemite γ-Fe2O3 nano-objects is reduced significantly, thus the SPM component of the RT spectrum is absent at the corresponding 77 K spectrum. However, the SPM relaxation still persists at this temperature, and it is evident by the presence of two very broad magnetically split components (red and orange) used to fit this spectrum. These components acquire the characteristic MPs of maghemite γ-Fe2O3 (Table 1), influenced though by the SPM relaxation (high and asymmetric ΔBhf values). This large broadening screens the clear appearance of the magnetically resolved goethite α-FeOOH phase in this spectrum, however the contributions from the metallic iron α-Fe and hematite α-Fe2O3 phases are more evident and are included in the fitting model.

T

IS

Γ/2

QS or 2ε

BhfC

ΔBhf or
ΔBhfhfC/ΔBhf>BhfC

Area

Assignement/Color

K

mm/s

mm/s

mm/s

kOe

mm/s

%

300

0.38

0.14

-0.20

517

1

3

Hematite/Cyan

0.00

0.14

0.00

330

0

8

α-Fe/Blue

0.35

0.14

-0.01

502

11

2

Maghemite/Brown

0.38

0.14

-0.26

381

12/0

2

Goetite/Green

0.37

0.14

-0.02

500

29/0

9

COL Maghemite/Magenta

0.35

0.14

0.01

288

147

25

COL Maghemite /Orange

0.35

0.26

0.66

0

0

51

SPM Maghemite/Red

77

0.42

0.15

0.41

524

0

3

Hematite/Cyan

0.13

0.18

0.00

339

0

10

α-Fe/Blue

0.47

0.14

-0.05

524

41/6

58

COL Maghemite-Goethite/Red

0.54

0.14

0.24

267

117/80

29

COL Maghemite/Orange

Table 1: Mössbauer hyperfine parameters as resulting from the best fits of the corresponding spectra of the sample recorded at 300 and 77 K. IS is the isomer shift (given relative to α-Fe at 300 K), Γ/2 is the half line-width, QS is the quadrupole splitting, 2ε is the quadrupole shift, Bhf is the hyperfine magnetic field, ΔBhf is the spreading of Bhf around the central BhfC value (when this parameter is used) and Area is the relative spectral absorption area of each component used to fit the spectra. Typical errors are ± 0.02 mm/s for IS, Γ/2, 2ε and QS, ±3 kOe for Bhf and ± 5% for Area. In the cases where two ΔBhf values are given, they correspond to asymmetric spreading around (lower/higher) the BhfC value.

Lastly, and due to the strong magnetic character of the solid, Figure 8 presents the corresponding M vs. H loop measurement at room temperature. The contributions of the ferromagnetic metallic iron α-Fe and ferrimagnetic maghemite γ-Fe2O3 phases are evident from the sigmoidal shape of this loop. However, saturation of the M values is not achieved up to H=2 T, a characteristic which reflects the SPM relaxation evident by Mössbauer spectroscopy measurements. The maximum M value at H=2 T reaches Mmax ≈ 34 Am2/kg, which is lower than the nominal saturation M values of both metallic iron α-Fe (218 Am2/kg) and maghemite γ-Fe2O3 (76 Am2/kg) [17], revealing on the one hand the presence of the antiferromagnetic hematite α-Fe2O3 and goethite α-FeOOH phases in the sample, that do not contribute to M, and on the other hand the reduction of M due to SPM relaxation of the ultrafine sized nanomaghemite γ-Fe2O3. The coercive field reaches HC ≈ 0.009 T (90 Oe), a value which again reflects the finite size effect of the nanomaghemite γ-Fe2O3 induced by their SPM relaxation.

Figure 8: Magnetization vs. applied magnetic field hysteresis loop of the magnetic solid at 300 K. The inset reveals the details of the loop at low magnetic field values around zero.

4. Conclusions

Hypergolic materials synthesis defines a new preparative technique in materials science that allows the fast, spontaneous and exothermic synthesis of a wide range of nanomaterials at ambient conditions. In this frame, our group has recently provided several examples of carbon materials syntheses but fewer ones in the direction of inorganics, the latter mainly focusing on the action of fuming nitric acid HNO3 on organometallic precursors, such as metallocenes and metallocene dichlorides. Here special attention is given to the investigation of additional chemical options towards the hypergolic synthesis of inorganic materials with unusual shapes. The proposed alternatives include, but not limited to, (1) the hypergolic ignition of titanium (IV) dimethylamide Ti[N(CH3)2]4 by fuming nitric acid HNO3 towards the formation of titania TiO2 nanoparticles with twin morphology, (2) the hypergolic ignition of molten iron (III) chloride hexahydrate FeCl3·6H2O by sodium hydride NaH towards the formation of thin maghemite γ-Fe2O3 nanosheets. Worth noting, tin (IV) dimethylamide Sn[N(CH3)2]4 reacts similarly to titanium (IV) dimethylamide Ti[N(CH3)2]4 with fuming nitric acid HNO3 to correspondingly afford conductive stannic oxide SnO2, whereas cobalt (II) chloride hexahydrate CoCl2·6H2O and copper (II) nitrate hexahydrate Cu(NO3)2·6H2O react similarly to iron (III) chloride hexahydrate FeCl3·6H2O with sodium hydride NaH to correspondingly afford metallic cobalt Co and copper (II) oxide CuO, respectively. Therefore, metal (IV) dimethylamides and low melting point hydrated transition metal salts (chlorides or nitrates) appear as a new and general class of precursors towards the hypergolic synthesis of inorganic materials with interesting morphologies.

Conflict of interest

The author declared that he has no conflicts of interest to this work.

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