Metal Nanoparticles

This invention relates to a process for the synthesis of high purity metal nanoparticles, the nanoparticles produced and their use, for example as catalysts or carriers.

Metal nanoparticles are an increasingly important industrial material. Due to their high surface area and high reactivity, metal nanoparticles may be used in a variety of applications, many of which arise from the improved behaviour and properties of nanomaterials. Particular applications for nanoparticles include catalysts, carriers, array waveguides, biosensors, nanoantennas, optical filters, drug delivery, synthesis of carbon nanotubes and metal hydrides, and hydrogen gas synthesis.

By nanoparticles and nano-thickness is meant a size below 1 micrometer, typically below 500nm and generally above 5nm.

Many techniques are currently used for nanoparticle synthesis, for example plasma or laser-driven gas phase reactions, evaporation-condensation mechanisms and wet chemical techniques. However, the existing methods all have drawbacks and no single technique currently provides a reliable, low-cost, simple method for production of metal nanoparticles of a controlled size. Typical problems with the existing methods include poor crystallinity or an unpredictable distribution of phases within the nanoparticles, and/or an inability to control the distribution of sizes around a desired nanoparticle size. Some methods also require expensive equipment or reagents.

Laser ablation synthesis, for example, has limitations in size control, as discussed by Amendola ef a/, in Phys. Chem. Chem. Phys. 1 1 :3805-3821(2009). Methods like plasma chemical vapour deposition (CVD), are expensive, require very high temperatures and also have problems with size control of the

nanoparticles. Wet chemistry methods require a stabiliser and/or surfactant, which increases the complexity and cost of synthesis and requires the activation of the formed nanoparticles in an additional activation step before they can be used. In addition, the precursors used in wet methods are typically metal alkoxides which are expensive, and metal chlorides, which lead to chlorine contamination and are therefore not optimal for microelectronics, nanoelectronics and most other applications of interest. In view of the problems of producing stable metal nanoparticles, there is a need for a simple, reliable and low cost method for producing crystalline metal nanoparticles without the use of a separate surfactant and which allows for control of the average particle size while minimizing the amount of variance in particle sizes.

Synthesis of different novel nanoparticles is a fundamental focal point of chemical research, and this interest is mandated by development in all areas of industry and technology. Synthesis of metal and alloy powders nanoparticles has been going on for centuries. Several procedures have been described for the synthesis of metal/bimetal nanoparticles; their catalytic and magnetic properties have been reported. A range of increasingly important chemical syntheses for nanoparticles are described. These syntheses are "chimie-douce" soft chemical, sol-gel autocombustion, template assisted synthesis, electrochemical reduction, aqueous route, Kirkendall effect, Magnetic-field-directed growth of nanocrystal and decomposition of metal organic precursor. Different strategies to produce well dispersed metal/bimetal nanocrystalline particules with tuneable size and shape such as spherical, nanopolyhedra, nanoplates, and nanodisks have been proposed. Usually chemical reduction methods were used to synthesize metal/bimetal nanoparticles. Typical reducing agents include polyols , NaBH ₄ or ascorbic acid and Gas phase synthesis .

Among various methods, chemical reduction of metal ions using surfactants or polymers as protective reagents is one of the promising ways to prepare metal nanoparticles. The polyol process is commonly used for preparation of easily reducible metals. The polyols, such as ethylene glycol, diethylene glycol or a mixture of them, can act as the reducing agents as well as solvents in which the metal salts can be dissolved.

Summary of invention

In one aspect, the present invention provides a process for the production of metal nanoparticles comprising:

i. mixing an organic solvent with at least one metal organic precursor; and

ii. heating the resulting mixture in a pressurised container. Preferably the process of the invention uses an organic solvent comprising an aromatic or polycyclic, preferably polyaromatic alcohol and/or an amine. The metal organic precursor preferably comprises at least one metal hydrocarbyl compound, e.g. a metal acetate or metal acetyl-acetonate. The mixture can comprise organic precursors of at least two different metals or metal salts. It is preferred that at least one metal organic precursor comprises a transition metal selected from groups 4, 6 and 8 to 11 , especially Co, Ni, Au, Ag, Pd, Pt, Cu, Rh and Ru.

In one embodiment, the mixture, e.g. a solution, is heated in the temperature range of 100 to 400 °C, preferably 160 to 300 °C. The mixture is typically heated for a time period of 1 to 72 hours, preferably 15 to 60 hours, more preferably 20 to 55 hours and most preferably around 48 hours.

The process may further comprise:

iii. removing remaining organic residue.

In one embodiment of the invention the remaining organic residue may be removed by rinsing the metal nanoparticles with a solvent, typically an organic solvent. For example absolute ethanol and/or dichlorometane.

Preferably the mixture formed in step (i) of the process of the invention does not comprise surfactants and/or stabilisers.

In another aspect, the invention provides metal nanoparticles produced by the process of the invention.

In a further aspect the invention provides the use of metal nanoparticles produced by the process of the invention, e.g. as catalysts or carriers.

In yet a further aspect, the invention provides nanoparticles of hexagonal close packed (hep) nickel. Detailed Description

The present invention provides a process for synthesising highly crystalline metal nanoparticles in a one pot reaction. There is no need to use surfactants and/or stabilisers in the current method, and the particles produced have high purity and do not carry heteroatoms.

The process of the invention can be performed essentially in the absence of water. In non-aqueous conditions, traditional hydrolysis and condensation reactions are replaced by direct condensation or non-hydrolytic hydroxylation reactions. Organic solvents of varying viscosity and coordinating ability have been found to influence the final structure of the product. In the process of the invention at least one metal organic precursor is mixed with an organic solvent to form a mixture.

The organic solvents suitable for this process include any aryl or polycyclic alcohol and/or amine solvent in which the metal organic precursor(s) are soluble. Preferably the solvent will comprise an aromatic or polyaromatic alcohol or amine. Preferred alcohols include aryl and polycyclic monools, diols and triols, but are preferably monools. More preferably these are aromatic and/or polyaromatic monools. Preferred amines include aryl and polycyclic amines, diamines and triamines, but are preferably monoamines. More preferably these are aromatic and/or polyaromatic monoamines. Most preferably the solvent will comprise or consist of benzyl alcohol (C ₆ H ₅ CH ₂ 0H), benzyl amine (C ₆ H ₅ CH ₂ NH2) or a naphthyl alcohol or amine.

The term "polyaromatic" has its usual meaning herein, meaning a polycyclic aromatic compound, i.e. an aromatic cyclic compound with more than one loop or ring structure.

The term "aryl" has its usual meaning herein, meaning any functional group or substituent derived from a simple aromatic ring. For example, phenyl, thienyl, indolyl, naphthyl.

The choice of organic solvent can influence the crystal structure of the nanoparticle product. Aromatic alcohol solvents have been found to produce hexagonal close packed (hep) structures in cobalt nanoparticles, while aromatic amine solvents produce face centred cubic (fee) structured cobalt nanoparticles (see Examples 1 and 2 below).

Where bulky solvents, e.g. aryl or polycyclic solvents, are used, the size (approximately 4-50nm) of the resulting nanoparticles may be advantageously controlled by selection of the solvent.

For any metal ion, any convenient metal organic precursor can be used if it is soluble. For example, it is possible to use nitrates, aryl-carboxylates and oxalates (/dioxalates) as metal precursors. Aryl-carboxylate and oxalate precursors should normally react in the same way as β-diketonate. Preferred compounds are salts of organic acids, especially hydrocarbyl salts such as acetates and acetylacetonates. Particularly preferred are metal acetates and/or

acetylacetonates.

In theory, an organic precursor of any metal can be used in the process of the invention, but it is preferred that the metal is a transition metal. More preferably there is used at least one metal organic precursor of a metal selected from the group consisting of Co, Ni, Au, Ag, Pd, Pt, Cu, Rh and Ru.

It is possible to prepare bimetallic or trimetallic nanoparticles using the process of the invention, so organic precursors of more than one metal may be used. In one embodiment, organic precursors of at least two metals, for example Co and Pt), are used. In another embodiment, organic precursors of at least three metals are used.

The bimetallic particle formation solution can be formed in non-aqueous media. The solvent used and metal salts can be combined simultaneously or sequentially to induce nanoparticle formation.

Preferred metal organic precursors are:

Co(acetylacetonate) ₂ ;

Co(acetate) ₂ ;

N i (a cetylaceto nate ) ₂ ;

Ni(acetate) ₂ , tetra hydrate;

Au( 111 )(acetylacetonate)(methyl) ₂ ;

Ag(l)(acetate);

Pd( I l)(acetylacetonate) ₂ ;

Pt(ll) (acetylacetonate) ₂ ;

Cu(ll)(acetylacetonate) ₂ ;

Cu( I) (acetate);

Rh(lll)(acetylacetonate) ₃ ;

Rh(ll) ₂ (acetate) ₄ , dimer;

Ru(lll)(acetylacetonate) ₃ .

It is most preferred if one or more of these precursors are combined with benzyl amine and/or benzyl alcohol. There must be a sufficient amount of solvent to dissolve the metal precursor, preferably at least 60% of the metal precursor is dissolved, more preferably 80-90%, and most preferably 95-100% of the metal precursor is dissolved.

The solvent and precursor are preferably mixed and loaded into the pressurized container under an inert atmosphere, for example, in a glove box.

The mixture of organic solvent and metal organic precursor is heated in the pressurised container.

Preferably the mixture is heated in the temperature range of 100 to 400 °C, preferably 160 to 300 °C, more preferably 160-240 °C and most preferably 180-200 °C. The mixture is typically heated for a time period of 1 to 72 hours, preferably 15 to 60 hours, more preferably 20 to 55 hours, and most preferably approximately 48 hours. In the preferred reaction conditions the mixture is heated at 200 °C for 48 hours.

Under equivalent reaction conditions, preferably with a reaction time of 48 hours, and where a substrate is disposed in the autoclave, it is possible to deposit a nano-thickness surface coating onto the substrate, e.g. a sheet, bead, rod, or mesh. For many applications, especially as catalysts, it is desirable to use such surface coated substrates and this modification of the process of the invention forms a further aspect of the invention. Viewed from this aspect the invention provides a method of providing a nano-thickness surface metal coating on a substrate, said method comprising:

i. mixing an organic solvent comprising an aryl or polycyclic alcohol and/or amine with at least one metal organic precursor; ii. heating the resulting mixture in a pressurised container containing or providing said substrate, and

iii. optionally removing organic residue from the resulting metal coated substrate.

The coating may cover at least 50% of the surface of the substrate, for example at least 60%, 70%, 80% of the surface of the substrate. Preferably the coating will cover at least 90% of the surface of the substrate, for example at least 95%, 98% or 99% of the substrate surface.

In another aspect the coating may consist of discrete metal nanoparticles or aggregates of metal nanoparticles. The nanoparticles typically have diameters in the range of 1-100 nm, preferably 2-50 nm, more preferably 3-20 nanometers. For example 4- 5 nm, such as 5-10 nm. The metal nanoparticle aggregates typically have an overall diameter in the range 50-500 nm, for example they may be approximately 100, 200, 300 or 400 nm in diameter.

Viewed from this aspect the invention provides a method of providing metal nanoparticles on the surface of a substrate, said method comprising:

i. mixing an organic solvent comprising an aryl or polycyclic alcohol and/or amine with at least one metal organic precursor; ii. heating the resulting mixture in a pressurised container containing or providing said substrate, and iii. optionally removing organic residue from the resulting metal nanoparticle coated substrate.

The resulting coated substrates and their use form further aspects of the invention.

The pressurized container is a vessel capable of withstanding the internal pressures generated during the reaction (see Walton ef al. in Chem. Soc. Rev. 31 : 230-238 (2002), Figure 1 ). For example, the container should be able to withstand internal pressures of 2-300 bar. Typically the pressurised container used is an autoclave. The reactants are used in amounts appropriate to the volume of the autoclave. In the examples the autoclaves used are of a size appropriate to laboratory research, but the skilled person would be able to scale up the process of the invention for commercial autoclaves.

After the reaction, any remaining organic residue can be removed from the nanoparticle product by standard rinsing and separation techniques. For example, washing with ethanol and/or dichloromethane and centrifuging.

The current process allows "one pot" synthesis of metal nanoparticles at low temperatures without the utilization of surfactant and/or stabiliser. Usually metal nanoparticles synthesised by the existing techniques are not stable in air and oxidise immediately in the presence of oxygen or an oxidising source. In contrast, the metal nanoparticles produced by the current process are stable under air and in oxygen at room temperature (i.e. approximately 18-25 °C, such as 20-22 °C), preferably for a period of at least 1-24 months, for example 2-18 months, 3-12 months or 4-10 months, preferably at least approximately 6 months.

The use of a surfactant to improve the stability of the nanoparticles during the current process is unnecessary. Nanoparticles produced by the existing wet chemical methods have a coating of surfactant on their surface, which must be removed by calcination at high temperature (600-1000 °C). This high temperature treatment generally induces agglomeration/coalescence of the nanoparticles and also hinders its numerous applications.

Stabilisers are generally used in existing methods to control the

agglomeration/coalescence of the nanoparticles, thus the formed nanoparticles have a coating of stabiliser on their surface. This must be removed in a series of treatments, which lead to contamination and an organic surface residue which is detrimental for applications. The presence of surfactants/stabilisers usually passivates the surface of the nanoparticles, preventing their integration in an industrial process or application. The additional treatments which are necessary to remove stabilisers/surfactants also incur additional costs in terms of time and expense.

Therefore it is a particular advantage that the process of the invention does not require the use of surfactant and/or stabiliser, as the oxidation-resistant nanoparticles of the current invention do not require calcination or other activation steps before they can be used.

The metal nanoparticles produced by the process of the invention differ from those produced by existing methods by virtue of their high crystaiiinity and stability to oxidation.

Particles of cobalt are generally in the range of 8-15 nm in diameter, while nickel nanoparticles are approximately 50 nm in diameter.

However, depending on the growth conditions, it was observed that the synthesis inside a nanoporous inert structure such as γ-alumina particles induces a confinement effect (Example 1 1 describe the synthesis of metal Co nanoparticles on and into nanoporous γ-alumina). It was also possible to produce in the same condition Ni metal fee nanoparticles of approximately 5 nm in diameter (Figure 2).

CoPt ₃ as a bimetallic (example 8 and 9) compound was synthesized at 180°C using Pt(acac) ₂ and benzyl alcohol or benzylamine as solvent to obtain bimetallic nanoparticles. Nanoparticles synthesized by both solvents were moderately monodispersed. The formation of "solid solution" type alloys such as CoPt ₃ bimetallic nanoparticles was confirmed by XRD as shown in figures 12 and 13. From a full-width at half-maximum of diffraction peak due to CoPt ₃ metal at 2Θ = 40.51° and 2Θ = 40.95° for both samples, respective average crystallite sizes of 5.51 and 4.63 nm of bimetallic CoPt ₃ were estimated using the Scherrer equation.

In developing the process of the invention, the inventors have also produced nickel nanoparticles which have a hexagonal close packed structure. The surface chemistry and properties of these particles will differ from face-centred cubic (fee) nickel nanoparticles. Description of Figures

Figure 1. Pressurized container 100: Stopper, 101 : Container, 102: Teflon sealing ring, 103: Glass tube, 104: Upper part of the stainless-steal sealing bolt, 105: Lower part of the stainless-steal sealing bolt.

Figure 2. TEM image of Ni metal fee nanoparticles produced in a nanoporous structure.

Figure 3. X-ray diffraction (XRD) patterns showed the Co metal cubic structure in nanoparticles produced in Example 1.

Figure 4. X-ray diffraction (XRD) patterns showed the Co metal cubic structure in nanoparticles produced in Example 2.

Figure 5. X-ray diffraction (XRD) patterns showed the Co metal hep structure in nanoparticles produced in Example 3.

Figure 6. TEM image of Co metal hep nanoparticles produced in example 3.

Figure 7. X-ray diffraction (XRD) patterns showed the Ni metal cubic structure in nanoparticles produced in Example 4.

Figure 8. X-ray diffraction (XRD) patterns showed the Ni metal cubic structure in nanoparticles produced in Example 5.

Figure 9. X-ray diffraction (XRD) patterns showed the Ni metal cubic structure and the Ni metal hexagonal structure in nanoparticles produced in Example 6.

Figure 10. X-ray diffraction (XRD) patterns showed the Pt metal cubic structure in nanoparticles produced in Example 7.

Figure 11. TEM image of Pt metal fee nanoparticles produced in example 7.

Figure 12. X-ray diffraction (XRD) patterns showed the CoPt ₃ metal cubic structure and Pt metal cubic structure in nanoparticles produced in Example 8.

Figure 13. X-ray diffraction (XRD) patterns showed the CoPt ₃ metal cubic structure and Pt metal cubic structure in nanoparticles produced in Example 9.

Figure 14. X-ray diffraction (XRD) patterns showed the Ag metal cubic structure in nanoparticles produced in example 10.

Figure 15. X-ray diffraction (XRD) patterns showed the Co metal structure

(indicated with arrows) in nanoparticles produced with γ-alumina in example 11. Figure 16. High resolution image of the Co metal nanoparticles loaded into γ- alumina particles produced with γ-alumina in example 11.

All XRD patterns were produced using Cu-alpha radiation. Examples

The X-ray diffractometer used to collect the data shown in figures 3, 5, 7, 8, 9, 10, 12, 13, 14 and 15 is a Scintag PDS 2000 diffractometer with a Cu Ka X-ray source (λ = 1.54 A) in step-scan mode with a scanning rate of 0.02 deg s ^"1 in the 2Θ range from 3° to 90°. For figure 4 a Philips X'Pert four-circle MPD diffractometer with Cu Ka X-ray source (λ = 1.54 A) was used.

Example 1 : Cobalt metal cubic fee nanoparticles synthesis using

Co(acetylacetonate) ₂ and benzyl amine.

The synthesis procedures were carried out in a glove box (0 ₂ and H ₂ 0 < 1 ppm). In a typical synthesis, Co(acetylacetonate) ₂ (97%, Aldrich) (acetylacetonate: CH ₃ COCHCO CH ₃ ) 500 mg were added to 20 mL benzyl amine (<99.5%, Aldrich) (Benzyl amine: C ₆ H ₅ CH ₂ NH ₂ ). Once the solution clarified, the reaction mixture was transferred into a stainless steel autoclave and carefully sealed. Thereafter, the autoclave was taken out of the glove box and heated in a furnace at 180 °C for 48 hours. The resulting milky suspensions were centrifuged at 5000 turns/minute for 10 minutes. The precipitate was thoroughly washed once with ethanol

(CH ₃ CH ₂ OH) and then centrifuged at 5000 turns/minute for 10 minutes; then washed twice with dichloromethane (CH ₂ CI ₂ ) and centrifuged at 5000 turns/minute for 10 minutes. The precipitate was subsequently dried in air at 60 °C.

Figure 3 shows X-ray diffraction (XRD) patterns for the product, showing the Co metal cubic structure.

Example 2: Cobalt metal cubic fee nanoparticles synthesis using Co(acetate) ₂ and benzyl amine.

The synthesis procedures were carried out in a glove box (0 ₂ and H ₂ 0 < 1 ppm). In a typical synthesis, Co(acetate) ₂ anhydrous, (Alfa Aesar) (acetate:

CH ₃ COO ^" ) 500 mg were added to 20 mL benzyl amine (<99.5%, Aldrich) (Benzyl amine: C ₆ H ₅ CH ₂ NH ₂ ). Following stirring, the reaction mixture was transferred into a stainless steel autoclave and carefully sealed. Thereafter, the autoclave was taken out of the glove box and heated in a furnace at 240 °C for 72 hours. The resulting milky suspensions were centrifuged at 5000 turns/minute for 10 minutes. The precipitate was thoroughly washed once with ethanol (CH ₃ CH ₂ OH) and then centrifuged at 5000 turns/minute for 10 minutes; then washed twice with dichloromethane (CH ₂ CI ₂ ) and centrifuged at 5000 turns/minute for 10 minutes. The precipitate was subsequently dried in air at 60 °C.

Figure 4 shows X-ray diffraction (XRD) patterns for the product, showing the Co metal cubic structure.

Example 3: Co metal hexagonal hep nanoparticle synthesis using

Co(acetylacetonate) ₂ and benzyl alcohol.

The synthesis procedures were carried out in a glove box (0 ₂ and H ₂ 0 < 1 ppm). In a typical synthesis, Co(acetylacetonate) ₂ (97%, Aldrich) (acetylacetonate: CH ₃ COCHCO ^" CH ₃ ) 350 mg were added to 20 mL benzyl alcohol anhydrous

(ReagentPlus >99%, Aldrich) (Benzyl alcohol: C ₆ H ₅ CH ₂ OH). Following stirring, the reaction mixture was transferred into a stainless steel autoclave and carefully sealed. Thereafter, the autoclave was taken out of the glove box and heated in a furnace at 180 °C for 48 hours. The resulting milky suspensions were centrifuged at 10000 turns/minute for 10 minutes. The precipitate thoroughly washed once with ethanol (CH ₃ CH ₂ OH) and then centrifuged at 10000 turns/minute for 10 minutes; then washed twice with dichloromethane (CH ₂ CI ₂ ) and centrifuged at 10000 turns/minute for 10 minutes. The precipitate was subsequently dried in air at 60 °C.

Figure 5 shows X-ray diffraction (XRD) patterns, showing the Co metal hep structure. Figure 6 shows the Cobalt hep product under the TEM.

Example 4: Ni metal cubic fee nanoparticles synthesis using Ni(acetylacetonate) ₂ and benzyl amine.

The synthesis procedures were carried out in a glove box (0 ₂ and H ₂ 0 < 1 ppm). In a typical synthesis, Ni(acetylacetonate) ₂ (95%, Aldrich) (acetylacetonate: CH ₃ COCHCO CH ₃ ) 500 mg were added to 20 mL benzyl amine (<99.5%, Aldrich) (Benzyl amine: C ₆ H ₅ CH ₂ NH ₂ ). Following stirring, the reaction mixture was transferred into a stainless steel autoclave and carefully sealed. Thereafter, the autoclave was taken out of the glove box and heated in a furnace at 180 °C for 48 hours. The resulting milky suspensions were centrifuged at 10000 turns/minute for 10 minutes. The precipitate was thoroughly washed once with ethanol

(CH ₃ CH ₂ OH) and then centrifuged at 10000 turns/minute for 10 minutes; then washed twice with dichloromethane (CH ₂ CI ₂ ) and centrifuged at 10000 turns/minute for 10 minutes. The precipitate was subsequently dried in air at 60 °C. Figure 7 shows X-ray diffraction (XRD) patterns, showing the Ni metal cubic structure of the product.

Example 5: Ni metal cubic fee nanoparticles synthesis using Ni(acetylacetonate) ₂ and benzyl alcohol.

The synthesis procedures were carried out in a glove box (0 ₂ and H ₂ 0 < 1 ppm). In a typical synthesis, Nickel (acetylacetonate) ₂ (97%, Aldrich)

(acetylacetonate: CH ₃ COCHCO ^~ CH ₃ ) 500 mg were added to 20 imL benzyl alcohol anhydrous (ReagentPlus >99%, Aldrich) (Benzyl alcohol: C ₆ H ₅ CH ₂ OH). Following stirring, the reaction mixture was transferred into a stainless steel autoclave and carefully sealed. Thereafter, the autoclave was taken out of the glove box and heated in a furnace at 180 °C for 48 hours. The resulting milky suspensions were centrifuged at 10000 turns/minute for 10 minutes. The precipitate was thoroughly washed once with ethanol (CH ₃ CH ₂ OH), then centrifuged at 10000 turns/minute for 10 minutes, and then washed twice with dichloromethane (CH ₂ CI ₂ ) and centrifuged at 10000 turns/minute for 10 minutes. The precipitate was subsequently dried in air at 60 °C.

Figure 8 shows X-ray diffraction (XRD) patterns of the product showing the Ni metal cubic structure.

Example 6: Ni metal hexagonal hep nanoparticles synthesis using Ni(acetate) ₂ , tetrahydrate and benzyl amine.

The synthesis procedures were carried out in a glove box (0 ₂ and H ₂ 0 < 1 ppm). In a typical synthesis, Nickel (acetate) ₂ , tetrahydrate (99.999, STREM) (acetate: CH ₃ COO ^" ) 500 mg were added to 20 ml_ benzyl amine (<99.5%, Aldrich) (Benzyl amine: C ₆ H ₅ CH ₂ NH ₂ ). Following stirring, the reaction mixture was transferred into a stainless steel autoclave and carefully sealed. Thereafter, the autoclave was taken out of the glove box and heated in a furnace at 240 °C for 48 hours. The resulting milky suspensions were centrifuged at 10000 turns/minute for 10 minutes. The precipitate was thoroughly washed once with ethanol

(CH ₃ CH ₂ OH), then centrifuged at 10000 turns/minute for 10 minutes, and then washed twice with dichloromethane (CH ₂ CI ₂ ) and centrifuged at 10000 turns/minute for 10 minutes. The precipitate was subsequently dried in air at 60 °C.

Figure 9 shows X-ray diffraction (XRD) patterns of the product showing the Ni metal hexagonal structure. Example 7: Pt metal cubic fee nanoparticles synthesis using Pt(acetylacetonate) ₂ and benzyl alcohol.

The synthesis procedures were carried out in a glove box (0 ₂ and H ₂ 0 < 1 ppm). In a typical synthesis, Pt (acetylacetonate) ₂ (98%, STREM) (acetylacetonate: CH ₃ COCHCO ^" CH ₃ ) 500 mg were added to 20 mL benzyl alcohol anhydrous (ReagentPlus >99%, Aldrich) (Benzyl alcohol: C ₆ H ₅ CH ₂ OH). Following stirring, the reaction mixture was transferred into a stainless steel autoclave and carefully sealed. Thereafter, the autoclave was taken out of the glove box and heated in a furnace at 180 °C for 48 hours. The resulting milky suspensions were centrifuged at 10000 turns/minute for 10 minutes. The precipitate was thoroughly washed once with ethanol (CH ₃ CH ₂ OH), then centrifuged at 10000 turns/minute for 10 minutes, and then washed twice with dichloromethane (CH ₂ CI ₂ ) and centrifuged at 10000 turns/minute for 10 minutes. The precipitate was subsequently dried in air at 60 °C.

Figure 10 shows X-ray diffraction (XRD) patterns of the product showing the

Pt metal cubic structure. Figure 11 shows the Pt fee product under the TEM .

Example 8: CoPt ₃ metal nanoparticles synthesis using Co(acetylacetonate) ₂ , Pt(acetylacetonate) ₂ and benzyl amine.

The synthesis procedures were carried out in a glove box (0 ₂ and H ₂ 0 < 1 ppm). In a typical synthesis, Co(acetylacetonate) ₂ (97%, Aldrich) (acetylacetonate: CH ₃ COCHCO CH ₃ ) 394 mg and Pt(acetylacetonate) ₂ (98%, STREM) 603 mg were added to 20 mL benzyl amine (<99.5%, Aldrich) (Benzyl amine: C ₆ H ₅ CH ₂ NH ₂ ). Following stirring, the reaction mixture was transferred into a stainless steel autoclave and carefully sealed. Thereafter, the autoclave was taken out of the glove box and heated in a furnace at 180 °C for 48 hours. The resulting milky suspensions were centrifuged at 10000 turns/minute for 10 minutes. The precipitate was thoroughly washed once with ethanol (CH ₃ CH ₂ OH) and then centrifuged at 10000 turns/minute for 10 minutes, then washed twice with dichloromethane (CH ₂ CI ₂ ) and centrifuged at 10000 turns/minute for 10 minutes. The precipitate was subsequently dried in air at 60 °C.

Figure 12 shows X-ray diffraction (XRD) patterns of the product showing the CoPt ₃ metal cubic structure and Pt metal cubic structure. Example 9: CoPt ₃ metal nanoparticles synthesis using Co(acetylacetonate) _2l Pt(acetylacetonate) ₂ and benzyl alcohol.

The synthesis procedures were carried out in a glove box (0 ₂ and H ₂ 0 < 1 ppm). In a typical synthesis, Co(acetylacetonate) ₂ (97%, Aldrich) (acetylacetonate: CH ₃ COCHCO CH ₃ ) 394 mg and Pt(acetylacetonate) ₂ (98%, STREM) 603 mg were added to 20 mL benzyl aicoho) anhydrous (ReagentPlus >99%, Aldrich) (Benzyl alcohol: C ₆ H ₅ CH ₂ OH). Following stirring, the reaction mixture was transferred into a stainless steel autoclave and carefully sealed. Thereafter, the autoclave was taken out of the glove box and heated in a furnace at 180 °C for 48 hours. The resulting milky suspensions were centrifuged at 10000 turns/minute for 10 minutes. The precipitate was thoroughly washed once with ethanol (CH ₃ CH ₂ OH) and then centrifuged at 10000 turns/minute for 10 minutes, then washed twice with dichloromethane (CH ₂ CI ₂ ) and centrifuged at 10000 turns/minute for 10 minutes. The precipitate was subsequently dried in air at 60 °C.

Figure 13 shows X-ray diffraction (XRD) patterns of the product, showing the CoPt ₃ metal cubic structure and Pt metal cubic structure.

Example 10: Ag metal nanoparticles synthesis using Ag(acetate) and benzyl alcohol.

The synthesis procedures were carried out in a glove box (0 ₂ and H ₂ 0 <

1 ppm). In a typical synthesis, Ag(acetate) (99%, STREM) (acetate: CH ₃ COO ^" ) 500 mg to 20 mL benzyl alcohol anhydrous (ReagentPlus >99%, Aldrich) (Benzyl alcohol: C ₆ H ₅ CH ₂ OH). Following stirring, the reaction mixture was transferred into a stainless steel autoclave and carefully sealed. Thereafter, the autoclave was taken out of the glove box and heated in a furnace at 240 °C for 48 hours. The resulting milky suspensions were centrifuged at 10000 turns/minute for 10 minutes. The precipitate was thoroughly washed once with ethanol (CH ₃ CH ₂ OH) and then centrifuged at 10000 turns/minute for 10 minutes, then washed twice with dichloromethane (CH ₂ CI ₂ ) and centrifuged at 10000 turns/minute for 10 minutes. The precipitate was subsequently dried in air at 60 °C.

Figure 14 shows X-ray diffraction (XRD) patterns of the product, showing the Ag metal cubic structure.

Example 1 1 : Co metal hexagonal hep nanoparticle synthesis into γ-alumina using Co(acetylacetonate) ₂ and benzyl alcohol. The synthesis procedures were carried out in a glove box (0 ₂ and H ₂ 0 < 1 ppm). In a typical synthesis, Co(acetylacetonate) ₂ (97%, Aldrich) (acetylacetonate: CH ₃ COCHCO ^" CH ₃ ) 500 mg and 500mg of γ-alumina nanoporous particles (with diameter ranging from 20 to ΙΟΟμηι and pore of about 16nm) were added to 20 mL benzyl alcohol anhydrous (ReagentPlus >99%, Aldrich) (Benzyl alcohol:

C ₆ H ₅ CH ₂ OH). Following stirring, the reaction mixture was transferred into a stainless steel autoclave and carefully sealed. Thereafter, the autoclave was taken out of the glove box and heated in a furnace at 180 °C for 48 hours. The resulting milky suspensions were centrifuged at 10000 turns/minute for 10 minutes. The precipitate thoroughly washed once with ethanol (CH ₃ CH ₂ OH) and then centrifuged at 0000 turns/minute for 10 minutes; then washed twice with dichloromethane (CH ₂ CI ₂ ) and centrifuged at 10000 turns/minute for 10 minutes. The precipitate was subsequently dried in air at 60 °C.

Figure 15 shows X-ray diffraction (XRD) patterns, showing the Co metal hep structure and γ-alumina structure. Figure 16 shows the Cobalt hep product loaded into the nanoporous γ-alumina under the TEM.