A PROCESS FOR THE SYNTHESIS OF NANOPARTICLES OF TRANSITION METAL CHALCOGENIDES

Abstract

A process for the synthesis of transition metal chalcogenides (TMC) having formula (I). More particularly, the present work relates to a one pot single phase process for the synthesis of a TMC system having formula (I) by wet chemistry. Formula (I) is represented as Ax-By.

Description

FIELD OF THE INVENTION

The present invention relates to a process for the synthesis of transition metal chalcogenides (TMC) having formula (I). More particularly, the present work relates to a one-pot single phase process for the synthesis of TMC system having formula (I) by wet chemistry.

BACKGROUND AND PRIOR ART OF THE INVENTION

Transition-metal chalcogenides represent an important class of materials with rich phase diagram and industrial applications. The electronic (optical, magnetic, and electrical) and thermal properties are so sensitive to the crystalline phase, stoichiometry, shape, size that it is essential to reach a good control over the chemistry of phase formation. TMC consisting of metal atoms (Fe, Co, and Ni) and chalcogen atoms (S, Se, Te) have renewed interest as very attractive candidates for applications in devices including fuel-cells, solar-cells, light-emitting-diodes, sensors, memory-devices, thermoelectric devices, supercapacitors, Li-ion batteries, magnetic materials etc. Among the TMC, Fe_xSe_y compounds (with x: y varying from 1:2 to 1:1) are of great importance because of their interesting and unique magnetic, electrical, thermal, and optical properties which are strongly related on the stoichiometric ratio between Fe and Se as well as their crystalline structure. Family of iron selenides have four stable phases: FeSe₂, Fe₃Se₄, Fe₇Se₈, and FeSe having orthorhombic (O) marcasite, monoclinic (M) and hexagonal (H) NiAs type, and tetragonal (T) PbO type crystal structure, respectively. Existence of multiple phases with abundantly different crystal structures indicates the complexity of the system and therefore, phase-selective syntheses were quite challenging for this system. In solid state method, as reported by Grivel et al. (Supercond. Sci. Technol. 24 (2011) 015007) there was phase transformation of Fe—Se system with respect to temperature in a sequence of FeSe₂→Fe₃Se₄→Fe₇Se₈—β-FeSe at 300° C., 320° C., ˜340° C., 350° C.-370° C., respectively. In this article the phase boundaries were not sharply defined as a function of temperature. Often at a particular temperature, phases evolved out of the other phases leading to overall impurity.

Numerous solution processes have been applied to synthesize these compounds. For example, Fe₃Se₄ and Fe₇Se₈ nanoparticles (NPs) were obtained via the thermal decomposition method at 340 ° C-350° C., Fe₃Se₄ were synthesized at 300° C. by one-pot high-temperature organic-solution-phase method, flower-like FeSe₂ NPs were synthesized via a solvothermal approach at 200° C., FeSe_x (x=1,2) NPs were synthesized via the hot-injection method at 330° C. and FeSe₂ NPs were synthesized via hydrothermal method at 140° C. for 13 h. The FeSe NPs were synthesized by solvothermal reaction in an autoclave at 220° C. for 24 h. These methods involved the high temperature, long reaction time, complex apparatus, expensive chemicals, or drastic conditions to synthesis the Fe—Se NPs.

Thus, adopting a simple, low-temperature, short-time, and low-cost method with well-defined shape and high crystallinity of Fe—Se NPs is much desired. To overcome the prior drawbacks the present invention provides a one pot single phase process for the synthesis of transition metal chalcogenides (TMC) system having formula I.

OBJECTIVES OF THE INVENTION

The objective of the present invention is to provide a one pot single phase process for the synthesis of transition metal chalcogenides (TMC) having formula (I).

SUMMARY OF THE INVENTION

Accordingly, the present invention provides a one pot single phase process for the synthesis of transition metal chalcogenides (TMC) system having formula (I) by using wet chemistry. This method comprises mixing both precursors of transition metal and chalcogen in the presence of a reducing agent and an accelerating agent at a temperature in the range of 100° C. to 300° C. for a time period varied from 30 min to 10 h to obtain transition metal chalcogenides (TMC) having formula (I).

1The transition metal chalcogenides (TMC) system having formula (I) is represented as

A_x-B_y   Formula (I)

wherein,

• A is selected from iron, chromium, manganese, cobalt, or nickel.
• B is selected from selenium, sulphur, or tellurium.
• The A_x-B_y is selected from AB₂, A₃B₄, A₇B₈ or AB,
• wherein x and y are in ranges from 1:2 to 1:1.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1: Powder X-ray diffraction patterns collected at various temperatures during the heating ramp a. 25° C. b. 190° C. c. 360° C. d. 394° C. and e. 486° C. for prior art.

FIG. 2: Powder X-ray diffraction patterns collected at various temperatures during the heating ramp for present invention.

FIG. 3: Iron-Selenium phase diagram.

FIG. 4: XRD patterns of the as-synthesized a) FeSe₂ NPs, b) Fe₃Se₄ NPs, c) Fe₇Se₈ NPs and d) FeSe NPs.

FIG. 5: Magnetization (M) vs. applied magnetic field (H) hysteresis loops of a) FeSe₂ b) Fe₃Se₄ c) Fe₇Se₈ and d) FeSe measured by the vibrating sample magnetometer at 300 K.

FIG. 6: Magnetization (M) vs. applied magnetic field (H) hysteresis loops of a) FeSe₂ b) Fe₃Se₄ c) Fe₇Se₈ and d) FeSe measured by the vibrating sample magnetometer at 10 K.

FIG. 7: TEM measurements of as-synthesized NPs.

FIG. 8: Thermal Gravimetric Analysis (TGA).

FIG. 9: Raman spectra.

FIG. 10: TEM images of as-synthesized NPs with different organic solvents.

FIG. 11: XRD patterns of the as-synthesized Co₃Se₄ NPs.

FIG. 12: XRD patterns of the as-synthesized Ni₃Se₄ NPs.

FIG. 13: XRD patterns of the as-synthesized MnSe NPs.

FIG. 14: XRD patterns of the as-synthesized Fe₃Se₄ NPs with different crystallite size.

FIG. 15: Magnetization (M) vs. applied magnetic field (H) hysteresis loops of Fe₃Se₄ NPs with different crystallite size measured by the vibrating sample magnetometer at 300 K.

FIG. 16: Coercive field (H_c) and remanence magnetization (M_r) vs. crystallite size of Fe₃Se₄ NPs.

DETAILED DESCRIPTION OF THE INVENTION

The invention will now be described in detail in connection with certain preferred and optional embodiments, so that various aspects thereof may be more fully understood and appreciated.

The present invention provides a one-pot single phase process for the synthesis of a transition metal chalcogenide (TMC) nanoparticles (NPs) system having formula (I) by using wet chemical method, the process comprising mixing and stirring both a transition metal precursor and a chalcogen precursor in the presence of a reducing agent and an accelerating agent and stirring at a temperature in the range of 100° C. to 300° C. for a time period varied from 30 min to 10 h to obtain the TMC NPs system having formula (I).

The TMC NPs system having formula (I) is represented as

A_x-B_y   Formula (I)

wherein,

A is selected from the group consisting of iron, chromium, manganese, cobalt, and nickel;

B is selected from the group consisting of selenium, sulphur, and tellurium; A_x-B_y is selected from AB₂, A₃B₄, A₇B₈ and AB;

wherein the ratio of x and y are in ranges from 1:2 to 1:1.

The system of formula (I) is selected from FeSe₂, Fe₃Se₄, Fe₇Se₈, FeSe, Co₃Se₄, Ni₃Se₄ and MnSe.

The size of as-synthesized TMC NPs are in the range of 5 nm to 350 nm. The shape of as-synthesized TMC NPs is selected from nano-rod, nano-sphere, nano-sheet, nano-platelet, nano-cube, and mixed shape.

Any organic solvent, which has the ability to make complex with transition metal (Fe) and chalcogen (Se) precursors, and simultaneously reduce them can be used as a reducing agent for TMC system. Moreover, any organic solvent can use as an accelerating agent which have the ability to make complex with chalcogen (Se powder). The particular temperature required for pure phase formation will strongly depends on the organic solvent. As going towards the stronger reducing and accelerating agent, the temperature and time for that particular phase changes.

The reducing agent is selected from oleylamine (OLA), oleic acid, 1-octadecene (1-ODE), octadecylamine, oleyl alcohol, pentylamine, ethylamine and n-octadecane. The accelerating agent is selected from 1-octadecene, oleic acid, oleylamine, octadecylamine, oleyl alcohol, pentylamine, and ethylamine.

The transition metal precursor is selected from Tris(acetylacetonato) iron (III) (Fe(acac)₃), Cobalt(III) acetylacetonate, Nickel(II) acetylacetonate and Manganese(III)acetylacetonate.

The chalcogen precursor is Se powder.

• • In one of the features, the present invention provides a one pot single phase process for the synthesis of transition metal chalcogenides (TMC) nanoparticles system particularly Fe—Se system comprising the steps of:
    • a) mixing Se powder and Fe(acac)₃ at room temperature (25° C. to 30° C.) in the presence of an organic solvent under the blanket of inert gas with constant magnetic stirring;
    • b) raising the temperature to 40° C. followed by stirring for 30 min and taking the first sample of only Se powder;
    • c) further increasing the temperature to 50° C. followed by stirring for 30 min and taking the second sample of only Se powder and
    • d) increasing the temperature up to 340° C. with the rate of 10° C./30 min and taking the sample at every 10° C. rise in temperature, as the temperature increases, FeSe₂ starts forming followed by Fe₃Se₄, Fe₇Se₈ and FeSe.

In each step 2 mL aliquots are withdrawn using a long needle-glass syringe. All the samples are stored in small glass vials and naturally quenched to room temperature (RT) for further investigation.

In another feature of the present invention, the organic solvent is selected from oleylamine (OLA); oleylamine & 1-octadecene (OLA & 1-ODE) and oleylamine (OLA) & pre-dissolved Se powder in 1-octadecene (1-ODE).

Three separate reactions are carried out with above procedure except the solvent conditions; in one reaction only OLA has been used as a solvent, in second reaction a combination of OLA and 1-ODE (in 3:2 ratio) has been used as a solvent; and in the last reaction Se powder was pre-dissolved in 1-ODE and used that as a Se precursor with OLA and Fe(acac)₃.

FIG. 1 depicts diffraction patterns collected at various temperatures during the heating ramp for prior art. The phase boundaries were not sharply defined as a function of temperature. Often at a particular temperature, phases evolved out of the other phases leading to overall impurity.

FIG. 2 depicts diffraction patterns collected at various temperatures during the heating ramp for present invention. Phase boundaries were mostly sharply defined and well isolated as a function of temperatures and phase impurities were avoided. The diffraction pattern shows the phase evolution from FeSe₂ to Fe₃Se₄ followed by Fe₇Se₈ and FeSe.

TABLE 1
Results of diffraction patterns collected at
various temperatures during the heating ramp.
	Fe	Se		Temperature-
Reaction	Precursor	precursor	Solvent	range	Phase
A	Fe(acac)3	Se powder	OLA	RT-100° C.	Se
				110-130° C.	Se +
					FeSe2
				140-220° C.	FeSe2
				230-240° C.	FeSe2 +
					Fe3Se4
				250-270° C.	Fe3Se4
				280-340° C.	Fe7Se8
B	Fe(acac)3	Se powder	OLA +	RT-100° C.	Se
		(Se was pre-	1-ODE	110-230° C.	FeSe2
		dissolved in		240-250° C.	FeSe2 +
		1-ODE at			Fe3Se4
		30° C. for		260° C.	Fe3Se4 +
		6 h)			FeSe2
				270° C.	Fe7Se8
				280-300° C.	FeSe

FIG. 3 depicts Iron-Selenium phase diagram. Phases 1 to 5 show the results of five prolonged reactions. The experiments were done by varying the amount of Se from 37.5 to 100 at % with constant Fe precursor in presence of OLA and 1-ODE together from RT to 340° C. The phase transformation has been confirmed by doing the WAXS (wide angle X-ray scattering) of all the samples, taken at every 10° C. rise in temperature from 30° C.-340° C. and the data are compared with the JCPDS files to conform the phases.

TABLE 2
Results of phases formed at minimal possible temperature with pertinent time.
Phases	Solvent	Ramping Rate	Temp.	Time	Remarks
FeSe2	OLA	2° C. min−1	150° C.	2 h	Single phase
					FeSe2 NPs
Fe3Se4	OLA	2° C. min−1	230° C.	8 h	Fe3Se4 + FeSe2
		2° C. min−1	240° C.	6 h	(impurity phase)
		2° C. min−1	250° C.	5 h
		120° C.-0.5 h +	250° C.	4 h	Fe3Se4 + FeSe2
		2° C. min−1 up to 200° C. +			(impurity phase)
		2° C. min−1 up to 250° C.
		2° C. min−1	260° C.	5 h
		120° C.-0.5 h +	260° C.	2 h	Single phase
		2° C. min−1 up to 200° C. +			Fe3Se4 NPs
		2° C. min−1 up to 250° C.
Fe7Se8	OLA	2° C. min−1	270° C.	4 h	Fe3Se4 + FeSe2
					(impurity phase)
		5° C. min−1 up to 230° C. +	270° C.	4 h	Fe7Se8 + Fe3Se4
		2° C. min−1 up to 270° C.			(impurity phase)
		2° C. min−1	280° C.	4 h, 5 h
		5° C. min−1 up to 230° C. +	280° C.	4 h	Single phase
		2° C. min−1 up to 280° C.			Fe7Se8 NPs
	OLA	5° C. min−1 up to 230° C. +	280° C.	4 h	Fe7Se8
		2° C. min−1 up to 280° C.
	OLA + 1-ODE	5° C. min−1 up to 230° C. +	280° C.	4 h	FeSe + Fe7Se8
		2° C. min−1 up to 280° C.			(impurity phase)
	OLA + 1-ODE	5° C. min−1 up to 230° C. +	280° C.	4 h	Single phase
		2° C. min−1 up to 280° C.			FeSe NPs
					(Se powder was
					pre-dissolved
					in 1-ODE)

FIG. 4 depicts XRD patterns of the as-synthesized a) FeSe₂ NPs, b) Fe₃Se₄ NPs, c) Fe₇Se₈ NPs, and d) FeSe NPs. All the XRD peaks are in good agreement with the JCPDS (Joint Committee on Powder Diffraction Standards) data files—(74-0247) for FeSe₂, (73-2021) for Fe₃Se₄, (71-0586) for Fe₇Se₈ and (85-0735) for FeSe without ambiguous reflections. The XRD and magnetic measurements prove the high purity of as-synthesized NPs. Crystallite size of FeSe₂=23 nm, Fe₃Se₄=35 nm, Fe₇Se₈=29 nm, FeSe=46 nm as estimated from the XRD pattern using Scherrer's formula.

FIG. 5 depicts magnetization (M) vs. magnetic field (H) hysteresis loops of a) FeSe₂ b) Fe₃Se₄ c) Fe₇Se₈ and d) FeSe measured by the vibrating sample magnetometer at 300 K in an applied magnetic field up to ±60 kOe. The M-H curves reveal prominent M-H characteristics indicating the synthesis of pure phase. Figure a) shows the M-H curve of FeSe₂ NPs revealing paramagnetic behavior with coercivity (H_c) 146 Oe. Figure b-c) shows the M-H curves of Fe₃Se₄ and Fe₇Se₈ NPs having ferrimagnetic behavior. These hysteresis loops show the coercivity 1.6 kOe and 1.8 kOe, respectively. In Figure d) the hysteresis loop of FeSe reveals ferromagnetic nature of NPs having coercivity (H_c) 282 Oe.

FIG. 6 depicts M-H hysteresis loops of a) FeSe₂ b) Fe₃Se₄ c) Fe₇Se₈ and d) FeSe measured by the vibrating sample magnetometer at 10 K. The coercivity (H_c) of FeSe₂ NPs rises to 200 Oe with ferromagnetic behavior. The H_c value of Fe₃Se₄ nanorods raises nearly 20-fold to about 32 kOe. The value of Fe₇Se₈ nanorods rises more than 7-fold to about 13.8 kOe. The coercivity (H_c) of FeSe nanorods increases to about 4.4 kOe.

TABLE 3
Magnetic parameters measured at 300K and 10K for Fe—Se system. Hc and
σR represents the coercivity and remanence respectively obtained
from hysteresis loops at various temperature.
	Hc (Oe)	σR (emu/g)
Phases	300K	10K	300K	10K
FeSe2	146	200	~0	0.4
Fe3Se4	1600	32000	1.2	7.3
Fe7Se8	1800	13800	2	8.6
FeSe	300	4400	0.1	0.4

FIG. 7 shows TEM measurements of as-synthesized NPs. Typical TEM images of as-synthesized a)FeSe₂, b)Fe₃Se₄, c)Fe₇Se₈ and d)FeSe NPs shows the rod like features and inset shows the iron selenide nanocacti with rod like features growing on the surface [Scale bar in the insets are 100 nm]. a′) to d′) shows the lattice fringes space at 2.5 Å, 2.7 Å, 5.4 Å and 5.5 Å represents the (111), (−202), (101) and (001) of Fe—Se system respectively [The inset SAED pattern]. The diffraction pattern obtained for all the nanostructures were matched well with the crystal planes of Fe—Se system and have been assigned to (002), (101), (111) planes for FeSe₂, (−202), (011) planes for Fe₃Se₄, (203), (101), (206) planes for Fe₇Se₈ and (001), (101) planes for FeSe. Thus, d-spacing calculated in TEM are in good agreement with those given in the standard JCPDS for all the phases of Fe—Se system.

FIG. 8 shows Thermal Gravimetric Analysis (TGA). All the samples were undergone with different step decomposition. The first step in all samples is related to the loss of all organic fragments capped on NPs, this step was up to 460° C. The FeSe₂ NPs further go through three more step decomposition. The steps assigned to the decomposition of FeSe₂ NPs to Fe₃Se₄; Fe₃Se₄ NPs to the Fe₇Se₈ followed by the conversion of Fe₇Se₈ to FeSe and final step, the decomposition of FeSe NPs started at 875° C. and remains up to 1000° C. The Fe₃Se₄ NPs further go through final step, assigned to the decomposition of Fe₃Se₄ started at 725° C. and gradually decreases up to 1000° C. The Fe₇Se₈ NPs go through final step, assigned to the decomposition of Fe₇Se₈ started at 770° C. and gradually decreases up to 1000° C. The FeSe NPs go through final step assigned to the decomposition of FeSe started at 875° C. and gradually decreases up to 1000° C.

FIG. 9 shows Raman Spectra of all the samples having six characteristic peaks at 225, 244, 292, 410, 496, and 611 cm⁻¹. The presences of Fe—Se near 225 cm⁻¹, 292 cm⁻¹and 610 cm⁻¹, as well as Fe—O at 410 cm⁻¹ are identified for all the samples.

FIG. 10 shows TEM images of as-synthesized NPs in the presence of different organic solvents a) n-octadecane, b) 1-octadecene, c) octadecylamine and d) oleylamine. TEM data shows the strong depends of size, shape, and stability on solvent. Figure shows the as-synthesized nanospheres in presence of n-octadecane, nanoplatelets in 1-octadecene, nano-spheres in octadecylamine and nanocacti with rod like features growing on the surface in OLA.

To control the size of transition metal chalcogenides (Fe₃Se₄), the reaction parameters are optimized to find suitable synthesis conditions to crystallize various sizes of Fe₃Se₄ compound by following the one-pot thermal decomposition method as shown in table 4 and the observed data shows that as the reaction temperature increases crystallite size also increases, table 5.

TABLE 4
Summary of the experimental conditions to control the
size of the Fe3Se4 NPs.
		Fe	Se	Step 1	Step 2
Reac-	Sol-	pre-	pre-	Temp.	Time	Temp.	Time	Re-
tion	vent	cursor	cursor	(° C.)	(min)	(° C.)	(min)	sults
1	OLA	Fe(acac)3	Se	120	30	260	120	S1
2			powder			300	80	S2
3						330	70	S3

Table 5 describes list of calculated crystallite size along different planes of all the as-synthesized Fe₃Se₄ NPs, indicating the influence of the temperature on the crystallite size of the products evolve out of solution chemistry.

TABLE 5
List of calculated crystallite size along different planes of
all the as-synthesized Fe3Se4 NPs
	Crystallite size along following planes: d (±3 nm)
Sample	(−112)	(202)	(204)
S1	33	25	22
S2	37	31	24
S3	42	35	26

FIG. 11 depicts XRD patterns of the as-synthesized Co₃Se₄ NPs. The XRD peaks are in good agreement with the 99989-ICSD (Inorganic Crystal Structure Database) data file without ambiguous reflections.

FIG. 12 depicts XRD patterns of the as-synthesized Ni₃Se₄ NPs. The XRD peaks are in good agreement with the JCPDS (Joint Committee on Powder Diffraction Standards) data files—(65-1220) without ambiguous reflections.

FIG. 13 depicts XRD patterns of the as-synthesized MnSe NPs. The XRD peaks are in good agreement with the JCPDS (Joint Committee on Powder Diffraction Standards) data files—(65-7705) without ambiguous reflections.

FIG. 14 depicts XRD patterns of the as-synthesized Fe₃Se₄ NPs with different crystallite size. The XRD peaks are in good agreement with the JCPDS (Joint Committee on Powder Diffraction Standards) data files—(73-2021) without ambiguous reflections.

FIG. 15 depicts M-H hysteresis loops of 51, S2 and S3 of Fe₃Se₄ measured by the vibrating sample magnetometer at 300 K in an applied magnetic field up to ±60 kOe.

FIG. 16 depicts coercive field (H_c) vs crystallite size (left) and remanence magnetization (M_r) vs crystallite size (right) for Fe₃Se₄ NPs.

EXAMPLES

Following examples are given by way of illustration therefore should not be construed to limit the scope of the invention.

Example 1: Synthesis of the Fe—Se System to Examine the Phase Transformation

Synthesis of the Fe—Se System in OLA and 1-ODE. To study the effect of stoichiometry on the phase-transformation five prolonged reactions were performed by varying the amount of Se from 37.5 to 100 wt %, the stoichiometry of Fe/Se ranging from 1:0.75 (0.35 g, 0.059 g) to 1:2 (0.35 g, 0.158 g). All the reactions were carried out in the presence of 10 mL of 1-ODE and 15 mL of OLA in a 100 mL three-neck round-bottom (RB) flask under the blanket of nitrogen with constant magnetic stirring. The temperature was raised from 30 to 340° C. at a ramping rate of 2° C. min ⁻¹. For every 10° C. rise in the temperature, hold-time was ˜30 min. In each step, 2 mL aliquots were withdrawn using a long needle glass syringe to study the phase evolution. All the samples were stored in small glass vials and naturally quenched to RT for further investigation by wide-angle X-ray scattering (WAXS). The phase diagram was plotted after assembling the WAXS results, which inferred the effect of stoichiometry along with temperature on phase transformation of the Fe—Se system.

Example 2: Synthesis of the Fe—Se System in OLA

To study the effect of solvents on phase transformation one synthesis was done by following the same procedure as mentioned above except that only the OLA (15 mL) was used as an organic solvent with the stoichiometry of 1:1.

Example 3: Synthesis of the Fe—Se System in OLA and Predissolved Se Powder in 1-ODE

In order to examine the effect of solvents, one more reaction was done with the same procedure as mentioned earlier except that the Se powder was predissolved in 1-ODE under a

nitrogen environment with constant magnetic stirring at 30° C. for 6 h.

Example 4: Synthesis of FeSe₂ NPs

In a conventional reaction, 0.353 g (1 mmol) of Fe(acac)₃ and 0.158 g (2 mmol) of Se powders were added to 15 ml of OLA in a 100 mL three-neck round bottom (RB) flask. The mixture was stirred under a flow of high-purity nitrogen gas at 30° C. Then the temperature was raised to 150° C. at a ramping rate of 2° C. min⁻¹ and kept at 150° C. for 2 h. A thermometer was placed inside the RB-flask and the temperature was kept stable within ±1.0° C. during the 2 h long dwell-time at 150° C. The solution was cooled to RT by removing the heating source. After cooling, 20 ml of 2-propanol was added to the solution to give a black precipitate, which was separated from the solution by centrifugation. The obtained NPs were rewashed with the mixture of 15 ml hexane and 10 ml 2-propanol. Finally, the product was dried in a vacuum at 28° C. and utilized for further characterization.

Example 5: Synthesis of Fe₃Se₄ NPs

A 0.53 g (1.5 mmol) portion of Fe(acac)₃ and 0.158 g (2 mmol) of Se powder were mixed in 15 mL of OLA in a 100 mL three-neck RB flask. The mixture was heated to 120° C. and maintained for 30 min. Then, the temperature was raised at a heating rate of 2° C. min⁻¹ up to 200° C. and 5° C. min⁻¹ was used to reach a maximum temperature of 260° C.; at which the sample was maintained for 2 h.

Example 6: Synthesis of Fe₇Se₈ NPs

A 0.618 g (1.75 mmol) of Fe(acac)₃ and 0.158 g (2 mmol) of Se powder were added in 15 mL of OLA in a 100 mL three-neck RB flask. The mixture was heated to the designed temperature at a ramping rate of 5° C. min⁻¹ from 30° C. to 230° C. and then after ramping rate was decreased to 2° C. min⁻¹ up to 280° C., and kept for 4 h.

Example 7: Synthesis of FeSe NPs

This synthesis is similar to the synthesis of Fe₇Se₈ NPs with stoichiometry 1:1 except that the Se powder was pre-dissolved in 11 mL of 1-ODE at 30° C. with constant magnetic stirring for 6 h.

Example 8: Synthesis with Different Solvents

These syntheses are similar to the above synthesis except that 1-octadecene, octadecylamine and n-octadecane was used instead of OLA.

Example 9: Synthesis of Co₃Se₄ NPs

A 1.5 mmol portion of Cobalt(III) acetylacetonate (Co(acac)₃) and 2 mmol of Se powder were mixed in 15 mL of OLA in a 100 mL three-neck RB flask. The mixture was heated to 120° C. and maintained for 30 min. Then, the temperature was raised at a heating rate of 2° C. min⁻¹ up to 200° C. and 5° C. min⁻¹ was used to reach a maximum temperature of 300° C.; at which the sample was maintained for 2 h.

Example 10: Synthesis of Ni₃Se₄ NPs

A 1.5 mmol portion of Nickel(II) acetylacetonate (Ni(acac)₂) and 2 mmol of Se powder were mixed in 15 mL of OLA in a 100 mL three-neck RB flask. The mixture was heated to 120° C. and maintained for 30 min. Then, the temperature was raised at a heating rate of 2° C. min⁻¹ up to 200° C. and 5° C. min⁻¹ was used to reach a maximum temperature of 300° C.; at which the sample was maintained for 2 h.

Example 11: Synthesis of MnSe NPs

A 2 mmol portion of Manganese(III)acetylacetonate (Mn(acac)₃) and 2 mmol of Se powder were mixed in 15 mL of OLA in a 100 mL three-neck RB flask. The mixture was heated to 120° C. and maintained for 30 min. Then, the temperature was raised at a heating rate of 2° C. min⁻¹ up to 200° C. and 5° C. min⁻¹ was used to reach a maximum temperature of 300° C.; at which the sample was maintained for 2 h.

Advantages of the invention:

• • 1. The present method is simpler and economical than solid state route and required relatively lower temperature.
  • 2. This method is capable of giving high purity in phases and by this route it is easy to control the size, shape, and crystalline structure.
  • 3. It is possible to control the size of NPs by varying the temperature with pertinent time as well as shape by changing the solvents.
  • 4. This route is not only applicable for these 4 phases but also for other iron chalcogenide phases.
  • 5. Various other transition metal chalcogenides consisting of metal atoms (Fe, Cr, Mn, Co, and Ni) and chalcogen atoms (S, Se, Te) can also be synthesized by this route after optimizing the reaction conditions (temperature, precursors, solvents).

Claims

1. A one pot single phase process for the synthesis of a transition metal chalcogenide nanoparticle system having formula (I) by using wet chemical method, the process comprising: mixing and stirring both a transition metal precursor and a chalcogen precursor in the presence of a reducing agent and an accelerating agent andstirring at a temperature in the range of 100° C. to 300° C. for a time period varied from 30 min to 10 h to obtain the transition metal chalcogenide nanoparticle system having formula (I),wherein the formula (I) is represented as Ax-By   Formula (I)wherein,A is selected from the group consisting of iron, chromium, manganese, cobalt, and nickel;B is selected from the group consisting of selenium, sulphur, and tellurium; andAx-By is selected from the group consisting of AB2, A3B4, A7B8 and AB;wherein the ratio of x and y is from 1:2 to 1:1.

2. The process as claimed in claim 1, wherein said system of formula (I) is selected from the group consisting of FeSe2, Fe3Se4, Fe7Se8, FeSe, Co3Se4, Ni3Se4 and MnSe.

3. The process as claimed in claim 1, wherein the size of as-synthesized transition metal chalcogenide nanoparticle is in the range of 5 nm to 350 nm.

4. The process as claimed in claim 1, wherein the shape of as-synthesized transition metal chalcogenide nanoparticle is selected from the group consisting of nano-rod, nano-sphere, nano-sheet, nano-platelet, nano-cube and mixed shape.

5. The process as claimed in claim 1, wherein the reducing agent is selected from the group consisting of oleylamine, oleic acid, 1-octadecene, octadecylamine, oleyl alcohol, pentylamine, ethylamine and n-octadecane.

6. The process as claimed in claim 1, wherein the accelerating agent is selected from the group consisting of 1-octadecene, oleic acid, oleylamine, octadecylamine, oleyl alcohol, pentylamine, and ethylamine.

7. The process as claimed in claim 1, wherein the transition metal precursor is selected from the group consisting of Tris(acetylacetonato) iron (III), Cobalt(III) acetylacetonate, Nickel(II) acetylacetonate and Manganese(III)acetylacetonate.

8. The process as claimed in claim 1, wherein the chalcogen precursor is Se powder.

9. A one pot single phase process for the synthesis of transition metal chalcogenides nanoparticles system wherein said system is Fe—Se system comprising the steps of: a) mixing Se powder and Fe(acac)3 at a temperature in the range of 25° C. to 30° C. in the presence of an organic solvent under the blanket of inert gas with constant magnetic stirring;b) raising the temperature to 40° C. followed by stirring for 30 min and taking the first sample of only Se powder;c) further increasing the temperature to 50° C. followed by stirring for 30 min and taking the second sample of only Se powder; andd) increasing the temperature up to 340° C. with the rate of 10° C./30 min and taking the sample at every 10° C. rise in temperature, as the temperature increases, wherein FeSe2 starts forming followed by Fe3Se4, Fe7Se8 and FeSe.

10. The process as claimed in claim 9, wherein said organic solvent is selected from the group consisting of oleylamine; oleylamine and 1-octadecene; and oleylamine and pre-dissolved Se powder in 1-octadecene.