Electrode material and method of synthesizing

Abstract

The present disclosure provides a phosphate framework electrode material for sodium ion battery and a method for synthesizing such electrode material. A surfactant and precursors including a sodium precursor, a phosphate precursor, a transition metal precursor are dissolved in a solvent and stirred for sufficient mixing and reaction. The precursors are reacted to yield a precipitate of particles of Na.sub.xA.sub.bM.sub.y(PO.sub.4).sub.zX.sub.n compound and with the surfactant attached to the particles. The solvent is then removed and the remaining precipitate is sintered to crystallize the particles. During sintering, the surfactant is decomposed to form a carbon network between the crystallized particles and the crystallized particles and the carbon matrix are integrated to form the electrode material.

Claims

1. A method for synthesizing an electrode material, the method comprising: preparing a precipitate of particles by a step consisting of dissolving a surfactant, a sodium precursor, a phosphate precursor and a transition metal precursor in a solvent to cause reaction of the sodium, phosphate and transition metal precursors to yield the precipitate of particles, wherein the surfactant is attached to the particles; removing the solvent; and sintering the precipitate to crystallize the particles, wherein during sintering the surfactant is decomposed to form a carbon matrix between the crystallized particles; wherein the crystallized particles and the carbon matrix are integrated to form the electrode material; wherein the crystallized particles have a grain size between 20 nm and 200 nm; and wherein the particles include Na.sub.3V.sub.2(PO.sub.4).sub.3.

2. The method of claim 1, wherein the surfactant is selected from the group consisting of sodium dodecyl sulfate (SDS), octyltrimethyl ammonium bromide (OTAB), dodecyltrimethyl ammonium bromide (DOTAB), cetyltrimethyl ammonium bromide (CTAB), and gluconic acid lactone.

3. The method of claim 1, wherein the sodium precursor is a sodium salt.

4. The method of claim 1, wherein the phosphate precursor is an ammonium phosphate salt or a phosphoric acid.

5. The method of claim 1, wherein the solvent is one of alcohol and a mixture of de-ionized water and alcohol.

6. The method of claim 1, wherein the transitional metal precursor is selected from a metal acetate, metal nitrate, metal chloride, metal acetyl acetonate, metal hydroxide, and combinations thereof.

7. The method of claim 1, wherein the carbon matrix forms a carbon layer coated on the crystallized particles, and wherein the carbon layer has a thickness of 2 to 10 nm.

8. The method of claim 1, wherein removing the solvent consists of drying the precipitate.

9. The method of claim 1, wherein sintering is carried out in one of a flowing oxidizing atmosphere, an inert atmosphere and a reducing atmosphere.

10. The method of claim 1, wherein removing the solvent consists of separating the precipitate from the solvent.

11. A method for synthesizing an electrode material, the method comprising: preparing a precipitate of particles by a step consisting of dissolving a surfactant, a sodium precursor, a phosphate precursor, a transition metal precursor, and a compound having fluorine in a solvent to cause reaction of the sodium, phosphate and transition metal precursors to yield the precipitate of particles, wherein the surfactant is attached to the particles; removing the solvent; and sintering the precipitate to crystallize the particles, wherein during sintering the surfactant is decomposed to form a carbon matrix between the crystallized particles; wherein the crystallized particles and the carbon matrix are integrated to form the electrode material; wherein the crystallized particles have a grain size between 20 nm and 200 nm; and wherein the particles include Na.sub.3V.sub.2(PO.sub.4).sub.2F.sub.3 and NaVPO.sub.4F.

12. A method for synthesizing an electrode material, the method comprising: preparing a precipitate of particles by a step consisting of dissolving a surfactant, a sodium precursor, a phosphate precursor, a transition metal precursor, and a compound having manganese in a solvent to cause reaction of the sodium, phosphate and transition metal precursors to yield the precipitate of particles, wherein the surfactant is attached to the particles; removing the solvent; and sintering the precipitate to crystallize the particles, wherein during sintering the surfactant is decomposed to form a carbon matrix between the crystallized particles; wherein the crystallized particles and the carbon matrix are integrated to form the electrode material; wherein the crystallized particles have a grain size between 20 nm and 200 nm; and wherein the particles include Na.sub.2V.sub.0.5Mn.sub.0.5PO.sub.4F.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) These and other aspects of the present disclosure will be described in detail with reference to the accompanying drawings, in which:

(2) FIG. 1 is a block diagram showing a method of synthesizing an electrode material according to one embodiment of the present disclosure;

(3) FIG. 2 is a chart showing a Rietveld refinement pattern of X-ray diffraction data of a Na.sub.3V.sub.2(PO.sub.4).sub.3/C sample synthesized as an electrode material according to one embodiment of the present disclosure;

(4) FIG. 3A is an FESEM image of a Na.sub.3V.sub.2(PO.sub.4).sub.3/C sample synthesized using C16 surfactant;

(5) FIG. 3B is an enlarged view of FIG. 3A

(6) FIG. 4A is a TEM image of a mesoporous Na.sub.3V.sub.2(PO.sub.4).sub.3/C particle;

(7) FIG. 4B is an enlarged view of FIG. 4A;

(8) FIG. 4C is an image of SAED pattern showing single crystalline nature of mesoporous Na.sub.3V.sub.2(PO.sub.4).sub.3/C particles;

(9) FIG. 5 is a chart showing N.sub.2 absorption/desorption isotherms of a Na.sub.3V.sub.2(PO.sub.4).sub.3/C sample;

(10) FIG. 6A is a chart showing galvanostatic charge/discharge cycle curves of Na.sub.3V.sub.2(PO.sub.4).sub.3/C material used as cathode under different current rates;

(11) FIG. 6B is a chart showing long term cyclability curve of Na.sub.3V.sub.2(PO.sub.4).sub.3/C material used as cathode at 1C;

(12) FIG. 7A is a chart showing galvanostatic charge/discharge cycle curves of Na.sub.3V.sub.2(PO.sub.4).sub.3/C material used as anode under different current rates;

(13) FIG. 7B is a chart showing long term cyclability curve of Na.sub.3V.sub.2(PO.sub.4).sub.3/C material used as anode at 1C.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

(14) FIG. 1 illustrates a method 100 of synthesizing an electrode material according to one embodiment of the present disclosure. At block 102, a surfactant and metal precursors including a sodium precursor, a phosphate precursor and a transitional metal precursor are dissolved in a solvent to cause reaction of the precursors in the solvent. The solvent may be alcohol and/or a mixture of de-ionized water and alcohol. The mixture of the precursors may be stirred to help uniform mixing of the reactants at atomic level. The reaction yields a precipitate of amorphous sodium-transitional metal-phosphate compound particles with the surfactant attached thereto. At block 104, the solvent is removed and at block 106, the remaining precipitate is sintered, e.g. in a flowing, inert gas or a reducing atmosphere. During the sintering process, the surfactant remaining on the particles is decomposed to form an integrated conductive carbon matrix between the crystallized nanoparticles, and the crystallized nanoparticles and the carbon matrix are integrated to form the electrode material in bulk form.

(15) The above method enables homogeneous mixing of the precursors and control of the particle size and morphology. The carbon matrix decomposed from the surfactant and formed between the nanoparticles prevents the particle agglomeration and growth during the sintering process. The carbon matrix also forms an in-situ coating of electrically conductive carbon layer on the crystallized nanoparticles. The carbon matrix therefore can greatly improve the electrical conductivity to make the electrode material suitable for rechargeable sodium ion battery applications.

(16) The above method may be used to synthesize the entire phosphate polyanion family of electrode materials for the sodium ion battery applications. The base formula for these compounds takes the form of:
Na.sub.xA.sub.bM.sub.y(PO.sub.4).sub.zX.sub.n/C
where Na.sub.xA.sub.bM.sub.y(PO.sub.4).sub.zX.sub.n denotes the structure of Na-Transitional Metal-Phosphate nanoparticle, in which, M is a transition metal obtained from a compound selected from a group consisting of metal acetates, metal nitrate metal chloride and metal acetyl acetonate; A is an additional doped or mixed cation(s) obtained from a compound selected from a group consisting of group 1 elements, transition metals, ammonium and hydrogen; X is a substituted anion or polyanion(s) obtained from a compound selected from a group consisting of fluorine, hydroxide, vanadate, arsenate, chloride, pyrophosphate; x, b, y, z and n denote the numbers of ions of a corresponding element, in which: 1x3; 0b1; 1y2; 1z3; 0n3;
and C denotes a carbon matrix formed between the Na.sub.xA.sub.bM.sub.y(PO.sub.4).sub.zX.sub.n nanoparticles.

(17) The sodium precursor may be a sodium salt. The phosphate precursor may be an ammonium di-hydrogen phosphate or a phosphoric acid. The transitional metal precursor comprises a compound selected from the group consisting of metal acetates, metal nitrate, metal chloride, metal acetyl acetonate and metal hydroxide. The surfactant provides the necessary carbon content to form the carbon matrix during sintering to integrate with the crystallized nanoparticles. The surfactant comprises a compound selected from the group consisting of Sodium dodecyl sulfate (SDS), octyltrimethyl ammonium bromide (OTAB), dodecyltrimethyl ammonium bromide (DOTAB), cetyltrimethyl ammonium bromide (CTAB) and gluconic acid lactone.

(18) Sample electrode material synthesized by the above method include, but not limited to, Na.sub.3V.sub.2(PO.sub.4).sub.3/C, Na.sub.3V.sub.2(PO.sub.4).sub.2F.sub.3/C, Na.sub.2FePO.sub.4F/C, NaVPO.sub.4F/C, Na.sub.2FePO.sub.4(OH)/C, Na.sub.2Fe.sub.0.5Mn.sub.0.5PO.sub.4F/C, Na.sub.2Ti.sub.0.5Mn.sub.0.5PO.sub.4F/C, Na.sub.2V.sub.0.5Mn.sub.0.5PO.sub.4F/C, NaFePO.sub.4/C, Na.sub.3Ti.sub.2(PO.sub.4).sub.3/C. These materials possess unique properties of small crystallite size, high purity, high crystallinity, large surface-to-volume ratio, and promising structural stability after prolonged charge-discharge cycles required to use in sodium ion rechargeable batteries.

(19) Note that for materials containing additional cation, e.g. Fe in Na.sub.2Fe.sub.0.5Mn.sub.0.5PO.sub.4F/C, Ti in Na.sub.2Ti.sub.0.5Mn.sub.0.5PO.sub.4F/C and V in Na.sub.2V.sub.0.5Mn.sub.0.5PO.sub.4F/C and for those containing anion/polyanion e.g. F in Na.sub.3V.sub.2(PO.sub.4).sub.2F.sub.3/C, compounds or precursors containing the respective cation/anion are added and dissolved in the solvent for reaction together with the sodium precursor, phosphate precursor and transitional metal precursor.

(20) The crystallized particles have a grain size between about 20 nm to 200 nm, and the carbon layer coated on the particles has a thickness of about 2 to 10 nm. The carbon matrix portion in the electrode material is not more than about 5% in weight, and forms a carbon coating layer covering the crystallized nanoparticles in a surface area of about 10 to 100 m.sup.2/gram. Therefore, electrode materials provided by embodiments of the present disclosure have electrically conductive carbon matrix sufficiently mixed and integrated with the crystallized Na-transitional metal-Phosphate nanoparticles. The crystallized Na-transitional metal-Phosphate nanoparticles provide enhanced sodium intercalation/deintercalation. In the meantime, the interconnected carbon matrix between the nanoparticles provides electrical conductivity suitable for rechargeable sodium ion battery applications.

(21) A Na.sub.3V.sub.2(PO.sub.4).sub.3/C (NVP/C) material formed according to the above method is now taken as a non-limiting example to illustrate the characteristics and performances for use as electrode in rechargeable sodium ion batteries. It should be appreciated that other types of phosphate framework material synthesized by the method according to embodiments of the present disclosure may be taken for performance study in a similar manner.

(22) FIGS. 2 to 5 show test results of structural characterization study and morphological analysis of NVP/C material synthesized according to an embodiment of the present disclosure.

(23) FIG. 2 depicts a powder X-ray diffraction pattern (PXRD) of a porous NVP/C electrode material sample. Rietveld refinement of the PXRD pattern is performed to show the pure phase formation of NVP/C, without any impurity. This characteristic is evidenced by the close match of the calculated/fitted curve 22 and measured curve 24 and the difference 23 of curves 22 and 24.

(24) FIGS. 3A and 3B are field emission scanning electron microscope (FESEM) images of NVP/C sample, showing a network of NVP particles with an irregular morphology and various sized ranging from 500 to 900 nm. Transmission Electron Microscopy (TEM) analysis reveals that the NVP nano grains are well dispersed in the carbon matrix.

(25) FIGS. 4A and 4B show clear lattice fringes of NVP particle with a uniform carbon layer 42 of about 8 nm formed on NVP particle 44. A selected area electron diffraction (SAED) pattern (FIG. 4C) shows single crystalline nature of the NVP nanoparticles which is consistent with the PXRD pattern shown in FIG. 2.

(26) Nitrogen absorption/desorption isotherms 52, 54 shown in FIG. 5 indicate that the nanostructured NVP/C prepared according to embodiments of the present disclosure exhibits a distinct large hysteresis loop 56 and this type of behavior is a typical characteristic of mesoporous materials, namely a type-TV isotherm due to capillary condensation in the mesoporous channels and/or cages.

(27) FIGS. 6A, 6B, 7A and 7B show test results of electrochemical behaviour study of an NVP/C material synthesized according to embodiment of the present disclosure. The NVP/C material may be used as either a cathode or an anode for sodium ion battery.

(28) Galvanostatic cycling curves obtained under current density of 117 mAg.sup.1 from C/10 to 40C, for porous NVP/C material as a cathode in a Na-ion battery is shown in FIG. 6A. Here 1C refers to a capacity of 117 mAg.sup.1 in one hour. As shown, the voltage profile has a flat charge plateau at about 3.39V before it rises steeply to the cutoff voltage of 3.9V, with a direct voltage drop to 3.36V followed by a very flat voltage plateau that spreads over a long range of sodium composition (up to 1.88 mole of Na.sup.+) and then falls steeply to the cutoff voltage of 2.3V, leading to the storage capacity of 117 mAhg.sup.1. Accordingly, the flat voltage profile for a wide range of sodium ion molar concentrations observed for the NVP/C material synthesized according to embodiment of the present disclosure is much higher than conventional electrode material used for the same applications. During subsequent cycles, the observed voltage profiles remain unaltered, demonstrating excellent reversibility of the cycling process. As shown in FIG. 6B, at 1C rate the capacity can remain around 70 mAhg.sup.1 for at least 500 cycles.

(29) When an NVP/C material synthesized according to embodiment of the present disclosure is used as an anode in a sodium-ion battery, as shown in FIGS. 7A and 7B. A flat voltage profile was observed during the different charge/discharge current rates. Excellent long term cyclability was also observed when employed as anode.

(30) As illustrated above, with respect to specific but non-limiting sample of NVP/C, an electrode material has Nasicon-type, phosphate framework nanoparticles integrated with carbon matrix between the particles.

(31) Although embodiments of the present disclosure have been illustrated in conjunction with the accompanying drawings and described in the foregoing detailed description, it should be appreciated that the present disclosure is not limited to the embodiments disclosed. Therefore, the present disclosure should be understood to be capable of numerous rearrangements, modifications, alternatives and substitutions without departing from the spirit of the disclosure as set forth and recited by the following claims.