Three-dimensional nanosized porous metal oxide electrode material of lithium ion battery and preparation method thereof

Abstract

A preparation method of a three-dimensional nanosized porous metal oxide electrode material of lithium ion battery, which soaks a dried polymer colloidal crystal microsphere template in a metal salt solution as a precursor solution for a period of time, and obtains a precursor template complex after filtration and drying; heats the precursor template complex to a certain temperature at a low heating rate and keeps the temperature, and then obtains the three-dimensional nanosized porous metal oxide electrode material of lithium ion battery after cooling to room temperature. A metal oxide electrode material is manufactured, with the three-dimensional nanosized porous metal oxide electrode material thereby improving the ionic conductivity of the negative electrode material of lithium ion battery, and shortens the diffusion path of the lithium ions during an electrochemical reaction process, and improves the rate discharge performance of lithium ion battery greatly.

Claims

1. A preparation method of a three-dimensional nanosized porous metal oxide electrode material for a lithium ion battery, wherein the method comprises the following steps: (1) soaking a dried polymer microsphere colloid crystal template composed of microspheres with a size of 27510 nm in a metal salt solution as a precursor, where the metal salt solution is selected from a group consisting of: an ethylene glycol/methanol mixed solution of Fe.sup.3+, an ethylene glycol/methanol mixed solution of Fe.sup.3+ and Co.sup.2+ with a total metal ion concentration of 1.5 mols/Liter (the molar ratio, Fe.sup.3+: Co.sup.2+=2:1), and an ethanol solution of SnCl.sub.2.2H.sub.2O with a total metal ion concentration of 0.5 mol/L, where the soaking is conducted for 5-10 hours, and obtaining a polystyrene (PS) precursor template complex after filtration and drying; and (2) heating the polystyrene (PS) precursor template complex to a temperature that falls in a range of 450-600 C. at a rate of 1-5 C./min and keeping the temperature in the range of 450-600 C. for 10 hours, and then obtaining based on the selected precursor, respectively, from step 1at least one of a-Fe.sub.2O.sub.3, CoFe.sub.2O.sub.4, or SnO.sub.2 ordered three-dimensional nanosized porous metal oxide electrode material for the lithium ion battery after cooling to room temperature, wherein an aperture of the three-dimensional nanosized porous metal oxide electrode material has an aperture size of from 105 to 225 nm and an aperture wall thickness of from 20 to 30 nm and the least one of a-Fe.sub.2O.sub.3, CoFe.sub.2O.sub.4, or SnO.sub.2 ordered three-dimensional nanosized porous metal oxide electrode material having an initial discharge capacity of at least 1704 mAh.Math.g.sup.1 and a coulombic efficiency of at least 80% after 20 cycles.

2. The preparation method of a three-dimensional nanosized porous metal oxide electrode material for a lithium ion battery according to claim 1, wherein the polymer microsphere template is prepared by the following method: preparing a polymer microsphere emulsion with the polymer emulsion polymerization method, and then obtaining the polymer microsphere template with ordered arrangement by co-precipitation or centrifugation.

3. The preparation method of a three-dimensional nanosized porous metal oxide electrode material for a lithium ion battery according to claim 2, wherein the polymer microsphere emulsion is a polystyrene microsphere emulsion.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is a schematic view of one embodiment of the preparation method of a three-dimensional nanosized porous metal oxide electrode material of lithium ion battery according to the present invention.

(2) FIG. 2 is a scanning electron micrograph of the polystyrene colloidal crystal microsphere template with close arrangement obtained by the embodiment shown in FIG. 1 with the natural sedimentation method.

(3) FIG. 3a is a scanning electron micrograph of the three-dimensional nanosized porous metal oxide electrode material -Fe.sub.2O.sub.3 of lithium ion battery prepared with the polystyrene colloidal crystal microsphere template shown in FIG. 2.

(4) FIG. 3b is a cycle performance view of the three-dimensional nanosized porous metal oxide electrode material -Fe.sub.2O.sub.3 of lithium ion battery shown in FIG. 3a.

(5) FIG. 4 is a scanning electron micrograph of the polystyrene colloidal crystal microsphere template with close arrangement obtained by the embodiment shown in FIG. 1 with the centrifugation method.

(6) FIG. 5a is a scanning electron micrograph of the three-dimensional nanosized porous metal oxide electrode material CoFe.sub.2O.sub.4 of lithium ion battery prepared with the polystyrene colloidal crystal microsphere template shown in FIG. 4.

(7) FIG. 5b is a cycle performance view of the three-dimensional nanosized porous metal oxide electrode material CoFe.sub.2O.sub.4 of lithium ion battery shown in FIG. 5a.

(8) FIG. 6a is a scanning electron micrograph of the three-dimensional nanosized porous metal oxide electrode material SnO.sub.2 of lithium ion battery prepared with the polystyrene colloidal crystal microsphere template shown in FIG. 4.

(9) FIG. 6b is a cycle performance view of the three-dimensional nanosized porous metal oxide electrode material SnO.sub.2 of lithium ion battery shown in FIG. 6a.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT

(10) In order to understand the technical content of the present invention clearly, the present invention is further exemplified by reference to the following examples. It is only intended to make the content of the present invention to be better understood, and not to limit the protection scope of the present invention.

Embodiment 1

(11) Preparation and Performance Test of a Three-Dimensional Nanosized Porous Metal Oxide Electrode Material -Fe.sub.2O.sub.3 of Lithium Ion Battery

(12) (1) Preparation of a Polystyrene Colloidal Crystal Microsphere Template

(13) A 27510 nm polystyrene microsphere emulsion is prepared by the emulsion polymerization method, the microspheres are arranged by the natural sedimentation method to be a polystyrene colloidal crystal microsphere template (as shown in FIG. 2), the scanning electron micrograph shows that the polystyrene colloidal crystal microsphere template presents a multilayer, orderly, regular, close arrangement in a large area, has fewer defects and a relatively strong sense of hierarchicy.

(14) (2) Obtaining a Three-Dimensional Nanosized Porous Metal Oxide Electrode Material -Fe.sub.2O.sub.3

(15) The dried polystyrene colloidal crystal microsphere template is soaked in an ethylene glycol/methanol mixed solution of Fe.sup.3+ as a precursor solution for 5 hours, a precursor template complex is obtained after filtration and drying; the precursor template complex is heated to 450 C. at 1 C./min and the temperature is kept for 10 hours, and then the three-dimensional nanosized porous metal oxide electrode material of lithium ion battery is obtained after cooling to room temperature.

(16) The ethylene glycol/methanol mixed solution of Fe.sup.3+ as a precursor solution is poured into the gaps of the above-mentioned polystyrene colloidal crystal microsphere template, the three-dimensional nanosized porous -Fe.sub.2O.sub.3 is prepared after the incineration, which has a relative complete crystal form, and a three-dimensional porous network nanostructure (as shown in FIG. 3a), the diameter of a single aperture is approximately 11510 nm; the aperture wall is composed of -Fe.sub.2O.sub.3 crystal nanoparticles, and 2030 nm in thickness.

(17) (3) Performance Test of a Three-Dimensional Nanosized Porous Metal Oxide Electrode Material -Fe.sub.2O.sub.3 of Lithium Ion Battery

(18) The electrochemical tests show that the initial discharge and charge capacities reach 1880 and 1130 mAh.Math.g.sup.1, respectively, after 20 cycles, the reversible capacity is still as high as 631 mAh.Math.g.sup.1, and the coulombic efficiency remains above 90%, presenting a relatively high specific capacity and a good cycle performance (as shown in FIG. 3b).

Embodiment 2

(19) Preparation and Performance Test of a Three-Dimensional Nanosized Porous Metal Oxide Electrode Material CoFe.sub.2O.sub.4 of Lithium Ion Battery

(20) (1) Preparation of a Polystyrene Colloidal Crystal Microsphere Template

(21) A 27510 nm polystyrene microsphere emulsion is prepared by the emulsion polymerization method, the microspheres are arranged by the centrifugation method to be a polystyrene colloidal crystal microsphere template (as shown in FIG. 4), the scanning electron micrograph shows that the polystyrene colloidal crystal microsphere template presents a multilayer, orderly, regular, close arrangement in a large area, has fewer defects and a relatively strong sense of hierarchicy.

(22) (2) Obtaining a Three-Dimensional Nanosized Porous Metal Oxide Electrode Material CoFe.sub.2O.sub.4

(23) An ethylene glycol/methanol mixed solution with a total metal ion concentration of 1.5 mol.Math.L-1 (the molar ratio, Fe.sup.3+:Co.sup.2+=2:1) is prepared as a precursor solution. The dried PS colloidal crystal template is soaked in the precursor solution for 7 hours, a complex of the precursor and the template is obtained after vacuum filtration; the precursor template complex is heated to 550 C. at 3 C./min and the temperature is kept for 10 hours, and then the three-dimensional nanosized porous metal oxide electrode material of lithium ion battery is obtained after cooling to room temperature.

(24) The ethylene glycol/methanol mixed solution with a total metal ion concentration of 1.5 mol.Math.L-1 (the molar ratio, Fe.sup.3+:Co.sup.2+=2:1) as a precursor solution is poured into the gaps of the above-mentioned polystyrene colloidal crystal microsphere template, the three-dimensional nanosized porous CoFe.sub.2O.sub.4 is prepared after the incineration, which has a relative complete crystal form, and a three-dimensional porous network nanostructure (as shown in FIG. 5a), the diameter of a single aperture is approximately 13010 nm; the aperture wall is composed of CoFe.sub.2O.sub.4 crystal nanoparticles, and 2030 nm in thickness.

(25) (3) Performance Test of a Three-Dimensional Nanosized Porous Metal Oxide Electrode Material CoFe.sub.2O.sub.4 of Lithium Ion Battery

(26) The electrochemical tests show that the initial discharge and charge capacities reach 1782 and 1147 mAh.Math.g.sup.1, respectively, after 20 cycles, the reversible capacity is still as high as 610 mAh.Math.g.sup.1, and the coulombic efficiency remains above 80%, presenting a relatively high specific capacity and a good cycle performance (as shown in FIG. 5b).

Embodiment 3

(27) Preparation and Performance Test of a Three-Dimensional Nanosized Porous Metal Oxide Electrode Material SnO.sub.2 of Lithium Ion Battery

(28) (1) Preparation of a Polystrene Colloidal Crystal Microsphere Template

(29) A 27510 nm polystyrene microsphere emulsion is prepared by the emulsion polymerization method, the microspheres are arranged by the centrifugation method to be a polystyrene colloidal crystal microsphere template (as shown in FIG. 4), the scanning electron micrograph shows that the polystyrene colloidal crystal microsphere template presents a multilayer, orderly, regular, close arrangement in a large area, has fewer defects and a relatively strong sense of hierarchicy.

(30) (2) Obtaining a Three-Dimensional Nanosized Porous Metal Oxide Electrode Material SnO.sub.2

(31) An ethanol solution of SnCl.sub.2.2H.sub.2O with a total metal ion concentration of 0.5 mol/L is prepared as a precursor solution. The dried PS colloidal crystal template is soaked in the precursor solution for 10 hours, a complex of the precursor and the template is obtained after vacuum filtration; the precursor template complex is heated to 600 C. at 5 C./min and the temperature is kept for 10 hours, and then the three-dimensional nanosized porous metal oxide electrode material of lithium ion battery is obtained after cooling to room temperature.

(32) The ethanol solution of SnCl.sub.2.2H.sub.2O with a total metal ion concentration of 0.5 mol/L as a precursor solution is poured into the gaps of the above-mentioned polystyrene colloidal crystal microsphere template, the three-dimensional nanosized porous SnO.sub.2 is prepared after the incineration, which has a relative complete crystal form, and a three-dimensional porous network nanostructure (as shown in FIG. 6a), the diameter of a single aperture is approximately 21510 nm; the aperture wall is composed of SnO.sub.2 crystal nanoparticles, and 2030 nm in thickness.

(33) (3) Performance Test of a Three-Dimensional Nanosized Porous Metal Oxide Electrode Material SnO.sub.2 of Lithium Ion Battery

(34) The electrochemical tests show that the initial discharge and charge capacities reach 1704 and 769 mAh.Math.g.sup.1, respectively, after 20 cycles, the reversible capacity is still as high as 416 mAh.Math.g.sup.1, and the coulombic efficiency remains above 90%, much higher than the theoretical capacity of graphite (as shown in FIG. 6b).

(35) The present invention prepares a three-dimensional nanosized porous metal oxide electrode material of lithium ion battery with the template method, firstly a polymer microsphere emulsion is prepared with the polymer emulsion polymerization method, and then the polymer colloidal crystal microsphere template with regular arrangement is obtained by co-precipitation or centrifugation, then a metal salt solution as a precursor solution is poured into the gaps between the microspheres, and they are transformed into a metal complex or a solid metal compound before the template is removed; then a three-dimensional nanosized porous metal oxide electrode material with regular structure is obtained by removing the template with the method of incinerating at a low heating rate. The electrode material prepared has a good electrochemical performance. Such a method may also be used for the preparation of three-dimensional nanosized porous metal oxide electrode materials of other elements in other fields, which have a relatively uniform three-dimensional porous nanostructure, and a relatively wide application fields.

(36) On the basis that the metal oxide electrode material has a high specific capacity, by the preparation of a porous nanostructure, the present invention improves the specific surface area and the ionic conductivity of the metal oxide electrode material greatly, and shortens the diffusion path of the lithium ions during an electrochemical reaction process, to make the electrode material react completely in the electrode reaction process, so as to further improve the specific capacity and the rate performance of the metal oxide electrode material, therefore the material is suitable for large-scale popularization.

(37) That is to say, the present invention improves the ionic conductivity and the reactivity of the electrode material of lithium ion battery in the electrochemical reaction process by changing its micro morphology, so as to improve the characteristics of the material, such as the utilization rate, the rate performance and the specific capacity.

(38) It is noted that, the precursor solution can be a salt solution of one metal, and can be a salt solution of many metals (e.g., Embodiment 2), if a salt solution of many metals is used as a precursor solution, the three-dimensional nanosized porous metal oxide electrode material of lithium ion battery obtained is essentially the three-dimensional nanosized porous multiple-metal-oxide electrode material of lithium ion battery.

(39) To sum up, the three-dimensional nanosized porous metal oxide electrode material of lithium ion battery of the present invention improves the ionic conductivity of the negative electrode material of lithium ion battery, and shortens the diffusion path of the lithium ions during an electrochemical reaction process, improves the rate discharge performance of lithium ion battery greatly, and its preparation method is designed uniquely, operated simply and conveniently, and suitable for large-scale popularization.

(40) In the present specification, the present invention has been described according to the particular embodiments. But it is obvious that these embodiments can be modified or changed without departure from the spirit and scope of the present invention. Therefore, the specification and drawings described above are exemplary only and not intended to be limiting.