CN100457608C - Sol-gel method of ferresodium flurophosphate for sodium ion battery - Google Patents
Sol-gel method of ferresodium flurophosphate for sodium ion battery Download PDFInfo
- Publication number
- CN100457608C CN100457608C CNB2006100968732A CN200610096873A CN100457608C CN 100457608 C CN100457608 C CN 100457608C CN B2006100968732 A CNB2006100968732 A CN B2006100968732A CN 200610096873 A CN200610096873 A CN 200610096873A CN 100457608 C CN100457608 C CN 100457608C
- Authority
- CN
- China
- Prior art keywords
- sodium
- sol
- gel
- ion battery
- hours
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 title claims abstract description 17
- 229910001415 sodium ion Inorganic materials 0.000 title claims abstract description 17
- 238000003980 solgel method Methods 0.000 title claims abstract description 14
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims abstract description 18
- 238000002360 preparation method Methods 0.000 claims abstract description 11
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 claims abstract description 8
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 claims abstract description 8
- 238000002156 mixing Methods 0.000 claims abstract description 7
- 239000012153 distilled water Substances 0.000 claims abstract description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 238000001354 calcination Methods 0.000 claims abstract description 5
- 238000006243 chemical reaction Methods 0.000 claims abstract description 5
- 235000011114 ammonium hydroxide Nutrition 0.000 claims abstract description 4
- 238000010438 heat treatment Methods 0.000 claims abstract description 4
- 239000011775 sodium fluoride Substances 0.000 claims abstract description 4
- 235000013024 sodium fluoride Nutrition 0.000 claims abstract description 4
- 239000004317 sodium nitrate Substances 0.000 claims abstract description 4
- 235000010344 sodium nitrate Nutrition 0.000 claims abstract description 4
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 claims abstract description 3
- 238000001035 drying Methods 0.000 claims abstract 3
- PNGLEYLFMHGIQO-UHFFFAOYSA-M sodium;3-(n-ethyl-3-methoxyanilino)-2-hydroxypropane-1-sulfonate;dihydrate Chemical compound O.O.[Na+].[O-]S(=O)(=O)CC(O)CN(CC)C1=CC=CC(OC)=C1 PNGLEYLFMHGIQO-UHFFFAOYSA-M 0.000 claims description 12
- 239000000243 solution Substances 0.000 claims description 7
- 238000001291 vacuum drying Methods 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 3
- MVFCKEFYUDZOCX-UHFFFAOYSA-N iron(2+);dinitrate Chemical compound [Fe+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MVFCKEFYUDZOCX-UHFFFAOYSA-N 0.000 claims description 3
- 239000004570 mortar (masonry) Substances 0.000 claims description 3
- 229940001516 sodium nitrate Drugs 0.000 claims description 3
- 241000628997 Flos Species 0.000 claims description 2
- 235000019219 chocolate Nutrition 0.000 claims description 2
- 206010013786 Dry skin Diseases 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 15
- 239000007774 positive electrode material Substances 0.000 abstract description 13
- 238000000034 method Methods 0.000 abstract description 7
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 abstract description 6
- 229910052786 argon Inorganic materials 0.000 abstract description 3
- 239000007789 gas Substances 0.000 abstract description 3
- 239000011734 sodium Substances 0.000 abstract description 3
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 abstract 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 2
- VCJMYUPGQJHHFU-UHFFFAOYSA-N iron(3+);trinitrate Chemical compound [Fe+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O VCJMYUPGQJHHFU-UHFFFAOYSA-N 0.000 abstract 2
- 229910052708 sodium Inorganic materials 0.000 abstract 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 abstract 1
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 abstract 1
- 238000001816 cooling Methods 0.000 abstract 1
- 238000000227 grinding Methods 0.000 abstract 1
- 235000019837 monoammonium phosphate Nutrition 0.000 abstract 1
- 238000011068 loading method Methods 0.000 description 10
- 239000002245 particle Substances 0.000 description 8
- 230000004087 circulation Effects 0.000 description 7
- 239000000203 mixture Substances 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000009792 diffusion process Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 229910021385 hard carbon Inorganic materials 0.000 description 2
- 229910001416 lithium ion Inorganic materials 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- IJJWOSAXNHWBPR-HUBLWGQQSA-N 5-[(3as,4s,6ar)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]-n-(6-hydrazinyl-6-oxohexyl)pentanamide Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)NCCCCCC(=O)NN)SC[C@@H]21 IJJWOSAXNHWBPR-HUBLWGQQSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 1
- 229910013553 LiNO Inorganic materials 0.000 description 1
- 229910013716 LiNi Inorganic materials 0.000 description 1
- 229910014411 LiNi1/2Mn1/2O2 Inorganic materials 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 239000010405 anode material Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 239000010406 cathode material Substances 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 238000004146 energy storage Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- DWYMPOCYEZONEA-UHFFFAOYSA-L fluoridophosphate Chemical compound [O-]P([O-])(F)=O DWYMPOCYEZONEA-UHFFFAOYSA-L 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000010532 solid phase synthesis reaction Methods 0.000 description 1
- 229910052596 spinel Inorganic materials 0.000 description 1
- 239000011029 spinel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000011232 storage material Substances 0.000 description 1
- 238000012876 topography Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000011240 wet gel Substances 0.000 description 1
Images
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Landscapes
- Battery Electrode And Active Subsutance (AREA)
Abstract
The present invention relates to a sol-gel method capable of preparing sodium ferrous fluophosphate for sodium ion battery, belonging to the preparation method of secondary cell positive electrode material in energy source material. Said method includes the following step: mixing sodium nitrate, sodium fluoride, ferric nitrate and ammonium dihydrogen phosphate according to the ratio of 0.1 mol: 0.1 mol:0.1mol:0.1mol, dissolving them in distilled water so as to obtain a solution, adding citric acid, using ammonia water to regulate pH value, its reaction temperature is 80 deg.C, converting the above-mentioned solution into a cardinal red transparent sol, heating it to obtain a viscous gel, drying said gel for 8 hr in a drying box to obtain a black-brown floccules, grinding and prefiring at 300 deg.C for 3 hr under the condition of argon gas protection in the furnace, taking out and tabletting, continuously calcining at 750 deg.C under the protection of argon gas, heat-insulating for 6 hr, cooling to room temperature so as to obtain the invented sodium ferrous fluophosphate.
Description
One, technical field
This invention be used for the method for the hexafluorophosphoric acid Naferon of sodium-ion battery with Prepared by Sol Gel Method, belong to the preparation method of the secondary battery positive electrode material in the energy and material.
Two, technical background
It is low that sodium-ion battery has material cost, and therefore characteristics such as safety performance excellence are considered to substitute the clang ionization cell as moving the better selection that reaches electrical source of power.In recent years, the research of external sodium-ion battery negative material is flourish, it is reported that materials such as treated graphite, carbon black, hard carbon all have higher reversible capacity (more than the 300mAh/g).With respect to the obtained good progress of negative material, the optional leeway of positive electrode current material is less, and specific discharge capacity lower (being lower than 90mAh/g).Therefore, can the research of positive electrode material make a breakthrough, and is the key point of development sodium-ion battery.
At home, the research work of sodium-ion battery positive electrode material does not appear in the newspapers as yet, for seeking good sodium-ion battery positive electrode material, has occurred some significant research work abroad.Bach etc. have studied under the sodium ion low temperature has the Mn of spinel structure
2.2Co
0.27O
4Embedded performance in the material is found to discharge and recharge with the electric current of C/8 multiplying power, and capacity is held in the discharge in the 15th week still 95mAh/g.Concrete document is [S.Bach, M.Millet, J.P.Periera-Ramos, L.Sanchez, P.Lavela, and J.L.Tirado, Electrochemical and Solid-State Letters, 2 (1999) 545].The loading capacity of this material and cyclical stability are still not fully up to expectations, and the performance under middle high temperature is unsatisfactory.U.S. Valence Technology, the research that the Barker of Incorporated etc. carry out transistion metal compound, they find NaVPO
4The F effect is better, cooperates with hard carbon material and makes sodium-ion battery, and battery operated voltage is 3.7V, and is very consistent with lithium ion battery, and the capacity of positive electrode material is 82mAh/g, after 30 charge and discharge cycles cell container be the 1st time 50%.Concrete document is [J.Barker, M.Y.Saidi, and J.L.Swoyer, A Sodium-Ion Cell Based on theFluorophosphate Compound NaVPO
4F, Electrochemical and Solid-State Letters, 6 (2003) A1-A4].Though NaVPO
4F can obtain comparatively stable sparking voltage, but its loading capacity and stable circulation performance still have much room for improvement.
Sol-gel method can be accomplished uniform mixing on molecule or atomic level, can accomplish the better chemical measure control, and characteristics such as it is low to have a synthesis temperature, and the reaction times is short, and crystal growth is intact.This method can also effectively be controlled size of particles, can obtain the small-particle of size homogeneous.Sol-gel method is widely used in the preparation of anode material for lithium-ion batteries, as people such as Gopukumar with LiNO
3, MnNO
3, NiNO
3Being raw material, is complexing agent with the Padil, synthesizes LiNi by sol-gel method
0.5Mn
0.5O
2[Gopukumar S, Chung K Y, Kim K B.Novelsynthesis of layered LiNi
1/2Mn
1/2O
2As cathode material for lithiumrechargeable cells[J] .ElectrochimicaActa, 2004,49 (5): 803-810.].
Three, summary of the invention
The objective of the invention is to, propose a kind of can preparing and have more high discharge capacity and the stable circulation performance and sodium-ion battery positive electrode material that have high-specific surface area and high electrochemical activity.
This invention seeks to improve the solution of sodium-ion battery positive electrode material performance from two aspects.At first, the present invention is with NaFePO
4This novel composition metal fluorophosphate of F is as positive electrode material, and this storeroom group is the serial Na of 14/mmm
3m
2(PO
4)
2F
3, will possess and NaVPO
4Thermostability that F is identical and discharge stability, and higher specific discharge capacity and stable circulation performance will be arranged.Secondly, this invention is prepared the positive electrode material with high-specific surface area and high electrochemical activity by changing the structure and the surface topography of hexafluorophosphoric acid Naferon, has bigger sodium ion embedded quantity in the hope of making it, thereby improves the capacity of battery.Moreover the gentle controlled sol-gel method of reaction conditions is used in this invention, helps the industrialization operation in enormous quantities of material preparation, will further promote the practicalization of low-cost and high-performance energy storage material.
Sol-gel method can be accomplished uniform mixing on molecule or atomic level, can accomplish the better chemical measure control, and characteristics such as it is low to have a synthesis temperature, and the reaction times is short, and crystal growth is intact.This method can also effectively be controlled size of particles, can obtain the small-particle of size homogeneous, helps the raising of material electrochemical performance.Concrete technical scheme is as follows:
With SODIUMNITRATE; iron nitrate; biphosphate is pressed; Sodium Fluoride is according to the mixed of 0.1mol: 0.1mol: 0.1mol: 0.1mo; form mixed aqueous solution with 500-1000ml distilled water; the citric acid of 0.05～0.1mol is dissolved in the 500ml distilled water in advance forms citric acid solution; join then in the above-mentioned mixed aqueous solution and form mixing solutions; join with the ammoniacal liquor of 50% volume ratio again and regulate the pH value in the mixing solutions at 7-8; the water-bath control reaction temperature is 80 ℃; after changing into the scarlet vitreosol; continue heating and formed the heavy-gravity gel in 40 minutes; taking-up is transferred in the vacuum drying oven; in 80 ℃ of vacuum-dryings 8 hours; obtain the chocolate floss, agate mortar grinds, in tube furnace in the hydrogen atmosphere in 300 ℃ of following pre-burnings 3 hours; take out; make disk shape (middle 20mm, thickness 5mm) with tabletting machine, continue 750 ℃ of calcination under hydrogen shield; insulation 6h, it is stand-by to cool to room temperature with the furnace.
By experiment, sodium-ion battery of the present invention uses the charge and discharge platform of positive electrode material near 3.7V and 2.5V, and loading capacity is 91mAh/g first, and the loading capacity decay is slow, and it is 89.78% that the loading capacity after 20 circulations maintains the 81.7mAh/g capability retention.
Four, description of drawings
Fig. 1 is the hexafluorophosphoric acid Naferon SEM figure of Prepared by Sol Gel Method
Fig. 2 is the first charge-discharge curve of hexafluorophosphoric acid Naferon
Fig. 3 is the discharge cycles capacity of hexafluorophosphoric acid Naferon
Five, specific embodiments
Now provide with next specific embodiment, utilize sol-gel method to obtain hexafluorophosphoric acid Naferon positive electrode material.Present technique is mainly formed by colloidal sol, the wet gel preparation, and the xerogel preparation, several steps such as calcining are formed.
1. colloidal sol preparation
Use electronic analytical balance to take by weighing SODIUMNITRATE, iron nitrate, primary ammonium phosphate, each 0.01mol of Sodium Fluoride, mix, the 100ml dissolved in distilled water, glass stick stirred 20 minutes, add 1mol/L citric acid 10ml again, mixture is regulated pH value to 7 with the ammoniacal liquor of 50% (volume ratio).With mixture water-bath control reaction temperature is 80 ℃, does not stop therebetween to stir, and mixture will change into the scarlet vitreosol after 30 minutes.
2. xerogel preparation
After formation changes into the scarlet vitreosol, continue heating and formed the heavy-gravity gel in 40 minutes, taking-up was transferred in the vacuum drying oven, in 80 ℃ of vacuum-dryings 8 hours.Take out, use agate mortar grind 30 minutes powdered, stand-by.
3. calcining
Is the following 300 ℃ of following pre-burnings of 99.99% argon gas atmosphere 3 hours with the gained xerogel in the tube furnace moderate purity, continues to be heated to 750 ℃, is incubated 6 hours, cools to room temperature with the furnace and can get product.
In order to study the structure and the chemical property of the prepared hexafluorophosphoric acid Naferon of present technique, we take following experimental technique.
Hexafluorophosphoric acid Naferon to Prepared by Sol Gel Method carries out scanning electron microscopic observation, and as shown in Figure 1, even particle distribution, median size are 0.3 μ m, and ubiquity agglomeration between particle forms the coacervate of particle diameter about 6 μ m.The sample of preparation is assembled into Experimental cell as positive active material, and with the 20mA/g constant current charge-discharge, the first charge-discharge curve of gained as shown in Figure 2.Its charge and discharge platform is near 3.7V and 2.5V, and loading capacity is 91mAh/g first, than the material of solid phase method preparation first loading capacity exceed 31mAh/g.The increase of capacity first is because each coacervate is all formed by the small-particle accumulation of diameter in submicron, thereby make material have loose porous microtexture, this microtexture can allow material can fully contact with electrolytic solution in as electrode, thereby enlarge the ionic diffusion area, increase ion diffusion speed, improve radial diffusion coefficient, demonstrated better electrochemical performance.Fig. 3 is loading capacity and the cycle index graph of a relation of Prepared by Sol Gel Method hexafluorophosphoric acid Naferon under onesize current density, as seen from the figure, the loading capacity decay in initial circulation several times of this material is very fast, repeatedly after the circulation, cyclical stability increases, capacity attenuation is slow, and the loading capacity after 20 circulations maintains 81.7mAh/g, and capability retention is 89.78%.
Claims (1)
1. the preparation method of the sol-gel method of a hexafluorophosphoric acid Naferon that is used for sodium-ion battery; it is characterized in that; with SODIUMNITRATE; iron nitrate; primary ammonium phosphate; Sodium Fluoride is dissolved in the 500-1000ml distilled water by the mixed of 0.1mol: 0.1mol: 0.1mol: 0.1mol and forms mixed aqueous solution; the citric acid of 0.05～0.1mol is dissolved in the 500ml distilled water in advance forms citric acid solution; join then in the above-mentioned mixed aqueous solution and form mixing solutions; ammoniacal liquor with 50% volume ratio joins adjusting pH value 7～8 in the mixing solutions again; 80 ℃ of temperature of reaction; after changing into the scarlet vitreosol; continue heating and formed the heavy-gravity gel in 40 minutes; taking-up is transferred in the vacuum drying oven; in 80 ℃ of dryings 8 hours; obtain the chocolate floss, agate mortar grinds, and takes out in 3 hours in 300 ℃ of following pre-burnings in the hydrogen atmosphere in tube furnace; make the disk shape with tabletting machine; continuation is 750 ℃ of calcination under hydrogen shield, are incubated 6 hours, are chilled to room temperature with stove and obtain the hexafluorophosphoric acid Naferon.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100968732A CN100457608C (en) | 2006-10-23 | 2006-10-23 | Sol-gel method of ferresodium flurophosphate for sodium ion battery |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2006100968732A CN100457608C (en) | 2006-10-23 | 2006-10-23 | Sol-gel method of ferresodium flurophosphate for sodium ion battery |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1948137A CN1948137A (en) | 2007-04-18 |
| CN100457608C true CN100457608C (en) | 2009-02-04 |
Family
ID=38017782
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2006100968732A Expired - Fee Related CN100457608C (en) | 2006-10-23 | 2006-10-23 | Sol-gel method of ferresodium flurophosphate for sodium ion battery |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100457608C (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105428649A (en) * | 2015-12-09 | 2016-03-23 | 天津大学 | Nano-carbon coated sodium ferrous fluorophosphates and preparation method of hydrothermal method |
| CN105810902B (en) * | 2016-03-11 | 2018-09-04 | 天津大学 | A kind of method of solvent hot preparation nano-carbon coated fluorophosphoric acid Naferon |
| CN107658438A (en) * | 2017-08-29 | 2018-02-02 | 天津大学 | Prepare fluorophosphoric acid Naferon porous spongy structural material and method |
| CN110299528B (en) * | 2019-07-02 | 2020-12-25 | 中南大学 | Fluorinated phosphate ferric sodium pyrophosphate @ C @ RGO composite material, preparation method thereof and application thereof in sodium ion battery |
| CN116081594B (en) * | 2023-02-23 | 2024-07-09 | 武汉工程大学 | Preparation method of sodium ion battery anode material |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1630126A (en) * | 2004-10-11 | 2005-06-22 | 湘潭大学 | sodium ion battery and method for manufacturing the same |
| US20050142056A1 (en) * | 2000-04-27 | 2005-06-30 | Jeremy Barker | Lithium metal fluorophosphate and preparation thereof |
| CN1723578A (en) * | 2001-04-06 | 2006-01-18 | 威伦斯技术公司 | Sodium ion batteries |
-
2006
- 2006-10-23 CN CNB2006100968732A patent/CN100457608C/en not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050142056A1 (en) * | 2000-04-27 | 2005-06-30 | Jeremy Barker | Lithium metal fluorophosphate and preparation thereof |
| CN1723578A (en) * | 2001-04-06 | 2006-01-18 | 威伦斯技术公司 | Sodium ion batteries |
| CN1630126A (en) * | 2004-10-11 | 2005-06-22 | 湘潭大学 | sodium ion battery and method for manufacturing the same |
Non-Patent Citations (4)
| Title |
|---|
| A Sodium-Ion Cell Based on the FluorophosphateCompoundNaVPO4F. J. Barker, M. Y. Saidi and J. L. Swoyer.Electrochemical and Solid-State Letters,No.6. 2003 |
| A Sodium-Ion Cell Based on the FluorophosphateCompoundNaVPO4F. J. Barker, M. Y. Saidi and J. L. Swoyer.Electrochemical and Solid-State Letters,No.6. 2003 * |
| High capacity anode materials for rechargeablesodium-ionbatteries. D. A. Stevens, J. R. Dahn.J. Electrochem. soc.,Vol.147 No.4. 2000 |
| High capacity anode materials for rechargeablesodium-ionbatteries. D. A. Stevens, J. R. Dahn.J. Electrochem. soc.,Vol.147 No.4. 2000 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1948137A (en) | 2007-04-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN102738465B (en) | Preparation method of lithium iron manganese phosphate cathode composite material | |
| CN100448071C (en) | Lithium battery positive electrode material and preparation method thereof | |
| CN103956485B (en) | Lithium iron phosphate electrode material of a kind of three-dimensional hierarchical structure and preparation method thereof | |
| CN105428648B (en) | A kind of preparation method of battery anode material of lithium iron phosphate | |
| CN101826617B (en) | Preparation method of lithium iron phosphate | |
| CN101504979A (en) | A novel preparation method for LiFePO4/C composite positive pole material | |
| CN101013751A (en) | Ball-shaped lithium-ion battery anode material doped with rare earth and method for making same | |
| CN101752562B (en) | Compound doped modified lithium ion battery anode material and preparation method thereof | |
| CN102306772A (en) | Method for preparing fluorine sodium ferrous phosphate positive electrode material of mixed ion battery | |
| CN105977458A (en) | Nano diamond powder and graphene composite electrode material and preparation method thereof | |
| CN103078113A (en) | Vanadium-titanium ion-codoped lithium iron phosphate material and preparation method thereof | |
| CN101673819A (en) | Method for preparing manganese lithium phosphate/carbon composite material by manganese phosphate | |
| CN101913655A (en) | Method for preparing lithium manganate cathode material by microwave sintering | |
| CN102104143A (en) | Hydrothermal synthesis method of composite material for high-performance power battery | |
| CN102208647A (en) | Lithium ferrous silicate anode material coated with crystalline carbon and preparation method thereof | |
| CN102097616A (en) | Preparation method of high-energy and high-power density nano-scale lithium iron phosphate powder | |
| CN107221664A (en) | Carbon coating ferric phosphate soda-lime glass ceramic composite and preparation method thereof and it is used as the application of secondary battery positive electrode material | |
| CN103531794B (en) | Lithium ferrous phosphate as anode material of lithium ion battery and preparation method thereof | |
| CN100457608C (en) | Sol-gel method of ferresodium flurophosphate for sodium ion battery | |
| CN102945953A (en) | Novel preparation method of high temperature-type long-life lithium ion battery anode material LiMn2-x-yMIxMIIyO4 | |
| CN110620217A (en) | Zinc-doped lithium iron phosphate/carbon composite material and preparation method thereof | |
| CN102332582B (en) | Preparation method for novel lithium vanadium phosphate/bamboo charcoal composite cathode material | |
| CN103515600A (en) | Ti3SiC2 and carbon composite modified LiFePO4 lithium ion battery anode material and preparation method thereof | |
| CN103117391A (en) | Preparation method of molybdenum-doped carbon-coated lithium iron phosphate, namely positive electrode material | |
| CN1948138A (en) | High temperature solid phase method of ferrosodium flurophosphate for sodium ion battery |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| EE01 | Entry into force of recordation of patent licensing contract |
Assignee: Jiangsu King Lithium Cell Co.,Ltd. Assignor: Nanjing University of Aeronautics and Astronautics Contract record no.: 2012320000220 Denomination of invention: Sol-gel method of ferresodium flurophosphate for sodium ion battery Granted publication date: 20090204 License type: Exclusive License Open date: 20070418 Record date: 20120314 |
|
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20090204 Termination date: 20161023 |
|
| CF01 | Termination of patent right due to non-payment of annual fee |