US20160126540A1 - Lithium ionic energy storage element and method for making the same - Google Patents
Lithium ionic energy storage element and method for making the same Download PDFInfo
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- US20160126540A1 US20160126540A1 US14/798,004 US201514798004A US2016126540A1 US 20160126540 A1 US20160126540 A1 US 20160126540A1 US 201514798004 A US201514798004 A US 201514798004A US 2016126540 A1 US2016126540 A1 US 2016126540A1
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- Prior art keywords
- lithium
- positive electrode
- active substance
- carbon
- energy storage
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- 229910052744 lithium Inorganic materials 0.000 title claims abstract description 75
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 title claims abstract description 69
- 238000004146 energy storage Methods 0.000 title claims abstract description 36
- 238000000034 method Methods 0.000 title claims abstract description 25
- 239000013543 active substance Substances 0.000 claims abstract description 90
- HPGPEWYJWRWDTP-UHFFFAOYSA-N lithium peroxide Chemical compound [Li+].[Li+].[O-][O-] HPGPEWYJWRWDTP-UHFFFAOYSA-N 0.000 claims abstract description 79
- 229910001416 lithium ion Inorganic materials 0.000 claims abstract description 53
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 51
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 claims abstract description 40
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 40
- 239000000463 material Substances 0.000 claims abstract description 34
- 239000003792 electrolyte Substances 0.000 claims abstract description 26
- FUJCRWPEOMXPAD-UHFFFAOYSA-N lithium oxide Chemical compound [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 claims abstract description 25
- 229910001947 lithium oxide Inorganic materials 0.000 claims abstract description 25
- 239000000203 mixture Substances 0.000 claims abstract description 13
- 229910000676 Si alloy Inorganic materials 0.000 claims abstract description 7
- 229910001128 Sn alloy Inorganic materials 0.000 claims abstract description 7
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 74
- 238000002156 mixing Methods 0.000 claims description 36
- YQCIWBXEVYWRCW-UHFFFAOYSA-N methane;sulfane Chemical compound C.S YQCIWBXEVYWRCW-UHFFFAOYSA-N 0.000 claims description 29
- 239000002131 composite material Substances 0.000 claims description 28
- ZUHZGEOKBKGPSW-UHFFFAOYSA-N tetraglyme Chemical compound COCCOCCOCCOCCOC ZUHZGEOKBKGPSW-UHFFFAOYSA-N 0.000 claims description 20
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 claims description 15
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims description 15
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims description 14
- 229910044991 metal oxide Inorganic materials 0.000 claims description 13
- 239000011230 binding agent Substances 0.000 claims description 12
- 239000006229 carbon black Substances 0.000 claims description 12
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 claims description 12
- WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 claims description 11
- 229910002804 graphite Inorganic materials 0.000 claims description 11
- 239000010439 graphite Substances 0.000 claims description 11
- 229910001290 LiPF6 Inorganic materials 0.000 claims description 8
- 239000002033 PVDF binder Substances 0.000 claims description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 239000001301 oxygen Substances 0.000 claims description 8
- 229920002981 polyvinylidene fluoride Polymers 0.000 claims description 8
- 239000011248 coating agent Substances 0.000 claims description 7
- 238000000576 coating method Methods 0.000 claims description 7
- 239000002270 dispersing agent Substances 0.000 claims description 7
- 229910052782 aluminium Inorganic materials 0.000 claims description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 6
- 239000011888 foil Substances 0.000 claims description 6
- 150000003949 imides Chemical class 0.000 claims description 6
- 229910021385 hard carbon Inorganic materials 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 239000011593 sulfur Substances 0.000 claims description 5
- 239000002946 graphitized mesocarbon microbead Substances 0.000 claims description 4
- 229920002134 Carboxymethyl cellulose Polymers 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 238000011049 filling Methods 0.000 claims description 3
- 239000001768 carboxy methyl cellulose Substances 0.000 claims 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 claims 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 claims 1
- 238000007600 charging Methods 0.000 description 46
- 238000007599 discharging Methods 0.000 description 46
- 229910001323 Li2O2 Inorganic materials 0.000 description 25
- 239000002931 mesocarbon microbead Substances 0.000 description 19
- 238000012360 testing method Methods 0.000 description 9
- 239000002002 slurry Substances 0.000 description 8
- 238000002441 X-ray diffraction Methods 0.000 description 6
- 238000007086 side reaction Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000002484 cyclic voltammetry Methods 0.000 description 3
- 238000010325 electrochemical charging Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000007774 positive electrode material Substances 0.000 description 3
- VJHCJDRQFCCTHL-UHFFFAOYSA-N acetic acid 2,3,4,5,6-pentahydroxyhexanal Chemical compound CC(O)=O.OCC(O)C(O)C(O)C(O)C=O VJHCJDRQFCCTHL-UHFFFAOYSA-N 0.000 description 2
- YHWCPXVTRSHPNY-UHFFFAOYSA-N butan-1-olate;titanium(4+) Chemical compound [Ti+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] YHWCPXVTRSHPNY-UHFFFAOYSA-N 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- GNTDGMZSJNCJKK-UHFFFAOYSA-N divanadium pentaoxide Chemical compound O=[V](=O)O[V](=O)=O GNTDGMZSJNCJKK-UHFFFAOYSA-N 0.000 description 2
- 238000009713 electroplating Methods 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 238000009830 intercalation Methods 0.000 description 2
- 150000002641 lithium Chemical class 0.000 description 2
- 238000004088 simulation Methods 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- -1 LiPF6 Chemical class 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 230000002687 intercalation Effects 0.000 description 1
- 230000016507 interphase Effects 0.000 description 1
- WBJZTOZJJYAKHQ-UHFFFAOYSA-K iron(3+) phosphate Chemical compound [Fe+3].[O-]P([O-])([O-])=O WBJZTOZJJYAKHQ-UHFFFAOYSA-K 0.000 description 1
- 229910000399 iron(III) phosphate Inorganic materials 0.000 description 1
- SHXXPRJOPFJRHA-UHFFFAOYSA-K iron(iii) fluoride Chemical compound F[Fe](F)F SHXXPRJOPFJRHA-UHFFFAOYSA-K 0.000 description 1
- 229910000625 lithium cobalt oxide Inorganic materials 0.000 description 1
- 229910002102 lithium manganese oxide Inorganic materials 0.000 description 1
- MHCFAGZWMAWTNR-UHFFFAOYSA-M lithium perchlorate Chemical compound [Li+].[O-]Cl(=O)(=O)=O MHCFAGZWMAWTNR-UHFFFAOYSA-M 0.000 description 1
- 229910001486 lithium perchlorate Inorganic materials 0.000 description 1
- 229910001496 lithium tetrafluoroborate Inorganic materials 0.000 description 1
- BFZPBUKRYWOWDV-UHFFFAOYSA-N lithium;oxido(oxo)cobalt Chemical compound [Li+].[O-][Co]=O BFZPBUKRYWOWDV-UHFFFAOYSA-N 0.000 description 1
- VLXXBCXTUVRROQ-UHFFFAOYSA-N lithium;oxido-oxo-(oxomanganiooxy)manganese Chemical compound [Li+].[O-][Mn](=O)O[Mn]=O VLXXBCXTUVRROQ-UHFFFAOYSA-N 0.000 description 1
- URIIGZKXFBNRAU-UHFFFAOYSA-N lithium;oxonickel Chemical compound [Li].[Ni]=O URIIGZKXFBNRAU-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000007773 negative electrode material Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000006479 redox reaction Methods 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000007784 solid electrolyte Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Images
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- H01M4/525—Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
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Definitions
- the invention relates to a lithium ionic energy storage element, in particular to a lithium ionic energy storage element comprising a positive electrode active substance including a lithium ion donor and a positive electrode frame active substance.
- lithium ionic batteries are regarded as a portable chemical power source with a high efficiency in next generation because they have advantages of high energy density, light weight and less pollution.
- the lithium ionic batteries are widely used in the fields of digital cameras, smart phones and notebooks. As the energy density of the lithium ionic battery is enhanced, the fields of use are extended. There is a higher need for the performance of the lithium ionic battery as the requirement of high capacity and long life of the lithium ionic battery for the mobile electric equipment is increased
- a lithium ionic battery comprises a negative electrode, a positive electrode and an electrolyte.
- the positive electrode active substance is not only used as an electrode material to take part in the chemical reaction, but also used as a lithium source.
- the positive electrode active substance is generally lithium metallic oxides which contain lithium atoms intercalated therein.
- lithium metallic oxides such as lithium cobalt oxide, lithium nickel oxide and lithium manganese oxide are available commercially.
- the above lithium metallic oxides cannot exhibit a proper combinative property of high initial electrical capacity, high thermal stability and excellent electrical capacity sustainability after a lithium ionic battery is charged and discharged repeatedly.
- the lithium ionic battery is limited by the capacity capacity (mA/g) of the positive electrode of the lithium metallic oxides, so that it cannot exhibit a higher capacitycapacity. Therefore, the lithium sources have to be increased if it is desired to increase the capacity of the lithium ionic battery.
- Several methods were proposed, wherein one of the methods is coating lithium metal used as lithium source on the negative electrode, and another method is forming lithium metal as a third electrode on the negative electrode by electroplating.
- the above two methods are difficult to perform and the coating and electroplating film are not uniform because the lithium metal is very active.
- lithium metal has disadvantages of safety and stability
- the current commercial lithium ion secondary battery is used a working system having a positive electrode material containing lithium ions and a negative electrode material for intercalating lithium ions.
- the energy density of the lithium ion secondary battery has to be enhanced, because the electric devices have a large energy demand.
- the stability of the positive electrode material structure is not high and the amount of lithium ions intercalation is not large, so that the capacity per gram cannot be further enhanced.
- FeF 3 , FePO 4 and V 2 O 5 were proposed.
- the above materials are preferable to be the positive electrode material for a high energy density, because they have good electrical capacity and a higher platform voltage.
- the above materials do not contain lithium ions, so they have to combine with lithium metal. As a result, they would be only used in half cell tests but fail to be used in a full cell.
- the present invention provides a lithium ionic energy storage element comprising a positive electrode having a first current collector and a positive electrode active substance provided on the first current collector; a negative electrode having a second current collector and a negative electrode active substance provided on the second current collector, wherein the negative electrode active substance is a material selected from the group consisting of carbon-containing materials, Si alloy and Sn alloy; and an electrolyte, wherein the positive electrode active substance comprises a lithium ion donor including lithium peroxide, lithium oxide or the mixture thereof and a positive electrode frame active substance.
- the present invention also relates to a positive electrode active substance used in a lithium ionic energy storage element, the positive electrode active substance comprising a lithium ion donor and a positive electrode frame active substance, wherein the lithium ion donor includes lithium peroxide, lithium oxide or a combination of lithium peroxide and lithium oxide; and the positive electrode frame active substance is a material selected from the group consisting of anatase titanium dioxide, carbon-sulfur composite, carbon-containing materials and carbon fluoride or is lithium metallic oxides.
- the present invention also relates to a method for making a lithium ionic energy storage element.
- a positive electrode frame active substance e.g. anatase titanium dioxide and a binder, e.g. PVDF are mixed with a predetermined weight ratio to form a mixture, and the mixture is added into a dispersant, e.g. N-methyl-2-pyrrolidone to form a slurry.
- a dispersant e.g. N-methyl-2-pyrrolidone
- the slurry is coating on an aluminum foil to form a film by a blade coater.
- the film is baked in an oven at a temperature of 80-90° C. to remove a solvent, and raise the temperature to 120-130° C.
- conductive carbon for example super P carbon black, KS6 graphite or a combination thereof may be added.
- a lithium ionic energy storage element is formed by assembling the positive electrode with lithium peroxide/anatase titanium dioxide, a negative electrode having a negative electrode active substance, e.g. graphitized mesocarbon microbeads (MCMB) and a porous separate strip interposed between the positive electrode and the negative electrode, and an electrolyte, e.g. a concentration of 1M LiPF 6 dissolving in a mixing solution of ethylene carbonate (EC) and diethyl carbonate (DEC) with mixing ratio 1:1 by volume is filled into the porous separate strip.
- MCMB graphitized mesocarbon microbeads
- the present invention relates to a method for making a lithium ionic energy storage element.
- a positive electrode frame active substance e.g. carbon-sulfur composite and a binder, e.g. carboxymethyl cellulose (CMC) are mixed with a predetermined weight ratio to form a mixture, and the mixture is added into a dispersant, e.g. N-methyl-2-pyrrolidone to form a slurry.
- the slurry is coating on an aluminum foil to form a film by a blade coater.
- the film is baked in an oven at a temperature of 80-90° C. to remove a solvent, and raise the temperature to 120-130° C. for a period of time to form a positive electrode with lithium peroxide/carbon-sulfur composite.
- conductive carbon for example super P carbon black, KS6 graphite or a combination thereof may be added.
- a lithium ionic energy storage element is formed by assembling the positive electrode with lithium peroxide/carbon-sulfur composite, a negative electrode having a negative electrode active substance, e.g. hard carbon and a porous separate strip interposed between the positive electrode and the negative electrode, and an electrolyte, e.g. a concentration of 1M lithium bis(trifluoromethanesulfonly)imide dissolving in a mixing solution of tetraethylene glycol dimethyl ether (TEGDME) and 1,3-dioxolane (DOL) with mixing ratio 1:1 by volume is filled into the porous separate strip.
- TEGDME tetraethylene glycol dimethyl ether
- DOL 1,3-dioxolane
- the lithium ionic energy storage element of the present invention comprises a lithium ion donor having lithium peroxide and/or lithium oxide and a positive electrode frame active substance, wherein lithium peroxide and/or lithium oxide can be decomposed to produce lithium ions by electrochemical charging, and lithium ions intercalate repeatedly in and out of the positive electrode frame active substance and the negative electrode active substance in a full cell.
- the full cell can exhibit a high capacity.
- FIG. 1 shows a schematic view of a unit cell structure of a lithium ionic energy storage element an embodiment according to the invention.
- FIG. 2 shows a first cycle curve of voltage against electric capacity of a half cell of lithium peroxide charging/discharging of the invention.
- FIG. 3 shows a second cycle and a third cycle curves of voltage against electric capacity of a half cell of lithium peroxide charging/discharging of the invention.
- FIG. 4 shows a first cycle curve of voltage against electric capacity of a half cell of lithium peroxide charging/discharging under various ratio of a conductive carbon of the invention.
- FIG. 5 shows cyclic voltammetry response of lithium peroxide charging/discharging under various ratio of a conductive carbon of the invention.
- FIG. 6 shows the influent of voltage against electric capacity of lithium peroxide in the different current density.
- FIG. 7( a ) shows XRD pattern of TiO 2 synthetized from tetrabutyl titanate of the invention.
- FIG. 7( b ) shows XRD pattern of TiO 2 by simulation.
- FIG. 8 shows a charging/discharging curve of prelithiation period of Li 2 O 2 /TiO 2 half cell.
- FIG. 9 shows a charging/discharging curve of subsequent cycles of Li 2 O 2 /TiO 2 half cell.
- FIG. 10 shows a charging/discharging curve of prelithiation period of Li 2 O 2 /TiO 2 versus MCMB full cell.
- FIG. 11 shows a charging/discharging curve of subsequent cycles of Li 2 O 2 /TiO 2 versus MCMB full cell.
- FIG. 12 shows a charge/discharge curve of prelithiation period of Li 2 O 2 /TiO 2 versus MCMB with disassembling process of coin cell.
- FIG. 13 shows a charge/discharge curve of subsequent cycles of Li 2 O 2 /TiO 2 versus MCMB with disassembling process of coin cell.
- FIG. 14 shows a charging/discharging curve of Li 2 O 2 (30 wt. %) with current density of 100 mA/g Li 2 O 2 vs. Li metal of half cell.
- FIG. 15 shows a charge/discharge curve of carbon-sulfur composite of half cell.
- FIG. 16 shows a charge/discharge curve of prelithiation period of lithium peroxide/carbon-sulfur composite vs. Li/Li + of half cell.
- FIG. 1 shows a schematic view of a unit cell structure of a lithium ionic energy storage element an embodiment according to the invention.
- the lithium ionic energy storage element comprises a plurality of unit cell structures 100 , each unit cell structure 100 comprises a porous separate strip 104 interposed between the positive electrode 106 and the negative electrode 108 .
- the porous separate strip 104 is coated with a binder 105 to enhance the binding of the cell structure's 100 components to each other.
- the positive electrode 106 has a first current collector 110 and a positive electrode active substance 114 provided on the first current collector 110 and the negative electrode 108 has a second current collector 112 and a negative electrode active substance 116 provided on the second current collector 112 .
- the positive electrode active substance 114 comprises a lithium ion donor including lithium peroxide, lithium oxide or a combination thereof and a positive electrode frame active substance, e.g. anatase titanium dioxide or carbon-sulfur composite.
- the carbon-sulfur composite has a weight ratio of carbon with sulfur is 0.4-1.
- the negative electrode active substance 116 may be carbon-containing materials, e.g. graphitized mesocarbon microbeads (MCMB).
- MCMB graphitized mesocarbon microbeads
- the negative electrode active substance 116 may be carbon-containing materials, e.g. hard carbon.
- the positive electrode active substance 114 used in a lithium ionic energy storage element comprising a lithium ion donor and a positive electrode frame active substance, wherein the lithium ion donor includes lithium peroxide, lithium oxide or a combination of lithium peroxide and lithium oxide; and the positive electrode frame active substance is a material selected from the group consisting of anatase titanium dioxide, carbon-sulfur composite, carbon-containing materials and carbon fluoride or is lithium metallic oxides.
- the lithium ion donor of the invention may include but not be limited to lithium peroxide.
- lithium oxide is also suitable to be the lithium ion donor.
- lithium peroxide and lithium oxide are mixed for the use.
- the positive electrode frame active substance may use carbon-containing material, and thus both of the positive electrode and negative electrode use carbon-containing materials to form lithium ion electric capacity accordingly.
- Carbon fluorides (CF x ) that have a high mass capacity ratio are suitable to be the positive electrode frame active substance of the invention.
- Si alloy or Sn alloy that has a very high theoretical electrical capacity is also suitable to be negative electrode active substance 116 of the invention.
- An electrolyte that is suitable to a lithium ionic energy storage element with lithium peroxide/anatase titanium dioxide system comprises an inorganic compound such as LiPF 6 , LiClO 4 or LiBF 4 and an organic solvent that is a material selected from the group consisting of ethylene carbonate (EC) and diethyl carbonate (DEC).
- an electrolyte comprises a concentration of 1M lithium bis(trifluoromethanesulfonly)imide dissolving in a mixing solution of tetraethylene glycol dimethyl ether (EGDME) and 1,3-dioxolane (DOL) with mixing ratio 1:1 by volume that is suitable to a lithium ionic energy storage element with lithium peroxide/carbon-sulfur system.
- lithium peroxide of the positive electrode active substance 114 is decomposed to lithium ions and oxygen to intercalate into carbon-containing materials of the negative electrode 108 when unit cell is charged, and the lithium ions located in the negative electrode 108 diffuse to the positive electrode 106 and intercalate in the positive electrode active substance through the electrolyte when unit cell is discharged.
- the lithium ionic energy storage element of the present invention comprises a lithium ion donor having lithium peroxide and/or lithium oxide and a positive electrode frame active substance, wherein lithium peroxide and/or lithium oxide can be decomposed to produce lithium ions by electrochemical charging, and lithium ions intercalate repeatedly in and out of the positive electrode frame active substance and the negative electrode active substance in a full cell without containing Li ions. Because the conductivity of lithium peroxide is not high, a conductive carbon may be added to enhance the conductivity of lithium peroxide.
- the present invention provides a method for making a lithium ionic energy storage element.
- a positive electrode frame active substance e.g. anatase titanium dioxide, a conductive carbon, for example super P carbon black, KS6 graphite or a combination thereof and a binder, e.g. PVDF are mixed with a predetermined weight ratio to form a mixture, and the mixture is added into a dispersant, e.g. N-methyl-2-pyrrolidone (NMP) to form a slurry.
- NMP N-methyl-2-pyrrolidone
- the slurry is coating on an aluminum foil to form a film by a blade coater.
- the film is baked in an oven at a temperature of 80° C. for 6 hours to remove a solvent, and raise the temperature to 120° C. for 4-6 hours to form a positive electrode with lithium peroxide/anatase titanium dioxide.
- a lithium ionic energy storage element is formed by assembling the positive electrode with lithium peroxide/anatase titanium dioxide, a negative electrode having a negative electrode active substance, e.g. graphitized mesocarbon microbeads (MCMB) and a porous separate strip interposed between the positive electrode and the negative electrode, and an electrolyte, e.g. a concentration of 1M LiPF 6 dissolving in a mixing solution of ethylene carbonate (EC) and diethyl carbonate (DEC) with mixing ratio 1:1 by volume is filled into the porous separate strip.
- the lithium ion donor of the invention may include but not be limited to lithium peroxide.
- lithium oxide is also suitable to be the lithium ion donor.
- the positive electrode frame active substance may use carbon-containing material, and thus both of the positive electrode and negative electrode use carbon-containing materials to form a lithium ion electric capacity accordingly.
- Carbon fluorides (CFx) that have a high mass capacity ratio are suitable to be the positive electrode frame active substance of the invention.
- Si alloy or Sn alloy that has a very high theoretical electrical capacity is also suitable to be negative electrode active substance 116 of the invention.
- the present invention relates to a method for making a lithium ionic energy storage element.
- a positive electrode frame active substance e.g. carbon-sulfur composite, a conductive carbon, for example super P carbon black, KS 6 graphite or a combination thereof and a binder, e.g. carboxymethyl cellulose (CMC) are mixed with a predetermined weight ratio to form a mixture, and the mixture is added into a dispersant, e.g. N-methyl-2-pyrrolidone to form a slurry.
- the slurry is coating on an aluminum foil to form a film by a blade coater.
- the film is baked in an oven at a temperature of 80-90° C. to remove a solvent, and raise the temperature to 120-130° C. for a period of time to form a positive electrode with lithium peroxide/carbon-sulfur composite.
- the lithium ion donor of the invention may include but not be limited to lithium peroxide.
- lithium oxide is also suitable to be the lithium ion donor.
- lithium peroxide and lithium oxide are mixed for the use.
- the positive electrode frame active substance may use carbon-containing material, and thus both of the positive electrode and negative electrode use carbon-containing materials to form a lithium ion electric capacity accordingly.
- Carbon fluorides (CFx) that have a high mass capacity ratio are suitable to be the positive electrode frame active substance of the invention.
- Si alloy or Sn alloy that has a very high theoretical electrical capacity is also suitable to be negative electrode active substance 116 of the invention.
- a lithium ionic energy storage element is formed by assembling the positive electrode with lithium peroxide/carbon-sulfur composite, a negative electrode having a negative electrode active substance, e.g. hard carbon and a porous separate strip interposed between the positive electrode and the negative electrode, and an electrolyte, e.g. a concentration of 1M lithium bis(trifluoromethanesulfonly)imide dissolving in a mixing solution of tetraethylene glycol dimethyl ether (TEGDME) and 1,3-dioxolane (DOL) with mixing ratio 1:1 by volume is filled into the porous separate strip.
- TEGDME tetraethylene glycol dimethyl ether
- DOL 1,3-dioxolane
- FIG. 2 shows a first cycle curve of voltage against electric capacity of a half cell of lithium peroxide charging/discharging of the invention.
- FIG. 3 shows a second cycle and a third cycle curves of voltage against electric capacity of a half cell of lithium peroxide charging/discharging of the invention.
- a half cell that is used for test is formed by assembling a positive electrode formed with mixing lithium peroxide, super P carbon black and PVDF by weight ratio of 10:80:10; and a porous separate strip filled with an electrolyte, e.g. a concentration of 1M LiPF 6 dissolving in a mixing solution of ethylene carbonate (EC) and diethyl carbonate (DEC) with mixing ratio 1:1 by volume.
- Conditions of operation comprise charging/discharging current of 100 mA/g Li 2 O 2 and charging/discharging voltage of 2-4.6V.
- FIG. 4 shows a first cycle curve of voltage against electric capacity of a half cell of lithium peroxide charging/discharging under various ratio of a conductive carbon of the invention.
- Conditions of operation comprise charging/discharging current of 10 mA/g Li2O2 and charging/discharging voltage of 2-4.8V.
- FIG. 5 shows cyclic voltammetry response of lithium peroxide charging/discharging under various ratio of a conductive carbon of the invention.
- Condition of operation comprises a scan rate of cyclic voltammetry of 0.4 mV/s. The resultant current is 0 mA in the different voltage.
- FIG. 6 shows the influent of voltage against electric capacity of lithium peroxide in the different current density.
- a half cell that is used for test is formed by assembling a positive electrode formed with mixing lithium peroxide, a conductive carbon (super P carbon black and KS6 graphite with mixing ratio 1:1 by weight) and PVDF by weight ratio of 30:60:10; and a porous separate strip filled with an electrolyte, e.g. a concentration of 1M LiPF6 dissolving in a mixing solution of ethylene carbonate (EC) and diethyl carbonate (DEC) with mixing ratio 1:1 by volume.
- EC ethylene carbonate
- DEC diethyl carbonate
- Conditions of operation comprise charging/discharging current of 10 mA/g Li 2 O 2 , 30 mA/g Li 2 O 2 and 50 mA/g Li 2 O 2 and charging/discharging voltage of 2-4.8V.
- FIG. 7( a ) shows XRD pattern of TiO 2 synthetized from tetrabutyl titanate of the invention.
- FIG. 7( b ) shows XRD pattern of TiO 2 by simulation. An error of degree (2 ⁇ ) of XRD pattern of TiO 2 of FIG. 7( a ) is obtained within 3% compared with XRD pattern of TiO 2 of FIG. 7( b ) .
- lithium peroxide of the positive electrode is a functional material for use in one time, i.e. only may be decomposed by charging in one time. Therefore, another positive electrode active substance, for example anatase titanium dioxide or carbon-sulfur composite is required to use for receiving Li ions that may diffuse to the positive electrode from the negative electrode in a discharging process.
- another positive electrode active substance for example anatase titanium dioxide or carbon-sulfur composite is required to use for receiving Li ions that may diffuse to the positive electrode from the negative electrode in a discharging process.
- the initial lithium peroxide may be decomposed to produce Li ions by charging of the invention that is called as a charging period of prelithiation, and Li ions diffuse to the positive electrode from the negative electrode by discharging that is called as a discharging period of prelithiation.
- the subsequent Li ions intercalate in and out in the positive electrode and negative electrode that is called as a regular working system.
- FIG. 8 shows a charging/discharging curve of prelithiation period of Li 2 O 2 /TiO 2 half cell.
- FIG. 9 shows a charging/discharging curve of subsequent cycles of Li 2 O 2 /TiO 2 half cell.
- lithium peroxide may be charged to 4.8V against Li/Li + by applying the current density of 50 mA/gLi 2 O 2 .
- the resultant charging/discharging curves of half cells are shown in FIG.
- FIG. 8 shows a charging curve of Li 2 O 2 with electric capacity of 365 mA/gLi 2 O 2 during charging period of prelithiation and a discharing curve of TiO 2 with two discharging platforms of 1.8V and 2.7V during discharging period of prelithiation, wherein the discharging platform of 2.7V has electric capacity of 100 mAh/gTiO 2 that may be an oxidation-reduction reaction or regeneration of lithium peroxide, and it is regarded as a side reaction, i.e. the additional electric capacity may not belong to TiO 2 .
- the resultant electric capacity may be about 280 mAh/gTiO 2 after 100 mAh/gTiO 2 of the electric capacity of the side reaction is deducted from 380 mAh/gTiO 2 .
- FIG. 10 shows a charging/discharging curve of prelithiation period of Li 2 O 2 /TiO 2 versus MCMB full cell.
- FIG. 11 shows a charging/discharging curve of subsequent cycles of Li 2 O 2 /TiO 2 versus MCMB full cell.
- the weight of each Li 2 O 2 , super P carbon black and KS graphite is 0.4219 g (22%) and the weight of PVDF is 0.1406 g (7%) and the weight of titanium dioxide is 0.4858 g (27%).
- lithium peroxide may be charged to 4.8V against MCMB by applying the current density of 50 mA/gLi 2 O 2 .
- the resultant charging/discharging curves of half cells are shown in FIG. 10 and FIG. 11 .
- Li ions prelithiation in the positive is successful.
- oxygen is produced in the process, and will affect the electrochemical performance. It is important to have an oxygen removal step for removing oxygen produced in a first cycle of charge and discharge the lithium ionic energy storage element.
- a battery active step is performed in a first cycle of charging and discharging the lithium ionic battery after filling the electrolyte into the porous separate strip to form a solid electrolyte interphase (SEI) on the negative electrode, and the electrolyte decomposes in part at the same time.
- SEI solid electrolyte interphase
- FIG. 12 shows a charge/discharge curve of prelithiation period of Li 2 O 2 /TiO 2 versus MCMB with disassembling process of coin cell
- FIG. 13 shows a charge/discharge curve of subsequent cycles of Li 2 O 2 /TiO 2 versus MCMB with disassembling process of coin cell. The effect of removing oxygen is not obvious from FIG. 12 .
- carbon-sulfur composite may be used for the positive electrode frame active substance of the positive electrode active substance.
- Lithium peroxide is mixed with carbon-sulfur composite to replace Li metal.
- a full cell is assembled by the positive electrode having the positive electrode active substance comprising lithium peroxide and carbon-sulfur composite and the negative electrode having the negative electrode active substance comprising hard carbon.
- Li-sulfur battery uses ethers as an electrolyte
- a half cell that is used for test is formed by assembling a positive electrode formed with mixing lithium peroxide, a conductive carbon and binder by weight ratio of 30:60:10; and a porous separate strip filled with an electrolyte, e.g. a concentration of 1M lithium bis(trifluoromethanesulfonly)imide dissolving in a mixing solution of tetraethylene glycol dimethyl ether (TEGDME) and 1,3-dioxolane (DOL) with mixing ratio 1:1 by volume.
- TEGDME tetraethylene glycol dimethyl ether
- DOL 1,3-dioxolane
- Conditions of operation comprise charging/discharging current density of 100 mA/g Li 2 O 2 vs. Li metal and charging/discharging voltage of 2-4.3V in the embodiment, shown as FIG. 14 .
- the cut off voltage of charging is 4.3V.
- the half cell is charged for 9 hours by 100 mA/gLi 2 O 2 after testing. It can be found the decomposition of lithium peroxide in Li-sulfur battery electrolyte system has the overpotential about 4.1V and the resultant electric capacity about 980 mAh/gLi 2 O 2 .
- FIG. 15 shows a charge/discharge curve of carbon-sulfur composite of half cell.
- the carbon-sulfur composite of the half cell has a weight ratio of carbon with sulfur is 0.4-1.
- FIG. 16 shows a charge/discharge curve of prelithiation period of lithium peroxide/carbon-sulfur composite vs. Li/Li + of half cell.
- a half cell that is used for test is formed by assembling a positive electrode formed with mixing lithium peroxide/carbon-sulfur composite, a conductive carbon and a binder dissolving in a dispersant of N-methyl-2-pyrrolidone; and a porous separate strip filled with an electrolyte, e.g.
- lithium bis(trifluoromethanesulfonly)imide dissolving in a mixing solution of tetraethylene glycol dimethyl ether (TEGDME) and 1,3-dioxolane (DOL) with mixing ratio 1:1 by volume.
- TEGDME tetraethylene glycol dimethyl ether
- DOL 1,3-dioxolane
- lithium peroxide may be charged with current density of 100 mA/gLi 2 O 2 to 4.3V against Li/Li + by applying the current density of 50 mA/gLi 2 O 2 .
- the resultant charging/discharging curves of half cells are shown in FIG. 16 .
- the lithium ionic energy storage element of the present invention comprises a lithium ion donor having lithium peroxide and/or lithium oxide and a positive electrode frame active substance, wherein lithium peroxide and/or lithium oxide can be decomposed to produce lithium ions by electrochemical charging, and lithium ions intercalate repeatedly in and out of the positive electrode frame active substance and the negative electrode active substance in a full cell.
- the full cell can exhibit a high capacity.
- the positive electrode frame active substance of the positive electrode active substance can be a material selected from the group consisting of anatase titanium dioxide, carbon-sulfur composite, carbon-containing materials and carbon fluoride, but not limited to the above groups, as long as the materials that are stable and have excellent electric capacity are suitable as the positive electrode frame active substance.
- Even lithium metallic oxides may be the positive electrode frame active substance to mix with lithium peroxide and/or lithium oxide as the positive electrode active substance that can exhibit a higher capacity than the full cell using lithium metallic oxides only as the positive electrode active substance.
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Abstract
A lithium ionic energy storage element comprises a positive electrode having a first current collector and a positive electrode active substance provided on the first current collector; a negative electrode having a second current collector and a negative electrode active substance provided on the second current collector, wherein the negative electrode active substance is a material selected from the group consisting of carbon-containing materials, Si alloy and Sn alloy; and an electrolyte, wherein the positive electrode active substance comprises a lithium ion donor including lithium peroxide, lithium oxide or the mixture thereof and a positive electrode frame active substance. The invention also relates to a method for making a lithium ionic energy storage element.
Description
- 1. Field of the Invention
- The invention relates to a lithium ionic energy storage element, in particular to a lithium ionic energy storage element comprising a positive electrode active substance including a lithium ion donor and a positive electrode frame active substance.
- 2. Description of the Related Art
- In various energy storage technologies, lithium ionic batteries are regarded as a portable chemical power source with a high efficiency in next generation because they have advantages of high energy density, light weight and less pollution. Nowadays, the lithium ionic batteries are widely used in the fields of digital cameras, smart phones and notebooks. As the energy density of the lithium ionic battery is enhanced, the fields of use are extended. There is a higher need for the performance of the lithium ionic battery as the requirement of high capacity and long life of the lithium ionic battery for the mobile electric equipment is increased
- Typically, a lithium ionic battery comprises a negative electrode, a positive electrode and an electrolyte. The positive electrode active substance is not only used as an electrode material to take part in the chemical reaction, but also used as a lithium source. The positive electrode active substance is generally lithium metallic oxides which contain lithium atoms intercalated therein. Currently, lithium metallic oxides such as lithium cobalt oxide, lithium nickel oxide and lithium manganese oxide are available commercially. However, the above lithium metallic oxides cannot exhibit a proper combinative property of high initial electrical capacity, high thermal stability and excellent electrical capacity sustainability after a lithium ionic battery is charged and discharged repeatedly.
- The lithium ionic battery is limited by the capacity capacity (mA/g) of the positive electrode of the lithium metallic oxides, so that it cannot exhibit a higher capacitycapacity. Therefore, the lithium sources have to be increased if it is desired to increase the capacity of the lithium ionic battery. Several methods were proposed, wherein one of the methods is coating lithium metal used as lithium source on the negative electrode, and another method is forming lithium metal as a third electrode on the negative electrode by electroplating. However, the above two methods are difficult to perform and the coating and electroplating film are not uniform because the lithium metal is very active.
- Because lithium metal has disadvantages of safety and stability, the current commercial lithium ion secondary battery is used a working system having a positive electrode material containing lithium ions and a negative electrode material for intercalating lithium ions. In recent years, the energy density of the lithium ion secondary battery has to be enhanced, because the electric devices have a large energy demand. However, the stability of the positive electrode material structure is not high and the amount of lithium ions intercalation is not large, so that the capacity per gram cannot be further enhanced.
- Several materials, for example FeF3, FePO4 and V2O5 were proposed. The above materials are preferable to be the positive electrode material for a high energy density, because they have good electrical capacity and a higher platform voltage. However, the above materials do not contain lithium ions, so they have to combine with lithium metal. As a result, they would be only used in half cell tests but fail to be used in a full cell.
- Therefore, the inventor conducted researches according to the scientific approach in order to improve and resolve the above drawback, and finally proposed the present invention, which is reasonable and effective.
- It is an object of present invention to provide a lithium ionic energy storage element. It can exhibit a high capacity by using a positive electrode active substance which comprises a lithium ion donor and a positive electrode frame active substance.
- In order to achieve the above object, the present invention provides a lithium ionic energy storage element comprising a positive electrode having a first current collector and a positive electrode active substance provided on the first current collector; a negative electrode having a second current collector and a negative electrode active substance provided on the second current collector, wherein the negative electrode active substance is a material selected from the group consisting of carbon-containing materials, Si alloy and Sn alloy; and an electrolyte, wherein the positive electrode active substance comprises a lithium ion donor including lithium peroxide, lithium oxide or the mixture thereof and a positive electrode frame active substance.
- The present invention also relates to a positive electrode active substance used in a lithium ionic energy storage element, the positive electrode active substance comprising a lithium ion donor and a positive electrode frame active substance, wherein the lithium ion donor includes lithium peroxide, lithium oxide or a combination of lithium peroxide and lithium oxide; and the positive electrode frame active substance is a material selected from the group consisting of anatase titanium dioxide, carbon-sulfur composite, carbon-containing materials and carbon fluoride or is lithium metallic oxides.
- The present invention also relates to a method for making a lithium ionic energy storage element. At first, lithium peroxide, a positive electrode frame active substance, e.g. anatase titanium dioxide and a binder, e.g. PVDF are mixed with a predetermined weight ratio to form a mixture, and the mixture is added into a dispersant, e.g. N-methyl-2-pyrrolidone to form a slurry. Next, the slurry is coating on an aluminum foil to form a film by a blade coater. The film is baked in an oven at a temperature of 80-90° C. to remove a solvent, and raise the temperature to 120-130° C. for a period of time to form a positive electrode with lithium peroxide/anatase titanium dioxide. In order to increase conductivity of lithium peroxide, conductive carbon, for example super P carbon black, KS6 graphite or a combination thereof may be added.
- A lithium ionic energy storage element is formed by assembling the positive electrode with lithium peroxide/anatase titanium dioxide, a negative electrode having a negative electrode active substance, e.g. graphitized mesocarbon microbeads (MCMB) and a porous separate strip interposed between the positive electrode and the negative electrode, and an electrolyte, e.g. a concentration of 1M LiPF6 dissolving in a mixing solution of ethylene carbonate (EC) and diethyl carbonate (DEC) with mixing ratio 1:1 by volume is filled into the porous separate strip.
- Further, the present invention relates to a method for making a lithium ionic energy storage element. At first, lithium peroxide, a positive electrode frame active substance, e.g. carbon-sulfur composite and a binder, e.g. carboxymethyl cellulose (CMC) are mixed with a predetermined weight ratio to form a mixture, and the mixture is added into a dispersant, e.g. N-methyl-2-pyrrolidone to form a slurry. Next, the slurry is coating on an aluminum foil to form a film by a blade coater. The film is baked in an oven at a temperature of 80-90° C. to remove a solvent, and raise the temperature to 120-130° C. for a period of time to form a positive electrode with lithium peroxide/carbon-sulfur composite. In order to increase conductivity of lithium peroxide, conductive carbon, for example super P carbon black, KS6 graphite or a combination thereof may be added.
- A lithium ionic energy storage element is formed by assembling the positive electrode with lithium peroxide/carbon-sulfur composite, a negative electrode having a negative electrode active substance, e.g. hard carbon and a porous separate strip interposed between the positive electrode and the negative electrode, and an electrolyte, e.g. a concentration of 1M lithium bis(trifluoromethanesulfonly)imide dissolving in a mixing solution of tetraethylene glycol dimethyl ether (TEGDME) and 1,3-dioxolane (DOL) with mixing ratio 1:1 by volume is filled into the porous separate strip.
- Compared to the conventional lithium ionic battery comprising lithium metallic oxides, the lithium ionic energy storage element of the present invention comprises a lithium ion donor having lithium peroxide and/or lithium oxide and a positive electrode frame active substance, wherein lithium peroxide and/or lithium oxide can be decomposed to produce lithium ions by electrochemical charging, and lithium ions intercalate repeatedly in and out of the positive electrode frame active substance and the negative electrode active substance in a full cell. The full cell can exhibit a high capacity.
-
FIG. 1 shows a schematic view of a unit cell structure of a lithium ionic energy storage element an embodiment according to the invention. -
FIG. 2 shows a first cycle curve of voltage against electric capacity of a half cell of lithium peroxide charging/discharging of the invention. -
FIG. 3 shows a second cycle and a third cycle curves of voltage against electric capacity of a half cell of lithium peroxide charging/discharging of the invention. -
FIG. 4 shows a first cycle curve of voltage against electric capacity of a half cell of lithium peroxide charging/discharging under various ratio of a conductive carbon of the invention. -
FIG. 5 shows cyclic voltammetry response of lithium peroxide charging/discharging under various ratio of a conductive carbon of the invention. -
FIG. 6 shows the influent of voltage against electric capacity of lithium peroxide in the different current density. -
FIG. 7(a) shows XRD pattern of TiO2 synthetized from tetrabutyl titanate of the invention. -
FIG. 7(b) shows XRD pattern of TiO2 by simulation. -
FIG. 8 shows a charging/discharging curve of prelithiation period of Li2O2/TiO2 half cell. -
FIG. 9 shows a charging/discharging curve of subsequent cycles of Li2O2/TiO2 half cell. -
FIG. 10 shows a charging/discharging curve of prelithiation period of Li2O2/TiO2 versus MCMB full cell. -
FIG. 11 shows a charging/discharging curve of subsequent cycles of Li2O2/TiO2 versus MCMB full cell. -
FIG. 12 shows a charge/discharge curve of prelithiation period of Li2O2/TiO2 versus MCMB with disassembling process of coin cell. -
FIG. 13 shows a charge/discharge curve of subsequent cycles of Li2O2/TiO2 versus MCMB with disassembling process of coin cell. -
FIG. 14 shows a charging/discharging curve of Li2O2 (30 wt. %) with current density of 100 mA/g Li2O2 vs. Li metal of half cell. -
FIG. 15 shows a charge/discharge curve of carbon-sulfur composite of half cell. -
FIG. 16 shows a charge/discharge curve of prelithiation period of lithium peroxide/carbon-sulfur composite vs. Li/Li+ of half cell. - The technical content of invention will be explained in more detail below with reference to a few figures. However, the figures are intended solely for illustration and not to limit the inventive concept.
-
FIG. 1 shows a schematic view of a unit cell structure of a lithium ionic energy storage element an embodiment according to the invention. In the embodiment, the lithium ionic energy storage element comprises a plurality ofunit cell structures 100, eachunit cell structure 100 comprises a porousseparate strip 104 interposed between thepositive electrode 106 and thenegative electrode 108. The porousseparate strip 104 is coated with abinder 105 to enhance the binding of the cell structure's 100 components to each other. Thepositive electrode 106 has a firstcurrent collector 110 and a positive electrodeactive substance 114 provided on the firstcurrent collector 110 and thenegative electrode 108 has a secondcurrent collector 112 and a negative electrodeactive substance 116 provided on the secondcurrent collector 112. The positive electrodeactive substance 114 comprises a lithium ion donor including lithium peroxide, lithium oxide or a combination thereof and a positive electrode frame active substance, e.g. anatase titanium dioxide or carbon-sulfur composite. The carbon-sulfur composite has a weight ratio of carbon with sulfur is 0.4-1. In lithium peroxide/anatase titanium dioxide system, the negative electrodeactive substance 116 may be carbon-containing materials, e.g. graphitized mesocarbon microbeads (MCMB). In lithium peroxide/carbon-sulfur composite system, the negative electrodeactive substance 116 may be carbon-containing materials, e.g. hard carbon. - In the embodiment, the positive electrode
active substance 114 used in a lithium ionic energy storage element, the positive electrodeactive substance 114 comprising a lithium ion donor and a positive electrode frame active substance, wherein the lithium ion donor includes lithium peroxide, lithium oxide or a combination of lithium peroxide and lithium oxide; and the positive electrode frame active substance is a material selected from the group consisting of anatase titanium dioxide, carbon-sulfur composite, carbon-containing materials and carbon fluoride or is lithium metallic oxides. - The lithium ion donor of the invention may include but not be limited to lithium peroxide. For example, lithium oxide is also suitable to be the lithium ion donor. Alternative, lithium peroxide and lithium oxide are mixed for the use. In addition, the positive electrode frame active substance may use carbon-containing material, and thus both of the positive electrode and negative electrode use carbon-containing materials to form lithium ion electric capacity accordingly. Carbon fluorides (CFx) that have a high mass capacity ratio are suitable to be the positive electrode frame active substance of the invention. Si alloy or Sn alloy that has a very high theoretical electrical capacity is also suitable to be negative electrode
active substance 116 of the invention. - An electrolyte that is suitable to a lithium ionic energy storage element with lithium peroxide/anatase titanium dioxide system comprises an inorganic compound such as LiPF6, LiClO4 or LiBF4 and an organic solvent that is a material selected from the group consisting of ethylene carbonate (EC) and diethyl carbonate (DEC). In addition, an electrolyte comprises a concentration of 1M lithium bis(trifluoromethanesulfonly)imide dissolving in a mixing solution of tetraethylene glycol dimethyl ether (EGDME) and 1,3-dioxolane (DOL) with mixing ratio 1:1 by volume that is suitable to a lithium ionic energy storage element with lithium peroxide/carbon-sulfur system.
- In a charge/discharge mode of the
unit cell structure 100 of the embodiment, lithium peroxide of the positive electrodeactive substance 114 is decomposed to lithium ions and oxygen to intercalate into carbon-containing materials of thenegative electrode 108 when unit cell is charged, and the lithium ions located in thenegative electrode 108 diffuse to thepositive electrode 106 and intercalate in the positive electrode active substance through the electrolyte when unit cell is discharged. - At first, electric property of lithium peroxide is investigated. The lithium ionic energy storage element of the present invention comprises a lithium ion donor having lithium peroxide and/or lithium oxide and a positive electrode frame active substance, wherein lithium peroxide and/or lithium oxide can be decomposed to produce lithium ions by electrochemical charging, and lithium ions intercalate repeatedly in and out of the positive electrode frame active substance and the negative electrode active substance in a full cell without containing Li ions. Because the conductivity of lithium peroxide is not high, a conductive carbon may be added to enhance the conductivity of lithium peroxide.
- The present invention provides a method for making a lithium ionic energy storage element. At first, lithium peroxide, a positive electrode frame active substance, e.g. anatase titanium dioxide, a conductive carbon, for example super P carbon black, KS6 graphite or a combination thereof and a binder, e.g. PVDF are mixed with a predetermined weight ratio to form a mixture, and the mixture is added into a dispersant, e.g. N-methyl-2-pyrrolidone (NMP) to form a slurry. Next, the slurry is coating on an aluminum foil to form a film by a blade coater. The film is baked in an oven at a temperature of 80° C. for 6 hours to remove a solvent, and raise the temperature to 120° C. for 4-6 hours to form a positive electrode with lithium peroxide/anatase titanium dioxide.
- A lithium ionic energy storage element is formed by assembling the positive electrode with lithium peroxide/anatase titanium dioxide, a negative electrode having a negative electrode active substance, e.g. graphitized mesocarbon microbeads (MCMB) and a porous separate strip interposed between the positive electrode and the negative electrode, and an electrolyte, e.g. a concentration of 1M LiPF6 dissolving in a mixing solution of ethylene carbonate (EC) and diethyl carbonate (DEC) with mixing ratio 1:1 by volume is filled into the porous separate strip. The lithium ion donor of the invention may include but not be limited to lithium peroxide. For example, lithium oxide is also suitable to be the lithium ion donor. Alternative, lithium peroxide and lithium oxide are mixed for the use. In addition, the positive electrode frame active substance may use carbon-containing material, and thus both of the positive electrode and negative electrode use carbon-containing materials to form a lithium ion electric capacity accordingly. Carbon fluorides (CFx) that have a high mass capacity ratio are suitable to be the positive electrode frame active substance of the invention. Si alloy or Sn alloy that has a very high theoretical electrical capacity is also suitable to be negative electrode
active substance 116 of the invention. - Further, the present invention relates to a method for making a lithium ionic energy storage element. At first, lithium peroxide, a positive electrode frame active substance, e.g. carbon-sulfur composite, a conductive carbon, for example super P carbon black, KS6 graphite or a combination thereof and a binder, e.g. carboxymethyl cellulose (CMC) are mixed with a predetermined weight ratio to form a mixture, and the mixture is added into a dispersant, e.g. N-methyl-2-pyrrolidone to form a slurry. Next, the slurry is coating on an aluminum foil to form a film by a blade coater. The film is baked in an oven at a temperature of 80-90° C. to remove a solvent, and raise the temperature to 120-130° C. for a period of time to form a positive electrode with lithium peroxide/carbon-sulfur composite.
- The lithium ion donor of the invention may include but not be limited to lithium peroxide. For example, lithium oxide is also suitable to be the lithium ion donor. Alternative, lithium peroxide and lithium oxide are mixed for the use. In addition, the positive electrode frame active substance may use carbon-containing material, and thus both of the positive electrode and negative electrode use carbon-containing materials to form a lithium ion electric capacity accordingly. Carbon fluorides (CFx) that have a high mass capacity ratio are suitable to be the positive electrode frame active substance of the invention. Si alloy or Sn alloy that has a very high theoretical electrical capacity is also suitable to be negative electrode
active substance 116 of the invention. - A lithium ionic energy storage element is formed by assembling the positive electrode with lithium peroxide/carbon-sulfur composite, a negative electrode having a negative electrode active substance, e.g. hard carbon and a porous separate strip interposed between the positive electrode and the negative electrode, and an electrolyte, e.g. a concentration of 1M lithium bis(trifluoromethanesulfonly)imide dissolving in a mixing solution of tetraethylene glycol dimethyl ether (TEGDME) and 1,3-dioxolane (DOL) with mixing ratio 1:1 by volume is filled into the porous separate strip.
-
FIG. 2 shows a first cycle curve of voltage against electric capacity of a half cell of lithium peroxide charging/discharging of the invention.FIG. 3 shows a second cycle and a third cycle curves of voltage against electric capacity of a half cell of lithium peroxide charging/discharging of the invention. A half cell that is used for test is formed by assembling a positive electrode formed with mixing lithium peroxide, super P carbon black and PVDF by weight ratio of 10:80:10; and a porous separate strip filled with an electrolyte, e.g. a concentration of 1M LiPF6 dissolving in a mixing solution of ethylene carbonate (EC) and diethyl carbonate (DEC) with mixing ratio 1:1 by volume. Conditions of operation comprise charging/discharging current of 100 mA/g Li2O2 and charging/discharging voltage of 2-4.6V. -
FIG. 4 shows a first cycle curve of voltage against electric capacity of a half cell of lithium peroxide charging/discharging under various ratio of a conductive carbon of the invention. A half cell that is used for test is formed by assembling a positive electrode formed with mixing lithium peroxide, a conductive carbon (super P carbon black and KS6 graphite with mixing ratio 1:1 by weight) and PVDF by weight ratio of X:Y:10, wherein X=80, 60, 45, 30 and 10, and Y=10, 30, 45, 60 and 80; and a porous separate strip filled with an electrolyte, e.g. a concentration of 1M LiPF6 dissolving in a mixing solution of ethylene carbonate (EC) and diethyl carbonate (DEC) with mixing ratio 1:1 by volume. Conditions of operation comprise charging/discharging current of 10 mA/gLi2O2 and charging/discharging voltage of 2-4.8V. -
FIG. 5 shows cyclic voltammetry response of lithium peroxide charging/discharging under various ratio of a conductive carbon of the invention. A half cell that is used for test is formed by assembling a positive electrode formed with mixing lithium peroxide, a conductive carbon (super P carbon black and KS6 graphite with mixing ratio 1:1 by weight) and PVDF by weight ratio of X:Y:10, wherein X:Y=10:80 and 30:60; and a porous separate strip filled with an electrolyte, e.g. a concentration of 1M LiPF6 dissolving in a mixing solution of ethylene carbonate (EC) and diethyl carbonate (DEC) with mixing ratio 1:1 by volume. Condition of operation comprises a scan rate of cyclic voltammetry of 0.4 mV/s. The resultant current is 0 mA in the different voltage. -
FIG. 6 shows the influent of voltage against electric capacity of lithium peroxide in the different current density. A half cell that is used for test is formed by assembling a positive electrode formed with mixing lithium peroxide, a conductive carbon (super P carbon black and KS6 graphite with mixing ratio 1:1 by weight) and PVDF by weight ratio of 30:60:10; and a porous separate strip filled with an electrolyte, e.g. a concentration of 1M LiPF6 dissolving in a mixing solution of ethylene carbonate (EC) and diethyl carbonate (DEC) with mixing ratio 1:1 by volume. Conditions of operation comprise charging/discharging current of 10 mA/g Li2O2, 30 mA/g Li2O2 and 50 mA/g Li2O2 and charging/discharging voltage of 2-4.8V.FIG. 7(a) shows XRD pattern of TiO2 synthetized from tetrabutyl titanate of the invention.FIG. 7(b) shows XRD pattern of TiO2 by simulation. An error of degree (2θ) of XRD pattern of TiO2 ofFIG. 7(a) is obtained within 3% compared with XRD pattern of TiO2 ofFIG. 7(b) . - The above tests show the various combinations of lithium peroxide, a conductive carbon and binder, and the influence of charging and discharging of lithium peroxide in the different current density. However, lithium peroxide of the positive electrode is a functional material for use in one time, i.e. only may be decomposed by charging in one time. Therefore, another positive electrode active substance, for example anatase titanium dioxide or carbon-sulfur composite is required to use for receiving Li ions that may diffuse to the positive electrode from the negative electrode in a discharging process.
- The initial lithium peroxide may be decomposed to produce Li ions by charging of the invention that is called as a charging period of prelithiation, and Li ions diffuse to the positive electrode from the negative electrode by discharging that is called as a discharging period of prelithiation. The subsequent Li ions intercalate in and out in the positive electrode and negative electrode that is called as a regular working system.
- Please refer to
FIG. 8 andFIG. 9 .FIG. 8 shows a charging/discharging curve of prelithiation period of Li2O2/TiO2 half cell.FIG. 9 shows a charging/discharging curve of subsequent cycles of Li2O2/TiO2 half cell. During charging period of prelithiation, lithium peroxide may be charged to 4.8V against Li/Li+ by applying the current density of 50 mA/gLi2O2. During discharging period of prelithiation and subsequent charging/discharging, TiO2 may be charged and discharged at 1V-3V against Li/Li+ by 0.1C (1C=335 mAh/g). The resultant charging/discharging curves of half cells are shown inFIG. 8 andFIG. 9 .FIG. 8 shows a charging curve of Li2O2 with electric capacity of 365 mA/gLi2O2 during charging period of prelithiation and a discharing curve of TiO2 with two discharging platforms of 1.8V and 2.7V during discharging period of prelithiation, wherein the discharging platform of 2.7V has electric capacity of 100 mAh/gTiO2 that may be an oxidation-reduction reaction or regeneration of lithium peroxide, and it is regarded as a side reaction, i.e. the additional electric capacity may not belong to TiO2. Moreover, the resultant electric capacity may be about 280 mAh/gTiO2 after 100 mAh/gTiO2 of the electric capacity of the side reaction is deducted from 380 mAh/gTiO2. - Next, please refer to
FIG. 10 andFIG. 11 .FIG. 10 shows a charging/discharging curve of prelithiation period of Li2O2/TiO2 versus MCMB full cell.FIG. 11 shows a charging/discharging curve of subsequent cycles of Li2O2/TiO2 versus MCMB full cell. In the embodiment, a negative electrode is formed with mixing MCMB: super P carbon black: KS graphite: binder=70:7.5:7.5:15 by weight; and a positive electrode is formed with mixing lithium peroxide, a conductive carbon, binder and titanium dioxide by A/C ratio=1 versus weight of MCMB powder with calculation of A/C ratio between Li2O2/TiO2 cathode and MCMB anode as formulas: -
Li2O2 vs MCMB: (372 mAh/g*0.5 g*0.7)/(410 mAh/g*xg)=1 -
x=0.4219 g Li2O2 -
TiO2 vs MCMB: (350 mAh/g*0.5 g*0.7)/(335 mAh/g*yg)=1 -
y=0.4858 g TiO2 - According to the formulas based on the electric capacity of MCMB, the weight of each Li2O2, super P carbon black and KS graphite is 0.4219 g (22%) and the weight of PVDF is 0.1406 g (7%) and the weight of titanium dioxide is 0.4858 g (27%). During charging period of prelithiation, lithium peroxide may be charged to 4.8V against MCMB by applying the current density of 50 mA/gLi2O2. During discharging period of prelithiation and subsequent charging/discharging, TiO2 may be charged and discharged at 0-3V against MCMB by 0.1 C (1 C=335 mAh/g). The resultant charging/discharging curves of half cells are shown in
FIG. 10 andFIG. 11 . - It could be found from the above experiments that Li ions prelithiation in the positive is successful. However, oxygen is produced in the process, and will affect the electrochemical performance. It is important to have an oxygen removal step for removing oxygen produced in a first cycle of charge and discharge the lithium ionic energy storage element. In manufacturing a large scale of lithium ionic battery such as battery with aluminum foil soft pack (pouch cell), a battery active step is performed in a first cycle of charging and discharging the lithium ionic battery after filling the electrolyte into the porous separate strip to form a solid electrolyte interphase (SEI) on the negative electrode, and the electrolyte decomposes in part at the same time. Next, the original electrolyte is withdrawn by evacuation, and a new electrolyte is filled. Accordingly, a regular charging and discharging the lithium ionic battery can be performed.
FIG. 12 shows a charge/discharge curve of prelithiation period of Li2O2/TiO2 versus MCMB with disassembling process of coin cell, andFIG. 13 shows a charge/discharge curve of subsequent cycles of Li2O2/TiO2 versus MCMB with disassembling process of coin cell. The effect of removing oxygen is not obvious fromFIG. 12 . However, there is not an acute decease in electric capacity during the subsequent charge/discharge of TiO2 that can prove the subsequent charge/discharge of TiO2 is affected by the side reaction of the prelithiation discharging period. The source of the side reaction is the oxygen produced from the decomposition of lithium peroxide during the prelithiation charging period. - In another embodiment, carbon-sulfur composite may be used for the positive electrode frame active substance of the positive electrode active substance. Lithium peroxide is mixed with carbon-sulfur composite to replace Li metal. A full cell is assembled by the positive electrode having the positive electrode active substance comprising lithium peroxide and carbon-sulfur composite and the negative electrode having the negative electrode active substance comprising hard carbon. Before assembling a full cell, the electrochemical properties of lithium peroxide and carbon-sulfur composite in ethers should be determined Because Li-sulfur battery uses ethers as an electrolyte, a half cell that is used for test is formed by assembling a positive electrode formed with mixing lithium peroxide, a conductive carbon and binder by weight ratio of 30:60:10; and a porous separate strip filled with an electrolyte, e.g. a concentration of 1M lithium bis(trifluoromethanesulfonly)imide dissolving in a mixing solution of tetraethylene glycol dimethyl ether (TEGDME) and 1,3-dioxolane (DOL) with mixing ratio 1:1 by volume. Conditions of operation comprise charging/discharging current density of 100 mA/g Li2O2 vs. Li metal and charging/discharging voltage of 2-4.3V in the embodiment, shown as
FIG. 14 . The cut off voltage of charging is 4.3V. The half cell is charged for 9 hours by 100 mA/gLi2O2 after testing. It can be found the decomposition of lithium peroxide in Li-sulfur battery electrolyte system has the overpotential about 4.1V and the resultant electric capacity about 980 mAh/gLi2O2. -
FIG. 15 shows a charge/discharge curve of carbon-sulfur composite of half cell. The carbon-sulfur composite of the half cell has a weight ratio of carbon with sulfur is 0.4-1. Conditions of operation comprise charging/discharging current density of 0.1 C (1 C=1672 mAh/gs) vs. Li/Li+ and charging/discharging voltage of 1.5V-3V in the embodiment, shown asFIG. 15 . -
FIG. 16 shows a charge/discharge curve of prelithiation period of lithium peroxide/carbon-sulfur composite vs. Li/Li+ of half cell. In the embodiment, a half cell that is used for test is formed by assembling a positive electrode formed with mixing lithium peroxide/carbon-sulfur composite, a conductive carbon and a binder dissolving in a dispersant of N-methyl-2-pyrrolidone; and a porous separate strip filled with an electrolyte, e.g. a concentration of 1M lithium bis(trifluoromethanesulfonly)imide dissolving in a mixing solution of tetraethylene glycol dimethyl ether (TEGDME) and 1,3-dioxolane (DOL) with mixing ratio 1:1 by volume. During charging period of prelithiation, lithium peroxide may be charged with current density of 100 mA/gLi2O2 to 4.3V against Li/Li+ by applying the current density of 50 mA/gLi2O2. During discharging period of prelithiation and subsequent charging/discharging, carbon-sulfur composite may be charged and discharged against Li/Li+ by 0.1 C (1 C=1672 mAh/gs). The resultant charging/discharging curves of half cells are shown inFIG. 16 . - The lithium ionic energy storage element of the present invention comprises a lithium ion donor having lithium peroxide and/or lithium oxide and a positive electrode frame active substance, wherein lithium peroxide and/or lithium oxide can be decomposed to produce lithium ions by electrochemical charging, and lithium ions intercalate repeatedly in and out of the positive electrode frame active substance and the negative electrode active substance in a full cell. The full cell can exhibit a high capacity. The positive electrode frame active substance of the positive electrode active substance can be a material selected from the group consisting of anatase titanium dioxide, carbon-sulfur composite, carbon-containing materials and carbon fluoride, but not limited to the above groups, as long as the materials that are stable and have excellent electric capacity are suitable as the positive electrode frame active substance. Even lithium metallic oxides may be the positive electrode frame active substance to mix with lithium peroxide and/or lithium oxide as the positive electrode active substance that can exhibit a higher capacity than the full cell using lithium metallic oxides only as the positive electrode active substance.
- The invention is not limited to these embodiments, but various variations and modifications may be made without departing from the scope of the invention.
Claims (15)
1. A positive electrode active substance used in a lithium ionic energy storage element, the positive electrode active substance comprising a lithium ion donor and a positive electrode frame active substance, wherein the lithium ion donor includes lithium peroxide, lithium oxide or a combination of lithium peroxide and lithium oxide; and the positive electrode frame active substance is a material selected from the group consisting of anatase titanium dioxide, carbon-sulfur composite, carbon-containing materials, carbon fluoride and—is lithium metallic oxides.
2. A lithium ionic energy storage element comprising:
a positive electrode having a first current collector and a positive electrode active substance provided on the first current collector;
a negative electrode having a second current collector and a negative electrode active substance provided on the second current collector, wherein the negative electrode active substance is a material selected from the group consisting of carbon-containing materials, Si alloy and Sn alloy; and
an electrolyte interposed between the positive electrode and the negative electrode, wherein the positive electrode active substance comprises a lithium ion donor including lithium peroxide, lithium oxide or a combination of lithium peroxide and lithium oxide and a positive electrode frame active substance.
3. The lithium ionic energy storage element as claimed in claim 2 , wherein the positive electrode frame active substance of the positive electrode active substance is a material selected from the group consisting of anatase titanium dioxide, carbon-sulfur composite, carbon-containing materials, carbon fluoride and lithium metallic oxides.
4. The lithium ionic energy storage element as claimed in claim 3 , wherein the carbon-sulfur composite of the positive electrode frame active substance has a weight ratio of carbon with sulfur is 0.4-1.
5. The lithium ionic energy storage element as claimed in claim 2 , wherein the positive electrode frame active substance is lithium metallic oxides.
6. The lithium ionic energy storage element as claimed in claim 2 , wherein the positive electrode active substance contains conductive carbon comprising super P carbon black, KS6 graphite or a combination thereof.
7. A method for making a lithium ionic energy storage element comprising steps:
(a) mixing a lithium ion donor, a positive electrode frame active substance and a binder with a predetermined weight ratio to form a mixture, and adding the mixture into a dispersant to form a positive electrode active substance, wherein the lithium ion donor includes lithium peroxide, lithium oxide or a combination thereof;
(b) coating the positive electrode active substance on an aluminum foil to form a film, and baking the film to form a positive electrode; and
(c) forming a lithium ionic energy storage element by assembling the positive electrode, a negative electrode having a negative electrode active substance and a porous separate strip interposed between the positive electrode and the negative electrode, and filling an electrolyte into the porous separate strip.
8. The method as claimed in claim 7 , further comprising an oxygen removal step for removing oxygen produced in a first cycle of charge and discharge the lithium ionic energy storage element after filling the electrolyte into the porous separate strip.
9. The method as claimed in claim 7 , wherein the positive electrode frame active substance of the step (a) is a material selected from the group consisting of anatase titanium dioxide, carbon-sulfur composite, carbon-containing materials and carbon fluoride.
10. The method as claimed in claim 7 , wherein the positive electrode frame active substance of the step (a) is lithium metallic oxides.
11. The method as claimed in claim 7 , further comprising adding a conductive carbon into the mixture of the step (a), wherein the conductive carbon is super P carbon black, KS6 graphite or a combination thereof.
12. The method as claimed in claim 7 , wherein the binder in the step (a) is polyvinylidene fluoride or carboxymethyl cellulose.
13. The method as claimed in claim 7 , wherein the negative electrode active substance of the step (c) is a material selected from the group consisting of graphitized mesocarbon microbeads, hard carbon, Si alloy and Sn alloy.
14. The method as claimed in claim 7 , wherein the electrolyte of the step (c) is a concentration of 1M LiPF6dissolving in a mixing solution of ethylene carbonate and diethyl carbonate; or a concentration of 1M lithium bis(trifluoromethanesulfonly)imide dissolving in a mixing solution of tetraethylene glycol dimethyl ether and 1,3-dioxolane.
15. The method as claimed in claim 7 , wherein the dispersant of the step (a) is N-methyl-2-pyrrolidone.
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US20140217992A1 (en) * | 2013-02-05 | 2014-08-07 | Hrl Laboratories, Llc | Separators for lithium-sulfur batteries |
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Owner name: AMITA TECHNOLOGIES INC LTD., TAIWAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:CHERNG, JING-YIH;HWANG, BING-JOE;WANG, HSUAN-FU;AND OTHERS;SIGNING DATES FROM 20150630 TO 20150713;REEL/FRAME:036072/0374 |
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STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |