LITHIUM SECONDARY BATTERIES

Abstract

The invention provides a lithium secondary battery including an ionic provider added to the positive electrode and/or a lithium receiver added to the negative electrode. The ionic provider and/or the ionic provider does not involve in the electrochemical reaction of the lithium secondary battery during charging and discharging. The ionic provider can absorb thermal energy caused by the rising temperature of the lithium secondary battery to release the reactive cation. The reactive cation will insert the location with lithium-ion extraction of the positive electrode to make the lattice structure of the positive active material be stable. Therefore, the release of atomic oxygen is avoided. The lithium receiver receives the diffused lithium from the negative electrode to reduce the lithium concentration of the negative electrode. Therefore, it will present a stable state with lower energy to effectively suppress the thermal runaway.

Claims

1. A lithium secondary battery, comprising: a positive electrode having a positive active material; a negative electrode having a negative active material; an electrolyte system providing ionic conductivity between the positive electrode and the negative electrode to allow lithium ions to move between the positive electrode and the negative electrode to perform an electrochemical reaction for charging and discharging; and an ionic provider, added in the positive electrode and being inactive during the electrochemical reaction, wherein the ionic provider includes an anionic group and a reactive cation bonded to the anionic group, and the ionic provider releases the reactive cation by absorbing thermal energy to react with the positive active material and deactivate the positive active material; wherein the reactive cation is sodium or potassium.

2. The lithium secondary battery of claim 1, wherein the anionic group is NO.sub.3.sup.-, NO.sub.2.sup.-, NO.sup.-, Al(OH).sub.4.sup.-, PO.sub.4.sup.3-, P.sub.2O.sub.7.sup.4-; HCO.sub.3.sup.-, AlSiO.sub.4.sup.-, B.sub.4O.sub.7.sup.2-, CO.sub.3.sup.2-, CF.sub.3SO.sub.3.sup.-, SiO.sub.3.sup.-, PSS.sup.-, HPO.sub.4.sup.2.sup.-, SO.sub.3.sup.2-, H.sub.2PO.sub.2.sup.-, HPO.sub.3.sup.2.sup.-, P.sub.2O.sub.6.sup.-, P.sub.3O.sub.9.sup.3.sup.-, BO.sub.2.sup.-, BO.sup.3-, P.sub.4O.sub.13.sup.6-, SO.sub.7.sup.2-, S.sub.2O.sub.3.sup.2.sup.-, SO.sub.5.sup.2-, S.sub.2O.sub.8.sup.2.sup.-, S.sub.2O.sub.6.sup.2.sup.-, S.sub.2O.sub.4.sup.2.sup.-, P.sub.3O.sub.10.sup.5.sup.-, B.sub.2O.sub.5.sup.4.sup.-, H.sub.2PO.sub.4.sup.-, SO.sub.3C.sub.4F.sub.9.sup.-, SO.sub.2CF.sub.3.sup.- or S.sub.2O.sub.5.sup.2.sup.-.

3. The lithium secondary battery of claim 1, wherein the anionic group is asymmetrical.

4. The lithium secondary battery of claim 1, wherein the ionic provider is distributed between positive active material particles or is coated on a surface of the positive electrode.

5. The lithium secondary battery of claim 1, further comprises a lithium receiver distributed between negative active material particles or coated on a surface of the negative electrode, wherein the lithium receiver is capable of reacting with lithium to form lithium alloy or lithium compound, but does not involve in the electrochemical reaction; wherein an electric potential which the lithium receiver is reacted with lithium is different from an electric potential which the negative active material of the negative electrode is reacted with lithium.

6. The lithium secondary battery of claim 5, wherein the lithium receiver is an inorganic material or an organic polymer, wherein the inorganic material comprises Li.sub.4Ti.sub.5O.sub.12, Fe.sub.4(P.sub.2O.sub.7).sub.3, FeS.sub.2, Cu.sub.2P.sub.2O.sub.7, TiS.sub.2 or a mixture thereof; wherein the organic polymer comprises polyimide (PI), polyimide derivatives or a mixture thereof.

7. The lithium secondary battery of claim 1, wherein the ionic provider is not dissociable in a polar solution.

8. A lithium secondary battery, comprising: a positive electrode having a positive active material; a negative electrode having a negative active material; an electrolyte system providing ionic conductivity between the positive electrode and the negative electrode to allow lithium ions to move between the positive electrode and the negative electrode to perform an electrochemical reaction for charging and discharging; and a lithium receiver disposed in the negative electrode, wherein the lithium receiver is capable of reacting with lithium to form lithium alloy or lithium compound, but does not involve in the electrochemical reaction; wherein an electric potential which the lithium receiver is reacted with lithium is different from an electric potential which the negative active material of the negative electrode is reacted with lithium.

9. The lithium secondary battery of claim 8, wherein the lithium receiver is an inorganic material or an organic polymer, wherein the inorganic material comprises Li.sub.4Ti.sub.5O.sub.12, Fe.sub.4(P.sub.2O.sub.7).sub.3, FeS.sub.2, Cu.sub.2P.sub.2O.sub.7, TiS.sub.2 or a mixture thereof; wherein the organic polymer comprises polyimide (PI), polyimide derivatives or a mixture thereof.

10. The lithium secondary battery of claim 8, wherein the lithium receiver is distributed between negative active material particles or is coated on a surface of the negative electrode.

11. The lithium secondary battery of claim 8, further comprises an ionic provider disposed in the positive electrode and being inactive during the electrochemical reaction, wherein the ionic provider includes an anionic group and a reactive cation bonded to the anionic group, and the ionic provider releases the reactive cation by absorbing thermal energy to react with the positive active material and deactivate the positive active material; wherein the reactive cation is sodium or potassium.

12. The lithium secondary battery of claim 11, wherein the anionic group is NO.sub.3.sup.-, NO.sub.2.sup.-, NO.sup.-, Al(OH).sub.4.sup.-, PO.sub.4.sup.3-, P.sub.2O.sub.7.sup.4-, HCO.sub.3.sup.-, AlSiO.sub.4.sup.-, B.sub.4O.sub.7.sup.2-, CO.sub.3.sup.2-, CF.sub.3SO.sub.3.sup.-, SiO.sub.3.sup.-, PSS.sup.-, HPO.sub.4.sup.2.sup.-, SO.sub.3.sup.2-, H.sub.2PO.sub.2.sup.-, HPO.sub.3.sup.2.sup.-, P.sub.2O.sub.6.sup.-, P.sub.3O.sub.9.sup.3.sup.-, BO.sub.2.sup.-, BO.sup.3-, P.sub.4O.sub.13.sup.6.sup.-, SO.sub.7.sup.2-, S.sub.2O.sub.3.sup.2.sup.-, SO.sub.5.sup.2-, S.sub.2O.sub.8.sup.2.sup.-, S.sub.2O.sub.6.sup.2.sup.-, S.sub.2O.sub.4.sup.2.sup.-, P.sub.3O.sub.10.sup.5.sup.-, B.sub.2O.sub.5.sup.4.sup.-, H.sub.2PO.sub.4.sup.-, SO.sub.3C.sub.4F.sub.9.sup.-, SO.sub.2CF.sub.3.sup.- or S.sub.2O.sub.5.sup.2.sup.-.

13. The lithium secondary battery of claim 11, wherein the anionic group is asymmetrical.

14. The lithium secondary battery of claim 11, wherein the ionic provider is distributed between positive active material particles or is coated on a surface of the positive electrode.

15. The lithium secondary battery of claim 11, wherein the ionic provider is not dissociable in a polar solution.

16. A lithium secondary battery, comprising: a positive electrode having a positive active material; a negative electrode having a negative active material; an electrolyte system providing ionic conductivity between the positive electrode and the negative electrode to allow lithium ions to move between the positive electrode and the negative electrode to perform an electrochemical reaction for charging and discharging; an ionic provider, added in the positive electrode and being inactive during the electrochemical reaction, wherein the ionic provider includes an anionic group and a reactive cation bonded to the anionic group, and the ionic provider releases the reactive cation by absorbing thermal energy to react with the positive active material and deactivate the positive active material, wherein the reactive cation is sodium or potassium; and a lithium receiver disposed in the negative electrode, wherein the lithium receiver is capable of reacting with lithium to form lithium alloy or lithium compound, but does not involve in the electrochemical reaction; wherein an electric potential which the lithium receiver is reacted with lithium is different from an electric potential which the negative active material of the negative electrode is reacted with lithium.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0018] The present invention will become more fully understood from the detailed description given hereinbelow illustration only, and thus are not limitative of the present invention, and wherein:

[0019] FIG. 1 is an XRD diffraction pattern of an embodiment of the positive electrode, in which with and without Na.sub.3PO.sub.4 served as the ionic provider, in accordance with the present invention.

[0020] FIG. 2 is an XRD diffraction pattern of an embodiment of the positive electrode, in which with and without KNO.sub.3 or NaNO.sub.3 served as the ionic provider, in accordance with the present invention.

[0021] FIG. 3 is a thermogram of the differential scanning calorimeter with or without the ionic provider in accordance with the present invention.

DETAILED DESCRIPTION OF THE INVENTION

[0022] The present invention will be described with respect to particular embodiments and with reference to certain drawings but the invention is not limited thereto but only by the claims. Any reference signs in the claims shall not be construed as limiting the scope. The drawings described are only schematic and are non-limiting. In the drawings, the size of some of the elements may be exaggerated and not drawn on scale for illustrative purposes.

[0023] The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the general inventive concept. As used herein, the singular forms “a” , “an” and “the” are intended to include the plural forms as well, unless the context clearly indicates otherwise. Unless otherwise defined, all terms (including technical and scientific terms) used herein have the same meaning as commonly understood by one of ordinary skill in the art to which example embodiments belong. It will be further understood that terms, such as those defined in commonly used dictionaries, should be interpreted as having a meaning that is consistent with their meaning in the context of the relevant art and should not be interpreted in an idealized or overly formal sense unless expressly so defined herein.

[0024] Reference throughout this specification to “one embodiment” or “an embodiment” means that a particular feature, structure or characteristic described in connection with the embodiment is included in at least one embodiment of the present invention. Thus, appearances of the phrases “in one embodiment” or “in an embodiment” in various places throughout this specification are not necessarily all referring to the same embodiment, but may. Furthermore, the particular features, structures or characteristics may be combined in any suitable manner, as would be apparent to one of ordinary skill in the art from this disclosure, in one or more embodiments.

[0025] This invention discloses a lithium secondary battery capable of suppressing thermal runaway effectively, which includes a positive electrode having a positive active material, a negative electrode having a negative active material, and an electrolyte system providing ionic conductivity between the positive electrode and the negative electrode. The lithium ions are allowed to move between the positive electrode and the negative electrode to perform the electrochemical reaction for charging and discharging. An ionic provider is added in the positive electrode. The ionic provider is inactive during the electrochemical reaction, i.e. does not involve in the electrochemical reaction. The ionic provider includes an anionic group and a reactive cation bonded to the anionic group. The ionic provider releases the reactive cation after absorbing thermal energy. The reactive cation will insert the location with lithium-ion extraction of the positive active material to make the lattice structure of the positive active material be stable. Therefore, the release of atomic oxygen is avoided to suppress the thermal runaway of the lithium secondary battery. The thermal energy absorbed by the ionic provider may be provided by the lithium secondary battery when the temperature of the lithium secondary battery reaches to a first temperature. The strength of the bonding between the reaction cation and the anionic group can be adjusted by selecting the materials thereof by those skilled in the art. At the first temperature, the ionic provider can obtain enough kinetic energy to break the bonding of the reaction cation and the anionic group, so that the reaction cation can move freely. Thus, it is not necessary for the ionic provider of this invention to be dissociated in a polar solution, i.e. the ionic provider is not dissociable in a polar solution. The reactive cation is driven by thermal energy to make the reactive cation be released from the ionic provider to pass to the positive electrode by diffusion in an ionized state.

[0026] The reactive cation may be selected from sodium or potassium. The ionic provider is disposed on the positive electrode of the lithium secondary battery and the ionic provider is adjacent or directly contacted to the positive active material particle of the positive electrode. For example, the ionic provider is mixed with the positive active material particles of the positive electrode to form a random distribution between the positive active material particles. Alternatively, the ionic provider is coated on the surface of the positive electrode.

[0027] Before the ionic provider receives or absorbs enough thermal energy, the anionic group is bonded with the reactive cation, such as sodium or potassium. When the ionic provider absorbs enough thermal energy, the bonding of the reaction cation and the anionic group is broken. Then the reaction cation is separated from the anionic group, so that the reaction cation can move freely. The reactive cation will react with the positive active material to deactivate the positive active material. The deactivation may be achieved by insertion of the reactive cation into the location with lithium-ion extraction of the positive active material to make the positive active material become stable from unstable resulting from lithium-ion extraction. Also, the location with lithium-ion extraction of the positive active material is inserted by the reactive cation, such as sodium or potassium, the lattice structure of the positive active material is stable. Therefore, with the deactivation, the release of a large amount of atomic oxygen from the positive active material, caused by the lithium-ion extraction, is avoided. Moreover, due to the location with lithium-ion extraction of the positive active material is inserted by the reactive cation, the lithium can not be accepted by the positive active material. The positive active material will become a deactivating state for the electrochemical reaction. In this embodiment, the temperature (i.e. the first temperature) is acted as the triggering mechanism of whether the reactive cation of the ionic provider is in a free state, so as to achieve of inserting the location with lithium-ion extraction of the positive electrode. Further, in this way, the voltage of the lithium secondary battery is lowered to achieve harmlessness.

[0028] In this embodiment, the anionic group is selected from non-single chemical element (i.e., not a single type of atom) which has a certain bonding length, such as NO.sub.3.sup.-, NO.sub.2.sup.-, NO.sup.-, Al(OH).sub.4.sup.-, PO.sub.4.sup.3-, P.sub.2O.sub.7.sup.4-, HCO.sub.3.sup.-, AlSiO.sub.4.sup.-, B.sub.4O.sub.7.sup.2-, CO.sub.3.sup.2-, CF.sub.3SO.sub.3.sup.-, SiO.sub.3.sup.-, PSS , HPO.sub.4.sup.2-, SO.sub.3.sup.2-, H.sub.2PO.sub.2.sup.-, HPO.sub.3.sup.2.sup.-, P.sub.2O.sub.6.sup.-, P.sub.3O.sub.9.sup.3.sup.-, BO.sub.2.sup.-, BO.sup.3-, P.sub.4O.sub.13.sup.6.sup.-, SO.sub.7.sup.2-, S.sub.2O.sub.3.sup.2.sup.-, SO.sub.5.sup.2-, S.sub.2O.sub.8.sup.2.sup.-, S.sub.2O.sub.6.sup.2.sup.-, S.sub.2O.sub.4.sup.2.sup.-, P.sub.3O.sub.10.sup.5-, B.sub.2O.sub.5.sup.4-, H.sub.2PO.sub.4.sup.-, SO.sub.3C.sub.4F.sub.9.sup.-, SO.sub.2CF.sub.3.sup.- or S.sub.2O.sub.5.sup.2-. The anionic group can be symmetrical or asymmetrical. The ability to release sodium or potassium of the asymmetrical anionic group is better than that of the symmetrical anionic group. For example, Na.sub.4P.sub.2O.sub.7 has better ability to release sodium than that of Na.sub.3PO.sub.4. Also, in case of the reactive cation is sodium, the ionic provider may be NaAlOH.sub.4, Na.sub.3PO.sub.4, Na.sub.4P.sub.2O.sub.7, NaHCO.sub.3, NaAlSiO.sub.4, Na.sub.2B.sub.4O.sub.7, Na.sub.2CO.sub.3, CF.sub.3SO.sub.3Na, NaSiO.sub.3, NaPSS (poly(sodium styrene sulfonate)), Na.sub.2HPO.sub.4, Na.sub.2SO.sub.3, Na.sub.2S.sub.2O.sub.5, NaNO.sub.3, NaNO.sub.2, NaNO or an oxide of sodium. In addition, because potassium ions have a larger ionic radius than that of sodium ions, and the electronegativity of potassium ions is lower than that of sodium ions, potassium ions are less attractive to shared electrons. Therefore, potassium ions are more likely to become free state after absorbing thermal energy to diffuse to the location with lithium-ion extraction of the positive electrode.

[0029] In this invention, a lithium receiver, or so-called new lithium host, is disposed in the negative electrode of the lithium secondary battery. The lithium receiver is capable of reacting with lithium to form lithium alloy or lithium compound, but does not involve in the electrochemical reaction of the positive and negative electrodes of the lithium secondary battery during charging and discharging. It means that the lithium receiver is inactive during lithium alloying or lithium-ion insertion in the negative electrode. The electric potential which the lithium receiver is reacted with lithium is different from the electric potential which the negative active material of the negative electrode is reacted with lithium. For example, the electric potential which the lithium receiver is reacted with lithium, to form lithium alloy or lithium compound, is higher than from the electric potential which the negative active material of the negative electrode is reacted with lithium, to form lithium alloy or lithium compound. Therefore, the lithium receiver does not involve in charging and discharging of the lithium secondary battery. The lithium receiver is disposed on the negative electrode of the lithium secondary battery and the lithium receiver is adjacent or directly contacted to the negative active material. For example, the lithium receiver is mixed with the negative active material particles of the negative electrode to distribute between the negative active material particles or is coated on the surface of the negative electrode.

[0030] During the charging operation of the lithium secondary battery, the excessive deposition and diffusion of lithium ions to the negative electrode. The negative electrode will become to demonstrate the material characteristics of lithium from the characteristics of the raw material. That is extremely unstable. However, lithium atoms will diffuse from the negative electrode to the lithium receiver driven by the concentration difference and the thermal energy of the lithium secondary battery at a second temperature. The lithium concentration at the negative electrode is reduced to demonstrate the material properties near to the original raw material. Therefore, it will present a stable state with lower energy. The second temperature may be the same or different with the first temperature. The negative active material of the negative electrode may be carbon, silicon or lithium metal. The lithium receiver may be an inorganic material, such as Li.sub.4Ti.sub.5O.sub.12, Fe.sub.4(P.sub.2O.sub.7).sub.3, FeS.sub.2, Cu.sub.2P.sub.2O.sub.7 , TiS.sub.2 or a mixture thereof. FeS.sub.2 is alloyed with lithium at 1.5-2.5 volts, and the carbon, silicon or lithium metal performs electrochemical reaction with lithium at 0-0.1 volts. Therefore, the lithium receiver is inactive during lithium alloying or lithium-ion insertion in the negative electrode.

[0031] Alternatively, the lithium receiver may be an organic polymer, which can withstand the temperature above 150° C. The organic polymer is alloyed with lithium at 1.5-3.5 volts. The negative active material can be pretreated to avoid the above operating voltage of the organic polymer. In case of the negative active material is carbon or silicon, the carbon or silicon is lithiated to avoid the above operating voltage of the organic polymer. Also, The organic polymer may be polyimide(PI), polyimide derivatives such as polyetherimide (PEI), polyaryletherketone(PAEK) or a mixture thereof. For example, PI is alloyed with lithium at 2.5 volts.

[0032] The lithium secondary battery may include the ionic provider, the lithium receiver or both. The lithium secondary battery of this invention may further include a separator, which is composed of an electrically insulating material with holes to allow the ions pass through or an ionic conductive and electrically insulating material, such as a solid electrolyte. The negative active material of the negative electrode may be carbon material, silicon-based material, a mixture of both, or lithium metal. Examples of the carbon material may include graphitized carbon materials and amorphous carbon materials, such as natural graphite, modified graphite, graphitized mesocarbon microbeads, soft carbon (such as coke) and hard carbon. The silicon-based material include silicon, silicon oxide, silicon-carbon composites, and silicon alloy. The positive active material of the positive electrode may be lithium cobalt manganese oxide, wherein the weight percentage of nickel is more than 75%, such NCM811.

[0033] Various experiments are carried out below to verify the effect of this invention. The electrolyte used in this experiment is a non-aqueous electrolyte, such as an organic electrolyte, a colloidal electrolyte, a polymer electrolyte, or a carbonate solvent, such as EC(ethylene carbonate), PC(polycarbonate), added with salts, such as LiPF.sub.6, LiBF.sub.4, etc.

[0034] Please refer to FIG. 1, which is the XRD diffraction pattern with and without Na.sub.3PO.sub.4 served as the ionic provider. The composition of the sample 1 is 76.61% NCM811, 3.26% electrically conductive material, 1.63% adhesive and 18.5% electrolyte by weight. The composition of sample 2 is 38.305% NCM811, 1.63% electrically conductive material, 0.815% adhesive, 9.25% electrolyte and 50% Na.sub.3PO.sub.4 by weight. The production method of the sample 1 is to mix 76.61% NCM811, 3.26% electrically conductive material, 1.63% adhesive and 18.5% electrolyte by weight and coat on a positive current collector to form a positive active material layer. Then a separator, a negative active material layer and a negative current collector are sequentially stacked on the surface of the positive active material layer. A sealing frame sandwiched between the positive current collector and the negative current collector is used to seal the positive active material layer, the separator and the negative active material layer between the positive current collector, the sealing frame and the negative current collector to form a laminated battery sheet. The laminated battery sheet is formed with a 100% SOC(state of charge). Then the formed positive active material layer is scraped off and pressed under 0.9 N for 1 minute to form a sheet. After a heat treatment process, the sample 1 is obtained. The heat treatment process is performed under 130° C. for 30 minutes. The production method of the sample 2 is to mix 76.61% NCM811, 3.26% electrically conductive material, 1.63% adhesive and 18.5% electrolyte by weight and coat on a positive current collector to form a positive active material layer. Then a separator, a negative active material layer and a negative current collector are sequentially stacked on the surface of the positive active material layer. A sealing frame sandwiched between the positive current collector and the negative current collector is used to seal the positive active material layer, the separator and the negative active material layer between the positive current collector, the sealing frame and the negative current collector to form a laminated battery sheet. The laminated battery sheet is formed with a 100% SOC(state of charge). Then the formed positive active material layer is scraped off to mix and grind with Na.sub.3PO.sub.4 with the same weight. The mixture is pressed under 0.9 N for 1 minute to form a sheet. After the same heat treatment process, the sample 2 is obtained. Cu is used as target and the scanning parameters were from a range of about 10-80 degrees and a continuous scan at a rate of about 4 degrees/min. It can be seen from the FIG. 1 that compared to sample 1, the characteristic peak of lithium is greatly reduced and the characteristic peak of sodium is presented of sample 2.

[0035] Please refer to FIG. 2, which is the XRD diffraction pattern with and without KNO.sub.3 or NaNO.sub.3 served as the ionic provider. The sample 3 or 4 is produced in the same manner as described in sample 2 except that Na.sub.3PO.sub.4 is replaced with KNO.sub.3 or NaNO.sub.3. Cu is used as target and the scanning parameters were from a range of about 10-80 degrees and a continuous scan at a rate of about 4 degrees/min. It can be seen from the FIG. 2 that compared to sample 1, the characteristic peak of lithium is greatly reduced and the characteristic peak of potassium or sodium is presented of sample 3 or 4.

[0036] The following samples are taken for the gas production test. The composition of sample 5 is 76.61% NCM811, 3.26% electrically conductive material, 1.63% adhesive and 18.5% electrolyte by weight. The production method of the sample 5 is to mix NCM811, electrically conductive material, adhesive and electrolyte to form an electrode film. Then the electrode film is used to form a coin cell. The coin cell is formed with a 100% SOC(state of charge) thereof. Then the electrode film is directly taken out as sample 5. The composition of sample 6 is 66.61% NCM811, 3.26% electrically conductive material, 1.63% adhesive, 18.5% electrolyte and 10% Na.sub.3PO.sub.4 by weight. The production method of the sample 6 is to mix NCM811, electrically conductive material, adhesive, electrolyte and Na.sub.3PO.sub.4 to form an electrode film. The electrode film is used as a positive electrode of a coin cell. The coin cell is formed with a 100% SOC(state of charge) thereof. Then the electrode film is directly taken out as sample 6. Sample 5 and sample 6 are analysed by GC-MS(gas chromatography-mass spectrometry) respectively. In this analysis, sample 5 and sample 6 are placed into special sample bottles for GC-MS analysis. In a glove box, the oxygen in the sample bottles is replaced with argon. Then, use parafilm to seal the sample bottles to avoid air infiltration. In GC-MS analysis, the headspace extraction temperature is 200° C., and extraction time is 20 minutes. Then sample 1 ml to heat from 40° C. to 250° C. As following Table 1, after the above GC-MS analysis, the generated oxygen of sample 6 with ionic provider can be reduced by 22.2% compared with sample 5.

TABLE-US-00001 Item ionic provider proportion of ionic provider generated oxygen index sample 5(base) none none 1 sample 6 Na.sub.3PO.sub.4 10% 77.8%

[0037] Please refer to FIG. 3, which is a thermogram of the differential scanning calorimeter with or without the ionic provider. An appropriate amount of these samples (Sample 5 and Sample 6) are taken by a spatula. Then place them on the DSC special sample tray, and seal the sample tray. The DSC test is carried out on the samples under the temperature rising from 30° C. to 300° C. at a rate of 5° C./min. It can be seen from the FIG. 3 that the sample 6 with the ionic provider can shift the trigger temperature of the exothermic reaction backward. Therefore, the lithium secondary battery is allowed to withstand higher temperature.

[0038] The following Table 2 is the difference table of generated gas between samples with and without the lithium receiver. The composition of the sample 7 is 62.153% C/SiO, 2.049% electrically conductive material, 4.098% adhesive and 31.7% electrolyte by weight. The production method of the sample 7 is to mix 62.153% C/SiO, 2.049% electrically conductive material, 4.098% adhesive and 31.7% electrolyte by weight and coat on a negative current collector to form a negative active material layer. Then a separator, a positive active material layer and a negative current collector are sequentially stacked on the surface of the negative active material layer. A sealing frame sandwiched between the positive current collector and the negative current collector is used to seal the positive active material layer, the separator and the negative active material layer between the positive current collector, the sealing frame and the negative current collector to form a laminated battery sheet. The laminated battery sheet is formed with a 100% SOC(state of charge). Then the formed negative active material layer is scraped off and pressed under 0.9 N for 1 minute to form a sheet to obtain the sample 7. The composition of the sample 8 is 31.0765% C/SiO, 1.0245% electrically conductive material, 2.049% adhesive, 15.85% electrolyte and 50% CaHPO.sub.4 by weight. The production method of the sample 8 is to mix 62.153% C/SiO, 2.049% electrically conductive material, 4.098% adhesive and 31.7% electrolyte by weight and coat on a negative current collector to form a negative active material layer. Then a separator, a positive active material layer and a negative current collector are sequentially stacked on the surface of the negative active material layer. A sealing frame sandwiched between the positive current collector and the negative current collector is used to seal the positive active material layer, the separator and the negative active material layer between the positive current collector, the sealing frame and the negative current collector to form a laminated battery sheet. The laminated battery sheet is formed with a 100% SOC(state of charge). Then the formed negative active material layer is scraped off to mix and grind with CaHPO.sub.4 with the same weight. The mixture is pressed under 0.9 N for 1 minute to form a sheet to obtain the sample 8. The production method of the sample 9 is almost the same with the production method of the sample 8. Only CaHPO.sub.4 is replaced with Cu.sub.2P.sub.2O.sub.7. Samples 7 to 9 are analysed by GC-MS(gas chromatography-mass spectrometry) respectively for oxygen, carbon monoxide and gaseous alkane. In GC-MS analysis, the headspace extraction temperature is 200° C., and extraction time is 20 minutes. Then sample 1 ml to heat from 40° C. to 250° C. As following Table 2, after the above GC-MS analysis, the generated oxygen of sample 8 with non-ionic provider is increased compared with sample 7, and the generated oxygen of sample 9 with ionic provider is reduced compared with sample 7.

TABLE-US-00002 Item ionic provider generated oxygen index generated CO index generated CO&CH index generated H.sub.2 index sample 7(base) none 1 - - - sample 8 CaHPO.sub.4 108.93% - - - sample 9 Cu.sub.2P.sub.2O.sub.7 77.81% - - -

[0039] The following Table 3 is the difference table of generated gas between samples with and without the lithium receiver. The composition of sample 10 is 62.153% C/SiO, 2.049% electrically conductive material, 4.098% adhesive and 31.7% electrolyte by weight. The production method of the sample 10 is to mix 62.153% C/SiO, 2.049% electrically conductive material, 4.098% adhesive and 31.7% electrolyte by weight to form an electrode film. The electrode film is used as a positive electrode of a coin cell. The coin cell is formed with a 100% SOC(state of charge) thereof. Then the electrode film is directly taken out as sample 10. The composition of sample 11 is 52.153% C/SiO, 2.049% electrically conductive material, 4.098% adhesive, 31.7% electrolyte and 10% Cu.sub.2P.sub.2O.sub.7 by weight. The production method of the sample 11 is to mix all the above-mentioned materials to form an electrode film. The electrode film is used as a positive electrode of a coin cell. The coin cell is formed with a 100% SOC(state of charge) thereof. Then the electrode film is directly taken out as sample 11. The production method of the sample 12 is almost the same with the production method of the sample 11. Only Cu.sub.2P.sub.2O.sub.7 is replaced with Fe.sub.4(P.sub.2O.sub.7).sub.3. Samples 10 to 12 are analysed by GC-MS/GC-TCD(gas chromatography-thermal conductivity detector) respectively. In this analysis, samples 10 to 12 are placed into special sample bottles for GC-MS/GC-TCD analysis. In a glove box, the oxygen in the sample bottles is replaced with argon. Then, use parafilm to seal the sample bottles to avoid air infiltration. GC-MS is used to analyse oxygen, carbon monoxide and gaseous alkane and GC-TCD is used to analyse hydrogen. In the analysis, the headspace extraction temperature is 200° C., and extraction time is 20 minutes. Then sample 1 ml to heat from 40° C. to 250° C. As following Table 3, the generated gas of samples 11 to 12 with ionic provider can be greatly reduced compared with sample 10.

TABLE-US-00003 Item ionic provider generated oxygen index generated CO index generated CO&CH index generated H.sub.2 index sample 10(base) none 1 1 1 1 sample 11 Cu.sub.2P.sub.2O.sub.7 18.40% 5.70% 3.50% 40.60% sample 12 Fe.sub.4(P.sub.2O.sub.7).sub.3 3.10% 6.30% 3.60% 65.60%

[0040] Accordingly, the present invention provides a lithium secondary battery capable of suppressing thermal runaway. An ionic provider is added to the positive electrode and/or a lithium receiver is added to the negative electrode. The ionic provider can absorb thermal energy caused by the rising temperature of the lithium secondary battery to release the reactive cation. The reactive cation will insert the location with lithium-ion extraction of the positive electrode to make the lattice structure of the positive active material be stable. Therefore, the release of atomic oxygen is avoided. For the negative electrode, the lithium receiver is used to receive the excessive lithium to demonstrate the material properties near to the original raw material of the negative electrode. Therefore, it will present a stable state to effectively suppress the thermal runaway.

[0041] The invention being thus described, it will be obvious that the same may be varied in many ways. Such variations are not to be regarded as a departure from the spirit and scope of the invention, and all such modifications as would be obvious to one skilled in the art are intended to be included within the scope of the following claims.