WO2019143306A1 - Gel (cross linked) polymeric binder for high performance lithium ion batteries - Google Patents
Gel (cross linked) polymeric binder for high performance lithium ion batteries Download PDFInfo
- Publication number
- WO2019143306A1 WO2019143306A1 PCT/TR2018/050017 TR2018050017W WO2019143306A1 WO 2019143306 A1 WO2019143306 A1 WO 2019143306A1 TR 2018050017 W TR2018050017 W TR 2018050017W WO 2019143306 A1 WO2019143306 A1 WO 2019143306A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- polymer
- cross linked
- polymeric binder
- gel
- formula
- Prior art date
Links
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/62—Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
- H01M4/621—Binders
- H01M4/622—Binders being polymers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/13—Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulators; Processes of manufacture thereof
- H01M4/134—Electrodes based on metals, Si or alloys
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/02—Electrodes composed of, or comprising, active material
- H01M4/36—Selection of substances as active materials, active masses, active liquids
- H01M4/38—Selection of substances as active materials, active masses, active liquids of elements or alloys
- H01M4/386—Silicon or alloys based on silicon
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
Definitions
- the present invention relates to a gel polymer binder used for high performance lithium ion batteries.
- the present invention relates to a gel polymer binder containing polyvinyl alcohol or polyhydroxyethyl methacrylate units and a polyfluorene- phenylene copolymer, which is conjugated with carboxylic acid for cross linking and electrolyte reception.
- a Si-based composite anode is generated by using a compound comprising Si particles (active agent), carbon (conductive agent) and a polymeric binder; and most researches are directed towards developing and modifying various pure forms; silicon nanotubes, nanoporous silicon and Si thin thrombocytes are used for preventing the recycling capacity of Si-based electrode materials.
- silicone materials have improved electrochemical performance, the wide surface areas of Si structures arising from their small sizes usually increase the surface failure percentages, therefore several problems need to be solved in order to commercialize these for LIB’s. Such failures cause weak cycles and consequently, supportive inactive compounds such as binders and conductive agents, which consume the capacity, in excessive amounts are required for establishing contacts among the particles.
- the synthesis of nano sized Si materials requires complex preparation procedures, thereby inevitably increasing production costs.
- the polymers used as binders in electrodes can suppress the volumetric expansions and the resulting internal stresses created by the reaction of the commercially used graphite with lithium, and can maintain the structure.
- the binding polymers (CMC, PVDF, EPDM) used for graphite in metals which are tried instead of graphite and which exhibit over 200% volumetric change as a result of their reaction with lithium, do not possess the flexibility and binding performance that can tolerate the volumetric changes exhibited due to the metals (Al, Si, Sn, Sb) being able to hold more lithium. Therefore, the use of polymers in metals exhibiting such high volumetric changes, which are to be used as active agents in the electrodes of lithium ion batteries, poses great significance.
- Electrode active materials used in lithium ion batteries are not sufficiently conductive and, accordingly, that the electrode structure deforms at high charge -discharge speeds.
- additives which increase conductivity are added to the electrode active agents.
- These additives can be carbon-based materials (such as carbon black, graphene, super-P conductive) or conductive polymers (PT, PANI).
- carbon-based materials such as carbon black, graphene, super-P conductive
- PT, PANI conductive polymers
- the addition of carbon-based materials in addition to the polymers used as binders for the purpose of increasing conductivity increases costs and the weight of the battery, and nowadays it became important to provide conductive properties to the polymers used as binders.
- an improved polymeric binder for forming silicon electrodes is disclosed.
- This polymer includes a poly 9, 9-dioctylfluorene and 9-fluorenone copolymer.
- electrode materials include an electrode active material combined with a binder that is formed of cross linked polymeric material, optionally polyvinyl alcohol cross linked with lithium tetraborate.
- the developed material optionally includes silicon, silicon carbon composites, lithium alloys, lithium metal oxides, lithium metal phosphates, transition metal oxides, nitride materials and fluorine materials.
- an anode for use in a lithium-ion battery consists of a polymeric gel binder made of at least two polymers having carboxylic acid groups and silicon particles.
- the anode of said invention contains polyvinyl alcohol.
- the exemplary patent documents focus on the formation of cross linked gel by using polyvinyl alcohol groups against polyacrylic acid.
- fluorene (F) has been included in order to form the electronic structure of the polymer, which is a polyfluorene type of conductive polymer, and different groups have been used to be copolymerized in order to increase the adhesion strength between the polymer binders.
- the gel polymer binders included in the disclosed documents are not flexible or conductive and they have high production costs. Therefore, it is necessary to develop the gel cross polymeric binder of the present invention.
- the objective of the present invention is to provide a gel polymeric binder with cross links, which is flexible, conductive and which incurs low production costs.
- the objective of the present invention is to provide a new gel polymeric binder with cross links, which is induced by an interaction between the polyfluorene- phenylene carboxylic acid (PF-co-PPC) copolymer and polyvinyl alcohol (PVA) units.
- PF-co-PPC polyfluorene- phenylene carboxylic acid
- PVA polyvinyl alcohol
- Another objective of the present invention is to provide a gel polymeric binder which has a high charging capacity.
- Yet another objective of the present invention is to provide a gel polymeric binder which has both ionic and electrical conductivity in a single polymer chain.
- the present invention provides a new polymeric binder with cross links, which is induced by an interaction between the polyfluorene-phenylene carboxylic acid (PF-co-PPC) copolymer and polyvinyl alcohol (PVA) units.
- PF-co-PPC has a conjugated aromatic structure which has carboxylic acid groups for the hydrogen bonds which can partake in the specific interactions with the hydroxyl group of PVA.
- PF-co-PPC/PVA gives Si composite electrodes with high mechanical resistance on Si and provides a battery performance which is distinctly improved when compared to conventional binders.
- the developed Si-based composite anode provides a perfect cyclic performance with a high charging capacity.
- conjugated (conductive) polymer which includes carboxylic acid groups is obtained through polymerization with suitable duration, temperature and catalysts, by using various derivatives of dioctylfluorene boronic ester and various derivatives of dibromobenzoic acid (Diagram 1).
- the polymers obtained herein are Ri and R 2 , methylene groups and their C number can vary between 1 - 17.
- the m number (polymer repeating unit) of the obtained polymer can vary between 1 -1.000.000 (Formula 1).
- the conductive polymer with carboxylic acid content as shown in Formula I and Formula II is handled with a strong base (NaOH or KOH) and is converted into sodium/potassium carboxylate salt form (Diagram 2).
- the polymer which is converted into sodium/potassium carboxylate salt form is cross linked with a polymer containing hydroxyl group, such as polyvinyl alcohol or polyhydroxyethylmethacrylate, through a thermal process at 25-250 0 C, thereby obtaining a porous structure.
- a polymer containing hydroxyl group such as polyvinyl alcohol or polyhydroxyethylmethacrylate
- the molecular weight of the polyvinyl alcohol or polyhydroxyethylmethacrylate (commercial polymers), which are used herein, should be between 1-150.000.
- the surface area of the porous structure has been measured via the BET porosimetry method and has been found to be 100- 800 m 2 /g. Thanks to the created pores, the silicon used in the lithium ion battery has been prevented from degrading due to volumetric expansion.
- the obtained cross linked material is shown in formula IV.
- electrodes are produced by using the conductive and flexible polymers from which the electrode active agents are synthesized.
- the synthesized polymer has conductive and flexible groups.
- the polymers which are commercially used in lithium batteries are not flexible or conductive. Thanks to the conductivity provided to the electrode via the conductive polymer of the present invention, the carbon based materials which are commercially used in electrodes to increase conductivity are not used herein.
- the electrode structure maintains its integrity thanks to the flexibility provided by the developed polymer. Because, due to the operating mechanism of the battery, Li + ions move between anode and cathode electrodes, they settle inside these electrode structures and this causes volumetric swelling in the electrode structure. The structure, which is not flexible enough, breaks and disbands due to swelling.
- the flexible polymers obtained with the present invention are able to compensate such volumetric swellings.
- the active material is able to maintain its structure during the swelling and shrinking observed when the battery is charged or discharged. This enables the electrode to endure long cycles.
- the capacity of the electrode is mostly utilized since the structure is prevented from being pulverized. This, in turn, extends the life and capacity of the battery.
Abstract
The present invention relates to a gel polymer binder containing polyvinyl alcohol units and a polyfluorene-phenylene copolymer, which is conjugated with carboxylic acid for enabling cross linking and electrolyte reception.
Description
GEL (CROSS LINKED) POLYMERIC BINDER FOR HIGH
PERFORMANCE LITHIUM ION BATTERIES
Technical Field of Invention The present invention relates to a gel polymer binder used for high performance lithium ion batteries.
More specifically, the present invention relates to a gel polymer binder containing polyvinyl alcohol or polyhydroxyethyl methacrylate units and a polyfluorene- phenylene copolymer, which is conjugated with carboxylic acid for cross linking and electrolyte reception.
Prior Art
Due to the use of silicon (Si) as the negative electrode material instead of the conventional graphite anode, significant volume changes (>400%) occur during lithiation, which is quite harmful for the cycle stability of Lithium Ion Batteries (LIBs). The mechanical stress caused by this repeated volume change breaks the anode composite and separates the components of LIBs from each other; this, in turn, causes a weak electrical contact between the Si particles and leads to a significant degradation of the electrode during the cycle. Even worse, this negative effect becomes more apparent when the electrode is generated for practical, high energy cells which require the active agents to be highly loaded on the current collector.
Generally, a Si-based composite anode is generated by using a compound comprising Si particles (active agent), carbon (conductive agent) and a polymeric binder; and most researches are directed towards developing and modifying various pure forms; silicon nanotubes, nanoporous silicon and Si thin thrombocytes are used for preventing the recycling capacity of Si-based electrode materials. Even though silicone materials have improved electrochemical
performance, the wide surface areas of Si structures arising from their small sizes usually increase the surface failure percentages, therefore several problems need to be solved in order to commercialize these for LIB’s. Such failures cause weak cycles and consequently, supportive inactive compounds such as binders and conductive agents, which consume the capacity, in excessive amounts are required for establishing contacts among the particles. Furthermore, the synthesis of nano sized Si materials requires complex preparation procedures, thereby inevitably increasing production costs.
The chemical cross linking of alginate, acidic and hyper branched polymeric bonds is proposed as increasing the stability of LIBs through Si-based electrodes. On the other hand, even though the chemically cross linked polymers which are connected to each other in three dimensions exhibit high mechanical resistance against tension and unrecoverable deformation due to strong interaction among polymer chains, the nature of the chemical cross linking also increases the rigidity of the polymer. This causes a gradual and irreversible breaking of the grid, thereby causing the cell performance to be faulty during long term battery operation.
The polymers used as binders in electrodes can suppress the volumetric expansions and the resulting internal stresses created by the reaction of the commercially used graphite with lithium, and can maintain the structure. However, the binding polymers (CMC, PVDF, EPDM) used for graphite in metals, which are tried instead of graphite and which exhibit over 200% volumetric change as a result of their reaction with lithium, do not possess the flexibility and binding performance that can tolerate the volumetric changes exhibited due to the metals (Al, Si, Sn, Sb) being able to hold more lithium. Therefore, the use of polymers in metals exhibiting such high volumetric changes, which are to be used as active agents in the electrodes of lithium ion batteries, poses great significance.
Another problem experienced with the electrode active materials used in lithium ion batteries is that they are not sufficiently conductive and, accordingly, that the electrode structure deforms at high charge -discharge speeds. For this reason, additives which increase conductivity are added to the electrode active agents. These additives can be carbon-based materials (such as carbon black, graphene, super-P conductive) or conductive polymers (PT, PANI). However, the addition of carbon-based materials in addition to the polymers used as binders for the purpose of increasing conductivity increases costs and the weight of the battery, and nowadays it became important to provide conductive properties to the polymers used as binders.
So, it is of great importance that the polymer or polymers to be used to are flexible, conductive and quite reasonable in terms of production costs.
In the known art, polymeric binders for lithium ion batteries have been developed.
In the US patent document numbered US2013288126 of the known art, a family of carboxylic acid groups containing fluorene copolymers is used as binders of silicon particles in the fabrication of negative electrodes for use with lithium ion batteries. In the document, the polyvinylalcohol ether backbone structure of the conductive polymer binder is also present.
In the US patent document numbered US2012119155 of the known state of the art, an improved polymeric binder for forming silicon electrodes is disclosed. This polymer includes a poly 9, 9-dioctylfluorene and 9-fluorenone copolymer.
In the International patent document numbered WO2016145341 of the known art, electrode materials are disclosed that include an electrode active material combined with a binder that is formed of cross linked polymeric material, optionally polyvinyl alcohol cross linked with lithium tetraborate. The developed material optionally includes silicon, silicon carbon composites, lithium alloys, lithium metal oxides, lithium metal phosphates, transition metal oxides, nitride materials and fluorine materials.
In the US patent document numbered US2016164099 of the known art, an anode for use in a lithium-ion battery consists of a polymeric gel binder made of at least two polymers having carboxylic acid groups and silicon particles. The anode of said invention contains polyvinyl alcohol. The exemplary patent documents focus on the formation of cross linked gel by using polyvinyl alcohol groups against polyacrylic acid. In order to optimize its electronic and mechanical properties, first, fluorene (F) has been included in order to form the electronic structure of the polymer, which is a polyfluorene type of conductive polymer, and different groups have been used to be copolymerized in order to increase the adhesion strength between the polymer binders.
Yet, the gel polymer binders included in the disclosed documents are not flexible or conductive and they have high production costs. Therefore, it is necessary to develop the gel cross polymeric binder of the present invention.
Objectives and Brief Description of the Invention The objective of the present invention is to provide a gel polymeric binder with cross links, which is flexible, conductive and which incurs low production costs.
The objective of the present invention is to provide a new gel polymeric binder with cross links, which is induced by an interaction between the polyfluorene- phenylene carboxylic acid (PF-co-PPC) copolymer and polyvinyl alcohol (PVA) units.
Another objective of the present invention is to provide a gel polymeric binder which has a high charging capacity.
Yet another objective of the present invention is to provide a gel polymeric binder which has both ionic and electrical conductivity in a single polymer chain.
The present invention provides a new polymeric binder with cross links, which is induced by an interaction between the polyfluorene-phenylene carboxylic acid (PF-co-PPC) copolymer and polyvinyl alcohol (PVA) units. PF-co-PPC has a conjugated aromatic structure which has carboxylic acid groups for the hydrogen bonds which can partake in the specific interactions with the hydroxyl group of PVA. PF-co-PPC/PVA gives Si composite electrodes with high mechanical resistance on Si and provides a battery performance which is distinctly improved when compared to conventional binders. The developed Si-based composite anode provides a perfect cyclic performance with a high charging capacity. Detailed Description of the Invention
In the present invention, conjugated (conductive) polymer which includes carboxylic acid groups is obtained through polymerization with suitable duration, temperature and catalysts, by using various derivatives of dioctylfluorene boronic ester and various derivatives of dibromobenzoic acid (Diagram 1). The polymers obtained herein are Ri and R2, methylene groups and their C number can vary between 1 - 17. The m number (polymer repeating unit) of the obtained polymer can vary between 1 -1.000.000 (Formula 1).
Diagram 1:
As an alternative to the reaction illustrated in Diagram 1, the synthesis and application of polymethacrylic acid (PMAA) polyhydroxyethylmethacrylate (PHEMA) exhibit similarities to the polymer mentioned in Formula I (Formula II).
The conductive polymer with carboxylic acid content as shown in Formula I and Formula II is handled with a strong base (NaOH or KOH) and is converted into sodium/potassium carboxylate salt form (Diagram 2).
Diagram 2:
The polymer which is converted into sodium/potassium carboxylate salt form is cross linked with a polymer containing hydroxyl group, such as polyvinyl alcohol or polyhydroxyethylmethacrylate, through a thermal process at 25-250 0 C, thereby obtaining a porous structure. The molecular weight of the polyvinyl alcohol or polyhydroxyethylmethacrylate (commercial polymers), which are used herein, should be between 1-150.000. The surface area of the porous structure has been measured via the BET porosimetry method and has been found to be 100- 800 m2/g. Thanks to the created pores, the silicon used in the lithium ion battery
has been prevented from degrading due to volumetric expansion. The obtained cross linked material is shown in formula IV.
In the present invention, electrodes are produced by using the conductive and flexible polymers from which the electrode active agents are synthesized. The synthesized polymer has conductive and flexible groups. The polymers which are commercially used in lithium batteries are not flexible or conductive. Thanks to the conductivity provided to the electrode via the conductive polymer of the present invention, the carbon based materials which are commercially used in electrodes to increase conductivity are not used herein. Moreover, the electrode structure maintains its integrity thanks to the flexibility provided by the developed polymer. Because, due to the operating mechanism of the battery, Li+ ions move between anode and cathode electrodes, they settle inside these electrode structures and this causes volumetric swelling in the electrode structure. The structure, which is not flexible enough, breaks and disbands due to swelling. The flexible polymers obtained with the present invention are able to compensate such volumetric swellings. Thus the active material is able to maintain its structure during the swelling and shrinking observed when the battery is charged or discharged. This enables the electrode to endure long cycles. Furthermore, the capacity of the electrode is mostly utilized since the structure is prevented from being pulverized. This, in turn, extends the life and capacity of the battery.
Claims
1. The present invention is a gel cross linked polymeric binder according to formula IV ;
2. The invention is a method for obtaining gel cross linked polymeric binder;
characterized in that it comprises the steps of; obtaining the conjugated (conductive) polymer, which includes carboxylic acid groups, as in formula I through polymerization performed by using the derivatives of dioctylfluorene boronic ester and dibromobenzoic acid; or as in formula II though the synthesis and application of polymethacrylic acid (PMAA) polyhydroxyethyl methacrylate (PHEMA), wherein
Rl and R2 are: methylene groups and the carbon (C) number is: 1-17,
m is: 1-1,000,000
converting the obtained conductive polymer, which contains carboxylic acid, into sodium/potassium carboxylate salt form by handling said polymer with strong bases such as NaOH or KOH, and; obtaining a cross linked polymeric binder with a porous structure as in formula IV, by enabling the polymer which is converted into the sodium/potassium carboxylate salt form, to be cross linked with a polymer such as polyvinyl alcohol or polyhydroxyethylmethacrylate through a thermal process at 25-250 °C.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2019527846A JP2020510953A (en) | 2018-01-19 | 2018-01-19 | Gel (crosslinked) polymer binder for high performance lithium ion batteries |
PCT/TR2018/050017 WO2019143306A1 (en) | 2018-01-19 | 2018-01-19 | Gel (cross linked) polymeric binder for high performance lithium ion batteries |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/TR2018/050017 WO2019143306A1 (en) | 2018-01-19 | 2018-01-19 | Gel (cross linked) polymeric binder for high performance lithium ion batteries |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2019143306A1 true WO2019143306A1 (en) | 2019-07-25 |
Family
ID=64100708
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/TR2018/050017 WO2019143306A1 (en) | 2018-01-19 | 2018-01-19 | Gel (cross linked) polymeric binder for high performance lithium ion batteries |
Country Status (2)
Country | Link |
---|---|
JP (1) | JP2020510953A (en) |
WO (1) | WO2019143306A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114539537A (en) * | 2022-02-21 | 2022-05-27 | 中化国际(控股)股份有限公司 | Binder for lithium ion battery electrode material and preparation method thereof |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20120119155A1 (en) | 2009-05-18 | 2012-05-17 | The Regents Of The University Of California | Electronically conductive polymer binder for lithium-ion battery electrode |
US20130260239A1 (en) * | 2010-06-02 | 2013-10-03 | Gao Liu | Si Composite Electrode with Li Metal Doping for Advanced Lithium-ion Battery |
US20130288126A1 (en) | 2009-05-18 | 2013-10-31 | The Regents Of The University Of California | Electronically conductive polymer binder for lithium-ion battery electrode |
US20160164099A1 (en) | 2013-07-29 | 2016-06-09 | The Penn State Research Foundation | Elastic gel polymer binder for silicon-based anode |
WO2016145341A1 (en) | 2015-03-11 | 2016-09-15 | Navitas Systems, Llc | Crosslinked polymeric battery materials |
WO2017119861A1 (en) * | 2016-01-07 | 2017-07-13 | Enwair Enerji Teknolojileri A. S. | Usage of conductive and flexible polymers in lithium batteries |
-
2018
- 2018-01-19 JP JP2019527846A patent/JP2020510953A/en active Pending
- 2018-01-19 WO PCT/TR2018/050017 patent/WO2019143306A1/en active Application Filing
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20120119155A1 (en) | 2009-05-18 | 2012-05-17 | The Regents Of The University Of California | Electronically conductive polymer binder for lithium-ion battery electrode |
US20130288126A1 (en) | 2009-05-18 | 2013-10-31 | The Regents Of The University Of California | Electronically conductive polymer binder for lithium-ion battery electrode |
US20130260239A1 (en) * | 2010-06-02 | 2013-10-03 | Gao Liu | Si Composite Electrode with Li Metal Doping for Advanced Lithium-ion Battery |
US20160164099A1 (en) | 2013-07-29 | 2016-06-09 | The Penn State Research Foundation | Elastic gel polymer binder for silicon-based anode |
WO2016145341A1 (en) | 2015-03-11 | 2016-09-15 | Navitas Systems, Llc | Crosslinked polymeric battery materials |
WO2017119861A1 (en) * | 2016-01-07 | 2017-07-13 | Enwair Enerji Teknolojileri A. S. | Usage of conductive and flexible polymers in lithium batteries |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114539537A (en) * | 2022-02-21 | 2022-05-27 | 中化国际(控股)股份有限公司 | Binder for lithium ion battery electrode material and preparation method thereof |
Also Published As
Publication number | Publication date |
---|---|
JP2020510953A (en) | 2020-04-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US11326010B2 (en) | Agent for dispersing electrically conductive carbon material, and dispersion of electrically conductive carbon material | |
US20160164099A1 (en) | Elastic gel polymer binder for silicon-based anode | |
EP3493304B1 (en) | Conductive resin composition for electrodes, electrode composition, electrode using same and lithium ion battery | |
WO2013002504A2 (en) | Novel polymer electrolyte and lithium secondary battery including same | |
CN109004220B (en) | Boric acid compound modified lithium ion battery silicon cathode and preparation method thereof | |
CN110336037B (en) | Water-based binder for lithium ion battery cathode material and preparation method thereof | |
JP2017050152A (en) | Sulfur-based positive electrode active material, positive electrode and lithium ion secondary battery | |
KR20190059119A (en) | An all solid lithium-polymer secondary battery and method of manufacturing them a secondary battery including a positive electrode | |
JP6621994B2 (en) | Negative electrode material for lithium secondary battery and method for producing the same, composition for negative electrode active material layer for lithium secondary battery using the negative electrode material, negative electrode for lithium secondary battery, and lithium secondary battery | |
CN107408698B (en) | Negative active material and method for preparing same | |
CN114122400A (en) | Negative pole piece and lithium ion battery containing same | |
Liu et al. | Influence of binder on impedance of lithium batteries: a mini-review | |
JP2008198408A (en) | Nonaqueous electrolyte secondary battery | |
WO2019143306A1 (en) | Gel (cross linked) polymeric binder for high performance lithium ion batteries | |
CN113169303A (en) | Binder for electrochemical device, electrode mixture, electrode, electrochemical device, and secondary battery | |
US10312505B2 (en) | Usage of conductive and flexible polymers in lithium batteries | |
CN111384398A (en) | Composite conductive adhesive suitable for silicon-based negative electrode of lithium ion battery | |
CN112786879B (en) | Negative electrode material for sodium ion battery and sodium ion battery | |
KR20110078307A (en) | Metal based zn negative active material and lithium secondary battery comprising thereof | |
WO2023282248A1 (en) | Composition for electrode formation | |
KR20200107733A (en) | Secondary battery, fuel battery and separator for secondary battery or fuel battery and manufacturing method of separator for secondary battery or fuel battery | |
WO2023282246A1 (en) | Composition for forming electrode | |
US20240006613A1 (en) | Porous solid compound, method for preparing same, cathode for lithium secondary battery comprising porous solid compound, and lithium secondary battery | |
KR102611099B1 (en) | Method for Anode for lithium secondary battery comprising silicon-metal silicide-carbon composition and Anode for lithium secondary battery manufactured thereby | |
CN115403033B (en) | Conductive agent for lithium ion battery, negative electrode and preparation method thereof, and lithium ion battery |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
ENP | Entry into the national phase |
Ref document number: 2019527846 Country of ref document: JP Kind code of ref document: A |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 18796790 Country of ref document: EP Kind code of ref document: A1 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 18796790 Country of ref document: EP Kind code of ref document: A1 |