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Shape-conformable alkali metal battery having a conductive and deformable quasi-solid polymer electrode

An alkali metal, quasi-solid technology, used in battery electrodes, active material electrodes, non-aqueous electrolyte batteries, etc., can solve problems such as low diffusion coefficient, inability to effectively and efficiently transport electrons and heat, and long recharge time.

Active Publication Date: 2020-01-10
NANOTEK INSTR
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The past two decades have witnessed continuous improvements in Li-ion batteries in terms of energy density, rate capability, and safety, but Li metal batteries with significantly higher energy densities have been largely ignored for some reason.
However, the use of graphite-based anodes in Li-ion batteries has several significant disadvantages: low specific capacity (372 mAh / g theoretical capacity compared to 3,860 mAh / g for Li metal), long Li intercalation time (e.g. Li entry and Low solid-state diffusion coefficients away from graphite and inorganic oxide particles) require long recharge times (e.g. 7 hours for electric vehicle batteries), cannot deliver high pulse power (power density << 1kW / kg), and require the use of pre-lithium cathodes (e.g. lithium cobalt oxide), thus limiting the choice of available cathode materials
[0010] (1) The actual capacity achievable with current cathode materials (such as lithium iron phosphate and lithium transition metal oxides) has been limited to the range of 150-250mAh / g, and in most cases, less than 200mAh / g
[0011] (2) Intercalation and deintercalation of lithium into and out of these commonly used cathodes relies on Li in the -8 to 10 -14 cm 2 / s) in solid particles (resulting in very low power densities (another longstanding problem with today's Li-ion batteries))
[0012] (3) Current cathode materials are electrically and thermally insulating and cannot effectively and efficiently transport electrons and heat
Conversely, thicker samples tend to become extremely brittle or have poor structural integrity and will also require the use of large amounts of binder resin

Method used

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  • Shape-conformable alkali metal battery having a conductive and deformable quasi-solid polymer electrode
  • Shape-conformable alkali metal battery having a conductive and deformable quasi-solid polymer electrode
  • Shape-conformable alkali metal battery having a conductive and deformable quasi-solid polymer electrode

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0154] Example 1: Preparation of Graphene Oxide (GO) and Reduced Graphene Oxide (RGO) Nanosheets from Natural Graphite Powder

[0155] Natural graphite from Huadong Graphite Co. (Qingdao, China) was used as starting material. GO was obtained by following the well-known modified Hummers method involving two oxidation stages. In a typical procedure, the first oxidation is achieved under the following conditions: 1100 mg of graphite is placed in a 1000 mL long-necked flask. Then, add 20 g of K in the flask 2 S 2 o 8 , 20g of P 2 o 5 and 400 mL of concentrated H 2 SO 4 Aqueous solution (96%). The mixture was heated at reflux for 6 hours and then left undisturbed at room temperature for 20 hours. Graphite oxide was filtered and rinsed with copious amounts of distilled water until neutral pH. A wet cake material is recovered at the end of this first oxidation.

[0156] For the second oxidation process, place the previously collected wet cake in a solution containing 69 mL...

example 2

[0160] Example 2: Preparation of pristine graphene sheets (essentially 0% oxygen)

[0161] Recognizing the possibility that the high number of defects in GO sheets act to reduce the conductivity of individual graphene planes, we decided to investigate whether using pristine graphene sheets (non-oxidized and oxygen-free, non-halogenated and halogen-free, etc.) and thermally conductive conductive additives. Pre-lithiated native graphene has also been used as an anode active material. Native graphene sheets are produced using direct sonication or liquid-phase production processes.

[0162] In a typical procedure, 5 grams of graphite flakes ground to a size of approximately 20 μm or less were dispersed in 1,000 mL of deionized water (containing 0.1% by weight of FSO) to obtain a suspension. An ultrasonic energy level of 85 W (Branson S450 ultrasonic generator) was used for the expansion, separation and size reduction of the graphene sheets for a period of 15 minutes to 2 hours...

example 3

[0164] Example 3: Preparation of pre-lithiated graphene fluoride sheets as anode active materials for lithium-ion batteries

[0165] We have used several methods to produce GF, but only one method is described here as an example. In a typical procedure, highly expanded graphite (HEG) is prepared from an intercalation compound С 2 F·xClF 3 preparation. HEG is further fluorinated by chlorine trifluoride vapor to produce fluorinated highly expanded graphite (FHEG). A pre-cooled Teflon reactor was filled with 20-30 mL of liquid pre-cooled ClF 3 , the reactor was closed and cooled to liquid nitrogen temperature. Then, no more than 1 g of HEG was placed in a container with 3 The gas enters the reactor and is located in the pores within the reactor. Formed within 7-10 days with approximate formula C 2 Gray beige product of F.

[0166] Subsequently, a small amount of FHEG (approximately 0.5 mg) was mixed with 20-30 mL of organic solvents (methanol and ethanol, respectively) an...

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Abstract

Provided is method of preparing an alkali metal cell, the method comprising: (a) combining a quantity of an active material, a quantity of an electrolyte, and a conductive additive to form a deformable and conductive electrode material, wherein the conductive additive, containing conductive filaments, forms a 3D network of electron-conducting pathways and the electrolyte contains an alkali salt and an ion-conducting polymer dissolved or dispersed in a solvent; (b) forming the electrode material into a quasi-solid polymer electrode, wherein the forming includes deforming the electrode materialinto an electrode shape without interrupting the 3D network of electron-conducting pathways such that the electrode maintains an electrical conductivity no less than 10-6 S / cm; (c) forming a second electrode; and (d) forming an alkali metal cell by combining the quasi-solid electrode and the second electrode. The second electrode may also be a quasi-solid polymer electrode.

Description

[0001] Cross References to Related Applications [0002] This application claims priority to U.S. Patent Application No. 15 / 608,597, filed May 30, 2017, and U.S. Patent Application No. 15 / 610,136, filed May 31, 2017, which are incorporated herein by reference. technical field [0003] The present invention relates generally to the field of alkali metal batteries, including rechargeable lithium metal batteries, sodium metal batteries, lithium ion batteries, sodium ion batteries, lithium ion capacitors and sodium ion capacitors. Background technique [0004] Historically, today's most popular rechargeable energy storage device—the lithium-ion battery—was actually derived from rechargeable "lithium metal batteries" using lithium (Li) metal or Li alloys as the anode and Li intercalation compounds as the cathode. developed. Li metal is an ideal anode material due to its light weight (the lightest metal), high electronegativity (−3.04 V vs. standard hydrogen electrode), and high ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M2/16H01M4/02H01M4/04H01M10/05C25D9/06C25D9/08C25D7/06
CPCH01M4/13H01M4/134H01M4/139H01M4/1395H01M4/38H01M4/381H01M4/382H01M4/40H01M4/405H01M4/62H01M4/622H01M4/625H01M4/626H01M10/052H01M10/054H01M2004/021H01M2004/027H01M2004/028C25D7/0614Y02E60/10C25D9/08H01M10/0565H01M2300/0085
Inventor 阿茹娜·扎姆张博增
Owner NANOTEK INSTR
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