CN110372358A - A kind of electric field induction crystalline A l3+、Be2+The K of doping2MgSi5O12Potassium fast-ionic conductor and preparation method - Google Patents

A kind of electric field induction crystalline A l3+、Be2+The K of doping2MgSi5O12Potassium fast-ionic conductor and preparation method Download PDF

Info

Publication number
CN110372358A
CN110372358A CN201910617293.0A CN201910617293A CN110372358A CN 110372358 A CN110372358 A CN 110372358A CN 201910617293 A CN201910617293 A CN 201910617293A CN 110372358 A CN110372358 A CN 110372358A
Authority
CN
China
Prior art keywords
potassium
fast
hours
potassium ion
minutes
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
CN201910617293.0A
Other languages
Chinese (zh)
Inventor
水淼
舒杰
任元龙
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ningbo University
Original Assignee
Ningbo University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ningbo University filed Critical Ningbo University
Priority to CN201910617293.0A priority Critical patent/CN110372358A/en
Publication of CN110372358A publication Critical patent/CN110372358A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/16Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silicates other than clay
    • C04B35/20Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on silicates other than clay rich in magnesium oxide, e.g. forsterite
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/05Accumulators with non-aqueous electrolyte
    • H01M10/054Accumulators with insertion or intercalation of metals other than lithium, e.g. with magnesium or aluminium
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/05Accumulators with non-aqueous electrolyte
    • H01M10/056Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes
    • H01M10/0561Accumulators with non-aqueous electrolyte characterised by the materials used as electrolytes, e.g. mixed inorganic/organic electrolytes the electrolyte being constituted of inorganic materials only
    • H01M10/0562Solid materials
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3205Alkaline earth oxides or oxide forming salts thereof, e.g. beryllium oxide
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/32Metal oxides, mixed metal oxides, or oxide-forming salts thereof, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3217Aluminum oxide or oxide forming salts thereof, e.g. bauxite, alpha-alumina
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/34Non-metal oxides, non-metal mixed oxides, or salts thereof that form the non-metal oxides upon heating, e.g. carbonates, nitrates, (oxy)hydroxides, chlorides
    • C04B2235/3418Silicon oxide, silicic acids, or oxide forming salts thereof, e.g. silica sol, fused silica, silica fume, cristobalite, quartz or flint
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/02Composition of constituents of the starting material or of secondary phases of the final product
    • C04B2235/30Constituents and secondary phases not being of a fibrous nature
    • C04B2235/44Metal salt constituents or additives chosen for the nature of the anions, e.g. hydrides or acetylacetonate
    • C04B2235/442Carbonates
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/65Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes
    • C04B2235/656Aspects relating to heat treatments of ceramic bodies such as green ceramics or pre-sintered ceramics, e.g. burning, sintering or melting processes characterised by specific heating conditions during heat treatment
    • C04B2235/6562Heating rate
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/96Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M2300/00Electrolytes
    • H01M2300/0017Non-aqueous electrolytes
    • H01M2300/0065Solid electrolytes
    • H01M2300/0068Solid electrolytes inorganic
    • H01M2300/0071Oxides
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Electrochemistry (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Condensed Matter Physics & Semiconductors (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Secondary Cells (AREA)
  • Conductive Materials (AREA)

Abstract

A kind of electric field induction crystalline A l3+、Be2+The K of doping2MgSi5O12Potassium fast-ionic conductor and preparation method, it is characterized in that: stoichiometric equation K2+2x+yMgBexAlySi5‑x‑yO12, in which: x=0.05-0.15;Y=0.05-0.15;Room temperature potassium ion conductivity is more than 510‑4S/cm.Using Al3+、Be2+Part replaces Si4+Ion generates gap potassium ion in crystal and reduces potassium ion migration activation energy;Pass through the Be of small ionic radii2+Doping adjusts the size of the migrating channels of potassium ion to adapt to the fast transferring of potassium ion;And during the preparation process in K2MgSi5O12The surface of particle is modified, and easy-sintering characteristic is formed.The induction crystallization of strong dc electric field is introduced simultaneously to accelerate the speed of crystallization, reduce the temperature of crystallization and improve crystallization integrity degree.These synergistic effects are so that the room temperature potassium ion conductivity of the potassium fast-ionic conductor is more than 510‑4S/cm is more nearly the potassium ion conductivity of liquid electrolyte.

Description

A kind of electric field induction crystalline A l3+、Be2+The K of doping2MgSi5O12Potassium fast-ionic conductor and Preparation method
Technical field
The present invention relates to a kind of solid potassium fast-ionic conductor manufacturing fields.
Background technique
Lithium ion battery has volume, weight energy than high, voltage is high, self-discharge rate is low, memory-less effect, cycle life The absolute advantages such as length, power density height possess in global mobile power source market and exceed 30,000,000,000 dollar/year shares and far more than other The occupation rate of market of battery is electrochmical power source [Wu Yuping, Wan Chunrong, Jiang Changyin, the lithium ion two of most market development prospect Primary cell, Beijing: Chemical Industry Press, 2002.].Lithium ion secondary battery is most of using liquid both at home and abroad at present Electrolyte, liquid lithium ionic cell have some unfavorable factors, and such as: liquid organic electrolyte may be revealed, in excessively high temperature Lower generation explosion can not apply the occasion high in some pairs of security requirements to cause safety accident;Liquid electrolyte lithium from The sub- generally existing Capacity fading problem of battery, after a period of use due to electrode active material in the electrolyte molten Solution, reaction and degradation failure [Z.R.Zhang, Z.L.Gong, and Y.Yang, J.Phys.Chem.B, 108,2004, 17546.].And all-solid-state battery it is highly-safe, substantially without Capacity fading, wherein fast as the solid that electrolyte uses Ion conductor also acts the effect of diaphragm, simplifies the structure of battery;Further, since also simplifying life without completely cutting off air To the requirement of equipment during production, the configuration design of battery is also more convenient and flexible, and [Wen Zhaoyin, Zhu Xiujian know hero etc., entirely perhaps The research of solid secondary batteries, the 12nd Chinese solid-state ionics academic meeting paper collection, 2004.].
In all-solid lithium-ion battery, migration rate of the carrier in fast-ionic conductor is often far smaller than electrode surface Electric charge transfer and ion diffusion rates in positive electrode and become the rate determining step in entire electrode reaction dynamics, Therefore it is the core key for constructing high performance lithium ion battery that developing, which has the inorganic fast ionic conductor of higher li ionic conductivity, Place.From the point of view of current lithium fast-ionic conductor Development Status: LLTO (Li, La) TiO3Fast-ionic conductor has very high transgranular Conductivity is (10-3S/cm or so) and relatively high room temperature total conductivity (10-4S/cm-10-5S/cm), but LLTO decomposes electricity It forces down, the above all-solid-state battery of discharge voltage 3.7V and unstable to lithium anode can not be constituted;It is more with NASICON type Brilliant LiM2(PO4)3(M=Ti, Ge, Zr) is by tetrahedron PO4With octahedra MO6The grid structure collectively constituted, generation finish Hole and fillable coordination on structure, allow to regulate and control a large amount of Li ion, are a kind of up-and-coming high-lithium ion electricity Conductance fast-ionic conductor.By the substitution of aliovalent ion, introduce hole in the structure or calking lithium ion can further improve from Subconductivity [Xiaoxiong Xu, Zhaoyin Wen, ZhonghuaGu, et al., Solid State Ionics, 171, 2004,207-212.].Such as woods ancestral Zuxiang, Li Shichun [woods ancestral Zuxiang, Li Shichun, silicate journal, 9 (3), 1981,253-257.] It was found that Li1+xTi2-xGaxP3O12, Li1+2xTi2-xMgxP3O12, Li1+xGe2-xCrxP3012, Li1+xGe2-xAlxP3O12, Li1+ xTi2-xInxP3O12Etc. systems or other such as Li1+2x+2yAlxMgyTi2-x-ySixP3-xO12, Li1+x+yAlxTi2-xSiyP3-yO12, Li1+ xAlxTi2-xP3O12Etc. systems all have higher lithium ion conductivity.But the room temperature lithium ion conductivity of these systems usually exists 10-4S/cm-10-6Between S/cm, requirement of the non-film lithium ion battery to electrolytic conductivity can't be met very well.In addition NASICON system is equally unstable to lithium anode.Ramaswamy Murugan is equal to 2007 in German application term A kind of novel lithium ion fast-ionic conductor Li has been reported on periodical7La3Zr2O12Its lithium ion conductivity at normal temperature is more than 1 × 10-4S·cm-1, decomposition voltage is more than 5.5V, and lithium metal can be used as cathode, be that one kind has very much to air and moisture stabilization The fast ion solid electrolyte of the lithium of application potential (Ramaswamy Murugan, Venkataraman Thangadurai, Werner Weppner, (2007) " Fast lithium ion conduction in garnet-type Li7La3Zr2O12" Angewandte Chemie-International Edition 46 (41): 7778-7781.).However 5.0 × 10 will often be reached to the higher occasion conductivity of current requirements-4S/cm or so just can satisfy normal battery operation It needs, in addition the solid electrolyte synthesis temperature is at 1350 DEG C or so, and temperature is high, and energy consumption is high.
It additionally needs and is pointed out that the consumption of lithium rises rapidly as secondary cell is quickly applied in power battery, Reserves of the elemental lithium in the earth's crust very it is low only PPM grade, rare lithium resource make future lithium ion battery cost it is continuous on It rises.The electrochemical energy storing device for seeking a kind of alternative low cost becomes urgent problem to be solved.Sodium and potassium element are in the earth The electrochemical properties very high and with lithium of abundance have certain similar, be following to be expected to replace most having for lithium ion all-solid-state battery uncommon The selection of prestige.However the building essential potassium ion conductor of potassium ion all-solid-state battery is also substantially at space state at present. Therefore screening has the potassium fast ion conducting material of high conductance to the inexpensive kalium ion battery of building and full-solid potassium ion Battery has great importance.
Summary of the invention
The technical problem to be solved by the present invention is to a kind of electric fields provided for existing background technique to induce crystalline A l3 +、Be2+The K of doping2MgSi5O12Potassium fast-ionic conductor and preparation method.Using Al3+、Be2+Part replaces Si4+Ion, in crystal Middle generation high concentration gap potassium ion helps to reduce potassium ion migration to generate more potassium ions collaboration migration of short distance Activation energy;Pass through the Be of small ionic radii2+Doping adjusts the size of the migrating channels of potassium ion to adapt to quickly moving for potassium ion It moves;And during the preparation process in K2MgSi5O12The surface of particle is modified, and is formed easy-sintering characteristic, is conducive to improve the potassium Fast-ionic conductor reduces crystal boundary gap when preparing bulk devices, increases consistency to improve the potassium of block potassium fast-ionic conductor Ionic conductivity;The induction crystallization of strong dc electric field is introduced simultaneously to accelerate the speed of crystallization, reduce the temperature of crystallization and improve crystallization Integrity degree.These synergistic effects are so that the room temperature potassium ion conductivity of the potassium fast-ionic conductor is more than 510-4S/cm, more adjunction The potassium ion conductivity of nearly liquid electrolyte.
The present invention reaches by the following technical solutions, which provides a kind of room temperature potassium ion conductivity and be more than 5·10-4The potassium fast-ionic conductor of S/cm, stoichiometric equation K2+2x+yMgBexAlySi5-x-yO12, in which: x=0.05- 0.15;Y=0.05-0.15.
In the technical scheme, by solid K2CO3∶MgO∶Al2O3∶SiO2: BeO is according to K2+2x+yMgBexAlySi5-x-yO12's The ratio uniform of nonstoichiometric molar ratio mixes, and the dehydrated alcohol that quality is mixture quality 3%-9% is added, in the ball mill With revolving speed ball milling 10-50 hours of 100-500 revs/min, after ball milling gas pressure be 3Pa-20Pa temperature be 60 DEG C- It is 2-10 hours dry in 120 DEG C of vacuum drying ovens, it grinds in alms bowl and re-grinds 10-30 minutes in agate after taking-up, the powder after grinding Rate in air atmosphere with 5-30 DEG C/min is warming up to furnace cooling after 550-650 DEG C of heat preservation 3-10 hours;After cooling Powder agate grind alms bowl in regrind 10-30 minutes, the powder after grinding is in air atmosphere with 5-15 in platinum crucible DEG C/min rate be warming up to 1250-1350 DEG C of heat preservation 25-48 hours after take out burner hearth cool down rapidly;By material after cooling It filters, dry after being impregnated 5-15 minutes in the sodium hydroxide solution of 0.1-0.3M after crushing and grinding 30-50 minutes in grinding Dry doubling is in a press 1 × 107Pa-8×107The pressure of Pa pushes flakiness, by thin slice obtained embedment half full of porcelain boat In SiO 2 powder, which is put into the oxygen in the tube furnace of both ends setting 800-1100V DC voltage in 10-60Pa Rate in atmosphere with 5-10 DEG C/min is warming up to furnace cooling after 700-800 DEG C of heat preservation 30-60 hours;The potassium ion is made Fast-ionic conductor thin slice.If Fig. 1 is that group becomes K2.15MgBe0.05Al0.05Si4.9O12The XRD spectrum of potassium fast-ionic conductor, spectral line Meet PDF card 82-0548 K2MgSi5O12It is 7.310 through LCR821 impedance analyzer measurement conductivity mutually without miscellaneous phase-4S/ cm。
Compared with the prior art, the advantages of the present invention are as follows: use Al3+、Be2+Part replaces Si4+Ion, in crystal High concentration gap potassium ion is generated, to generate more potassium ions collaboration migration of short distance, helping, which reduces potassium ion migration, lives Change energy;Pass through the Be of small ionic radii2+Doping adjusts the size of the migrating channels of potassium ion to adapt to the fast transferring of potassium ion; It will be particularly beneficial that during the preparation process in K2MgSi5O12The surface of particle is modified, and is formed easy-sintering characteristic, is conducive to mention The high potassium fast-ionic conductor reduces crystal boundary gap when preparing bulk devices, increase consistency is led to improve the fast ion of block potassium The potassium ion conductivity of body;The induction crystallization of strong dc electric field is introduced simultaneously to accelerate the speed of crystallization, reduce the temperature of crystallization and mention Highly crystalline integrity degree.These synergistic effects are so that the room temperature potassium ion conductivity of the potassium fast-ionic conductor is more than 510-4S/cm, It is very beneficial for the building of full-solid potassium ion battery.
Detailed description of the invention
Fig. 1 is K2.15MgBe0.05Al0.05Si4.9O12The XRD spectrum of potassium fast-ionic conductor.
Specific embodiment
Below in conjunction with embodiment, present invention is further described in detail.
Embodiment 1: by solid K2CO3∶MgO∶Al2O3∶SiO2: BeO is according to K2.15MgBe0.05Al0.05Si4.89O12Chemistry The ratio uniform of stoichiometric mole ratio mixes, and the dehydrated alcohol that quality is mixture quality 3% is added, in the ball mill with 120 turns/ Revolving speed ball milling 10 hours of minute, drying 3 is small in 60 DEG C of vacuum drying ovens (gas pressure is in 5Pa in baking oven) after ball milling When, it grinds in alms bowl and re-grinds 12 minutes in agate after taking-up, the powder after grinding is in air atmosphere with 7 DEG C/min of rate Furnace cooling after being warming up to 550 DEG C of heat preservations 3 hours;Powder after cooling is ground in alms bowl in agate and is regrind 10 minutes, is ground Powder afterwards takes out furnace after being warming up to 1250 DEG C of heat preservations 25 hours with 5 DEG C/min of rate in platinum crucible in air atmosphere Thorax cools down rapidly;Material after cooling is crushed in grinding and is impregnated in the sodium hydroxide solution of 0.1M after grinding 30 minutes It filters, dry and in a press 1.5 × 10 after five minutes7The pressure of Pa pushes flakiness, and thin slice obtained embedment is partly filled In the SiO 2 powder of full porcelain boat, which is put into the oxygen in the tube furnace of both ends setting 820V DC voltage in 15Pa Furnace cooling after being warming up to 700 DEG C of heat preservations 30 hours in atmosphere with 5 DEG C/min of rate;The potassium ion fast-ionic conductor is made Thin slice.
Embodiment 2: by solid K2CO3∶MgO∶Al2O3∶SiO2: BeO is according to K2.45MgBe0.15Al0.15Si4.7O12Chemistry The ratio uniform of stoichiometric mole ratio mixes, and the dehydrated alcohol that quality is mixture quality 9% is added, in the ball mill with 400 turns/ Revolving speed ball milling 40 hours of minute, after ball milling dry 10 in 110 DEG C of vacuum drying ovens (gas pressure is in 20Pa in baking oven) Hour, it grinds in alms bowl and re-grinds 30 minutes in agate after taking-up, the powder after grinding is in air atmosphere with 30 DEG C/min of speed Rate is warming up to furnace cooling after 600 DEG C of heat preservations 10 hours;Powder after cooling is ground in alms bowl in agate and is regrind 30 minutes, is ground Powder after mill takes out after being warming up to 1330 DEG C of heat preservations 45 hours with 13 DEG C/min of rate in platinum crucible in air atmosphere Burner hearth cools down rapidly;Material after cooling is crushed in grinding and is soaked in the sodium hydroxide solution of 0.3M after grinding 50 minutes Bubble is filtered after 15 minutes, is dried and in a press 7.5 × 107The pressure of Pa pushes flakiness, and thin slice obtained is embedded to In half SiO 2 powder full of porcelain boat, which is put into the tube furnace of both ends setting 1100V DC voltage in 60Pa Oxygen atmosphere in 10 DEG C/min of rate be warming up to 800 DEG C heat preservation 60 hours after furnace cooling;Be made the potassium ion fastly from Sub- conductor sheet.
Embodiment 3: by solid K2CO3∶MgO∶Al2O3∶SiO2: BeO is according to K2.3MgBe0.1Al0.1Si4.8O12Chemistry meter The ratio uniform mixing for measuring molar ratio, is added the dehydrated alcohol that quality is mixture quality 6%, in the ball mill with 300 revs/min The revolving speed ball milling of clock 30 hours, drying 6 is small in 100 DEG C of vacuum drying ovens (gas pressure is in 15Pa in baking oven) after ball milling When, it grinds in alms bowl and re-grinds 20 minutes in agate after taking-up, the powder after grinding is in air atmosphere with 20 DEG C/min of rate Furnace cooling after being warming up to 600 DEG C of heat preservations 7 hours;Powder after cooling is ground in alms bowl in agate and is regrind 20 minutes, is ground Powder afterwards takes out furnace after being warming up to 1300 DEG C of heat preservations 35 hours with 10 DEG C/min of rate in platinum crucible in air atmosphere Thorax cools down rapidly;Material after cooling is crushed in grinding and is ground and is impregnated in the sodium hydroxide solution of 0.2M after forty minutes It filters, dry and in a press 5 × 10 after ten minutes7The pressure of Pa pushes flakiness, and thin slice obtained embedment is partly filled In the SiO 2 powder of full porcelain boat, which is put into the oxygen in the tube furnace of both ends setting 900V DC voltage in 50Pa Furnace cooling after being warming up to 750 DEG C of heat preservations 45 hours in atmosphere with 7 DEG C/min of rate;The potassium ion fast-ionic conductor is made Thin slice.
Embodiment 4: by solid K2CO3∶MgO∶Al2O3∶SiO2: BeO is according to K2.27MgBe0.1Al0.07Si4.83O12Chemistry The ratio uniform of stoichiometric mole ratio mixes, and the dehydrated alcohol that quality is mixture quality 6% is added, in the ball mill with 500 turns/ Revolving speed ball milling 40 hours of minute, after ball milling dry 10 in 120 DEG C of vacuum drying ovens (gas pressure is in 20Pa in baking oven) Hour, it grinds in alms bowl and re-grinds 20 minutes in agate after taking-up, the powder after grinding is in air atmosphere with 20 DEG C/min of speed Rate is warming up to furnace cooling after 610 DEG C of heat preservations 7 hours;Powder after cooling is ground in alms bowl in agate and is regrind 20 minutes, is ground Powder after mill takes out after being warming up to 1310 DEG C of heat preservations 45 hours with 10 DEG C/min of rate in platinum crucible in air atmosphere Burner hearth cools down rapidly;Material after cooling is crushed in grinding and is soaked in the sodium hydroxide solution of 0.2M after grinding 50 minutes Bubble is filtered after ten minutes, is dried and in a press 3 × 107The pressure of Pa pushes flakiness, by thin slice obtained embedment half In SiO 2 powder full of porcelain boat, which is put into the tube furnace of both ends setting 1000V DC voltage 50Pa's Furnace cooling after being warming up to 750 DEG C of heat preservations 40 hours in oxygen atmosphere with 10 DEG C/min of rate;The fast ion of the potassium ion is made Conductor sheet.
By solid K2CO3∶MgO∶Al2O3∶SiO2: BeO is according to K2.3MgBe0.09Al0.12Si4.79O12Stoichiometric molar The ratio uniform of ratio mixes, and the dehydrated alcohol that quality is mixture quality 3% is added, in the ball mill with 100 revs/min of turn Fast ball milling 15 hours, it is 10 hours dry in 60 DEG C of vacuum drying ovens (gas pressure is in 20Pa in baking oven) after ball milling, it takes out It grinds in alms bowl and re-grinds 20 minutes in agate afterwards, the powder after grinding is warming up in air atmosphere with 10 DEG C/min of rate 550 DEG C heat preservation 3 hours after furnace cooling;Powder after cooling is ground in alms bowl in agate and is regrind 20 minutes, the powder after grinding It is rapid that body takes out burner hearth after being warming up to 1350 DEG C of heat preservations 40 hours with 10 DEG C/min of rate in platinum crucible in air atmosphere It is cooling;Material after cooling is crushed in grinding and is ground and is impregnated 10 minutes in the sodium hydroxide solution of 0.1M after forty minutes It filters, dry and in a press 6 × 10 afterwards7The pressure of Pa pushes flakiness, and thin slice obtained embedment half is full of porcelain boat SiO 2 powder in, by the porcelain boat be put into both ends setting 800V DC voltage tube furnace in the oxygen atmosphere of 10Pa Furnace cooling after being warming up to 750 DEG C of heat preservations 40 hours with 5 DEG C/min of rate;The potassium ion fast-ionic conductor thin slice is made.

Claims (1)

1. a kind of electric field induces crystalline A l3+、Be2+The K of doping2MgSi5O12Potassium fast-ionic conductor, it is characterized in that: stoichiometric equation For K2+2x+yMgBexAlySi5-x-yO12, in which: x=0.05-0.15;Y=0.05-0.15;Room temperature potassium ion conductivity is more than 5 10-4S/cm;Its preparation process is by solid K2CO3∶MgO∶Al2O3∶SiO2: BeO is according to K2+2x+yMgBexAlySi5-x-yO12Change Learn stoichiometric mole ratio ratio uniform mixing, be added quality be mixture quality 3%-9% dehydrated alcohol, in the ball mill with 100-500 revs/min of revolving speed ball milling 10-50 hours, after ball milling gas pressure be 3Pa-20Pa temperature be 60 DEG C- It is 2-10 hours dry in 120 DEG C of vacuum drying ovens, it grinds in alms bowl and re-grinds 10-30 minutes in agate after taking-up, the powder after grinding Rate in air atmosphere with 5-30 DEG C/min is warming up to furnace cooling after 550-650 DEG C of heat preservation 3-10 hours;After cooling Powder agate grind alms bowl in regrind 10-30 minutes, the powder after grinding is in air atmosphere with 5-15 in platinum crucible DEG C/min rate be warming up to 1250-1350 DEG C of heat preservation 25-48 hours after take out burner hearth cool down rapidly;By material after cooling It filters, dry after being impregnated 5-15 minutes in the sodium hydroxide solution of 0.1-0.3M after crushing and grinding 30-50 minutes in grinding Dry doubling is in a press 1 × 107Pa-8×107The pressure of Pa pushes flakiness, by thin slice obtained embedment half full of porcelain boat In SiO 2 powder, which is put into the oxygen in the tube furnace of both ends setting 800-1100V DC voltage in 10-60Pa After rate in atmosphere with 5-10 DEG C/min is warming up to 700-800 DEG C of heat preservation 30-60 hours furnace cooling be made the potassium fastly from Sub- conductor.
CN201910617293.0A 2019-06-27 2019-06-27 A kind of electric field induction crystalline A l3+、Be2+The K of doping2MgSi5O12Potassium fast-ionic conductor and preparation method Withdrawn CN110372358A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201910617293.0A CN110372358A (en) 2019-06-27 2019-06-27 A kind of electric field induction crystalline A l3+、Be2+The K of doping2MgSi5O12Potassium fast-ionic conductor and preparation method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201910617293.0A CN110372358A (en) 2019-06-27 2019-06-27 A kind of electric field induction crystalline A l3+、Be2+The K of doping2MgSi5O12Potassium fast-ionic conductor and preparation method

Publications (1)

Publication Number Publication Date
CN110372358A true CN110372358A (en) 2019-10-25

Family

ID=68252483

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201910617293.0A Withdrawn CN110372358A (en) 2019-06-27 2019-06-27 A kind of electric field induction crystalline A l3+、Be2+The K of doping2MgSi5O12Potassium fast-ionic conductor and preparation method

Country Status (1)

Country Link
CN (1) CN110372358A (en)

Similar Documents

Publication Publication Date Title
CN102780031B (en) A kind of Mg 2+, Al 3+, Zr 4+, F -ion co-doped garnet-type solid electrolyte
CN102867988B (en) B3+, Al3 +, Ti4 +, Y3+ F-codoped solid electrolyte Li7La3Zr2Ol2
CN102780028B (en) Four-component iron co-doped garnet type solid electrolyte
CN102867987B (en) A B3+, al3+, mg2+, Y3+, F- codoped solid electrolyte Li7La3Zr2O12
CN102769147B (en) Mg<2+>, Al<3+>, Zr<4+> and S<2-> ion co-doped garnet type solid electrolyte
CN110372350A (en) A kind of B3+、Al3+The K of ion collaboration doping6Si2O7Potassium fast-ionic conductor and preparation method
CN102867985B (en) B<3+>, Al<3+>, Mg<2+>, Y<3+> and S<2-> co-doped solid electrolyte Li7La3Zr2O12
CN102780029B (en) A kind of three component cation codope carbuncle type solid lithium-ion electrolytes
CN110265706A (en) A kind of electric field induction crystallization P5+、Al3+、B3+The K of ion collaboration doping6Si2O7Potassium fast-ionic conductor and preparation method thereof
CN110372357A (en) A kind of P5+、Al3+、B3+The K of ion collaboration doping2MgSi5O12Potassium fast-ionic conductor and preparation method thereof
CN110372348A (en) A kind of electric field induction crystallization K6.15Zn0.05B0.2Al0.1P0.05Zr0.05Si1.6O7Potassium fast-ionic conductor and preparation method
CN110372358A (en) A kind of electric field induction crystalline A l3+、Be2+The K of doping2MgSi5O12Potassium fast-ionic conductor and preparation method
CN110526697A (en) A kind of liquid phase synthesis K6.25Be0.1Al0.1P0.05Ti0.05Si1.7O7Potassium fast-ionic conductor and preparation method thereof
CN110371996A (en) A kind of Al3+、B3+The K of ion collaboration doping2MgSi5O12Potassium fast-ionic conductor and preparation method thereof
CN102856584B (en) A B3+, al3+, ti4+, Y3+and S2- codoped solid electrolyte Li7La3Zr2O12
CN102867986B (en) One B3+, al3+, ti4+and Y3+cationic co-doped solid electrolyte Li7La3Zr2O12
CN110304912A (en) A kind of electric field induction crystallization P5+、Be2+Cooperate with the K of doping2MgSi5O12Potassium fast-ionic conductor and preparation method thereof
CN110357598A (en) A kind of P5+、Be2+The K of ion collaboration doping2MgSi5O12Potassium fast-ionic conductor and preparation method thereof
CN110371995A (en) A kind of electric field induction crystallization P5+、Al3+、Be2+Cooperate with the K of doping2MgSi5O12Potassium fast-ionic conductor and preparation method thereof
CN110357599A (en) A kind of P5+、Al3+、Be2+、Zn2+The K of ion collaboration doping2MgSi5O12Potassium fast-ionic conductor and preparation method thereof
CN102780030B (en) Four-component cation and anion co-doped garnet-type solid electrolyte
CN110336008A (en) A kind of P5+、Al3+、Be2+、Zn2+The K of ion collaboration doping6Si2O7Potassium fast-ionic conductor and preparation method thereof
CN110372349A (en) A kind of P5+、Al3+、Be2+The K of ion collaboration doping6Si2O7Potassium fast-ionic conductor and preparation method thereof
CN110371997A (en) A kind of P5+、Al3+、Be2+The K of ion collaboration doping2MgSi5O12Potassium fast-ionic conductor and preparation method thereof
CN110350250A (en) A kind of P5+、Al3+、B3+The K of ion collaboration doping6Si2O7Potassium fast-ionic conductor and preparation method thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WW01 Invention patent application withdrawn after publication

Application publication date: 20191025

WW01 Invention patent application withdrawn after publication