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 PDFInfo
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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
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.
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