CN108975910A - A kind of sodium niobate base ferroelectric ceramics and its preparation method and application with temperature-stable electric field induced strain - Google Patents

A kind of sodium niobate base ferroelectric ceramics and its preparation method and application with temperature-stable electric field induced strain Download PDF

Info

Publication number
CN108975910A
CN108975910A CN201810798533.7A CN201810798533A CN108975910A CN 108975910 A CN108975910 A CN 108975910A CN 201810798533 A CN201810798533 A CN 201810798533A CN 108975910 A CN108975910 A CN 108975910A
Authority
CN
China
Prior art keywords
temperature
electric field
sodium niobate
ferroelectric ceramics
field induced
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.)
Pending
Application number
CN201810798533.7A
Other languages
Chinese (zh)
Inventor
靳立
王亮
徐卓
魏晓勇
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.)
Xian Jiaotong University
Original Assignee
Xian Jiaotong 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 Xian Jiaotong University filed Critical Xian Jiaotong University
Priority to CN201810798533.7A priority Critical patent/CN108975910A/en
Publication of CN108975910A publication Critical patent/CN108975910A/en
Pending 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
    • C04B35/495Shaped 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 vanadium, niobium, tantalum, molybdenum or tungsten oxides or solid solutions thereof with other oxides, e.g. vanadates, niobates, tantalates, molybdates or tungstates
    • 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
    • C04B35/622Forming processes; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10NELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10N30/00Piezoelectric or electrostrictive devices
    • H10N30/80Constructional details
    • H10N30/85Piezoelectric or electrostrictive active materials
    • H10N30/853Ceramic compositions
    • H10N30/8536Alkaline earth metal based oxides, e.g. barium titanates
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10NELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10N30/00Piezoelectric or electrostrictive devices
    • H10N30/80Constructional details
    • H10N30/85Piezoelectric or electrostrictive active materials
    • H10N30/853Ceramic compositions
    • H10N30/8542Alkali metal based oxides, e.g. lithium, sodium or potassium niobates
    • 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
    • C04B2235/3201Alkali metal oxides or oxide-forming salts thereof
    • 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
    • C04B2235/3208Calcium oxide or oxide-forming salts thereof, e.g. lime
    • 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
    • C04B2235/3215Barium oxides or oxide-forming salts thereof
    • 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
    • C04B2235/3231Refractory metal oxides, their mixed metal oxides, or oxide-forming salts thereof
    • C04B2235/3232Titanium oxides or titanates, e.g. rutile or anatase
    • 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
    • C04B2235/3231Refractory metal oxides, their mixed metal oxides, or oxide-forming salts thereof
    • C04B2235/3244Zirconium oxides, zirconates, hafnium oxides, hafnates, or oxide-forming salts thereof

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Compositions Of Oxide Ceramics (AREA)

Abstract

A kind of sodium niobate ferroelectric ceramics and its preparation method and application with temperature-stable electric field induced strain disclosed by the invention, belongs to ferroelectric ceramic material preparation technical field, and the chemical composition of the ceramic medium material is (1-x) NaNbO3‑xBa0.85Ca0.15Zr0.1Ti0.9O3, wherein x is 0.13~0.15.The material system can obtain a kind of consistency height, the Electrostrictive strain with temperature-stable at a lower temperature using solid reaction process preparation synthesis.Between 30 DEG C to 120 DEG C, under 60kV/cm electric field action, low hysteresis Electrostrictive strain maximum value is between 0.10%~0.12%, and change rate is less than 12%.Ingredient and processing step of the invention is simple, easily operated, reproducible.It can be applied to have temperature stability on the high-precision driver of high request, there is great economic value.

Description

It is a kind of with the sodium niobate base ferroelectric ceramics of temperature-stable electric field induced strain and its preparation Methods and applications
Technical field
The invention belongs to ferroelectric ceramic material preparation technical fields, and in particular to one kind has temperature-stable electric field induced strain Sodium niobate ferroelectric ceramics and its preparation method and application.
Background technique
In high-precision driver, often through electroluminescent the answering for obtaining hysteresis degree very little to ferroelectric material application electric field Become, this strain precision can control in dozens to a few hundred nanometers, have important value in highly sophisticated device.From the angle of application For degree, other than with biggish electric field induced strain, the temperature stability of the strain is also to evaluate the material application value One important indicator.For ferroelectric material, its polarization intensity can all decline when the temperature increases, so as to cause phase same electric field The reduction strained under intensity.Such as from room temperature to 120 DEG C, the change rate of strain should can meet the material less than 20% It is used in high-temperature section.
It in the prior art, is that the material is free at quasi- similar shape phase boundary for generate that the ferroelectric material of Large strain utilizes more The energy minimum principle of potential barrier, to ensure that its high strain.But the problem of being the largest is exactly that the phase boundary can be with the change of temperature And change, very poor temperature stability is also shown so as to cause corresponding strain.
Summary of the invention
The purpose of the present invention is to provide a kind of sodium niobate ferroelectric ceramics and its system with temperature-stable electric field induced strain Preparation Method and application, this method operating procedure are simple, easily operated, reproducible;It makes pottery through sodium niobate ferroelectricity made from this method Ceramic material consistency height, the Electrostrictive strain with temperature-stable, thus can be applied to have height to temperature stability It is required that high-precision field of drivers.
The present invention is to be achieved through the following technical solutions:
The invention discloses a kind of sodium niobate ferroelectric ceramics with temperature-stable electric field induced strain, sodium niobate ferroelectricity potteries The chemical composition of porcelain is (1-x) NaNbO3-xBa0.85Ca0.15Zr0.1Ti0.9O3, wherein x=0.13~0.15.
Preferably, the sodium niobate ferroelectric ceramics is between 30 DEG C~120 DEG C, and under 60kV/cm electric field action, low hysteresis is electroluminescent Flexible strain maximum value is 0.10%~0.12%, and change rate is less than 12%.
The invention also discloses a kind of preparation method of sodium niobate ferroelectric ceramics with temperature-stable electric field induced strain, packets Include following steps:
1) (1-x) NaNbO is pressed3-xBa0.85Ca0.15Zr0.1Ti0.9O3, the chemical composition of x=0.13~0.15 weighs raw material Na2CO3、Nb2O5、BaCO3、CaCO3、ZrO2And TiO2;After weighed raw material is mixed through ball milling, dry, be ground up, sieved processing, Then in 1250 DEG C of progress pre-burnings, 6h is kept the temperature, room temperature is naturally cooled to, comes out of the stove, again ball milling, synthesize NN-xBCZT powder;
2) the NN-xBCZT powder of step 1) synthesis dried, grinding, cross 120 meshes, NN-xBCZT powder quality is added 5% poly-vinyl alcohol solution is uniformly mixed, and sieving takes the powder between 60~100 mesh;
3) after standing powder made from step 2) for 24 hours, it is pressed into blank, blank is risen to 600 DEG C by room temperature, heat preservation 2h;
4) by step 3) treated blank sintering processes 4h at 1450 DEG C, room temperature is cooled to the furnace, being made has width Temperature stablizes the sodium niobate ferroelectric ceramics of electric field induced strain.
Preferably, in step 2), the concentration of poly-vinyl alcohol solution is 5%.
It preferably, in step 3), is put into the powder after stewing process in the stainless steel mould that diameter is 8mm, Cylindric blank is pressed under 250MPa pressure.
Preferably, in step 4), blank is put into crucible, is covered, and use similar powder as material is buried and be sintered place Reason.
It preferably, further include the sodium niobate ferroelectricity pottery to obtained with temperature-stable electric field induced strain after step 4) The operation that porcelain is tested for the property, specifically: burned sodium niobate ferroelectric ceramics piece is polishing to a thickness of 0.8mm, is dried in the air naturally Dry, lower surface coats silver paste on it, is placed in furnace and is warming up to 600 DEG C, keeps the temperature 20min, and cooled to room temperature carries out dielectric Performance and strain property test.
The invention also discloses the above-mentioned sodium niobate ferroelectric ceramics with temperature-stable electric field induced strain in preparation high-precision Application in microdrive.
Compared with prior art, the invention has the following beneficial technical effects:
The chemical composition of sodium niobate ferroelectric ceramic material disclosed by the invention with temperature-stable electric field induced strain is (1- x)NaNbO3-xBa0.85Ca0.15Zr0.1Ti0.9O3(NN-xBCZT), wherein x is 0.13~0.15.The present invention utilizes sodium niobate (NaNbO3, NN) base ferroelectric ceramics high-curie temperature (> 400 DEG C), introduce Ba0.85Ca0.15Zr0.1Ti0.9O3(BCZT) constituent element is logical It crosses component design and to 120 DEG C or more while keeping the system component from room temperature to being 120 DEG C (1-x) NN-xBCZT adjusting Single phase structure, to obtain the electric field induced strain with temperature-stable, to meet the application demand of high-precision driver.The material Material system can be at a lower temperature using solid reaction process preparation synthesis, and consistency is high, and with temperature-stable Electrostrictive strain.
Further, between 30 DEG C~120 DEG C, under 60kV/cm electric field action, low hysteresis Electrostrictive strain is maximum Value is between 0.10%~0.12%, and change rate is less than 12%.
The method operating procedure of disclosure of the invention is simple, reproducible, low for equipment requirements, is suitble to amplification production.
Sodium niobate ferroelectric ceramic material disclosed by the invention can be applied to the high-precision for having high request to temperature stability On driver, there is great economic value.
Detailed description of the invention
Fig. 1 is that electric field induced strain variation with temperature of the NN-0.13BT sample of embodiment 1 between 30 DEG C~120 DEG C is closed It is curve;Wherein, a is 30 DEG C, and b is 60 DEG C, and c is 90 DEG C, and d is 120 DEG C;
Fig. 2 is that electric field induced strain variation with temperature of the NN-0.15BT sample of embodiment 2 between 30 DEG C~120 DEG C is closed It is curve;Wherein, a is 30 DEG C, and b is 60 DEG C, and c is 90 DEG C, and d is 120 DEG C;
Fig. 3 a is the maximum strain variation with temperature relationship of embodiment 1 and embodiment 2;
Fig. 3 b is the maximum strain variation with temperature rate of embodiment 1 and embodiment 2.
Specific embodiment
Below with reference to specific embodiment, the present invention is described in further detail, it is described be explanation of the invention and It is not to limit.
Embodiment 1
A kind of sodium niobate ferroelectric ceramic material with temperature-stable electric field induced strain, chemical composition are as follows:
0.87NaNbO3-0.13Ba0.85Ca0.15Zr0.1Ti0.9O3, it is abbreviated as NN-0.13BT, is denoted as sample 1, is labeled as # 1。
Above-mentioned sample 1 the preparation method is as follows:
1) according to chemical expression 0.87NaNbO3-0.13Ba0.85Ca0.15Zr0.1Ti0.9O3Weigh Na2CO3、Nb2O5、 BaCO3、CaCO3、ZrO2And TiO2.It is put into ball grinder after weighed raw material is mixed, ball milling solvent isopropanol and oxidation is added Zirconium ball, ball milling 6 hours, rotational speed of ball-mill was 250 revs/min, then mixture is put into 80 DEG C of drying in baking oven, was ground being put into mortar Mill crosses 80 meshes;In 1250 DEG C of progress pre-burnings in Muffle furnace, 6 hours are kept the temperature, room temperature is naturally cooled to, comes out of the stove;Ball again Mill synthesizes 0.87NaNbO3-0.13Ba0.85Ca0.15Zr0.1Ti0.9O3
2) 0.87NaNbO for synthesizing step 1)3-0.13Ba0.85Ca0.15Zr0.1Ti0.9O3Powder drying, then in mortar In it is finely ground, cross 120 meshes, be added mass percent be 5% polyvinyl alcohol (PVA) solution, the PVA solution concentration be 5%, mix It closes uniformly, sieving takes the powder between 60~100 mesh.
3) powder after being granulated in step 2) is stood 24 hours, then powder is put into the stainless steel mould that diameter is 8mm In, cylindric blank is depressed in 250MPa pressure;
4) green body in step 3) is put into Muffle furnace, temperature rises to 600 DEG C, keeps the temperature 2 hours, carries out organic matter row It removes;
5) green body after dumping in step 4) is put into crucible, covers, buries material with similar powder and bury burning, at 1450 DEG C Middle sintering keeps the temperature 4 hours, with furnace cooled to room temperature;
6) potsherd burned in step 5) is polishing to a thickness of 0.8mm, naturally dry, the silver of lower surface coating on it Slurry is placed in furnace and is warming up to 600 DEG C, keeps the temperature 20min, cooled to room temperature;The dielectric properties and strain property of test sample.
Referring to Fig. 1, full test electric field is 60kV/cm, test frequency 1Hz.As can be seen that NN-0.13BT sample is answered Become S to increase with the increase of electric field, voltage from zero to maximum value again to zero during, strain curve shows very little Hysteresis, electric field induced strain hysteresis degree is all < 10% at listed temperature.Meet the requirement of high-precision strain controlling.
Embodiment 2
A kind of sodium niobate ferroelectric ceramic material with temperature-stable electric field induced strain, chemical composition are as follows:
0.85NaNbO3-0.15Ba0.85Ca0.15Zr0.1Ti0.9O3, it is abbreviated as NN-0.15BT, is denoted as sample 2, is labeled as # 2。
Above-mentioned sample 2 the preparation method is as follows:
1) according to chemical expression 0.85NaNbO3-0.15Ba0.85Ca0.15Zr0.1Ti0.9O3Weigh Na2CO3、Nb2O5、 BaCO3、CaCO3、ZrO2And TiO2.It is put into ball grinder after weighed raw material is mixed, ball milling solvent isopropanol and oxidation is added Zirconium ball, ball milling 6 hours, rotational speed of ball-mill was 250 revs/min, then mixture is put into 80 DEG C of drying in baking oven, was ground being put into mortar Mill crosses 80 meshes;In 1250 DEG C of progress pre-burnings in Muffle furnace, 6 hours are kept the temperature, room temperature is naturally cooled to, comes out of the stove;Ball again Mill synthesizes 0.85NaNbO3-0.15Ba0.85Ca0.15Zr0.1Ti0.9O3Powder.
2) 0.85NaNbO for synthesizing step 1)3-0.15Ba0.85Ca0.15Zr0.1Ti0.9O3After powder drying, in mortar It is finely ground, 120 meshes are crossed, polyvinyl alcohol (PVA) solution that mass percent is 5% is added, which is 5%, and mixing is equal Even, sieving takes the powder between 60~100 mesh.
3) powder after being granulated in step 2) is stood 24 hours, then powder is put into the stainless steel mould that diameter is 8mm In, cylindric blank is depressed in 250MPa pressure;
4) green body in step 3) is put into Muffle furnace, temperature rises to 600 DEG C, keeps the temperature 2 hours, carries out organic matter row It removes;
5) green body after dumping in step 4) is put into crucible, covers, buries material with similar powder and bury burning, at 1450 DEG C Middle sintering keeps the temperature 4 hours, with furnace cooled to room temperature;
6) potsherd burned in step 5) is polishing to a thickness of 0.8mm, naturally dry, the silver of lower surface coating on it Slurry is placed in furnace and is warming up to 600 DEG C, keeps the temperature 20min, cooled to room temperature;The dielectric properties and strain property of test sample.
Referring to fig. 2, full test electric field is 60kV/cm, test frequency 1Hz.As can be seen that NN-0.15BT sample is answered Become S to increase with the increase of electric field, voltage from zero to maximum value again to zero during, strain curve shows very little Hysteresis, electric field induced strain hysteresis degree is all < 10% at listed temperature.Meet the requirement of high-precision strain controlling.
It is sample 1 and sample 2 the maximum strain variation with temperature relationship between 30 DEG C~120 DEG C referring to Fig. 3 a, referring to Fig. 3 b is sample 1 and sample 2 maximum strain variation with temperature rate, maximum value 0.12%, minimum value between 30 DEG C~120 DEG C 0.10%, change rate is less than 12%.
In conclusion present invention proposition is generated using the single phase structure of ferroelectric material with temperature-stable electric field induced strain Thinking.As long as guaranteeing material Curie temperature with higher, then its emergent property should have below this temperature Good temperature stability, because its polarization intensity has good temperature stability in the following wider range of this temperature.Base In above-mentioned characteristic, it is high that the sodium niobate ferroelectric ceramics produced by the present invention with temperature-stable electric field induced strain can be applied to preparation Precision microdrive field.

Claims (8)

1. a kind of sodium niobate ferroelectric ceramics with temperature-stable electric field induced strain, which is characterized in that the sodium niobate ferroelectric ceramics Chemical composition be (1-x) NaNbO3-xBa0.85Ca0.15Zr0.1Ti0.9O3, wherein x=0.13~0.15.
2. the sodium niobate ferroelectric ceramics according to claim 1 with temperature-stable electric field induced strain, which is characterized in that should Sodium niobate ferroelectric ceramics is between 30 DEG C~120 DEG C, and under 60kV/cm electric field action, low hysteresis Electrostrictive strain maximum value is 0.10%~0.12%, change rate is less than 12%.
3. a kind of preparation method of the sodium niobate ferroelectric ceramics with temperature-stable electric field induced strain, which is characterized in that including with Lower step:
1) (1-x) NaNbO is pressed3-xBa0.85Ca0.15Zr0.1Ti0.9O3, the chemical composition of x=0.13~0.15 weighs raw material Na2CO3、Nb2O5、BaCO3、CaCO3、ZrO2And TiO2;After weighed raw material is mixed through ball milling, dry, be ground up, sieved processing, Then in 1250 DEG C of progress pre-burnings, 6h is kept the temperature, room temperature is naturally cooled to, comes out of the stove, again ball milling, synthesize NN-xBCZT powder;
2) the NN-xBCZT powder of step 1) synthesis dried, grinding, cross 120 meshes, NN-xBCZT powder quality 5% is added Poly-vinyl alcohol solution is uniformly mixed, and sieving takes the powder between 60~100 mesh;
3) after standing powder made from step 2) for 24 hours, it is pressed into blank, blank is risen to 600 DEG C by room temperature, keeps the temperature 2h;
4) by step 3) treated blank sintering processes 4h at 1450 DEG C, room temperature is cooled to the furnace, being made has wide temperature Stablize the sodium niobate ferroelectric ceramics of electric field induced strain.
4. the preparation method of the sodium niobate ferroelectric ceramics according to claim 3 with temperature-stable electric field induced strain, It is characterized in that, in step 2), the concentration of poly-vinyl alcohol solution is 5%.
5. the preparation method of the sodium niobate ferroelectric ceramics according to claim 3 with temperature-stable electric field induced strain, It is characterized in that, in step 3), is to be put into the powder after stewing process in the stainless steel mould that diameter is 8mm, is pressed in 250MPa Cylindric blank is pressed under power.
6. the preparation method of the sodium niobate ferroelectric ceramics according to claim 3 with temperature-stable electric field induced strain, It is characterized in that, in step 4), blank is put into crucible, cover, and use similar powder as material is buried and be sintered.
7. the preparation method of the sodium niobate ferroelectric ceramics according to claim 3 with temperature-stable electric field induced strain, It is characterized in that, further includes the sodium niobate ferroelectric ceramics progress to obtained with temperature-stable electric field induced strain after step 4) The operation of performance test, specifically: burned sodium niobate ferroelectric ceramics piece is polishing to a thickness of 0.8mm, naturally dry, at it Upper and lower surface coats silver paste, is placed in furnace and is warming up to 600 DEG C, keeps the temperature 20min, and cooled to room temperature carries out dielectric properties and answers Become performance test.
8. the sodium niobate ferroelectric ceramics of any of claims 1 or 2 with temperature-stable electric field induced strain is micro- in preparation high-precision Application in driver.
CN201810798533.7A 2018-07-19 2018-07-19 A kind of sodium niobate base ferroelectric ceramics and its preparation method and application with temperature-stable electric field induced strain Pending CN108975910A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810798533.7A CN108975910A (en) 2018-07-19 2018-07-19 A kind of sodium niobate base ferroelectric ceramics and its preparation method and application with temperature-stable electric field induced strain

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810798533.7A CN108975910A (en) 2018-07-19 2018-07-19 A kind of sodium niobate base ferroelectric ceramics and its preparation method and application with temperature-stable electric field induced strain

Publications (1)

Publication Number Publication Date
CN108975910A true CN108975910A (en) 2018-12-11

Family

ID=64549985

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810798533.7A Pending CN108975910A (en) 2018-07-19 2018-07-19 A kind of sodium niobate base ferroelectric ceramics and its preparation method and application with temperature-stable electric field induced strain

Country Status (1)

Country Link
CN (1) CN108975910A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113908869A (en) * 2021-10-15 2022-01-11 安徽医科大学 Preparation method of photocatalytic composite micro-driver

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102815938A (en) * 2012-08-27 2012-12-12 天津大学 Barium titanate-based lead-free electrostrictive ceramics and preparation method thereof
CN104761259A (en) * 2015-03-10 2015-07-08 西安交通大学 Linear electrostrictive-strain leadless piezoelectric ceramic material and preparation method thereof
CN105439560A (en) * 2015-12-02 2016-03-30 陕西科技大学 High energy density ceramic material and preparation method
CN107500762A (en) * 2017-09-15 2017-12-22 西安交通大学 A kind of low hysteresis High-temperature stabilization strain ferroelectric ceramic material and preparation method thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102815938A (en) * 2012-08-27 2012-12-12 天津大学 Barium titanate-based lead-free electrostrictive ceramics and preparation method thereof
CN104761259A (en) * 2015-03-10 2015-07-08 西安交通大学 Linear electrostrictive-strain leadless piezoelectric ceramic material and preparation method thereof
CN105439560A (en) * 2015-12-02 2016-03-30 陕西科技大学 High energy density ceramic material and preparation method
CN107500762A (en) * 2017-09-15 2017-12-22 西安交通大学 A kind of low hysteresis High-temperature stabilization strain ferroelectric ceramic material and preparation method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113908869A (en) * 2021-10-15 2022-01-11 安徽医科大学 Preparation method of photocatalytic composite micro-driver
CN113908869B (en) * 2021-10-15 2023-05-26 安徽医科大学 Preparation method of photocatalysis composite micro driver

Similar Documents

Publication Publication Date Title
CN104761259B (en) A kind of linear electric field induced strain lead-free piezoceramic material and preparation method thereof
CN106588006B (en) A kind of high dielectric property barium strontium titanate, preparation method and the dielectric ceramic using its preparation
CN102167585B (en) Multielement-doped bismuth titanate group lead-free piezoceramic material and preparation method thereof
CN113582667B (en) Low-temperature cofiring high-energy-storage antiferroelectric ceramic material and preparation method and application thereof
Li et al. Middle-low temperature sintering and piezoelectric properties of CuO and Bi2O3 doped PMS-PZT based ceramics for ultrasonic motors
CN108546125A (en) A kind of piezoceramic material and preparation method thereof towards hot environment application
Wei et al. Improvement of the piezoelectric and ferroelectric properties of (K, Na) 0.5 NbO3 ceramics via two-step calcination–milling route
CN110357624B (en) High-dielectric-constant glass frit modified strontium zirconate doped potassium-sodium niobate lead-free transparent ceramic material and preparation method thereof
CN109970443B (en) Rubidium and cerium co-doped bismuth calcium niobate based high-temperature piezoelectric ceramic and preparation method thereof
CN106145941A (en) A kind of rich zirconium lead zirconate titanate bismuth ferrite multiferroic ceramic material
CN107986770A (en) Doping vario-property bismuth ferrite-lead titanate piezoelectric ceramics and preparation method thereof
CN114478006A (en) KNNS-BNZ + CuO piezoceramic material and preparation method and application thereof
US11958781B2 (en) Potassium sodium bismuth niobate tantalate zirconate ferrite ceramics with non-stoichiometric Nb5+ and preparation method therefor
CN114085079A (en) High-energy-storage non-equimolar-ratio high-entropy perovskite oxide ceramic material and preparation method thereof
CN108069712A (en) One kind has temperature-stable Electrostrictive strain ceramic material and preparation method thereof
CN107056290B (en) Method for regulating Curie temperature of ferroelectric ceramic
CN106045499A (en) Preparation method of zirconium-doped and lanthanum-doped sodium titanate-barium titanate ceramics
CN108975910A (en) A kind of sodium niobate base ferroelectric ceramics and its preparation method and application with temperature-stable electric field induced strain
KR102380196B1 (en) BiFeO3-BaTiO3 BASED ENVIRONMENT FRIENDLY LEAD-FREE PIEZOCERAMICS WITH PHYSICAL PROPERTIES AND MANUFACTURING METHOD THEREOF
CN107417267A (en) Bismuth ferrite multiferroic ceramics and preparation method thereof
CN115376825B (en) NN-based energy storage ceramic block material with high energy storage density and energy storage efficiency and preparation method thereof
CN115010483B (en) Piezoelectric ceramic material insensitive to strain and components, and preparation method and application thereof
CN107512910A (en) A kind of ternary relaxor ferroelectric piezoelectric niobium lutetium lead plumbate lead nickle niobate lead titanates and its preparation method and application
CN1331803C (en) (Balx-ySrxYy) TiO3 based dielectrical ceramic material and preparation process thereof
KR101866717B1 (en) BiFeO3-BaTiO3-BiGaO3 LEAD-FREE CERAMICS COMPOSITIONS AND MANUFACTURING 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
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20181211