CN1884197A - Process for preparing double perovskite type magnetic materials Sr2MWO6 (M is Co or Ni) - Google Patents
Process for preparing double perovskite type magnetic materials Sr2MWO6 (M is Co or Ni) Download PDFInfo
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- CN1884197A CN1884197A CN 200610016947 CN200610016947A CN1884197A CN 1884197 A CN1884197 A CN 1884197A CN 200610016947 CN200610016947 CN 200610016947 CN 200610016947 A CN200610016947 A CN 200610016947A CN 1884197 A CN1884197 A CN 1884197A
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Abstract
The invention discloses a preparing method of double-calcium titanium magnetic material Sr2MWO6 (M=Co or Ni), which is characterized by the following: adopting strontium nitrate, cobalt nitrate, nickel nitrate and ammonium paratungstate as strontium, cobalt, nickel and tungsten source; utilizing citrate as complexing agent, ethandiol as disperser; reacting these materials at 1000-1300 deg.c for 20-40 h to obtain the product.
Description
Technical field
The present invention relates to a kind of double perovskite magnetic material Sr
2MWO
6The preparation method of (M=Co or Ni).
Background technology
Since people such as Japanese Kobayashi in 1998 find structure of double perovskite oxide S r
2FeMoO
6The polycrystalline sample is since room temperature also has bigger magneto-resistance effect, and this compounds particular structure and electromagnetic performance make it have good application prospects at aspects such as Magnetic Sensor, magnetic memory devices.Particularly some structure of double perovskite oxide compounds have the semi-metal characteristic, and spin-polarized degree is expected to use as the spinning electron injecting material near 100%.But existing structure of double perovskite oxide compound still can not satisfy under room temperature downfield condition and has big magneto-resistance effect, and people prepare novel magnetic resistance material to obtain the more excellent material of performance always in recent years.Wherein, the ionic radius of W elements and cobalt, nickel element and molybdenum element and ferro element are more approaching, and W elements has with the similar out-shell electron of molybdenum and arranges.Therefore, double-perovskite oxide S r
2MWO
6(M=Co, structure Ni) and performance number get people and further study.
Up to the present, to Sr
2MWO
6(M=Co or Ni) synthetic main solid phase method (crystal journal, 1951,4,503 of adopting; Acta Crystallogr.1951,4,503), (physics and chemical solid, 1999,60,1173; J.Phys.Chem.Solids), (materials chemistry, 2003,15,1655; Chem.Mater.2003,15,1655); Double decomposition synthesizes (materials chemistry, 2005,17,2310; Chem.Mater.2005,17,2310).Have the temperature of reaction height, the time is long, needs repeated multiple times grinding and sintering or SrWO
4Drawbacks such as impurity is difficult to remove.
Summary of the invention
For solving the deficiencies in the prior art, the invention provides a kind of double perovskite magnetic material Sr
2MWO
6The preparation method of (M=Co or Ni), the monomer of employing is strontium nitrate, Xiao Suangu, nickelous nitrate, ammonium paratungstate; Complexing agent is a citric acid; Dispersion agent is an ethylene glycol; Solvent is a deionized water.
Its preparation process and condition are as follows:
Strontium nitrate, Xiao Suangu or nickelous nitrate, ammonium paratungstate are dissolved in the deionized water, add complexing agent and dispersion agent, stir, form colloidal sol; Complexing agent wherein: dispersion agent: metal ion summation: the mol ratio of deionized water is 2-10: 2-10: 1-5: 30-100; Strontium ion: bore ion or nickel ion: the mol ratio of tungsten ion is 2: 1: 1.In 60～70 ℃ of heating, until forming gel, xerogel is made in 80～120 ℃ of oven dry then with transparent colloidal sol.Xerogel in 700 ℃ of pre-burnings 6～10 hours, is obtained oxide powder.The oxide powder that pre-burning obtains is put into corundum crucible, and sintering 20～40 hours in 1000～1300 ℃ of air atmosphere adopts the furnace cooling mode to be cooled to room temperature in retort furnace, can obtain double perovskite magnetic material Sr
2MWO
6(M=Co, Ni).
The present invention utilizes sol-gel technique, makes initial metal ion reach the homodisperse of atomic level, and it is low to make that therefore the preparation process of the whole material of the present invention has temperature of reaction, and the reaction times is short, and method is easy, is easy to realize industrialized characteristics.In addition, method synthetics purity height of the present invention, even particle size has particularly been removed and has been difficult to the SrWO that avoids in the solid state reaction
4Dephasign.
Embodiment
Embodiment 1: double-perovskite oxide S r
2CoWO
6Preparation
Adopt the sol-gel method sintetics, get 4.26g strontium nitrate (20.00mmol) respectively, 2.94g Xiao Suangu (10.00mmol), 2.73g ammonium paratungstate (0.83mmol), with each nitrate of 22mL deionized water dissolving and ammonium salt, add 16.81g citric acid (80mmol) and 4mL ethylene glycol and obtain colloidal sol.With colloidal sol in 60 ℃ of heating, until forming gel; Xerogel is made in 120 ℃ of oven dry.With 700 ℃ of pre-burnings of xerogel 6 hours, obtain oxide powder.The powder that pre-burning obtains is put into corundum crucible, and 1200 ℃ of air atmosphere sintering are 20 hours in retort furnace, adopt the furnace cooling mode to be cooled to room temperature, obtain double-perovskite oxide S r
2CoWO
6The product particle size is even, and diameter range is tetragonal system at 1.5～2.0 μ.
Embodiment 2: double-perovskite oxide S r
2NiWO
6Preparation
Adopt the sol-gel method sintetics, get 4.26g strontium nitrate (20.00mmol) respectively, 2.96g nickelous nitrate (10.00mmol), 2.73g ammonium paratungstate (0.83mmol), with each nitrate of 14mL deionized water dissolving and ammonium salt, add 16.81g citric acid (80mmol) and 4mL ethylene glycol and obtain colloidal sol.With colloidal sol in 70 ℃ of heating, until forming gel; Xerogel is made in 80 ℃ of oven dry.With 700 ℃ of pre-burnings of xerogel 10 hours, obtain oxide powder.The powder that pre-burning obtains is put into corundum crucible, and 1200 ℃ of air atmosphere sintering are 20 hours in retort furnace, adopt the furnace cooling mode to be cooled to room temperature, obtain double-perovskite oxide S r
2NiWO
6The product particle size is even, and diameter range is tetragonal system at 0.4～0.6 μ.
Embodiment 3: double-perovskite oxide S r
2CoWO
6Preparation
Adopt the sol-gel method sintetics, get 2.13g strontium nitrate (10.00mmol) respectively, 1.47g Xiao Suangu (5.00mmol), 1.37g ammonium paratungstate (0.42mmol), with each nitrate of 10mL deionized water dissolving and ammonium salt, add 8.42g citric acid (40mmol) and 6mL ethylene glycol and obtain colloidal sol.With colloidal sol in 65 ℃ of heating, until forming gel; Xerogel is made in 100 ℃ of oven dry.With 700 ℃ of pre-burnings of xerogel 8 hours, obtain oxide powder.The powder that pre-burning obtains is put into corundum crucible, and 1300 ℃ of air atmosphere sintering are 30 hours in retort furnace, adopt the furnace cooling mode to be cooled to room temperature, obtain double-perovskite oxide S r
2CoWO
6The product particle size is even, and diameter range is tetragonal system at 3～4 μ.
Embodiment 4: double-perovskite oxide S r
2NiWO
6Preparation
Adopt the sol-gel method sintetics, get 4.26g strontium nitrate (20.00mmol) respectively, 2.96g nickelous nitrate (10.00mmol), 2.73g ammonium paratungstate (0.83mmol), with each nitrate of 22mL deionized water dissolving and ammonium salt, add 16.81g citric acid (80mmol) and 10mL ethylene glycol and obtain colloidal sol.With colloidal sol in 60 ℃ of heating, until forming gel; Xerogel is made in 100 ℃ of oven dry.With 700 ℃ of pre-burnings of xerogel 10 hours, obtain oxide powder.The powder that pre-burning obtains is put into corundum crucible, and 1250 ℃ of air atmosphere sintering are 28 hours in retort furnace, adopt the furnace cooling mode to be cooled to room temperature, obtain double-perovskite oxide S r
2NiWO
6The product particle size is even, and diameter range is tetragonal system at 0.5～0.7 μ.
Embodiment 5: double-perovskite oxide S r
2NiWO
6Preparation
Adopt the sol-gel method sintetics, get 4.26g strontium nitrate (20.00mmol) respectively, 2.96g nickelous nitrate (10.00mmol), 2.73g ammonium paratungstate (0.83mmol), with each nitrate of 40mL deionized water dissolving and ammonium salt, add 8.42g citric acid (40mmol) and 10mL ethylene glycol and obtain colloidal sol.With colloidal sol in 70 ℃ of heating, until forming gel; Xerogel is made in 110 ℃ of oven dry.With 700 ℃ of pre-burnings of xerogel 6 hours, obtain oxide powder.The powder that pre-burning obtains is put into corundum crucible, and 1100 ℃ of air atmosphere sintering are 30 hours in retort furnace, adopt the furnace cooling mode to be cooled to room temperature, obtain double-perovskite oxide S r
2NiWO
6The product particle size is even, and diameter range is tetragonal system at 0.2～0.4 μ.
Embodiment 7: double-perovskite oxide S r
2CoWO
6Preparation
Adopt the sol-gel method sintetics, get 4.26g strontium nitrate (20.00mmol) respectively, 2.94g Xiao Suangu (10.00mmol), 2.73g ammonium paratungstate (0.83mmol), with each nitrate of 30mL deionized water dissolving and ammonium salt, add 16.81g citric acid (80mmol) and 5mL ethylene glycol and obtain colloidal sol.With colloidal sol in 65 ℃ of heating, until forming gel; Xerogel is made in 120 ℃ of oven dry.With 700 ℃ of pre-burnings of xerogel 10 hours, obtain oxide powder.The powder that pre-burning obtains is put into corundum crucible, and 1250 ℃ of air atmosphere sintering are 35 hours in retort furnace, adopt the furnace cooling mode to be cooled to room temperature, obtain double-perovskite oxide S r
2CoWO
6The product particle size is even, and diameter range is tetragonal system at 2～3 μ.
Embodiment 6: double-perovskite oxide S r
2NiWO
6Preparation
Adopt the sol-gel method sintetics, get 8.52g strontium nitrate (40.00mmol) respectively, 5.92g nickelous nitrate (20.00mmol), 5.46g ammonium paratungstate (1.66mmol), with each nitrate of 120mL deionized water dissolving and ammonium salt, add 33.62g citric acid (160mmol) and 20mL ethylene glycol and obtain colloidal sol.With colloidal sol in 65 ℃ of heating, until forming gel; Xerogel is made in 120 ℃ of oven dry.With 700 ℃ of pre-burnings of xerogel 7 hours, obtain oxide powder.The powder that pre-burning obtains is put into corundum crucible, and 1000 ℃ of air atmosphere sintering are 40 hours in retort furnace, adopt the furnace cooling mode to be cooled to room temperature, obtain double-perovskite oxide S r
2NiWO
6The product particle size is even, and diameter range is tetragonal system at 0.2～0.3 μ.
Embodiment 8: double-perovskite oxide S r
2CoWO
6Preparation
Adopt the sol-gel method sintetics, get 4.26g strontium nitrate (20.00mmol) respectively, 2.94g Xiao Suangu (10.00mmol), 2.73g ammonium paratungstate (0.83mmol), with each nitrate of 80mL deionized water dissolving and ammonium salt, add 25.22g citric acid (120mmol) and 15mL ethylene glycol and obtain colloidal sol.With colloidal sol in 70 ℃ of heating, until forming gel; Xerogel is made in 100 ℃ of oven dry.With 700 ℃ of pre-burnings of xerogel 6 hours, obtain oxide powder.The powder that pre-burning obtains is put into corundum crucible, and 1200 ℃ of air atmosphere sintering are 40 hours in retort furnace, adopt the furnace cooling mode to be cooled to room temperature, obtain double-perovskite oxide S r
2CoWO
6Even particle size, diameter range are tetragonal system at 2～3 μ.
Claims (1)
1, a kind of double perovskite magnetic material Sr
2MWO
6The preparation method of (wherein M=Co or Ni) is characterized in that the monomer of employing is strontium nitrate, Xiao Suangu, nickelous nitrate, ammonium paratungstate; Complexing agent is a citric acid; Dispersion agent is an ethylene glycol; Solvent is a deionized water; Its preparation process and condition are as follows:
Strontium nitrate, Xiao Suangu or nickelous nitrate, ammonium paratungstate are dissolved in the deionized water, add complexing agent and dispersion agent, stir, form colloidal sol; Complexing agent wherein: dispersion agent: metal ion summation: the mol ratio of deionized water is 2-10: 2-10: 1-5: 30-100; Strontium ion: cobalt ion or nickel ion: the mol ratio of tungsten ion is 2: 1: 1; In 60～70 ℃ of heating, until forming gel, xerogel is made in 80～120 ℃ of oven dry then with transparent colloidal sol; Xerogel in 700 ℃ of pre-burnings 6～10 hours, is obtained oxide powder; The oxide powder that pre-burning obtains is put into corundum crucible, and sintering 20～40 hours in 1000～1300 ℃ of air atmosphere adopts the furnace cooling mode to be cooled to room temperature in retort furnace, can obtain double perovskite magnetic material Sr
2MWO
6(M=Co or Ni).
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103193279A (en) * | 2013-04-12 | 2013-07-10 | 吉林大学 | Method for preparing high electric magnetic resistance material strontium cobalt molybdenum oxide |
| CN103865532A (en) * | 2014-03-31 | 2014-06-18 | 长安大学 | Double-ion-doped antimonate luminescent material and preparation method thereof |
| CN111933730A (en) * | 2020-08-20 | 2020-11-13 | 西安电子科技大学 | Nuclear radiation detector based on lead-free perovskite single crystal and preparation method thereof |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4419575C1 (en) * | 1994-06-03 | 1995-10-19 | Starck H C Gmbh Co Kg | Metal tungstate for prodn. of lead perovskite electro-ceramics and X=ray improving luminescent materials |
| JP4430619B2 (en) * | 2003-01-14 | 2010-03-10 | パナソニック株式会社 | Low thermal expansion material |
| CN1238303C (en) * | 2004-07-01 | 2006-01-25 | 上海交通大学 | Negative thermal-expansion coefficient adjustable laminated ceramic matrix composite and preparing method thereof |
| JP5234237B2 (en) * | 2004-08-31 | 2013-07-10 | 住友金属鉱山株式会社 | Transparent conductive film and method for producing the same, transparent electrode, infrared absorption reflection film, antifogging film, and electromagnetic shielding film |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103193279A (en) * | 2013-04-12 | 2013-07-10 | 吉林大学 | Method for preparing high electric magnetic resistance material strontium cobalt molybdenum oxide |
| CN103865532A (en) * | 2014-03-31 | 2014-06-18 | 长安大学 | Double-ion-doped antimonate luminescent material and preparation method thereof |
| CN103865532B (en) * | 2014-03-31 | 2016-03-23 | 长安大学 | Stibnate luminescent material of a kind of double ion doping and preparation method thereof |
| CN111933730A (en) * | 2020-08-20 | 2020-11-13 | 西安电子科技大学 | Nuclear radiation detector based on lead-free perovskite single crystal and preparation method thereof |
| CN111933730B (en) * | 2020-08-20 | 2024-02-23 | 西安电子科技大学 | Nuclear radiation detector based on leadless perovskite monocrystal and preparation method thereof |
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