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A kind of preparation method of nitrogen-doped bismuth ferrite nanopowder

A technology of nano-powder and bismuth ferrite, which is applied in nanotechnology, nanotechnology, chemical instruments and methods, etc., can solve the problems of few researches on doping substitution, and achieve the effect of avoiding ferroelectric-paraelectric phase transition

Active Publication Date: 2016-08-24
SOUTH CHINA UNIV OF TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, there are not many studies on the doping substitution of O sites.

Method used

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  • A kind of preparation method of nitrogen-doped bismuth ferrite nanopowder
  • A kind of preparation method of nitrogen-doped bismuth ferrite nanopowder
  • A kind of preparation method of nitrogen-doped bismuth ferrite nanopowder

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Experimental program
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Effect test

Embodiment 1

[0029] Weigh 1.213g of bismuth nitrate pentahydrate and 1.01g of ferric nitrate nonahydrate at a molar ratio of 1:1 and dissolve them in 50ml of dilute nitric acid; 3+ The concentration is about 0.025mol / L, and then according to Fe 3+ The ions are added with tartaric acid at a molar ratio of 1:1, and finally by Fe and Fe 3+ The molar ratio of ions is 1.2:1. Add urea to the above solution; preheat the obtained solution in an oil bath at 55°C for 1 hour, then raise the temperature to 105°C and stir the reaction until it is completely evaporated to dryness to form xerogel; The gel is ground into powder, pre-fired in a muffle furnace at 300°C for 2 hours, then heated to 600°C for 1 hour, and then cooled naturally with the furnace; put the sintered powder into a dilute nitric acid solution with a concentration of 1M / L and stir to clean it 1 h, then repeatedly rinsed with deionized water and suction filtered, and finally vacuum-dried at 80° C. to obtain nitrogen-doped bismuth ferri...

Embodiment 2

[0032] Weigh 1.213g of bismuth nitrate pentahydrate and 1.01g of ferric nitrate nonahydrate at a molar ratio of 1:1 and dissolve them in 50ml of dilute nitric acid; 3+ The concentration is about 0.025mol / L, and then according to Fe 3+ The ions are added with tartaric acid at a molar ratio of 1:1, and finally by Fe and Fe 3+ The molar ratio of ions is 0.9:1, and urea is added to the above solution; the resulting solution is preheated for 1.5h under stirring in an oil bath at 60°C, and then heated to 110°C and fully stirred until the reaction is completely evaporated to dryness to form xerogel; The dry gel is ground into powder, pre-fired in a muffle furnace at 350°C for 2 hours, then heated to 650°C for 1 hour, and then cooled naturally with the furnace; put the sintered powder into a dilute nitric acid solution with a concentration of 1M / L and stir Wash for 1 hour, then repeatedly rinse with deionized water and suction filter, and finally vacuum dry at 90° C. to obtain nitrog...

Embodiment 3

[0035] Weigh 1.213g of bismuth nitrate pentahydrate and 1.01g of ferric nitrate nonahydrate at a molar ratio of 1:1 and dissolve them in 50ml of dilute nitric acid; 3+ The concentration is about 0.025mol / L, and then according to Fe 3+ The ions are added with tartaric acid at a molar ratio of 1:1, and finally by Fe and Fe 3+ Add urea to the above solution at a molar ratio of ions of 0.5:1; preheat the resulting solution in an oil bath at 65°C for 2 hours, then raise the temperature to 110°C and stir the reaction until it is completely evaporated to dryness to form a xerogel; The gel is ground into powder, pre-fired in a muffle furnace at 400°C for 2 hours, then heated to 750°C for 2 hours, and then cooled naturally with the furnace; put the sintered powder into a dilute nitric acid solution with a concentration of 1M / L and stir to clean it 1.5h, then repeatedly washed with deionized water and suction filtered, and finally vacuum-dried at 110°C to obtain nitrogen-doped bismuth ...

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Abstract

The invention discloses a method for preparing nitrogen-doped bismuth ferrite nano powder. The method comprises the following steps: (1) respectively dissolving bismuth nitrate pentahydrate and iron nitrate nonahydrate which are weighed according to a mole number of 1:1 in dilute nitric acid, adding tartaric acid and urea, dissolving by stirring to obtain a solution; (2) preheating the solution for 1 to 3h in a 55-65 DEG C oil bath by stirring, and then reacting by sufficiently stirring at a temperature of 105 to 115 DEG C until the solution is fully evaporated to dryness to form a dry gel; (3) grinding the dry gel into powder, presintering for 1 to 3h in a muffle furnace at a temperature of 300 to 500 DEG C, sintering for 0.5 to 2h at a temperature of 600 to 800 DEG C, and performing furnace cooling; and (4) putting the sintered powder into a dilute nitric acid solution to stir for 1 to 3h, repeatedly washing with deionized water and performing suction filtration, and drying in a vacuum at a temperature of 60 to 100 DEG C. The bismuth ferrite structure of the product provided by the invention keeps unchanged as a whole and the ferromagnetism appears.

Description

technical field [0001] The invention relates to the field of multiferroic materials with both ferromagnetic and ferroelectric properties, in particular to a preparation method of nitrogen-doped bismuth ferrite nanopowder. Background technique [0002] In recent years, multiferroic materials, as one of the most promising new materials, have attracted great interest from researchers in the field of materials and condensed matter physics. Since multiferroic materials combine magnetic and ferroelectric materials, there is a new degree of freedom in device design. Therefore, multiferroic materials show promise for practical applications in multiple fields. Among many single-phase multiferroic materials, bismuth ferrite (BiFeO 3 ) is one of the most researched materials at present. It is a typical multiferroic material with a high ferromagnetic transition temperature T N ~643K and ferroelectric transition temperature Tc~1103K, it is currently the only single-phase multiferroic...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C01G49/00B82Y30/00
Inventor 张弜陈龙胜张家敏陈熹
Owner SOUTH CHINA UNIV OF TECH