Method for forming a magnetoelectric nanocomposite
US-12100538-B2 · Sep 24, 2024 · US
US12183494B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12183494-B2 |
| Application number | US-202418791804-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 1, 2024 |
| Priority date | May 7, 2021 |
| Publication date | Dec 31, 2024 |
| Grant date | Dec 31, 2024 |
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A magnetoelectric multiferroic nanocomposite. The nanocomposite comprises a ferroelectric perovskite oxide and a rare-earth substituted mixed ternary transition metal ferrite of the formula A1−xBxRyFe2−yO4. The nanocomposite has a high dielectric constant, low dielectric loss, both stable over a wide frequency range. These properties may make the nanocomposite desirable for applications in microelectronic devices, sensors and antennas.
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The invention claimed is: 1. A method of forming a nanocomposite, comprising: mixing ferroelectric perovskite oxide particles and rare-earth substituted mixed ternary transition metal ferrite particles to form a particle mixture, wherein the mixing includes combining a solution of Thulium oxide with a solution of transition metal nitrate salts to form the perovskite oxide particles and the rare-earth substituted mixed ternary transition metal ferrite particles; milling the particle mixture to form a precursor powder; pressing the precursor powder to form a pellet; and sintering the pellet to form the nanocomposite; wherein the rare-earth substituted mixed ternary transition metal ferrite particles are of formula A 1−x B x R y Fe 2−y O 4 , wherein A and B represent different transition metals; 0<x<1; R is Thulium; 0<y<0.2; and the rare-earth substituted mixed ternary transition metal ferrite particles are superparamagnetic at 0 to 50° C. 2. The method of claim 1 , wherein the ferroelectric perovskite oxide particles are lead-free BaTiO 3 . 3. The method of claim 1 , wherein the ferroelectric perovskite oxide particles have a mean particle size of less than 1000 nm. 4. The method of claim 1 , wherein A is cobalt. 5. The method of claim 1 , wherein B is zinc. 6. The method of claim 1 , wherein 0.1≤x<0.5. 7. The method of claim 1 , wherein the rare-earth substituted mixed ternary transition metal ferrite particles are substantially free of nickel. 8. The method of claim 1 , wherein R is thulium. 9. The method of claim 1 , wherein 0.001≤y≤0.1. 10. The method of claim 1 , wherein the rare-earth substituted mixed ternary transition metal ferrite particles have a mean particle size of 10 nm to 5 μm. 11. The method of claim 1 , wherein a molar ratio of the rare-earth substituted mixed ternary transition metal ferrite particles to the ferroelectric perovskite oxide particles is 0.05:1 to 0.5:1. 12. The method of claim 1 , wherein the nanocomposite has a dielectric constant (ε′) of 10 to 15 for frequencies of 10 0 to 10 6 Hz at 0 to 140° C. 13. The method of claim 1 , wherein the nanocomposite has a dielectric loss tangent of 0 to 0.1 for frequencies of 10 0 to 10 6 Hz at 0 to 140° C. 14. The method of claim 1 , wherein the nanocomposite has a band gap of 1.40 to 2.5 eV. 15. The method of claim 1 , wherein the nanocomposite has a saturation magnetization of 0.1 to 20 emu/g at 0 to 50° C. and a magnetic coercivity of 10 to 2000 Oe at 0 to 50° C. 16. A method of forming a nanocomposite, comprising: mixing ferroelectric perovskite oxide particles and rare-earth substituted mixed ternary transition metal ferrite particles to form a particle mixture, wherein the mixing includes combining a solution of a rare earth oxide with a solution of transition metal nitrate salts to form the perovskite oxide particles and the rare-earth substituted mixed ternary transition metal ferrite particles; milling the particle mixture to form a precursor powder; pressing the precursor powder to form a pellet; and sintering the pellet to form the nanocomposite; wherein the rare-earth substituted mixed ternary transition metal ferrite particles are of formula A 1−x B x R y Fe 2−y O 4 , wherein A and B represent different transition metals: 0<x<1; R is a rare-earth element; 0<y<0.2; and the rare-earth substituted mixed ternary transition metal ferrite particles are superparamagnetic at 0 to 50° C., wherein the pressing is performed at 900 to 1100 MPa. 17. The method of claim 1 , wherein the sintering is performed at 850 to 1350° C. for 1 to 6 hours. 18. A method of forming a nanocomposite, comprising: mixing ferroelectric perovskite oxide particles and rare-earth substituted mixed ternary transition metal ferrite particles to form a particle mixture, wherein the mixing includes combining a solution of a rare earth oxide with a solution of transition metal nitrate salts to form the perovskite oxide particles and the rare-earth substituted mixed ternary transition metal ferrite particles; milling the particle mixture to form a precursor powder; pressing the precursor powder to form a pellet; and sintering the pellet to form the nanocomposite; wherein the rare-earth substituted mixed ternary transition metal ferrite particles are of formula A 1−x B x R y Fe 2−y O 4 , wherein A and B represent different transition metals: 0<x<1; R is a rare-earth element; 0<y<0.2; and the rare-earth substituted mixed ternary transition metal ferrite particles are superparamagnetic at 0 to 50° C., wherein the rare-earth substituted mixed ternary transition metal ferrite particles are prepared by: mixing a cobalt (II) source, a zinc (II) source, an iron (III) source, and a thulium source in a solvent to form a precursor solution; adding a base to the precursor solution to form a reaction mixture having a pH of 11 to 12; ultrasonically treating the reaction mixture at a frequency of 18 to 25 kHz and a power of 50 to 100 W to form a precipitate; and drying the precipitate to form the rare-earth substituted mixed ternary transition metal ferrite particles. 19. The method of claim 18 , wherein: the cobalt (II) source is cobalt nitrate; the zinc (II) source is zinc nitrate; the iron (III) source is iron nitrate; the thulium source is thulium oxide; the base is sodium hydroxide; and the ultrasonic treatment is performed for 30 to 120 minutes.
Electromagnets; Actuators including electromagnets {(electric coils H01F5/00; devices for holding workpieces using electric force B23Q3/15; load-engaging elements for lifting articles electromagnetically B66C1/06; electromagnetic couplings F16D27/00; magnetic brakes F16D63/002; electromagnetically operated valves F16K11/24, F16K31/00; analysing materials by magnetic means G01N27/72, G01N27/80; electromagnets for winding mechanical clocks G04C1/02; electromagnetic relays H01H51/00; windings for salient poles of dynamo-electric machines H02K3/18; electromagnets for telegraphic communication H04L; for arc lamps H05B31/28)} · CPC title
Nanomagnetism, e.g. magnetoimpedance, anisotropic magnetoresistance, giant magnetoresistance or tunneling magnetoresistance · CPC title
Manufacture or treatment of nanostructures · CPC title
Oxides (H01F1/36 and H01F1/38 take precedence) · CPC title
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