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PbPdO2 material with oriented growth along [400] crystal orientation and preparation method thereof

A technology of orientation growth and grain growth, applied in the direction of single crystal growth, crystal growth, single crystal growth, etc., can solve the problem of no film found

Active Publication Date: 2017-02-08
HEFEI UNIV OF TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0003] In 2009, X.L.Wang et al prepared PbPdO doped with 25at.% Co element by pulsed laser deposition method 2 Thin film, X-ray diffraction analysis shows that the film mainly grows along the conventional [211] crystal direction, and it is found that the material has electroresistance effect and giant magnetoresistance effect, but it is not found along the [400] crystal direction or other crystal directions Oriented film
From 2010 to 2016, many research groups in the world studied the PbPdO 2 Conducted research on the doping of Co, Mn, Cu, Zn and other transition metal elements, and prepared PbPdO with large grain size by solid-state reaction and pulsed laser deposition. 2 Materials, it is found that these materials have low-temperature ferromagnetism and giant magnetoresistance effects, and there is no report that the method used by them grows along the [400] crystal direction or other crystal orientations, nor does it change the concentration of dopant ions to control the growth of crystals along a specific crystal orientation

Method used

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  • PbPdO2 material with oriented growth along [400] crystal orientation and preparation method thereof
  • PbPdO2 material with oriented growth along [400] crystal orientation and preparation method thereof
  • PbPdO2 material with oriented growth along [400] crystal orientation and preparation method thereof

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preparation example Construction

[0051] The preferred solution is a PbPdO with controllable crystal orientation 2 The preparation method of material, concrete steps are as follows:

[0052] Step a, taking anhydrous lead nitrate, palladium nitrate dihydrate and ferric nitrate nonahydrate respectively, wherein the atomic ratio of Pb:Pd:Fe is 4.21:(0.75-0.95):(0.05-0.25);

[0053] Step b, weighing ethylene glycol methyl ether, ethylene glycol and deionized water, and uniformly mixing to form a mixed solvent; further, when weighing 0.0535-0.2675 grams of iron nitrate nonahydrate (molar mass is 0.00013-0.00066mol) , Weigh 0.6715~0.5301 grams of palladium nitrate dihydrate (molar mass is 0.00252~0.00199mol), 3.7294 grams of nonahydrate lead nitrate (molar mass is 0.01115mol, and remain unchanged), 18mL (17.37 grams) of ethylene glycol Methyl ether, 5 mL (5.5775 g) of ethylene glycol, 1 mL (1 g) of deionized water, 3 mL (2.73 g) of concentrated nitric acid;

[0054] Add the anhydrous lead nitrate weighed in step a...

Embodiment 1

[0064]Weigh 0.01115mol of anhydrous lead nitrate, 0.00252mol of palladium nitrate dihydrate and 0.00013mol of iron nitrate nonahydrate, the atomic ratio is about Pb:Pd:Fe=4.21:0.95:0.05; weigh 18mL of ethylene glycol methyl ether, 5mL ethylene glycol and 1mL deionized water, uniformly mix the three solutions into a mixed solvent, add the weighed anhydrous lead nitrate and stir until completely dissolved, then add the weighed ferric nitrate nonahydrate and stir until completely dissolved, forming Dissolve the mixed solution of lead nitrate anhydrous and ferric nitrate nonahydrate; Weigh 0.01863mol citric acid monohydrate as a complexing agent, add to the mixed solution of lead nitrate anhydrous and ferric nitrate nonahydrate and stir until completely dissolved, Form the mixed solution that dissolves lead nitrate anhydrous, ferric nitrate nonahydrate and citric acid monohydrate; Measure 3mL concentrated nitric acid, dissolve the palladium nitrate dihydrate that has been weighed c...

Embodiment 2

[0067] Weigh respectively 0.01115mol anhydrous lead nitrate, 0.00225mol dihydrate palladium nitrate and 0.00040mol nonahydrate iron nitrate, the atomic ratio is about Pb:Pd:Fe=4.21:0.85:0.15; respectively weigh 18mL ethylene glycol methyl ether, 5mL ethylene glycol and 1mL deionized water, uniformly mix the three solutions into a mixed solvent, add the weighed anhydrous lead nitrate and stir until completely dissolved, then add the weighed ferric nitrate nonahydrate and stir until completely dissolved, forming Dissolve the mixed solution of lead nitrate anhydrous and ferric nitrate nonahydrate; Weigh 0.01863mol citric acid monohydrate as a complexing agent, add to the mixed solution of lead nitrate anhydrous and ferric nitrate nonahydrate and stir until completely dissolved, Form the mixed solution that dissolves lead nitrate anhydrous, ferric nitrate nonahydrate and citric acid monohydrate; Measure 3mL concentrated nitric acid, dissolve the palladium nitrate dihydrate that has...

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Abstract

The invention provides a crystal orientation-controllable PbPdO2 material and a preparation method thereof. The PbPdO2 material is characterized in that the growth orientation of crystal grains corresponding to the strongest diffraction peak is [400] crystal orientation. The preparation method comprises the following steps of weighing a compound containing Fe (iron), a compound containing Pb (plumbum) and a compound containing Pd (palladium); mixing the compound containing the Fe, the compound containing the Pb, a mixing solvent and a complexing agent, so as to obtain mixing liquid containing Fe and Pb; mixing the compound containing the Pd and strong acid, so as to obtain mixing liquid containing the strong acid; mixing the mixing liquid, so as to obtain a sol; coating the sol onto a substrate, drying, and pre-burning, so as to obtain a pre-burning thin film; calcining the pre-burning thin film, so as to obtain a product. The PbPdO2 material and the preparation method have the beneficial effects that under the condition of no reliance on a lattice constant substrate with high matching degree, the PbPdO2 material is induced to perform preferable oriented growth along the [400] crystal orientation successfully, and a nanometer particle film is formed.

Description

technical field [0001] The present invention relates to the technical field of zero bandgap semiconductors, in particular to PbPdO 2 semiconductor material, as an induced PbPdO 2 A technology for the growth of materials along the [400] crystal direction, specifically a PbPdO grown along the [400] crystal direction 2 Materials and their preparation methods. Background technique [0002] Over the past ten years, PbPdO 2 As a layered transition metal oxide material, it has been extensively studied by researchers due to its unique structure and properties. T.C.Ozawa et al. first synthesized single-phase PbPdO by solid-state reaction method 2 and Cu-doped PbPdO 2 material, the proposed PbPdO 2 The crystal structure is a body-centered orthorhombic structure, and its thermoelectric properties have been studied, and it is believed that there is a metal-insulation transition temperature (T MI ). In 2008, X.L.Wang theoretical calculations at the University of Wollongong in Aus...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C30B29/22C30B28/04C30B29/64
CPCC30B28/04C30B29/22C30B29/64
Inventor 苏海林刘俊梅超吴玉程黄荣俊
Owner HEFEI UNIV OF TECH