BLSFMC/CMFO film with resistance switch effect and preparation method thereof
A resistive switching and thin film technology, applied in the field of BLSFMC/CMFO thin film and its preparation, can solve the problems of difficult to meet strong magnetoelectric coupling, practical application limitations, high remanent polarization value, etc., and achieve good chemical stability and moderate saturation magnetization. value, the effect of high insulation
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0035] The BLSFMC / Co 1-x mn x Fe 2 o 4 The preparation method of composite film, comprises the following steps:
[0036] Step 1: Add Co(NO 3 ) 2 ·6H 2 O, C 4 h 6 MnO 4 4H 2 O and Fe(NO 3 ) 3 9H 2 O is (1-x) in molar ratio: x: 2 is dissolved in the mixed solution of ethylene glycol methyl ether and acetic anhydride, stirs evenly, obtains Co 1-x mn x Fe 2 o 4 Precursor;
[0037] Step 2: Coating Co on the FTO / Glass substrate by spin coating method 1-x mn x Fe 2 o 4 Precursor, get Co 1- x mn x Fe 2 o 4 Wet film, the wet film is baked at 195-200°C to obtain a dry film after uniform glue, and then annealed at 550-600°C to obtain crystalline Co 1-x mn x Fe 2 o 4 film;
[0038] Step 3: To be crystalline Co 1-x mn x Fe 2 o 4 After natural cooling of the film, the crystalline Co 1-x mn x Fe 2 o 4 Repeat step 2 on the film to reach the desired thickness, that is, to obtain Co 1-x mn x Fe 2 o 4 film;
[0039] Step 4: Bi(NO 3 ) 3 ·5H 2 O, La(NO...
Embodiment 1
[0051] Step 1, Co(NO 3 ) 2 ·6H 2 O and Fe(NO 3 ) 3 9H 2 O is dissolved in the mixed solution of ethylene glycol methyl ether and acetic anhydride at a molar ratio of 1:2, and stirred evenly for 2 hours to obtain CoFe 2 o 4 Precursor, CoFe 2 o 4 The concentration of metal ions in the precursor solution is 0.3mol / L, and the volume ratio of ethylene glycol methyl ether and acetic anhydride is 3:1;
[0052] Step 2, spin coating CoFe on FTO / Glass substrate by spin coating method 2 o 4 Precursor solution, the homogenization speed is 4000r / min, the homogenization time is 15s, and the CoFe 2 o 4 Wet film, bake the wet film at 200°C for 8 minutes to obtain a dry film, and then anneal at 600°C for 30 minutes to obtain crystalline CoFe 2 o 4 film;
[0053] Step 3, to be crystalline CoFe 2 o 4 After natural cooling of the film, the crystalline CoFe 2 o 4 Repeat step 2 on the film to achieve the desired thickness, that is, to obtain CoFe 2 o 4 film;
[0054] Step 4, th...
Embodiment 2
[0058] Step 1, Co(NO 3 ) 2 ·6H 2 O, C 4 h 6 MnO 4 4H 2 O and Fe(NO 3 ) 3 9H2 O is dissolved in the mixed solution of ethylene glycol methyl ether and acetic anhydride with a molar ratio of 0.8:0.2:2, and stirred evenly for 2h to obtain Co 0.8 mn 0.2 Fe 2 o 4 Precursor, Co 0.8 mn 0.2 Fe 2 o 4 The concentration of metal ions in the precursor solution is 0.3mol / L, and the volume ratio of ethylene glycol methyl ether and acetic anhydride is 3:1;
[0059] Step 2, Spin Coating Co on FTO / Glass Substrate by Spin Coating 0.8 mn 0.2 Fe 2 o 4 Precursor solution, the homogenization speed is 4000r / min, the homogenization time is 15s, and the Co 0.8 mn 0.2 Fe 2 o 4 Wet film, bake the wet film at 200°C for 8 minutes to obtain a dry film, and then anneal at 600°C for 30 minutes to obtain crystalline Co 0.8 mn 0.2 Fe 2 o 4 film;
[0060] Step 3, to be crystalline Co 0.8 mn 0.2 Fe 2 o 4 After natural cooling of the film, the crystalline Co 0.8 mn 0.2 Fe 2 o 4 ...
PUM
Property | Measurement | Unit |
---|---|---|
electrical resistivity | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com