Energy augmentation structures, energy emitters or energy collectors containing the same, and their use in solar cells and other energy conversion devices
US-2024115878-A1 · Apr 11, 2024 · US
US9873773B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9873773-B2 |
| Application number | US-201615134708-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 21, 2016 |
| Priority date | Apr 23, 2015 |
| Publication date | Jan 23, 2018 |
| Grant date | Jan 23, 2018 |
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Disclosed are a composite material and a method for preparing the same. The composite material is consisted of TiO 2 and BaZn 1.2 Co 0.8 Fe 16 O 27 . The composite material of the invention has the advantages of high absorption frequency band, good compatibility and wide frequency band, and it is applicable for the shell protection material of a mobile phone or a TV set, thereby absorbing the electromagnetic wave band that is the most harmful to human bodies, without influencing the normal communication function of an electronic device, for example, a mobile phone.
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What is claimed is: 1. A composite material, comprising TiO 2 -coated BaZn 1.2 Co 0.8 Fe 16 O 27 particulates. 2. The composite material according to claim 1 , wherein, a weight ratio of TiO 2 to BaZn 1.2 Co 0.8 Fe 16 O 27 is (0.1-10):(1-10). 3. The composite material according to claim 1 , wherein, the composite material is a powder with a micrometer-level grain size. 4. The composite material according to claim 1 , wherein, a reflection loss of the composite material at 7.76-13.68 GHz is less than −10 dB, and a reflection loss thereof at 10.3 GHz is −47.6 dB. 5. An electronic device shell, which is made from a raw material comprising the composite material according to claim 1 . 6. The electronic device shell according to claim 5 , wherein, the weight ratio of TiO 2 to BaZn 1.2 Co 0.8 Fe 16 O 27 is (0.1-10):(1-10). 7. The electronic device shell according to claim 5 , wherein, the composite material is a powder with a micrometer-level grain size. 8. The electronic device shell according to claim 5 , wherein, the reflection loss of the composite material at 7.76-13.68 GHz is less than −10 dB, and the reflection loss thereof at 10.3 GHz is -47.6 dB. 9. The electronic device shell according to claim 5 , wherein, the electronic device is a mobile phone. 10. A method for preparing a composite material, comprising the steps of: dissolving Ba(NO 3 ) 2 , Zn(NO 3 ) 2 .6H 2 O, Co(NO 3 ) 2 .6H 2 O and Fe(NO 3 ) 3 .9H 2 O in distilled water at a molar ratio of 1:1.2:0.8:16, adding a citric acid at a molar ratio of 10:1 relative to Ba(NO 3 ) 2 , stirring till complete dissolution, adjusting a pH value of a resultant solution to neutrality, evaporating the solution to prepare a sol, drying to obtain a gel, and then calcining the gel to obtain BaZn 1.2 Co 0.8 Fe 16 O 27 ; and adding BaZn 1.2 Co 0.8 Fe 16 O 27 into a TiO 2 sol, stirring and filtering, washing the obtained filter residue, drying the obtained filter residue to obtain a precursor, and drying the precursor to obtain the composite material which comprises TiO 2 -coated BaZn 1.2 Co 0.8 Fe 16 O 27 particulates. 11. The method according to claim 10 , wherein, Ba(NO 3 ) 2 is analytically pure Ba(NO 3 ) 2 , Zn(NO 3 ) 2 .6H 2 O is analytically pure Zn(NO 3 ) 2 .6H 2 O, Co(NO 3 ) 2 .6H 2 O is analytically pure Co(NO 3 ) 2 .6H 2 O, Fe(NO 3 ) 3 .9H 2 O is analytically pure Fe(NO 3 ) 3 .9H 2 O. 12. The method according to claim 10 , wherein, the evaporation is constant-temperature evaporation in 70° C. water bath. 13. The method according to claim 10 , wherein, before being calcined at 1300° C., the gel is ground into powder. 14. The method according to claim 10 , wherein, the filter residue is washed with absolute ethyl alcohol. 15. The method according to claim 14 , wherein, the filter residue washed with absolute ethyl alcohol is dried at 80° C. 16. The method according to claim 10 , wherein, the TiO 2 sol is prepared by: dissolving 2 parts by weight of butyl titanate and 1 part by weight of glacial acetic acid in 10 parts by weight of absolute ethyl alcohol, and stirring to obtain a transparent solution; and adding 4 parts by weight of an ethanol solution with a volume fraction of 75% dropwise into the transparent solution slowly, and stirring to obtain the TiO 2 sol. 17. The method according to claim 10 , wherein, the calcining is performed at 1300° C. 18. The method according to claim 10 , wherein, a weight ratio of TiO 2 to BaZn 1.2 Co 0.8 Fe 16 O 27 is (0.1-10):(1-10).
Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties · CPC title
Titanium dioxide · CPC title
Use of inorganic substances as compounding ingredients · CPC title
Shaped ceramic products characterised by their composition {(porous ceramic products C04B38/00; ceramic articles characterised by particular shape, see the relevant classes, e.g. linings for casting ladles, tundishes, cups or the like B22D41/02; ceramic substrates for microelectronic semi-conductors H10W70/692)}; Ceramics compositions ({shaping of ceramics B28B;} containing free metal bonded to carbides, diamond, oxides, borides, nitrides, silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides or sulfides other than as macroscopic reinforcing agents C22C); Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products {(infiltration of sintered ceramic preforms with molten metal C04B41/51; chemical preparation of powders of inorganic compounds C01)} · CPC title
of metals · CPC title
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