CN112723409A - SrTiO3Method for preparing polyhedron - Google Patents
SrTiO3Method for preparing polyhedron Download PDFInfo
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- CN112723409A CN112723409A CN202011237201.5A CN202011237201A CN112723409A CN 112723409 A CN112723409 A CN 112723409A CN 202011237201 A CN202011237201 A CN 202011237201A CN 112723409 A CN112723409 A CN 112723409A
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- C01G23/006—Alkaline earth titanates
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- C01P2002/70—Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data
- C01P2002/72—Crystal-structural characteristics defined by measured X-ray, neutron or electron diffraction data by d-values or two theta-values, e.g. as X-ray diagram
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Abstract
The invention belongs to the field of inorganic non-metallic materials, and particularly relates to SrTiO3A preparation method of polyhedron. The invention takes strontium hydroxide and titanium dioxide as raw materials, and sodium chloride and sodium bicarbonate as molten salt. The method comprises the following steps: (1) mixing strontium hydroxide and titanium dioxide raw materials with sodium chloride and sodium bicarbonate composite molten salt; (2) carrying out wet grinding and drying treatment on the obtained mixed material; (3) reacting the obtained powder particles at 700-900 ℃ for 5-10 h; (4) washing and drying the obtained product to finally obtain SrTiO with high crystallinity, good dispersity and jointly exposed crystal faces of (001) and (110)3Polyhedral powder material. The method has simple operation steps, no other by-products, mass preparation and convenient industrial production.
Description
Technical Field
The invention belongs to the field of inorganic non-metallic materials, and particularly relates to SrTiO3A preparation method of polyhedron.
Background
SrTiO3Is typically of perovskite (ABO)3Type) structure, which has a high dielectric constant and low dielectric loss, good piezoelectric properties, ferroelectricity and thermal stability, and a suitable optical forbidden bandwidth and energy band structure, has wide and important applications in the fields of electronic devices, industrial ceramics, energy sources, catalysis, and the like.
The research shows that the materialThe physicochemical properties of the material depend to a large extent on its micro-morphology and structure. For example, TiO2The nano-rods, the nano-fibers and the cubes all present irregular TiO2The particles have more excellent photoelectrochemical properties. At present, SrTiO with cubic, nanorod, micro-nano flower-shaped and other morphological structures3Have been widely reported. With the progress of research, the physical and chemical properties of the material can be remarkably improved by regulating and controlling the specific exposed crystal face of the material and utilizing the synergistic effect between the crystal faces. The main reason for this is that the electron structures of different exposed crystal planes differ from each other due to different atomic arrangements. Typically, a semiconductor energy band presents anisotropy in a three-dimensional direction of a space, and a crystal plane electric field can be formed by changing an exposed crystal plane of a semiconductor, so that the effective separation of photo-generated electrons and holes is realized, and the photoelectric catalytic performance of the semiconductor energy band is improved. Thus, SrTiO is prepared3The polyhedron has important significance for improving the photoelectrochemistry and other properties of the polyhedron.
The literature (Scientific Reports 2014,4, 5084; Nano Research 2014,7,1311) Reports a method of using TiCl4And SrCl2Taking organic alcohol (propylene glycol, glycerol or butanetriol) as a surfactant as a raw material, adjusting the pH of the solution by using LiOH, and hydrothermally synthesizing SrTiO3A preparation method of the octadecahedron. However, the preparation process of the method is complex, and the TiCl serving as the reaction raw material needs to be controlled in an ice-water bath4The dropping speed of the solution is high, meanwhile, the reaction time is long, the temperature needs to be kept at 180 ℃ for 48 hours, and organic matter residues exist on the surface of the material and need to be removed by high-temperature annealing treatment. The invention patent (publication number CN105727922B) discloses a Li-doped SrTiO3The preparation method of the octodecahedron nano-particles comprises the steps of preparing titanium hydroxide by using titanium sulfate and potassium hydroxide, and then mixing the titanium hydroxide with strontium nitrate solution, potassium hydroxide solution and halite octahedron LiTiO2The nano particles are stirred and mixed to carry out hydrothermal reaction. The method not only needs to use an easy-explosion reagent, but also has the dropping speed of the raw materials and the LiTiO2The morphology has strict requirements. In addition, strontium carbonate formed by mixing carbon dioxide into the precursor needs to be removed by acetic acid cleaning.
Disclosure of Invention
Aiming at the technologyThe invention provides a SrTiO3The simple synthesis method of the polyhedron has simple operation steps, does not need organic surfactant, strong alkali and acid washing treatment, can be prepared in large batch and is convenient for industrial production.
The invention aims to prepare SrTiO3Polyhedral and provides a simple and effective synthesis method.
The invention takes strontium hydroxide and titanium dioxide as raw materials and sodium chloride and sodium bicarbonate as molten salt to prepare SrTiO3High crystallinity, good dispersibility, and polyhedral structure with exposed (001) and (110) crystal faces. The method comprises the following specific steps:
(1) weighing strontium hydroxide and titanium dioxide in a stoichiometric ratio as raw materials; mixing sodium chloride and sodium bicarbonate according to the weight ratio of 3-8: 1 to obtain composite molten salt; and mixing the raw materials and the composite molten salt according to the proportion of 1: mixing at a molar ratio of 8-20 to obtain a mixture;
(2) adding an ethanol water solution or pure water into the mixture for wet grinding, and drying after the mixture is fully mixed;
(3) adding the dried powder particles into a crucible, heating to 700-900 ℃ at a heating rate of 5 ℃/min in an air atmosphere, reacting for 5-10 h, and naturally cooling to room temperature after the reaction is finished;
(4) washing the obtained product with deionized water, and drying to obtain SrTiO3Polyhedral powder material.
Compared with the prior art, the invention has the beneficial effects that:
(1) SrTiO prepared by the invention3The polyhedron has high crystallinity and good dispersibility;
(2) the preparation method has the advantages of simple preparation flow, low equipment requirement, low raw material cost, large-scale synthesis and easy industrial production;
(3) the invention does not need to use organic surface active agent, and has no environmental pollution.
Drawings
FIG. 1 shows SrTiO synthesized in example 13XRD pattern of polyhedral particles.
FIG. 2 shows SrTiO synthesized in example 13SEM pictures of polyhedral particles.
FIG. 3 shows SrTiO synthesized in example 23SEM pictures of polyhedral particles.
FIG. 4 shows SrTiO synthesized in example 33TEM pictures of polyhedral particles.
FIG. 5 shows SrTiO synthesized in example 43TEM and SAED pictures of polyhedral particles.
FIG. 6 shows SrTiO synthesized in example 43Polyhedral particle and SrTiO synthesized by traditional solid phase method3Photocatalytic reduction of CO by particles2Performance is compared to the graph.
Detailed Description
Example 1
(1) Weighing strontium hydroxide (0.304g) and titanium dioxide (0.2g) in a stoichiometric ratio; sodium chloride (1.16g) and sodium bicarbonate (0.42g) were mixed as a 4: 1 to obtain composite molten salt; and mixing the raw materials and the composite molten salt according to the proportion of 1: 10 mol ratio mixing;
(2) adding an ethanol aqueous solution into the mixture for wet grinding, and drying after the mixture is fully mixed;
(3) adding the fully dried powder particles into a crucible, heating to 700 ℃ at a heating rate of 5 ℃/min in an air atmosphere, reacting for 10h, and naturally cooling to room temperature after the reaction is finished;
(4) washing the obtained product with deionized water, and drying to obtain SrTiO3Polyhedral powder material.
FIG. 1 shows SrTiO prepared3The polyhedron XRD pattern has all diffraction peaks corresponding to standard card JCPDS #35-0734 one by one and is pure cubic phase SrTiO3A material. The diffraction peak intensity is high, the half-peak width is narrow, and the prepared SrTiO is illustrated3The degree of polyhedral crystallinity is high.
FIG. 2 shows SrTiO prepared3The crystal surface of the polyhedron SEM picture is smooth, has no obvious defects, shows good crystallinity, and SrTiO3Has an eighteen-hedron structure, good dispersibility and particle size of 200-500 nm.
Example 2
This example is the same as example 1 except that the aqueous ethanol solution was replaced with pure water during wet ball milling.
FIG. 3 shows SrTiO prepared3Polyhedral SEM picture, change of milling dispersant to synthetic SrTiO compared to example 13The polyhedral structure, dispersibility and particle size of the particles have no obvious influence.
Example 3
This example is the same as example 1 except that sodium chloride (1.74g) and sodium bicarbonate (0.42g) were weighed in 6: 1 to obtain composite molten salt; and mixing the raw materials and the composite molten salt according to the proportion of 1: and (4) mixing at a ratio of 14.
FIG. 4 shows SrTiO prepared3Polyhedral TEM picture, SrTiO3The polyhedral structure of (A) is not changed along with the change of process parameters, and the dispersity of particles is improved along with the increase of the proportion of molten salt.
Example 4
This example is identical to the procedure of example 1, except that the reaction temperature is 900 ℃ and the holding time is 5 hours.
FIG. 5 shows SrTiO prepared according to the present invention3And (3) polyhedral TEM and SAED pictures, wherein the TEM picture shows a typical polyhedral structure, and shows that the change of reaction temperature and time does not influence the synthesis of SrTiO in a sodium chloride and sodium bicarbonate composite molten salt system3Structural features of polyhedrons. SrTiO in SAED picture3The diffraction spots are in periodic ordered lattice arrangement, which shows that the prepared SrTiO3Is a single crystal. Obtaining the crystal face distance by taking the reciprocal after measuring the distance between the target diffraction point and the diffraction center, comparing with a standard card JCPDS #35-0734, and determining the SrTiO in the corresponding TEM picture3The exposed crystal planes of the polyhedrons are the (001) and (110) crystal planes.
Photocatalytic reduction of CO2And (3) performance comparison test:
0.1g of SrTiO prepared by the invention is weighed respectively3Polyhedrons and SrTiO prepared by traditional solid-phase sintering method3Placing the particles as photocatalyst in a photocatalytic reaction device, vacuumizing to remove oxygen-containing gaseous molecules, introducing high-purity carbon dioxide into the photocatalytic reaction device to make the pressure reach one atmosphere, adding 0.4mAfter distilling water, SrTiO is irradiated by a 300W xenon lamp3Carbon dioxide reduction reaction is carried out.
FIG. 6 shows SrTiO synthesized in example 43Polyhedral nano-particle and SrTiO synthesized by traditional solid phase method3Photocatalytic reduction of CO by particles2Performance is compared to the graph. SrTiO3Photocatalytic reduction of CO2The products of (A) are CO and CH4,SrTiO3Polyhedral CO and CH4The yield is obviously higher than that of a sample prepared by a solid phase method, and the synthesis of the polyhedron is favorable for improving SrTiO3The photocatalytic performance of (a).
The invention has been described in detail with reference to specific embodiments and illustrative examples, but the description is not intended to be construed in a limiting sense. It will be understood by those skilled in the art that various equivalent substitutions or modifications may be made to the technical solution of the present invention and the embodiments thereof without departing from the spirit and scope of the present invention, which fall within the scope of the present invention. The scope of the invention is defined by the appended claims.
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Cited By (2)
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CN116239078A (en) * | 2023-05-10 | 2023-06-09 | 中国科学院过程工程研究所 | A device and method for producing hydrogen by photolysis of water |
CN117042570A (en) * | 2023-10-10 | 2023-11-10 | 宁德时代新能源科技股份有限公司 | Perovskite thin film, perovskite precursor liquid, perovskite battery and electricity utilization device |
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CN103449511A (en) * | 2013-04-09 | 2013-12-18 | 深圳信息职业技术学院 | Strontium titanate submicron crystal and preparation method thereof |
CN104229874A (en) * | 2014-09-17 | 2014-12-24 | 上海应用技术学院 | Preparation method of strontium titanate nano-powder |
CN104399452A (en) * | 2014-10-20 | 2015-03-11 | 江苏科技大学 | Method for one-step microwave synthesis of La-Cr co-doped strontium titanate |
CN106745205A (en) * | 2016-11-23 | 2017-05-31 | 吕梁学院 | A kind of synthetic method of bar-shaped Mg2+ doping SrTiO3 |
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CN103449511A (en) * | 2013-04-09 | 2013-12-18 | 深圳信息职业技术学院 | Strontium titanate submicron crystal and preparation method thereof |
CN104229874A (en) * | 2014-09-17 | 2014-12-24 | 上海应用技术学院 | Preparation method of strontium titanate nano-powder |
CN104399452A (en) * | 2014-10-20 | 2015-03-11 | 江苏科技大学 | Method for one-step microwave synthesis of La-Cr co-doped strontium titanate |
CN106745205A (en) * | 2016-11-23 | 2017-05-31 | 吕梁学院 | A kind of synthetic method of bar-shaped Mg2+ doping SrTiO3 |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
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CN116239078A (en) * | 2023-05-10 | 2023-06-09 | 中国科学院过程工程研究所 | A device and method for producing hydrogen by photolysis of water |
CN116239078B (en) * | 2023-05-10 | 2023-08-22 | 中国科学院过程工程研究所 | A device and method for producing hydrogen by photolysis of water |
US11975967B1 (en) | 2023-05-10 | 2024-05-07 | Institute Of Process Engineering, Chinese Academy Of Sciences | Device for hydrogen production from water photolysis and method therefor |
CN117042570A (en) * | 2023-10-10 | 2023-11-10 | 宁德时代新能源科技股份有限公司 | Perovskite thin film, perovskite precursor liquid, perovskite battery and electricity utilization device |
CN117042570B (en) * | 2023-10-10 | 2024-03-29 | 宁德时代新能源科技股份有限公司 | Perovskite thin film, perovskite precursor liquid, perovskite battery and electricity utilization device |
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