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Preparation method for CLSTON type visible photocatalytic overall water splitting catalyst

A catalyst and visible light technology, applied in chemical instruments and methods, physical/chemical process catalysts, oxygen preparation, etc., can solve the problems of low efficiency of water splitting by visible light and insufficient use of solar energy, and achieve high efficiency of total water splitting, Promotes the separation of photogenerated electrons and holes and improves efficiency

Inactive Publication Date: 2015-09-09
BOHAI UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The present invention aims to provide a method for preparing a catalytic material for total visible light water splitting, so as to solve the current problems of low efficiency of visible light full photolytic water splitting and insufficient use of solar energy

Method used

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  • Preparation method for CLSTON type visible photocatalytic overall water splitting catalyst
  • Preparation method for CLSTON type visible photocatalytic overall water splitting catalyst
  • Preparation method for CLSTON type visible photocatalytic overall water splitting catalyst

Examples

Experimental program
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Effect test

Embodiment 1

[0045] Put calcium chloride, lanthanum chloride, scandium chloride, tantalum pentachloride and urea in a molar ratio of 1:1:1:1:100, accurately weigh them and put them into methanol aqueous solution (volume ratio of alcohol to water is 1:1) Stir to dissolve. Put the above mixture into a large crucible and put it directly into a muffle furnace. The heating rate of the programmed temperature rise is 10 ℃ / min, the high temperature setting temperature is 600 ℃, and the holding time of the high temperature stage is 12 h. After natural cooling, the obtained Precursor. The precursor was nitrided in an ammonia atmosphere, the nitriding temperature was 800°C, and the time was 24 hours. After cooling, CLSTON powder was obtained. The purity of its products is not less than 99.73%, and the impurity content: carbon is less than 0.06%; chlorine is less than 0.13%. With CLSTON as the main catalyst, after stirring for 24 hours under 300 W xenon light (stirring speed 1000 rpm), the cocatalys...

Embodiment 2

[0047] Calcium nitrate, lanthanum nitrate, scandium nitrate, tantalum pentaethoxide and citric acid in a molar ratio of 1:1:1:1:50, accurately weighed and put into methanol aqueous solution (volume ratio of alcohol to water: 1:1) Stir to dissolve. Put the above mixture into a large crucible and put it directly into a muffle furnace. The heating rate of the programmed temperature rise is 10 ℃ / min, the high temperature setting temperature is 800 ℃, the holding time of the high temperature stage is 6 h, and after natural cooling, the obtained Precursor. The precursor was nitrided in an ammonia atmosphere, the nitriding temperature was 850°C, and the time was 8 hours. After cooling, CLSTON powder was obtained. The purity of its products is not less than 99.93%, and the impurity content: carbon is less than 0.04%; chlorine is less than 0.02%. With CLSTON as the main catalyst, after stirring for 24 hours under 300 W xenon light (stirring speed 1000 rpm), the cocatalyst RhCrO x mi...

Embodiment 3

[0049] Calcium nitrate, lanthanum nitrate, scandium nitrate, tantalum pentaethoxide and citric acid in a molar ratio of 1:1:1:1:50, accurately weighed and put into methanol aqueous solution (volume ratio of alcohol to water: 1:1) Stir to dissolve. Put the above mixture into a large crucible and put it directly into a muffle furnace. The heating rate of the programmed temperature rise is 10 ℃ / min, the high temperature setting temperature is 900 ℃, and the holding time of the high temperature stage is 4 h. After natural cooling, the obtained Precursor. The precursor was nitrided in an ammonia atmosphere, the nitriding temperature was 900°C, and the time was 6 hours. After cooling, CLSTON powder was obtained. The purity of its products is not less than 99.87%, and the impurity content: carbon is less than 0.06%; chlorine is less than 0.03%. With CLSTON as the main catalyst, after stirring for 24 hours under 300 W xenon light (stirring speed 1000 rpm), the cocatalyst RhCrO x mi...

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Abstract

The invention discloses a preparation method for a visible photocatalytic overall water splitting catalyst. The preparation method comprises: sufficiently dissolving soluble calcium salt, soluble lanthanum salt, soluble scandium salt, soluble tantalum salt and a burning auxiliary agent in a methanol-water mixed solution, performing temperature programming in a muffle furnace so as to perform a burning reaction, keeping the high temperature stage for certain time, and performing natural cooling so as to form a predecessor; then, performing nitrogenization high-temperature treatment on the predecessor so as to obtain CLSTON perovskite type nitrogen oxide powder. CLSTON is used as a main catalyst, after light stirring, firstly, the CLSTON is loaded with a co-catalyst, and then, the CLSTON loaded with the co-catalyst is cladded with a nitrogen inhibitor so as to prepare the overall water splitting catalyst responding to the visible light. The preparation method disclosed by the invention has the advantages of high efficiency, high stability, high catalytic overall water splitting efficiency, and the like, is environmentally-friendly, has the catalytic activity of the visible light, can sufficiently transform and utilize solar energy, and is easy to apply and popularize, and the raw materials are easily available.

Description

technical field [0001] The invention belongs to the technical field of preparation of inorganic non-metallic materials, and in particular relates to a preparation method of a CLSTON type visible light total water splitting catalyst. Background technique [0002] Photocatalytic overall water splitting is a hot research topic in the field of photocatalysis. Usually, nanostructured photocatalyst particles dissolved in solution are used. Through contact with these particles in solution, a series of chemical catalytic reactions occur, and finally water is completely decomposed to generate hydrogen and oxygen. This approach differs from the usual method of producing hydrogen and oxygen using separate catalyst-coated electrodes. The main advantage of photocatalytic total water splitting is that it uses photocatalytic materials that are cheaper than those required for photoelectrochemical (PEC) cells. Therefore, it is more affordable for widespread and large-scale use, and the pro...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J27/24C01B3/04C01B13/02
CPCY02E60/36Y02P20/133
Inventor 张杰许家胜
Owner BOHAI UNIV