Preparation method of h-BN-based catalyst for hydrogen production by photolysis of water
A technology for photo-splitting water for hydrogen production and catalyst, applied in chemical instruments and methods, physical/chemical process catalysts, hydrogen production, etc., can solve the problems of low hydrogen production efficiency, poor photocatalyst activity, etc. , the effect of improving photocatalytic activity and improving photocatalytic efficiency
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0046] The invention provides a technical solution: a preparation method of an h-BN-based photolysis water hydrogen production catalyst, comprising the following steps:
[0047] S1. Weigh boric acid (0.15g), urea (5g), and PEG2000 (0.5g), disperse them in deionized water, stir to disperse fully, evaporate the water to dryness, and obtain the precursor of h-BN;
[0048] S2. Put the above-mentioned h-BN precursor in a tube furnace, raise the temperature to 900°C at 4°C / min under an argon atmosphere, and calcinate for 4 hours to obtain carbon-doped h-BN;
[0049] S3, take by weighing the nickel chloride hexahydrate of 1.0mmol, the indium trichloride of 2.0mmol, the thiourea of 4.0mmol, join the N of 70ml, N-dimethylformamide and ethylene glycol (volume ratio 1: 1 ) in a mixed solvent, fully stirred and dissolved to form NiIn 2 S 4 The precursor solution;
[0050] S4. Weigh 0.2g of the above-prepared carbon-doped h-BN and add it to NiIn 2 S 4 In the precursor solution, stir...
Embodiment 2
[0053] The invention provides a technical solution: a preparation method of an h-BN-based photolysis water hydrogen production catalyst, comprising the following steps:
[0054] S1. Weigh boric acid (0.3g), thiourea (3g), and activated carbon (12g), disperse them in deionized water, stir to disperse fully, evaporate the water to dryness, and obtain the precursor of h-BN;
[0055] S2. Put the above-mentioned h-BN precursor in a tube furnace, raise the temperature to 900°C at 4°C / min under an argon atmosphere, and calcinate for 4 hours to obtain carbon / sulfur co-doped h-BN;
[0056] S3. Weigh 1.0mmol of zinc nitrate hexahydrate, 2.0mmol of indium sulfate nonahydrate, and 4.0mmol of thioacetamide, add them to 60ml of water, fully stir and dissolve to form ZnIn 2 S 4 The precursor solution;
[0057] S4. Weigh 0.5g of the above-prepared carbon / sulfur co-doped h-BN and add it to NiIn 2 S 4 In the precursor solution, stir to make it fully dispersed;
[0058] S5. In a high-pressu...
Embodiment 3
[0060] S1. Weigh fluoroboric acid (0.5g), melamine (5g), and sucrose (5g), and disperse them in deionized water, stir to disperse fully, evaporate the water to dryness, and obtain the precursor of h-BN;
[0061] S2. Put the above-mentioned h-BN precursor in a tube furnace, raise the temperature to 900°C at 4°C / min under an argon atmosphere, and calcinate for 4 hours to obtain fluorine-doped h-BN;
[0062] S3. Weigh 1.0mmol of cadmium nitrate tetrahydrate, 2.0mmol of indium trichloride, and 4.0mmol of sodium sulfide, add them to 50ml of ethanol, fully stir and dissolve to form CdIn 2 S 4 The precursor solution;
[0063] S4. Weigh 0.1g of the above-prepared fluorine co-doped h-BN and add it to CdIn 2 S 4 In the precursor solution, stir to make it fully dispersed;
[0064] S5. In a high-pressure reactor, at 150 degrees, hydrothermally react for 12 hours, wash and dry to obtain CdIn 2 S 4 / Fluorine-doped h-BN composites.
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 
