Ag-(010) crystal face BiVO4 photocatalyst and preparation method thereof
A photocatalyst, crystal face technology, applied in chemical instruments and methods, physical/chemical process catalysts, metal/metal oxide/metal hydroxide catalysts, etc. high, photo-generated carriers are difficult to migrate, etc., to achieve good application prospects and simple operation.
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Embodiment 1
[0021] Step 1: Add Bi(NO 3 ) 3 ·5H 2 O dissolved in dilute HNO with a concentration of 1mol / L 3 Add NH after stirring for 30min 4 VO 3 , Stirred for 120 min to form precursor liquid A; among them Bi(NO 3 ) 3 ·5H 2 O and NH 4 VO 3 The molar ratio is 1:1, Bi in precursor A 3+ The concentration is 0.1mol / L;
[0022] Step 2: Hydrothermally react the precursor solution A at 70°C for 15 hours. After the reaction, the precipitate is washed and dried at 70°C for 9 hours to obtain a monoclinic phase with exposed (010) crystal plane and (110) crystal plane. The spatial structure group is BiVO for I2 / a 4 Surface heterojunction powder;
[0023] Step 3, the (010) crystal plane BiVO 4 The powder is dissolved in deionized water to obtain BiVO with a concentration of 6.25g / L 4 Aqueous solution, press AgNO 3 The quality is BiVO 4 5% to BiVO 4 Add AgNO to the aqueous solution 3 Dissolve in BiVO under dark state and stirring 4 In the aqueous solution, the precursor liquid B is prepared;
[0024] Step 4...
Embodiment 2
[0026] Step 1: Add Bi(NO 3 ) 3 ·5H 2 O dissolved in dilute HNO with a concentration of 1mol / L 3 Medium, add NH after stirring for 10min 4 VO 3 , Stirred for 100min to form precursor liquid A; where Bi(NO 3 ) 3 ·5H 2 O and NH 4 VO 3 The molar ratio is 1:1, Bi in precursor A 3+ The concentration is 0.2mol / L;
[0027] Step 2: Hydrothermally react the precursor solution A at 80°C for 14h. After the reaction, wash the precipitate and dry it at 60°C for 10h to obtain a monoclinic phase with exposed (010) crystal plane and (110) crystal plane. The spatial structure group is BiVO for I2 / a 4 Surface heterojunction powder;
[0028] Step 3, the (010) crystal plane BiVO 4 The powder is dissolved in deionized water to obtain BiVO with a concentration of 6.25g / L 4 Aqueous solution, press AgNO 3 The quality is BiVO 4 10% to BiVO 4 Add AgNO to the aqueous solution 3 Dissolve in BiVO under dark state and stirring 4 In the aqueous solution, the precursor liquid B is prepared;
[0029] Step 4. Put the ...
Embodiment 3
[0031] Step 1: Add Bi(NO 3 ) 3 ·5H 2 O dissolved in dilute HNO with a concentration of 2mol / L 3 Medium, add NH after stirring for 50min 4 VO 3 , Stirred for 140min to form precursor liquid A; where Bi(NO 3 ) 3 ·5H 2 O and NH 4 VO 3 The molar ratio is 1:1, Bi in precursor A 3+ The concentration is 0.3mol / L;
[0032] Step 2: Hydrothermally react the precursor solution A at 85°C for 13 hours. After the reaction, the precipitate is washed and dried at a constant temperature of 80°C for 8 hours to obtain a monoclinic phase with exposed (010) crystal plane and (110) crystal plane. The spatial structure group is BiVO for I2 / a 4 Surface heterogeneous powder;
[0033] Step 3, the (010) crystal plane BiVO 4 The powder is dissolved in deionized water to obtain BiVO with a concentration of 6.25g / L 4 Aqueous solution, press AgNO 3 The quality is BiVO 4 15% to BiVO 4 Add AgNO to the aqueous solution 3 Dissolve in BiVO under dark state and stirring 4 In the aqueous solution, the precursor liquid B...
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