Making method and application of mycotoxin photoelectrochemical sensor for in situ generation of CdS
A mycotoxin and photoelectrochemical technology, applied in the direction of material electrochemical variables, scientific instruments, instruments, etc., can solve the problems of complex sample pretreatment, large amount of sample required, single target, etc., to achieve shortened production time and high sensitivity and specific detection, the effect of a wide linear range
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Embodiment 1
[0039] Example 1Preparation method and application of a photoelectrochemical sensor for in-situ generation of CdS mycotoxins
[0040] (1) The conductive glass was ultrasonically cleaned with acetone, ethanol and ultrapure water in sequence, and dried with nitrogen gas; 6 μL, 2 mg / mL ceria-doped reduced graphene oxide composite nanomaterial was added dropwise to the conductive glass. surface, dried at room temperature, calcined at 400°C for 30min, and cooled to obtain ceria-doped reduced graphene oxide composite nanomaterial GS-CeO 2 Modified glass electrodes;
[0041] (2) In GS-CeO 2 On the modified glass electrode surface, add 5 μL, 0.1 μg / mL mycotoxin antibody solution dropwise, rinse the electrode surface with ultrapure water, and dry it in a refrigerator at 4 °C;
[0042] (3) Continue to drop 3 μL of BSA solution with a mass fraction of 1% to seal the non-specific active sites on the electrode surface, rinse the electrode surface with ultrapure water, and dry it in a r...
Embodiment 2
[0046] Example 2 Preparation method and application of a photoelectrochemical sensor for in-situ generation of CdS mycotoxins
[0047] (1) The conductive glass was ultrasonically cleaned with acetone, ethanol and ultrapure water in sequence, and dried with nitrogen gas; 6 μL, 3 mg / mL ceria-doped reduced graphene oxide composite nanomaterial was added dropwise to the conductive surface of the conductive glass. surface, dried at room temperature, calcined at 450 °C for 45 min, and cooled to obtain ceria-doped reduced graphene oxide composite nanomaterial GS-CeO 2 Modified glass electrodes;
[0048] (2) In GS-CeO 2 On the modified glass electrode surface, add 5 μL, 0.5 μg / mL mycotoxin antibody solution dropwise, rinse the electrode surface with ultrapure water, and dry it in a refrigerator at 4 °C;
[0049] (3) Continue to drop 3 μL of BSA solution with a mass fraction of 2% to seal the non-specific active sites on the electrode surface, rinse the electrode surface with ultra...
Embodiment 3
[0053] Example 3 Preparation method and application of a photoelectrochemical sensor for in-situ generation of CdS mycotoxins
[0054] (1) The conductive glass was ultrasonically cleaned with acetone, ethanol and ultrapure water in sequence, and dried with nitrogen; 6 μL, 4 mg / mL ceria-doped reduced graphene oxide composite nanomaterial was dropped onto the conductive surface of the conductive glass , dried at room temperature, calcined at 500°C for 60 min, and cooled to obtain ceria-doped reduced graphene oxide composite nanomaterial GS-CeO 2 Modified glass electrodes;
[0055] (2) In GS-CeO 2 On the modified glass electrode surface, add 5 μL, 1 μg / mL mycotoxin antibody solution dropwise, rinse the electrode surface with ultrapure water, and dry it in a refrigerator at 4 °C;
[0056] (3) Continue to drop 3 μL of BSA solution with a mass fraction of 3% to seal the non-specific active sites on the electrode surface, rinse the electrode surface with ultrapure water, and dry ...
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