Preparation method and application of photoelectrochemical N-terminal pro-brain natriuretic peptide sensor based on mesoporous flower-like tin oxide composite material
A photoelectrochemical and composite material technology, applied in the preparation and application of photoelectrochemical N-terminal forebrain natriuretic peptide sensors based on mesoporous flower-like tin oxide composite materials, can solve the problems of cumbersome steps, low sensitivity, and long detection cycle , to achieve high surface activity, enhanced sensitivity, and improved photoelectric performance
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Embodiment 1
[0032] Example 1 Preparation of SnO 2 / NCQDs / Bi 2 S 3 The specific steps are:
[0033] (1) Add 0.01 g of thioacetamide to 10 mL of isopropanol, stir until the thioacetamide is dissolved, then add 7 μL of tin chloride, stir to mix evenly and the solution is clear, transfer the solution to 50 mL In the reaction kettle, place it in a blast drying oven at 180 °C to react for 24 h. After the reaction is completed, the obtained product is washed with ultrapure water and ethanol for 3 times, and dried at 80 °C for 12 h to obtain SnO 2 powder, transfer the powder to a muffle furnace, calcinate at 500°C for 0.5 h, cool to room temperature, collect the powder for grinding, and obtain calcined SnO 2 , the calcined SnO 2 The powder was dispersed in ultrapure water and ultrasonicated for 20 s to obtain SnO 2 suspension;
[0034] (2) Cut the ITO electrode to a size of 2.5 cm × 0.8 cm, ultrasonically clean it with acetone, ethanol and ultrapure water for 30 min, and dry it in an oven a...
Embodiment 2
[0036] Embodiment 2 prepares SnO 2 / NCQDs / Bi 2 S 3 The specific steps are:
[0037] (1) Add 0.02 g of thioacetamide to 20 mL of isopropanol, stir until the thioacetamide is dissolved, then add 14 μL of tin chloride, stir to make it evenly mixed and the solution is clear, transfer the solution to 50 mL In the reaction kettle, place it in a blast drying oven at 180 °C to react for 24 h. After the reaction is completed, the obtained product is washed with ultrapure water and ethanol for 3 times, and dried at 80 °C for 12 h to obtain SnO 2 powder, transfer the powder to a muffle furnace, calcinate at 500°C for 1 h, and collect the powder after cooling to room temperature for grinding to obtain calcined SnO 2 , the calcined SnO 2 The powder was dispersed in ultrapure water and ultrasonicated for 20 s to obtain SnO 2 suspension;
[0038] (2) Cut the ITO electrode to a size of 2.5 cm × 0.8 cm, ultrasonically clean it with acetone, ethanol and ultrapure water for 30 min, and dry...
Embodiment 3
[0040] Embodiment 3 prepares SnO 2 / NCQDs / Bi 2 S 3 The specific steps are:
[0041] (1) Add 0.01 g of thioacetamide to 10 mL of isopropanol, stir until the thioacetamide is dissolved, then add 7 μL of tin chloride, stir to mix evenly and the solution is clear, transfer the solution to 50 mL In the reaction kettle, place it in a blast drying oven at 180 °C to react for 24 h. After the reaction is completed, the obtained product is washed with ultrapure water and ethanol for 3 times, and dried at 80 °C for 12 h to obtain SnO 2 powder, transfer the powder to a muffle furnace, calcinate at 500 °C for 2 h, and collect the powder after cooling to room temperature for grinding to obtain calcined SnO 2 , the calcined SnO 2 The powder was dispersed in ultrapure water and ultrasonicated for 20 s to obtain SnO 2 suspension;
[0042] (2) Cut the ITO electrode to a size of 2.5 cm × 0.8 cm, ultrasonically clean it with acetone, ethanol and ultrapure water for 30 min, and dry it in an ...
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