Preparation method and application of a photoelectrochemical cardiac troponin i sensor based on multi-level micron cubic zinc stannate composite material
A technology of cardiac troponin and cubic zinc stannate, which is applied in the fields of material electrochemical variables, scientific instruments, analytical materials, etc., can solve the problems of long detection period, low sensitivity, complicated steps, etc., and achieves improved photoelectric performance, enhanced sensitivity, Enhance the effect of photoelectric activity
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Embodiment 1
[0034] Example 1 Preparation of Zn 2 SnO 4 / N,S-GQDs / CdS specific steps are:
[0035] (1) Add 0.03 g polypyrrole / nitrogen-deficient graphitic carbon nitride PPy / g-C to 10 mL ultrapure water and 10 mL ethanol mixture 3 N 4 -VN template, sonicate for 0.5 h, then continue to add 1.25 mmol zinc chloride and 0.625 mmol tin chloride, after that, add 5 mL 1.0 mol / L NaOH solution dropwise, stir for 15 min, transfer the suspension to 50 mL poly In a tetrafluoroethylene-lined autoclave, heat the reaction at 200 °C for 24 h, centrifuge and wash the resulting product three times with ethanol and ultrapure water, and finally dry to obtain Zn 2 SnO 4 powder, which is dissolved in ultrapure water to obtain Zn 2 SnO 4 suspension;
[0036] (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 with nitrogen, then add 10 µL of Zn 2 SnO 4 The suspension was modified onto the ITO electrode and dried...
Embodiment 2
[0038] Embodiment 2 prepares Zn 2 SnO 4 / N,S-GQDs / CdS specific steps are:
[0039] (1) Add 0.1 g polypyrrole / nitrogen-deficient graphitic carbon nitride PPy / g-C to 10 mL ultrapure water and 10 mL ethanol mixture 3 N 4 -VN template, sonicate for 0.5 h, then continue to add 1.25 mmol zinc chloride and 0.625 mmol tin chloride, after that, add 5 mL 1.0 mol / L NaOH solution dropwise, stir for 15 min, transfer the suspension to 50 mL poly In a tetrafluoroethylene-lined autoclave, heat the reaction at 200 °C for 24 h, centrifuge and wash the resulting product three times with ethanol and ultrapure water, and finally dry to obtain Zn 2 SnO 4 powder, which is dissolved in ultrapure water to obtain Zn 2 SnO 4 suspension;
[0040] (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 with nitrogen, then add 10 µL of Zn 2 SnO 4 The suspension was modified onto the ITO electrode and dried at ...
Embodiment 3
[0042] Embodiment 3 prepares Zn 2 SnO 4 / N,S-GQDs / CdS specific steps are:
[0043] (1) Add 0.3 g polypyrrole / nitrogen-deficient graphitic carbon nitride PPy / g-C to 10 mL ultrapure water and 10 mL ethanol mixture 3 N 4 -VN template, sonicate for 1 h, then continue to add 2.5 mmol zinc chloride and 1.25 mmol tin chloride, after that, add 5 mL 1.0 mol / L NaOH solution dropwise, stir for 30 min, transfer the suspension to 50 mL poly In a tetrafluoroethylene-lined autoclave, heat the reaction at 200°C for 28 h, centrifuge and wash the resulting product three times with ethanol and ultrapure water, and finally dry to obtain Zn 2 SnO 4 powder, which is dissolved in ultrapure water to obtain Zn 2 SnO 4 suspension;
[0044] (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 with nitrogen, then add 10 µL of Zn 2 SnO 4 The suspension was modified onto the ITO electrode and dried at room ...
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