A kind of ultraviolet dose detector based on nucleic acid material and its preparation method
A detector and nucleic acid technology, applied in the field of ultraviolet detection, can solve the problems of low photoresponsivity, low measurement accuracy, low sensitivity, etc., and achieve the effects of sensitive response, simple process and easy miniaturization
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Embodiment 1
[0032] First, single-layer graphene was grown on a 25-micron-thick copper foil by chemical vapor deposition, and the graphene was transferred to a patterned Cr / Au (thickness of 5 / 300 mm) prepared by thermal evaporation technology in advance by electrochemical exfoliation. 40 nm) material electrode SiO 2 / Si substrate to obtain graphene transistor devices.
[0033] Then, modify a layer of benzoic acid N-hydroxysuccinimide ester on the graphene surface as a probe connector, the solvent used is dimethyl sulfoxide, the modified concentration is 5 mmol / L, and the modified reaction temperature is 25 Celsius, the reaction time is 1.5 hours, washed with ethanol and distilled water three times respectively, and dried under high-purity nitrogen.
[0034] Next, modify the rectangular DNA origami structure (DNA Origami) on the surface of the device. The buffer solution used is tris hydroxymethylaminomethane acetate and ethylenediaminetetraacetic acid buffer solution. The modified concent...
Embodiment 2
[0037] First, single-layer graphene was grown on a 25-micron-thick copper foil by chemical vapor deposition, and the graphene was transferred to a patterned Cr / Au (thickness of 5 / 300 mm) prepared by thermal evaporation technology in advance by electrochemical exfoliation. 40 nm) material electrode SiO 2 / Si substrate to obtain graphene transistor devices.
[0038] Then, modify a layer of benzoic acid N-hydroxysuccinimide ester on the graphene surface as a probe connector, the solvent used is dimethyl sulfoxide, the modified concentration is 5 mmol / L, and the modified reaction temperature is 25 Celsius, the reaction time is 1.5 hours, washed with ethanol and distilled water three times respectively, and dried under high-purity nitrogen.
[0039] Next, modify the rectangular DNA origami structure (DNA Origami) on the surface of the device. The buffer solution used is Tris hydroxymethylaminomethane acetate and EDTA buffer solution. The modified concentration is 2 nmol / liter. The...
Embodiment 3
[0042] First, single-layer graphene was grown on a 25-micron-thick copper foil by chemical vapor deposition, and the graphene was transferred to a patterned Cr / Au (thickness of 5 / 300 mm) prepared by thermal evaporation technology in advance by electrochemical exfoliation. 40 nm) material electrode SiO 2 / Si substrate to obtain graphene transistor devices.
[0043] Then, modify a layer of benzoic acid N-hydroxysuccinimide ester on the graphene surface as a probe connector, the solvent used is dimethyl sulfoxide, the modified concentration is 5 mmol / L, and the modified reaction temperature is 25 Celsius, the reaction time is 1.5 hours, washed with ethanol and distilled water three times respectively, and dried under high-purity nitrogen.
[0044] Next, modify the rectangular DNA origami structure (DNA Origami) on the surface of the device. The buffer solution used is Tris hydroxymethylaminomethane acetate and EDTA buffer solution. The modified concentration is 10 nmol / liter. The ...
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