Polydopamine-silver particle-polydopamine type surface-enhanced Raman spectroscopic substrate and preparation method thereof
A surface-enhanced Raman and polydopamine-based technology, applied in the field of nanomaterials, can solve problems such as harsh conditions, cumbersome operation steps, and large environmental pollution, and achieve excellent resistance, simple experimental environment, and stable performance.
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Embodiment 1
[0028] Take the quartz plate as the base, cut it into 5mm×5mm rectangular pieces, and use 10 pieces as a group. Use acetone, absolute ethanol, and deionized water to clean ultrasonically for 30 minutes, and then blow dry with nitrogen for use. The obtained clean quartz plate is used as an attachment substrate.
[0029] Using a glass petri dish with a diameter of 6 mm (before the experiment, it must be ultrasonically cleaned with acetone, absolute ethanol, and deionized water for 30 minutes, and then vacuum-dried in an oven at 95 ° C) as a container, prepare a Tris buffer solution with a concentration of 10 mM, and use 0.1 mM hydrochloric acid solution to adjust the pH value of the Tris buffer solution to 8.5, using the Tris buffer solution with a concentration of 10 mM and a pH value of 8.5 as a solvent to prepare 10 mL of a dopamine-Tris solution with a concentration of 2 mg / mL. Immerse the quartz substrate into the above prepared solution (10mL), keep the liquid level of the...
Embodiment 2
[0034] Take the quartz plate as the base, cut it into 5mm×5mm rectangular pieces, and use 10 pieces as a group. Use acetone, absolute ethanol, and deionized water to clean ultrasonically for 40 minutes, and then blow dry with nitrogen for use. The obtained clean quartz plate is used as an attachment substrate.
[0035] Using a glass petri dish with a diameter of 6 mm (before the experiment, it must be ultrasonically cleaned with acetone, absolute ethanol, and deionized water for 30 minutes, and then vacuum-dried in an oven at 95 ° C) as a container, prepare a Tris buffer solution with a concentration of 10 mM, and use 0.1 mM hydrochloric acid solution to adjust the pH value of the Tris buffer solution to 8.5, using the Tris buffer solution with a concentration of 10 mM and a pH value of 8.5 as a solvent to prepare 10 mL of a dopamine-Tris solution with a concentration of 2 mg / mL. Immerse the quartz substrate in the prepared solution above, keep the liquid level of the solution...
Embodiment 3
[0040] Using the silicon wafer as the base, cut it into rectangular pieces of 5mm×5mm, and take 10 pieces as a group. Use acetone, absolute ethanol, and deionized water to ultrasonically clean for 30 min, respectively, and then blow dry with nitrogen for use. The obtained clean silicon wafer is used as an attachment substrate.
[0041] Using a glass petri dish with a diameter of 6 mm (before the experiment, it must be ultrasonically cleaned with acetone, absolute ethanol, and deionized water for 30 minutes, and then vacuum-dried in an oven at 95 ° C) as a container, prepare a Tris buffer solution with a concentration of 10 mM, and use 0.1 mM hydrochloric acid solution to adjust the pH value of the Tris buffer solution to 8.5, using the Tris buffer solution with a concentration of 10 mM and a pH value of 8.5 as a solvent to prepare 10 mL of a dopamine-Tris solution with a concentration of 2 mg / mL. Immerse the silicon substrate into the above prepared solution (10mL), keep the l...
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