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Preparation and testing method of a core-shell enhanced Raman spectroscopy substrate

A Raman spectroscopy substrate, Raman spectroscopy technology, applied in Raman scattering, measurement devices, material analysis by optical means, etc., can solve problems such as single functionality, and achieve the effect of a simple method

Active Publication Date: 2020-08-11
DONGHUA UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] However, almost all previous reports on core-shell nanoparticle-enhanced Raman spectroscopy are aimed at single-functional, multi-functional core-shell structure-enhanced Raman spectroscopy substrates with probe molecular selectivity and multiple stimuli responsiveness. No relevant reports yet

Method used

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  • Preparation and testing method of a core-shell enhanced Raman spectroscopy substrate
  • Preparation and testing method of a core-shell enhanced Raman spectroscopy substrate
  • Preparation and testing method of a core-shell enhanced Raman spectroscopy substrate

Examples

Experimental program
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Effect test

Embodiment 1

[0030] Add 440mg of anhydrous sodium citrate to 2.5×10 -4 M HAuCl 4 ·3H 2 In 100mL boiling aqueous solution of O, stir vigorously for 15 minutes and cool down to obtain a water dispersion solution of gold nanoparticles, with a concentration of about 50 μg mL -1 ; 0.4mL 50μg mL -1 Aqueous dispersion of gold nanoparticles with 2mL of 2mg mL -1 (PVP) 2 -(PNIPAM-b-PAA) 2The aqueous solution and 1.6mL deionized water were mixed evenly, and after standing for two days, centrifuged three times, and the precipitate was redispersed in 4mL aqueous solution to obtain (PVP) 2 -(PNIPAM-b-PAA) 2 loaded gold nanoparticles.

[0031] figure 1 and figure 2 Is the Au@(PVP) 2 -(PNIPAM-b-PAA) 2 Schematic diagram of the structure of nanoparticles and TEM images under different conditions. From figure 1 and figure 2 It can be seen that changing the temperature and pH can well change the thickness and aggregation state of the shell.

[0032] Configure 5μg mL -1 Au@(PVP) 2 -(PNIPAM-...

Embodiment 2

[0035] Configure 5μg mL -1 Au@(PVP) 2 -(PNIPAM-b-PAA) 2 with 10 -6 The mixed solution of M R6G was put into a capillary tube after standing for 24 hours for Raman spectroscopy test. The test conditions of Raman spectroscopy are: excitation wavelength of 633nm, laser energy of 17mW, and exposure time of 10s. The temperature of the solution is controlled by a hot stage, and the pH is controlled by adding NaOH or HCl solution to the mixture. The temperature control range is 25-55°C, and the pH control range is 5-13.

[0036] This example examines Au@(PVP) under different temperature and pH conditions 2 -(PNIPAM-b-PAA) 2 Raman spectrum signal enhancement effect on R6G molecules. Via R6G 1359cm -1 The enhancement factor calculated from the peak intensity at the peak is plotted against the temperature and pH, and the Figure 4 . From Figure 4 It can be seen from the figure that Au@(PVP) 2 -(PNIPAM-b-PAA) 2 The enhancement of the Raman signal of R6G molecules shows a gr...

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Abstract

The invention provides a preparation method of a core-shell surface enhanced Raman spectrometry substrate. According to the preparation method, chloroauric acid is added into boiling water to carry out reactions to obtain spherical gold nano particles; non-linear hydrophilic segmented copolymer (PVP)2-(PNIPAM-b-PAA)2 is synthesized through reversible addition-fragmentation chain transfer polymerization and single electron transfer active free radical polymerization; gold nano particles are mixed with a water solution of (PVP)2-(PNIPAM-b-PAA)2, after still standing and adsorption, the system is subjected to centrifugal washing to remove free polymers, nano particles Au@(PVP)2-(PNIPAM-b-PAA)2 with a core-shell structure are obtained, and the nano particles are the core-shell surface enhanced Raman spectrometry substrate. The invention also provides a Raman spectrum test method of the core-shell surface enhanced Raman spectrometry substrate. The prepared substrate has probe molecule selectivity, temperature responding property, and pH responding property, the method is simple, and the substrate can be used to super-sensitively detect an analyte in a complicated environment.

Description

technical field [0001] The invention belongs to the technical field of surface-enhanced Raman spectroscopy, and in particular relates to a method for preparing and testing a core-shell-enhanced Raman spectroscopy substrate with probe molecule selectivity and temperature and pH responsiveness. Background technique [0002] Surface-enhanced Raman spectroscopy is a spectroscopic method for highly sensitive detection of analytes based on the enhancement of Raman signals by active substrates. Since its discovery, it has been widely used in interface and surface science, material analysis, biology, medicine, and food safety. , environmental monitoring and other fields. Among them, surface-enhanced Raman spectroscopy based on core-shell nanoparticles is considered to be a substrate with great application potential. This is because, on the one hand, the active substrate material as the core, such as a noble metal, can produce a strong electromagnetically enhanced Raman effect in th...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): G01N21/65
CPCG01N21/658
Inventor 孙胜童武培怡
Owner DONGHUA UNIV