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A kind of preparation method of Raman spectroscopic detection substrate

A Raman spectroscopic detection and substrate technology, applied in the field of analysis and detection, can solve problems such as high cost and unfavorable large-scale production, and achieve the effects of being conducive to large-scale production, simple operation and low cost

Active Publication Date: 2020-07-10
SHANGHAI JIAOTONG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the three-dimensional ordered substrate realized by high-cost processes such as photolithography and coating (patent number: 201711131759.3 is too expensive to be conducive to mass production.

Method used

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  • A kind of preparation method of Raman spectroscopic detection substrate
  • A kind of preparation method of Raman spectroscopic detection substrate
  • A kind of preparation method of Raman spectroscopic detection substrate

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0030] (1) TiO 1.04 Preparation of nanorods: adding NaCl and titanium isopropoxide to 5 mol / L hydrochloric acid solution to make the concentrations of the two reach 0.7 mol / L and 0.042 mol / L respectively, and dissolve NaCl and titanium isopropoxide under high-speed stirring. Transfer the solution to a hydrothermal reaction kettle, clean the FTO glass in piranha liquid, and place it in the solution at an angle. After sealing, react at 150°C for 18 hours. After the reaction, the FTO glass was taken out and rinsed with deionized water. Annealed at 500°C for 30 minutes.

[0031] (2) Preparation and assembly of gold nanoparticles: the TiO prepared in (1) 1.04 The surface of the nanorod substrate was aminated with a freshly prepared amination solution (40 μL triethoxysilane, 0.5 mL deionized water and 0.5 mL ethanol) for 20 minutes, and after amination, the sample was dried at 60 °C for 10 minutes. minute. The supplies were then rinsed three times with deionized water. The sam...

Embodiment 2

[0037] The implementation process of this embodiment is the same as that of Embodiment 1 except for the following differences.

[0038] TiO prepared in (1) 1.04 The surface of the nanorod substrate was aminated with a freshly prepared amination solution (40 μL triethoxysilane, 0.5 mL deionized water and 0.5 mL ethanol) for 20 minutes, and after amination, the sample was dried at 60 °C for 10 minutes. minute. The supplies were then rinsed three times with deionized water. The sample was placed in 100 mL of 0.015 mol / L sodium citrate solution, and the solution was boiled using a constant temperature magnetic stirrer. Then stir rapidly and add 0.5mL 2mol / L chloroauric acid solution. After ten minutes of reaction, the solution was observed to change from colorless to wine red. Finally, the samples were removed and rinsed with deionized water.

[0039] The obtained result is different from the size and density of the gold nanoparticles in Example 1. The result is as image 3 a...

Embodiment 3

[0041] The implementation process of this embodiment is the same as that of Embodiment 1 except for the following differences.

[0042] TiO prepared in (1) 1.04 The surface of the nanorod substrate was aminated with a freshly prepared amination solution (40 μL triethoxysilane, 0.5 mL deionized water and 0.5 mL ethanol) for 20 minutes, and after amination, the sample was dried at 60 °C for 10 minutes. minute. The supplies were then rinsed three times with deionized water. The sample was placed in 100 mL of 0.015 mol / L sodium citrate solution, and the solution was boiled using a constant temperature magnetic stirrer. Then stir rapidly and add 1mL of 2mol / L chloroauric acid solution. After ten minutes of reaction, the solution was observed to change from colorless to wine red. Finally, the samples were removed and rinsed with deionized water.

[0043] The obtained result is different from the size and density of the gold nanoparticles in Example 1. The results obtained can ...

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Abstract

The invention provides a preparation method for a raman spectrum detection substrate. The method comprises the following steps: preparing a precursor solution; cleaning an FTO glass, and then bias placing into the precursor solution, and annealing at 500 DEG C after the hydrothermal reaction at 150 DEG C, thereby forming a TiO1.04 nanorod on the FTO glass surface; soaking the TiO1.04 nanorod in anamination solution, performing surface treatment, and then drying and cleaning, placing into a sodium citrate solution, boiling, adding a chloroauric acid solution under a boiling state, reacting till the solution becomes wine red from colorless, taking out and cleaning. Compared with the prior art, the invention has the advantages that the preparation for the raman spectrum detection substrate with low cost and high sensitivity can be realized and the preparation method is beneficial to large-scale production; compared with a granular raman substrate, the raman substrate basing on a glass substrate has the advantages that the operation in detecting and self-degradation is simpler; the raman substrate can be reused and can keep ultrahigh detection sensitivity; the substrate can keep stable for a long time.

Description

technical field [0001] The invention relates to a preparation method of a Raman spectrum detection substrate, belonging to the technical field of analysis and detection. Background technique [0002] Surface-enhanced Raman spectroscopy (SERS) can quickly detect most organic molecules. At present, the main forms of SERS substrates are noble metal particles and noble metal-semiconductor. In addition to the localized surface plasmon resonance (LSPR) effect produced by the noble metal, the noble metal-semiconductor substrate also has an electron transfer (CT) effect between the semiconductor and the detected molecules. Therefore, modifying noble metal particles on semiconductor materials can increase the "hot spots" to enhance LSPR, and further enhance Raman spectroscopy through electron migration between semiconductors and detected molecules. [0003] Li Juan et al. (patent number: 201610038980.3 assemble silver nanoparticles on the surface of titanium dioxide microspheres, w...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): G01N21/65
CPCG01N21/658
Inventor 程秀兰王晓东余旭丰曾源李君
Owner SHANGHAI JIAOTONG UNIV