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A kind of preparation method of silver nanocluster

A technology of silver nanoclusters and silicon nanowires, which is applied in Raman scattering, material excitation analysis, etc., and can solve problems such as unfavorable silver nanocluster applications

Active Publication Date: 2017-10-17
TECHNICAL INST OF PHYSICS & CHEMISTRY - CHINESE ACAD OF SCI
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, this method usually uses NaBH 4 reduction method, the obtained silver nanoclusters contain a small amount of NaBH 4 or its reaction products, which is not conducive to the application of silver nanoclusters in biological in situ analysis

Method used

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  • A kind of preparation method of silver nanocluster
  • A kind of preparation method of silver nanocluster
  • A kind of preparation method of silver nanocluster

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] 20 μL of 1.5 mM AgNO 3 The aqueous solution was mixed with 50 μL of 100 μM DNA (5’-AATTCCCCCCCCCCCCCTTAA-3’) in 20 mM PB7.4 buffer, 110 μL of 20 mM PB7.0 buffer was added, shaken vigorously for 30 s, and placed in ice water for 15 min. The 20mM PB7.0 buffer is a chloride ion-free phosphate buffer at pH 7.0; the PB7.4 buffer is a chloride ion-free phosphate buffer at pH 7.4.

[0030] The silicon nanowire array was placed in a 4% HF solution for 30 min, washed with deoxygenated water, and ultrasonicated to obtain a suspension of silicon nanowires with surface silicon-hydrogen bonds at 4 μg / mL. Add 20 μL of this suspension immediately to the above AgNO 3 and DNA mixture, shake vigorously for 30s, place in a refrigerator at 4°C for 10 hours, take the supernatant, and obtain silver nanoclusters with an emission wavelength of 570 nm. Luminescence spectra of the obtained silver nanoclusters figure 1 and TEM figure 2 shown.

[0031] The preparation method of the silicon n...

Embodiment 2

[0035] Dissolve 96 μL of 1.5 mM AgNO 3 The aqueous solution was mixed with 90 μL of 100 μM DNA (5’-CCCACCACCCCTCCCA-3’) in 20 mM PB7.4 buffer, 34 μL of 20 mM PB7.0 buffer was added, shaken vigorously for 1 min, and placed in ice water for 30 min.

[0036] The silicon nanowire array was placed in a 2% HF solution for 40 min, washed with deoxygenated water, and ultrasonicated to obtain a suspension of silicon nanowires with silicon-hydrogen bonds on the surface at 4 μg / mL. Add 20 μL of this suspension immediately to the above AgNO 3 and DNA mixture, shake vigorously for 1 min, place in a 4°C refrigerator for 5 hours, take the supernatant, and obtain silver nanoclusters with emission wavelengths of 625 nm and 823 nm. Luminescence spectra of the obtained silver nanoclusters Figure 4 with 5 shown.

[0037] Preparation method of silicon nanowire array: Take n(100) silicon wafers of different sizes, perform ultrasonic cleaning with anhydrous acetone, absolute ethanol, and distil...

Embodiment 3

[0039]Dissolve 36 μL of 1.5 mM AgNO 3 The aqueous solution was mixed with 90 μL of 100 μM DNA (5’-CCCCCCCCCCCC-3’) in 20 mM PB7.4 buffer, 34 μL of 20 mM PB7.0 buffer was added, shaken vigorously for 2 min, and placed in ice water for 10 min.

[0040] The silicon nanowire array was placed in 8% HF solution for 10 min, washed with deoxygenated water, and ultrasonicated to obtain a suspension of silicon nanowires with silicon-hydrogen bonds on the surface at 4 μg / mL. 20 μL of this suspension was immediately added to the above-mentioned AgNO3 and DNA mixture, shaken vigorously for 3 minutes, placed in a refrigerator at 4°C for 8 hours, and the supernatant was taken to obtain silver nanoclusters with an emission wavelength of 630 nm. result with figure 2 resemblance.

[0041] Preparation method of silicon nanowire array: Take n(100) silicon wafers of different sizes, ultrasonically clean them with 50% acetone, 60% ethanol, and distilled water for 15 minutes in sequence, and plac...

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Abstract

The invention discloses a preparation method of a silver nanocluster, comprising the following steps: 1. mixing an AgNO3 solution with a DNA solution according to a molar ratio of AgNO3 to DNA of 6:1-16:1, adding a first buffer solution with certain volume, quickly shaking for 30s-2min, and standing for 10-30min; 2. putting a silicon nanowire array into a 2-8% hydrofluoric acid (HF) solution for 10-40min, washing with deoxidizing water, and carrying out ultrasonic treatment to obtain a silicon nanowire solution with surface having a hydrogen bond; and 3. adding the silicon nanowire with surface having the hydrogen bond to the mixed solution obtained in step 1, quickly shaking for 30s-3min, standing for 5-10 hours, and discarding the lower-layer silicon nanowire, thus obtaining the silver nanocluster. According to the invention, the hydrogen bond on the surface of the silicon nanowire is used as a reducing agent to prepare the silver nanocluster, the silicon nanowire can be removed just by standing, and the obtained silver nanocluster can be directly used for subsequent biological application, without being affected by a little quantity of NaBH4 or reaction products thereof in common methods.

Description

technical field [0001] The invention belongs to the field of preparation of nano clusters, in particular to the technical field of preparation of noble metal nano clusters. Background technique [0002] Noble metal nanoclusters composed of a small number of metal atoms have important potential applications in chemical sensing, bioimaging, and bioin situ analysis due to their unique fluorescent properties. Therefore, in recent years, many preparation methods for noble metal clusters have been developed, mainly including template method, monolayer protection method, etching method and so on. Among them, silver nanoclusters using DNA as a template have the advantages of simple preparation method, easy regulation of emission wavelength, low toxicity, good biocompatibility and photostability, which make the silver nanoclusters using DNA as a template useful in biological imaging and chemical detection. Many excellent works (J.H.Yu, S.Choi, R.M.Dickson, Angew.Chem.Int.Ed. 2009, 4...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): G01N21/65
CPCB22F9/24
Inventor 穆丽璇师文生
Owner TECHNICAL INST OF PHYSICS & CHEMISTRY - CHINESE ACAD OF SCI