SILVER OXIDE MESO CRYSTAL CONTAINING SILVER PEROXIDE AND MANUFACTURING METHOD THEREFOR

20170354950 · 2017-12-14

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Inventors

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International classification

Abstract

A method for preparing a meso crystal of silver oxide containing silver peroxide is provided. A quantum crystal of silver thiosulfate complex on a substrate or a particle made of copper metal or copper alloy is subjected to treating by an alkaline aqueous solution containing halogen ion to obtain a meso crystal of silver oxide containing the silver peroxide. The meso crystal of silver oxide having nanometer scale, containing a silver peroxide, the silver oxide nanocrystal being a superstructure three-dimensionally arranged in the shape of a neuron provided with properties being negatively charged in water and able to be reduced to a silver nanoparticle by a laser radiation.

Claims

1. A method for preparing a meso crystal of silver oxide containing silver peroxide, comprising; forming a silver thiosulfate complex crystal on a substrate or a particle made of copper metal or copper alloy, and treating the substrate or the particle made of copper metal or copper alloy by an alkaline aqueous solution containing halogen ion to obtain a meso crystal of silver oxide containing the silver peroxide.

2. The method for preparing a meso crystal of silver oxide according to claim 1, wherein the silver thiosulfate complex crystal is a quantum crystal of metal complex formed on the substrate or the particle made of copper metal or copper alloy, while the alkaline aqueous solution containing halogen ion is a sodium hypochlorite aqueous solution, and wherein a meso structure is a superstructure of silver oxide containing silver peroxide, made by self-organization and three-dimensionally arrangement in the shape of neuron.

3. A meso crystal of silver oxide having nanometer scale, containing a silver peroxide, the silver oxide nanocrystal being a superstructure three-dimensionally arranged in the shape of a neuron.

4. The meso crystal of silver oxide according to claim 3 provided with properties being negatively charged in water.

5. The meso crystal of silver oxide according to claim 3 provided with properties able to be reduced to a silver nanoparticle by a laser radiation.

6. The meso crystal of silver oxide according to claim 4 provided with properties able to be reduced to a silver nanoparticle by a laser radiation.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0016] FIG. 1 is an illustrative diagram indicating the method for producing novel SERS substrate described in the Example 1, and the upper left substrate is made by MyTech Co., Ltd. and 2 kinds of the SEM image are shown in the right side.

[0017] FIG. 2 is a SEM image of recrystallized substrate obtained in case of alkali treating (sodium hypochlorite treating) the quantum crystal substrate in the presence of halogen ion (upper figure), and a graph indicating the results of EDS spectrum (elemental analysis) of the recrystallized substrate.

[0018] FIG. 3 indicates a result of the XPS measurement of the recrystallized substrate treated by alkali.

[0019] FIG. 4 indicates a result of the XPS measurement of the recrystallized substrate treated by etching.

DESCRIPTION OF EMBODIMENTS

[0020] The present invention is based on an idea that if the silver thiosulfate complex quantum crystal is treated by a sodium hypochlorite aqueous solution, a neuronal nano structure (meso structure) of the silver oxide containing silver chloride is formed by the chemical reaction mentioned below. The meso crystal structure has a negative charge in the aqueous solution, and thus the meso pores structure (fine pores having a diameter of 2-50 nanometers resulting from space between the particles) tends to efficiently absorb a protein having positive charge to form a charge-transfer complex, while a part of the silver oxide or the silver peroxide on its surface can be reducted into silver metal due to a laser irradiation, and as a result a surface plasmon enhancing effect occurs by the laser irradiation.

[0021] As described below in detail, the present inventor forms the silver complex quantum crystal by allowing the silver thiosulfate aqueous solution to agglomerate on a copper alloy using a chemical reduction method. If such silver complex is alkali treated (sodium hypochlorite treated) in the presence of halogen ion, a superstructure (meso structure) of needle-like nano crystal of silver oxide containing silver peroxide is formed with a help from formation of nucleus of silver chloride by the chemical reaction as mentioned below (FIG. 2).


Na.sub.2S.sub.2O.sub.3+4NaClO+H.sub.2O.fwdarw.Na.sub.2SO.sub.4+H.sub.2SO.sub.4+4NaCl


Ag.sup.++NaCl.fwdarw.AgCl+Na.sup.+


Ag.sup.++3NaOCl.fwdarw.2AgCl+NaClO.sub.3+2Na.sup.+


Ag.sup.++OH.sup.−.fwdarw.AgOH


2Ag.sup.++2OH.fwdarw.Ag.sub.2O+H.sub.2O

[0022] This needle-like nano crystal has a negative charge in water while a free DNA resulting from undifferentiated cell in a sample has a positive charge due to the fact that the DNA twines around a histone. Thus, the protein resulting from the undifferentiated cell has a positive charge and thus selectively be absorbed on the needle-like nano structure. In addition, the needle-like nano crystal group of silver halide or composite of silver oxide containing halogen is changed into silver metal nanoparticles by a reductive reaction due to a laser irradiation. Thus, a surface plasmon enhancing effect occurs by the laser irradiation. As a result, a chromatin peak occurs in the surface-enhanced Raman scattering (SERS) spectrum for detecting the undifferentiated cell as typified by the absorbed free DNA.

[0023] The present invention will be described by way of Examples. However, the present invention should not be construed as being limited by the Examples. Next will be specifically described the embodiments of the present invention by reference to figures below.

[0024] (Example of Manufacturing Protein Absorption Chip)

[0025] As shown in FIG. 4, 1000 ppm of silver thiosulfate aqueous solution was prepared, and one drop of the aqueous solution was put onto a phosphor-bronze plate. After 3 minutes the drop was blown away, the quantum crystals were obtained as shown in SEM image in the right side. The SEM image shows that the resulting crystal is a thin hexagonal cylinder-like crystal having 100 nm of thickness, wherein asperities of several nano order were formed on the surface. A facet characteristic of metal nano crystal was not found. First, a hexagonal quantum crystal is formed, and the crystals are growing with keeping its shape. From EDS spectrum (elemental analysis), it is found that elements originating from the silver or the complex ligand were detected.

[0026] (Consideration of Preparation of the Quantum Crystal)

[0027] It was confirmed from the SEM image (FIG. 1) that in case of 1000 ppm of silver thiosulfate complex aqueous solution, the quantum crystals were formed as crystals like hexagonal cylinder having about 100 nm of diameter, and that each of the hexagonal cylinder-like quantum crystals has asperities of several nanometer order. However, a facet characteristic of metal nano crystal was not found. In light of detection of EDS elemental analysis that the elements originating from the silver or the complex ligand were found, it is assumed that 1) the resulting quantum crystals are entirety made of the silver complex nano crystal, and 2) the asperities formed on its surface shows formation of the quantum dots from clusters due to expansion of the silver contained in the complex. In the present invention, the followings would be important for forming the quantum crystals; 1) the complex aqueous solution would be in the dilute range of 500-2000 ppm, 2) an electrode potential of supported metal would be slightly base, that is, not noble with respect to an equilibrium potential of the metal complex aqueous solution, 3) the metal complex would agglomerate by the difference in electrode potential. 1000 ppm of silver thiourea complex aqueous solution could show the same function as that of silver thiosulfate solution.

[0028] (Consideration of the Meso Crystal of Silver Oxide: No. 1)

[0029] When drops of 5% of sodium hypochlorite aqueous solution were put onto the quantum crystal substrate to treat the substrate for two minutes and subsequently the drops were removed. The crystal structure was observed as shown in FIG. 2. As seen in FIG. 2, the needle-like crystals, the rugby ball-like clusters and the large cluster were found. From analyzation by EDS spectrum (element analysis), any chlorine was not observed, and the silver and the oxygen was dominantly found in FIG. 2, although both of the needle-like crystals would be formed of the composite crystal of silver chloride and silver oxide, from the following reaction.


Na.sub.2S.sub.2O.sub.3+4NaClO+H.sub.2O.fwdarw.Na.sub.2SO.sub.4+H.sub.2SO.sub.4+4NaCl   (1)


Ag.sup.++NaCl.fwdarw.AgCl+Na.sup.+  (2)


Ag.sup.++3NaOCl.fwdarw.2AgCl+NaClO.sub.3+2Na.sup.+  (3)


Ag.sup.++OH.sup.−AgOH   (4)


2Ag.sup.++2OH.fwdarw.Ag.sub.2O+H.sub.2O tm (5)

[0030] Thus, it is thought that the meso crystal according to the present invention can be formed from the silver ion and the thiosulfate ion by an alkali oxidation reaction in the presence of chlorine ion. It is normal that the silver oxide is only formed in the normal aqueous solution. However, it is surprising that the silver peroxide is dominantly formed from the XPS measurements mentioned below.

(Consideration of the Meso Crystal of Silver Oxide: No.2)

[0031] XPS Measurements:

[0032] 25 μl of sodium hypochlorite aqueous solution was given onto the quantum crystal substrate for two minutes to form the meso crystal recrystallized on the substrate. The substrate was analyzed as to Ag and O by XPS measurement without etching (Type of used equipment: ULVAC-PHI, Inc./PH15000 VersaProbe II (scanning X-ray photoelectron spectrometer)). In comparison, Ag contained in powder of silver oxide and Ag contained in powder of silver chloride were analyzed. On the other hand, the recrystallization substrate is etched by argon gas cluster ion gun for 5 minutes and subjected to the XPS measurement as to Ag and O. The XPS measurement of FIGS. 3 and 4 were analized based on the result of the EDS of FIG. 2, wherein the peak observed at around 529 eV indicates O peak caused by the silver peroxide (AgO) and the peak observed at around 530 eV indicates O peak caused by the silver oxide (Ag.sub.2O). Although the content of oxygen decreases by etching, the O peak caused by the silver peroxide (AgO) at around 529 eV keeps larger than that of the O peak caused by the silver oxide (Ag.sub.2O) at 530 eV, which means that the silver peroxide may be formed near the substrate. We assumed that the catalyst action and the electrode potential of the substrate would cause the above phenomenon, during formation of the meso crystal. In the meanwhile, the EDS measurement with respect to the recrystallization substrate was carried out by JAPAN ELECTRON OPTICS LABORATORY CO., LTD/JSM-7001F (Electron field emission analysis electron scanning microscope) (type of used equipment).

INDUSTRIAL APPLICABILITY

[0033] According to the present invention, it is quite important that the meso crystal can be obtained in the field of the silver oxide. The larger activity of the meso crystal obviously realizes the application of the silver oxide to be expanded and increased. In addition, the performance of silver oxide can be fully improved by preventing the metal oxide nanoparticles from agglomeration and segregation, whereby limitation of the performance could be omitted away.