JP2008106315A - Metal nanoparticle and production method therefor - Google Patents
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- JP2008106315A JP2008106315A JP2006290971A JP2006290971A JP2008106315A JP 2008106315 A JP2008106315 A JP 2008106315A JP 2006290971 A JP2006290971 A JP 2006290971A JP 2006290971 A JP2006290971 A JP 2006290971A JP 2008106315 A JP2008106315 A JP 2008106315A
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- 239000010931 gold Substances 0.000 claims abstract description 36
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- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 claims description 10
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- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 6
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- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims description 3
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- 229920001223 polyethylene glycol Polymers 0.000 claims description 3
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- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 claims description 3
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- HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 3
- 229940038773 trisodium citrate Drugs 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
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- AVTYONGGKAJVTE-OLXYHTOASA-L potassium L-tartrate Chemical compound [K+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O AVTYONGGKAJVTE-OLXYHTOASA-L 0.000 description 1
- 239000001508 potassium citrate Substances 0.000 description 1
- 229960002635 potassium citrate Drugs 0.000 description 1
- QEEAPRPFLLJWCF-UHFFFAOYSA-K potassium citrate (anhydrous) Chemical compound [K+].[K+].[K+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O QEEAPRPFLLJWCF-UHFFFAOYSA-K 0.000 description 1
- 235000011082 potassium citrates Nutrition 0.000 description 1
- LJCNRYVRMXRIQR-OLXYHTOASA-L potassium sodium L-tartrate Chemical compound [Na+].[K+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O LJCNRYVRMXRIQR-OLXYHTOASA-L 0.000 description 1
- 239000001472 potassium tartrate Substances 0.000 description 1
- 229940111695 potassium tartrate Drugs 0.000 description 1
- 235000011005 potassium tartrates Nutrition 0.000 description 1
- YPSNMKHPDJVGEX-UHFFFAOYSA-L potassium;sodium;3-carboxy-3-hydroxypentanedioate Chemical compound [Na+].[K+].OC(=O)CC(O)(C([O-])=O)CC([O-])=O YPSNMKHPDJVGEX-UHFFFAOYSA-L 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
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- 229940100890 silver compound Drugs 0.000 description 1
- 150000003379 silver compounds Chemical class 0.000 description 1
- HELHAJAZNSDZJO-OLXYHTOASA-L sodium L-tartrate Chemical compound [Na+].[Na+].[O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O HELHAJAZNSDZJO-OLXYHTOASA-L 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 239000001476 sodium potassium tartrate Substances 0.000 description 1
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Landscapes
- Manufacture Of Metal Powder And Suspensions Thereof (AREA)
- Powder Metallurgy (AREA)
Abstract
Description
本発明は、粒子の吸光スペクトルがシャープで局在プラズモン共鳴（ＬＰＲ）センサに好適に利用可能な金属ナノ粒子及びその製造方法に関するものであり、更に詳しくは、上記ＬＰＲセンサの金属ナノ粒子として好適な粒子特性を有する、金、銀、又はそれらを含むナノ粒子及びその製造方法に関するものである。本発明は、例えば、バイオセンシングに対する応用として、透過電子顕微鏡のための生体染色剤、また、金又は銀ナノ粒子の色の特徴を用いたイムノクロマトグラフィーによるバイオセンサー、更に、微細な回路パターンを形成するための配線形成用材料や車の塗料としても好適に利用することが可能な、粒子の吸光スペクトルがシャープで分散性の良好な金属ナノ粒子及びその製造方法を提供するものである。 The present invention relates to a metal nanoparticle that has a sharp absorption spectrum of particles and can be suitably used for a localized plasmon resonance (LPR) sensor, and a method for producing the metal nanoparticle, and more specifically, suitable as a metal nanoparticle of the LPR sensor. The present invention relates to gold, silver, or nanoparticles containing the same, and a method for producing the same. The present invention is applied to biosensing, for example, a biological stain for a transmission electron microscope, a biosensor by immunochromatography using the color characteristics of gold or silver nanoparticles, and a fine circuit pattern. The present invention provides a metal nanoparticle having a sharp absorption spectrum and good dispersibility, and a method for producing the same, which can be suitably used as a wiring forming material and a vehicle paint.
局在プラズモン共鳴（ＬＰＲ）センサは、金属ナノ粒子を固定した基板に光を照射し、金属ナノ粒子を透過した光の吸光度を測定することにより、金属ナノ粒子近傍の媒質の変化を検出するものである。このＬＰＲセンサに利用される金属ナノ粒子としては、可視光においてＬＰＲ吸収を示す金ナノ粒子及び銀ナノ粒子が主に用いられている。このセンサにおいては、金ナノ粒子又は銀ナノ粒子表面に、有機薄膜を介するか又は直接的に、抗体が固定されている。固定された抗体と被検物中の抗原とが選択的に結合することにより、金属ナノ粒子近傍の媒質の屈折率変化が生じるため、プラズモン共鳴条件が変化する。これを、吸収スペクトルの変化、屈折率の変化などを測定することにより検出する。 A localized plasmon resonance (LPR) sensor detects changes in the medium near a metal nanoparticle by irradiating the substrate on which the metal nanoparticle is fixed with light and measuring the absorbance of the light transmitted through the metal nanoparticle. It is. As the metal nanoparticles used in this LPR sensor, gold nanoparticles and silver nanoparticles that exhibit LPR absorption in visible light are mainly used. In this sensor, an antibody is immobilized on the gold nanoparticle or silver nanoparticle surface via an organic thin film or directly. The selective binding of the immobilized antibody and the antigen in the test substance causes a change in the refractive index of the medium in the vicinity of the metal nanoparticles, so that the plasmon resonance condition changes. This is detected by measuring a change in absorption spectrum, a change in refractive index, and the like.
これまでに、金属ナノ粒子を合成する種々の技術が報告されている。先行技術として、例えば、液相で、ポリオール法（非特許文献１）、電気化学法（非特許文献２）、界面活性剤を利用する方法（非特許文献３）、レーザーを用いる方法（非特許文献４）等を利用して、金属ナノ粒子を合成する方法が提案されている。金属ナノ粒子をバイオセンサーに利用するためには、精密な吸光特性の検出が必要であり、そのために、いろいろな観点から、吸光特性の良好な金属ナノ粒子を合成するための金属ナノ粒子の合成過程の研究がなされている。 So far, various techniques for synthesizing metal nanoparticles have been reported. Prior arts include, for example, a polyol method (Non-Patent Document 1), an electrochemical method (Non-Patent Document 2), a method using a surfactant (Non-Patent Document 3), and a method using a laser (Non-Patent Document 1). A method of synthesizing metal nanoparticles using literature 4) has been proposed. In order to use metal nanoparticles for biosensors, it is necessary to precisely detect the light absorption characteristics. For this reason, synthesis of metal nanoparticles to synthesize metal nanoparticles with good light absorption characteristics from various viewpoints. Processes are being studied.
例えば、簡便な手法で、Ａｇナノ粒子を合成したり（特許文献１）、貴金属化合物と界面活性剤とから貴金属コロイド粒子を製造したり（特許文献２）、アスペクト比の再現性の良い金ナノロッドを作製したり（特許文献３）、マイクロ流路を用いて、粒度分布がシャープで、結晶性の高い高結晶性ナノ銀粒子スラリーを作製したり（特許文献４）、界面活性剤を含む溶液中で電気化学的反応によってロッド状の金属ナノロッドを作製したり（特許文献５）、超音波撹拌により有機無機ハイブリッドナノ複合材を作製すること（特許文献６）、等が行われている。 For example, Ag nano particles can be synthesized by a simple method (Patent Document 1), noble metal colloidal particles can be produced from a noble metal compound and a surfactant (Patent Document 2), or gold nanorods with good aspect ratio reproducibility. (Patent Document 3), or using a micro-channel, a highly crystalline nano silver particle slurry having a sharp particle size distribution and high crystallinity (Patent Document 4), or a solution containing a surfactant In particular, rod-shaped metal nanorods are produced by electrochemical reaction (Patent Document 5), and organic-inorganic hybrid nanocomposites are produced by ultrasonic stirring (Patent Document 6).
また、溶液中において超音波付与を行うと、急激な撹拌効果や気泡の圧縮・膨張によるキャビテーションによってソノケミカル反応が生じ、微粒子の還元反応、結晶の核生成、粒成長などに影響を与えることが知られている（非特許文献５）。また、超音波は、生成した微粒子と保護剤との結合状態の促進、それによる粒子間の結合の緩和にも効果を発揮すると考えられる。そのため、先行技術として、例えば、超音波を利用して、金の前駆体を還元させて金のナノ粒子を作製したり（特許文献７）、超音波照射により、粒子表面に金属ナノ粒子を析出させて複合粒子を作製したり（特許文献８）、超音波振動を加えることにより準安定金属酸化物よりなるナノ複合構造体を製造すること（特許文献９）、等が報告されている。 In addition, when ultrasonic waves are applied in a solution, a sonochemical reaction occurs due to a rapid stirring effect or cavitation due to bubble compression / expansion, which may affect fine particle reduction reaction, crystal nucleation, and grain growth. It is known (Non-Patent Document 5). In addition, it is considered that ultrasonic waves are effective in promoting the bonding state between the generated fine particles and the protective agent and thereby relaxing the bonding between the particles. Therefore, as a prior art, for example, using gold, the gold precursor is reduced to produce gold nanoparticles (Patent Document 7), or metal nanoparticles are deposited on the particle surface by ultrasonic irradiation. It is reported that a composite particle is produced (Patent Document 8), or that a nanocomposite structure made of a metastable metal oxide is produced by applying ultrasonic vibration (Patent Document 9).
上記特許文献６では、ナノ複合材の製造過程で、超音波を使用しているが、超音波は、無機粒子の分散液を超音波撹拌に付し、その少なくとも一つの一次元長が０．１〜２５０ｎｍの平均サイズを有するナノサイズ化させた無機粒子の分散液を生成するために使用されている。また、上記特許文献７では、分散用の液相に対して、水和物としての金の前駆体と分散助剤との混合物を添加し、その後、超音波照射により、液相内に金の前駆体を微小に分散させること、更に、金の前駆体を還元させて金のナノ粒子を生成すること、が行われている。 In the above-mentioned Patent Document 6, ultrasonic waves are used in the manufacturing process of the nanocomposite. However, the ultrasonic waves are obtained by subjecting a dispersion of inorganic particles to ultrasonic agitation, and at least one one-dimensional length of which is 0.00. It has been used to produce a dispersion of nanosized inorganic particles having an average size of 1-250 nm. Further, in Patent Document 7, a mixture of a gold precursor as a hydrate and a dispersion aid is added to a liquid phase for dispersion, and then, by irradiation with ultrasonic waves, Finely dispersing the precursor and further reducing the gold precursor to produce gold nanoparticles.
また、上記特許文献８では、基粒子及び金属前駆体が混在する溶媒に超音波を照射することにより、基粒子の表面に、金属前駆体が還元した金属であるナノメートルオーダの金属微粒子を析出させること、が行われている。更に、上記特許文献９では、準安定金属酸化物粒子を溶媒中に混合せしめた混合液に対して、超音波振動を加えることにより、粒子凝集体を作製することが行われている。 Moreover, in the said patent document 8, the metal particle of the nanometer order which is the metal which the metal precursor reduced is deposited on the surface of a base particle by irradiating the ultrasonic wave to the solvent in which a base particle and a metal precursor are mixed. To make it happen. Furthermore, in the said patent document 9, producing a particle aggregate by applying ultrasonic vibration with respect to the liquid mixture which mixed the metastable metal oxide particle in the solvent.
しかし、上述の方法では、超音波照射は、粒子の機械的な分散、金属前駆体の還元、粒子凝集体の形成等を目的として使用されているが、これまで、超音波を利用してナノ粒子の吸光スペクトルをシャープに改質させること、及びそれにより吸光スペクトルをシャープに改質させたナノ粒子に関する事項については知られていない。 However, in the above-described method, ultrasonic irradiation is used for the purpose of mechanical dispersion of particles, reduction of metal precursors, formation of particle aggregates, and the like. Nothing is known about sharply modifying the absorption spectrum of the particles and about the nanoparticles that have thus sharply modified the absorption spectrum.
このような状況の中で、本発明者らは、上記従来技術に鑑みて、金属粒子の粒径や形状及び連結などの粉体特性を精密に制御することは、ＬＰＲセンサの実用化に向けて必要であるとの見地から、金属粒子の粒径や形状及び連結などの粉体特性を精密に制御することにより、それらの粉体特性を改善して粒子の吸光スペクトルをシャープに改質させた金属ナノ粒子を製造する方法を開発することを目標として鋭意研究を積み重ねた結果、金属ナノ粒子の合成過程において、反応液に超音波を照射することにより所期の目的を達成できることを見出し、本発明を完成するに至った。本発明は、バイオセンサー等の各種センサとしての使用が可能な、より精度の良いＬＰＲ吸収を示すＬＰＲセンサ用金属ナノ粒子を製造できる新しい金属ナノ粒子の製造方法及びその金属ナノ粒子を提供することを目的とするものである。 Under such circumstances, in view of the above prior art, the present inventors precisely controlled the powder characteristics such as the particle size, shape and connection of the metal particles for the practical application of the LPR sensor. From the point of view of necessity, the powder characteristics such as the particle size, shape and connection of the metal particles are precisely controlled to improve the powder characteristics and sharply modify the absorption spectrum of the particles. As a result of intensive research aimed at developing a method for producing metal nanoparticles, it was found that the intended purpose can be achieved by irradiating the reaction solution with ultrasonic waves in the synthesis process of metal nanoparticles, The present invention has been completed. The present invention provides a novel method for producing metal nanoparticles capable of producing metal nanoparticles for LPR sensors that can be used as various sensors such as biosensors and exhibit LPR absorption with higher accuracy, and the metal nanoparticles. It is intended.
上記課題を解決するための本発明は、以下の技術的手段から構成される。
（１）粒子の吸光スペクトルをシャープに改質させた金、銀、又はそれらを含むナノ粒子からなる局在プラズモン共鳴（ＬＰＲ）センサ用ナノ粒子であって、１）粒子の粒径が５〜１００ｎｍで、２）一辺が略４０ｎｍ程度の三角形の粒子を含み、３）光子相関法による測定で頂点４０ｎｍ付近にシャープな粒度分布を有する、ことを特徴とするＬＰＲセンサ用ナノ粒子。
（２）粒子の吸光スペクトルをシャープに改質させた金、銀、又はそれらを含むナノ粒子を製造する方法であって、１）還元水溶液中に金属塩を溶解した反応液を作製した後、該反応液に超音波を照射することによりナノ粒子を生成させる、２）それにより、ａ）粒子の粒径が５〜１００ｎｍで、ｂ）一辺が略４０ｎｍ程度の三角形の粒子を含み、ｃ）光子相関法による測定で頂点４０ｎｍ付近にシャープな粒度分布を有する、金、銀、又はそれらを含むナノ粒子を作製する、ことを特徴とするナノ粒子の製造方法。
（３）前記（１）又は（２）記載の粒子の吸光スペクトルをシャープに改質させた金、銀、又はそれらを含むナノ粒子を含有することを特徴とするナノ粒子含有スラリー、塗料又は塗膜。
（４）前記（１）又は（２）記載の粒子の吸光スペクトルをシャープに改質させた金、銀、又はそれらを含むナノ粒子を基板に固定した構造を有することを特徴とする局在プラズモン共鳴（ＬＰＲ）センサ。
（５）金属塩として、塩化金酸又は硝酸銀を用いる、前記（２）記載の方法。
（６）還元水溶液が、還元剤として、過酸化水素、テトラヒドロほう酸ナトリウム、蟻酸、又はアスコルビン酸を含む、前記（２）記載の方法。
（７）反応液が、分散剤として、ポリビニルピロリドン、ポリビニルアルコール、ポリエチレングリコール、ポリアクリル酸、ドデシル硫酸ナトリウム及びヘキサメタリン酸ナトリウムからなる群より選択される少なくとも１種を含む、前記（２）記載の方法。
（８）反応液に、金属イオンの錯化剤として、クエン酸塩を加える、前記（２）記載の方法。
（９）反応液に、２０−５０ｋＨｚの低周波数の超音波を照射する、前記（２）記載の方法。
（１０）上記超音波照射を間欠的に行う、前記（９）記載の方法。
The present invention for solving the above-described problems comprises the following technical means.
(1) A nanoparticle for a localized plasmon resonance (LPR) sensor composed of gold, silver, or a nanoparticle containing the same having a sharply modified absorption spectrum of the particle, and 1) the particle size is 5 to 5 A nanoparticle for an LPR sensor, which is 100 nm, 2) includes triangular particles having a side of about 40 nm, and 3) has a sharp particle size distribution near a vertex of 40 nm as measured by a photon correlation method.
(2) A method for producing gold, silver, or nanoparticles containing them with sharply modified absorption spectra of particles, 1) after preparing a reaction solution in which a metal salt is dissolved in a reducing aqueous solution, The reaction liquid is irradiated with ultrasonic waves to generate nanoparticles, 2) thereby including a) a triangular particle having a particle diameter of 5 to 100 nm and b) a side of about 40 nm, and c) A method for producing nanoparticles, comprising producing gold, silver, or nanoparticles containing them having a sharp particle size distribution in the vicinity of a vertex of 40 nm as measured by a photon correlation method.
(3) A nanoparticle-containing slurry, paint or coating, characterized by containing gold, silver, or nanoparticles containing them, wherein the absorption spectrum of the particles according to (1) or (2) is sharply modified film.
(4) Localized plasmon characterized by having a structure in which gold, silver, or nanoparticles containing them, in which the absorption spectrum of the particle according to (1) or (2) is sharply modified, are fixed to a substrate Resonance (LPR) sensor.
(5) The method according to (2) above, wherein chloroauric acid or silver nitrate is used as the metal salt.
(6) The method according to (2) above, wherein the reducing aqueous solution contains hydrogen peroxide, sodium tetrahydroborate, formic acid, or ascorbic acid as a reducing agent.
(7) The reaction solution according to (2), wherein the reaction solution contains at least one selected from the group consisting of polyvinyl pyrrolidone, polyvinyl alcohol, polyethylene glycol, polyacrylic acid, sodium dodecyl sulfate, and sodium hexametaphosphate as a dispersant. Method.
(8) The method according to (2) above, wherein citrate is added as a complexing agent for metal ions to the reaction solution.
(9) The method according to (2) above, wherein the reaction liquid is irradiated with ultrasonic waves having a low frequency of 20-50 kHz.
(10) The method according to (9), wherein the ultrasonic irradiation is intermittently performed.
次に、本発明について更に詳細に説明する。
本発明は、粒子の吸光スペクトルをシャープに改質させた金、銀、又はそれらを含むナノ粒子からなる局在プラズモン共鳴（ＬＰＲ）センサ用ナノ粒子であって、粒子の粒径が５〜１００ｎｍで、一辺が略４０ｎｍ程度の平板状の三角形の粒子を含み、光子相関法による測定で頂点４０ｎｍ付近にシャープな粒度分布を有する、ことを特徴とするものである。
Next, the present invention will be described in more detail.
The present invention relates to a nanoparticle for a localized plasmon resonance (LPR) sensor comprising gold, silver, or a nanoparticle containing the same having a sharply modified absorption spectrum of the particle, and the particle size of the particle is 5 to 100 nm. Thus, it includes flat triangular particles having a side of about 40 nm, and has a sharp particle size distribution in the vicinity of the apex of 40 nm as measured by the photon correlation method.
また、本発明は、粒子の吸光スペクトルをシャープに改質させた金、銀、又はそれらを含むナノ粒子を製造する方法であって、還元水溶液中に金属塩を溶解した反応液を作製した後、該反応液に超音波を照射することによりナノ粒子を生成させ、それにより、上述の特定の粉体特性を有するナノ粒子を作製すること、を特徴とするものである。 In addition, the present invention is a method for producing gold, silver, or nanoparticles containing them, in which the absorption spectrum of particles is sharply modified, and after preparing a reaction solution in which a metal salt is dissolved in a reducing aqueous solution The reaction liquid is irradiated with ultrasonic waves to generate nanoparticles, thereby producing nanoparticles having the specific powder characteristics described above.
すなわち、本発明は、金属ナノ粒子の合成過程において、反応液に強力超音波を照射することにより、粒子の吸光特性を改質し、粒子の吸光スペクトルをシャープに改質させたナノ粒子を合成するものであり、その粒子が、金、銀、又はそれらを含むナノ粒子であることを特徴とする吸光スペクトルをシャープに改質させたナノ粒子の製造方法及びそのナノ粒子を提供するものである。 That is, the present invention synthesizes nanoparticles with a sharply modified absorption spectrum by irradiating the reaction solution with intense ultrasonic waves during the synthesis process of metal nanoparticles. The present invention provides a method for producing nanoparticles having sharply modified absorption spectrum, characterized in that the particles are gold, silver, or nanoparticles containing them, and the nanoparticles. .
本発明において、「粒子の吸光スペクトルをシャープに改質させた」とは、従来材と比較して、１）粒子の単分散性を向上させることにより粒子の吸光スペクトルがシャープになること、及び／又は、２）粒子の粒度分布又は形状を揃えることにより吸光スペクトルがシャープになること、を意味する。一般に、粒子が凝集することによって吸光スペクトルが広がる傾向になるが、粒子間の相互作用（粒子間距離等）により、粒子の吸光スペクトルが異なる（文献：M. Gluodenis et al., J. Phys. Chem. B, 106, 9484 （2002）)。 In the present invention, “the absorption spectrum of the particles is sharply modified” means that, compared with the conventional material, 1) the absorption spectrum of the particles becomes sharp by improving the monodispersity of the particles, and 2) Means that the absorption spectrum becomes sharper by aligning the particle size distribution or shape of the particles. In general, agglomeration of particles tends to broaden the absorption spectrum, but the absorption spectrum of particles varies depending on the interaction between particles (interparticle distance, etc.) (Reference: M. Gluodenis et al., J. Phys. Chem. B, 106, 9484 (2002)).
そのため、粒子は、粒子の凝集状態によって、それぞれ固有の吸光スペクトルを持つようになり、積算して表現される粒子の溶液の吸光スペクトルでは、粒子の凝集が多いと、吸光スペクトルが広くなる。また、本発明において、粒子の粒度分布により吸光スペクトルがシャープになる理由は、粒子の溶液に超音波を照射することにより、過飽和度が上がり、核が一度に生成し、後から生成する核生成を無視できるようになり、結果として、粒度分布が狭くなり、また、溶液の均一性も増加するため、形状も一定のものに近づくためである。 Therefore, each particle has a specific absorption spectrum depending on the aggregation state of the particle. In the absorption spectrum of the solution of particles expressed by integration, the absorption spectrum becomes wider when the particle aggregation is large. In the present invention, the reason why the absorption spectrum becomes sharper due to the particle size distribution of the particles is that, by irradiating the particle solution with ultrasonic waves, the degree of supersaturation increases, nuclei are generated at once, and nucleation generated later As a result, the particle size distribution becomes narrow and the uniformity of the solution also increases, so that the shape approaches a constant one.
次に、本発明について、具体例に則して詳細に説明する。本発明の金、銀及びそれらを含むナノ粒子の合成方法は、例えば、０．０５から５ｍｍｏｌ／ｌの濃度範囲のナノ粒子の原料となる金属塩と、ナノ粒子の保護剤となる、例えば、ポリビニルピロリドン（ＰＶＰ―Ｋ９０）を、０．００１から１ｍｍｏｌ／ｌの濃度範囲で蒸留水に加え、１時間撹拌することにより溶解させる。更に、金属イオンの錯化剤であるクエン酸塩を０．５から１０ｍｍｏｌ／ｌを加えて、３０分撹拌する。これらの合成過程において、上記合成条件は、例示的に示したものであり、これらは、必要に応じて、適宜変更することができる。 Next, the present invention will be described in detail based on specific examples. The method for synthesizing gold, silver and nanoparticles containing them according to the present invention includes, for example, a metal salt that is a raw material for nanoparticles in a concentration range of 0.05 to 5 mmol / l, and a protective agent for the nanoparticles. Polyvinylpyrrolidone (PVP-K90) is added to distilled water in a concentration range of 0.001 to 1 mmol / l and dissolved by stirring for 1 hour. Further, 0.5 to 10 mmol / l of citrate which is a metal ion complexing agent is added and stirred for 30 minutes. In these synthesis processes, the above synthesis conditions are exemplarily shown, and these can be appropriately changed as necessary.
この溶液を１０から６０℃に設定した水槽内にある反応容器に添加し、強力超音波による照射を行う。本発明における超音波の効果とは、気液界面が振動により不安定化すること、超音波による液相内での極めて大きな加速度運動（１×１０４−６Ｇ：Ｇは重力加速度）を受け、更には、超音波キャビテーションにより生じる衝撃波や、マイクロジェットにより離散すること等の作用（文献：特開２００６−２１３５３６号公報）により、激しい撹拌効果が生じる。この撹拌効果により、溶液の均一性及び核の生成の活性化、結晶性の向上、更に、生成した粒子表面上への保護剤の結合促進などが生起し、粒子の吸光特性が改質されると考えられる。また、この吸光特性は、粒子の凝集性にも影響され、また、粒子表面での保護剤の立体障壁性の向上、粒子の分散性にも影響される。 This solution is added to a reaction vessel in a water tank set at 10 to 60 ° C., and irradiation with high intensity ultrasonic waves is performed. The effect of ultrasonic waves in the present invention is that the gas-liquid interface is destabilized by vibration and receives extremely large acceleration motion (1 × 10 4-6 G: G is gravitational acceleration) in the liquid phase by ultrasonic waves. Furthermore, a vigorous agitation effect is produced by actions such as shock waves generated by ultrasonic cavitation and discrete action by microjets (reference: Japanese Patent Application Laid-Open No. 2006-213536). This agitation effect causes the uniformity of the solution and the activation of nucleation, the improvement of crystallinity, and the promotion of the binding of the protective agent to the surface of the generated particles, thereby modifying the light absorption characteristics of the particles. it is conceivable that. The light absorption characteristics are also affected by the cohesiveness of the particles, and also by the improvement of the steric barrier property of the protective agent on the particle surface and the dispersibility of the particles.
撹拌効果のような物理的作用による上述の粒子の吸光特性は、低い周波数の超音波において顕著であり、本発明では、２０−５０ｋＨｚ程度の低い周波数の超音波が好適に用いられる。更に、超音波キャビテーションなどにより生成した気泡の合体によって生成される大きな気泡を抑制するために、間欠的に照射することが望ましい。その間隔は、５から１０秒稼働、１から５秒停止が望ましい。超音波照射中に、還元剤である０．０２から２ｗｔ％濃度範囲の過酸化水素、０．１から５ｍｍｏｌ／ｌのテトラヒドロほう酸ナトリウムを添加し、金属ナノ粒子を生成させる。本発明は、窒素ガスやアルゴンガス、更に、水素ガスを反応容器中に流すことにより還元が促進される。 The above-mentioned light absorption characteristics of the particles due to physical action such as the stirring effect are remarkable in low frequency ultrasonic waves. In the present invention, low frequency ultrasonic waves of about 20-50 kHz are preferably used. Further, it is desirable to irradiate intermittently in order to suppress large bubbles generated by coalescence of bubbles generated by ultrasonic cavitation or the like. The interval is preferably 5 to 10 seconds of operation and 1 to 5 seconds of stoppage. During the ultrasonic irradiation, hydrogen peroxide in a concentration range of 0.02 to 2 wt% and 0.1 to 5 mmol / l sodium tetrahydroborate as a reducing agent are added to form metal nanoparticles. In the present invention, the reduction is promoted by flowing nitrogen gas, argon gas, or hydrogen gas into the reaction vessel.
本発明で用いられる金属ナノ粒子の金属としては、可視光領域で局在プラズモン共鳴（ＬＰＲ）を起こす金属が好ましい。具体的には、金、銀等の貴金属が挙げられる。その金及び銀の化合物としては、金の場合には塩化金酸、銀の場合には硝酸銀を用いることが望ましい。生成される金属微粒子の粒径は、５〜１００ｎｍが好ましい。 The metal of the metal nanoparticle used in the present invention is preferably a metal that causes localized plasmon resonance (LPR) in the visible light region. Specific examples include noble metals such as gold and silver. As the gold and silver compounds, it is desirable to use chloroauric acid in the case of gold and silver nitrate in the case of silver. The particle size of the generated metal fine particles is preferably 5 to 100 nm.
分散剤としては、ポリビニルピロリドン、ポリビニルアルコール、ポリエチレングリコール、ポリアクリル酸、ドデシル硫酸ナトリウム及びヘキサメタリン酸ナトリウムからなる群より選択される少なくとも１種を含むことが好ましい。還元剤としては、過酸化水素、テトラヒドロほう酸ナトリウム、蟻酸、アスコルビン酸を用いることが望ましい。また、金属イオンの錯化剤としては、好適には、例えば、クエン酸ナトリウム、クエン酸カリウム、クエン酸ナトリウムカリウム、酒石酸ナトリウム、酒石酸カリウム、酒石酸ナトリウムカリウム等を用いることができる。 The dispersant preferably contains at least one selected from the group consisting of polyvinyl pyrrolidone, polyvinyl alcohol, polyethylene glycol, polyacrylic acid, sodium dodecyl sulfate and sodium hexametaphosphate. As the reducing agent, it is desirable to use hydrogen peroxide, sodium tetrahydroborate, formic acid, or ascorbic acid. As the metal ion complexing agent, for example, sodium citrate, potassium citrate, sodium potassium citrate, sodium tartrate, potassium tartrate, sodium potassium tartrate and the like can be preferably used.
本発明の方法によって合成される粒子の吸光スペクトルをシャープに改質させた金属ナノ粒子は、合成過程で超音波照射しない場合と比較して、１）粒子の粒径が５〜１００ｎｍであり、２）一辺が略４０ｎｍ程度の平板状で三角形の粒子を含み、３）光子相関法による測定で頂点４０ｎｍ付近にシャープな粒度分布を有し、４）粒子の吸光スペクトルがシャープに改質されている、という特性を有している。 Compared to the case where the absorption spectrum of the particles synthesized by the method of the present invention is sharply modified, the metal nanoparticles are 1) the particle diameter is 5 to 100 nm, compared with the case where no ultrasonic irradiation is performed in the synthesis process. 2) Includes flat and triangular particles with a side of approximately 40 nm, 3) has a sharp particle size distribution near the apex of 40 nm as measured by the photon correlation method, and 4) sharply modifies the absorption spectrum of the particles. It has the characteristic of being.
後記する実施例に示されるように、作製した銀ナノ粒子の溶液を石英板上に塗布し、乾燥させた試料のＸ線回析から、ピークは小さいが、３８度に銀の立方晶系を示す（１１１）面のピークが見られる。また、紫外可視分光スペクトルでは、例えば、５２４から５７５ｎｍ付近に頂点があり、３３３から３３６ｎｍ付近に粒子が平板状である特徴のピークが見られる。また、透過電子顕微鏡写真による観察では、一辺が略４０ｎｍ程度の三角形の粒子で平板の側面を持つ粒子が見られる。 As shown in the examples described later, the solution of the prepared silver nanoparticles was applied on a quartz plate, and from the X-ray diffraction of the dried sample, the peak was small, but a silver cubic system was formed at 38 degrees. The peak of the (111) plane shown is seen. Further, in the ultraviolet-visible spectrum, for example, a peak having a peak in the vicinity of 524 to 575 nm and a tabular particle in the vicinity of 333 to 336 nm is seen. Further, in observation with a transmission electron micrograph, a triangular particle having a side of about 40 nm and a plate having a flat side surface can be seen.
また、作製した金ナノ粒子の紫外可視分光スペクトルでは、５２０ｎｍ付近に頂点を有しており、その頂点の強度は、合成過程で超音波照射した方が超音波照射しないものより大きい。本発明では、金属ナノ粒子の合成過程において、反応液に強力超音波を照射することにより、金属粒子の粒径や形状及び連結などの粉体特性を精密に制御することで、粒子の吸光スペクトルがシャープに改質されたナノ粒子を合成することが可能となる。本発明の金属ナノ粒子は、通常の方法で作製した金属ナノ粒子と比べて、より精度の良いＬＰＲ吸収を示すナノ粒子として、局在プラズモン共鳴（ＬＰＲ）センサ等に適用可能なナノ粒子として有用である。 Further, the ultraviolet-visible spectroscopic spectrum of the produced gold nanoparticles has a vertex near 520 nm, and the strength of the vertex is higher when the ultrasonic irradiation is performed during the synthesis process than when the ultrasonic irradiation is not performed. In the present invention, in the process of synthesizing the metal nanoparticles, by irradiating the reaction solution with high-intensity ultrasonic waves, it is possible to precisely control the powder properties such as the particle size, shape, and connection of the metal particles, and thereby the absorption spectrum of the particles. It becomes possible to synthesize nanoparticles that have been sharply modified. The metal nanoparticles of the present invention are useful as nanoparticles that can be applied to localized plasmon resonance (LPR) sensors, etc., as nanoparticles exhibiting more accurate LPR absorption than metal nanoparticles prepared by a normal method. It is.
本発明では、上記粒子の吸光スペクトルをシャープに改質させた金、銀、又はそれらを含むナノ粒子を含有する当該ナノ粒子含有スラリー、塗料又は塗膜が提供される。本発明は、上記ナノ粒子以外の成分については、特に制限されるものではなく、適宜のスラリー、塗料又は塗膜に適用される。本発明において、粒子の吸光スペクトルをシャープに改質させたとは、例えば、図２、５に例示される紫外可視分光スペクトルのスペクトル曲線の頂点が合成過程で超音波照射しない従来法で作製したナノ粒子と比べて、吸光スペクトルがシャープに改質されたことを意味する。 In this invention, the said nanoparticle containing slurry, coating material, or coating film containing the gold | metal | money which changed the absorption spectrum of the said particle sharply, silver, or the nanoparticle containing them is provided. In the present invention, the components other than the above-mentioned nanoparticles are not particularly limited, and can be applied to an appropriate slurry, paint or coating film. In the present invention, the sharp modification of the absorption spectrum of the particles means, for example, a nano-particle produced by a conventional method in which the vertex of the spectrum curve of the UV-visible spectrum illustrated in FIGS. It means that the absorption spectrum is sharply modified compared to the particles.
本発明により、次のような効果が奏される。
（１）本発明により、金属ナノ粒子の粒径や形状及び連結などの粉体特性を精密に制御して粒子の吸光スペクトルをシャープに改質させたナノ粒子を製造し、提供することができる。
（２）本発明のナノ粒子を用いることにより、局在プラズモン共鳴（ＬＰＲ）センサの実用化を実現することができるＬＰＲセンサ用ナノ粒子を提供することができる。
（３）合成過程で超音波照射していない従来法で作製したナノ粒子と比較して、粒子の吸光スペクトルをシャープに改質させた金属ナノ粒子を製造し、提供することができる。
（４）上記粒子の吸光スペクトルをシャープに改質させた金、銀、又はそれらを含むナノ粒子を含むスラリー、塗料又は塗膜を提供できる。
The present invention has the following effects.
(1) According to the present invention, it is possible to manufacture and provide nanoparticles in which the powder properties such as the particle size, shape and connection of metal nanoparticles are precisely controlled to sharply modify the absorption spectrum of the particles. .
(2) By using the nanoparticles of the present invention, it is possible to provide nanoparticles for an LPR sensor that can realize the practical application of a localized plasmon resonance (LPR) sensor.
(3) Compared with nanoparticles prepared by a conventional method that is not irradiated with ultrasonic waves in the synthesis process, metal nanoparticles having sharply modified absorption spectra of the particles can be produced and provided.
(4) It is possible to provide a slurry, a paint, or a coating film containing gold, silver, or nanoparticles containing them, in which the absorption spectrum of the particles is sharply modified.
次に、本発明を実施例に基づいて具体的に説明するが、本発明は、以下の実施例に限定されるものではない。 EXAMPLES Next, although this invention is demonstrated concretely based on an Example, this invention is not limited to a following example.
０．１ｍｍｏｌ／ｌの硝酸銀、０．０８７５ｍｍｏｌ／ｌのポリビニルピロリドン（ＰＶＰ−Ｋ９０）を５０ｍｌの蒸留水に加え、１時間撹拌することにより、これらを溶解させた。これに、更に、３０ｍｍｏｌ／ｌのクエン酸三ナトリウムを３ｍｌ加えて、更に、３０分撹拌した。この溶液５０ｍｌを２５℃に設定した水槽内にある反応容器に添加し、大気中、２０ｋＨｚ４５０Ｗ中５０％出力、９秒ＯＮ、３秒ＯＦＦのパルス照射、総稼働時間が１５分の超音波照射条件にて、還元剤として、３０ｗｔ％の０．１２ｍｌ過酸化水素、１００ｍｍｏｌ／ｌのテトラヒドロほう酸ナトリウムを０．４ｍｌ添加し、銀ナノ粒子を生成させた。 These were dissolved by adding 0.1 mmol / l silver nitrate and 0.0875 mmol / l polyvinylpyrrolidone (PVP-K90) to 50 ml distilled water and stirring for 1 hour. To this was further added 3 ml of 30 mmol / l trisodium citrate, and the mixture was further stirred for 30 minutes. 50 ml of this solution is added to a reaction vessel in a water tank set at 25 ° C., 50% output in air, 20 kHz, 450 W, 9 seconds ON, 3 seconds OFF pulse irradiation, total operating time 15 minutes ultrasonic irradiation conditions As a reducing agent, 0.4 ml of 30 wt% 0.12 ml hydrogen peroxide and 100 mmol / l sodium tetrahydroborate was added to form silver nanoparticles.
作製した銀ナノ粒子を含む溶液は、青色を呈しており、１ヶ月を経過しても安定な状態であった。図１に、作製したナノ粒子の溶液を、石英板上に塗布し、乾燥させた試料のＸ線回折を示す。ピークは小さいが、３８度に銀の立方晶系を示す（１１１）面のピークが見られる。図２に、作製した銀ナノ粒子の紫外可視分光スペクトルを示す。５７５ｎｍに頂点があり、３３３ｎｍに粒子が平板状である特徴のピークが見られる。更に、図３に、作製した銀ナノ粒子の透過電子顕微鏡写真を示す。一辺が略４０ｎｍ程度の三角形の粒子が見られ、一部、長方形に見られるものがあるが、これは、平板の側面から見た像であると考えられる。 The produced solution containing silver nanoparticles was blue and was stable even after one month. FIG. 1 shows X-ray diffraction of a sample obtained by applying the prepared nanoparticle solution on a quartz plate and drying the solution. Although the peak is small, a peak on the (111) plane showing a silver cubic system at 38 degrees can be seen. FIG. 2 shows an ultraviolet-visible spectrum of the produced silver nanoparticles. There is a peak at 575 nm and a characteristic feature that the particles are tabular at 333 nm. Furthermore, the transmission electron micrograph of the produced silver nanoparticle is shown in FIG. Triangular particles with a side of about 40 nm are seen, and some of them are seen as rectangles. This is considered to be an image seen from the side of the flat plate.
また、合成過程で超音波を照射しないで作製した試料の場合には、６６０ｎｍに吸収のピークが存在し、溶液は青緑を呈していた。更に、光子相関法により測定した上記銀ナノ粒子の粒度分布の結果を図４に示す。なお、溶液の粘度を、音叉型振動式粘度計（ＳＶ−１０、Ａ＆Ｄ社製）により測定した。その結果、溶液の粘度は２０ｍＰａｓであった。ここでは、粒子が平板状をしているため、粒度分布の標準偏差又は標準偏差を平均値で除した変動係数で比較することはできないが、頂点４０ｎｍ付近の分布を比較すると、明らかに合成過程で超音波照射をした場合の粒子の分布の方がシャープな粒度分布をしていた。 In the case of a sample prepared without irradiating ultrasonic waves during the synthesis process, an absorption peak was present at 660 nm, and the solution was blue-green. Furthermore, the result of the particle size distribution of the silver nanoparticles measured by the photon correlation method is shown in FIG. The viscosity of the solution was measured with a tuning fork type vibration viscometer (SV-10, manufactured by A & D). As a result, the viscosity of the solution was 20 mPas. Here, since the grains are flat, it is impossible to compare the standard deviation of the particle size distribution or the coefficient of variation obtained by dividing the standard deviation by the average value. In the case of ultrasonic irradiation, the particle distribution was sharper.
０．１ｍｍｏｌ／ｌの硝酸銀、０．３５ｍｍｏｌ／ｌのポリビニルピロリドン（ＰＶＰ−Ｋ９０）を５０ｍｌの蒸留水に加え、１時間撹拌することにより、これらを溶解させた。これに、更に、３０ｍｍｏｌ／ｌのクエン酸三ナトリウムを３ｍｌ加えて、更に、３０分間撹拌した。この溶液５０ｍｌを２５℃に設定した水槽内にある反応容器に添加し、大気中、２０ｋＨｚ４５０Ｗ中５０％出力、９秒ＯＮ、３秒ＯＦＦのパルス照射、総稼働時間が１５分の超音波照射条件にて、還元剤として、３０ｗｔ％の０．１２ｍｌ過酸化水素、１００ｍｍｏｌ／ｌのテトラヒドロほう酸ナトリウムを０．４ｍｌ添加し、銀ナノ粒子を生成させた。 These were dissolved by adding 0.1 mmol / l silver nitrate and 0.35 mmol / l polyvinylpyrrolidone (PVP-K90) to 50 ml distilled water and stirring for 1 hour. To this was further added 3 ml of 30 mmol / l trisodium citrate, and the mixture was further stirred for 30 minutes. 50 ml of this solution is added to a reaction vessel in a water tank set at 25 ° C., 50% output in air, 20 kHz, 450 W, 9 seconds ON, 3 seconds OFF pulse irradiation, total operating time 15 minutes ultrasonic irradiation conditions As a reducing agent, 0.4 ml of 30 wt% 0.12 ml hydrogen peroxide and 100 mmol / l sodium tetrahydroborate was added to form silver nanoparticles.
作製した銀ナノ粒子を含む溶液は、紫色を呈しており、１ヶ月を経過しても安定な状態であった。図５に、作製したナノ粒子の紫外可視分光スペクトルを示す。５２４ｎｍに頂点があり、３３６ｎｍに粒子が平板状である特徴のピークが見られる。更に、図６に、作製したナノ粒子の透過電子顕微鏡写真を示す。合成過程で超音波照射して作製した粒子の場合には、それぞれの粒子が分散して存在しているように見えた。一辺が略４０ｎｍ程度の三角形の粒子が見られ、それぞれ分離している。更に、合成過程で超音波照射しないで作製した粒子の場合には、４９０ｎｍに吸収のピークが存在し、なだらかなピークとなった。更に、光子相関法により測定した３０日後の上記銀ナノ粒子の粒度分布の結果を図７に示す。合成過程で超音波照射しないで作製した粒子の方は、凝集のためか粒度分布がＴＥＭ観察による粒子径より大きな値となっていた。 The produced solution containing silver nanoparticles had a purple color and was stable even after one month. FIG. 5 shows an ultraviolet-visible spectrum of the produced nanoparticles. A peak having a peak at 524 nm and a tabular grain shape at 336 nm is observed. Furthermore, the transmission electron micrograph of the produced nanoparticles is shown in FIG. In the case of particles produced by ultrasonic irradiation during the synthesis process, each particle appeared to be dispersed. Triangular particles with a side of approximately 40 nm are seen and separated. Further, in the case of particles produced without irradiating ultrasonic waves during the synthesis process, an absorption peak was present at 490 nm, which was a gentle peak. Furthermore, the result of the particle size distribution of the silver nanoparticles after 30 days measured by the photon correlation method is shown in FIG. Particles produced without sonication during the synthesis process had a particle size distribution larger than the particle diameter obtained by TEM observation because of aggregation.
０．１ｍｍｏｌ／ｌの塩化金酸、０．３５ｍｍｏｌ／ｌのポリビニルピロリドン（ＰＶＰ−Ｋ９０）を５０ｍｌの蒸留水に加え、１時間撹拌することにより、これらを溶解させた。この溶液５０ｍｌを２５℃に設定した水槽内にある反応容器に添加し、大気中、２０ｋＨｚ４５０Ｗ中５０％出力、９秒ＯＮ、３秒ＯＦＦのパルス照射、総稼働時間が１５分の超音波照射条件にて、金属イオンの錯化剤として、３０ｍｍｏｌ／ｌのクエン酸三ナトリウムを３ｍｌ加えて、また、還元剤として、３０ｗｔ％の０．１２ｍｌ過酸化水素、１００ｍｍｏｌ／ｌのテトラヒドロほう酸ナトリウムを０．４ｍｌ添加し、金ナノ粒子を生成させた。図８に、作製した金ナノ粒子の紫外可視分光スペクトルを示す。合成過程で超音波照射して作製した粒子の場合には５２０ｎｍに、超音波照射しないで作製した粒子の場合には５１０ｎｍに頂点があった。その頂点の強度は、超音波照射して作製した粒子の方が大きかった。 These were dissolved by adding 0.1 mmol / l chloroauric acid and 0.35 mmol / l polyvinylpyrrolidone (PVP-K90) to 50 ml of distilled water and stirring for 1 hour. 50 ml of this solution is added to a reaction vessel in a water tank set at 25 ° C., 50% output in air, 20 kHz, 450 W, 9 seconds ON, 3 seconds OFF pulse irradiation, total operating time 15 minutes ultrasonic irradiation conditions 3 ml of 30 mmol / l trisodium citrate was added as a metal ion complexing agent, and 0.12 ml of 30 wt% 0.12 ml hydrogen peroxide and 100 mmol / l sodium tetrahydroborate were added as a reducing agent in an amount of 0. 4 ml was added to produce gold nanoparticles. FIG. 8 shows an ultraviolet-visible spectrum of the produced gold nanoparticles. In the case of particles produced by ultrasonic irradiation in the synthesis process, the vertex was at 520 nm, and in the case of particles produced without ultrasonic irradiation, the vertex was at 510 nm. The intensity of the vertex was higher for particles produced by ultrasonic irradiation.
以上詳述したように、本発明は、金属ナノ粒子及びその製造方法に係るものであり、本発明により、金属ナノ粒子の粒径や形状及び連結などの粉体特性を精密に制御して粒子の吸光スペクトルをシャープに改質させたナノ粒子を製造し、提供することができる。また、本発明のナノ粒子を用いることにより、局在プラズモン共鳴（ＬＰＲ）センサの実用化を実現することができるＬＰＲセンサ用ナノ粒子を提供することができる。また、合成過程で超音波照射していない従来法で作製したナノ粒子と比較して、粒子の吸光スペクトルをシャープに改質させた金属ナノ粒子を製造し、提供することができる。更に、上記粒子の吸光スペクトルをシャープに改質させた金、銀、又はそれらを含むナノ粒子を含むスラリー、塗料又は塗膜を提供できる。
本発明は、合成過程で超音波照射を適用しない従来法で作製した従来材のナノ粒子と比較して、粒子の吸光スペクトルをシャープに改質させた金、銀、又はそれらを含む５〜１００ｎｍのナノ粒子を製造し、提供することを可能とする新しい技術を提供するものとして有用である。
As described above in detail, the present invention relates to metal nanoparticles and a method for producing the same, and according to the present invention, the particle characteristics, shape, and connection properties of the metal nanoparticles are precisely controlled. Nanoparticles having a sharply modified absorption spectrum can be produced and provided. In addition, by using the nanoparticle of the present invention, it is possible to provide a nanoparticle for an LPR sensor capable of realizing practical use of a localized plasmon resonance (LPR) sensor. Moreover, compared with the nanoparticle produced by the conventional method which is not irradiated with an ultrasonic wave in the synthesis process, the metal nanoparticle which sharply modified the absorption spectrum of the particle can be produced and provided. Furthermore, the slurry, coating material, or coating film containing gold | metal | money which changed the absorption spectrum of the said particle | grain sharply, silver, or the nanoparticle containing them can be provided.
The present invention is gold, silver having a sharply modified absorption spectrum of particles, or 5 to 100 nm containing them, compared to conventional nanoparticles prepared by a conventional method in which ultrasonic irradiation is not applied in the synthesis process. It is useful as a new technology that makes it possible to produce and provide nano-particles.
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| JP2005290478A (en) * | 2004-03-31 | 2005-10-20 | Tamura Kaken Co Ltd | Method for producing nano-particle of gold |
| JP2006176869A (en) * | 2004-12-21 | 2006-07-06 | Lambda Vision Inc | Particulate aggregate and method for producing the same |
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| JP2005290478A (en) * | 2004-03-31 | 2005-10-20 | Tamura Kaken Co Ltd | Method for producing nano-particle of gold |
| JP2006176869A (en) * | 2004-12-21 | 2006-07-06 | Lambda Vision Inc | Particulate aggregate and method for producing the same |
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