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Preparation of Stable Silver Nanoparticles Having Wide Red-To-Near-Infrared Extinction.具有宽红光至近红外消光特性的稳定银纳米颗粒的制备。
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本文引用的文献

1
Plasmon-induced spatial electron transfer between single Au nanorods and ALD-coated TiO2: dependence on TiO2 thickness.
Chem Commun (Camb). 2015 Oct 1;51(76):14373-6. doi: 10.1039/c5cc05898h. Epub 2015 Aug 13.
2
Dense Deposition of Gold Nanoclusters Utilizing a Porphyrin/Inorganic Layered Material Complex as the Template.
Langmuir. 2015 Aug 25;31(33):9142-7. doi: 10.1021/acs.langmuir.5b02254. Epub 2015 Aug 12.
3
Titanium oxide nanosheets: graphene analogues with versatile functionalities.二氧化钛纳米片:具有多种功能的石墨烯类似物。
Chem Rev. 2014 Oct 8;114(19):9455-86. doi: 10.1021/cr400627u. Epub 2014 Apr 22.
4
Au/TiO2 superstructure-based plasmonic photocatalysts exhibiting efficient charge separation and unprecedented activity.基于 Au/TiO2 超结构的等离子体光催化剂表现出高效的电荷分离和前所未有的活性。
J Am Chem Soc. 2014 Jan 8;136(1):458-65. doi: 10.1021/ja410994f. Epub 2013 Dec 17.
5
Gold nanorods and their plasmonic properties.金纳米棒及其等离子体特性。
Chem Soc Rev. 2013 Apr 7;42(7):2679-724. doi: 10.1039/c2cs35367a.
6
Size and structure matter: enhanced CO2 photoreduction efficiency by size-resolved ultrafine Pt nanoparticles on TiO2 single crystals.尺寸和结构很重要:通过在 TiO2 单晶体上进行尺寸分辨的超细微 Pt 纳米颗粒来提高 CO2 光还原效率。
J Am Chem Soc. 2012 Jul 11;134(27):11276-81. doi: 10.1021/ja304075b. Epub 2012 Jun 28.
7
Plasmonic-metal nanostructures for efficient conversion of solar to chemical energy.用于高效将太阳能转化为化学能的等离子体金属纳米结构。
Nat Mater. 2011 Nov 23;10(12):911-21. doi: 10.1038/nmat3151.
8
Photoinduced electron transfer between the anionic porphyrins and viologens in titania nanosheets and monodisperse mesoporous silica hybrid films.TiO2 纳米片中卟啉阴离子和聚甲亚胺阳离子间的光诱导电子转移及单分散介孔硅杂化薄膜。
ACS Appl Mater Interfaces. 2011 Apr;3(4):931-5. doi: 10.1021/am101281n. Epub 2011 Mar 21.
9
Controlling the synthesis and assembly of silver nanostructures for plasmonic applications.用于等离子体应用的银纳米结构的合成与组装控制。
Chem Rev. 2011 Jun 8;111(6):3669-712. doi: 10.1021/cr100275d. Epub 2011 Mar 11.
10
Influence of excitation wavelength (UV or visible light) on the photocatalytic activity of titania containing gold nanoparticles for the generation of hydrogen or oxygen from water.激发波长(紫外光或可见光)对含金纳米粒子的二氧化钛光催化水分解生成氢气或氧气活性的影响。
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在层状钛酸盐透明薄膜的层间空间原位合成无聚集的金纳米颗粒。

In Situ Synthesis of Gold Nanoparticles without Aggregation in the Interlayer Space of Layered Titanate Transparent Films.

作者信息

Sasaki Kazuhisa, Matsubara Kazuki, Kawamura Shiori, Saito Kenji, Yagi Masayuki, Yui Tatsuto

机构信息

Department of Material Science and Technology, Faculty of Engineering, Niigata University.

Department of Material Science and Technology, Faculty of Engineering, Niigata University;

出版信息

J Vis Exp. 2017 Jan 17(119):55169. doi: 10.3791/55169.

DOI:10.3791/55169
PMID:28117791
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5352274/
Abstract

Combinations of metal oxide semiconductors and gold nanoparticles (AuNPs) have been investigated as new types of materials. The in situ synthesis of AuNPs within the interlayer space of semiconducting layered titania nanosheet (TNS) films was investigated here. Two types of intermediate films (i.e., TNS films containing methyl viologen (TNS/MV) and 2-ammoniumethanethiol (TNS/2-AET)) were prepared. The two intermediate films were soaked in an aqueous tetrachloroauric(III) acid (HAuCl4) solution, whereby considerable amounts of Au(III) species were accommodated within the interlayer spaces of the TNS films. The two types of obtained films were then soaked in an aqueous sodium tetrahydroborate (NaBH4) solution, whereupon the color of the films immediately changed from colorless to purple, suggesting the formation of AuNPs within the TNS interlayer. When only TNS/MV was used as the intermediate film, the color of the film gradually changed from metallic purple to dusty purple within 30 min, suggesting that aggregation of AuNPs had occurred. In contrast, this color change was suppressed by using the TNS/2-AET intermediate film, and the AuNPs were stabilized for over 4 months, as evidenced by the characteristic extinction (absorption and scattering) band from the AuNPs.

摘要

金属氧化物半导体与金纳米颗粒(AuNPs)的组合已作为新型材料进行了研究。本文研究了在半导体层状二氧化钛纳米片(TNS)薄膜的层间空间中原位合成AuNPs。制备了两种类型的中间膜(即含有甲基紫精的TNS膜(TNS/MV)和2-氨基乙硫醇的TNS膜(TNS/2-AET))。将这两种中间膜浸泡在四氯金(III)酸(HAuCl4)水溶液中,从而使大量的Au(III)物种容纳在TNS膜的层间空间内。然后将得到的两种类型的膜浸泡在硼氢化钠(NaBH4)水溶液中,随即膜的颜色立即从无色变为紫色,这表明在TNS层间形成了AuNPs。当仅使用TNS/MV作为中间膜时,膜的颜色在30分钟内从金属紫色逐渐变为灰紫色,这表明发生了AuNPs的聚集。相比之下,使用TNS/2-AET中间膜可抑制这种颜色变化,并且AuNPs稳定了4个多月,这由AuNPs的特征消光(吸收和散射)带证明。