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一步短时间合成Ag@SiO₂核壳纳米颗粒。

A one-step short-time synthesis of Ag@SiO2 core-shell nanoparticles.

作者信息

Lismont Marjorie, Páez Carlos A, Dreesen Laurent

机构信息

GRASP-Biophotonics, Département de Physique, B5a, Université de Liège, B-4000 Liège, Belgium.

Nanomatériaux, Catalyse et Electrochimie, Département de Chimie Appliquée, Génie chimique, B6a, Université de Liège, B-4000 Liège, Belgium.

出版信息

J Colloid Interface Sci. 2015 Jun 1;447:40-9. doi: 10.1016/j.jcis.2015.01.065. Epub 2015 Feb 7.

Abstract

A performance of shell-thickness precise control in silver-silica coating core-shell nanoparticles is presented. 60nm sized citrate-stabilized silver nanoparticles are directly silica coated using a modified Stöber process. Tetraethyl orthosilicate is used as a silica precursor and ammonium hydroxide as catalyst in an alcoholic solvent to promote the seeded silica growth. By simply varying the synthesis reaction time from 4 to 60min, the silica shell thickness is increased from 5.1nm to 76.4nm. This well-controlled synthesis is then transposed to 40, 80 and 100nm sized silver cores in order to show the independence of the silica shell growth on the nanoparticle core size. Optical properties, i.e. localized surface plasmon resonance, of the produced silver-silica core-shell are also investigated.

摘要

介绍了一种在银-二氧化硅包覆核壳纳米颗粒中实现壳层厚度精确控制的方法。使用改良的施托伯法对60nm尺寸的柠檬酸盐稳定的银纳米颗粒直接进行二氧化硅包覆。在醇类溶剂中,使用正硅酸四乙酯作为二氧化硅前驱体,氢氧化铵作为催化剂,以促进二氧化硅的种子生长。通过简单地将合成反应时间从4分钟改变到60分钟,二氧化硅壳层厚度从5.1nm增加到76.4nm。然后将这种良好控制的合成方法应用于40nm、80nm和100nm尺寸的银核,以表明二氧化硅壳层生长与纳米颗粒核尺寸无关。还研究了所制备的银-二氧化硅核壳的光学性质,即局域表面等离子体共振。

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