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硫化镉量子点的单层行为及朗缪尔-布洛杰特操控

Monolayer behavior and Langmuir-Blodgett manipulation of CdS quantum dots.

作者信息

Shen Yu-Jen, Lee Yuh-Lang, Yang Yu-Min

机构信息

Department of Chemical Engineering, National Cheng Kung University, Tainan 70101, Taiwan.

出版信息

J Phys Chem B. 2006 May 18;110(19):9556-64. doi: 10.1021/jp060416k.

Abstract

Cadmium sulfide (CdS) quantum dots (QDs) were prepared and surface modified by dodecanthiol or mercaptosuccinic acid (MSA) to render a surface with alkyl chains (C(12)-CdS) or carboxylic acid groups (MSA-CdS), respectively. Due to the hydrophobic property of C(12)-CdS, the nanoparticles disperse well in chloroform and stay stable at the air/water interface. However, 3-dimensional (3D) aggregative domains and particle-free pores were formed in the monolayer due to poor particle-water interaction. For the MSA-CdS nanoparticles, the surface was hydrophobized through physical adsorption of a cationic surfactant, cetyltrimethylammonium bromide (CTAB). The capped MSA on the CdS plays an important role in enhancing the adsorption of CTAB and improving the stability of the QDs at the air/water interface. Due to the reversible adsorption of CTAB on MSA-CdS, a hydrophilic area can be exposed in the water-contacting region of a nanoparticle when it stays at the air/water interface. Thus, the CTAB-MSA-CdS QD behaves as an amphiphilic compound at the air/water interface and has properties superior to those of C(12)-CdS QDs in fabrication of layer-by-layer 2D structure of particulate films. The distinct behaviors of the two QDs at the air/water interface and the related effect on the properties of LB films were studied using a number of methods, including pressure-area (pi-A) isotherm, relaxation and hysteresis experiments, in-situ observation of Brewster angle microscopy (BAM), the postdeposition analysis of atomic force microscopy (AFM), and UV-vis spectroscopy.

摘要

制备了硫化镉(CdS)量子点(QDs),并用十二烷硫醇或巯基琥珀酸(MSA)对其进行表面改性,分别得到具有烷基链(C(12)-CdS)或羧酸基团(MSA-CdS)的表面。由于C(12)-CdS的疏水性,纳米颗粒在氯仿中分散良好,并在空气/水界面保持稳定。然而,由于颗粒与水的相互作用较差,在单层中形成了三维(3D)聚集域和无颗粒孔隙。对于MSA-CdS纳米颗粒,通过阳离子表面活性剂十六烷基三甲基溴化铵(CTAB)的物理吸附使表面疏水化。CdS上封端的MSA在增强CTAB的吸附和提高量子点在空气/水界面的稳定性方面起着重要作用。由于CTAB在MSA-CdS上的可逆吸附,当纳米颗粒停留在空气/水界面时,在其与水接触的区域可以暴露出一个亲水区域。因此,CTAB-MSA-CdS量子点在空气/水界面表现为两亲性化合物,在制备颗粒膜的逐层二维结构方面具有优于C(12)-CdS量子点的性能。使用多种方法研究了两种量子点在空气/水界面的不同行为以及对LB膜性能的相关影响,包括压力-面积(π-A)等温线、弛豫和滞后实验、布鲁斯特角显微镜(BAM)原位观察、原子力显微镜(AFM)沉积后分析以及紫外-可见光谱。

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