Analytical separation of Au/Ag core/shell nanoparticles by capillary electrophoresis.

J Chromatogr A

Department of Applied Chemistry, National University of Kaohsiung, No. 700, Kaohsiung University Rd., Nan Tzu District, Kaohsiung 811, Taiwan, ROC.

Published: November 2006

This paper demonstrates that capillary electrophoresis (CE) can be employed for characterizing the sizes of a series of Au/Ag core/shell nanoparticles (NPs). We effected the CE separation of Au/Ag core/shell NPs using a mixed buffer of sodium dodecyl sulphate (SDS) (40 mM) and 3-(cyclohexylamino)propanesulfonic acid (10 mM) at pH 9.7 and an applied voltage of 20 kV. A linear relationship (R(2)>0.99) existed between the electrophoretic mobilities and the sizes of the Au/Ag core/shell NPs within the diameter range from 25 to 90 nm; the relative standard deviations of these electrophoretic mobilities were <0.9%. From the good correlation between the results obtained by CE and those provided by scanning electron microscopy, we confirmed that this CE method is a valid one for characterizing the sizes of Au/Ag core/shell NP samples. In addition, when the Au/Ag core/shell NPs were separated through CE and detected using an on-line photodiode array detector, this approach allowed the chemical characterization of the NP species. This CE approach should allow the rapid and cost-effective characterization of a number of future nanomaterials.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.chroma.2006.08.033DOI Listing

Publication Analysis

Top Keywords

au/ag core/shell
16
separation au/ag
8
core/shell nanoparticles
8
capillary electrophoresis
8
core/shell nps
8
electrophoretic mobilities
8
analytical separation
4
au/ag
4
core/shell
4
nanoparticles capillary
4

Similar Publications

Gatifloxacin (GAT), an antibiotic belonging to the fluoroquinolone (FQ) class, is a toxicant that may contaminate food products. In this study, a method of ultrasensitive immunochromatographic detection of GAT was developed for the first time. An indirect format of the lateral flow immunoassay (LFIA) was performed.

View Article and Find Full Text PDF

In contrast to homogeneous enzyme catalysis, nanozymes are nanosized heterogeneous catalysts that perform reactions on a rigid surface. This fundamental difference between enzymes and nanozymes is often overlooked in kinetic studies and practical applications. In this article, using 14 nanozymes of various compositions (core@shell, metal-organic frameworks, metal, and metal oxide nanoparticles), we systematically demonstrate that nontypical features of nanozymes, such as multiple catalytic activities, chemical transformations, and aggregation, need to be considered in nanozyme catalysis.

View Article and Find Full Text PDF

Tandem neural networks for inverse design can only make single predictions, which limits the diversity of predicted structures. Here, we use conditional variational autoencoder (cVAE) for the inverse design of core-shell nanoparticles. cVAE is a type of generative neural network that generates multiple valid solutions for the same input condition.

View Article and Find Full Text PDF
Article Synopsis
  • - Atomically precise metal nanoclusters (NCs) are interesting for their unique structures and catalytic potential, but they have issues like instability and self-aggregation.
  • - This research presents a method to stabilize metal NCs by anchoring them to a metal oxide matrix, creating a hollow core-shell structure through thermal treatment.
  • - The resulting metal NPs@metal oxide heterostructures show improved catalytic activity and stability for reducing aromatic nitro compounds, suggesting a new approach to utilize the instability of metal NCs in catalysis.
View Article and Find Full Text PDF

We reported the gold/silver core-shell nanoparticles (Au@Ag NPs) functionalized with β-cyclodextrin (β-CD) as versatile nano-agents demonstrated for human urine-based biosensing of cysteamine and catalytic conversion from nitrobenzene (NB) to aniline. First, the hybrid bimetallic nanoparticles, i.e.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!