A surfactant-free route to single-crystalline CeO2 nanowires.

Chem Commun (Camb)

College of Chemistry, Chemical Engineering and Materials Science, Shandong Normal University, Jinan 250014, China.

Published: July 2005

A surfactant-free route was successfully established to synthesize CeO2 single-crystalline nanowires using H2O2 as oxidizer and template agent.

Download full-text PDF

Source
http://dx.doi.org/10.1039/b500708aDOI Listing

Publication Analysis

Top Keywords

surfactant-free route
8
route single-crystalline
4
single-crystalline ceo2
4
ceo2 nanowires
4
nanowires surfactant-free
4
route established
4
established synthesize
4
synthesize ceo2
4
ceo2 single-crystalline
4
single-crystalline nanowires
4

Similar Publications

A surfactant-free ammonia and carbamide precursor-modulated engineering of self-assembled flower-like 3D NiO nanostructures based on ordered β-Ni(OH) and turbostratic Ni(OH)(NO) nanoplate-structured intermediates is reported. By employing complementary structural and spectroscopic techniques, fundamental insights into structural and chemical transformations from intermediates to NiO nanoparticles (NPs) are provided. FTIR, Raman and DSC analyses show that the transformation of intermediates to NiO NPs involves subsequent loss of NO and OH species through a double-step phase transformation at 306 and 326 °C corresponding to the loss of free interlayer ions and HO species, respectively, followed by the loss of chemically bonded OH and NO ions.

View Article and Find Full Text PDF
Article Synopsis
  • This study demonstrates the creation of submicron metal nanocapsules through spontaneous emulsification of organometallic precursors, utilizing water, solvent, and metal precursor ratios to produce either stable or metastable emulsions.
  • The research focused on transition metals like Au, Pd, and Pt, which formed nanoparticle shells in different morphologies depending on the emulsions used, particularly highlighting a unique Au-Pd structure within a continuous metal shell.
  • The resulting water-stable, surfactant-free nanocapsules were evaluated as catalysts, showing promising activity in hydrolyzing ammonia-borane, thus paving the way for using gold colloids in hydrogen release applications.
View Article and Find Full Text PDF

Generally, inorganic nano/microparticles produced by chemical routes are covered by organic surfactants or polymers to control their agglomeration during their synthesis. However, these surfactants and polymers negatively affect their catalytic activity because these molecules mask the surface. This work presents the synthesis of surfactant-free CuInS and CuInSe (sf-CuInS2 and sf-CuInSe2) nano/microparticles through simple reactions without surfactant or polymer coatings using LiBH under a thermodynamically favourable condition.

View Article and Find Full Text PDF

In this study, we report the synthesis of PbS particles having dimensions in the quantum-dot regime (13.17 to 26.91 nm) using a cyclohexane:isopropanol:dimethyl-sulfoxide surfactant-free microemulsion (CID-SFME) scheme without a capping agent.

View Article and Find Full Text PDF

Alternative routes of surfactant application - An update.

Semin Fetal Neonatal Med

December 2023

Menzies Institute for Medical Research, University of Tasmania, Hobart, Australia; Department of Paediatrics, Royal Hobart Hospital, Hobart, Australia.

Non-invasive modes of respiratory support have been shown to be the preferable way of primary respiratory support of preterm infants with respiratory distress syndrome (RDS). The avoidance of invasive mechanical ventilation can be beneficial for preterm infants in reduction of morbidity and even mortality. However, it is well-established that some infants managed with non-invasive respiratory support from the outset have symptomatic RDS to a degree that warrants surfactant administration.

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!