Please use this identifier to cite or link to this item: http://dx.doi.org/10.14279/depositonce-6273
Main Title: Time-resolved in situ studies on the formation mechanism of iron oxide nanoparticles using combined fast-XANES and SAXS
Author(s): Kabelitz, Anke
Guilherme, Ana
Joester, Maike
Reinholz, Uwe
Radtke, Martin
Bienert, Ralf
Schulz, Katrin
Schmack, Roman
Krähnert, Ralph
Emmerling, Franziska
Type: Article
Language Code: en
Abstract: The reaction of iron chlorides with an alkaline reagent is one of the most prominent methods for the synthesis of iron oxide nanoparticles. We studied the particle formation mechanism using triethanolamine as reactant and stabilizing agent. In situ fast-X-ray absorption near edge spectroscopy and small-angle X-ray scattering provide information on the oxidation state and the structural information at the same time. In situ data were complemented by ex situ transmission electron microscopy, wide-angle X-ray scattering and Raman analysis of the formed nanoparticles. The formation of maghemite nanoparticles (gamma-Fe2O3) from ferric and ferrous chloride was investigated. Prior to the formation of these nanoparticles, the formation and conversion of intermediate phases (akaganeite, iron(II, III) hydroxides) was observed which undergoes a morphological and structural collapse. The thus formed small magnetite nanoparticles (Fe3O4) grow further and convert to maghemite with increasing reaction time.
URI: https://depositonce.tu-berlin.de//handle/11303/6934
http://dx.doi.org/10.14279/depositonce-6273
Issue Date: 2015
Date Available: 25-Oct-2017
DDC Class: 540 Chemie und zugeordnete Wissenschaften
Creative Commons License: https://creativecommons.org/licenses/by/3.0/
Journal Title: CrystEngComm
Publisher: Royal Society of Chemistry
Publisher Place: Cambridge
Volume: 17
Issue: 44
Publisher DOI: 10.1039/c5ce01585e
Page Start: 8463
Page End: 8470
ISSN: 1466-8033
Appears in Collections:Fachgebiet Technische Chemie » Publications

Files in This Item:
File SizeFormat 
c5ce01585e.pdf3.26 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons