The decomposition of iron(III) acetylacetonate in high-boiling polyols such as diethylene glycole is an efficient way to produce water-soluble iron oxide nanoparticles (IONPs) with small sizes. We present an extension of this method by introducing ethylene diamine (EDA) or diethylene triamine (DTA) as a structure-directing agent and adding polyvinylpyrrolidone (PVP) as a stabilizing agent. The synthesis was studied with respect to effects of the chain length of the polyol used as solvent, the chain length of the structure-directing agent, the presence of PVP, the heating rate, and the nature of the precursor. By varying these parameters, we were able to show, that probably an interplay of the structure-directing agent and the polyol plays an important role for the stabilization and growth of the different facets of the IONP crystal. The chain length of the polyol used as solvent alters the influence of EDA or DTA as stabilizer of {111} facets, leading to IONPs with spherical, tetrahedral, or nanoplate morphology and mean diameters ranging from 4 nm up to 25 nm. PVP in the reaction medium narrows down particle size and shape distributions and promotes the formation of very stable, water-based colloidal solutions. The saturation magnetization of the particles was determined by a superconducting quantum interference device (SQUID) and their ability to act as a T2-contrast agent was tested by magnetic resonance imaging (MRI).
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http://dx.doi.org/10.1016/j.jcis.2013.11.023 | DOI Listing |
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January 2025
School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, China.
A key issue in photoelectrochemical applications is the modification of the behavior of photogenerated charge barriers. An effective strategy to improve the photoelectrochemical performance of semiconductor materials is to use the facet effect to promote spatial charge separation. In this work, three different morphologies of lead chromate (PbCrO) crystals are prepared by a simple hydrothermal method that used ammonium fluoride as the structure-directing agents.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
State Key Lab of New Ceramics and Fine Processing, School of Materials Science and Engineering, Tsinghua University, Beijing 100084, PR China.
Supported noble metal catalysts have a high catalytic activity and selectivity. However, fast surface reconstruction and sintering of noble metal particles during a high-temperature reaction process pose a major challenge to the stability of the catalysts. In this study, sinter-resistant supported noble metal catalysts were prepared by constructing an oxide nanotrap.
View Article and Find Full Text PDFJ Biomater Appl
January 2025
Biomedical Engineering Graduate Program, Toronto Metropolitan University, Toronto, ON, Canada.
This study explores mesoporous bioactive glasses (MBGs) that show promise as advanced therapeutic delivery platforms owing to their tailorable porous properties enabling enhanced drug loading capacity and biomimetic chemistry for localized, sustained release. This work systematically investigates the complex relationship between MBG composition and surfactant templating on structural evolution, bioactive response, resultant drug loading efficiency and release. A total of 12 samples of sol-gel-derived MBG were synthesized using cationic and non-ionic structure-directing agents (cetyltrimethylammonium bromide, Pluronic F127 and P123) while modulating the SiO/CaO content, generating MBG with surface areas of 60-695 m/g.
View Article and Find Full Text PDFMaterials (Basel)
December 2024
Institute of Nuclear Physics Polish Academy of Sciences, 31-342 Krakow, Poland.
The resistivity of the silica SBA-15 type can be significantly improved by forming a thin layer of carbon on the pore surface. This is possible through the carbonization reaction of a surfactant used as a structure-directing agent in the synthesis of mesostructured silica materials. The synthesis of this type of silica-carbon composite (SBA-C) is based on the use of sulfuric acid to create a carbon layer from surfactant molecules encapsulated in silica mesopores.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Nanomaterials Laboratory, Department of Polymers and Functional Materials, CSIR-Indian Institute of Chemical Technology, Uppal Road, Tarnaka, Hyderabad 500 007, India.
Herein, porous SnO microspheres in a three-dimensional (3D) hierarchical architecture were successfully synthesized via a facile hydrothermal route utilizing d-(+)-glucose and cetyltrimethylammonium bromide (CTAB), which act as reducing and structure-directing agents, respectively. Controlled adjustment of the CTAB to glucose mole ratio, reaction temperature, reaction time, and the calcination parameters all provided important clues toward optimizing the final morphologies of SnO with exceptional structural stability and reasonable monodispersity. Electron microscopy analysis revealed that microspheres formed were hierarchical self-assemblies of numerous primary SnO nanoparticles of ∼3-8 nm that coalesce together to form nearly monodispersed and ordered spherical structures of sizes in the range of 230-250 nm and are appreciably porous.
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