journal article·2007-12-01

Single-Source Precursor to Complex Metal Oxide Monoliths with Tunable Microstructures and Properties: The Case of Mg-Containing Materials

Lu Zou, Xu Xiang, Jun Fan, Feng Li

Chemistry of Materials· Volume 19· Issue 26
Publisher page

Abstract

Synthesis of complex metal oxide monoliths (MgAl 2 O 4, MgFe 2 O 4, and In 2– x Mg x O 3 ) with macropore frameworks through a novel single-source inorganic precursor route is successfully established. The synthesis approach mainly involves the formation of two-phase composite (desired complex metal oxide and MgO phases) monoliths induced by high-temperature sintering of layered double hydroxide (LDH) precursors, followed by a selective leaching of self-generated MgO sacrificial template from the sintered two-phase composites. The materials have been characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR), thermogravimetric and differential thermal analysis (TG-DTA), scanning electron microscopy (SEM), and energy dispersive X-ray spectrometry (EDX). The results indicate that the microstructures (morphologies, particle sizes, spacing among particles, and compositions) of resultant macroporous monoliths could be finely tuned by changing precursor compositions and sintering temperatures of precursors. Further investigation shows that these as-prepared monoliths display promising surface superhydrophobicity for organically modified MgAl 2 O 4 spinels, ferromagnetism for MgFe 2 O 4 ferrites, and semiconductor optical behaviors for Mg-doped In 2 O 3 . We believe that this method has a wide scope of application for the preparation of monoliths of complex metal oxides of macroporous type from suitable layered double hydroxides as the precursors.
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Research context

OpenAlex topics: Layered Double Hydroxides Synthesis and Applications · Magnesium Oxide Properties and Applications · Mesoporous Materials and Catalysis

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, P.O. Box 98, Beijing 100029, P. R. China

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