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Low temperature synthesis and formation mechanism of carbon encapsulated nanocrystals by electrophilic oxidation of ferrocene
Affiliation:1. Museo Nacional de Ciencias Naturales-CSIC, C/ José Gutiérrez Abascal 2, 28006 Madrid, Spain;2. University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom;3. Statens Naturhistoriske Museum, Øster Voldgade 5-7, 1350 København K, Denmark;4. Rue Girardet 68, 2400 Le Locle, Switzerland;5. University of Bristol, Queen''s Road, Bristol BS8 1RJ, United Kingdom;1. Universidad de la República, Facultad de Ciencias, Laboratorio de Electroquímica Fundamental, Núcleo Interdisciplinario Ingeniería Electroquímica, Igua 4225, CP 11400 Montevideo, Uruguay;2. Universidad de la República, Crystallography, Solid State and Materials Laboratory (Cryssmat-Lab), DETEMA, Centro NanoMat, Polo Tecnológico de Pando, Espacio Interdisciplinario, Facultad de Química, Montevideo, Uruguay
Abstract:A novel method is developed for low temperature synthesis of carbon encapsulated spherical Fe7S8, equiaxed Fe3O4 and spherical porous FeOOH nanocrystals with a core–shell structure via a solid–solid reaction of ferrocene with (NH4)2S2O8, (NH4)2Cr2O7 and NH4ClO4 in an autoclave, respectively. Samples were characterized by X-ray diffraction, scanning electron microscopy and transmission electron microscopy. It is found that the median size of Fe7S8, Fe3O4 and FeOOH nanocrystals is about 28.99, 52.68 and 25.66 nm, respectively. The hollow worm-like carbon shell provides exclusive rooms for tens to hundreds of nanocrystals separated from each other. The cooperative effect of ammonium and strong oxidizing ion on electrophilic oxidation of ferrocene contributes to the in situ formation of carbon shell on the nanocrystals. The metal–π interaction of iron atom with cyclopentadienone oligomers enables ordered self-assembling of carbon rings, resulting in the formation of graphitizable carbon shell with roughly parallel fringes at low temperature.
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