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    Synthesis of Rhombic Dodecahedral Fe<sub>3</sub>O<sub>4</sub> Nanocrystals with Exposed High-Energy {110} Facets and Their Peroxidase-like Activity and Lithium Storage Properties

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    Large quantities of monodispersed single-crystal rhombic dodecahedral (RD) Fe<sub>3</sub>O<sub>4</sub> nanocrystals (NCs) bounded by high-energy {110} facets were prepared by using a one-pot toluene–water two-phase interfacial reaction method. By adjusting the Fe­(acac)<sub>3</sub> concentration and the volume of hydrazine hydrate, their sizes could be controlled in the range from 60 to 100 nm. The formation of these RD Fe<sub>3</sub>O<sub>4</sub> NCs with exposed high-energy {110} surfaces might be the result of selective stabilization of such unstable facets by the C<sub>17</sub>H<sub>33</sub>­COO<sup>–</sup> based on FT-IR analysis. The magnetic measurement revealed that the saturation magnetization (<i>M</i><sub>s</sub>) of the RD Fe<sub>3</sub>O<sub>4</sub> NCs was 85 emu/g at room temperature. When used as peroxidase mimetics, the prepared RD Fe<sub>3</sub>O<sub>4</sub> NCs showed excellent peroxidase-like catalytic activity toward oxidation of the substrate 3,3′,5,5′-tetramethylbenzidine and degradation of the aniline compound methylene blue dye in the presence of H<sub>2</sub>O<sub>2</sub>. When tested as anode materials for lithium-ion batteries, these as-obtained RD Fe<sub>3</sub>O<sub>4</sub> NCs showed a high initial discharge capacity of 1147 mA h g<sup>–1</sup> at the current density of 0.2 C, a good cycle performance (362 mA h g<sup>–1</sup> at 0.2 C after 100 cycles and 191 mA h g<sup>–1</sup> at 1 C up to 130 cycles), and good rate capability at high current rates of 1–4 C
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