Issue 10, 2014

Direct conversion of multilayer molybdenum trioxide to nanorods as multifunctional electrodes in lithium-ion batteries

Abstract

In this study we prepared molybdenum trioxide (MoO3) nanorods having average lengths of 0.5–1.5 μm and widths of approximately 100–200 nm through a one-step mechanical break-down process involving favorable fracturing along the crystal direction. We controlled the dimensions of the as-prepared nanorods by applying various imposing times (15–90 min). The nanorods prepared over a reaction time of 90 min were, on average, much shorter and narrower relative to those obtained over 30 min. Evaluations of lithium-ion storage properties revealed that the electrochemical performance of these nanorods was much better than that of bulk materials. As cathodes, the nanorods could deliver a high specific capacity (>315 mA h g−1) with losses of less than 2% in the first cycle at a rate of 30 mA g−1; as anodes, the specific capacity was 800 mA h g−1 at a rate of 50 mA g−1. Relative to α-MoO3 microparticles, these nanorods displayed significantly enhanced lithium-ion storage properties with higher reversible capacities and better rate performance, presumably because their much shorter diffusion lengths and higher specific surface areas allowed more-efficient insertion/deinsertion of lithium ions during the charge/discharge process. Accordingly, enhanced physical and/or chemical properties can be obtained through appropriate nanostructuring of materials.

Graphical abstract: Direct conversion of multilayer molybdenum trioxide to nanorods as multifunctional electrodes in lithium-ion batteries

Supplementary files

Article information

Article type
Paper
Submitted
07 Feb 2014
Accepted
07 Mar 2014
First published
10 Mar 2014

Nanoscale, 2014,6, 5484-5490

Author version available

Direct conversion of multilayer molybdenum trioxide to nanorods as multifunctional electrodes in lithium-ion batteries

M. A. Ibrahem, F. Wu, D. A. Mengistie, C. Chang, L. Li and C. W. Chu, Nanoscale, 2014, 6, 5484 DOI: 10.1039/C4NR00692E

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