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A manganese oxyiodide cathode for rechargeable lithium batteries

Abstract

The increasing demand for portable electronic devices is driving the development of compact lightweight batteries of high energy density1. Lithium-ion batteries tend to be the systems of choice, as they offer higher energy densities and longer operational lifetimes than other rechargeable battery systems1,2. But commercially available lithium-ion batteries make use of layered LiCoO2 cathodes3,4, and the high cost and toxicity of cobalt therefore motivate the development of cheaper and environmentally benign cathode materials. In this regard, manganese oxides are attractive alternatives, and the spinel LiMn2O4 has been investigated intensively as a cathode5,6; however, the fading on cycling of its energy-storage capacity poses problems. More recently, attention has been focused on the synthesis of layered LiMnO2 as a cathode material, but its cycling characteristics remain to be established7,8,9. Here we report the synthesis and electrochemical performance of a new manganese oxide cathode, the oxyiodide Li1.5Na0.5MnO2.85I0.12. Our material exhibits a high reversible capacity of 260 mA h g−1 in the range 1.5–4.3 V with excellent cycling characteristics. Furthermore, the amorphous nature of the material (as determined by X-ray diffraction) and smooth discharge behaviour may help to overcome the problems associated with lattice distortions that have plagued manganese oxides with more crystalline structures5,6,7,8,9

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Figure 1: X-ray powder diffraction patterns of the product obtained by reducing permanganate with LiI.
Figure 3: Charge and discharge–charge curves (8 cycles) of Li1.5Na0.5MnO2.85I0.12 recorded at a current density of 0.1 mA cm−2.
Figure 4
Figure 2: Vacuum-annealed Li1.5Na0.5MnO2.85I0.12.

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Acknowledgements

This research was supported by the National Science Foundation.

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Correspondence to Arumugam Manthiram.

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Kim, J., Manthiram, A. A manganese oxyiodide cathode for rechargeable lithium batteries. Nature 390, 265–267 (1997). https://doi.org/10.1038/36812

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