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An all-in-one nanopore battery array 已有1人参与
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An all-in-one nanopore battery array Chanyuan Liu, Eleanor I. Gillette, Xinyi Chen, Alexander J. Pearse, Alexander C. Kozen, Marshall A. Schroeder, Keith E. Gregorczyk, Sang Bok Lee & Gary W. Rubloff AffiliationsContributionsCorresponding authors Nature Nanotechnology 9, 1031–1039 (2014) doi:10.1038/nnano.2014.247 Received 09 April 2014 Accepted 24 September 2014 Published online 10 November 2014 Article tools Citation Reprints Rights & permissions Article metrics Abstract Abstract• References• Author information• Supplementary information A single nanopore structure that embeds all components of an electrochemical storage device could bring about the ultimate miniaturization in energy storage. Self-alignment of electrodes within each nanopore may enable closer and more controlled spacing between electrodes than in state-of-art batteries. Such an ‘all-in-one’ nanopore battery array would also present an alternative to interdigitated electrode structures that employ complex three-dimensional geometries with greater spatial heterogeneity. Here, we report a battery composed of an array of nanobatteries connected in parallel, each composed of an anode, a cathode and a liquid electrolyte confined within the nanopores of anodic aluminium oxide, as an all-in-one nanosize device. Each nanoelectrode includes an outer Ru nanotube current collector and an inner nanotube of V2O5 storage material, forming a symmetric full nanopore storage cell with anode and cathode separated by an electrolyte region. The V2O5 is prelithiated at one end to serve as the anode, with pristine V2O5 at the other end serving as the cathode, forming a battery that is asymmetrically cycled between 0.2 V and 1.8 V. The capacity retention of this full cell (relative to 1 C values) is 95% at 5 C and 46% at 150 C, with a 1,000-cycle life. From a fundamental point of view, our all-in-one nanopore battery array unveils an electrochemical regime in which ion insertion and surface charge mechanisms for energy storage become indistinguishable, and offers a testbed for studying ion transport limits in dense nanostructured electrode arrays. |
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2014-12-18 15:37:47, 4.55 M
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