Issue 17, 2013

Li0.3V2O5 with high lithium diffusion rate: a promising anode material for aqueous lithium-ion batteries with superior rate performance

Abstract

Compared with non-aqueous lithium-ion batteries, aqueous lithium-ion batteries (ALIBs) have been widely regarded as a strategy to resolve the safety problems and reduce the manufacturing cost of lithium ion batteries. But the major challenge in ALIBs is the low capacity, especially at high current densities, due to the lack of suitable anode materials with high utilization efficiency of the theoretical capacity and fast lithium ion diffusion. Based on the calculation of Li+ diffusion coefficient (DLi+), Li0.3V2O5 is therefore first chosen as a novel anode material for ALIBs because of its rigid 3D tunnelled crystal structure with good electronic and ionic conductivity. When coupled with LiCoO2, its first discharge capacity is 182 mA h g−1 at a current density of 60 mA g−1 and remains at 112 mA h g−1 at a current density up to 180 mA g−1. These results are enabled by the facile ion diffusion and charge transfer during the process of charge–discharge at high rate, which is demonstrated sufficiently via the lithium insertion/extraction mechanisms investigated here for the first time. The feasibility of this material in ALIBs will offer guidelines for the future design of new materials with optimum intrinsic properties and beneficial structural elements to realize improvements in performances at high rate.

Graphical abstract: Li0.3V2O5 with high lithium diffusion rate: a promising anode material for aqueous lithium-ion batteries with superior rate performance

Supplementary files

Article information

Article type
Paper
Submitted
18 Dec 2012
Accepted
04 Mar 2013
First published
04 Mar 2013

J. Mater. Chem. A, 2013,1, 5423-5429

Li0.3V2O5 with high lithium diffusion rate: a promising anode material for aqueous lithium-ion batteries with superior rate performance

J. Bao, M. Zhou, Y. Zeng, L. Bai, X. Zhang, K. Xu and Y. Xie, J. Mater. Chem. A, 2013, 1, 5423 DOI: 10.1039/C3TA01548C

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