Optimization of Na-Ion Battery Systems Based on Polyanionic or Layered Positive Electrodes and Carbon Anodes

被引:79
作者
Dugas, R. [1 ,2 ]
Zhang, B. [1 ,2 ]
Rozier, P. [2 ,3 ,4 ]
Tarascon, J. M. [1 ,2 ,3 ]
机构
[1] Coll France, FRE 3677, Chim Solide Energie, F-75231 Paris 05, France
[2] FR CNRS 3459, Reseau Stockage Electrochem Energie RS2E, F-80039 Amiens, France
[3] ALISTORE European Res Inst, F-80039 Amiens, France
[4] Univ Toulouse 3, CIRIMAT CNRS UMR 5085, F-31062 Toulouse 09, France
基金
欧盟地平线“2020”;
关键词
CAPACITY; CATHODE;
D O I
10.1149/2.0051605jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
070208 [无线电物理];
摘要
The revival of the Na-ion battery concept has prompted intense research activities toward new Na-based insertion compounds and their implementation in full Na-ion cells. Herein, we report the optimization of full Na-ion cells consisting of either a layered oxide Na-x(Fe1/2Mn1/2)O-2 or a polyanionic Na3V2(PO4)(2)F-3 cathode associated with a hard carbon anode. From charge/discharge curves collected via 2 or 3-electrode measurements, the charge/discharge profiles of full cells are simulated to evaluate the maximum energy density these two systems can deliver. Similar energies of 235 W h kg(-1) are found for both systems provided that a fully sodiated Na-1(Fe1/2Mn1/2)O-2 layered phase is used. Experimental cells confirm these values, and cells based on polyanionic compounds surpass the layered cathodes in terms of energy retention, average voltage and rate capabilities. By using Na sources to compensate for carbon's irreversible capacity, energy densities as high as 265 W h kg(-1) can be reached with the Na3+xV2(PO4)(2)F-3/hard C system. Overall, such studies reveal that the gravimetric energy density advantage of layered over polyanionic compounds for Li-ion batteries vanishes by moving to Na-ion. We hope this information will be of great interest for battery manufacturers willing to enroll in the future commercialization of Na-ion batteries. (C) The Author(s) 2016. Published by ECS.
引用
收藏
页码:A867 / A874
页数:8
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