电池(电)
阳极
阴极
重量分析
材料科学
离子
电极
碳纤维
能量密度
氧化物
化学工程
电压
储能
工程物理
化学
电气工程
物理化学
复合材料
热力学
有机化学
冶金
功率(物理)
物理
复合数
工程类
作者
Romain Dugas,Biao Zhang,Patrick Rozier,J.‐M. Tarascon
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 Nax(Fe1/2Mn1/2)O2 or a polyanionic Na3V2(PO4)2F3 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 Na1(Fe1/2Mn1/2)O2 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)2F3 / 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.
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