Design of new electrode materials for Li-ion and Na-ion batteries from the bloedite mineral Na2Mg(SO4)2•4H2O

被引:83
作者
Reynaud, Marine [1 ]
Rousse, Gwenaelle [2 ]
Abakumov, Artem M. [3 ]
Sougrati, Moulay T. [4 ]
Van Tendeloo, Gustaaf [3 ]
Chotard, Jean-Noel [1 ]
Tarascon, Jean-Marie [1 ]
机构
[1] Univ Picardie Jules Verne, Lab Reactivite & Chim Solides, CNRS UMR 7314, F-80039 Amiens, France
[2] Univ Paris 06, Inst Mineral & Phys Milieux Condenses, CNRS UMR 7590, F-75252 Paris 05, France
[3] Univ Antwerp, B-2020 Antwerp, Belgium
[4] Univ Montpellier 2, CNRS UMR 5253, Inst Charles Gerhardt Lab Agr Interfaces & Mat En, F-34095 Montpellier 5, France
关键词
BIS(SULFATE) TETRAHYDRATE; TRIPLITE STRUCTURE; CRYSTAL-STRUCTURE; CO; ASTRAKANITE; DIFFRACTION; METAL; MN; FE; MG;
D O I
10.1039/c3ta13648e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Mineralogy offers a large database to search for Li- or Na-based compounds having suitable structural features for acting as electrode materials, LiFePO4 being one example. Here we further explore this avenue and report on the electrochemical properties of the bloedite type compounds Na2M(SO4)(2)center dot 4H(2)O (M = Mg, Fe, Co, Ni, Zn) and their dehydrated phases Na2M(SO4)(2) (M = Fe, Co), whose structures have been solved via complementary synchrotron X-ray diffraction, neutron powder diffraction and transmission electron microscopy. Among these compounds, the hydrated and anhydrous iron-based phases show electrochemical activity with the reversible release/uptake of 1 Na+ or 1 Li+ at high voltages of similar to 3.3 V vs. Na+/Na-0 and similar to 3.6 V vs. Li+/Li-0, respectively. Although the reversible capacities remain lower than 100 mA h g(-1), we hope this work will stress further the importance of mineralogy as a source of inspiration for designing eco-efficient electrode materials.
引用
收藏
页码:2671 / 2680
页数:10
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