Toward Stable Electrode/Electrolyte Interface of P2-Layered Oxide for Rechargeable Na-Ion Batteries

被引:40
作者
Zarrabeitia, Maider [1 ,2 ,3 ]
Chagas, Luciana Gomes [2 ,3 ,5 ]
Kuenzel, Matthias [2 ,3 ]
Gonzalo, Elena [1 ]
Rojo, Teofilo [1 ,4 ]
Passerini, Stefano [2 ,3 ]
Angel Munoz-Marquez, Miguel [1 ]
机构
[1] CIC Energigune, Parque Tecnol Alava,Albert Einstein 48, Minano 01510, Spain
[2] HIU, Helmholtzstr 11, D-89081 Ulm, Germany
[3] Karlsruhe Inst Technol, POB 3640, D-76021 Karlsruhe, Germany
[4] Univ Pais Vasco UPV EHU, Dept Quim Inorgan, POB 664, Leioa 48080, Spain
[5] Johnson Matthey Technol Ctr, Reading RG4 9NH, Berks, England
关键词
Na-layered oxide; solid permeable interface; carbonate-based electrolyte; ionic liquid electrolyte; Na-ion batteries; SOLID-ELECTROLYTE INTERPHASE; LIQUID ELECTROLYTES; HIGH-PERFORMANCE; HARD-CARBON; ELECTROCHEMICAL PROPERTIES; POSITIVE ELECTRODE; CATHODE MATERIAL; AUGER PARAMETER; SODIUM; P2-TYPE;
D O I
10.1021/acsami.9b07963
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The electrochemical properties of P2-Na2/3Mn0.8Fe0.1Ti0.1O2 layered oxide, which is a promising cathode material for rechargeable Na-ion batteries (NIBs), are evaluated with an optimized in-house ionic liquid (IL)-based electrolyte, and its performance is compared with that using carbonate-based electrolyte. The IL-based system reveals better electrochemical performance at room temperature than the carbonate electrolyte-based one at 0.1C and 1C, especially in terms of cycling stability, with a 97% capacity retention after 100 deep cycles (0.1C). The electrode/electrolyte interface is thoroughly studied in both systems by means of X-ray photoelectron spectroscopy and scanning electron microscopy so as proof that the formed interface is crucial to optimizing the electrochemical performance of NIBs. The carbonate-based system shows a thin, inhomogeneous, and unstable interface layer, while the IL-based one exhibits an even thinner but homogeneous and more stable interface, which may result in safer and longer-lasting NIBs.
引用
收藏
页码:28885 / 28893
页数:9
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