New insights into electrochemical anion intercalation into carbonaceous materials for dual-ion batteries: Impact of the graphitization degree

被引:82
作者
Heckmann, Andreas [1 ]
Fromm, Olga [1 ]
Rodehorst, Uta [1 ]
Munster, Patrick [1 ]
Winter, Martin [1 ,2 ]
Placke, Tobias [1 ]
机构
[1] Univ Munster, MEET Battery Res Ctr, Inst Phys Chem, Corrensstr 46, D-48149 Munster, Germany
[2] Forschungszentrum Julich, Helmholtz Inst Munster, IEK 12, Corrensstr 46, D-48149 Munster, Germany
关键词
X-RAY-DIFFRACTION; BIS(TRIFLUOROMETHANESULFONYL) IMIDE ANIONS; ALUMINUM CURRENT COLLECTOR; PLANE SURFACE-AREA; LITHIUM-ION; IN-SITU; HEXAFLUOROPHOSPHATE ANION; RECHARGEABLE BATTERY; GRAPHITE-ELECTRODES; POSITIVE ELECTRODE;
D O I
10.1016/j.carbon.2018.01.099
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
Within the past 5 years, dual-ion batteries and in particular their all-carbon/all-graphite versions, the dual-carbon or dual-graphite batteries, have received rising interest due to the use of carbonaceous active materials for both, the positive and the negative electrode. With regard to the capacity determining reactions at the positive electrode, related to the intercalation of anions, the influence of the carbon/graphite structure has been by far not fully understood. In this work, we present a comprehensive investigation on the structure - property relationship with special focus on the preparation and characterization of carbon materials with different degree of graphitization (DoG) and their electrochemical performance study as active material for the positive electrode in dual-ion batteries. We found that an increasing DoG directly leads to an enhanced specific discharge capacity, while the crystallite height exhibits only a negligible contribution to the capacity for the carbons examined in this work. A further observation is that the staging mechanism is a major step of the overall anion storage mechanism, even for carbons possessing a low DoG. Moreover, an increased DoG leads to a decreased voltage hysteresis between the charge and discharge step and, thus, to an enhanced voltage efficiency during charge/discharge cycling. (c) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:201 / 212
页数:12
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