A Raman spectroscopic study of graphene cathodes in high-performance aluminum ion batteries

被引:91
作者
Childress, Anthony S. [1 ]
Parajuli, Prakash [1 ]
Zhu, Jingyi [1 ]
Podila, Ramakrishna [1 ]
Rao, Apparao M. [1 ]
机构
[1] Clemson Univ, Dept Phys & Astron, Clemson Nanomat Inst, Kinard Lab 118, Clemson, SC 29634 USA
基金
美国国家科学基金会;
关键词
Aluminum ion battery; In situ Raman spectroscopy; Graphene; Graphite intercalation compound; Nitrogen doping; GRAPHITE-INTERCALATION COMPOUNDS; NITROGEN-DOPED GRAPHENE; LITHIUM INTERCALATION; FILM ELECTRODES; CHARGE-TRANSFER; APROTIC MEDIA; SCATTERING; MECHANISM; CHLORIDE; LIQUIDS;
D O I
10.1016/j.nanoen.2017.06.038
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
Few layer graphene is a promising cathode material for aluminum-ion batteries that use chloroaluminate (AlCl4-) ionic liquids as the electrolyte. A fundamental understanding of interactions between the few layer graphene cathode and the ionic liquid electrolyte is key for realizing the full potential of these systems. Through in situ Raman spectroscopy and density functional theory calculations, we show that the cathode is capable of achieving stage-one intercalation within the operating voltage window, leading to improved cell performance. We also show that the presence of structural defects in few layer graphene such as pores induced via plasma exposure or nitrogen dopants can deteriorate the cell performance by either decreasing the electrical connectivity or precluding stage-one intercalation respectively. The cathodes made with highly crystalline few layer graphene display high power and energy densities (similar to 200 W h kg(-1) at 200 W kg(-1) and similar to 160 W h kg(-1) at 5000 W kg(-1)), and are stable with no loss in performance up to 1000 cycles while fully charging to 2.4 V.
引用
收藏
页码:69 / 76
页数:8
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