阳极
兴奋剂
材料科学
碳纤维
高原(数学)
中子衍射
同步加速器
离子
纳米技术
化学
光电子学
结晶学
晶体结构
复合材料
光学
电极
复合数
物理化学
物理
数学分析
有机化学
数学
作者
Zhifei Li,Lu Ma,T. Wesley Surta,Clement Bommier,Zelang Jian,Zhenyu Xing,William F. Stickle,Michelle R. Dolgos,Khalil Amine,Jun Lü,Tianpin Wu,Xiulei Ji
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2016-07-18
卷期号:1 (2): 395-401
被引量:190
标识
DOI:10.1021/acsenergylett.6b00172
摘要
The capacity of hard carbon anodes in Na-ion batteries rarely reaches values beyond 300 mAh/g. We report that doping POx into local structures of hard carbon increases its reversible capacity from 283 to 359 mAh/g. We confirm that the doped POx is redox inactive by X-ray adsorption near edge structure measurements, thus not contributing to the higher capacity. We observe two significant changes of hard carbon's local structures caused by doping. First, the (002) d-spacing inside the turbostratic nanodomains is increased, revealed by both laboratory and synchrotron X-ray diffraction. Second, doping turns turbostratic nanodomains more defective along ab planes, indicated by neutron total scattering and the associated pair distribution function studies. The local structural changes of hard carbon are correlated to the higher capacity, where both the plateau and slope regions in the potential profiles are enhanced. Our study demonstrates that Na-ion storage in hard carbon heavily depends on carbon local structures, where such structures, despite being disordered, can be tuned toward unusually high capacities.
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