Pushing the theoretical limit of Li-CFx batteries using fluorinated nanostructured carbon nanodiscs

被引:62
作者
Ahmad, Yasser [1 ,2 ]
Dubois, Marc [1 ,2 ]
Guerin, Katia [1 ,2 ]
Hamwi, Andre [1 ,2 ]
Zhang, Wei [3 ]
机构
[1] Univ Blaise Pascal, Clermont Univ, Inst Chem Clermont Ferrand, F-63000 Clermont Ferrand, France
[2] CNRS, UMR 6296, ICCF, F-63171 Aubiere, France
[3] Beihang Univ, Univ Aeronaut & Astronaut Pekin, Beijing 100191, Peoples R China
关键词
TRIPLE ION FORMATION; GRAPHITE INTERCALATION COMPOUNDS; NUCLEAR-MAGNETIC-RESONANCE; SURFACE-FILM FORMATION; SOLID-STATE NMR; ELECTROCHEMICAL INSERTION; HYPERLITHIATED LI2F; DISCHARGE MECHANISM; IONIZATION ENERGIES; LITHIUM;
D O I
10.1016/j.carbon.2015.07.073
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
Li-CFx battery using a specific fluorinated nanocarbon as cathode material exhibits a capacity exceeding the expected theoretical value when used as an electrode material in primary lithium battery. Carbon nanodiscs were partially fluorinated by atomic fluorine released by thermal decomposition of TbF4, and the capacity of this material was up to 1180 mAh g(-1), whereas a theoretical value of 847 mAh g(-1) for the CF0.95 sample was calculated. The obtained value is also higher than the maximum one of 865 mAh g(-1) expected for CF1 carbon fluorides. The discharge mechanism was investigated using mainly SEM and solid state NMR in order to understand this "extra-capacity". Both the un-fluorinated carbon and the LiF covering, which is formed outside the carbon lattice during the discharge mechanism, play a key role for the achievement of the extra-capacity by the consumption of Li+ to form Li2F+ species stabilized by the carbon host structure formed after the electrochemical de-fluorination. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1061 / 1070
页数:10
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