机制(生物学)
GSM演进的增强数据速率
化学
材料科学
化学工程
化学物理
纳米技术
工程物理
计算机科学
电信
量子力学
物理
工程类
作者
Kevin Leung,Noah B. Schorr,Matthew T. Mayer,Timothy N. Lambert,Y. Shirley Meng,Katharine L. Harrison
标识
DOI:10.1021/acs.chemmater.0c04676
摘要
Graphite fluoride (CFx) cathodes coupled with lithium anodes yield one of the highest theoretical specific capacities (>860 mAh/g) among primary batteries. In practice, the observed discharge voltage (∼2.5 V) is significantly lower than thermodynamic limits (>4.5 V), the discharge rate is low, and so far Li/CFx has only been used in primary batteries. Understanding the discharge mechanism at atomic length scales will improve practical CFx energy density, rate capability, and rechargeability. So far, purely experimental techniques have not identified the correct discharge mechanism or explained the discharge voltage. We apply density functional theory calculations to demonstrate that a CFx-edge propagation discharge mechanism based on lithium insertion at the CF/C boundary in partially discharged CFx exhibits a voltage range of 2.5 to 2.9 V—depending on whether solvent molecules are involved. The voltages and solvent dependence agree with our discharge and galvanostatic intermittent titration technique measurements. The predicted discharge kinetics are consistent with CFx operations. Finally, we predict some Li/CFx rechargeability under the application of high potentials, along a charging pathway different from that of discharge. Our work represents a general, quasi-kinetic framework to understand the discharge of conversion cathodes, circumventing the widely used phase diagram approach which most likely does not apply to Li/CFx because equilibrium conditions are not attained in this system.
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