电解质
阴极
比能量
电池(电)
电极
电压
泄流深度
材料科学
自放电
锂(药物)
化学工程
容量损失
热扩散率
活化能
离子电导率
化学
热力学
电气工程
物理化学
功率(物理)
内分泌学
有机化学
工程类
物理
医学
作者
Wei Li,Bohong Wang,Yujie Chen,Yajun Deng,Christos N. Markides,Min Zeng
标识
DOI:10.1016/j.jclepro.2024.140719
摘要
The modeling research plays a crucial role in grasping the reaction mechanisms and forecasting the performance of lithium-sulfur (Li–S) batteries. A transient Li–S battery model including continuity, transportation, and reaction kinetics by simultaneously considering the discontinuous deposit of discharge product Li2S and the transport limitation in the concentrated electrolyte, is developed to reveal the discharge phenomena. The effects of operating conditions and electrolyte and electrode properties on the discharge behaviors including voltage-capacity curve, energy density, profiles of solid product (ɛLi2S) and porosity (ɛ) at the cathode are quantitatively studied. It is found that low discharge rate is beneficial to the discharge capacity and utilization of cathode sulfur. Enhancing precipitate (S8) solubility Ksp, S8 and ionic diffusivity Di improves voltage plateau and specific energy to varying degrees; the promotion of voltage plateau will be inconspicuous as electrode conductivity σ is enlarged over 0.1 S/m. With the rise of ɛ from 0.5 to 0.9, the specific capacity and the specific energy are expanded by around 5 times. When lengthening Lca from 20 μm to 60 μm, the specific capacity ascends from 944.5 to 991.5 mAh/g-S, whereas the growth rate of specific capacity and specific energy decreases gradually; the practical total energy almost increases linearly with thickness, yielding a 218.75% enhancement. With a certain period of relaxation, the recovered cell capacity after the high discharge rate is higher than that after the low discharge rate. This work may guide in designing electrodes and electrolytes and provide performance regulation strategies for Li–S batteries.
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