材料科学
锂(药物)
硫黄
锂硫电池
纳米技术
无机化学
化学工程
冶金
物理化学
电化学
电极
化学
医学
工程类
内分泌学
作者
Chen Li,Su Wang,Zhaokun Wang,Zuohang Li,Chenchen Zhang,Wei Ma,Xixi Shi,Hongzhou Zhang,Dawei Song,Lianqi Zhang
标识
DOI:10.1002/adfm.202414159
摘要
Abstract Low rate activation process is always used in conventional transition metal oxide cathode and fully activates active substances/electrolyte to achieve stable electrochemical performance. However, the related working mechanism in lithium‐sulfur (Li‐ battery is unclear due to the multiple complex chemical reaction steps including the redox of sulfur and the dissolution of polysulfides intermediate. Hence, the influencing mechanism of activation process on Li‐S battery is explored by adopting different current densities of 0.05, 0.2, and 1 C in initial three cycles before long‐term cycling tests at 0.2 C (denoted by 0.05, 0.2, and 1‐battery). 0.05‐battery presents the highest initial capacity in activation process, while 0.2‐battery presents superior electrochemical performances after 150 cycles. The similar trend can be found in more long‐term cycling rates such as 0.02, 0.1, 0.5, and 1 C. Potentiostatically Li 2 S precipitation test demonstrates that rapid generation of Li 2 S is achieved at higher current density, and S 8 ‐Li 2 S n ‐Li 2 S conversion is accelerated according to Tafel plots. However, interfacial electrochemical and physical characterizations suggest that serious lithium dendrite growth will be induced under high current density. Therefore, considering the reaction kinetics and interfacial properties, low rate activation process is unnecessary when cycling current lower than 1 C for Li‐S battery.
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