化学
热的
电池(电)
分析化学(期刊)
石墨
恒流
离子
滴定法
量热法
电流(流体)
指数函数
热力学
材料科学
无机化学
色谱法
物理
数学分析
数学
有机化学
功率(物理)
作者
Abdul Muiz Ahmad,Guillaume Thenaisie,Sang‐Gug Lee
标识
DOI:10.1016/j.powera.2022.100097
摘要
A fast entropy-variations (Δ S ) extraction method has been proposed based on calorimetry , which determines the heat associated with Δ S by analyzing the electro-thermal response of a battery to a sequence of constant current pulses, i.e., the galvanostatic intermittent titration technique (GITT). The rest times in GITT are reduced by only considering limited relaxation of the ionic concentration gradients inside the battery after the current interruptions while completely ignoring the thermal equilibrium conditions inside the calorimeter . The resulting thermal signal of the battery is analyzed using an algorithm that adopts exponential regression to characterize the generated heat energy corresponding to each current pulse. Additionally, the polarization heat inside the battery is investigated by taking into account the initial presence of the concentration gradients when a current pulse is applied. Thus, the optimized rest times between the successive current pulses can reduce the measurement time manyfold compared to the previously reported methods, which require the battery to reach both electrochemical and thermal equilibriums. This work shows that the Δ S profiles of a 1 Ah NMC811/graphite pouch cell with 2.5% state of charge (SOC) resolution can be extracted at least three times faster than the method with unoptimized rest times, in a highly repeatable manner.
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