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Thermodynamic Model Development For Lithium Intercalation Electrodes

机译:锂嵌入电极的热力学模型开发

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Staging is a characteristic phenomena observed in intercalation electrodes. During staging process the equilibrium potential of the electrode exhibits weak dependence on the solid phase Li concentration and does not follow the classical Nernst behavior. The coexistence of structurally different solid phases results in multiple plateaus in the equilibrium potential curve. Such complexities make the thermodynamic description of equilibrium potential as a function of concentration difficult, and so it is usually represented through an empirical expression. The objective of this work is to develop a frame work based on thermodynamic principles to describe the equilibrium potential of intercalation electrodes. Redlich-Kister thermodynamic equation was used to describe the excess Gibbs free energy, which in turn was used to evaluate the equilibrium potential as a function of concentration. The equilibrium potential expression for different lithium intercalation electrodes such as LiCoO_2, LiNi_(0.8)Co_(0.15)Al_(0.05)O_2, graphite and hard carbon were developed based on Redlich-Kister equation. The thermodynamic model was also used to estimate the activity of species directly from excess Gibbs free energy. The developed thermodynamic expressions along with the activity correction are incorporated into a single particle diffusion model for a Li-ion cell consisting of a graphite and LiCoO_2 electrode. The interactions between the Li-ions during intercalation/deintercalation process were incorporated into the present model by considering the chemical potential gradient corrected for activity as the driving force. The effect of inclusion of activity correction in the single particle model was studied for different discharge rates. It was observed that the activity correction term yielded increased capacity especially at higher rates. The effect of activity correction term was also found to be more significant in the LiCoO_2 electrode compared to the carbon electrode.
机译:分期是在插入电极中观察到的特征现象。在分阶段过程中,电极的平衡电势显示出对固相Li浓度的弱依赖性,并且不遵循经典的能斯特行为。结构不同的固相共存会导致平衡电位曲线出现多个平台。这种复杂性使得平衡势的热力学描述难以作为浓度的函数,因此通常通过经验表达式来表示。这项工作的目的是开发基于热力学原理的框架,以描述嵌入电极的平衡电位。用Redlich-Kister热力学方程式描述了多余的吉布斯自由能,然后用其评估了作为浓度函数的平衡势。基于Redlich-Kister方程,建立了LiCoO_2,LiNi_(0.8)Co_(0.15)Al_(0.05)O_2,石墨和硬碳等锂嵌入电极的平衡电势表达式。热力学模型还用于直接根据过量的吉布斯自由能估算物种的活性。所开发的热力学表达式以及活性校正被合并到由石墨和LiCoO_2电极组成的锂离子电池的单粒子扩散模型中。通过考虑针对活性校正的化学势梯度作为驱动力,将锂离子在嵌入/脱嵌过程中的相互作用纳入本模型。研究了不同排放速率下单颗粒模型中活性校正的影响。观察到,活动校正项产生了增加的容量,尤其是在较高速率下。还发现与碳电极相比,LiCoO_2电极中活性校正项的影响更为显着。

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