热失控
分离器(采油)
枝晶(数学)
电解质
锂(药物)
材料科学
不稳定性
各向异性
电极
电池(电)
热的
离子
储能
锂离子电池
化学物理
纳米技术
电流密度
扩散
化学工程
电化学
延伸率
发热
热扩散率
分子动力学
生物物理学
热稳定性
作者
Dong Liu,Weifeng Zhao,Guiquan Chen,Yelin Deng
标识
DOI:10.1002/ente.202500970
摘要
The growth of lithium dendrites poses a critical challenge to the safety and longevity of lithium‐metal batteries. A multiphysics‐coupled phase‐field model integrating electrochemical, mechanical, and thermal dynamics is employed to systematically investigate dendrite morphological evolution and inhibition mechanisms. Simulations of dendrite growth under varied conditions—including anisotropic strengths, pulse charging protocols, electrolyte concentrations, and stress‐temperature coupling—reveal three key findings. Reduced anisotropy intensity (δ < 0.01) suppresses primary dendrite elongation by 30% and increased current factor leads to increased stress in lithium dendrites. Thermal simulations further demonstrate localized temperature rises that enhance ion diffusion but risk thermal runaway upon separator penetration. High‐rate charging (5 C‐rate) exacerbates concentration gradients, amplifying dendritic instability by 40%. These results underscore the critical importance of optimizing interfacial energy modulation, pulse protocols, and thermal management to enhance battery safety. Actionable guidelines are provided for designing robust electrode architectures and operational frameworks to advance high‐energy‐density storage systems.
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