Wang Hua, Li Xintong, Li Tianyi, Chen Xi Chelsea, Chang Kai, Chen Lei, Yang Zhenzhen, Zhu Likun
Department of Mechanical and Energy Engineering, Indiana University Purdue University Indianapolis, Indianapolis, Indiana 46202, United States.
School of Mechanical Engineering, Purdue University, West Lafayette, Indiana 47907, United States.
ACS Appl Mater Interfaces. 2025 Jan 8;17(1):811-822. doi: 10.1021/acsami.4c11207. Epub 2024 Dec 16.
Solid-state Li-ion batteries are attracting attention for their enhanced safety features, higher energy density, and broader operational temperature range compared to systems based on liquid electrolytes. However, current solid-state Li-ion batteries face performance challenges, such as suboptimal cycling and poor rate capabilities, often due to inadequate interfacial contact between the solid electrolyte and electrodes. To address this issue, we incorporated a gallium-indium (Ga-In) liquid metal as the anode in a solid-state Li-ion battery setup, employing LiPSCl as the solid electrolyte. Operating at room temperature, this configuration achieved an initial capacity of 389 mAh g and maintained 88% of this capacity after 30 cycles at a 0.05 C rate. It also demonstrated a capacity retention of 66% after 500 cycles at a 0.5 C rate. In comparison to solid anode materials, such as tin, the Ga-In liquid metal exhibited superior cycling stability and rate capacity, which is due to the self-healing and fluid properties of the alloy that ensure stable interfacial contact with solid electrolytes. In situ X-ray diffraction (XRD) and ex situ scanning electron microscope (SEM) analyses revealed that indium does not directly participate in the lithiation/delithiation process. Instead, it helps maintain the alloy's low melting point, facilitating its return to a liquid state after delithiation. In a comparative analysis of stack pressure during cycling in cells utilizing Ga-In liquid metal and tin, the Ga-In liquid metal cell demonstrated an ability to buffer pressure increases associated with deformation. These findings suggest a promising approach for enhancing solid-state batteries by integrating liquid metal anodes, which improve interfacial contact and stability.
与基于液体电解质的系统相比,固态锂离子电池因其增强的安全特性、更高的能量密度和更宽的工作温度范围而备受关注。然而,目前的固态锂离子电池面临性能挑战,如循环性能欠佳和倍率性能较差,这通常是由于固体电解质与电极之间的界面接触不足所致。为解决这一问题,我们在固态锂离子电池装置中采用LiPSCl作为固体电解质,将镓铟(Ga-In)液态金属用作阳极。在室温下运行时,这种配置实现了389 mAh g的初始容量,在0.05 C倍率下循环30次后保持了该容量的88%。在0.5 C倍率下循环500次后,其容量保持率也达到了66%。与锡等固体阳极材料相比,Ga-In液态金属表现出卓越的循环稳定性和倍率性能,这归因于该合金的自愈和流体特性,确保了与固体电解质的稳定界面接触。原位X射线衍射(XRD)和非原位扫描电子显微镜(SEM)分析表明,铟并不直接参与锂化/脱锂过程。相反,它有助于维持合金的低熔点,便于在脱锂后恢复到液态。在对使用Ga-In液态金属和锡的电池循环过程中的堆叠压力进行的对比分析中,Ga-In液态金属电池展现出缓冲与变形相关的压力增加的能力。这些发现表明,通过集成液态金属阳极来增强固态电池是一种很有前景的方法,液态金属阳极可改善界面接触和稳定性。