Chen Brian, Hope-Glenn Niya, Wright Amanda, Messinger Robert J, Couzis Alexander
Department of Chemical Engineering, The City College of New York (CUNY), 160 Convent Avenue, New York, New York 10031, United States.
ACS Electrochem. 2025 Apr 22;1(5):574-587. doi: 10.1021/acselectrochem.4c00079. eCollection 2025 May 1.
Low-temperature and fast-charging lithium (Li)-ion batteries remain challenging due to the undesirable Li plating on graphite anodes under these conditions. Here, we present a kinetic mechanism that underpins electrochemical Li cation intercalation and Li metal plating reactions on graphite electrodes at low temperatures and fast rates. Variable-temperature (30 °C to -40 °C) and variable-rate (0.1 to 10 mA/cm) constant-current measurements were conducted on three-electrode cells comprised of Li metal counter, graphite working, and Li metal reference electrodes, as well as two-electrode cells. The local minima in the potential profiles, often associated with the nucleation overpotential for Li metal plating on graphite, must be disentangled from contributions from Li metal stripping at the counter electrode. Differential capacity analyses of three-electrode measurements of graphite potential show that the extent of electrochemical Li cation intercalation drops precipitously as temperature decreases below -20 °C. The temperature dependence of empirically defined rate constants for Li cation intercalation and Li plating determined from constant-current measurements revealed non-Arrhenius behavior for Li cation intercalation that suggests a two-step pre-equilibration mechanism, while typical Arrhenius behavior for Li plating suggests a unimolecular single-step process. A kinetic model based on Langmuir adsorption shows that the interfacial concentration of Li cations adsorbed on graphite active sites is critical in dictating the kinetics of the charging process. We show that rate limitations, either adsorption-limited or surface reaction-limited, manifest at different temperatures and rates during the charging process. The results yield new mechanistic understanding of how Li cations electrochemically compete for intercalation into and plating on graphite electrodes, as a function of temperature and charge rate.
低温和快速充电的锂离子电池仍然具有挑战性,因为在这些条件下石墨阳极上会出现不良的锂镀层。在此,我们提出一种动力学机制,该机制是低温和快速速率下石墨电极上电化学锂阳离子嵌入和锂金属镀层反应的基础。在由锂金属对电极、石墨工作电极和锂金属参比电极组成的三电极电池以及双电极电池上进行了变温(30℃至 -40℃)和变电流(0.1至10 mA/cm)恒流测量。电位分布中的局部最小值通常与石墨上锂金属镀层的成核过电位相关,必须将其与对电极上锂金属剥离的贡献区分开来。石墨电位的三电极测量的微分电容分析表明,当温度降至 -20℃以下时,电化学锂阳离子嵌入的程度会急剧下降。从恒流测量确定的锂阳离子嵌入和锂镀层的经验定义速率常数的温度依赖性揭示,锂阳离子嵌入具有非阿仑尼乌斯行为,这表明存在两步预平衡机制,而锂镀层的典型阿仑尼乌斯行为表明是单分子单步过程。基于朗缪尔吸附的动力学模型表明,吸附在石墨活性位点上的锂阳离子的界面浓度对于决定充电过程的动力学至关重要。我们表明,在充电过程中,吸附限制或表面反应限制的速率限制在不同温度和速率下表现出来。这些结果为锂阳离子如何根据温度和充电速率在石墨电极上进行电化学竞争嵌入和镀层提供了新的机理理解。