解开 Li2C2O4 的分解限制,实现高效阴极预硫酸盐化

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摘要

高能量密度锂离子电池的发展受到初始充放电过程中不可逆容量损失的阻碍。因此,预锂化技术在过去几十年中崭露头角,成为补充不可逆锂损耗的有力方法,从而最大限度地提高锂离子电池的能量利用率并延长其循环寿命。草酸锂(Li2C2O4)具有高锂含量和优异的空气稳定性,一直被认为是最有前途的锂补偿材料之一。然而,该材料缓慢的电化学分解动力学严重阻碍了其进一步的商业应用。在此,我们介绍了一种结合原子镍催化剂的再结晶策略,以调节质量传输和分解反应动力学。Li2C2O4 的分解电位从 ∼4.90V 显著下降到 ∼4.30V,与当前电池系统具有很高的兼容性。与裸 NCM//Li 电池相比,Ni/N-rGO 和 Li2C2O4 复合材料(Ni-LCO)改性电池可释放出 11.7 % 的额外容量。此外,这一比例在 NCM//SiOx 全电池中也得到了放大,使可逆容量提高了 30.4%。总之,这项工作将催化范例引入了预硫化技术,为高能量密度电池系统的开发打开了另一扇窗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Unlocking the decomposition limitations of the Li2C2O4 for highly efficient cathode preliathiations

The development of high-energy-density Li-ion batteries is hindered by the irreversible capacity loss during the initial charge-discharge process. Therefore, pre-lithiation technology has emerged in the past few decades as a powerful method to supplement the undesired lithium loss, thereby maximizing the energy utilization of LIBs and extending their cycle life. Lithium oxalate (Li2C2O4), with a high lithium content and excellent air stability, has been considered one of the most promising materials for lithium compensation. However, the sluggish electrochemical decomposition kinetics of the material severely hinders its further commercial application. Here, we introduce a recrystallization strategy combined with atomic Ni catalysts to modulate the mass transport and decomposition reaction kinetics. The decomposition potential of Li2C2O4 is significantly decreased from ∼4.90V to ∼4.30V with a high compatibility with the current battery systems. In compared to the bare NCM//Li cell, the Ni/N-rGO and Li2C2O4 composite (Ni-LCO) modified cell releases an extra capacity of ∼11.7 ​%. Moreover, this ratio can be magnified in the NCM//SiOx full cell, resulting in a 30.4 ​% higher reversible capacity. Overall, this work brings the catalytic paradigm into the pre-lithiation technology, which opens another window for the development of high-energy-density battery systems.

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