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Dynamic behaviour of interphases and its implication on high-energy-density cathode materials in lithium-ion batteries

机译:锂离子电池中相间的动态行为及其对高能量密度正极材料的影响

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摘要

Undesired electrode-electrolyte interactions prevent the use of many high-energy-density cathode materials in practical lithium-ion batteries. Efforts to address their limited service life have predominantly focused on the active electrode materials and electrolytes. Here an advanced three-dimensional chemical and imaging analysis on a model material, the nickel-rich layered lithium transition-metal oxide, reveals the dynamic behaviour of cathode interphases driven by conductive carbon additives (carbon black) in a common nonaqueous electrolyte. Region-of-interest sensitive secondary-ion mass spectrometry shows that a cathode-electrolyte interphase, initially formed on carbon black with no electrochemical bias applied, readily passivates the cathode particles through mutual exchange of surface species. By tuning the interphase thickness, we demonstrate its robustness in suppressing the deterioration of the electrode/electrolyte interface during high-voltage cell operation. Our results provide insights on the formation and evolution of cathode interphases, facilitating development of in situ surface protection on high-energy-density cathode materials in lithium-based batteries.
机译:不良的电极与电解质的相互作用会阻止在实际的锂离子电池中使用许多高能量密度的阴极材料。解决其有限使用寿命的努力主要集中在活性电极材料和电解质上。在此,对模型材料(富镍层状锂过渡金属氧化物)进行了高级的三维化学和成像分析,揭示了在常见的非水电解质中,导电碳添加剂(炭黑)驱动的阴极相间的动态行为。感兴趣的区域敏感的二次离子质谱分析表明,最初在炭黑上形成的阴极-电解质中间相没有施加任何电化学偏压,就很容易通过相互交换表面物种而钝化阴极颗粒。通过调整相间厚度,我们证明了其在抑制高压电池运行期间电极/电解质界面劣化方面的稳健性。我们的研究结果提供了有关阴极相间形成和演化的见解,从而促进了锂基电池中高能量密度阴极材料的原位表面保护的发展。

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