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Ethylene Carbonate-Based Electrolyte Decomposition and Solid-Electrolyte Interphase Formation on Ca Metal Anodes

机译:CA金属阳极上基于碳酸亚乙酯的电解质分解和固体电解质互相形成

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The formation of a solid electrolyte interphase (SEI) in multivalent ion batteries, resulting from the decomposition of organic solvents at the anode interface, is a major bottleneck to their development as it prevents ionic diffusion and reversible stripping and plating. To gain insight into SEI formation in these systems, we investigate the decomposition of pure ethylene carbonate (EC) and an EC/Ca(ClO4)(2) electrolyte on a Ca metal surface using density functional theory and ab initio molecular dynamics calculations. We first find that CaCO3, CaO, and Ca(OH)(2) are all primary inorganic SEI components. We then investigate the reaction mechanisms of this decomposition, finding that although a fast two-electron reduction producing CO32- and C2H4 is thermodynamically and kinetically favorable, a reaction producing C2H4O22- and CO dominates when multiple EC molecules are considered. Finally, we find similar results upon the inclusion of Ca(ClO4)(2) salt.
机译:由阳极界面处的有机溶剂分解产生的多价离子电池中的固体电解质间(SEI)是其开发的主要瓶颈,因为它防止离子扩散和可逆剥离和电镀。 为了进入这些系统中的SEI形成,我们使用密度函数理论和AB INITIO分子动力学计算研究纯碳酸酯(EC)和EC / CA(2)电解质对CA金属表面的分解。 我们首先发现Caco3,CaO和Ca(OH)(2)是所有主要无机SEI组件。 然后研究这种分解的反应机制,发现尽管产生CO 32和C2H4的快速两电子还原在热力学上和动力学上有利,但在考虑多个EC分子时,产生C 2 H 4 O 2 2的反应。 最后,在包含Ca(CLO 4)(2)盐时,我们发现类似的结果。

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