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Thermally Activated P2-O3 Mixed Layered Cathodes toward Synergistic Electrochemical Enhancement for Na Ion Batteries

机译:热活化的P2-O3混合层状阴极朝向Na离子电池的协同电化学增强

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摘要

Layer-structured oxide cathodes have a lot of phases, which can be varied depending on Na ion contents and finally determine their electrochemical properties. Therefore, the off-stoichiometry of layer-structured oxides with the Na ions may differentiate not only their capacities but also the cyclic stabilities, kinetics, and so on, highlighting the importance of Na ion content. However, Na2CO3 tends to be irreversibly formed on surface by making use of the Na ions lost from the lattice. Thereby, the O3 phase with stoichiometric Na content changes into the off-stoichiometric P2 phase bringing about significant disadvantages. To address this issue, a thermal activation process is suggested to simultaneously decompose Na2CO3 into electrochemically active Na ions and modulate the off-stoichiometric P2 phase into the stoichiometric O3 phase. This study indicates that minimizing the loss of Na ions and maintaining the lattice framework with higher contents of Na ions during the synthesis of Na-incorporating layered cathodes should be a key toward attaining electrochemical superiority.
机译:层结构氧化物阴极具有大量相,这可以根据Na离子含量而变化,并且最终确定其电化学性质。因此,具有Na离子的层结构氧化物的脱离化学计量不仅可以区分它们的容量,而且可以突出循环稳定性,动力学等,突出Na离子含量的重要性。然而,通过使用从晶格中损失的Na离子倾向于在表面上不可逆地形成。由此,O3相位具有化学计量Na含量的变化变为带来显着缺点的脱离化学计量的P2相。为了解决该问题,建议热激活过程将Na 2 CO 3同时分解成电化学活性Na离子,并调节脱离化学计量P2相进入化学计量O3相。该研究表明,在Na掺入层状阴极的合成期间,将Na离子的损失最小化并使晶格框架与较高的Na离子含量的含量应该是实现电化学优势的关键。

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