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Unraveling the stabilization mechanism of solid electrolyte interface on ZnSe by rGO in sodium ion battery

机译:在钠离子电池中rgo Znse上固体电解质界面的稳定机理

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Transition metal selenides have been widely studied as anode materials of sodium ion batteries(SIBs),however,the investigation of solid-electrolyte-interface(SEI)on these materials,which is critical to the electrochemical performance of SIBs,remains at its infancy.Here in this paper,ZnSe@C nanoparticles were prepared from ZIF-8 and the SEI layers on these electrodes with and without reduced graphene oxide(rGO)layers were examined in details by X-ray photoelectron spectroscopies at varied charged/discharged states.It is observed that fast and complicated electrolyte decomposition reactions on ZnSe@C leads to quite thick SEI film and intercalation of solvated sodium ions through such thick SEI film results in slow ion diffusion kinetics and unstable electrode structure.However,the presence of rGO could efficiently suppress the decomposition of electrolyte,thus thin and stable SEI film was formed.ZnSe@C electrodes wrapped by rGO demonstrates enhanced interfacial charge transfer kinetics and high electrochemical performance,a capacity retention of 96.4%,after 1000 cycles at 5 A/g.This study might offer a simple avenue for the designing high performance anode materials through manipulation of SEI film.
机译:过渡金属硒化硒已被广泛地研究了钠离子电池(SIBs)的阳极材料,然而,对这些材料的固体电解质界面(SEI)的研究对于SIBs的电化学性能至关重要,仍然处于初期。在本文中,通过在变化/放电状态下通过X射线光电子谱检查,从ZIF-8中制备ZnSe @ C纳米颗粒,并通过变化的/放电状态下的X射线光电子谱检查这些电极上的SEI层。被观察到,通过这种厚的SEI膜导致ZnSe @ C上的快速和复杂的电解质分解反应导致相当厚的SEI膜和溶剂化钠离子的插入导致慢离子扩散动力学和不稳定电极结构。然而,RGO的存在可以有效地抑制形成电解质的分解,从而形成薄且稳定的SEI膜。由RGO包裹的ZnSe至Colitors演示了增强的界面电荷转移动力学A. ND高电化学性能,容量保留96.4%,在5 A / G的1000次循环后。该研究可以通过操纵SEI薄膜为设计高性能阳极材料提供简单的途径。

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