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无定形 FeO/石墨烯复合纳米片具有增强的钠离子电池电化学性能。

Amorphous FeO/Graphene Composite Nanosheets with Enhanced Electrochemical Performance for Sodium-Ion Battery.

机构信息

State Key Laboratory of Chemical Resource Engineering, Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology , Beijing 100029, P. R. China.

出版信息

ACS Appl Mater Interfaces. 2016 Nov 16;8(45):30899-30907. doi: 10.1021/acsami.6b09444. Epub 2016 Nov 4.

Abstract

With the increasing use of sodium-ion batteries (SIBs), developing cost-effective anode materials, such as metal oxide, for Na-ion storage is one of the most attractive topics. Due to the obviously larger ion radius of Na than that of Li, most metal oxide electrode materials fail to exhibit the same high performance for SIBs like that of Li-ion batteries. Herein, iron oxide was employed to demonstrate a concept that rationally designing an amorphous structure should be useful to enhance Na-ion storage performance of a metal oxide. Amorphous FeO/graphene composite nanosheets (FeO@GNS) were successfully synthesized by a facile approach as anodes for SIBs. It reveals that amorphous FeO nanoparticles with an average diameter of 5 nm were uniformly anchored on the surface of graphene nanosheets by the strong C-O-Fe oxygen-bridge bond. Compared to well-crystalline FeO, amorphous FeO@GNS exhibited superior sodium storage properties such as high electrochemical activity, high initial Coulombic efficiency of 81.2%, and good rate performance. At a current density of 100 mA/g, amorphous FeO@GNS composites show a specific capacity of 440 mAh/g, which is obviously higher than the specific capacity of 284 mAh/g of crystalline FeO. Even at a high current density of 2 A/g, amorphous FeO@GNS composites still exhibit a specific capacity as high as 219 mAh/g. The excellent electrochemical performance should be attributed to the amorphous structures of FeO as well as strongly interfacial interaction between FeO and GNS, which not only accommodate more electrochemical active sites and provide the more transmission channels for sodium ions but also benefit electron transfer as well as effectively buffer the volume change of host materials during sodiation and desodiation. This concept for designing amorphous iron oxide anodes for SIBs is also expected to facilitate preparation of various amorphous nanostructure of other metal oxides and improve their Na-ion storage performance.

摘要

随着钠离子电池(SIBs)的应用日益广泛,开发具有成本效益的阳极材料,如金属氧化物,用于钠离子存储是最具吸引力的课题之一。由于钠离子的离子半径明显大于锂离子,大多数金属氧化物电极材料在钠离子电池中的表现不如锂离子电池那样出色。在此,我们选用氧化铁来证明合理设计非晶态结构的概念应该有助于提高金属氧化物的钠离子存储性能。通过一种简便的方法成功合成了非晶态 FeO/石墨烯复合纳米片(FeO@GNS)作为 SIBs 的阳极。结果表明,平均粒径为 5nm 的非晶态 FeO 纳米颗粒通过强 C-O-Fe 氧桥键均匀锚定在石墨烯纳米片的表面上。与结晶态 FeO 相比,非晶态 FeO@GNS 表现出优异的钠离子存储性能,如高电化学活性、初始库仑效率为 81.2%和良好的倍率性能。在 100mA/g 的电流密度下,非晶态 FeO@GNS 复合材料的比容量为 440mAh/g,明显高于结晶态 FeO 的 284mAh/g。即使在 2A/g 的高电流密度下,非晶态 FeO@GNS 复合材料仍表现出高达 219mAh/g 的比容量。优异的电化学性能应归因于 FeO 的非晶态结构以及 FeO 和 GNS 之间的强界面相互作用,这不仅为更多的电化学活性位点提供了更多的钠离子传输通道,而且有利于电子转移,并在钠化和脱钠过程中有效缓冲主体材料的体积变化。这种设计 SIBs 用非晶态氧化铁阳极的概念也有望促进其他金属氧化物的各种非晶态纳米结构的制备,并提高它们的钠离子存储性能。

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