Institute of Advanced Electrochemical Energy , Xi'an University of Technology , Xi'an 710048 , China.
ACS Appl Mater Interfaces. 2018 May 2;10(17):14716-14726. doi: 10.1021/acsami.8b01888. Epub 2018 Apr 18.
Sodium-ion batteries (SIBs), as the promising commercial energy system, are restricted by their sluggish kinetics and low sodium-ion storage. Metal selenide possesses good conductivity and capacity but still suffers from the stacked problem and volume expansion. Significantly, CoSe/C is successfully prepared with the assistance of citric acid as both a chelating agent and carbon precursor, displaying that cobblestone-like nanospheres with the radii (<25 nm) distribute uniformly in the carbon matrix. It is expected that the established Co-O-C bonds enhance the stability of the structure with faster ion shuttling. With the available electrolyte (NaCFSO/diethylene glycol dimethyl ether) in a potential window range from 0.5 to 3.0 V, the as-obtained sample shows the ultralong lifespan at 4.5 A g, retaining a capacity of 345 mA h g after 10 000 cycles. From the detailed kinetic analysis, it is clear that the surface-controlled electrochemical behavior mainly contributes to the excellent large-current cycling stability and Na storage capacity. The ex situ results support that the crystal and morphological structure remains stable. This work is anticipated to enhance the in-depth understanding of the CoSe/C anode and supply a facile manner to obtain electrode materials for SIBs.
钠离子电池(SIBs)作为有前途的商业能源系统,受到其缓慢动力学和低钠离子存储能力的限制。金属硒化物具有良好的导电性和容量,但仍然存在堆积问题和体积膨胀。值得注意的是,在柠檬酸的螯合作用和碳前体的辅助下,成功制备了 CoSe/C,其表现出具有半径(<25nm)的鹅卵石状纳米球均匀分布在碳基质中。预计建立的 Co-O-C 键会增强结构的稳定性,从而加快离子穿梭速度。在所提供的电解质(NaCFSO/diethylene glycol dimethyl ether)的电位窗口范围为 0.5 至 3.0V 时,所得样品在 4.5A g 的超高电流下表现出超长的寿命,在 10000 次循环后保留 345mA h g 的容量。从详细的动力学分析可以清楚地看出,表面控制的电化学行为主要有助于出色的大电流循环稳定性和 Na 存储能力。原位结果表明晶体和形态结构保持稳定。这项工作有望加深对 CoSe/C 阳极的理解,并为 SIBs 提供一种简单的方法来获得电极材料。