利用葡萄糖插层策略制造的花朵状掺杂铁的 NiSe2/C 混合球体可增强钠储存性能

Cheng Liu , Yi Wen , Gaoya Ren , Yaxuan Li , Qianqian Sun , Shenghui Shen , Zhujun Yao , Yefeng Yang
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引用次数: 0

摘要

二硒化镍(NiSe2)具有很高的理论容量,作为钠离子电池(SIB)的一种前景广阔的阳极材料,已经引起了广泛关注。然而,NiSe2 固有的低电导率、巨大的体积变化以及在钠化/解钠过程中的显著聚集仍然是其应用的重大障碍。在此,我们报告了通过葡萄糖插层策略制造的花状掺杂铁的 NiSe2/C 混合球(简称为 Fe-NiSe2/C),用于高效钠存储。这些 Fe-NiSe2/C 混合球由装饰有 Fe-NiSe2 纳米颗粒的薄多孔碳纳米片组成。在 NiSe2 纳米粒子中适度掺杂铁的同时,原位引入由插层葡萄糖衍生的碳纳米片,可通过花状结构中的快速离子通道以及 NiSe2 和碳纳米片之间紧密接触的界面加速离子/电子转移动力学,并通过减轻体积变化保持结构的完整性。因此,Fe-NiSe2/C 混合球的最佳阳极在 0.5 A g-1 的条件下可实现 415 mAh g-1 的高放电容量、出色的速率能力(5 A g-1 时为 243 mAh g-1)以及显著增强的循环稳定性(1 A g-1 时为 388 mAh g-1,循环 200 次)。这项研究为在过渡金属硒化物中实现量身定制的杂原子掺杂提供了一种高效而有价值的策略,同时还为先进的碱金属离子电池提供了导电碳质网络的原位组合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Flower-like Fe-doped NiSe2/C hybrid spheres fabricated by a glucose-intercalation strategy for enhanced sodium storage properties

Nickel diselenide (NiSe2), which has a high theoretical capacity, has attracted considerable attention as a promising anode material for sodium-ion batteries (SIBs). Nevertheless, the intrinsically low conductivity, large volume variation, and significant aggregation of NiSe2 during sodiation/desodiation remain significant obstacles to its application. Herein, we report flower-like Fe-doped NiSe2/C hybrid spheres (denoted as Fe-NiSe2/C) fabricated by a glucose intercalation strategy for efficient sodium storage. These Fe-NiSe2/C hybrid spheres are composed of thin porous carbon nanosheets decorated with Fe-NiSe2 nanoparticles. In situ introduced carbon nanosheets derived from intercalated glucose accompanied by moderate Fe doping in NiSe2 nanoparticles can provide accelerated ion/electron transfer kinetics through fast ion channels in the flower-like architecture and intimately contacted interfaces between NiSe2 and carbon nanosheets as well as maintain structural integrity by alleviating volume variation. Consequently, the optimal anode of the Fe-NiSe2/C hybrid spheres delivered a high discharge capacity of 415 mAh g−1 at 0.5 A g−1, outstanding rate capability (243 mAh g−1 at 5 A g−1), and significantly enhanced cycling stability (388 mAh g−1 at 1 A g−1 over 200 cycles). This work offers an efficient and valuable strategy for realizing tailored heteroatom doping in transition metal selenides, accompanied by an in situ combination of conductive carbonaceous networks for advanced alkali metal ion batteries.

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