阳极
碳化
多孔性
材料科学
化学工程
电化学
碳纤维
球体
电导率
纳米技术
兴奋剂
过渡金属
体积热力学
纳米颗粒
复合材料
化学
电极
扫描电子显微镜
催化作用
有机化学
热力学
物理
光电子学
物理化学
天文
复合数
工程类
作者
Yefeng Yang,Qianqian Sun,Tiantian Tang,Gaoya Ren,Yi Wen,Zhujun Yao
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2023-09-20
卷期号:37 (19): 15179-15188
被引量:1
标识
DOI:10.1021/acs.energyfuels.3c02802
摘要
As one type of promising anode material, transition-metal selenides have aroused great attention in the research field of sodium-ion batteries (SIBs) on account of their high theoretical capacity. Nevertheless, the intrinsically inferior conductivity, huge volume changes, as well as severe aggregation of transition-metal selenides that take place upon cycling lead to fast degradation of sodium storage performance. In this work, we report the confined construction of NiSe2 particles embedded in porous N-doped carbon spheres (NiSe2/NC) with polydopamine spheres as the functional template involving successive solvothermal, carbonization, and selenization processes. As expected, the porous N-doped carbon spheres could improve the conductivity, facilitate the migration of Na+, and also serve as a stable mechanical support to NiSe2 particles by effectively avoiding the aggregation of NiSe2 and mitigating the volume changes. Consequently, the NiSe2/NC hybrid spheres exhibit a high reversible capacity (489 mA h g–1 at 0.1 A g–1), superior rate capability (212 mA h g–1 at 5 A g–1), and outstanding cycling stability (351 mA h g–1 after 1600 cycles at 1 A g–1). The delicate design of NiSe2/NC hybrid spheres fundamentally offers a valuable guidance for the development of transition-metal selenides, as well as other high capacity anodes with decent electrochemical performance.
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