CoSe2 nanodots confined in multidimensional porous nanoarchitecture towards efficient sodium ion storage

材料科学 纳米点 阳极 石墨烯 储能 普鲁士蓝 电化学 纳米技术 电极 阴极 多孔性 化学工程 锂(药物) 离子 复合材料 有机化学 化学 工程类 医学 功率(物理) 物理 物理化学 量子力学 内分泌学
作者
Qian Xiao,Qilin Song,Ke Zheng,Zheng Li,Yanyan Zhu,Zhonghui Chen
出处
期刊:Nano Energy [Elsevier]
卷期号:98: 107326-107326 被引量:89
标识
DOI:10.1016/j.nanoen.2022.107326
摘要

Sodium ion batteries (SIBs) are a low-cost and promising alternative to lithium ion batteries, however, due to the large sodium ion size (Na+ vs Li+: 1.02 Å vs 0.76 Å), high ion diffusion barrier and huge volume variation of electrode materials, it remains a challenge to achieve satisfactory Na+ storage performance. To address these issues, herein, we deliberately designed a multidimensional porous anode for SIBs, which was constructed by zero-dimensional (0D) ultrasmall CoSe2 nanodots confined in one-dimensional (1D) porous carbon nanowires (CNWs) and well encapsulated within three-dimensional (3D) graphene (3DG/CoSe2@CNWs). The fabricated 3DG/CoSe2@CNWs nanoarchitecture exhibits plentiful reactive sites, interconnected conductive network, abundant ion transport channels, and double protective structure. Thus, it showed enhanced Na+ storage performance with high reversible capacities (543 mA h g−1 at 0.1 A g−1) and superior long-term cycling performance with a capacity retention of 86.1% at 2 A g−1, and when coupled with 3D graphene/Prussian blue (3DG/PB) cathodes, the full batteries also delivered enhanced electrochemical performance. Furthermore, its efficient Na+ storage mechanisms were proved by the reaction kinetics analysis and density functional theory calculations. Our work provides a new electrode design strategy based on multidimensional nanoarchitecture for high-performance energy storage devices.
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