阳极
法拉第效率
电解质
碳纤维
电池(电)
化学工程
电化学
储能
氮气
材料科学
磷
吸附
钠
扩散
兴奋剂
化学
无机化学
电极
复合材料
有机化学
冶金
热力学
光电子学
物理化学
工程类
功率(物理)
物理
复合数
作者
Sheng Wu,Peng Han-dong,Junling Xu,Le Huang,Yongsi Liu,Xiaocheng Xu,Yanxue Wu,Zhipeng Sun
出处
期刊:Carbon
[Elsevier]
日期:2024-01-01
卷期号:218: 118756-118756
被引量:18
标识
DOI:10.1016/j.carbon.2023.118756
摘要
Hard carbon (HC) is a prospective energy storage anode material in sodium-ion batteries (SIBs). However, their unimpressive rate capability and poor initial Coulombic efficiency (ICE) have driven the requirements for superior capability HC anode materials. In our work, nitrogen (N)/phosphorus (P) co-doped ultramicropores (≈0.5 nm) hard carbon spheres (NPUCS) with the boosted pyridinic-N content are successfully prepared. The ultramicropores structure (<0.7 nm) effectively prevents the electrolyte from contacting the carbon surface but allows the rapid diffusion of Na+ in the carbon layer, leading to high-efficiency sodium storage. Pyridinic-N has the highest reactivity, and could significantly promote the Na+ adsorption in HC. The NPUCS exhibits an excellent rate capability, providing capacities of 257.7 and 157.0 mA h g−1 at 0.1 and 5.0 A g−1 along with a high ICE to 75 %. Furthermore, when integrated into a full battery configuration, the prepared full battery displays a high energy density to 135.9 Wh kg−1 at 0.1 A g−1 with long-time stability (350 cycles at 0.2 A g−1). These excellent electrochemical behaviors highlight the potential of our approach for the synthesis of advanced HC anode for SIBs.
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