阳极
碳化
材料科学
化学工程
高原(数学)
插层(化学)
差示扫描量热法
电池(电)
碳纤维
阴极
电压
纳米技术
储能
离子
电极
化学
无机化学
复合材料
复合数
扫描电子显微镜
有机化学
电气工程
物理化学
功率(物理)
数学分析
工程类
物理
数学
热力学
量子力学
作者
Xiang Zhang,Xiaoli Dong,Xuan Qiu,Yongjie Cao,Congxiao Wang,Yonggang Wang,Yongyao Xia
标识
DOI:10.1016/j.jpowsour.2020.228550
摘要
Hard carbon is now one of the most promising anode materials for sodium-ion batteries, but achieving high reversible capacity at low voltage plateau (0–0.1 V) is still a major challenge, which can actually enhances the operating voltage as well as the energy density when coupled with cathodes. In this work, a series of hard carbon spheres (HCS) with controlled architectures for sodium ion batteries (SIBs) are prepared by carbonizing synthetic phenolic resin over a wide temperature range from 900 to 2800 °C. HCS treated at 1900 °C (HCS-1900) has a pure hard carbon structure with appropriate graphitic interlayer distance (0.358 nm) and microcrystal size (La ~ 1.61 nm, Lc ≈ 3.07 nm). It delivers a reversible capacity of 295 mAh g−1 and an ultra-large capacity of 248.2 mAh g−1 (84% of the reversible capacity) at low-voltage plateau, in which an intercalation mechanism is proposed for Na ion storage. Exquisite differential scanning calorimetry (DSC) analysis suggests that soliated hard carbon has better thermal stability than that of metallic Na.
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