阳极
磷
钠
碳纤维
兴奋剂
离子
生物量(生态学)
材料科学
多孔性
化学工程
无机化学
化学
光电子学
复合材料
电极
地质学
有机化学
冶金
复合数
物理化学
海洋学
工程类
作者
Pei Liang,Zhi Huo,Yangjie Liu,Bo Zheng,Yongmin Wu,Xiangyun Hu,Zhenhai Wen
标识
DOI:10.1002/batt.202400694
摘要
Biomass‐derived hard carbon, despite being promising for anode material of sodium‐ion batteries, usually suffer from low initial coulombic efficiency (ICE), poor rate capacity, and limited cycling stability caused by complex surface defects and low intrinsic conductivity. Herein, phosphorus‐doped porous hard carbon (HC@PC‐P) were synthesized by the thermal polymerization of soy lecithin on the surfaces of hard carbon derived from olive kernels. The incorporation of heteroatom phosphorus in the porous hard carbon framework expands the carbon lattice spacing, optimizes the graphitization degree, and increases electrical conductivity, guaranteeing ensuring rapid electron and ion transfer. These coupling effects enable HC@PC‐P anode to achieve a high reversible capacity of 350 mAh g‐1 at 0.1 A g‐1, an impressive initial coulombic efficiency of 89.6%, and remarkable long‐term cycling stability at 1 A g‐1 over 1000 cycles with negligible capacity fade. The mechanisms behind sodium storage and enhanced electrochemical performance were elucidated by ex‐situ Raman spectroscopy and kinetic analysis. Additionally, the assembled HC@PC‐P//Na3V2(PO4)3 full cell demonstrated a high energy density of 257.9 Wh kg‐1. This work provides a rational guide for designing advanced hard carbon anode materials for high‐energy sodium‐ion batteries.
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