阳极
磷化物
储能
碳纳米管
纳米技术
法拉第效率
材料科学
电解质
电池(电)
纳米管
化学工程
化学
电极
冶金
金属
工程类
功率(物理)
物理
物理化学
量子力学
作者
Lingbo Ren,Xinhua Zhou,Zhidong Hou,Zhixuan Luo,Yu Huyan,Chunguang Wei,Jian‐Gan Wang
标识
DOI:10.1016/j.jcis.2024.03.050
摘要
The conversion-type anode material of iron phosphide (FeP) promises enormous prospects for Na-ion battery technology due to its high theoretical capacity and cost-effectiveness. However, the poor reaction kinetics and large volume expansion of FeP significantly degrade the sodium storage, which remains a daunting challenge. Herein, we demonstrate a binder-free nanotube array architecture constructed by FeP@C hybrid on carbon cloth as advanced anodes to achieve fast and stable sodium storage. The nanotubular structure functions in multiple roles of providing short electron/ion transport distances, smooth electrolyte diffusion channels, and abundant active sites. The carbon layer could not only pave high-speed pathways for electron conductance but also cushion the volume change of FeP. Benefiting from these structural virtues, the FeP@C anode receives a high reversible capacity of 881.7 mAh/g at 0.1 A/g, along with a high initial Coulombic efficiency of 90% and excellent rate capability and cyclability in half and full cells. Moreover, the sodium energy reaction kinetics and mechanism of FeP@C are systematically studied. The present work offers a rational design and construction of high-capacity anode materials for high-energy–density Na-ion batteries.
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