磷化物
材料科学
阳极
电化学
锂(药物)
静电纺丝
化学工程
纳米纤维
纳米技术
碳纳米纤维
碳纤维
电极
复合数
复合材料
冶金
聚合物
碳纳米管
化学
金属
工程类
内分泌学
物理化学
医学
作者
Yang Yang,Wenbin Fu,Crystal Bell,Dong‐Chan Lee,Matthew Drexler,Yanna Nuli,Zhenqiang Ma,Alexandre Magasinski,Gleb Yushin,Faisal M. Alamgir
标识
DOI:10.1021/acsami.1c05989
摘要
Iron phosphide with high specific capacity has emerged as an appealing candidate for next-generation lithium-ion battery anodes. However, iron phosphide could undergo conversion reactions and generally suffer from a rapid capacity degradation upon cycling due to its structure pulverization. Chemomechanical breakdown of iron phosphide due to its rigidity has been a challenge to fully realizing its electrochemical performance. To address this challenge, we report here on an enticing opportunity: a flexible, free-standing iron phosphide anode with Fe2P nanoparticles confined in carbon nanofibers may overcome existing challenges. For the synthesis, we introduce a facile electrospinning strategy that enables in situ formation of Fe2P within a carbon matrix. Such a carbon matrix can effectively minimize the structure change of Fe2P particles and protect them from pulverization, allowing the electrodes to retain a free-standing structure after long-term cycling. The produced electrodes showed excellent electrochemical performance in lithium-ion half and full cells, as well as in flexible pouch cells. These results demonstrate the successful development of iron phosphide materials toward high capacity, light weight, and flexible energy storage.
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