Amorphous FeP@porous carbon nanofibers with sterically conductive networks for stable potassium-ion storage

被引:0
作者
Wan, Qi [1 ]
Zhao, Jie [1 ]
Liu, Yu [2 ]
Li, Linshu [1 ]
Yan, Juwei [1 ]
Tan, Qiwei [3 ]
Xu, Xun [1 ]
Zhang, Qingchun [1 ]
Wei, Xijun [1 ]
Ni, Ling [4 ]
Li, Ping [3 ]
机构
[1] Southwest Univ Sci & Technol, Sch Mat & Chem, State Key Lab Environm Friendly Energy Mat, Mianyang 621010, Sichuan, Peoples R China
[2] Univ Elect Sci & Technol China, Sch Mat & Energy, Chengdu 611731, Sichuan, Peoples R China
[3] Univ Sci & Technol Beijing, Inst Adv Mat & Technol, Beijing 100083, Peoples R China
[4] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, Qingdao 266101, Peoples R China
关键词
NANOPARTICLES; BATTERIES; ANODE; FILM;
D O I
10.1039/d5nr00116a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Structural instability in electrode materials is a critical barrier to the practical application of potassium-ion batteries (PIBs) in terms of long-term durability. To overcome this, we integrated amorphous FeP within continuous three-dimensional (3D) carbon fiber networks, fabricated through an electrospinning process. The amorphous structure of FeP facilitates isotropic volume expansion, effectively distributing stress uniformly across the electrode and mitigating degradation during cycling. Additionally, the loosely packed atomic arrangement and interconnected 3D conductive framework enable smoother potassium-ion diffusion, thereby enhancing the kinetic performance. Therefore, the well-designed amorphous FeP/porous carbon nanofibers (A-FeP@PCNFs) exhibit a remarkable specific capacity of 358.3 mA h g-1 at 0.1 A g-1 and demonstrate exceptional cycling durability, retaining a reversible capacity of 152.0 mA h g-1 after 2400 cycles at 3 A g-1. This innovative design offers a robust approach for developing excellent electrochemical performance anode materials with superior structural stability and rapid electrochemical response, advancing the potential of PIBs in energy storage applications.
引用
收藏
页码:10371 / 10379
页数:9
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