Insights into the Na+ Storage Mechanism of Phosphorus-Functionalized Hard Carbon as Ultrahigh Capacity Anodes

被引:244
作者
Li, Yu [1 ]
Yuan, Yifei [2 ]
Bai, Ying [1 ]
Liu, Yuanchang [1 ]
Wang, Zhaohua [1 ]
Li, Limin [1 ]
Wu, Feng [1 ,3 ]
Amine, Khalil [2 ]
Wu, Chuan [1 ,3 ]
Lu, Jun [2 ]
机构
[1] Beijing Inst Technol, Beijing Key Lab Environm Sci & Engn, Sch Mat Sci & Engn, Beijing 100081, Peoples R China
[2] Argonne Natl Lab, Chem Sci & Engn Div, 9700 South Cass Ave, Argonne, IL 60439 USA
[3] Collaborat Innovat Ctr Elect Vehicles Beijing, Beijing 100081, Peoples R China
关键词
first-principle calculations; hard carbon; phosphorous-functionalization; sodium ion batteries; ultrahigh capacity; SODIUM-ION BATTERIES; OXYGEN REDUCTION REACTION; LITHIUM-ION; PERFORMANCE; INSERTION; GRAPHENE; BEHAVIOR; CATHODE; NANOFIBERS; NANOTUBES;
D O I
10.1002/aenm.201702781
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hard carbon as a typical anode material for sodium ion batteries has received much attention in terms of its low cost and renewability. Herein, phosphorus-functionalized hard carbon with a specific honeycomb briquette shaped morphology is synthesized via electrospinning technology. When applied as an anode material for Na+ storage, it exhibits an impressively high reversible capacity of 393.4 mA h g(-1) with the capacity retention up to 98.2% after 100 cycles. According to first-principle calculation, the ultrahigh capacity of the as-prepared anode is ascribed to the enhancement of Na-absorption through formation of P=O and P-C bonds in graphitic layers when doped with phosphorus. Moreover, the increase of electron density around the Fermi level is found to be mainly caused by O atoms instead of P atoms.
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页数:7
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