杂原子
阳极
三聚氰胺
法拉第效率
碳纤维
材料科学
阴极
化学工程
热解
储能
电极
化学
纳米技术
有机化学
复合材料
工程类
复合数
物理化学
戒指(化学)
功率(物理)
物理
量子力学
作者
Ning Sun,Rui Zhao,Mengyao Xu,Shaohong Zhang,Razium Ali Soomro,Bin Xu
标识
DOI:10.1016/j.jpowsour.2023.232879
摘要
Although hard carbons are considered as promising anode candidates for commercial sodium-ion batteries (SIBs), the trade-off between high Na-storage capacity and initial coulombic efficiency (ICE) remains a critical challenge for their practical application. Herein, nitrogen/oxygen co-doped hard carbon microspheres (N/O–HCs) for SIBs are prepared by a simple solvothermal treatment to allow the efficient cross-linking of phenolic resin with melamine and followed high-temperature pyrolysis process. The heteroatom doping promotes structural disordering of hard carbons and generates more active sites for Na ion storage, whereas the cross-linking of melamine with phenol resin efficiently restricts the formation of surface defects. Therefore, the obtained N/O-HC-1200 electrode exhibits both high reversible Na-storage capacity of 319.7 mAh g−1 and much improved ICE of 81.6%. Moreover, the electrode demonstrates excellent cycle and rate performance with the capacity stabilized at 253.9 mAh g−1 at 1C over 1000 cycles. When coupled with NaFe1/3Ni1/3Mn1/3O2 cathode, the constructed full cell delivers a high energy density of 247.6 Wh kg−1 and outstanding rate capability with a retained capacity of 70 mAh g−1 at an ultrahigh current rate of 50C. The proposed work offers a new perspective on the surface chemistry and structural design of high-performance hard carbon anodes for SIBs.
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