Tuning the Closed Pore Structure of Hard Carbons with the Highest Na Storage Capacity

被引:501
作者
Meng, Qingshi [1 ,2 ]
Lu, Yaxiang [1 ,2 ]
Ding, Feixiang [1 ,2 ]
Zhang, Qiangqiang [1 ,2 ]
Chen, Liquan [1 ,2 ]
Hu, Yong-Sheng [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Phys, Beijing Natl Lab Condensed Matter Phys, Key Lab Renewable Energy,Beijing Key Lab New Ener, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
基金
英国工程与自然科学研究理事会;
关键词
SODIUM-ION BATTERIES; ANODE MATERIALS; MICROSPHERES; PHOSPHORUS;
D O I
10.1021/acsenergylett.9b01900
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
High-capacity anode materials are one of the bottlenecks to further improve the energy density of Na-ion batteries (NIBs). Except for introducing more defects to increase the sloping capacity, tuning the closed porous structure to boost the plateau capacity is another direction. Here by adopting phenol-formaldehyde resin (PF) as the carbon precursor and ethanol (EtOH) as the pore-forming agent, through precise chemical regulation of their relative content during a solvothermal process before further carbonization, carbon anodes with appropriate microstructure are achieved. It is found that the function of EtOH rests on generating steam vapor to create a pore cavity among cross-linked matrixes. The obtained optimal anodes exhibit a high Na storage capacity of ca. 410 mAh/g. When pairing with an O3-NaNi1/3Fe1/3Mn1/3O2 cathode, the full cell delivers a high initial Coulombic efficiency of 83% and energy density of ca. 300 Wh/kg. The proposed chemical regulation approach via a pore-forming strategy is simple and practical to enable high-energy-density NIBs.
引用
收藏
页码:2608 / +
页数:9
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