摘要
Soft carbons have attracted extensive interests as competitive anodes for fast-charging sodium-ion batteries(SIBs);however,the high-rate performance is still restricted by their large ion migration barriers and sluggish reaction kinetics.Herein,we show a molecular design approach toward the fabrication of nitrogen and phosphorus codoped mesoporous soft carbon(NPSC).The key to this strategy lies in the chemical cross-linking reaction between polyphosphoric acid and p-phenylenediamine,associated with pyrolysis induced in-situ self-activation that creates mesoporous structures and rich heteroatoms within the carbon matrix.Thanks to the enlarged interlayer spacing,reduced ion diffusion length,and plentiful active sites,the obtained NPSC delivers a superb rate capacity of 215 mAh g-1 at 10 A g-1 and an ultralong cycle life of 4,700 cycles at 5 A g^(-1).Remarkably,the full cell shows 99%capacity retention during 100 continuous cycles,and maximum energy and power densities of 191 Wh kg^(-1)and 9.2 kW kg^(-1),respectively.We believe that such a synthetic protocol could pave a novel venue to develop soft carbons with unique properties for advanced SIBs.
出处
《Research》
SCIE
EI
CSCD
2024年第2期329-337,共9页
研究(英文)
基金
supported by the National Natural Science Foundation of China(22279104,51902261,and 61935017)
the National Key Research and Development Program of China(2020YFA0709900)
the Guangdong Basic and Applied Basic Research Foundation(2020A1515110604)
the Natural Science Basic Research Program of Shaanxi(2021JQ-107)
the Natural Science Foundation of Ningbo(202003N4053 and 202003N4046)
the Provincial Innovation and Entrepreneurship Training Program for College Students(S202110699517).