材料科学
介孔材料
扩散
法拉第效率
化学工程
钛
基础(拓扑)
结晶
离子
电极
纳米技术
阳极
催化作用
物理化学
热力学
冶金
化学
工程类
数学分析
物理
量子力学
生物化学
数学
作者
Haichen Liang,Liangliang Liu,Nan Wang,Wei Zhang,Chin‐Te Hung,Xingmiao Zhang,Zhenghao Zhang,Linlin Duan,Dongliang Chao,Fei Wang,Yongyao Xia,Wei Li,Dongyuan Zhao
标识
DOI:10.1002/adma.202202873
摘要
Sodium-ion batteries (SIBs) are a promising candidate for grid-scale energy storage, however, the sluggish ion-diffusion kinetics brought by the large radius of Na+ seriously limits the performance of SIBs, let alone at low temperatures. Herein, a confined acid-base pair self-assembly strategy to synthesize unusual Ti0.88 Nb0.88 O4-x @C for high-performance SIBs operating at room and low temperatures is proposed. The confinement self-assembly of the acid-base pair around the micelles and confined crystallization by the carbon layer realize the formation of ordered and stoichiometric mesoporous frameworks with opened ion channels. Thus, the mesoporous Ti0.88 Nb0.88 O4-x @C exhibits rapid Na+ diffusion kinetics at 25 and -40 °C, which are one order higher than that of the nonporous one. A high reversible capacity of 233 mAh g-1 , excellent rate (a specific capacity of 103 mAh g-1 at 50 C), and cycling performances (<0.03% fading per cycle) can be observed at 25 °C. More importantly, even at -40 °C, the mesoporous Ti0.88 Nb0.88 O4-x @C can still deliver the 161 mAh g-1 capacity, a high initial Coulombic efficiency of 60% and outstanding cycling stability (99 mAh g-1 at 0.5 C after 500 cycles). It is believed this strategy opens a new avenue for constructing novel mesoporous electrode materials for low-temperature energy storage.
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