阳极
纳米片
化学
电极
动力学
储能
纳米技术
化学工程
纳米颗粒
电化学
工作(物理)
钠
阴极
软件部署
瞬态(计算机编程)
化学动力学
超短脉冲
自组装
作者
Yanhua Wan,Haichen Liang,Qiulong Wei,Linfan Duan,Pengcheng Qiu,Bin Ru,Wei Zhang,Xingmiao Zhang,Xiao Wang,Dongliang Chao,Fei Wang,Yonggang Wang,Dongyuan Zhao,Wei Li
摘要
Sodium-ion batteries represent promising energy storage devices, yet their deployment is severely hampered by sluggish ion-transport kinetics and unstable electrode-electrolyte interfacial chemistry that deteriorate rate capability and cycling lifespan, particularly under high-loading electrode configurations. Here, we report a structural anode design comprising double-shelled TiO2 spheres assembled from cross-distributed 2 nm thick nanosheets and uniformly encapsulated by a graphene-like armor. This architecture enables predominantly surface-controlled sodium storage behavior with ultrafast reaction kinetics and exceptional stability, overcoming the long-standing trade-off between capacity, rate performance, and cycle life. The rationally designed electrode achieves a practically relevant areal capacity of 2.13 mAh cm-2 and outstanding rate capability (121 mAh g-1 at 100 C). Remarkably, it remains more than 90% of its capacity over 3,000 cycles at 5 C under a high mass loading of 10.5 mg cm-2, outperforming conventional anode structures. This work establishes a structural design strategy for advanced anodes applicable in practical high-power batteries.
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