VOC Bonding of Heterointerface Boosting Kinetics of Free‐Standing Na5V12O32 Cathode for Ultralong Lifespan Sodium‐Ion Batteries

作者：Xuexia Song, Xifei Li, Hui Shan, Jingjing Wang, Wenbin Li, Kaihua Xu, Kun Zhang, Hirbod Maleki Kheimeh Sari, Lei Li, Wei Xiao, Jian Qin, Chong Xie, Xueliang Sun · 发表于：Advanced Functional Materials · 年份：2023 · DOI：10.1002/adfm.202303211 · 被引用次数：79 · 研究领域：Advancements in Battery Materials、Supercapacitor Materials and Fabrication、Transition Metal Oxide Nanomaterials

Abstract The flexible free‐standing cathodes with high energy density have been challenging toward wearable sodium‐ion batteries (SIBs). Herein, Na 5 V 12 O 32 nanobelts (NVO‐NBs)‐based heterostructure is fabricated with boosting the sodium‐ion kinetic characteristics to address the challenges. In the heterostructure, the controllable VOC bonds are generated at the interface originating from the chemical conversion of functional groups of the reduced graphene oxides (rGOs) with VO bonding of NVO through interfacial electronic interactions. The interfacial synergistic between the brilliant bonding properties and the inherent formation of a stress field at the heterointerface motivated by work function difference can reduce the Na + diffusion barrier, facilitate charge transfer, hence accelerates reaction kinetics and electron/ion transport, as well as modifying the electronic structure to realize a cherished adsorption energy of Na + . Therefore, the optimized NVO‐NBs‐based heterostructure exhibits exceptional rate capability (213 mAh g −1 at 0.2 C with 100 mAh g −1 at 10 C) and ultralong cycling stability (95.4%, 3000 cycles at 5 C). This work demonstrates that the controllable heterostructure interface with abundant chemical bonds is an effective approach to exploit potential cathodes for rechargeable batteries.