Dual-carbon coated Na3V2(PO4)3 derived from reduced graphene oxide and nanocellulose with porous structure for high performance sodium-ion batteries

石墨烯 纳米纤维素 碳化 材料科学 氧化物 多孔性 碳纤维 化学工程 基质(水族馆) 纳米技术 介孔材料 复合材料 纤维素 复合数 化学 扫描电子显微镜 有机化学 冶金 催化作用 工程类 地质学 海洋学
作者
Jiahao Li,Yanjun Chen,Tao Zhou,Hongen Shi,Zhichao Zheng,Yanzhong Wang,Li Guo
出处
期刊:Applied Surface Science [Elsevier]
卷期号:610: 155553-155553 被引量:33
标识
DOI:10.1016/j.apsusc.2022.155553
摘要

The intrinsic electronic conductivity of Na3V2(PO4)3 (NVP) limits its further application. Herein, a synergetic strategy for in situ synthesis of porous NVP using reduced graphene oxide (rGO) and nanocellulose as additional carbon sources is proposed. Specifically, the carbonization of GO forms a highly graphitized rGO substrate, which effectively hinders the agglomeration of NVP particles. Meanwhile, the disordered and thin carbon coating layers are generated by the carbonization of nanocellulose, constructing an interconnected conductive network with rGO substrate. The dual-carbon coated network significantly improves the electronic conductivity to enhance the kinetic characteristics. Furthermore, the active NVP grains form a porous structure by epitaxial homogenous growth on rGO, which is conducive to further utilization of active substances. The mesopores in the sample can serve as storage sites for Na+ to provide capacitive contributions to the reversible capacity, which makes the capacity exceeds the theoretical value of NVP. The optimized CNF-GC-3 delivers amazing electrochemical properties. It submits an impressive reversible specific capacity of 123.77 mAh/g at 1C and maintains 99.70 mAh/g after 700 cycles, corresponding to a capacity decay rate of 0.028 % per cycle. Even at 60C, it still exhibits a prominent discharge capacity of 95.59 mAh/g.
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