材料科学
电化学
石墨烯
阴极
兴奋剂
化学工程
电极
电导率
煅烧
纳米技术
光电子学
化学
物理化学
催化作用
生物化学
工程类
作者
Jie Wang,Yifeng Yuan,Xianhui Rao,Min’an Yang,Li Wang,Ailing Zhang,Yan Chen,Zhaolin Li,Hailei Zhao
标识
DOI:10.1007/s12613-023-2666-x
摘要
Na3V2(PO4)2O2F (NVPOF) has received considerable interest as a promising cathode material for sodium-ion batteries because of its high working voltage and good structural/thermal stability. However, the sluggish electrode reaction resulting from its low intrinsic electronic conductivity significantly restricts its electrochemical performance and thus its practical application. Herein, Nb-doped Na3V2−xNbx(PO4)2O2F/graphene (rGO) composites (x = 0, 0.05, 0.1) were prepared using a solvothermal method followed by calcination. Compared to the un-doped NVPOF/rGO, doping V-site with high-valence Nb element (Nb5+) (Na3V1.95Nb0.05(PO4)2O2F/rGO (NVN05POF/rGO)) can result in the generated V4+/V3+ mixed-valence, ensuring the lower bandgap and thus the increased intrinsic electronic conductivity. Besides, the expanded lattice space favors the Na+ migration. With the structure feature where NVN05POF particles are attached to the rGO sheets, the electrode reaction kinetics is further accelerated owing to the well-constructed electron conductive network. As a consequence, the as-prepared NVN05POF/rGO sample exhibits a high specific capacity of ∼72 mAh·g−1 at 10C (capacity retention of 65.2% (vs. 0.5C)) and excellent long-term cycling stability with the capacity fading rate of ∼0.099% per cycle in 500 cycles at 5C.
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