纳米点
材料科学
纳米技术
电化学
碳纳米管
纳米尺度
化学工程
纳米结构
碳纤维
动力学
微电极
扩散
超短脉冲
纳米颗粒
电催化剂
钠
钒
纳米线
成核
电容感应
化学气相沉积
阳极
模板方法模式
作者
Naohisa Okita,Keisuke Matsumura,Yuta Harada,Masahiro Fukuyama,Mai Tomita,Masaya Nakagawa,Yuto Iwasaki,Akari Ukai,Kangkang Ge,Etsuro Iwama,Wako Naoi,Patrick Rozier,Patrice Simon,Katsuhiko Naoi
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-10-07
卷期号:25 (41): 14872-14879
被引量:2
标识
DOI:10.1021/acs.nanolett.5c03272
摘要
Polyanion-substituted sodium vanadium phosphate (Na3V2(PO4)3, NVP) derivatives, including SO4, BO3, WO4, and SiO4 substitutions, were systematically synthesized and impregnated with a nanocarbon network via ultracentrifugation. Among them, nanosized (5-30 nm), highly crystalline, and well-dispersed sulfate-substituted NVP (NVPS) nanodots were directly nucleated onto multiwalled carbon nanotubes, enabling ultrafast electrochemical kinetics. This nanoscale architecture delivered exceptional rate capability, achieving 97 mAh g-1 at 1000C (3.6 s discharge), corresponding to 83% of the theoretical capacity, outperforming conventional NVP. The electrochemical kinetics analysis using a cavity microelectrode revealed reduced polarization, enhanced capacitive charge storage, and rapid sodium ion diffusion during intercalation/deintercalation, facilitated by the conformal interface between NVPS and MWCNT, possibly by sulfate-induced surface modifications. These findings establish polyanion substitution and ultracentrifugation-assisted materials processing as a transformative strategy for overcoming intrinsic transport limitations in NASICON-type phosphates, positioning NVPS as a benchmark material for next-generation high-power sodium-ion batteries and hybrid capacitors.
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