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Realizing a High‐Performance Na‐Storage Cathode by Tailoring Ultrasmall Na2FePO4F Nanoparticles with Facilitated Reaction Kinetics
In this paper, the synthesis of ultrasmall Na2FePO4F nanoparticles (≈3.8 nm) delicately embedded in porous N‐doped carbon nanofibers (denoted as Na2FePO4F@C) by electrospinning is reported. The as‐prepared Na2FePO4F@C fiber film tightly adherent on aluminum foil features great flexibility and is directly used as binder‐free cathode for sodium‐ion batteries, exhibiting admirable electrochemical performance with high reversible capacity (117.8 mAh g−1 at 0.1 C), outstanding rate capability (46.4 mAh g−1 at 20 C), and unprecedentedly high cyclic stability (85% capacity retention after 2000 cycles). The reaction kinetics and mechanism are explored by a combination study of cyclic voltammetry, ex situ structure/valence analyses, and first‐principles computations, revealing the highly reversible phase transformation of Na2FeIIPO4F ↔ NaFeIIIPO4F, the facilitated Na+ diffusion dynamics with low energy barriers, and the desirable pseudocapacitive behavior for fast charge storage. Pouch‐type Na‐ion full batteries are also assembled employing the Na2FePO4F@C nanofibers cathode and the carbon nanofibers anode, demonstrating a promising energy density of 135.8 Wh kg−1 and a high capacity retention of 84.5% over 200 cycles. The distinctive network architecture of ultrafine active materials encapsulated into interlinked carbon nanofibers offers an ideal platform for enhancing the electrochemical reactivity, electronic/ionic transmittability, and structural stability of Na‐storage electrodes.
Realizing a High‐Performance Na‐Storage Cathode by Tailoring Ultrasmall Na2FePO4F Nanoparticles with Facilitated Reaction Kinetics
In this paper, the synthesis of ultrasmall Na2FePO4F nanoparticles (≈3.8 nm) delicately embedded in porous N‐doped carbon nanofibers (denoted as Na2FePO4F@C) by electrospinning is reported. The as‐prepared Na2FePO4F@C fiber film tightly adherent on aluminum foil features great flexibility and is directly used as binder‐free cathode for sodium‐ion batteries, exhibiting admirable electrochemical performance with high reversible capacity (117.8 mAh g−1 at 0.1 C), outstanding rate capability (46.4 mAh g−1 at 20 C), and unprecedentedly high cyclic stability (85% capacity retention after 2000 cycles). The reaction kinetics and mechanism are explored by a combination study of cyclic voltammetry, ex situ structure/valence analyses, and first‐principles computations, revealing the highly reversible phase transformation of Na2FeIIPO4F ↔ NaFeIIIPO4F, the facilitated Na+ diffusion dynamics with low energy barriers, and the desirable pseudocapacitive behavior for fast charge storage. Pouch‐type Na‐ion full batteries are also assembled employing the Na2FePO4F@C nanofibers cathode and the carbon nanofibers anode, demonstrating a promising energy density of 135.8 Wh kg−1 and a high capacity retention of 84.5% over 200 cycles. The distinctive network architecture of ultrafine active materials encapsulated into interlinked carbon nanofibers offers an ideal platform for enhancing the electrochemical reactivity, electronic/ionic transmittability, and structural stability of Na‐storage electrodes.
Realizing a High‐Performance Na‐Storage Cathode by Tailoring Ultrasmall Na2FePO4F Nanoparticles with Facilitated Reaction Kinetics
Wang, Fanfan (Autor:in) / Zhang, Ning (Autor:in) / Zhao, Xudong (Autor:in) / Wang, Lixuan (Autor:in) / Zhang, Jian (Autor:in) / Wang, Tianshi (Autor:in) / Liu, Fanfan (Autor:in) / Liu, Yongchang (Autor:in) / Fan, Li‐Zhen (Autor:in)
Advanced Science ; 6
01.07.2019
10 pages
Aufsatz (Zeitschrift)
Elektronische Ressource
Englisch
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