Realizing a High-Performance Na-Storage Cathode by Tailoring Ultrasmall NaFePOF Nanoparticles with Facilitated Reaction Kinetics.

In this paper, the synthesis of ultrasmall NaFePOF nanoparticles (≈3.8 nm) delicately embedded in porous N-doped carbon nanofibers (denoted as NaFePOF@C) by electrospinning is reported. The as-prepared NaFePOF@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 at 0.1 C), outstanding rate capability (46.4 mAh g 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 NaFePOF ↔ NaFePOF, 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 NaFePOF@C nanofibers cathode and the carbon nanofibers anode, demonstrating a promising energy density of 135.8 Wh kg 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.