One dimensional pea-shaped NiSe_(2) nanoparticles encapsulated in N-doped graphitic carbon fibers to boost redox reversibility in sodium-ion batteries

In recent years,sodium-ion batteries(SIBs)have emerged as a promising technology for energy storage systems(ESSs)because of the abundance and affordability of sodium.Recently,metal selenides have been studied as promising high-performance conversion-type anode materials in SIBs.Among them,nickel se-lenide(NiSe_(2))has received considerable attention due to its high theoretical capacity of 495 mAh g^(-1)and conductivity.However,it still suffers from poor cycling stability because of the low electrochemical reactivity,large volume expansion,and structural instability during cycles.To address these challenges,NiSe_(2)nanoparticles encapsulated in N-doped graphitic carbon fibers(NiSe_(2)@NGCF)were synthesized by using ZIF-8 as a template.NiSe_(2)@NGCF showed a high discharge capacity of 558.3 mAh g^(-1)with a fading rate of 0.14%per cycle after 200 cycles at 0.5 A g^(-1)in 0.01-3.0 V.At a very high current density of 5 A g^(-1),the capacity still displayed excellent long-term cycle life with a discharge capacity of 406.1 mAh g^(-1)with a fading rate of 0.016%per cycle after 3000 cycles.The mechanism of the excellent electrochem-ical performance of NiSe_(2)@NGCF was thoroughly investigated by ex-situ XRD,TEM,and SEM analyses.Furthermore,NiSe_(2)@NGCF//Na_(3)V_(2)(PO_(4))_(3)full-cell also delivered an excellent reversible capacity of 378.7 mAh g^(−1)at 0.1 A g^(−1)after 50 cycles,demonstrating its potential for practical application in SIBs.

One-dimensional Li_(3)VO_(4)/carbon fiber composites for enhanced electrochemical performance as an anode material for lithium-ion batteries

Lithium vanadium oxide(Li_(3)VO_(4))has gained attention as an alternative anode material because of its higher theoretical capacity(592 mAh g^(−1)),moderate ionic conductivity(∼10^(−4)S cm^(−1)),and lower working voltage range(∼0.5–1.0 V vs.Li/Li^(+))in comparison to other metal oxides.However,there are disadvantages to using Li_(3)VO_(4)as an anode material,such as low initial Coulombic efficiency and poor rate performance that is attributed to its low electronic conductivity(<10^(−1)0 S cm^(−1)).In the present study,the synthesis of one-dimensional Li_(3)VO_(4)electrode was performed via a facile method by using oxidized vapor grown carbon fiber as a template and the formation of the outer shells of conductive carbon via chemical vapor deposition technique.In a half-cell configuration,the prepared Li_(3)VO_(4)composites exhib-ited an enhanced electrochemical performance with a reversible capacity of 516.2 mAh g^(−1)after 100 cycles at a rate of 0.5 C within the voltage range of 0.01–3.0 V.At a high rate of 5 C,a large reversible capacity of 322.6 mAh g^(−1)was also observed after 500 cycles.The full cell(LVO/VGCF16-C||LiCoO_(2))using LiCoO_(2)as the cathode showed competitive electrochemical performance,which demonstrates its high potential in commercial applications.

Enhanced electrochemical performance of graphitic carbon-wrapped spherical FeOF nanoparticles using maleopimaric acid as a cathode material for sodium-ion batteries

Sodium-ion batteries(SIBs)are considered one of the most promising energy storage systems for replacing lithium-ion batteries because of the high abundance and low cost of sodium.Iron oxyfluoride(FeOF)is a promising conversion-based cathode material for SIBs because of its high theoretical capacity of about855 mA h g^(-1),low-cost chemical compositions,and its lower sensitivity to the size of charged carrier ions.However,the poor electrical conductivity and ionic diffusion of FeOF result in a low rate capability and cyclability.In this work,FeOF nanoparticles wrapped by graphitic carbon layers were synthesized using abietic or maleopimaric acid as both the carbon source and organic ligand.In addition,the morphology of the FeOF particles was gradually controlled from rod to spherical shapes,simply depending on the rosin acids.The FeOF nanoparticles prepared with maleopimaric acid showed a large reversible discharge capacity of 356.7 mA h g^(-1)with a fading rate of 0.21%per cycle after 100 cycles at a current density of 100 mA g^(-1)and an excellent rate capability.