The design of a freestanding electrode is the key to the development of energy storage devices with superior electrochemical performance and mechanical durability. Herein, we propose a highly-scalable strategy for the facile synthesis of a freestanding alluaudite NaFe(SO)@porous carbon-nanofiber hybrid film, which is used as a self-supported and flexible electrode for sodium ion batteries. By the combined use of electrospinning and electrospraying, the freestanding hybrid film is constructed in the form of sulfate nanoparticles enwrapped in highly porous graphitic-like carbon-nanofibers. The multimodal porous architecture of the freestanding hybrid film ensures its superiority in mechanical flexibility and structural stability during repeated electrochemical processes, which meets the long-standing challenge of practical application. Moreover, both the highly conductive and porous framework and the nanoscale particles are favorable for promoting fast electron/ion transport capability. Compared with other carbon based supports such as graphene (GA), carbon nanotubes (CNTs) and active carbons (ACs), the flexible carbon nanofiber shows better interaction with electrochemical active materials and superior electrochemical properties. It retains over 95% of the capacity after five hundred cycles at alternate rates of 40C and 5C, which demonstrates the superior ultralong time and high-rate cycling capability. Therefore, the present work provides a facile and highly scalable strategy for the design and fabrication of high-performance freestanding sulfate cathodes for advanced sodium ion batteries.

No abstract

Pt catalyst supported on nanocapsule MWCNTs-Al(2)O(3) (multi-walled carbon nanotubes, MWCNTs) catalyst has been prepared by microwave-assisted polyol process (MAPP). The results of electrochemical measurements show that the nanocapsule Pt/MWCNTs-Al(2)O(3) catalyst has higher activity due to more uniform dispersion and smaller size of Pt nanoparticles, and higher stability ascribed to the stronger metal-support interaction (SMSI) between Pt nanoparticles and nanocapsule support than in Pt/MWCNTs. Furthermore, the carbon-riveted nanocapsule Pt/MWCNTs-Al(2)O(3) catalyst has been designed and synthesized on the basis of in situ carbonization of glucose. The physical characteristics such as X-ray diffraction (XRD), energy dispersive analysis of X-ray (EDAX), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) have indicated that α-Al(2)O(3) indeed entered into the inside of the MWCNTs and formed a nanocapsule support of MWCNTs with α-Al(2)O(3) as stuffing. The accelerated potential cycling tests (APCT) show that carbon-riveted nanocapsule Pt/MWCNTs-Al(2)O(3) possesses 10 times the stability of Pt/C and has 4.5 times the life-span of carbon-riveted Pt/TiO(2)-C reported in our previous work. The significantly enhanced stability for carbon-riveted nanocapsule Pt/MWCNTs-Al(2)O(3) catalyst is attributed to the reasons as follows: the inherently excellent mechanical resistance and stability of α-Al(2)O(3) and MWCNTs in acidic and oxidative environments; SMSI between Pt nanoparticles and the nanocapsule support; the anchoring effect of the carbon layers formed during the carbon-riveting process (CRP); the increase of Pt(0) composition during CRP.