RESUMEN
The electrochemical performance of carbon nanofiber (CNF) electrodes in vanadium redox flow batteries (VRFBs) is enhanced by optimizing the morphological and physical properties of low-cost electrospun CNFs. The surface area, porosity and electrical conductivity of CNFs are tailored by modifying the precursor composition, especially the sacrificing agent, Fe(acac)3, in the polymer precursor and carbonization temperature. A highly porous structure with a large surface area is generated by the catalytic growth of graphitic carbon spheres surrounding the iron nanoparticles which are removed by an acid etching process. The graphitic carbon layers formed at a high carbonization temperature improve the electrical conductivity of CNFs. The large surface area of 349 m2 g-1 together with the abundant mesopore-dominant structure leads to high wettability and high activity for redox reactions of the electrode, giving rise to enhanced electrochemical performance in VRFBs. It delivers an energy efficiency (EE) of 91.4% at a current density of 20 mA cm-2 and 79.3% at 100 mA cm-2, and maintains an average EE of 72.5% after 500 charge/discharge cycles at 100 mA cm-2.
RESUMEN
Metallic sodium (Na) is an appealing anode material for high-energy Na batteries. However, Na metal suffers from low coulombic efficiencies and severe dendrite growth during plating/stripping cycles, causing short circuits. As an effective strategy to improve the deposition behavior of Na metal, a 3D carbon foam is developed that is sputter-coated with gold nanoparticles (Au/CF), forming a functional gradient through its thickness. The highly porous Au/CF host is proven to have gradually varying sodiophilicity, which in turn facilitates initially preferential Na deposition on the gold-rich, sodiophilic region in a "bottom-up growth" mode, leading to uniform plating over the entire Au/CF host. This finding contrasts with dendrite formation in the pristine CF host, as proven by in situ microscopy. The Na-predeposited Au/CF (Na@Au/CF) composite anode operates steadily for 1000 h at a low overpotential of ≈20 mV at 2 mA cm-2 in a symmetric cell. When the composite anode is coupled with a Na3 V2 (PO4 )2 F3 cathode, the full cell has a high capacity of 102.1 mAh g-1 after 500 cycles at 2 C. The sodiophilicity gradient design that is explored in this study offers new insight into developing porous Na metal hosts with highly stable plating/stripping performance for next-generation Na batteries.
RESUMEN
Freestanding carbon-based electrodes with large surface areas and pore volumes are essential to fast ion transport and long-term energy storage. Many of the current porous carbon substrates are composed of particulates, making it difficult to form a self-supported structure. Herein, novel highly porous nitrogen-doped graphene fiber webs (N-GFWs) are prepared using a facile wet-spinning method. The wet chemical process facilitates simultaneous N-doping and surface wrinkling of graphene fibers in a one-pot process. The atomic structure and electrical conductivity of N-GFWs are tailored by tuning the degree of N-doping and thermal reduction for multi-battery charge storage in both lithium-oxygen batteries (LOBs) and lithium-sulfur batteries (LSBs). The N-GFW900 electrode presents an excellent electrocatalytic activity and the cathode with a high areal loading of 7.5 mg cm-2 delivers a remarkable areal capacity of 2 mA h cm-2 at 0.2 mA cm-2 for LOBs. The N-GFW700 interlayer with abundant oxygenated and nitrogen functional groups demonstrates effective entrapment of polysulfides in LSBs, delivering a much improved specific capacity after 200 cycles at 0.5C with a remarkable decay rate of 0.04%. The current approach paves the way for rational design of porous graphene-based electrodes, satisfying multifunctional requirements for high-energy storage applications.
