Holey tungsten oxynitride nanowires with superior conductivity, good biocompatibility, and good stability achieve excellent performance as anodes for both asymmetric supercapacitors and microbial fuel cells. Moreover, an innovative system is devised based on these as-prepared tungsten oxynitride anodes, which can simultaneously realize both energy conversion from chemical to electric energy and its storage.
The poor intrinsic conductivity of MoS2 presents a huge
barrier for the exploitation of its versatile properties, especially
as an electrochemical capacitor (EC) electrode and hydrogen evolution
reaction (HER) catalyst. Toward this challenge, TiN nanorods coated
by randomly oriented MoS2 nanosheets (TMSs) are engineered
as state-of-the-art electrodes for ECs and HER. In light of the synergistic
effects, TMS electrodes show favorable performance as both a binder-free
EC electrode and HER catalyst. Importantly, the optimal TMS achieves
an areal capacitance of 662.2 mF cm–2 at 1 mA cm–2 with superior rate capability and ultralong cycling
stability. As the catalyst for HER in 0.5 M H2SO4, it shows an overpotential of 146 mV at 10 mA cm–2, a favorable Tafel slope, and good electrocatalytic stability. All
of the results highlight the favorable integration of TiN and MoS2 and provide clear insight correlating the hybrid structure
and the corresponding electrochemical performance.
MnSe with high theoretical capacity and reversibility is considered as a promising material for the anode of sodium ion batteries. In this study, MnSe nanoparticles embedded in 1D carbon nanofibers (MnSe-NC) are successfully prepared via facile electrospinning and subsequent selenization. A carbon framework can effectively protect MnSe dispersed in it from agglomeration and can accommodate volume variation in the conversion reaction between MnSe and Na+ to guarantee cycling stability. The 1D fiber structure can increase the area of contact between electrode and electrolyte to shorten the diffusion path of Na+ and facilitate its transfer. According to the kinetic analysis, the storage process of sodium by MnSe-NC is a surface pseudocapacitive-controlled process with promising rate capability. Impressively, An MnSe-NC anode in sodium ion full cells is investigated by pairing with an Na3V2(PO4)2@rGO cathode, which exhibits a reversible capacity of 195 mA h g−1 at 0.1 A g−1.
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