Rechargeable aqueous zinc-ion batteries are highly desirable for grid-scale applications due to their low cost and high safety; however, the poor cycling stability hinders their widespread application. Herein, a highly durable zinc-ion battery system with a NaVO·1.63HO nanowire cathode and an aqueous Zn(CFSO) electrolyte has been developed. The NaVO·1.63HO nanowires deliver a high specific capacity of 352 mAh g at 50 mA g and exhibit a capacity retention of 90% over 6000 cycles at 5000 mA g, which represents the best cycling performance compared with all previous reports. In contrast, the NaVO nanowires maintain only 17% of the initial capacity after 4000 cycles at 5000 mA g. A single-nanowire-based zinc-ion battery is assembled, which reveals the intrinsic Zn storage mechanism at nanoscale. The remarkable electrochemical performance especially the long-term cycling stability makes NaVO·1.63HO a promising cathode for a low-cost and safe aqueous zinc-ion battery.
Rechargeable aqueous zinc-ion batteries have offered an alternative for large-scale energy storage owing to their low cost and material abundance. However, developing suitable cathode materials with excellent performance remains great challenges, resulting from the high polarization of zinc ion. In this work, an aqueous zinc-ion battery is designed and constructed based on H V O nanowire cathode, Zn(CF SO ) aqueous electrolyte, and zinc anode, which exhibits the capacity of 423.8 mA h g at 0.1 A g , and excellent cycling stability with a capacity retention of 94.3% over 1000 cycles. The remarkable electrochemical performance is attributed to the layered structure of H V O with large interlayer spacing, which enables the intercalation/de-intercalation of zinc ions with a slight change of the structure. The results demonstrate that exploration of the materials with large interlayer spacing is an effective strategy for improving electrochemical stability of electrodes for aqueous Zn ion batteries.
Electrocatalytic water splitting is one of the sustainable and promising strategies to generate hydrogen fuel but still remains a great challenge because of the sluggish anodic oxygen evolution reaction (OER). A very effective approach to dramatically decrease the input cell voltage of water electrolysis is to replace the anodic OER with hydrazine oxidation reaction (HzOR) due to its lower thermodynamic oxidation potential. Therefore, developing the low-cost and efficient HzOR catalysts, coupled with the cathodic hydrogen evolution reaction (HER) is tremendously important for energysaving electrolytic hydrogen production. Herein, a new-type copper-nickel nitride (Cu 1 Ni 2 -N) with rich Cu 4 N/Ni 3 N interface is rationally constructed on the carbon fiber cloth. The three-dimensional electrode exhibits extraordinary HER performance with an overpotential of 71.4 mV at 10 mA cm -2 in 1.0 M KOH, simultaneously delivering an ultralow potential of 0.5 mV at 10 mA cm -2 for HzOR in 1.0 M KOH/0.5 M hydrazine electrolyte. Moreover, the electrolytic cell utilizing the synthesized Cu 1 Ni 2 -N electrode as both the cathode and anode displays a cell voltage of 0.24 V at 10 mA cm -2 with an excellent stability over 75 h. The present work develops the promising copper-nickel-based nitride as a bifunctional electrocatalyst through hydrazine-assistance for energy-saving electrolytic hydrogen production.
The aqueous zinc ion batteries (ZIBs) composed of inexpensive zinc anode and nontoxic aqueous electrolyte are attractive candidates for large-scale energy storage applications. However, their development is limited by cathode materials, which often deliver inferior rate capability and restricted cycle life. Herein, the VO 2 nanorods show significant electrochemical performance when used as an intercalation cathode for aqueous ZIBs. Specifically, the VO 2 nanorods display high initial capacity of 325.6 mAh g −1 at 0.05 A g −1 , good rate capability, and excellent cycling stability of 5000 cycles at 3.0 A g −1 . Furthermore, the VO 2 unit cell expands in a, b, and c directions sequentially during the discharge process and contracts back reversibly during the charge process, and the zinc storage mechanism is revealed to be a highly reversible single-phase reaction by operando techniques and corresponding qualitative analyses. Our work not only opens a new door to the practical application of VO 2 in ZIB systems but also broadens the horizon in understanding the electrochemical behavior of rechargeable ZIBs.
Hydrogen evolution reaction performance of MoS can be enhanced through electric-field-facilitated electron transport. The best catalytic performance of a MoS nanosheet can achieve an overpotential of 38 mV (100 mA cm ) at gate voltage of 5 V, the strategy of utilizing the electric field can be used in other semiconductor materials to improve their electrochemical catalysis for future relevant research.
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