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Sodium superionic conductor (NASICON)‐type materials are getting more and more attention due to their high capacity and good cycling ability compared with other cathode materials in aqueous zinc ion batteries (AZIB). The present paper was to study the synthesis and electrochemical properties of two NASICON compounds of Na₃V₂(PO₄)₃and Na₃V₂(PO₄)₂F₃and to understand the impacts of fluorine. Both Na₃V₂(PO₄)₃and Na₃V₂(PO₄)₂F₃are synthesized by hydrothermal growth followed with annealing at 800°C in inert gas. With 3 mol/L Zn(CF₃SO₃)₂in water as electrolyte, Na₃V₂(PO₄)₃offered a high storage capacity, while Na₃V₂(PO₄)₂F₃demonstrated a high discharge voltage though low storage capacity. It was also found that the storage capacity of Na₃V₂(PO₄)₂F₃increases with increased cycles; however, the compound undergoes a gradual phase transition. It is discussed possible approaches to attain both high discharge voltage and large capacity with good cycling stability.

 

The ever‐increasing demand for clean sustainable energy has driven tremendous worldwide investment in the design and exploration of new active materials for energy conversion and energy‐storage devices. Tailoring the surfaces of and interfaces between different materials is one of the surest and best studied paths to enable high‐energy‐density batteries and high‐efficiency solar cells. Metal‐halide perovskite solar cells (PSCs) are one of the most promising photovoltaic materials due to their unprecedented development, with their record power conversion efficiency (PCE) rocketing beyond 25% in less than 10 years. Such progress is achieved largely through the control of crystallinity and surface/interface defects. Rechargeable batteries (RBs) reversibly convert electrical and chemical potential energy through redox reactions at the interfaces between the electrodes and electrolyte. The (electro)chemical and optoelectronic compatibility between active components are essential design considerations to optimize power conversion and energy storage performance. A focused discussion and critical analysis on the formation and functions of the interfaces and interphases of the active materials in these devices is provided, and prospective strategies used to overcome current challenges are described. These strategies revolve around manipulating the chemical compositions, defects, stability, and passivation of the various interfaces of RBs and PSCs.

 

A local electric field is induced to engineer the interface of vanadium pentoxide nanofibers (V₂O₅‐NF) to manipulate the charge transport behavior and obtain high‐energy and durable supercapacitors. The interface of V₂O₅‐NF is modified with oxygen vacancies (Vö) in a one‐step polymerization process of polyaniline (PANI). In the charge storage process, the local electric field deriving from the lopsided charge distribution around Vö will provide Coulombic forces to promote the charge transport in the resultant Vö‐V₂O₅/PANI nanocable electrode. Furthermore, an ≈7 nm porous PANI coating serves as the external percolated charge transport pathway. As the charge transfer kinetics are synergistically enhanced by the dual modifications, Vö‐V₂O₅/PANI‐based supercapacitors exhibit an excellent specific capacitance (523 F g⁻¹) as well as a long cycling lifespan (110% of capacitance remained after 20 000 cycles). This work paves an effective way to promote the charge transfer kinetics of electrode materials for next‐generation energy storage systems.

 

Abstract Ammonium vanadate with bronze structure (NH 4 V 4 O 10 ) is a promising cathode material for zinc-ion batteries due to its high specific capacity and low cost. However, the extraction of $${\text{NH}}_{{4}}^{ + }$$ NH 4 + at a high voltage during charge/discharge processes leads to irreversible reaction and structure degradation. In this work, partial $${\text{NH}}_{{4}}^{ + }$$ NH 4 + ions were pre-removed from NH 4 V 4 O 10 through heat treatment; NH 4 V 4 O 10 nanosheets were directly grown on carbon cloth through hydrothermal method. Deficient NH 4 V 4 O 10 (denoted as NVO), with enlarged interlayer spacing, facilitated fast zinc ions transport and high storage capacity and ensured the highly reversible electrochemical reaction and the good stability of layered structure. The NVO nanosheets delivered a high specific capacity of 457 mAh g −1 at a current density of 100 mA g −1 and a capacity retention of 81% over 1000 cycles at 2 A g −1 . The initial Coulombic efficiency of NVO could reach up to 97% compared to 85% of NH 4 V 4 O 10 and maintain almost 100% during cycling, indicating the high reaction reversibility in NVO electrode. 

Manganese dioxide (MnO 2 ) with a conversion mechanism is regarded as a promising anode material for lithium-ion batteries (LIBs) owing to its high theoretical capacity (∼1223 mA h g −1 ) and environmental benignity as well as low cost. However, it suffers from insufficient rate capability and poor cyclic stability. To circumvent this obstacle, semiconducting polypyrrole coated-δ-MnO 2 nanosheet arrays on nickel foam (denoted as MnO 2 @PPy/NF) are prepared via hydrothermal growth of MnO 2 followed by the electrodeposition of PPy on the anode in LIBs. The electrode with ∼50 nm thick PPy coating exhibits an outstanding overall electrochemical performance. Specifically, a high rate capability is obtained with ∼430 mA h g −1 of discharge capacity at a high current density of 2.67 A g −1 and more than 95% capacity is retained after over 120 cycles at a current rate of 0.86 A g −1 . These high electrochemical performances are attributed to the special structure which shortens the ion diffusion pathway, accelerates charge transfer, and alleviates volume change in the charging/discharging process, suggesting a promising route for designing a conversion-type anode material for LIBs. 

Iron hexacyanoferrate (FeHCF) particles were synthesized at room temperature with ethylenediaminetetraacetic acid (EDTA) at varying pH. The presence of EDTA produced faceted particles and increasing synthesis pH resulted in slower reaction kinetics and larger particles with lower water content and fewer anion vacancies determined by TGA and Mössbauer spectroscopy. Electrochemical testing of sodium metal half cells revealed higher capacity in FeHCF particles grown at lower pH with EDTA, obtaining a maximum discharge capacity of 151 mA h g −1 with 79% capacity retention after 100 cycles at 100 mA g −1 and a rate capability of 122 mA h g −1 at 3.2 A g −1 . In contrast, particles grown at higher pH had stunted low-spin Fe redox activity but with improved long-term cyclic stability. These findings demonstrate that small changes in synthesis pH can greatly affect the growth and electrochemical properties of FeHCF when using a pH sensitive chelating agent such as EDTA.