Metallic zinc is a promising anode candidate of aqueous zinc‐ion batteries owing to its high theoretical capacity and low redox potential. However, Zn anodes usually suffer from dendrite and side reactions, which will degrade their cycle stability and reversibility. Herein, we developed an in situ spontaneously reducing/assembling strategy to assemble a ultrathin and uniform MXene layer on the surface of Zn anodes. The MXene layer endows the Zn anode with a lower Zn nucleation energy barrier and a more uniformly distributed electric field through the favorable charge redistribution effect in comparison with pure Zn. Therefore, MXene‐integrated Zn anode exhibits obviously low voltage hysteresis and excellent cycling stability with dendrite‐free behaviors, ensuring the high capacity retention and low polarization potential in zinc‐ion batteries.

The electrochemical performance of vanadiumoxide-based cathodes in aqueous zinc-ion batteries (ZIBs) depends on their degree of crystallinity and composite state with carbon materials. An in situ electrochemical induction strategy was developed to fabricate a metal-organic-framework-derived composite of amorphous V 2 O 5 and carbon materials (a-V 2 O 5 @C) for the first time, where V 2 O 5 is in an amorphous state and uniformly distributed in the carbon framework. The amorphous structure endows V 2 O 5 with more isotropic Zn 2+ diffusion routes and active sites, resulting in fast Zn 2+ transport and high specific capacity. The porous carbon framework provides a continuous electron transport pathway and ion diffusion channels. As a result, the a-V 2 O 5 @C composites display extraordinary electrochemical performance. This work will pave the way toward design of ZIB cathodes with superior rate performance.

Aqueous zinc‐ion batteries (ZIBs) are considered to be a promising candidate for flexible energy storage devices due to their high safety and low cost. However, the scalable assembly of flexible ZIBs is still a challenge. Here, a scalable assembly strategy is developed to fabricate flexible ZIBs with an ultrathin all‐in‐one structure by combining blade coating with a rolling assembly process. Such a unique all‐in‐one integrated structure can effectively avoid the relative displacement or detachment between neighboring components to ensure continuous and effective ion‐ and/or loading‐transfer capacity under external deformation, resulting in excellent structural and electrochemical stability. Furthermore, the ultrathin all‐in‐one ZIBs can be tailored and edited controllably into desired shapes and structures, further extending their editable, stretchable, and shape‐customized functions. In addition, the ultrathin all‐in‐one ZIBs display the ability to integrate with perovskite solar cells to achieve an energy harvesting and storage integrated system. These enlighten a broad area of flexible ZIBs to be compatible with highly flexible and wearable electronics. The scaling‐up assembly strategy provides a route to design other ultrathin all‐in‐one energy storage devices with stretchable, editable, and customizable behaviors.

The co-insertion of dual ions can often offer

Metallic zinc is a promising anode candidate of aqueous zinc‐ion batteries owing to its high theoretical capacity and low redox potential. However, Zn anodes usually suffer from dendrite and side reactions, which will degrade their cycle stability and reversibility. Herein, we developed an in situ spontaneously reducing/assembling strategy to assemble a ultrathin and uniform MXene layer on the surface of Zn anodes. The MXene layer endows the Zn anode with a lower Zn nucleation energy barrier and a more uniformly distributed electric field through the favorable charge redistribution effect in comparison with pure Zn. Therefore, MXene‐integrated Zn anode exhibits obviously low voltage hysteresis and excellent cycling stability with dendrite‐free behaviors, ensuring the high capacity retention and low polarization potential in zinc‐ion batteries.

Please cite this article as: Xu, Y., Chen, X., Wang, Y., Yuan, Z., Stabbing r esistance of body ar mour panels impr egnated with shear thickening fluid, Composite Structures (2016), doi: http://dx.doi.org/10. 1016/ j.compstruct.2016.12.056 This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. Stabbing resistance of body armour panels impregnated with shear thickening fluid AbstractThis paper presents an investigation on the use of shear thickening fluid (STF) to improve stabbing resistance of soft ballistic body armour. STFs were produced from polyethylene glycol and silica nanoparticles. The effects of silica nanoparticle sizes and silica nanoparticle weight fraction were studied and STFs made with the different compositions were used to impregnate the Twaron ® woven fabrics. Systemic investigations into rheological behaviour of STF were carried out experimentally on STFs with different compositions. STF impregnated woven fabric panels were created and tested for stabbing resistance. Stabbing impact tests were conducted on 6 different types of STF impregnated fabric panels against 2 untreated fabric panels, and the results were studied against the benchmark fabrics without STF impregnation. Based on the same number of layers of fabric, the STF impregnation improves the stabbing resistance notably. For same panel areal density, the STF impregnated panels outperform the untreated fabric panel. The results of this research indicate the possibility of lighter ballistic panel materials for higher stabbing protection. It was also found that higher nanoparticle weight fraction and larger nanoparticle size of silica leads to better stabbing resistance performance among the STF impregnated panels.

The electrochemical performance of vanadiumoxide-based cathodes in aqueous zinc-ion batteries (ZIBs) depends on their degree of crystallinity and composite state with carbon materials. An in situ electrochemical induction strategy was developed to fabricate a metal-organic-framework-derived composite of amorphous V 2 O 5 and carbon materials (a-V 2 O 5 @C) for the first time, where V 2 O 5 is in an amorphous state and uniformly distributed in the carbon framework. The amorphous structure endows V 2 O 5 with more isotropic Zn 2+ diffusion routes and active sites, resulting in fast Zn 2+ transport and high specific capacity. The porous carbon framework provides a continuous electron transport pathway and ion diffusion channels. As a result, the a-V 2 O 5 @C composites display extraordinary electrochemical performance. This work will pave the way toward design of ZIB cathodes with superior rate performance.

The co‐insertion of dual ions can often offer enhanced electrochemical performance for the aqueous zinc batteries. Although the insertion of non‐metallic ions has been achieved in aqueous zinc batteries, the co‐insertion chemistry of non‐metallic cations is still a challenge. Here, a reversible H+/NH4+ co‐insertion/extraction mechanism was developed in an aqueous Zn/MnO2 battery system. The synergistic effect between the dual cations endows the aqueous batteries with the fast kinetics of ion diffusion and the reversible structure evolution of MnO2. As a result, the Zn/MnO2 battery displays excellent rate capability and cycling performance. This work will pave the way toward the design of aqueous rechargeable batteries with non‐metallic ions.