Dual-bionic nano-groove structured nanofibers for breathable and moisture-wicking protective respirators.

Coronavirus disease 2019 (COVID-19) pandemic makes protective respirators highly demanded. The respirator materials should filter out viral fine aerosols effectively, allow airflow to pass through easily, and wick away the exhalant moisture timely. However, the commonly used melt-blown nonwovens perform poorly in meeting these requirements simultaneously. Herein, dual-bionic nano-groove structured (NGS) nanofibers are fabricated to serve as protective, breathable and moisture-wicking respirator materials. The creativity of this design is that the tailoring of dual-bionic nano-groove structure, combined with the strong polarity and hydrophilicity of electrospinning polymer, not only endows the nanofibrous materials with improved particle capture ability but also enable them to wick away and transmit breathing moisture. Benefitting from the synthetic effect of hierarchical structure and the intrinsic property of polymers, the resulting NGS nanofibrous membranes show a high filtration efficiency of 99.96%, a low pressure drop of 110 Pa, and a high moisture transmission rate of 5.67 kg m-2 d-1 at the same time. More importantly, the sharp increase of breathing resistance caused by the condensation of exhaled moisture is avoided, overcoming the bottleneck faced by traditional nonwovens and paving a new way for developing protective respirators with high wear comfortability.

Binary Polyamide-Imide Fibrous Superelastic Aerogels for Fire-Retardant and High-Temperature Air Filtration.

Fibrous air filtration materials are highly desirable for particle removal from high-temperature emission sources. However, the existing commercial filter materials suffer from either low filtration efficiency or high pressure drop, due to the difficulty in achieving small fiber diameter and high porosity simultaneously. Herein, we report a facile strategy to fabricate mechanical robust fibrous aerogels by using dual-scale sized PAI/BMI filaments and fibers, which are derived from wet spinning and electrospinning technologies, respectively. The creativity of this design is that PAI/BMI filaments can serve as the enhancing skeleton and PAI/BMI fibers can assemble into high-porosity interconnected networks, enabling the improvement of both mechanical property and air filtration performance. The resultant dual-scale sized PAI/PBMI fibrous aerogels show a compressive stress of 8.36 MPa, a high filtration efficiency of 90.78% (particle diameter of 2.5 µm); for particle diameter over 5 µm, they have 99.99% ultra-high filtration efficiency, a low pressure drop of 20 Pa, and high QF of 0.12 Pa-1, as well as thermostable and fire-retardant properties (thermal decomposition temperature up to 342.7 °C). The successive fabrication of this material is of great significance for the govern of industrial dust.

Epoxy Cross-Linking Enhanced the Toughness of Polysaccharides as a Silicon Anode Binder for Lithium-Ion Batteries.

The large volume expansion of a silicon anode induces serious mechanical failure and limits its applications. Owing to the intrinsic weak van der Waals force and poor toughness, it is unable to solve this issue with the current commercial poly(vinylidene difluoride) (PVDF) binder. The development of a binder with strong binding strength with silicon (Si) is urgent. Herein, a hydroxyl-rich three-dimensional (3D) network binder is synthesized by chemical cross-linking reactions between epichlorohydrin (ECH) and sodium hyaluronate (SH), which exhibits dramatically enhanced toughness and cohesive properties. The Si anode with the novel SH-ECH as the binder delivers excellent electrochemical performance, especially cycling stability. The discharge capacity could maintain 800.4 mAh g-1 after 1000 cycles at a current of 0.2 C with the average capacity decay rate per cycle of 0.015%. Our results pave a new way for the tailoring of the chemical structures of natural polymers to realize lithium-ion batteries (LIBs) with superior electrochemical performance.

9,10-Anthraquinone/K2CuFe(CN)6: A Highly Compatible Aqueous Aluminum-Ion Full-Battery Configuration.

Temporally intermittent and spatially dispersed renewable energy sources strongly call for large-scale energy storage devices. Aqueous aluminum-ion batteries show great potential for application due to their safety and low cost. Thus far, however, the ideal full-battery configuration is beyond the scope due to shortcomings with regards to suitable anode and cathode materials. Herein, we report a pioneering aqueous aluminum-ion battery system consisting of a Prussian white cathode, 1 M Al2(SO4)3 aqueous electrolyte, and an organic 9,10-anthraquinone anode. The oxidation capability of the Prussian white cathode during the first charging allows for the fabrication of the full battery without pre-inserting aluminum ions, thus making the rocking-chair-type battery feasible. Importantly, the open-framework structure of the Prussian white and distinct enolization charge storage mechanism of 9,10-anthraquinone ensure fast reaction kinetics. The full battery exhibits cycling stability with a capacity retention of 89.1% over 100 cycles at 500 mA g-1, finishing a cycle in about 10 min. This work provides a pathway for developing rechargeable aqueous aluminum-ion batteries.