The rapidly growing fields of noncontact medical diagnosis, noninvasive epidermal sensing, and environmental monitoring bring forward the need for fast humidity sensors. However, achieving a rapid response to dynamic changes in humidity, such as for human respiration, is challenging. This is because the response can be limited by the diffusion of water, the sorption of water in the material, and the sensing method itself. Here, the water sorption and response mechanism for multilayer assemblies made from MXene nanosheets and polyelectrolytes for ultrafast humidity sensing are described. MXenes are a class of two-dimensional transition metal carbides (e.g., Ti 3 C 2 ) possessing hydrophilicity and metal-like conductivity. Herein we show that MXene/polyelectrolyte multilayer films prepared using layer-by-layer (LbL) assembly exhibit response and recovery times exceeding those of most humidity sensors. Quartz crystal microbalance and ellipsometry support the mechanism that, upon changing humidity, water molecules intercalate into (or deintercalate from) the MXene/polyelectrolyte multilayer, resulting in an increase (or a decrease) in the thickness and sheet-to-sheet distance, which then changes the tunneling resistance between MXene sheets. The ultrafast response was further demonstrated by monitoring real-time human respiration using a portable microcontroller for wireless sensing.

Mechanically and thermally robust separators offer an alternative approach for preventing battery failure under extreme conditions such as high loads and temperatures. However, the trade-off between electrochemical performance and mechanical and thermal stability remains an ongoing challenge. Here, we investigate aramid nanofiber (ANF) separators that possess high moduli and self-extinguishing characteristics. The ANF separators are formed from the dissolution of bulk Kevlar fibers and their subsequent vacuum-assisted self-assembly. Thermogravimetric analysis shows a high 5 wt % decomposition temperature of 447 °C, which is over ∼175 °C higher than commercial Celgard separators. The ANF separator also possesses a high Young’s modulus of 8.8 GPa, which is ∼1000% higher than commercial separators. Even when dry or when soaked in battery electrolyte, the ANF separators self-extinguish upon exposure to flame, whereas commercial separators melt or drip. We show that these features, although adventitious, present a trade-off with electrochemical performance in which a lithium nickel manganse cobalt (NMC) oxide-based battery possessed a reduced capacity of 123.4 mA h g–1. Considering the separator holistically, we propose that the ANF separator shows an excellent balance of the combined properties of high modulus, flame-resistance, thermal stability, and electrochemical stability and might be suitable for extreme environment applications with further testing.

Reduced graphene oxide/aramid nanofiber (rGO/ANF) supercapacitor electrodes have a good combination of energy storage and mechanical properties, but ion transport remains an issue toward achieving higher energy densities at high current because of the tightly packed electrode structure. Herein, carbon nanotubes (CNTs) are introduced to prevent rGO flake stacking to improve the rate capability of the rGO/ANF structural supercapacitor. The effect of CNTs on the rGO/ANF composite electrode’s mechanical and electrochemical properties is investigated by varying the composition. The addition of 20 wt % CNTs led to an increase in Young’s modulus up to 10.3 ± 1.8 GPa, while a maximum in ultimate strain and strength of 1.3 ± 0.14% and 55 ± 6.8 MPa, respectively, was found at a loading of 2.5 wt % CNTs. At low specific currents, the electrodes performed similarly (160–170 F g–1), but at high specific currents (5 A g–1), the addition of 20 wt % CNTs led to a significantly higher capacitance (76 F g–1) as compared to that of rGO/ANF electrodes without CNTs (26 F g–1). In addition, the energy density also improved significantly at high power from 1.4 to 5.1 W h L–1 with the addition of CNTs. The improvement in mechanical properties is attributed to the introduction of additional hydrogen-bonding and π–π interactions from the carboxylic acid-functionalized CNTs. The increase in capacitance at higher discharge rates is due to improved ion transport from the CNTs. Finally, in situ electrochemomechanical testing examines how capacitance varies with strain in these structural electrodes for the first time.

Strong electrodes with good energy storage capabilities are necessary to accommodate the current needs for structural and flexible electronics. To this end, conjugated polymers such as polyaniline (PANI) have attracted...