Cationic cellulose nanofiber solid electrolytes: A pathway to high lithium-ion migration and polysulfide adsorption for lithium-sulfur batteries.

Polyethylene oxide (PEO) solid electrolytes, acknowledged for their safety advantages over liquid counterparts, confront inherent challenges, including low ionic conductivity, restricted lithium ion migration, and mechanical fragility, notably pronounced in lithium­sulfur batteries due to the polysulfide shuttling phenomenon. To address these limitations, we integrate a quaternary ammonium cation-modified cellulose (QACC) nanofiber, electrospun with cellulose acetate (CA) from recycled cigarette filters, into the PEO electrolyte matrix. The nitrogen atom within the quaternary ammonium group exhibits a pronounced affinity for polysulfide compounds, effectively curtailing polysulfide migration. Concurrently, Lewis acid-base interactions between quaternary ammonium groups and lithium salt anions facilitate the release of additional Li+, achieving a lithium-ion transference number 1.5 times higher than its pure PEO counterpart. Furthermore, the introduction of a larger trifluoromethanesulfonimide (TFSI) group on the QACC macromolecule (TFSI-QACC) disrupts the ordered arrangement of PEO macromolecules, resulting in a noteworthy enhancement in ionic conductivity, reaching 2.07 × 10-4 S cm-1 at 60 °C, thus addressing the challenge of low PEO electrolyte conductivity. Moreover, the nanofiber enhances the mechanical strength of the PEO electrolyte from 0.49 to 7.50 MPa, mitigating safety concerns related to lithium dendrites puncturing the electrolyte. Consequently, the composite PEO demonstrates exemplary performance in lithium symmetrical batteries, enduring 500 h of continuous operation and completing 100 cycles at both room and elevated temperatures. This integrated approach, transitioning from waste to wealth, adeptly addresses a spectrum of challenges in the efficiency of solid-state electrolytes, holding considerable promise for advancing lithium­sulfur battery technology.

Smart Textiles with Self-Disinfection and Photothermochromic Effects.

Self-disinfecting textile materials employing combined photodynamic/photothermal effects enable the prevention of microbial infections, a property that has great potential in healthcare applications. However, smart textiles with stimulus responses to ambient temperature are marvelous materials for enhancing their photothermal applications with additional functions. It is still challenging to realize vivid and contrasting color changes as temperature indicators. Herein, through the in situ growth of PCN-224 metal-organic frameworks (MOFs), the electrospraying of a Ti3C2 MXene colloid, and the screen printing of a thermochromic dye, a smart photothermochromic self-disinfecting textile has been fabricated. An antibacterial inactivation study revealed 99.9999% inactivation toward gram-negative (Escherichia coli ATCC 8099) and gram-positive (Staphylococcus aureus ATCC 6538) bacteria in 30 min. A mechanism study revealed that light-driven singlet oxygen and heat are the main reasons for bacterial inactivation. Interestingly, the fabrics presented photothermal effects not only under a handheld 780 nm NIR laser but also under visible Xe lamp (λ ≥ 420 nm) illumination. The color of the fabrics (S-CF@PCN0.08) changed completely from dark green to dark red when the temperature exceeded 45 °C under Xe lamp illumination. Furthermore, the photothermochromic effect occurred in just 1 s under a 780 nm laser. Taken together, this smart photothermochromic self-disinfecting textile permits a new way to feedback the timely signal of temperature by color change and provides novel insights into the development of self-disinfecting textiles.