Shiao-Wei Kuo

Abstract Vitrimers offer a sustainable route to covalently crosslinked polymer networks with processability enabled by thermally activated bond-exchange reactions. However, the integration of programmable nanostructures into vitrimer networks remains challenging because of the competition between phase behavior and the curing process.

Engineering redox-active benzo[1,2-b:4,5-b']dithiophene-based conjugated polymers: tuning porosity and linker architecture for high-performance supercapacitors Conjugated polymers emerge as promising candidates for next-generation supercapacitor electrodes due to their high conductivity, redox activity, and π-conjugated frameworks.

Quinolone antibiotics (QAs), as a vital category of synthetic antimicrobial substances, are prevalently utilized in human treatments, livestock farming, and aquaculture owing to their broad-spectrum antimicrobial capabilities, absence of cross-resistance with other antimicrobial agents, and relatively mild toxic side-effects [1,2]. Nonetheless, the widespread use and inherent persistence of QAs have resulted in the presence of QAs residues in diverse environmental and food matrices [3].