In this study, a type of alkaline solid polyelectrolyte (ASPE) membrane was developed via the introduction of microcrystalline cellulose (MCC) and its modified product (QMCC) into the polyvinyl alcohol (PVA) matrix. In this process, green NaOH/urea-based solvent was used to achieve a good dispersion of MCC in the PVA matrix; meanwhile, the OH⁻ groups in the NaOH/urea-based solvent provided an alkaline environment for good ion conductivity. Compared to the MCC-incorporated ASPE, further improved conductivity was achieved when the MCC was modified with quantitative quaternary ammonium salt. TGA showed that the addition of QMCC improved the water retention of the matrix, which was beneficial to the OH⁻ conduction in the system. Compared to the control (50 mS cm⁻¹), a maximum conductivity of 238 mS cm⁻¹ was obtained after the incorporation of QMCC in the PVA matrix. Moreover, the tensile strength of the polymer electrolyte were also significantly increased with the addition of QMCC. Finally, this developed ASPE membrane was used in assembling a flexible Zn–air battery and showed a promising potential in the development of flexible electronic devices.

Hydrogen peroxide (H₂O₂) plays a very vital role in industrial and biological processes, but its high concentration may cause health hazards. Therefore, accurate detection of H₂O₂ is crucial for chemical and biological sensing applications. In this work, a ratiometric fluorescent probe was developed using a core–shell structural silica nanoparticle for the detection of H₂O₂. Firstly, a silica core structure with red fluorescence emission was constructed by encapsulating a Schiff base compound (SD). Afterwards, a mesoporous silica shell was fabricated, and the AIE featured fluorophore with a H₂O₂ response character was covalently linked on the surface of the mesoporous shell layer. As recognition sites on the shell, blue-emitting TB molecules specifically identified H₂O₂ through their phenylboronic acid ester group. The blue fluorescence of core–shell structural nanoprobes would be quenched in the presence of H₂O₂, while red fluorescence remained unchanged, ensuring the high sensitivity and specificity of the ratio sensing. This design has demonstrated significant potential for the reliable monitoring of hydrogen peroxide in biological and environmental applications.