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The greener alternatives to tactile‐integrated multimodal sensors with self‐powered and self‐healing abilities are highly desirable for all‐in‐one autonomous sensing systems, particularly impressive in diverse application ranges including smart home, healthcare, and e‐skin. The dynamically self‐healable, stretchable piezoresistive sensors, and triboelectric nanogenerators (TENGs) reported herein are constructed by a facile, industrially viable method of grafting imidazolium ions on epoxidized natural rubber (ENR) backbone. Owing to cation‐π and π–π interaction between the percolated carbon nanotubes (CNTs)‐network and the imidazolium ions formed by non‐covalent interactions, the interfacial adhesion between the filler and elastomer is shown to improve considerably. The sensors show high piezoresistive strain sensitivity, reversible ionic network‐assisted self‐healability (efficiency ≈80%) and wide‐ranging detectability for precise monitoring of human movements. Both the healed and pristine sensors feature low hysteresis and stable electrical outputs over a wide strain range (≤200%). While achieving rapid self‐healing efficiency, the substrates are shown to exhibit remarkable robustness for harsh climates owing to significant mechanical toughness. Supported by excellent triboelectric tactile sensitivity (2.12 V N−1), the multifunctional TENG‐enabled sensor yields superior power density (0.16 mW cm−2). Moreover, the TENG module exhibits high force sensitivity and ease of operation that are considered versatile for all‐weather integrated tactile solutions for future technology.
The greener alternatives to tactile‐integrated multimodal sensors with self‐powered and self‐healing abilities are highly desirable for all‐in‐one autonomous sensing systems, particularly impressive in diverse application ranges including smart home, healthcare, and e‐skin. The dynamically self‐healable, stretchable piezoresistive sensors, and triboelectric nanogenerators (TENGs) reported herein are constructed by a facile, industrially viable method of grafting imidazolium ions on epoxidized natural rubber (ENR) backbone. Owing to cation‐π and π–π interaction between the percolated carbon nanotubes (CNTs)‐network and the imidazolium ions formed by non‐covalent interactions, the interfacial adhesion between the filler and elastomer is shown to improve considerably. The sensors show high piezoresistive strain sensitivity, reversible ionic network‐assisted self‐healability (efficiency ≈80%) and wide‐ranging detectability for precise monitoring of human movements. Both the healed and pristine sensors feature low hysteresis and stable electrical outputs over a wide strain range (≤200%). While achieving rapid self‐healing efficiency, the substrates are shown to exhibit remarkable robustness for harsh climates owing to significant mechanical toughness. Supported by excellent triboelectric tactile sensitivity (2.12 V N−1), the multifunctional TENG‐enabled sensor yields superior power density (0.16 mW cm−2). Moreover, the TENG module exhibits high force sensitivity and ease of operation that are considered versatile for all‐weather integrated tactile solutions for future technology.
In this study, a novel biodegradable polymer electrolyte membrane with reduced fuel crossover, high selectivity, and high conductivity compared with Nafion 117 membrane in direct ethanol fuel cells (DEFCs) has been reported. Herein, polyvinyl alcohol/epoxidized natural rubber (PVA/ENR) blend membranes were synthesized via a simple solution casting method and applied in DEFCs. The structural and physicochemical features of the PVA/ENR blend membranes were examined using FESEM, FTIR, XRD, water absorption, ethanol uptake, swelling ratio and oxidative stability. ENR enhances the chemical, structural, and mechanical characteristics of PVA, making it a valuable material in fuel cell applications. The incorporation of ENR into the PVA matrix results in a compact morphology, excessive multifunctional groups, low fuel crossover, and high selectivity. The optimum membrane thickness achieves the highest selectivity, reaching up to 12.32 × 104 S s cm−3 at 30°C. Additionally, the maximum power density achieved is 19.52 mW cm−2, surpassing that of the Nafion membrane, which is only 14.55 mW cm−2 at 90°C. Furthermore, this biodegradable membrane can sustain operation for 1000 h at 90°C, owing to its ability to maintain hydration for an extended period. This study represents the first attempt to combine PVA and ENR in fuel cells.
Silica, as a high-quality reinforcing filler, can satisfy the requirements of high-performance green tread rubber with high wet-skid resistance, low rolling resistance, and low heat generation. However, the silica surface contains abundant silicon hydroxyl groups, resulting in a severe aggregation of silica particles in non-polar rubber matrix. Herein, we explored a carbon black (CB)/silica hybrid reinforcing strategy to prepare epoxidized natural rubber (ENR)-based vulcanizates. Benefiting from the reaction and interaction between the epoxy groups on ENR chains and the silicon hydroxyl groups on silica surfaces, the dispersion uniformity of silica in the ENR matrix was significantly enhanced. Meanwhile, the silica can facilitate the dispersity and reinforcing effect of CB particles in the ENR matrix. By optimizing the CB/silica blending ratios, we realized high-performance ENR vulcanizates with simultaneously improved mechanical strength, wear resistance, resilience, anti-aging, and damping properties, as well as reduced heat generation and rolling resistance. For example, compared with ENR vulcanizates with only CB fillers, those with CB/silica hybrid fillers showed ~10% increase in tensile strength, ~20% increase in elongation at break, and ~20% increase in tensile retention rate. These results indicated that the ENR compounds reinforced with CB/silica hybrid fillers are a promising candidate for high-performance green tread rubber materials.
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