TY - JOUR
T1 - Plasmonic hot-electron-assisted ultra-stretchable hydrogel electrodes for wearable cardiovascular monitoring and AI-driven predictive analytics
AU - Khan, Bangul
AU - Ahmed, Syed Bilal
AU - Khan, Bilawal
AU - Shehzad Khan, Muhammad
AU - Lyu, Liangyi
AU - Gunasekaran, Iyappan
AU - Ahmad, Rafi u Shan
AU - Liao, Junchen
AU - Elhousseini Hilal, Mohamed
AU - Khoo, Bee Luan
PY - 2026/5/6
Y1 - 2026/5/6
N2 - Wearable bioelectronic systems require soft, deformable materials that maintain high electrical conductivity and reliable interfacial charge transport under large mechanical strains. However, most existing hydrogel- or elastomer-based conductors involve trade-offs among mechanical compliance, electrical performance, and long-term biocompatibility, making it challenging to integrate all three properties within a single material platform. Here, we introduce a plasmonic hot-electron-assisted conductive PAM–PEDOT:PSS–Ag hydrogel, engineered to address these multifunctional requirements for continuous cardiovascular monitoring. Silver nanoparticles (Ag NPs) dispersed within the hydrogel matrix generate localised surface plasmon resonance (LSPR) under UV irradiation, producing smooth, spatially uniform heating and hot-electron injection throughout the precursor solution. This synergistic plasmonic heating effect accelerates polymerisation (∼420 s; 0.1167 h), enhances network homogeneity, and lowers interfacial charge-transfer resistance by promoting more ordered PEDOT:PSS chain assembly and improved crosslinking dynamics. As a result, the hydrogel exhibits ultrahigh stretchability (>2000%), stable conductivity (∼328.82 ± 1.78 mS m−1), and intrinsic antibacterial activity (≥99.7%). The material exhibits consistent electromechanical performance from −20 °C to 40 °C, showing tunable strain sensitivity governed by temperature-dependent network mechanics and ionic mobility. When used as epidermal electrodes, the hydrogel enables high-fidelity electrocardiogram (ECG) acquisition (SNR ≈ 25 dB) in human and rodent models. Integrated with machine-learning analytics, the platform supports accurate demographic prediction (96.2%), demonstrating a scalable material-device-data framework for next-generation personalised cardiovascular monitoring. This journal is © The Royal Society of Chemistry, 2026
AB - Wearable bioelectronic systems require soft, deformable materials that maintain high electrical conductivity and reliable interfacial charge transport under large mechanical strains. However, most existing hydrogel- or elastomer-based conductors involve trade-offs among mechanical compliance, electrical performance, and long-term biocompatibility, making it challenging to integrate all three properties within a single material platform. Here, we introduce a plasmonic hot-electron-assisted conductive PAM–PEDOT:PSS–Ag hydrogel, engineered to address these multifunctional requirements for continuous cardiovascular monitoring. Silver nanoparticles (Ag NPs) dispersed within the hydrogel matrix generate localised surface plasmon resonance (LSPR) under UV irradiation, producing smooth, spatially uniform heating and hot-electron injection throughout the precursor solution. This synergistic plasmonic heating effect accelerates polymerisation (∼420 s; 0.1167 h), enhances network homogeneity, and lowers interfacial charge-transfer resistance by promoting more ordered PEDOT:PSS chain assembly and improved crosslinking dynamics. As a result, the hydrogel exhibits ultrahigh stretchability (>2000%), stable conductivity (∼328.82 ± 1.78 mS m−1), and intrinsic antibacterial activity (≥99.7%). The material exhibits consistent electromechanical performance from −20 °C to 40 °C, showing tunable strain sensitivity governed by temperature-dependent network mechanics and ionic mobility. When used as epidermal electrodes, the hydrogel enables high-fidelity electrocardiogram (ECG) acquisition (SNR ≈ 25 dB) in human and rodent models. Integrated with machine-learning analytics, the platform supports accurate demographic prediction (96.2%), demonstrating a scalable material-device-data framework for next-generation personalised cardiovascular monitoring. This journal is © The Royal Society of Chemistry, 2026
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U2 - 10.1039/d5tb02743h
DO - 10.1039/d5tb02743h
M3 - RGC 21 - Publication in refereed journal
SN - 2050-750X
VL - 14
SP - 5408
EP - 5427
JO - Journal of Materials Chemistry B
JF - Journal of Materials Chemistry B
IS - 17
ER -