The development of waterproof ionogels with high stretchability and fast self-healing performance is essential for stretchable ionic conductors in sophisticated skin-inspired wearable sensors but can be rarely met in one material. Herein, a semicrystalline fluorinated copolymer ionogel (SFCI) with extremely high stretchability, underwater stability, and fast self-healability was fabricated, among which hydrophobic ionic liquids ([BMIM][TFSI]) were selectively enriched in fluoroacrylate segment domains of the fluorinated copolymer matrix through unique ion-dipole interactions. Benefiting from the reversible ion-dipole interactions between the [BMIM][TFSI] and fluoroacrylate segment domains as well as the physical cross-linking effects of semicrystalline oligoethylene glycol domains, the SFCI exhibited ultrastretchability (>6000%), fast room-temperature self-healability (>96% healing efficiency after cutting and self-healing for 30 min), and outstanding elasticity. In addition, the representative SFCI also exhibited high-temperature tolerance up to 300 °C, antifreezing performance as low as -35 °C, and high transparency (>93% visible-light transmittance). As a result, the as-obtained SFCI can readily be used as a highly stretchable ionic conductor in skin-inspired wearable sensors with waterproof performance for real-time detecting physiological human activities. These attractive features illustrate that the developed ultrastretchable and rapidly self-healable ionogels with unique waterproofness are promising candidates especially for sophisticated wearable strain sensing applications in complex and extreme environments.

Highly Stretchable, Fast Self-Healing, and Waterproof Fluorinated Copolymer Ionogels with Selectively Enriched Ionic Liquids for Human-Motion Detection.

Abstract The design of power supply systems for wearable applications requires both flexibility and durability. Thermoelectrochemical cells (TECs) with large Seebeck coefficient can efficiently convert low-grade heat into electricity, thus having attracted considerable attention in recent years. Utilizing hydrogel electrolyte essentially addresses the electrolyte leakage and complicated packaging issues existing in conventional liquid-based TECs, which well satisfies the need for flexibility. Whereas, the concern of mechanical robustness to ensure stable energy output remains yet to be addressed. Herein, a flexible quasi-solid-state TEC is proposed based on the rational design of a hydrogel electrolyte, of which the thermogalvanic effect and mechanical robustness are simultaneously regulated via the multivalent ions of a redox couple. The introduced redox ions not only endow the hydrogel with excellent heat-to-electricity conversion capability, but also act as ionic crosslinks to afford a dual-crosslinked structure, resulting in reversible bonds for effective energy dissipation. The optimized TEC exhibits a high Seebeck coefficient of 1.43 mV K −1 and a significantly improved fracture toughness of 3555 J m −2 , thereby can maintain a stable thermoelectrochemical performance against various harsh mechanical stimuli. This study reveals the high potential of the quasi-solid-state TEC as a flexible and durable energy supply system for wearable applications. 

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Regulating Thermogalvanic Effect and Mechanical Robustness via Redox Ions for Flexible Quasi-Solid-State Thermocells

/pdf/regulating-thermogalvanic-effect-and-mechanical-robustness-5516r6jk.pdf

A PEDOT:PSS thermoelectric fiber generator

Ionic thermoelectric (i-TE) material with mobile ions as charge carriers has the potential to generate large thermal voltages at low operating temperatures. This study highlights the role of ions in i-TE hydrogels employing a poly(vinyl alcohol) (PVA) polymer matrix and a number of ion providers, e.g., KOH, KNO3, KCl, KBr, NaI, KI, and CsI. The relationship between the intrinsic physical parameters of the ion and the thermoelectric performance is established, indicating the ability to influence the hydrogen bond by the ion is a crucial factor. Among these i-TE hydrogels, the PVA/CsI hydrogel exhibits the largest ionic Seebeck coefficient, reaching 52.9 mV K-1, which is the largest of all i-TE materials reported to date. In addition, our work demonstrates the influence of ions on polymer configuration and provides an avenue for ion selection in the Soret effect in ionic thermoelectrics.

Role of Ions in Hydrogels with an Ionic Seebeck Coefficient of 52.9 mV K-1.

Thermoelectric generators (TEGs) demonstrate great potential for flexible and wearable electronics due to the direct electrical energy harvested from waste heat. Good wearability requires high mech...

https://www.chinesechemsoc.org/doi/pdf/10.31635/ccschem.021.202101077

A Wavy-Structured Highly Stretchable Thermoelectric Generator with Stable Energy Output and Self-Rescuing Capability

Organic polymer thermoelectrics (TEs) that can realize direct heat-to-electricity conversion hold great potential in flexible and wearable applications and thus are receiving tremendous attention. Constructing polymer-based nanocomposites represents an effective approach in achieving high TE performance, while current studies on the underlying mechanisms for the improvement of TE properties in aspects of interfacial nanostructures are insufficient. In this work, flexible ternary nanocomposite films with unique interfacial architectures are developed by sequential electrochemical polymerization of conducting polymers and subsequent anion treatment. The optimized interfacial architectures contribute to enhanced π electron conjugation, which facilitates interfacial charge transfer and favours large-area charge transport. The anion treatment further enables the molecular chains to arrange in a more ordered configuration, leading to improved carrier mobility. As a result, the nanocomposites exhibit high power factors of more than 500 μW m−1 K−2 that outperform most of the literature-reported peer composites. The feasible interfacial architecting and anion treatment methods proposed in this study demonstrate high potential in designing high-performance TE nanocomposites.

Interfacial architecting with anion treatment for enhanced thermoelectric power of flexible ternary polymer nanocomposites

Thermocells (TECs) can directly convert thermal energy into electricity via the thermogalvanic effect of redox ions. The employment of hydrogel electrolytes allows for facile fabrication of flexible quasi-solid-state TECs with...

Peng Peng

Papers

A Wavy-Structured Highly Stretchable Thermoelectric Generator with Stable Energy Output and Self-Rescuing Capability

Regulating Thermogalvanic Effect and Mechanical Robustness via Redox Ions for Flexible Quasi-Solid-State Thermocells

Regulating Thermogalvanic Effect and Mechanical Robustness via Redox Ions for Flexible Quasi-Solid-State Thermocells

Interfacial architecting with anion treatment for enhanced thermoelectric power of flexible ternary polymer nanocomposites

Aqueous Eutectic Hydrogel Electrolytes Enable Flexible Thermocells with Wide Operation Temperature Range