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[Display omitted] • Anti-freezing conductive semi-IPN hydrogel was constructed by PAM, SA and LiCl. • Sodium alginate enhanced mechanical toughness (elongation at break ∼2100%). • LiCl contributed to sensitivity (GF = 17.45 in high strain) and anti-freezing property. • PAM/SA/3M LiCl hydrogel could maintain stretchable and conductive at −30 °C. As an ideal material for flexible sensors, electrically conductive hydrogels (ECHs) has been faced with water loss and easy freezing, which affects the conductive and tensile properties. Polyacrylamide/sodium alginate/LiCl (PAM/SA/LiCl) hydrogel was constructed to enhance the anti-freezing property without deficiencies of tensile and electrical performance. A semi-interpenetrating network (semi-IPN) was formed by PAM and SA through hydrogen bonding, which performed excellent mechanical property (fracture strain 2100%, fracture stress 110 KPa). LiCl contributed to the high ionic conductivity (up to 21.7 S/m) and sensitivity (Gauge Factor (GF) = 17.45). Double hydrogen bonding of SA and PAM, hydration of LiCl and ion interaction between SA and lithium ion improved the anti-freezing performance and mechanical property of the hydrogel together. The proportion of non-freezing water in system was proved to be significantly increased. The comprehensive properties of the hydrogels were evaluated and PAM/SA/3M LiCl hydrogel kept conductive without obvious loss of stretchability at −30 °C. The PAM/SA/LiCl hydrogel integrates remarkable toughness, conductivity, sensitivity and anti-freezing property, which is a suitable choice in smart wearable devices, soft robots and medical monitoring. [ABSTRACT FROM AUTHOR]

Conductive hydrogels usually suffer from weak mechanical properties and are easily destroyed, resulting in limited applications in flexible electronics. Concurrently, adding conductive additives to the hydrogel solution increases the probability of agglomeration and uneven dispersion issues. In this study, the biocompatible natural polymer chitosan was used as the network substrate. The rigid network employed was the Cit3−ion crosslinked chitosan (CS) network, and the MBA chemically crosslinked polyacrylamide (PAM) network was used as the flexible network. Tannic acid-reduced graphene oxide (TA-rGO), which has excellent conductivity and dispersibility, is used as a conductive filler. Thus, a CS/TA-rGO/PAM double network conductive hydrogel with excellent performance, high toughness, high conductivity, and superior sensing sensitivity was prepared. The prepared CS/TA-rGO/PAM double network conductive hydrogels have strong tensile properties (strain and toughness as high as 2009 % and 1045 kJ/cm3), excellent sensing sensitivity (GF value was 4.01), a wider strain detection range, high cycling stability and durability, good biocompatibility, and antimicrobial properties. The hydrogel can be assembled into flexible wearable devices that can not only dynamically detect human movements, such as joint bending, facial expression changes, swallowing, and saying, but also recognize handwriting and enable human-computer interaction. [ABSTRACT FROM AUTHOR]

In recent years, electrically conductive hydrogels (ECHs) have attracted extensive attention for their potential applications in flexible wearable sensors and human motion monitoring. However, many ECHs are prone to damage during use, limiting their application. In this study, a quick and simple one-pot in situ copolymerization method was used to introduce the double network (DN) structure with good mechanical properties into the conductive hydrogel, providing a new method for preparing the multi-function DN hydrogel. A novel conductive hydrogel was prepared by introducing sodium carboxymethyl cellulose (CMCNa) and polydopamine (PDA) reduced graphene oxide (D-rGO) into polyacrylamide (PAM) hydrogel. Among them, the well-dispersed D-rGO nanofillers provided a good electron conduction pathway. CMCNa/PAM matrix was physically and chemically crosslinked with Fe3+ and N, N′-methylene- bis -acrylamide (MBA), which made the hydrogel had better mechanical properties and pH sensitivity than pure PAM hydrogel. The conductive hydrogel designed by us had better sensitivity (gauge factor (GF) value was 6.44), wider strain detection range (0–500%), better cycle stability and durability compared with other conductive hydrogels by using a composite conductive mechanism of electron and ion conductivity. More notably, D-rGO/CMCNa/PAM hydrogel could detect large-scale changes in human movement (such as bending of fingers and wrists) and sensitive signals without obvious allergic reactions to human skin, which offered great possibilities for practical applications as flexible strain sensors. [Display omitted] [ABSTRACT FROM AUTHOR]