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Polyampholyte (PA) hydrogels are randomly copolymerized from anionic and cationic monomers, showing good mechanical properties owing to the existence of numerous ionic bonds in the networks. However, relatively tough PA gels can be synthesized successfully only at high monomer concentrations (CM), where relatively strong chain entanglements exist to stabilize the primary supramolecular networks. This study aims to toughen weak PA gels with relatively weak primary topological entanglements (at relatively low CM) via a secondary equilibrium approach. According to this approach, an as-prepared PA gel is first dialyzed in a FeCl3 solution to reach a swelling equilibrium and then dialyzed in sufficient deionized water to remove excess free ions to achieve a new equilibrium, resulting in the modified PA gels. It is proved that the modified PA gels are eventually constructed by both ionic and metal coordination bonds, which could synergistically enhance the chain interactions and enable the network toughening. Systematic studies indicate that both CM and FeCl3 concentration ( C FeCl 3 ) influence the enhancement effectiveness of the modified PA gels, although all the gels could be dramatically enhanced. The mechanical properties of the modified PA gel could be optimized at CM = 2.0 M and C FeCl 3 = 0.3 M, where the Young's modulus, tensile fracture strength, and work of tension are improved by 1800%, 600%, and 820%, respectively, comparing to these of the original PA gel. By selecting a different PA gel system and diverse metal ions (i.e., Al3+, Mg2+, Ca2+), we further prove that the proposed approach is generally appliable. A theoretical model is used to understand the toughening mechanism. This work well extends the simple yet general approach for the toughening of weak PA gels with relatively weak chain entanglements. [ABSTRACT FROM AUTHOR]

Many living tissues, such as muscle, become mechanically stronger with growth. Yet, synthetic hydrogels usually exhibit an opposite size‐mechanical property relation, that is, swelling‐weakening behavior. Herein, a series of swollen yet strengthened polyampholyte (PA) hydrogels are developed via a simple metal‐ion solution soaking strategy. In this strategy, a dynamic PA hydrogel (with ionic bonds) is dialyzed in ZrOCl2 solutions (Step‐I) and deionized water (Step‐II) successively to obtain equilibrated hydrogels. Due to the specific Zr4+ ions and PA network structure, Step‐I takes several months with sample size and mechanical performance increasing continuously, while Step‐II only needs several days. Through this strategy, the resultant hydrogel networks are reorganized and eventually constructed by ionic and metalligand bonds, enabling the swelling yet strengthening behavior. A systematic study confirms that dialysis time in Step‐I and corresponding ZrOCl2 concentration can significantly affect the multiphase microstructures of the hydrogels, resulting in different mechanical enhancements. The optimized hydrogel possesses 39.2 MPa of Young's modulus and 3.7 MPa of tensile strength, which are 302 and 5.5 times these of the original PA gel, respectively. Despite distinct swelling, these hydrogels still mechanically surpass many existing high‐performance hydrogels. This study opens a novel pathway for fabricating swollen yet strengthened hydrogels. [ABSTRACT FROM AUTHOR]

Despite existing in biological systems, developing synthetic polyampholyte (PA) hydrogels constructed by both ionic and metal–ligand bonds remains challenging. Herein, a simple secondary equilibrium approach is proposed to fabricate strong and tough PA hydrogels via the synergy of ionic and metal–ligand bonds. The original PA gels (constructed by ionic bonds) are first dialyzed in multivalent metal‐ion solutions to reach a swelling equilibrium and then moved to deionized water to dialyze excess free ions to achieve a new equilibrium. Through this approach, the original PA gel network can be optimized and eventually constructed by ionic and metal–ligand bonds, enabling a synergistic reinforcement. By selecting different original PA gel systems and diverse multivalent metal‐ions, the proposed approach is proved to be generalizable to fabricate strong and tough PA gels. Additionally, the hydrogels have stable ion‐conductivity even at the water‐equilibrium state, making them promising as strain sensors. The viscoelastic and elastic contributions to the mechanical properties of the hydrogels by a viscoelastic model are also discussed to further understand the strengthening and toughening mechanisms. The proposed strategy is simple but effective for achieving strong and tough PA‐based hydrogels. This study also provides new insights for PA hydrogels in electrolyte environments. [ABSTRACT FROM AUTHOR]

(Size: 5 cm height × 13 cm width). [Display omitted] • Developing a modified polyampholyte hydrogel with a swelling-strengthening behavior. • Hydrogel exhibiting high elastic modulus (18.5 MPa) and tensile strength (1.85 MPa). • Providing a simple pathway for achieving strong and stiff swollen hydrogels. Hydrogel networks are usually diluted upon swelling, weakening their mechanical performance. The mechanical weakness limits their practical applications. Herein, we report a modified polyampholyte (PA) hydrogel with a swelling-strengthening behavior via a secondary equilibrium strategy, based on the synergy of ionic and metal–ligand bonds in the network by introducing Zr4+ ions. Swelling and mechanical properties of the hydrogels are investigated, and the structure–property relationship is discussed. The modified PA gel possesses 18.5 MPa Young's modulus and 1.85 MPa tensile strength, highly surpassing the original PA gel. This work provides a simple route to achieve strong and stiff swollen hydrogels. [ABSTRACT FROM AUTHOR]

This work demonstrates a facile approach to achieve ultralong anti-dehydration lifespan and ion-conductivity in a swollen yet strengthened polyampholyte (PA) hydrogel via the synergy of ionic and two kinds of metal–ligand bonds. The gel is made into a flexible electronic skin as an environmental-adaptable strain sensor for monitoring human activity in the −60 to 80 ℃ range. [Display omitted] • Proposing a strengthened PA hydrogel via synergy of ionic and metal–ligand bonds. • Presenting a viscoelastic model of the mechanical properties of the hydrogels. • Achieving an ultralong anti-dehydration lifespan of > 300 days. • Achieving a high ion conductivity of 50 S/m and GF of 4.9 at 0%-300% strain. • Achieving 100% accuracy of body motions classification in physical exercises. In order to adapt environmental changes, a hydrogel that possesses high mechanical strength, long-lasting moisture, good temperature tolerance, and exceptional electrical conductivity simultaneously is extremely desirable but remains challenging. Inspired by muscles becoming more ion-rich and stronger after swelling with blood, herein we propose a simple secondary soaking method to achieve ultralong anti-dehydration lifespan and high conductivity in a swollen yet strengthened polyampholytes (PA) hydrogel via the synergy of ionic and two types of metal–ligand bonds. An as-prepared PA gel is first dialyzed in a ZnCl 2 solution to reach a swelling equilibrium, and then moved to a FeCl 3 solution to achieve a new equilibrium. Through this approach, the as-prepared PA gel network could be optimized and eventually constructed by ionic and two kinds of metal–ligand bonds, enabling a synergistic reinforcement. To understand the reinforcing mechanisms, we also discuss the viscoelastic and elastic contributions to the mechanical properties of the hydrogels by a viscoelastic model. Additionally, the hydrogels possess ultralong anti-dehydration lifespan (>300 days), high ion conductivity (≈50 S/m) and temperature- and humidity-responsiveness, exhibiting high potential as e-skin to monitor human activity. The proposed strategy is simple but effective for achieving anti-dehydration and highly ion-conductive tough hydrogels. [ABSTRACT FROM AUTHOR]

Tough hydrogels with adjustable stiffness are expected for adapting application as various biomaterials. Oppositely charged polyelectrolytes form tough and self-healing physical polyion-complex (PIC) hydrogels via formation of inter-chain ionic bonds with a wide distribution in bond strength. The strong bonds serve as permanent crosslinking to impart elasticity and the weak bonds as reversible sacrificial bonds to dissipate energy and to self-heal. In this work, we fabricate four PIC hydrogels using four positively charged trimethyl-ammonium monomers with slightly different chemical moieties and a same negatively charged polymer. The obtained PIC hydrogels all show high toughness but large difference in stiffness, extensibility, and self-recovery kinetics. With slight difference in the monomer structure of the polycations, the modulus of the hydrogels varies over two orders in magnitude, from 0.36 to 56 MPa, and the difference in elongation at break is up to five times. The presence of acryloyl moiety and methyl moiety increase the stiffness of the hydrogels. In the temperature range studied, all the four PIC hydrogels exhibit the rheological simple behaviours, following the time-temperature superposition principle. The four samples show quite different dynamic relaxation spectra over wide frequency range, revealing large difference in the strength distribution of dynamic ionic bonds. SEM observation reveals quite different phase separation structure for the four samples, in which the polymer chain stiffness should play an important role. This understanding of structure-properties of the PIC hydrogels will merit the designing of various supramolecular tough hydrogels and therefore broaden the scope of hydrogels for the applications as biomaterials. [ABSTRACT FROM AUTHOR]