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In situ mechanical reinforcement of polymer hydrogels via metal-coordinated crosslink mineralization
Biological organic-inorganic materials remain a popular source of inspiration for bioinspired materials design and engineering. Inspired by the self-assembling metal-reinforced mussel holdfast threads, we tested if metal-coordinate polymer networks can be utilized as simple composite scaffolds for direct in situ crosslink mineralization. Starting with aqueous solutions of polymers end-functionalized with metal-coordinating ligands of catechol or histidine, here we show that inter-molecular metal-ion coordination complexes can serve as mineral nucleation sites, whereby significant mechanical reinforcement is achieved upon nanoscale particle growth directly at the metal-coordinate network crosslink sites.
Physics-based prediction of moisture-capture properties of hydrogels
Not provided.
Porous hierarchically ordered hydrogels demonstrating structurally dependent mechanical properties
Not provided.
Additive manufacturing of micro-architected metals via hydrogel infusion
Not provided.
Chromophore amphiphile-polyelectrolyte hybrid hydrogels for photocatalytic hydrogen production
Abstract not provided
Dynamic intermolecular interactions through hydrogen bonding of water promote heat conduction in hydrogels
Dynamic intermolecular forces through hydrogen bonding between water and polymer chains are shown to enhance thermal transport in soft materials.
Dynamic behavior of chemically tunable mechano-responsive hydrogels
Here, using theory and simulation, we model the mechanical behavior of gels that encompass loops and dangling chain ends. If the loops remain folded and dangling ends are chemically inert, then these topological features just serve as defects. If, however, the loops unfold to expose the hidden (“cryptic”) binding sites and the ends of the dangling chains are reactive, these moieties can form bonds that improve the gel's mechanical properties. For gels with a lower critical solubility temperature (LCST), we systematically switch on the possible unfolding and binding events. To quantify the resulting effects, we derive equations for the gel's equilibrium and dynamic elastic moduli. We also use a finite element approach to simulate the gel's response to deformation and validate the analytic calculations. Herein, we show that the equilibrium moduli are highly sensitive to the presence of unfolding and binding transitions. The dynamical moduli are sensitive not only to these structural changes, but also to the frequency of deformation. For example, when reactive ends bind to exposed cryptic sites at T = 29 °C and relatively high frequency, the storage shear modulus is 119% greater than the corresponding equilibrium value, while the storage Young's modulus is 109% greater than at equilibrium. These findings provide guidelines for tuning the chemical reactivity of loops and dangling ends and the frequency of deformation to tailor the mechano-responsive behavior of polymer networks.
CryoEM reveals the complex self-assembly of a chemically driven disulfide hydrogel
We elucidate the mechanisms of chemically driven self-assembly processes, demonstrating how synchronous assembly–disassembly reactions can stabilize transient structures and create morphologies that differ from conventional assemblies.
Precursor design for additive manufacturing of ceramics through hydrogel infusion
Studies to understand how organic (resin formulations) and inorganic (salts and cation identities) precursors influence the quality of ceramics using HIAM.
Bridging dynamic regimes of segmental relaxation and center-of-mass diffusion in associative protein hydrogels
Not Available
High speed laser-induced refractive index change in ophthalmic HEMA hydrogel using a line focus
Laser-induced refractive index change (LIRIC) techniques typically focus femtosecond laser pulses to a tight spot to achieve the high intensities required to alter ophthalmic materials. A line-focus implementation using 800 nm pulses at 1 kHz repetition rate has been shown to greatly increase the effective writing speed of the process, but the high pulse energies used led to nonlinear propagation effects, presenting challenges for the fabrication of ophthalmic correctors. By taking advantage of the lower effective order of multiphoton absorption for 514 nm pulses, power levels may be reduced, allowing overlapped pulse writing. We demonstrate that this allows high-quality phase bars and devices to be made at high speeds.
The low-maintenance application of hydrogel electrolytes to Zn/MnO2 rechargeable batteries.
Abstract not provided.
Hydrogel Electrolytes Ensuring the Transportability and the 2nd Electron Reaction of Zn-MnO2 Alkaline Batteries.
Abstract not provided.
Optimization of Hydrogels for non-spillable Zn|MnO2 rechargeable batteries allowing for 2nd electron MnO2 cycling.
Abstract not provided.