Xingye Zhang

This work numerically reveals a novel strategy to modulate two ionic conductance state in a nanochannel via pressure-dependent fluidic motion inside the channel. Steady and transient simulations based on Poisson–Nernst–Planck–Stokes equations demonstrate that the two states with distinct ionic conductance and ion selectivity can be reversibly switched by external pressure, with a characteristic time of ~100 μs. Furthermore, the two conductance states are found to depend on the transversal electric field, which gives rise to two distinct intrachannel fluidic flow patterns, namely laminar flow and vortex flow, respectively. This finding suggests the potential of pressure-controlled ionic conductance switching for applications in nanofluidic ionic circuits, flow-regulated sensing, and integrated micro/nanoscale devices. It also provides insights into nonlinear ionic current–voltage behaviors.

Hydrogels are attractive due to their various applications in the fields of biomedical materials, cosmetics, and biosensors. To enhance UV protection and prevent skin penetration behaviors, inspired by the mussel adhesive proteins, the functional polydopamine (PDA) is employed herein to fabricate polydopamine/carboxymethyl cellulose/polyacrylic acid (PDA/CMC/PAA) adhesive hydrogels. To disperse PDA nanoparticles well in the PAA matrix, dopamine was self-polymerized in CMC solution to form PDA/CMC complex. Acrylic acid was polymerized in PDA/CMC complex solution and cross-linked to construct UV-resistant PDA/CMC/PAA hydrogel. The morphology, rheological behavior, mechanical properties and adhesion strength of PDA/CMC/PAA hydrogels were studied by scanning electron microscopy, rotational rheometer, universal test machine. Owing to the hydrogen bonding interaction between the PDA/CMC complex and PAA, the PDA/CMC/PAA hydrogels showed high resilience and compressive strength to withstand large deformation. The hydrogels exhibited strong adhesion to various substrate surfaces, such as stainless steel, aluminum, glass and porcine skin. The biocompatibility and UV-shielding properties were investigated through culture of cells and UV irradiation test. The adhesiveness of PDA promoted cell adhesion and provided the PDA/CMC/PAA hydrogels good biocompatibility with 96% of relative cell viability. The hydrogels possessed excellent UV-shielding ability to prevent collagen fibers from being destroyed during UV irradiation, which has promising potential in the practical applications for UV filtration membrane and skin care products.

For decades, lithium batteries have attracted much attention. Highly efficient, safe, and convenient batteries are worthy of being investigated and applied in modern life. However, most of the investigation is on the macroscopic device electrical properties such as current–voltage curves. Investigation on the microscopic electrical properties including potential distribution, electrolyte salt concentration distribution, and lithium ion concentration distribution within the batteries during the discharging is still needed. Here, a detailed study of the key electrical properties distributions inside the lithium battery in the discharging status is given. After comparing three widely used cathode materials (LiCoO₂, LiMn₂O₄, and LiFePO₄), LiFePO₄ is found to show the most stable working performance which is consistent with previous reports. This is probably attributed to its most uniform key electrical properties distributions, its high electric conductivity, and crystal structure. A structure is also proposed which might give a hint to stress and temperature release for a longer and safer application of batteries. This simulation study on the key parameters distribution inside the battery may help to achieve a better understanding and hence control on the lithium battery performance and reliability.