Magnetically-actuated functional gradient nanocomposites can be locally programmed to generate unprecedented mechanical gradients applied to various bioinspired load-bearing materials.
A soft body area sensor network presents a promising direction in wearable devices to integrate on-body sensors for physiological signal monitoring and flexible printed circuit boards (FPCBs) for signal conditioning/readout and wireless transmission. However, its realization currently relies on various sophisticated fabrication approaches such as lithography or direct printing on a carrier substrate before attaching to the body. Here, we report a universal fabrication scheme to enable printing and room-temperature sintering of the metal nanoparticle on paper/fabric for FPCBs and directly on the human skin for onbody sensors with a novel sintering aid layer. Consisting of polyvinyl alcohol (PVA) paste and nanoadditives in the water, the sintering aid layer reduces the sintering temperature. Together with the significantly decreased surface roughness, it allows for the integration of a submicron-thick conductive pattern with enhanced electromechanical performance. Various on-body sensors integrated with an FPCB to detect health conditions illustrate a system-level example.
Achieving a colossal room-temperature electrocaloric effect is essential for practical solid-state refrigeration applications with low-cost and highefficiency. Here, through the design of applying external stimuli (hydrostatic pressure and misfit strain), giant room-temperature electrocaloric effects in the bulk and thin film of metal-free organic perovskite [MDABCO](NH 4 )I 3 are obtained by using a combination of thermodynamic calculations and phasefield simulations. Under the hydrostatic pressure of 1 GPa, there emerges excellent room-temperature (300 K) electrocaloric performance with the temperature change (ΔT) of 8.41 K at 30 MV m −1 and electrocaloric strength (ΔT/ΔE) of 0.63 K m MV −1 at 10 MV m −1 , respectively. The prominent electrocaloric effects of MDABCO(NH 4 )I 3 may be related to its rapid change rates of free energy barrier height. Additionally, it can be found that some stripe domains and non-180° domain walls form in the [MDABCO](NH 4 )I 3 bulk, which is consistent with the experimental results. This work not only provides new insights into organic perovskite [MDABCO](NH 4 )I 3 , but also guides for further developing to realize remarkable room-temperature electrocaloric cooling.
For mechanically protective coatings, the coating material usually requires sufficient stiffness and strength to resist external forces and meanwhile matched mechanical properties with the underneath substrate to maintain the structural integrity. These requirements generate a conflict that limits the coatings from achieving simultaneous surface properties (e.g., high wear‐resistance) and coating/substrate interfacial durability. Herein this conflict is circumvented by developing a new manufacturing technique for functional gradient coatings (FGCs) with the material composition and mechanical properties gradually varying crossing the coating thickness. The FGC is realized by controlling the spatial distribution of magnetic‐responsive nanoreinforcements inside a polymer matrix through a magnetic actuation process. By concentrating the reinforcements with hybrid sizes at the surface region and continuously diminishing toward the coating/substrate interface, the FGC is demonstrated to exhibit simultaneously high surface hardness, stiffness, and wear‐resistance, as well as superb interfacial durability that outperforms the homogeneous counterparts over an order of magnitude. The concept of FGC represents a mechanically optimized strategy in achieving maximal performances with minimal use and site‐specific distribution of the reinforcements, in accordance with the design principles of many load‐bearing biological materials. The presented manufacturing technique for gradient nanocomposites can be extended to develop various bioinspired heterogeneous materials with desired mechanical performances.
We investigated the effects of CXC137, a tetramethylpyrazine piperazine derivate, on cell damage induced by N-methyl-D-aspartate (NMDA) in human derived neuroblastoma cells (SH-SY5Y) and its effect on memory dysfunction of rats with vascular dementia. It was found that the presence of CXC137 increased SH-SY5Y cells viability by inhibition of cell apoptosis induced by NMDA. These effects of CXC137 were accompanied by increases of the antioxidant superoxide dismutase activity and the level of reduced glutathione, and a decrease of lipid peroxidation product, malondialdehyde. The presence of CXC137 also showed to produce strong inhibition of cellular lactate dehydrogenase leakage, cell apoptosis and intracellular calcium overload. In a vascular dementia rat model established by bilateral common carotid arteries occlusion, treatment with CXC137 from 2 to 35 day of post-operation significantly improves the motor performance, spatial learning and memory capability of rats in both the prehensile traction test and Morris water maze test, an effect that was companied by reductions of the animal glutamic acid levels and the degree of brain mitochondrial swelling. These results suggest that CXC137 can improve the memory dysfunction in dementia and thus has important therapeutic potential for the treatment of dementia.
Despite the extraordinary electromechanical properties of relaxor ferroelectrics, correlating their properties to underlying atomic-scale structures remains a decisive challenge for these “mess” systems. Here, taking the lead-free relaxor ferroelectric Bi0.5Na0.5TiO3-based system as an example, we decipher the atomic-scale structure and its relationship to the polar structure evolution and large dynamic electromechanical response, using the direct atomic-scale point-by-point correlation analysis. With judicious chemical modification, we demonstrate the increased defect concentration is the main driving force for deviating polarizations with high-angle walls, leading to the increased random field. Meanwhile, the main driving force for deviating polarizations with low-angle walls changes from the anti-phase oxygen octahedral tilting to the multidirectional A-O displacement, leading to the decreased anisotropy field. Benefiting from the competitive and synergetic equilibrium of anisotropic field versus random field, the facilitated polarization rotation and extension versus facilitated domain switching are identified to be responsible for the giant electromechanical response. These observations lay a foundation for understanding the “composition-structure-property” relationships in relaxor ferroelectric systems, guiding the design of functional materials for electromechanical applications.
With the urgent need to explore low-cost, high-efficiency solid-state refrigeration technology, the electrocaloric effects of ferroelectric materials have attracted much attention in the past decades. With the development of modern computing technology, the phase-field method is widely used to simulate the evolution of microstructure at mesoscale and predict the properties of different types of ferroelectric materials. In this article, we review the recent progress of electrocaloric effects from phenomenological Landau thermodynamics theory to phase-field simulation by discussing the microcosmic composition, mesoscopic domain structures, macroscopic size/shape, and external stimulus of strain/stress. More importantly, in searching for new ferroelectric electrocaloric cooling materials, it is possible to find materials whose free energy barrier height changes rapidly with temperature, such materials have a faster change rate with polarization temperature in terms of ferroelectric macroscopic properties, from them could get superior electrocaloric effects. We compile a relatively comprehensive computational design on the high performance of electrocaloric effects in different types of ferroelectrics and offer a perspective on the computational design of electrocaloric refrigeration materials at the mesoscale microstructure level.
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