RESUMEN
The pursuit of harnessing superior mechanical properties achieved through the size effect on a macroscopic scale has been a prominent focus in engineering, as size-induced strengthening is enabled only in the nanoscale regime. This study presents a metal/ceramic/metal (MCM) nanocomposite reinforced by ceramic nanoarchitectures. Through proximity-field nanopatterning, the inch-scale production of nanoarchitecture films is enabled in a single fabrication step. The developed three-dimensional (3D) Ni/Al2O3/Ni nanocomposite film exhibits significantly high compressive strength, corresponding to an increase of approximately 30% compared with that calculated using the upper limits of the conventional rule of mixtures. The exceptional strength of the 3D MCM nanocomposite can be attributed to the extrinsic size effect of the ceramic nanoarchitectures. By combining size-induced strengthening of ceramics with the strengthening law for composites, a new type of strengthening model is derived and experimentally validated using the 3D MCM nanocomposite.
RESUMEN
When multiple intermolecular interactions occur simultaneously, complexed molecules undergo gelation by inter-cohesive bonding, inducing a pseudo-crosslinking effect to form a supramolecular gel. Among the number of substances that can induce supramolecular assembly, phenolic species such as 3,4-dihydroxy-l-phenylalanine (DOPA) are widely utilized for synthesizing adhesive materials. However, despite the strong adhesion capability of monomeric phenol, it lacks cohesive strength and rarely forms a supramolecular gel to secure its mechanical properties. In this study, to overcome this obstacle, we synthesized a supramolecular coacervate hydrogel by simply mixing poly(N-vinylpyrrolidone) (PVP) and tannic acid (TA), resulting in strong cohesive interactions by virtue of the larger molecular size of TA and reinforced molecular interactions attributed to the presence of galloyl groups with a high density. We further analyzed the rheological and adhesive properties of PVP-TA coacervate hydrogels, revealing that they could exhibit not only a self-healing property, but also super adhesive properties with an average adhesion strength of 3.71 MPa on a glass substrate, which is >4 times stronger than that of conventional PVP.
RESUMEN
Sn is one of the promising Li ion battery anode materials with high theoretical capacity and mechanical properties that allow for effective relaxation of Li diffusion-induced stresses. Sn is a low melting point metal with a low modulus and strength and has the ability to relax stresses via plasticity and creep deformations. In this study, concentration-dependent material properties are used in numerical simulations to model the Li diffusion-induced stress evolution in Sn micropillars. Simulation results using concentration-dependent material properties resulted in a completely different failure mode in comparison to that of concentration-independent simulation results. Tensile hoop stress needed for crack propagation was analyzed to be at the core for concentration-independent material properties, and switched to being at the surface for concentration-dependent simulation results. In addition, by incorporating these maximum tensile DIS results, the critical size for the failure of Sn micropillars was determined to be 5.3 µm at C/10 charging rate. This was then correlated with experimental observations, where fracture occurred in Sn micropillars with sizes larger than 6 µm, while 4.4 µm sized Sn micropillars survived the lithiation cycle.