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Jian Ping Gong

Publications and source records attributed to Jian Ping Gong.

7 recordsLinked to original sources

Defect screening and load transfer in minimal hard-soft double networks

Double network (DN) materials exhibit anomalous strength and toughness that far exceed the sum of their constituents. While widely exploited, the fundamental physical mechanisms underlying this synergy remain elusive. Here, we show that a minimal three-dimensional model of two coupled, disordered linear-elastic networks is sufficient to capture the essential physics of DN nonlinear mechanics. The model reproduces the full suite of unique mechanical behaviors, including yielding, necking, strain hardening, and the brittle-to-ductile transition. Mechanical contrast between the hard and soft networks drives inter-network load transfer, which screens defects and suppresses stress concentrations in the hard network. By defining a stress-concentration factor, K_sc, we find that the hard-network failure strain scales universally as 1/K_sc, directly bridging microscopic defect screening to macroscopic yielding. We further show that complete defect screening triggers the shift from localized necking to delocalized damage. Furthermore, the stable necking plateau is identified as an energetic selection governed by the balance between potential energy release and irreversible dissipation. These findings reveal that a simple linear-elastic framework can account for the rich nonlinear landscape of DN materials, providing a general principle for designing next-generation tough solids.

cond-mat.soft↗

Ultimately deformed double-network gels possess positive energetic elasticity

The elasticity of rubbery polymer networks has been considered to be entropy-driven. On the other hand, studies on single polymer chain mechanics have revealed that the elasticity of ultimately stretched polymer chains is dominated by the energetic contribution mainly originating from chemical bond deformation. Here, we experimentally found that the elasticity of the double-network gel transits from the entropy-dominated one to the internal energy-driven one with its uniaxial deformation through the thermodynamic analysis. Based on this finding, we developed a simple mechanical model that takes into account the energetic contribution and found that this model approximately reproduces the temperature dependence of the stress-strain curve of the double-network gel. This study demonstrates the importance of the chemical perspective in the mechanical analysis of highly deformed rubbery polymer networks.

cond-mat.soft↗

Color-switching hydrogels as integrated microfluidic pressure sensors

Precisely measuring pressure in microfluidic flows is essential for flow control, fluid characterization, and monitoring, but faces specific challenges such as \RE{achieving} sufficient resolution, non-invasiveness, or ease of use. Here, we demonstrate a fully integrated multiplexed optofluidic pressure sensor, entirely decoupled from the flow path, that enables local pressure measurements along any microfluidic channel without altering its flow geometry. The sensor itself relies on the compression of a soft mechano-actuated hydrogel, changing color in response to a pressure change. The hydrogel is separated from the fluid circulating in the channel by a thin membrane, allowing for the unrestricted use of different types of fluids. Imaging the gel through the transparent PDMS with a color camera provides a direct, easy, and contact-free determination of the fluid pressure at the sensing location for pressures as small as \SI{20}{\milli\bar} with a resolution of around \SI{10}{\milli\bar}. The sensitivity and accessible pressure range can be tuned via the mechanical properties \RE{of the sensing unit}. The photonic gel can also be used to acquire 2D pressure or deformation maps, taking advantage of the fast response time and fine spatial resolution.

physics.flu-dyn↗

Nonlinearity tunes crack dynamics in soft materials

Cracks in soft materials exhibit diverse dynamic patterns, involving straight, oscillation, branching, and supershear fracture. Here, we successfully reproduce these crack morphologies in a two-dimensional pre-strained fracture scenario and establish crack stability phase diagrams for three distinct nonlinear materials using a fracture phase field model. The contrasting phase diagrams highlight the crucial role of nonlinearity in regulating crack dynamics. In strain-softening materials, crack branching prevails, limiting the cracks to sub-Rayleigh states. Yet strain-stiffening stabilizes crack propagation, allowing for the presence of supershear fracture. Of particular interest is the large-strain linear elastic materials, where crack oscillation is readily triggered. The onset speed of such instability scales linearly with the characteristic wave speed near the crack tip, supporting the notion that such crack oscillations are a universal instability closely tied to the wave speed. The oscillation wavelength is shown to be a bilinear function of the nonlinear scale and crack driving force, with a minimum length scale associated with the dissipative zone. Moreover, our findings suggest that the increase in characteristic wave speed due to strain-stiffening can account for the observed transition of cracks from sub-Rayleigh to supershear regimes.

cond-mat.soft↗

The fracture of highly deformable soft materials: A tale of two length scales

The fracture of highly deformable soft materials is of great practical importance in a wide range of technological applications, emerging in fields such as soft robotics, stretchable electronics and tissue engineering. From a basic physics perspective, the failure of these materials poses fundamental challenges due to the strongly nonlinear and dissipative deformation involved. In this review, we discuss the physics of cracks in soft materials and highlight two length scales that characterize the strongly nonlinear elastic and dissipation zones near crack tips in such materials. We discuss physical processes, theoretical concepts and mathematical results that elucidate the nature of the two length scales, and show that the two length scales can classify a wide range of materials. The emerging multi-scale physical picture outlines the theoretical ingredients required for the development of predictive theories of the fracture soft materials. We conclude by listing open challenges and future investigation directions.

cond-mat.soft↗

Shearing-induced contact pattern formation in hydrogels sliding in polymer solution

The contact of a hydrogel during the rotational shearing on glass surface in concentrated polymer solution was observed in situ. Dynamic contact patterns that rotate in-phase with the rotational shearing of the gel were observed for the first time. The contact patterns with a periodicity in the circumferential direction appeared and developed into fine characters with the shearing time. The patterns appeared more quickly at elevated sliding velocity, polymer concentration, and normal pressure. Furthermore, the softness of the gel also substantially influenced the character of the patterns. The pattern formation was discussed in terms of the non-linear rheology of the polymer solution at the rotational soft interface.

cond-mat.soft↗

How super-tough gels break

Fracture of highly stretched materials challenges our view of how things break. We directly visualize rupture of tough double-network (DN) gels at >50\% strain. During fracture, crack tip shapes obey a $x\sim y^{1.6}$ power-law, in contrast to the parabolic profile observed in low-strain cracks. A new length-scale $\ell$ emerges from the power-law; we show that $\ell$ scales directly with the stored elastic energy, and diverges when the crack velocity approaches the shear wave speed. Our results show that DN gels undergo brittle fracture, and provide a testing ground for large-strain fracture mechanics.

cond-mat.soft↗