Fingering Instability Accelerates Population Growth of a Proliferating Cell Collective.

During the growth of a cell collective, such as proliferating microbial colonies and epithelial tissues, the local cell growth increases the local pressure, which in turn suppresses cell growth. How this pressure-growth coupling affects the growth of a cell collective remains unclear. Here, we answer this question using a continuum model of a cell collective. We find that a fast-growing leading front and a slow-growing interior of the cell collective emerge due to the pressure-dependent growth rate. The leading front can exhibit fingering instability, and we confirm the predicted instability criteria numerically with the leading front explicitly simulated. Intriguingly, we find that fingering instability is not only a consequence of local cell growth but also enhances the entire population's growth rate as positive feedback. Our work unveils the fitness advantage of fingering formation and suggests that the ability to form protrusions can be evolutionarily selected.

Decoupling between the translation and rotation of water in the proximity of a protein molecule.

The interaction between water and biomacromolecules is of fundamental interest in biophysics, biochemistry and physical chemistry. By combining neutron scattering and molecular dynamics simulations on a perdeuterated protein at a series of hydration levels, we demonstrated that the translational motion of water is slowed down more significantly than its rotation, when water molecules approach the protein molecule. Further analysis of the simulation trajectories reveals that the observed decoupling results from the fact that the translational motion of water is more correlated over space and more retarded by the charged/polar residues and spatial confinement on the protein surface, than the rotation. Moreover, around the stable protein residues (with smaller atomic fluctuations), water exhibits more decoupled dynamics, indicating a connection between the observed translation-rotation decoupling in hydration water and the local stability of the protein molecule.

Sharp selective scattering of red, green, and blue light achieved via gain material's loss compensation.

Frequency-selective scattering of light can be achieved by metallic nanoparticle's localized surface plasmon resonance (LSPR). And this property may find an application in a transparent projection screen: ideally, specially designed metallic nanoparticles dispersed in a transparent matrix only selectively scatter red, green and blue light and transmit the visible light of other colors. However, optical absorption and surface dispersion of a metallic nanoparticle, whose size is comparable or smaller than mean free path of electrons in the constituent material, degenerate the desired performance by broadening the resonance peak width (i.e., decreasing frequency-selectivity) and decreasing light scattering intensity. In this work, it is shown that the problem can be solved by introducing gain material. Numerical simulations are performed on nanostructures based on silver (Ag), gold (Au) or aluminum (Al) with or without gain material, to examine the effect of gain material and to search for suitable structures for sharp selective scattering of red, green and blue light. And it is found that introducing gain material greatly improves performance of the structures based on Ag or Au except the structures based on Al. The most suitable structures for sharp selective scattering of red, green and blue light are, respectively, found to be the core-shell structures of silica/Au (core/shell), silica/Ag and Ag/silica, all with gain material.

Putting scaling laws on a physical foundation.

As a cell changes size during the cell cycle, why does its density remain constant?

Effect of Surface Scattering of Electrons on Ratios of Optical Absorption and Scattering to Extinction of Gold Nanoshell.

Gold nanoshell's high light scattering and absorption at its resonance wavelength have found applications in biomedical imaging and photothermal therapy. However, at nanoscale, metallic material's dielectric function is affected by nanoparticle's size, mainly via a mechanism called surface scattering of conduction electrons. In this work, the effect of surface scattering of electrons on the ratios of optical absorption and scattering to extinction (which is the sum of the absorption and scattering) of gold nanoshell is investigated. Simulation results for several shell thicknesses are compared. It is found that the electrons' surface scattering increases the optical absorption ratio, and the thinner the shell thickness, the larger the increase in the difference of the absorption ratio between the situations with and without the surface scattering considered. The increase of absorption ratio is then verified by comparing simulation results to experimental measurements for three nanoshells. The parameters of the simulations to fit the experimental measurements show that the damping of conduction electrons in metallic shell geometry is larger than that predicted by the billiard scattering model.

Resonant scattering of green light enabled by Ag@TiO2 and its application in a green light projection screen.

The ability to selectively scatter green light is essential for an RGB transparent projection display, and this can be achieved by a silver-core, titania-shell nanostructure (Ag@TiO2), based on the metallic nanoparticle's localized surface plasmon resonance. The ability to selectively scatter green light is shown in a theoretical design, in which structural optimization is included, and is then experimentally verified by characterization of a transparent film produced by dispersing such nanoparticles in a polymer matrix. A visual assessesment indicates that a high-quality green image can be clearly displayed on the transparent film. For completeness, a theoretical design for selective scattering of red light based on Ag@TiO2 is also shown.

A Deformable and Highly Robust Ethyl Cellulose Transparent Conductor with a Scalable Silver Nanowires Bundle Micromesh.

Huge challenges remain regarding the facile fabrication of neat metallic nanowires mesh for high-quality transparent conductors (TCs). Here, a scalable metallic nanowires bundle micromesh is achieved readily by a spray-assisted self-assembly process, resulting in a conducting mesh with controllable ring size (4-45 µm) that can be easily realized on optional polymer substrates, rendering it transferable to various deformable and transparent substrates. The resultant conductors with the embedded nanowires bundle micromesh deliver superior and customizable optoelectronic performances, and can sustain various mechanical deformations, environmental exposure, and severe washing, exhibiting feasibility for large-scale manufacturing. The silver nanowires bundle micromesh with explicit conductive paths is embedded into an ethyl cellulose (EC) transparent substrate to achieve superior optoelectronic properties endowed by a low amount of incorporated nanowires, which leads to reduced extinction cross-section as verified by optical simulation. A representative EC conductor with a low sheet resistance of 25 Ω â–¡-1 , ultrahigh transmittance of 97%, and low haze of 2.6% is attained, with extreme deformability (internal bending radius of 5 µm) and waterproofing properties, opening up new possibilities for low-cost and scalable TCs to replace indium-tin oxide (ITO) for future flexible electronics, as demonstrated in a capacitive touch panel in this work.