Light intensity-induced phase transitions in graphene oxide doped polyvinylidene fluoride

The coupling of light with low-frequency functionalities of dielectrics and liquid crystals and an ability to turn “on” and “off” the pyro-, piezo-, or ferro- electric properties of materials on demand by optical means leads to fascinating science and device applications. Moreover, to achieve all-optical control in nano-circuits, the coupling of the light with mechanical degrees of freedom is highly desirable and has been elusive until recently. In this work, we report on the light intensity-induced structural phase transitions in graphene oxide doped piezoelectric polyvinylidene fluoride (PVDF) film observed by micro-Raman spectroscopy. Increasing the laser power results in a steady transformation of the Raman spectrum featured piezoelectric phase to one of non-piezoelectric structure. This effect is accompanied by volumetric change of a PVDF unit cell by a factor of two, useful for a photostriction materials application. Furthermore, we observed the reversible switching of α and phases as a function of the light intensity (laser power between 5.7–31.3 mW). This opens up a new route for multi-functionality control where strain, piezoelectric constants and polarization can be modified by light

Structural Origin of Recovered Ferroelectricity in BaTiO3_3 Nanoparticles

Nanoscale BaTiO$_3$ particles (~10 nm) prepared by ball-milling a mixture of oleic acid and heptane have been reported to have an electric polarization several times larger than that for bulk BaTiO$_3$. In this work, detailed local, intermediate, and long-range structural studies are combined with spectroscopic measurements to develop a model structure of these materials. The X-ray spectroscopic measurements reveal large Ti off-centering as the key factor producing the large spontaneous polarization in the nanoparticles. Temperature-dependent lattice parameter changes reveal the sharpening of the structural phase transitions in these BaTiO$_3$ nanoparticles compared to the pure nanoparticle systems. Sharp crystalline-type peaks in the barium oleate Raman spectra suggest that this component in the composite core-shell matrix, a product of mechanochemical synthesis, stabilizes an enhanced polar structural phase of the BaTiO$_3$ core nanoparticles.Comment: 5 figures in main text. 1 table and 3 figures in supplementary documen

Chemotactic response and adaptation dynamics in Escherichia coli

Adaptation of the chemotaxis sensory pathway of the bacterium Escherichia coli is integral for detecting chemicals over a wide range of background concentrations, ultimately allowing cells to swim towards sources of attractant and away from repellents. Its biochemical mechanism based on methylation and demethylation of chemoreceptors has long been known. Despite the importance of adaptation for cell memory and behavior, the dynamics of adaptation are difficult to reconcile with current models of precise adaptation. Here, we follow time courses of signaling in response to concentration step changes of attractant using in vivo fluorescence resonance energy transfer measurements. Specifically, we use a condensed representation of adaptation time courses for efficient evaluation of different adaptation models. To quantitatively explain the data, we finally develop a dynamic model for signaling and adaptation based on the attractant flow in the experiment, signaling by cooperative receptor complexes, and multiple layers of feedback regulation for adaptation. We experimentally confirm the predicted effects of changing the enzyme-expression level and bypassing the negative feedback for demethylation. Our data analysis suggests significant imprecision in adaptation for large additions. Furthermore, our model predicts highly regulated, ultrafast adaptation in response to removal of attractant, which may be useful for fast reorientation of the cell and noise reduction in adaptation.Comment: accepted for publication in PLoS Computational Biology; manuscript (19 pages, 5 figures) and supplementary information; added additional clarification on alternative adaptation models in supplementary informatio

Stoichiometric and ultra-stable nanoparticles of II-VI compound semiconductors

Nanoparticles of (CdSe)n are found extremely stable at n = 33 and 34 with structures distinctively different from the bulk fragments. They grow exclusively in large amount with a simple solution method. The diameter is determined as 1.5 nm. Such ultra-stable nanoparticles had been predicted both theoretically and experimentally after the discovery of carbon fullerenes, but not been produced macroscopically in any other element or compound system. First-principles calculations predict that the structures of (CdSe)33 and (CdSe)34 are puckered (CdSe)28-cages accommodating respectively (CdSe)5 an (CdSe)6 inside to form a three-dimensional network of essentially hetero-polar sp3-bonding