Hafnium oxide based ferroelectric thin films have shown potential as a promising alternative material for non-volatile memory applications. This work reports the switching stability of a Si-doped HfO2 film under bipolar pulsed-field operation. High field cycling causes a "wake-up" in virgin "pinched" polarization hysteresis loops, demonstrated by an enhancement in remanent polarization and a shift of negative coercive voltage. The rate of wake-up is accelerated by either reducing the frequency or increasing the amplitude of the cycling field. We suggest de-pinning of domains due to reduction of the defect concentration at bottom electrode interface as origin of the wake-up

Epidermal growth factor receptor (EGFR, also known as ErbB-1 or HER-1) is a membrane bound protein that has been associated with a variety of solid tumors and the control of cell survival, proliferation and metabolism. Quantification of EGFR expression level in cells membrane and the interaction kinetics with drugs are thus important for cancer diagnosis and treatment. Here we report mapping of the distribution and interaction kinetics of EGFR in their native environment with a surface plasmon resonance imaging (SPRi) technique. Monoclonal anti-EGFR antibody was used as a model drug in this study. The binding of the antibody to EGFR overexpressed A431 cells was monitored in real time, which was found to follow the first-order kinetics with association rate constant (ka) and dissociation rate constant (kd) to be (2.7 ± 0.6)×105 M-1s-1 and (1.4 ± 0.5)×10-4 s-1, respectively. The dissociation constant (KD) was determined to be (0.53 ± 0.26) nM with up to seven folds variation among different individual A431 cells. In addition, the averaged A431 cell surface EGFR density was found to be 636/μm2 with an estimation of 5×105 EGFR per cell. Additional measurement also revealed different EGFR positive cell lines (A431, HeLa and A549) show receptor density dependent anti-EGFR binding kinetics. The results demonstrate that SPRi is a valuable tool for direct quantification of membrane protein expression level and ligand binding kinetics at single cell resolution. Our findings show that the local environment affects the drug-receptor interactions and in-situ measurement of membrane protein binding kinetics is important.

Detection of a single or small amount of charges and molecules in biologically relevant aqueous solutions is a long-standing goal in analytical science and detection technology. Here we report on self-assembled nano-oscillators for charge and molecular binding detections in aqueous solutions. Each nano-oscillator consists of a nanoparticle linked to a solid surface via a molecular tether. By applying an oscillating electric field normal to the surface, the nanoparticles oscillate, which is detected individually with ∼0.1 nm accuracy by a plasmonic imaging technique. From the oscillation amplitude and phase, the charge of the nanoparticles is determined with a detection limit of ∼0.18 electron charges along with the charge polarity. We further demonstrate the detection of molecular binding with the self-assembled nano-oscillators.

A novel sugar-appended low-molecular-mass gelator, 4 00 -butoxy-4-hydroxy-p-terphenyl-β-D-glucoside (BHTG), was synthesized. It formed thermally reversible gels in a variety of aqueous and organic solvents. Three-dimensional networks made up of helical ribbons were observed in the mixture of H 2 O/1,4-dioxane (40/60 v/v). The handedness of the ribbons depended on the rate of gel formation. Fast-cooling process led to right-handed ribbons, while slow-cooling process led to left-handed ones. A combinatory analyses of microscopic, spectroscopic, and diffraction techniques revealed that BHTG formed a twisted interdigitated bilayer structure with a d spacing of 3.1 nm in gels through a kinetically controlled nucleation-growth process. There were two kinds of molecular orientations of BHTG in the nuclei, clockwise and anticlockwise, which dictated the growth of ribbons. One was metastable and formed first during the cooling process of gel formation. It was able to gradually transform into the more stable latter one with further decreasing temperature. Fast-cooling process did not leave enough time for the nuclei to evolve from metastable to stable state and the ribbons grown from them exhibited right-handedness. However, the metastable nuclei transformed into the stable one when cooled slowly and directed the molecules of BHTG to grow into left-handed aggregates.