We investigated what is really meant by so-called positional or frequency fluctuation of spectral features. To show the difference between the true frequency shift of a single band and apparent peak maximum shift caused by relative intensity changes of overlapped adjacent bands, we analyzed infrared (IR) spectra of the OH stretching band of ethylene glycol during the heating process and the C=O stretching band of acetone in a mixed solvent CHCl(3)/CCl(4) with varying solvent compositions. These spectra are well-known examples of so-called "band shift" phenomena often interpreted as the manifestation of gradual changes in the IR frequency associated with a specific chemical bond under the influence of molecular interactions. Analyses of IR spectra showed that the apparent positional shifts of peak maxima in these systems are actually due to relative contribution changes of two overlapped bands, instead of the gradual frequency shift of a single band induced by the change in the strength of molecular interactions. To further clarify our interpretation of "peak maximum shifts", we also analyzed simulated spectral datasets, comparing the true band frequency shift and change in the relative contributions of overlapped bands. It was found that principal component analysis (PCA) is a surprisingly sensitive tool to distinguish the two possible mechanisms of peak maximum shift. The new insight revealed by this study should help the interpretation of molecular interactions probed by vibrational spectroscopy.
In order to fabricate a digital microfluidic (DMF) chip, which requires a patterned array of electrodes coated with a dielectric film, we explored two simple methods: Ballpoint pen printing to generate the electrodes, and wrapping of a dielectric plastic film to coat the electrodes. For precise and programmable printing of the patterned electrodes, we used a digital plotter with a ballpoint pen filled with a silver nanoparticle (AgNP) ink. Instead of using conventional material deposition methods, such as chemical vapor deposition, printing, and spin coating, for fabricating the thin dielectric layer, we used a simple method in which we prepared a thin dielectric layer using pre-made linear, low-density polyethylene (LLDPE) plastic (17-μm thick) by simple wrapping. We then sealed it tightly with thin silicone oil layers so that it could be used as a DMF chip. Such a treated dielectric layer showed good electrowetting performance for a sessile drop without contact angle hysteresis under an applied voltage of less than 170 V. By using this straightforward fabrication method, we quickly and affordably fabricated a paper-based DMF chip and demonstrated the digital electrofluidic actuation and manipulation of drops.
A simple programmable contact printing method using ballpoint pens with silver nanoparticle (AgNP) and carbon nanotube (CNT) ink and a digital plotter were developed for quick patterning of electrodes on paper. This printing method enables sequential and programmable printing with two different inks and with ink consisting of high viscosity materials and is amenable to reproducibility of printed electrodes and customized designs. With this printing method, AgNP and CNT patterns with low electrical resistance and high density of the material can be printed. Using these AgNP and CNT inks, we fabricated disposable electrochemical sensors (ECSs) on paper. The ECSs were successfully used to detect glucose at various concentrations from 0 to 15 mM. The characteristics of the printed AgNP and CNT patterns, such as the printing resolution, surface morphology, and electrical properties, were also studied. The proposed contact printing method opens an avenue for printing paper-based electronics and devices.
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