Flexible Polyester Cellulose Paper Supercapacitor with a Gel Electrolyte

A low-cost polyester cellulose paper has been used as a substrate for a flexible supercapacitor device that contains aqueous carbon nanotube ink as the electrodes and a polyvinyl alcohol (PVA)-based gel as the electrolyte. Gel electrolytes have attracted much interest due to their solvent-holding capacity and good film-forming capability. The electrodes are characterized for their conductivity and morphology. Because of its high conductivity, the conductive paper is studied in supercapacitor applications as active electrodes and as separators after coating with polyvinylidene fluoride. Carbon nanotubes deposited on porous paper are more accessible to ions in the electrolyte than those on flat substrates, which results in higher power density. A simple fabrication process is achieved and paper supercapacitors are tested for their performance in both aqueous and PVA gel electrolytes by using galvanostatic and cyclic voltammetry methods. A high specific capacitance of 270 F g⁻¹ and an energy density value of 37 W h kg⁻¹ are achieved for devices with PVA gel electrolytes. Furthermore, this device can maintain excellent specific capacitance even under high currents. This is also confirmed by another counter experiment with aqueous sulfuric acid as the electrolyte. The cycle life, one of the most critical parameters in supercapacitor operations, is found to be excellent (6000 cycles) and less than 0.5 % capacitance loss is observed. Moreover, the supercapacitor device is flexible and even after twisting does not show any cracks or evidence of breakage, and shows almost the same specific capacitance of 267 F g⁻¹and energy density of 37 W h kg⁻¹. This work suggests that a paper substrate can be a highly scalable and low-cost solution for high-performance supercapacitors.     

Monitoring allostery in D2O: a necessary control in studies using hydrogen/deuterium exchange to characterize allosteric regulation

There is currently a renewed focus aimed at understanding allosteric mechanisms at atomic resolution. This current interest seeks to understand how both changes in protein conformations and changes in protein dynamics contribute to relaying an allosteric signal between two ligand binding sites on a protein (e.g., active and allosteric sites). Both nuclear magnetic resonance (NMR), by monitoring protein dynamics directly, and hydrogen/deuterium exchange, by monitoring solvent accessibility of backbone amides, offer insights into protein dynamics. Unfortunately, many allosteric proteins exceed the size limitations of standard NMR techniques. Although hydrogen/deuterium exchange as detected by mass spectrometry (H/DX-MS) offers an alternative evaluation method, any application of hydrogen/deuterium exchange requires that the property being measured functions in both H₂O and D₂O. Due to the promising future H/DX-MS has in the evaluation of allosteric mechanisms in large proteins, we demonstrate an evaluation of allosteric regulation in D₂O. Exemplified using phenylalanine inhibition of rabbit muscle pyruvate kinase, we find that binding of the inhibitor is greatly reduced in D₂O, but the effector continues to elicit an allosteric response.     

HDXFinder: automated analysis and data reporting of deuterium/hydrogen exchange mass spectrometry

Hydrogen/deuterium exchange in combination with mass spectrometry (H/D MS) is a sensitive technique for detection of changes in protein conformation and dynamics. However, wide application of H/D MS has been hindered, in part, by the lack of computational tools necessary for efficient analysis of the large data sets associated with this technique. We report a novel web-based application for automatic analysis of H/D MS experimental data. This application relies on the high resolution of mass spectrometers to extract all isotopic envelopes before correlating these envelopes with individual peptides. Although a fully automatic analysis is possible, a variety of graphical tools are included to aid in the verification of correlations and rankings of the isotopic peptide envelopes. As a demonstration, the rate constants for H/D exchange of peptides from rabbit muscle pyruvate kinase are mapped onto the structure of this protein.     

Isotope ratio monitoring gas chromatography/Mass spectrometry of D/H by high temperature conversion isotope ratio mass spectrometry

Of all the elements, hydrogen has the largest naturally occurring variations in the ratio of its stable isotopes (D/H). It is for this reason that there has been a strong desire to add hydrogen to the list of elements amenable to isotope ratio monitoring gas chromatography/mass spectrometry (irm-GC/MS). In irm-GC/MS the sample is entrained in helium as the carrier gas, which is also ionized and separated in the isotope ratio mass spectrometer (IRMS). Because of the low abundance of deuterium in nature, precise and accurate on-line monitoring of D/H ratios with an IRMS requires that low energy helium ions be kept out of the m/z 3 collector, which requires the use of an energy filter. A clean mass 3 (HD(+.)) signal which is independent of a large helium load in the electron impact ion source is essential in order to reach the sensitivity required for D/H analysis of capillary GC peaks. A new IRMS system, the DELTA(plus)XL(trade mark), has been designed for high precision, high accuracy measurements of transient signals of hydrogen gas. It incorporates a retardation lens integrated into the m/z 3 Faraday cup collector. Following GC separation, the hydrogen bound in organic compounds must be quantitatively converted into H(2) gas prior to analysis in the IRMS. Quantitative conversion is achieved by high temperature conversion (TC) at temperatures >1400 degrees C. Measurements of D/H ratios of individual organic compounds in complicated natural mixtures can now be made to a precision of 2 per thousand (delta notation) or, better, with typical sample amounts of approximately 200 ng per compound. Initial applications have focused on compounds of interest to petroleum research (biomarkers and natural gas components), food and flavor control (vanillin and ethanol), and metabolic studies (fatty acids and steroids). Copyright 1999 John Wiley & Sons, Ltd.     

Synthesis and characterization of "hairy urchin"-like polyaniline by using β-cyclodextrin as a template

A novel synthesis of "hairy urchin"-shaped polyaniline (PAni) and its surface coverage with nanospikes was achieved from a simple microemulsion polymerization technique in the presence of β-cyclodextrin (β-CD). The rodlike micelle phase was characterized, and the key factors affecting the formation of PAni nanostructures were systematically examined. Ferric chloride (FeCl(3)) has played a role as a structural directing agent to fabricate the polymer as hairy urchin-like structure/nanorods via a cooperative interaction between FeCl(3) and DoTAC in an aqueous medium. Host-guest inclusion complex of β-cyclodextrin with aniline was used as a monomer. It has been revealed that the formation of the supramolecular complexes of polyaniline with β-CD due to host-guest interaction is indispensable for the fabrication of these unique PAni nanostructures, and a suitable β-CD to aniline molar ratio is essential to their exclusive formation. Different varieties of PAni nanostructures such as hairy urchin, branched particles consisting of rodlike branches, and regular rodlike particles were obtained in the presence of FeCl(3). Also, in the absence of FeCl(3), a predominant product of regular spherical particles and wirelike aggregation exhibiting faceted surfaces were obtained. The structures of polyaniline hairy urchin-like nanorods were analyzed using transmission electron microscopy (TEM). The synthesized polymer was characterized by Fourier-transform infrared spectroscopy and X-ray diffraction technique. Additionally, the relationship between the morphology and the conductivity of the PAni nanostructures was investigated as well.     

An insight into phenomenal optical non‐linearities arising from synergistic relationship between selected BODIPYs and noble metal nanoparticles

Materials with large and quick non‐linear optical response, excellent photo thermal stability, cost effectiveness and off resonant non‐linear absorption (NLA) are essential requirements for a good optical limiting (OL). Among them, organic systems and π‐conjugated polymers are getting special interest because of their flexibility in structural modification that leads to the tuning of optical and electronic properties that are suitable for working under large bandwidth. Here, we report a drastic enhancement of non‐linear optical activity and exceptional OL action of two organic–inorganic hybrid system based on BODIPY and Au and Ag nanoparticles (NPs). The organic system taken was certain set of BODIPYs with different substitution at the para and meta positions. All the compounds were found to be exhibiting good reverse saturable absorption (RSA) behaviour and negative non‐linear refraction property. An attempt was made to improve the non‐linear optical (NLO) property of the BODIPY by forming nanohybrids with Au and Ag NPs, and the best NLO active candidate among the studied system was chosen for it. A significant enhancement in NLO property was observed on hybrid system formation. The optical limiting (OL) threshold of the hybrid (1 J/cm²) was reduced almost 1/5 times than that of the parent compound (5.2 J/cm²), and this value is comparable with the benchmark OL materials like C₆₀. The mechanism behind the NLA is found to be the combination of excited state absorption (ESA) and two‐photon absorption (TPA). The enhanced NLA and OL action of C? Ag/Au nanohybrids are attributed to the synergetic effect among the two parent components as well as the local field effects of NPs. Enhancement in non‐linear optical property is found to be stronger in hybrid system with Au NPs and is due to the resonant charge transfer and intense local field effect on exciting with 532‐nm pulse compared with that of Ag NPs. Both the parent compounds and the nanohybrids exhibit negative non‐linearity, and the non‐linear refraction is also found to be enhanced. The improved NLA and OL property of hybrid system guarantees successful usage of the strategy in OL applications.