Graphene functionalised by laser ablated V2O5 as highly sensitive NH3 sensor

Graphene has been recognized as a promising gas sensing material. The response of graphene-based sensors can be radically improved by introducing defects in graphene using, e. g., metal or metal oxide nanoparticles. We have functionalised CVD grown, single layer graphene by applying pulsed laser deposition (PLD) of V2O5 which resulted in a thin V2O5 layer on graphene with average thickness of ~0.6 nm. According to Raman analysis, PLD process also induced defects in graphene. Compared to unmodified graphene, the obtained chemiresistive sensor showed considerable improvement of sensing ammonia at room temperature. In addition, also the response time, sensitivity and reversibility were essentially enhanced due to graphene functionalisation by laser deposited V2O5. This can be explained by increased surface density of gas adsorption sites introduced by high energy atoms in laser ablation plasma and formation of nanophase boundaries between deposited V2O5 and graphene.Comment: 22 pages, 6 figure

Bionanomaterials from plant viruses

Plant virus capsids have emerged as useful biotemplates for material synthesis. All plant virus capsids are assembled with high-precision, three-dimensional structures providing nanoscale architectures that are highly monodisperse, can be produced in large quantities and that cannot replicate in mammalian cells (so are safe). Such exceptional characteristics make plant viruses strong candidates for application as biotemplates for novel and new material synthesis

Design, Development and Thermal Analysis of Reusable Li-Ion Battery Module for Future Mobile and Stationary Applications

open access articleThe performance, energy storage capacity, safety, and lifetime of lithium-ion battery cells of different chemistries are very sensitive to operating and environmental temperatures. The cells generate heat by current passing through their internal resistances, and chemical reactions can generate additional, sometimes uncontrollable, heat if the temperature within the cells reaches the trigger temperature. Therefore, a high-performance battery cooling system that maintains cells as close to the ideal temperature as possible is needed to enable the highest possible discharge current rates while still providing a sufficient safety margin. This paper presents a novel design, preliminary development, and results for an inexpensive reusable, liquid-cooled, modular, hexagonal battery module that may be suitable for some mobile and stationary applications that have high charge and or discharge rate requirements. The battery temperature rise was measured experimentally for a six parallel 18650 cylindrical cell demonstrator module over complete discharge cycles at discharge rates of 1C, 2C and 3C. The measured temperature rises at the hottest point in the cells, at the anode terminal, were found to be 6, 17 and 22 °C, respectively. The thermal resistance of the system was estimated to be below 0.2 K/W at a coolant flow rate of 0.001 Kg/s. The proposed liquid cooled module appeared to be an effective solution for maintaining cylindrical Li-ion cells close to their optimum working temperature

Electrochemical immunosensor modified with carbon nanofibers coupled to a paper platform for the determination of gliadins in food samples

The gluten-free diet is a unique, effective treatment for different conditions related to gluten consumption. Therefore, it is crucial the availability of new methodologies for the sensitive and specific determination of gluten content in food samples. Herein, a screen printed electrode modified with carbon nanofibers coupled to a paper immunoaffinity platform was reported for the determination of gliadin in foods samples. The paper microzone covalently functionalized with specific anti-gliadin antibodies was placed on the modified electrode surface for the electrochemical determination of gliadin. The surface of the electrode modified with carbon nanofibers was characterized by scanning electron microscopy (SEM) and cyclic voltammetry (CV), which showed the improved sensitivity of the modified surface. The developed device was evaluated using different flour samples obtaining a favorable response. The calculated limit of detection for the device in analyzed samples was 0.005 mg kg -1 and for the enzyme-linked immunosorbent assay was 1.5 mg kg -1 . The coefficient of variation (CV) for the determination of 20 μg kg -1 of gliadin was 4.11%. The disposable electrochemical sensor developed, represents an easy-to-use and low-cost strategy for the determination of gliadin in food samples.Fil: Marin Barroso, Evelyn del Valle. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; ArgentinaFil: Messina, Germán Alejandro. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina; ArgentinaFil: Bertolino, Franco Adrián. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina; ArgentinaFil: Raba, Julio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina; ArgentinaFil: Pereira, Sirley Vanesa. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - San Luis. Instituto de Química de San Luis. Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Instituto de Química de San Luis; Argentina; Argentin

Nonflammable Lithium Metal Full Cells with Ultra-high Energy Density Based on Coordinated Carbonate Electrolytes

Coupling thin Li metal anodes with high-capacity/high-voltage cathodes such as LiNi0.8Co0.1Mn0.1O2 (NCM811) is a promising way to increase lithium battery energy density. Yet, the realization of high-performance full cells remains a formidable challenge. Here, we demonstrate a new class of highly coordinated, nonflammable carbonate electrolytes based on lithium bis(fluorosulfonyl)imide (UFSI) in propylene carbonate/fluoroethylene carbonate mixtures. Utilizing an optimal salt concentr ation (4 M LiFSI) of the electrolyte results in a unique coordination structure of Li+-FSI-solvent cluster, which is critical for enabling the formation of stable interfaces on both the thin Li metal anode and high-voltage NCM811 cathode. Under highly demanding cell configuration and operating conditions (Li metal anode = 35 mu m, areal capacity/charge voltage of NCM811 cathode = 4.8 mAh cm(-2)/4 .6 V, and anode excess capacity [relative to the cathode] = 0.83), the Li metal-based full cell provides exceptional electrochemical performance (energy densities = 679 Wh kg(cell)(-1)/1,024 Wh L-cell(-1)) coupled with nonflammability

Rapid colour changes in Euglena sanguinea (Euglenophyceae) caused by internal lipid globule migration

The accumulation of red pigments under chronic stress is a response observed in most groups of oxygenic photoautotrophs. It is thought that the red pigments in the cell shield the chlorophyll located underneath from the light. Among these red pigments, the accumulation of carotenoids is one of the most frequent cases. However, the synthesis or degradation of carotenoids is a slow process and this response is usually only observed when the stress is maintained over a period of time. In the Euglenophyte Euglena sanguinea, this is due to the accumulation of a large amount of free and esterified astaxanthin (representing 80% of the carotenoid pool). While reddening is a slow and sometimes irreversible process in other phototrophs, reducing the efficiency of light harvesting by chlorophyll, in E. sanguinea it is highly dynamic, capable of shifting from red to green (and vice-versa) in 10-20 min. This change is not due to de novo carotenogenesis, but to the relocation of cytoplasmic lipid globules where astaxanthin accumulates. Thus, red globules migrate from the centre of the cell to peripheral locations when photoprotection is demanded. This protective system seems to be so efficient that other classical mechanisms are not operative in this species. For example, despite the presence and operation of the diadino-diatoxanthin cycle, nonphotochemical quenching (NPQ) is almost undetectable. Since E. sanguinea forms extensive floating colonies, reddening can be observed at much greater scale than at a cellular level, the mechanism described here being one of the fastest and most dramatic colour changes attributable to photosynthetic organisms at cell and landscape level. In sum, these data indicate an extremely dynamic and efficient photoprotective mechanism based on organelle migration more than on carotenoid biosynthesis that prevents excess light absorption by chlorophylls reducing the need for other protective processes related to energy dissipation.This work was supported by the Basque Government [UPV/EHU-GV IT-1018-16] [UPV/EHU PPG17/67 – GV IT-1040-16], and by the Spanish Ministry of Economy and Competitiveness (MINECO) and the European Research and Development Foundation (FEDER) through (i) [CTM2014-53902-C2-2-P] national grant and (ii) a “Juan de la Cierva-Incorporación” postdoctoral grant [IJCI-2014-22489] to BFM

Nanobead-reinforced outmost shell of solid-electrolyte interphase layers for suppressing dendritic growth of lithium metal

Department of Energy EngineeringDesign of catalyst support for high durability of oxygen electrocatalystPlating-stripping reversibility of lithium metal was improved by reinforcing the solid-electrolyte interphase (SEI) layer by inorganic nanobeads during formation of the SEI layer. The outmost SEI shell (OSS) was clearly identified, which is the SEI layer formed on current collectors (or lithium metal) before the first lithium metal deposition. The OSS was intrinsically brittle and fragile so that the OSS was easily broken by lithium metal dendrites growing along the progress of plating. Lithium metal deposit was not completely stripped back to lithium ions. On the other hand, lithium metal cells containing inorganic nanobeads in electrolyte showed high reversibility between plating and stripping. The nanobeads were incorporated into the OSS during the OSS formation. The nanobead-reinforced OSS having mechanically durable toughness suppressed dendritic growth of lithium metal, not allowing the dendrites to penetrate the OSS. In addition to the mechanical effect of nanobeads, the LiF-rich SEI layer formation was triggered by HF generated by the reaction of the moisture adsorbed on oxide nanobeads with PF6-. The LiF-rich composition was responsible for facile lithium ion transfer through the SEI layer and the OSS in the presence of nanobeads.clos

MRI-guided focused ultrasound surgery in musculoskeletal diseases: the hot topics

MRI-guided focused ultrasound surgery (MRgFUS) is a minimally invasive treatment guided by the most sophisticated imaging tool available in today's clinical practice. Both the imaging and therapeutic sides of the equipment are based on non-ionizing energy. This technique is a very promising option as potential treatment for several pathologies, including musculoskeletal (MSK) disorders. Apart from clinical applications, MRgFUS technology is the result of long, heavy and cumulative efforts exploring the effects of ultrasound on biological tissues and function, the generation of focused ultrasound and treatment monitoring by MRI. The aim of this article is to give an updated overview on a "new" interventional technique and on its applications for MSK and allied sciences