Jayati Datta

Energy efficient role of Ni/NiO in PdNi nano catalyst used in alkaline DEFC

The present investigation is based on a study of electro-oxidation of ethanol in alkaline medium over the carbon supported PdxNiy catalyst formulations synthesized by simultaneous reduction of the precursors using sodium borohydride as the reducing agent. X-ray diffraction studies of the PdNi/C nano-particles reveal formation of the face-centered cubic crystalline Pd, NiO and Ni(OH)2 on a meso porous carbon support whereas XPS confirmed the presence of metallic Ni and the oxide phases NiO, Ni(OH)2, NiOOH in the catalyst matrix. The structure and morphology of the binary matrix and the role of Ni and its oxide as a catalytically contributing entity in the oxidation process was ascertained by the help of respective analytical techniques like transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), voltammetry and chronoamperometry. Sequential oxidation steps were suggested involving dimeric (NiO)2 as one of the intermediate species during the oxidation reaction proceeding towards aldehyde formation and further to carbonate production via the intermediate formation of a six member ring, thereby increasing the reaction rates. This phenomenon has been discussed at molecular level using the results obtained from XPS analysis. The observations were further accomplished by extending the work to ion chromatography for quantitative analysis of the products formed during oxidation of ethanol. All the above results are congruent with the mechanistic interpretation and reflect the paramount significance of NiO existing in the binary catalyst matrix for accelerating ethanol oxidation reaction kinetics at a temperature 40 °C and above.

An investigation into the electro-oxidation of ethanol and 2-propanol for application in direct alcohol fuel cells (DAFCs)

A comparative study of the electro-oxidation of ethanol and 2-propanol was carried out on carbon-supported platinum particles. Cyclic voltammetry, steady state polarisation, and electrochemical impedance spectroscopy were used to investigate the oxidation reactions. A difference in the mechanistic behaviour of the oxidation of ethanol and 2-propanol on Pt was observed, thereby highlighting the fact that the molecular structure of the alcohol has great influence on its electroreactivity. The study emphasizes the fact that 2-propanol is a promising fuel candidate for a direct alcohol fuel cell.

Significant Role of Ru-Oxide Present in the Pt-Ru Alloy Catalyst for Ethanol Electro-Oxidation in Acid Medium

This work relates to the search for optimum Pt-Ru catalyst composition for electro-oxidation of ethanol. The structure, morphology, and composition of the synthesized Pt-Ru catalysts were investigated through techniques like X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive X-ray (EDX), and X-ray photoelectron spectroscopy (XPS) while cyclic-voltammetry, polarization, chronoamperometry, impedance spectroscopy were employed to study the electrocatalytic behavior of the catalyst. XPS spectrum of the binary sample suggests that the facile oxygen transfer from Ru to Pt site occurs, depending upon the respective valency state and the relative amount of oxide species present in the catalyst. The temperature dependence of ethanol oxidation afforded the determination of the activation energies of catalysts. The apparent reaction order with respect to ethanol was determined with the help of linear sweep voltammetry. The pronounced catalytic activity was observed for at around 12 at% Ru containing electrodes.

Studies on the photo-electrochemical behaviour of Bi2S3NPs embedded in a PANINFs matrix

A voltammetric technique was used to produce a thin coating of polyaniline nanofibers (PANINFs) on ITO-coated glass substrates. Thereafter, bismuth sulfide nanoparticles (Bi2S3NPs) were chemically deposited on the PANINFs layer. The composite films were firmly adhered to the substrate and uniformly distributed. The films were characterized by optical, electron microscopic and electrochemical techniques to identify their possible applications in liquid junction solar cells. The functional properties of the bare Bi2S3NPs were increased considerably by using PANINFs as the support materials in the composite matrix. The study of the electrochemical polarization of the synthesized films and subsequent anodic stripping voltammetry enabled the extent of the degradation of the films during polarization to be determined. Electrochemical studies revealed the n-type character of the composite film, which exhibited a substantially higher photo-conversion efficiency than the pure Bi2S3NPs film.

Catalytic Intervention of MoO3 toward Ethanol Oxidation on PtPd Nanoparticles Decorated MoO3–Polypyrrole Composite Support

Ethanol oxidation reaction has been studied in acidic environment over PtPd nanoparticles (NPs) grown on the molybdenum oxide-polypyrrole composite (MOPC) support. The attempt was focused on using reduced Pt loading on non-carbon support for direct ethanol fuel cell (DEFC) operated with proton exchange membrane (PEM). As revealed in SEM study, a molybdenum oxide network exists in polypyrrole caging and the presence of metal NPs over the composite matrix is confirmed by TEM analysis. Further physicochemical characterizations such as XRD, EDAX, and XPS are followed in order to understand the surface morphology and composition of the hybrid structure. Electrochemical techniques such as voltammetry, choroamperometry, and impedance spectroscopy along with performance testing of an in-house-fabricated fuel cell are carried out to evaluate the catalytic activity of the materials for DEFC. The reaction products are estimated by ion chromatographic analysis. Considering the results obtained from the above characterization procedures, the best catalytic performance is exhibited by the Pt-Pd (1:1) on MOPC support. A clear intervention of the molybdenum oxide network is strongly advocated in the EOR sequence which increases the propensity of the reaction by making the metallites more energy efficient in terms of harnessing sufficient numbers of electrons than with the carbon support.

Voltammetric deposition of BiCdTe composite films with improved functional properties for photo-electrochemical cells

Polycrystalline semiconductor films of BiCdTe composites were electro-deposited on ITO coated glass through a voltammetric technique under variable periodic cycles. The crystal structure and composition of the films were determined by X-ray diffraction, scanning electron microscopy, atomic force microscopy and energy dispersive X-ray analysis and the optical features were recorded using a UV-visible spectrometer. The band gap energy of the ternary films was found to be within the range of 1.5–1.7 eV. Electrochemical impedance spectroscopy provided important information regarding the interfacial properties of the films in polysulphide medium. The current–voltage measurements for the photo-electrochemical solar cells fabricated with the prepared films as anode components exhibited encouraging photo-response and improved functional properties. The BiCdTe composite films were further subjected to anodic corrosion studies followed by anodic stripping voltammetry and the stability of the films was compared with that of CdTe. An optimal composition of the film matrix shows a performance efficiency of 4.3%, significantly high photo current and considerably greater stability compared to the individual binary chalcogenide films.

Carbon-supported platinum catalysts for direct alcohol fuel cell anode

To achieve maximum utilization of precious platinum catalyst for ethanol electro-oxidation the highest possible surface to volume ratio of the dispersed metal is desirable. In this respect we have investigated the roughness factor of carbon-supported platinum catalysts prepared at different deposition current densities. It is observed that lowering the deposition current density can considerably reduce platinum particle size and thereby increase the roughness factor of the electrode. Further, use of PTFE in the deposition bath results in highly porous platinum dispersion. The combined effect of these two factors significantly enhances the electrocatalytic activity of platinum catalysts towards ethanol oxidation. Cyclic voltammetry, steady state polarization, and electrochemical impedance spectroscopy are used to investigate the kinetics and mechanism of ethanol electro-oxidation. SEM-EDX analysis has been performed to investigate the morphology and chemical composition of the synthesized catalyst layers.

CdTe nanoparticles decorated titania for dye sensitized solar cell: a novel co-sensitizer approach towards highly efficient energy conversion

A hybrid TiO2–CdTe multi-layer matrix was fabricated for validation in a dye sensitized solar cell (DSSC) operating with N3 dye as the sensitizer. The composite matrix was subjected to studies of structural and morphological information, and optical and spectral characterizations before sensitizing with dye. A CdTe–N3 dye conjugate sensitizer over the base TiO2 matrix improves the functional behavior of the anode by accelerating the charge transport and reducing the recombination within the DSSC framework. The photovoltaic measurements reveal that a moderate loading of CdTe NPs at the anode exhibits a solar conversion efficiency of 11.1% under an optimal illumination of 50 mW cm−2.

Multi-elemental chalcogenide n-BiCdSe films grown under controlled depth voltammetry: improved photo-electrochemical behaviour toward energy conversion

In this study, thin films of composite semiconductor (SC) n-BiCdSe were electrochemically synthesized by periodic voltammetry at room temperature using an aqueous acidic bath containing the respective precursor salts. The well-adherent and uniformly deposited thin films were subjected to optical measurements (UV-vis), scanning electron microscopy (SEM-EDAX) and X-ray diffraction studies to determine the optical properties, structure and morphology of the film matrices. The polycrystalline films were composed of agglomerated particles with spherical geometry, and their size was in the range of ∼30–40 nm. A series of electrochemical techniques were employed to determine the performance output of the films with respect to their photo-electrochemical (PEC) characteristics in a liquid junction solar cell. During fabrication of the films, voltammetric cycles were optimized to obtain the best-performing composite film, which exhibited a maximum photo-conversion efficiency of 2.6% and least photocurrent decay.

Catalytic intervention of transition metals in Pd based nanocatalyst for direct ethanol fuel cell

P is a common chronic inflammatory skin disease, characterized by abnormal differentiation and proliferation of keratinocytes, angiogenesis and infiltration of inflammatory cells that secrete Th1 and Th17 associated cytokines in the skin lesion, such as TNF-α, IL-17 and IL-20. Although mRNAs that encode cytokines are short-lived mRNAs in eukaryotes, the premRNAs, which contain AU-Rich Elements (AREs) in their 3’-untranslated regions, are recognized and stabilized by Human Antigen R (HuR), an RNA-binding protein, for post-transcription. Previous studies have suggested that HuR is involved in the stabilization of mRNAs in the psoriatic skin. HuR binds to and regulates IL-20 mRNA and relocalizes to the cytoplasm of psoriatic keratinocytes. Furthermore, HuR can bind numerous transcripts involved in the pathogenesis of psoriasis. Therefore, HuR may be a potential therapeutic target for psoriasis. In the present study, we tested several novel oligopeptides that targeted the RNA binding site of HuR as therapeutic agents for psoriasis. A mouse model of imiquimod (IMQ)-induced psoriasis-like dermatitis was generated in BALB/c mice by daily topical application of IMQ cream on the ear from days 0 to 9. The mice were treated with oligopeptides from days 5 to 10. The pathological features of psoriasis were scored daily using the thickness gauge and clinical Psoriasis Area and Severity Index (PASI). We found that the oligopeptide JS-1 could significantly ameliorate psoriasis pathogenesis in a dose-dependent manner. The oligopeptide affected the HuR downstream signaling pathway. Collectively, this study may provide an alternative therapeutic strategy for psoriasis.W are looking forward to the simple but strong method to enhance a sensitivity and responsibility of Graphene Oxide (GO) by forming a self-corrugated surface of GO. The self-corrugated surface was formed by the reaction of graphene oxide with Gallium chloride. The surface of GO is more corrugated with the concentration of gallium hydroxide during the dry of GO powder. The graphene oxide structure was distorted due to the three hydroxyl groups of gallium hydroxide. The properties of wrinkled GO were investigated by scanning electron microscope, energy dispersive spectroscopy, X-ray diffraction, Raman spectroscopy and atomic force microscope, respectively. This self-corrugated GO have superior advantages over normal GO for a higher sensitivity and responsibility for sensor applications.I in developing alternative energy sources is increasing due to depletion of oil resources and global warming. Therefore, fuel cells, which are new energy conversion and storage devices with low emission of pollutants, are emerging as an alternative. The process of producing hydrogen as a fuel of fuel cells requires a great deal of cost. Therefore, researches are being studying on reforming catalysts for converting natural gas rich in reserved into hydrogen energy and for use in fuel cells. In general, a transition metal (Ni, Co, Cu) or a noble metal (Ru, Pd, Pt) is used as a methane steam reforming catalyst. The noble metal catalyst has excellent catalytic activity and resistance to carbon deposition. But it is becoming a stumbling block to commercialization due to expensive cost. Ni-based catalysts are less expensive than noble metals and have a simple manufacturing process, but the problem of degradation due to carbon deposition and grain growth is pointed out as a disadvantage. In this study, Ni/MgO composite reforming catalyst activated Ni catalyst by exsolution was manufactured to improve durability. The size and amount of precipitated Ni particles were controlled by the reducing temperature and time. The catalytic activity and durability of the catalysts prepared as above were evaluated. The conversion rate of methane was measured and evaluated in the temperature range of 250-750oC and methane:water vapor = 1:2 atmospheres with catalyst in fixed bed reactor. The microstructure and distribution of the produced catalyst were confirmed by XRD and SEM.A well-defined 3D bicontinuous network structure in nanoscopic regular array has attracted considerable attention because of its potential applications such as photonic crystals, meta-materials, energy devices and superconductor. In this study, the asymmetric polystyrene-block-poly (methyl methacrylate) (PS-b-PMMA) thin films on the two different substrate with highmolecular-weight were prepared to be exposed a neutral solvent vapor to generate a hexagonal (HEX) cylindrical morphology to long-range ordered Gyroid (GYR). The interfacial interaction by different substrate interaction induced the two distinct GYR, [211] and [111] planes, which were directed from cylinders, like the parallel and perpendicular orientation on the selective and neutral substrate, respectively. Moreover, we further performed coarse-grained simulations of a block copolymer model to provide the molecular mechanisms. Our results based on experiments and simulations suggest a simple route for the controlled and well-defined GYR structures.T Fe-Mo based double perovskites have attracted much attention in the field of materials science due to their multiverse fascinating physical properties which make them suitable candidates for several technological applications. In the present work, the Sr2-xNdxFeMoO6 (0.0≤x≤0.3) samples have been investigated for their structural, magnetic and magnetocaloric properties. Polycrystalline Sr2-xNdxFeMoO6 (0.0≤x≤0.3) samples were prepared by using the conventional solid-state reaction method. To achieve the target double perovskite phase and to minimize the undesirable secondary phases, the samples were sintered in a reducing atmosphere, created by a gas mixture of 5% H2/95% Ar. The structure, microstructure and phase purity of the samples were investigated by X-ray Diffraction (XRD) and Scanning Electron Microscopy (SEM). XRD study confirmed the formation of tetragonal structure with Fm3m space group in all the synthesized samples. The Arrott plots and magnetization measurements showed a second order of ferromagnetic phase transition in all the fabricated samples. All the samples went through a paramagnetic to ferromagnetic phase transition at the Curie temperature (TC). A magnetocaloric effect was calculated in terms of isothermal magnetic entropy change. The value of the Relative Cooling Power (RCP) was observed to decrease with the increasing Nd content. A significant variation in the magnetocaloric properties of the samples was observed with the increasing Nd concentration. This investigation suggests that Sr2-xNdxFeMoO6 samples can be used as potential magnetic refrigerants for magnetocaloric applications.Purpose: Vorinostat (SAHA) is the most representative histone deacetylase inhibitor and a widely used anticancer drug, SAHA is applied in the treatment of hematological malignancies and most solid tumors. SAHA is challenging due to poor water solubility, low bioavailability and rapid elimination of drugs in vivo. In this study, we will prepare SAHA-Pluronic F127 Nanoparticles and investigated whether this could improve drug solubility, the effect of sustained release and inhibitory effect on cancer cells.C nanotube/polytetrafluoroethylene composite polymer targets (abbreviated as composite target) are proposed for use in the fabrication of plasma polymer fluorocarbon (abbreviated as PPFC) thin films using the mid-range frequency sputtering process. Large-area PPFC thin films were fabricated on roll-type PET substrate (polyethylene terephthalate, width 700 mm, thickness 100 μm) by a pilot-scale roll-to-roll sputtering system. The PPFC thin films exhibit an amorphous phase with a smooth surface and show a high water contact angle, optical transmittance and bendability. Mechanical property of PPFC thin films were studied using nanoindentation method and analyzed using X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy. As the carbon nanotube concentration in the composite target increases, a carbon cross-linked structure was formed which enhanced the film hardness and the modulus of the PPFC thin films.T monolayer graphene-Ag nanoparticles hybrids system is fabricated as the electro-optical coordinated controlled substrate of Surface-Enhanced Raman Scattering (SERS) spectroscopy. Plasmon-exciton coupling interactions of this hybrid system are systemically investigated and applied in the field of surface catalytic reactions, manipulated by the electrooptical synergy. Our experimental results demonstrate that plasmon-exciton coupling interaction co-driven surface catalytic reactions can not only be controlled via plasmon-exciton coupling, but also by gate voltages and electric current (or bias voltage). The gate voltage can tune the Density of State (DOS) of hot electrons and electric current can make the hot electrons with higher kinetic energy. Both of them can significantly promote plasmon-exciton co-driven surface catalytic reaction. Our electro-optical device based on plasmon-exciton coupling can be potentially applied in the fields of sensor, catalysis, energy and environment.C thin film coatings present unique optical properties. In this study, structural, chemical bonding and optical properties of the thin films in relation to the composition of reaction gas via sputtering process were investigated. All the thin films exhibited a polycrystalline character with cubic fluorite-structure for cerium dioxide along (111), (200) and (222) orientations. XPS analysis revealed that two oxidation states of CeO2 and Ce2O3 are present in the films prepared at lower argon-oxygen flow ratios, whereas the films are totally oxidized into CeO2 as the aforementioned ratio increases. Optical parameters (α, ε1, ε2, n and k) derived from UV-Vis reflectance data indicate that the thin films have indirect optical band gaps in the range of 2.25-3.1 eV. Density Functional Theory (DFT+U) implemented in the Cambridge Serial Total Energy Package (CASTEP) has been employed to model some optical properties of CeO2 cluster at ground state. The simulated electronic Density of State (DOS) of the relaxed structure of CeO2 demonstrates a band gap, agrees well with the measured optical band gap. The experimental and calculated absorption coefficient (α), have analogous trends and to some extent a similar range of values in the wave length. All in all, our theoretical findings consistently support the experimental results.A neuronal growth underlies the prefrontal cortical (PFC) pathology of many neurodegenerative disorders. Current treatments are inadequate and commonly cause severe side effects. Importantly, conventional pharmacotherapy strategies have limited efficacy in treating PFC dis-regulation in neurodegenerative disorders. Electrical stimulation is a modern treatment method which can include electroconvulsive therapy, Deep-Brain Stimulation (DBS) and epidural stimulation, etc. Previous studied showed that the application of electrical stimulations promotes neuritis outgrowth resulted to inter neuronal networking. Wide range of metallic microelectrodes composed of gold, steel, platinum etc. have been previously utilized to perform electrical stimulation however, rigidity, incompatible mechanical properties, high initial impedance and low chargetransfer capacity limit their application. Graphene and its derivatives are an exciting class of materials, which are utilized in microelectrodes due to having excellent mechanical stability, electrical conductivity, biocompatibility, flexibility and ability to fabricate and scale up. This work develops three-dimensional (3D) flexible electrode composed of 3D printed Reduced Liquid Crystalline Graphene Oxide (rLCGO) on a polyurethane (PU) substrate. The flexible conducting electrode is used as Host Template for Human Neural Stem Cells (hNSCs) development during proliferation and differentiation. The application of electrical stimulation on hNSC using graphene/PU electrodes revealed promising results to improve neurites guidance through 3D printed lines and enhanced cell-cell communication and networking.P method is superior in the fabrication of ultra-high-temperature ceramics with the designable composition and structure, low sintering temperature and easy densifying process. In this study, three kinds of hybrid precursors for ZrC/C, ZrC/SiC and ZrC/SiBNC multinary ceramics were synthesized via radical polymerization. ZrC/C ceramic precursor was synthesized using Cp2Zr (CH2CH=CH2) as monomer ZrC/SiC or ZrC/SiBNC precursor is obtained by further adding low molecular weight polycarbosilane (LPCS) or polyborosilazane (LPBSZ) for copolymerization. By controlling the preparation procedure, these hybrid polymers can dissolve in most organic solvent, which is essential to construct CMCs in complicated shapes and large sizes. After pyrolyzing at 1400oC, the synthesized precursors can convert into Zr-containing multinary ceramics, with ZrC nanoparticles finely dispersed in C, SiC or SiBNC matrix depending on the hybrid polymer. All of the three Zr-containing multinary ceramics can remain finely phase distribution at 1600oC, especially for ZrC/C and ZrC/SiC multinary ceramics, which can have a stabilized microstructure and little mass loss (less than 1.5 wt%) up to 2000oC in inert atmosphere. As for ZrC/SiBNC, the introduction of ZrC phase can restrict the decomposition of SiBNC matrix at 1800oC. Although the SiC and SiBNC components improve the oxidation resistance of ZrC, the oxidation weight increase of these multinary ceramics at about 500oC is still up to 5%.W synthesized cationic, one-dimensional fibril assemblies formed from coil-sheet poly(L-lysine)-block-poly(Lthreonine) (PLL-b-PLT) block co-polypeptides as anticancer agents. The 1D fibril assemblies can efficiently interact with negatively charged cellular and mitochondrial membranes via electrostatic interactions, leading to cell necrosis through membrane lysis and apoptosis via the lytic effect of mitochondria. This effect is similar to that of one-dimensional drug carriers that exhibit enhanced cell penetration. Compared to free PLL chains, PLL-b-PLT fibril assemblies exhibited more selective cytotoxicity against cancer cells, lower hemolytic activity, higher membranolytic activity and a different apoptotic pathway, which may be due to differences in the peptide-membrane interactions. The fibril assemblies significantly inhibited tumor growth, improved survival and suppressed tumor metastasis to the lung in C57BL/6 mice bearing syngeneic LL2 lung tumors. An additive antitumor activity was also observed when the tumor bearing mice were treated with PLL-b-PLT in combination with the common chemotherapeutic drug cisplatin. Collectively, these results support the feasibility of using one-dimensional fibril assemblies as potential anticancer therapeutics.C Vapor Deposition (CVD) synthesis of Carbon Nanotubes (CNTs) was carried out in a self-assembled apparatus consisting of a hot tube furnace. Magnesium oxide supported iron catalyst samples, containing varied proportions of iron loadings were prepared using impregnation method and spread uniformly over copper strips. Ceramic boats were placed in the furnace so as to expose the catalyst-loaded copper strips to industrial gases such as nitrogen, methane and hydrogen. Usage of horizontal tube furnace instead of conventional CVD reactor not only reduced the cost but also added to the simplicity of the apparatus. Additionally, ceramic boats are at least 50% cheaper than the commonly used quartz boats. FESEM tests on the resultant samples revealed that the CNTs ranged between 19.78 nm and 30.36 nm in diameter, which validates the nanotube structures. We demonstrate that increasing the iron loading in the catalyst samples enhanced the probability of CNT formation: 0% iron loading yielded no CNTs, while increasing the loading to 6.5% gave way to formation of Multi-Walled Carbon Nanotubes (MWCNTs). This study opens up an economical route for the mass production of MWCNTs.H structured materials consist of a bimodal structure with a periodic or harmonic distribution of fine and coarse grains allowing optimum combination of high strength and ductility to be attained. Harmonic structured materials have potential in variety of applications, where high wear and corrosion resistance are required. Therefore, effect of harmonically distributed fine and coarse grains on the corrosion and wear behavior of a SUS304L austenitic stainless steel was studied and compared with a non-harmonic structured SUS304L and a conventional 304 stainless steel. The corrosion study was performed using linear, potentiodynamic and cyclic polarization techniques as well as salt fog exposure test for 30 days in 3.5% NaCl solution. Improved pitting corrosion resistance was found in case of the harmonic structured steel as compared to that of the non-harmonic and the conventional 304 stainless steel. Harmonically distributed fine grained structure, less porosity and higher fraction of passive α-FeOOH are attributed to the improvement in corrosion resistance of the harmonic structured steel. The wear study was performed using fretting wear tests at varying loads under ball-on-flat contact configuration. Coefficient of friction and wear volume were found to be minimum at intermediate normal load of 5 N, whereas maximum at 10 N in case of the harmonic stainless steel compared to other two steels. Harmonically distributed fine grained structure attributes to the higher wear rate of the harmonic structured steel because of hard and soft interaction of the ball with the harmonically distributed fine and coarse grains.A Solid Oxide Electrolyzer Cells (SOECs) is an electrochemical device for producing hydrogen by electrolysis water vapor at a high temperature. SOEC is that they can operate reversibly as solid oxide fuel cells, producing electricity with high efficiency by consuming stored hydrogen. It can also be used in next-generation power generation and storage systems that produce hydrogen using surplus power. SOEC have disadvantage to provide high temperature/high-pressure water vapor to the hydrogen electrode and since oxygen is released very quickly at the air electrode, deterioration of cells and stacks is larger than SOFC and it is a stumbling block to commercialization. In this study, the effect of operating conditions on hydrogen electrode performance and deterioration of SOEC was investigated. To improve the durability of the hydrogen electrode the material technology for inhibiting oxidation of Ni/YSZ was studied. The polarization resistance and J-V characteristics are evaluated in both SOFC/SOEC. The partial pressure of water vapor is changed to 10, 30 and 50%. The change of voltage is observed under the condition of applying current density of 0.1 mA/cm2 to the cell. And the durability of the cell is evaluated by measuring the voltage change according to the SOFC-SOEC switching operation. In addition, to suppress the oxidation of the hydrogen electrode (Ni/YSZ) in a steam atmosphere, a composite hydrogen electrode was fabricated by applying anticorrosion technology and the possibility of oxidation suppression is examined.Methods: Morphology was studied by Transmission Electron Microscopy (TEM). 5 μl of freshly prepared micellar dispersions were placed on Formvar and allowed to dry for 5 min. To unveil the usefulness of such formulations concerning physical stability, formulations FM1-FM5 and meloxicam were dissolved in enteric and gastric medium. After 1 and 2 h we quantified meloxicam in gastric medium and after 3 and 4 h we quantified meloxicam in enteric medium. Quantification was performed using an UV spectrophotometer and absorbance taken at 363 nm. To determine encapsulation efficiency, FM1-FM5 was quantified immediately after preparation. Later on, micellar suspensions were centrifuged at 3000 g for 15 min using Amicon® Ultra 4 Centrifugal filter units, the supernatant was quantified and EE calculated based on the following equation: Finally, cytotoxicity of formulations was assessed in Caco-2 cells by Alamar Blue assay, performing a screening of crescent concentrations (0.625%, 1.25%, 2.5%, 5% and 10%) for each formulation.G Multiforme (GBM) is an aggressive brain tumor with poor prognosis, mainly because standard treatment is not always effective enough in reaching tumor cells. Blood-Brain Barrier (BBB) is pointed out as one of great challenges in this field. Considering the negative charge of BBB surface and its restricted permeability to small compounds, positively-charged nanoparticles have been developed to facilitate the transport of drugs through the BBB. This work aimed at studying the interaction of different cationic surfactants used in Lipid Nanoparticle (LN) formulations with BBB, using atomistic simulations. Surfactants incorporating natural structural motifs, specifically serine, were chosen instead of the conventional synthetic surfactants, due to the lower cytotoxicity and higher biodegradability, thus being environmental friendly. Molecular dynamics simulations were performed on 4 systems containing different serine-based surfactants, two of them are monomeric (16SerTFA and 12SerTFA) and the other two are dimeric ((12ser)2CON12 and (12ser)2N5), in a fully hydrated palmitoyloleoylphosphatidylcholine (POPC) lipid model, intended to mimic cell membranes of both the BBB and tumor. The systems were evaluated in terms of effects induced by the surfactants in this type of membranes and rationalize the interactions at molecular level. The results showed an integration of all surfactants into the POPC membrane. Longer chain length surfactants tended to induce the highest membrane stabilization, as evidenced by 16serTFA. Conversely, the dimeric (12ser)2CON12 led to the greater disturbance in the membrane structure, probably due to bridging phenomena. This may anticipate a better BBB cross ability of LN containing (12ser)2CON12. Overall, this computational study suggests the viability of cationic serine-based surfactants as appealing compounds in LN formulations for targeted GBM therapy.