Fabrication and Electrochemical Performance of Zn-Doped La_0.2Sr_0.25Ca_0.45TiO₃ Infiltrated with Nickel-CGO, Iron, and Cobalt as an Alternative Anode Material for Solid Oxide Fuel Cells

In solid oxide fuel cells, doped strontium titinates have been widely studied as anode materials due to their high n-type conductivity. They are used as current conducting backbones as an alternative to nickel-cermets, which suffer degradation due to coking, sulphur poisoning, and low tolerance to redox cycling. In this work, anode backbone materials were synthesized from La0.2Sr0.25Ca0.45TiO3−δ (LSCTA-), modified with 5 wt.% Zn, and infiltrated with nickel (Ni)/ceria gadolinium-doped cerium oxide (CGO), Fe, and Co. The electrodes were further studied for their electrochemical performance using electrochemical impedance spectroscopy (EIS) at open circuit voltage (OCV) in different hydrogen to steam ratios and at various operating temperatures (850–650 °C). Infiltration of electrocatalysts significantly reduced the polarization resistance and among the studied infiltrates, at all operating temperatures, Ni-CGO showed excellent electrode performance. The polarization resistances in 3% and 50% H2O/H2 atmosphere were found to be 0.072 and 0.025 Ω cm2, respectively, at 850 °C, and 0.091 and 0.076 Ω cm2, respectively, at 750 °C, with Ni-CGO. These values are approximately three orders of magnitude smaller than the polarization resistance (25 Ω cm2) of back bone material measured at 750 °C

Investigations on Anticancer Potentials by DNA Binding and Cytotoxicity Studies for Newly Synthesized and Characterized Imidazolidine and Thiazolidine-Based Isatin Derivatives

Imidazolidine and thiazolidine-based isatin derivatives (IST-01–04) were synthesized, characterized, and tested for their interactions with ds-DNA. Theoretical and experimental findings showed good compatibility and indicated compound–DNA binding by mixed mode of interactions. The evaluated binding parameters, i.e., binding constant (Kb), free energy change (ΔG), and binding site sizes (n), inferred comparatively greater and more spontaneous binding interactions of IST-02 and then IST-04 with the DNA, among all compounds tested under physiological pH and temperature (7.4, 37 °C). The cytotoxic activity of all compounds was assessed against HeLa (cervical carcinoma), MCF-7 (breast carcinoma), and HuH-7 (liver carcinoma), as well as normal HEK-293 (human embryonic kidney) cell lines. Among all compounds, IST-02 and 04 were found to be cytotoxic against HuH-7 cell lines with percentage cell toxicity of 75% and 66%, respectively, at 500 ng/µL dosage. Moreover, HEK-293 cells exhibit tolerance to the increasing drug concentration, suggesting these two compounds are less cytotoxic against normal cell lines compared to cancer cell lines. Hence, both DNA binding and cytotoxicity studies proved imidazolidine (IST-02) and thiazolidine (IST-04)-based isatin derivatives as potent anticancer drug candidates among which imidazolidine (IST-02) is comparatively the more promising

Investigations on the Morphological, Mechanical, Ablative, Physical, Thermal, and Electrical Properties of EPDM-Based Composites for the Exploration of Enhanced Thermal Insulation Potential

The most widely used filler in EPDM-based thermal insulation materials is asbestos which is hazardous to health and environment. The main motivation of this study was to develop improved EPDM-based materials by partially or completely replacing asbestos with other fillers. EPDM-Esprene501A and EPDM-Keltan®4869DE were used and the effect of three fillers (vulkasil-C, asbestos, carbon fiber fabric) on mechanical, ablative, physical, thermal, and electrical performances have been investigated. Samples were divided into phase -1, -2, and -3 by compounding EPDM with various percentages of fillers and other necessary ingredients. It was observed that asbestos and carbon fiber in the absence of vulkasil-C did not import enough reinforcement to EPDM-matrix. Experimental evidence showed that presence of vulkasil-C has not only enhanced mechanical properties but also improved thermal and ablation performance of EPDM-based composites. The swelling index was found comparatively lower with vulkasil-C than that with other fillers. Among two EPDMs, EPDM-Esprene based composites have shown comparatively better performance. Among all (phase-1–3) samples, E100K0VA (phase-2) has shown greater mechanical (stress 3.89 MPa; strain 774%), ablative (linear 0.1 mm/s; mass 0.05 g/s), and thermal (material left 91.0%) properties. Overall findings indicated improved properties of EPDM in the presence of vulkasil-C and may help to develop better heat resistant materials

Synthesis, photochemical and electrochemical studies on triphenyltin(IV) derivative of (Z)-4-(4-cyanophenylamino)-4-oxobut-2-enoic acid for its binding with DNA: Biological interpretation

(Z)-4-(4-cyanophenylamino)-4-oxobut-2-enoic acid (LH) and its new triphenyltin (IV) derivative (Ph3SnL) were synthesized and further investigated for their binding with ds.DNA under physiological conditions {pH: 4.7 (stomach); 7.4 (blood), 37 °C} using UV–Visible/fluorescence spectroscopy, cyclic voltammetry and viscosity measurement techniques. Spectral responses as well as experimental findings from all the techniques i.e., binding constant (Kb), binding site size (n) and free energy change (ΔG) correlated with each other and indicated formation of spontaneous compound–DNA complexes via intercalation of compounds into the DNA base pairs. Values of kinetic parameter, Kb, revealed comparatively greater binding of both the compounds with DNA at stomach pH (4.7). However among both compounds organotin complex (Ph3SnL) showed comparatively greater binding than that of its ligand (LH) as evident from its, Kb, values at both the pH values. In general, Kb values were evaluated greater for Ph3SnL at stomach pH {: Kb: 8.65 × 104 M−1 (UV); 5.49 × 104 M−1 (fluorescence); 8.85 × 104 M−1 (CV)}. Voltammetric responses of both compounds before and after the addition of DNA indicated that diffusion controlled processes are involved. Complex Ph3SnL exhibited the best antitumor activity

Exploration of anode candidacy of Ni0.2Co2.8O4 and integrated Ni0.2Co2.8O4/MWCNTs in supercapacitor and oxygen evolution reaction

In the current research work, Ni0.2Co2.8O4 and Ni0.2Co2.8/MWCNTs have been synthesized via facile sol-gel and wet impregnation method. The synthesized materials attained the crystalline structures as evident from X-ray diffraction analysis (XRD). The uniform morphology and well dispersion of Ni0.2Co2.8O4 onto MWCNTs was observed via scanning electron microscopy (SEM). The electrochemical investigations for supercapacitor application by cyclic voltammetry (CV), galvanostatic charge discharge (GCD), and electrochemical impedance spectroscopy (EIS) revealed that, among both materials, Ni0.2Co2.8O4/MWCNTs has high specific capacitance (CV; 505.8 Fg-1 at 5 mV/s, GCD; 1598 Fg-1 at 0.5 A/g), greater capacitance retention (85 %) at 1000 cycles and has lower charge transfer resistance (Rct; 3.48 Ω cm2). These findings reflected the potential candidacy of Ni0.2Co2.8O4/MWCNTs to be used as anode material in supercapacitor. Further investigations by CV and linear sweep voltammetry (LSV) for oxygen evolution reaction (OER) activity in 1.0 M KOH showed comparatively low over potential of 340 mV @100 mA/cm2 for the same integrated material. Additionally, the lower Tafel slope (47 mV/dec) and solution resistance authenticated it as an appropriate electrocatalyst for OER in water splitting. The CPE (controlled potential electrolysis) revealed the stability of both materials for OER in water oxidation