2 research outputs found
Highly Efficient CeO<sub>2</sub> Decorated Nano-ZSM‑5 Catalyst for Electrochemical Oxidation of Methanol
Cerium
oxide (CeO<sub>2</sub>) decorated nanocrystalline zeolite
(Nano-ZSM-5) nanocomposites with different weight ratios were prepared
by the calcination of a physical mixture of nanocrystalline CeO<sub>2</sub> and Nano-ZSM-5. Materials were characterized by the complementary
combination of X-ray diffraction, N<sub>2</sub>-adsorption, transmission
electron microscopic, and X-ray photoelectron spectroscopic techniques.
The material was investigated as a precious-metal-free electrode catalyst
for methanol oxidation. The electrochemical oxidation of methanol
was investigated at a CeO<sub>2</sub>/Nano-ZSM-5 modified glassy-carbon
electrode in alkaline medium using electrochemical impedance spectroscopy,
cyclic voltammetry, and chronoamperometry. Comparative investigations
were made with commercial Pt(20%)/C catalyst with respect to current
density, stability, and CO tolerance capacity. CeO<sub>2</sub>/Nano-ZSM-5
with a weight ratio of 30% exhibited remarkably high electrocatalytic
activity in the methanol oxidation in comparison to nanocrystalline
CeO<sub>2</sub> and commercial Pt (20%)/C catalyst. The material was
found to exhibit stable electrocatalytic activity even after 1000
cycles. High electrocatalytic activity in the methanol oxidation can
be attributed to the synergistic contribution provided by CeO<sub>2</sub> nanocrystals and Brønsted acidity of the high-surface-area
Nano-ZSM-5. Results demonstrate that the excellent current density
and high stability of CeO<sub>2</sub>/Nano-ZSM-5 would be valuable
for its commercial application in direct methanol fuel cells
Additional file 1: of Cytosolic phospholipase A2 (cPLA2) IVA as a potential signature molecule in cigarette smoke condensate induced pathologies in alveolar epithelial lineages
Supplementary data. Table S1. Primer Sequences of various genes. Table S2. CSC-induced mRNA expression of various cPLA2 groups in A-549 and WI-26 Cells. The values (mean ± SD of three different experiments) are in folds of control values. Figure S1. Schematic presentation of proposed plan of experimental design. Figure S2. Effect of CSC treatment at concentrations’ of 150 μg/ml (b) and 200 μg/ml (c) on cell morphology in lung epithelial type II (A-549) cells and type I (WI-26) cells. Figure 2a shows the normal morphology in two types of the cells (Magnification 5x). (DOCX 1098 kb