No abstract

No abstract

The recent revolution in nanoscience and global energy demand have motivated research in liquid fuel cells (LFCs) due to their enhanced efficiency, moving flexibility, and reduced contamination. In line with this advancement, a glassy carbon (GC) electrode was modified with platinum (PtNPs) and gold (AuNPs) nanoparticles to fabricate a nanosized anode for formic acid, methanol, and ethylene glycol electrooxidation (abbreviated, respectively, to FAO, MO, and EGO), of the key anodic reactions of LFCs. The deposition sequence of the catalyst’s layers was important where the Au/Pt/GC electrode (in which PtNPs were directly deposited onto the GC surface followed by AuNPs—surface coverage ≈ 32%) exhibited the best catalytic performance. The catalytic performance of the Au/Pt/GC anode excelled (at least threefold) its value obtained at the Pt/GC anode with regard to FAO and EGO, if the oxidation peak currents were compared. This enhancement got reduced to 1.4 times in the case of MO, but the large decrease (− 220 mV) in the onset potential of MO provided compensation. The role of AuNPs in the Au/Pt/GC catalyst was principal in boosting its catalytic performance as it immunized the underlying PtNPs against CO poisoning which is associated with the release of CO as an intermediate during the oxidation. Interestingly, AuNPs succeeded in interrupting the contiguity of the Pt surface sites required for CO adsorption during FAO, MO, and EGO and, thus, presage preventing the deterioration of the catalytic performance of their corresponding LFCs.

No abstract

No abstract

A glassy carbon (GC) electrode modified with multi-walled carbon nanotubes (MWCNTs) and platinum nanoparticles (PtNPs), Pt/MWCNTs-GC, has been introduced for formic acid electro-oxidation (FAO). A similar loading of PtNPs has been conserved for a proper comparison between the Pt/MWCNTs-GC and the unmodified Pt/GC electrodes. The modification with MWCNTs could enhance the loading of PtNPs onto the GC electrode in a way that minimizes its agglomeration and increases its dispersion in the CNTs network. This not only increases the surface area exposed to the reaction but also interrupts the contiguity of the Pt active sites minimizing the adsorption of the poisoning CO. As a result, both of the / and / ratios were increased by 12.5 and 2.5 times. Several techniques will be combined to track the catalyst activity and to determine its morphology.

No abstract

No abstract