2022
DOI: 10.1016/j.fuel.2022.125083
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Self-supported PdNi dendrite on Ni foam for improving monohydric alcohol and polyhydric alcohols electrooxidation

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Cited by 10 publications
(4 citation statements)
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“…The two main themes are the bifunctional mechanism and electronic effect. For the bifunctional mechanism, the addition of an oxophilic metal such as Ni to a noble metal catalyst enhances the catalytic activity by providing an increased amount of proximal hydroxide species adjacent to the GEOR active sites. ,, The enhanced activity is then a result of either the increased hydroxide species providing a more oxidative environment, participating in the GEOR or aiding the oxidative removal of inhibiting CO ad intermediates. For the electronic effect, the addition of non-noble transition metals to the lattice of noble metals such as Pt and Pd decreases the binding energy for inhibiting species such as CO and OH, and it can increase the number of available surface electrons and lower glycerol adsorption energy; the result being easier desorption of intermediates and, therefore, increased active sites during the GEOR as well as less C–C bond cleavage.…”
Section: Resultsmentioning
confidence: 99%
“…The two main themes are the bifunctional mechanism and electronic effect. For the bifunctional mechanism, the addition of an oxophilic metal such as Ni to a noble metal catalyst enhances the catalytic activity by providing an increased amount of proximal hydroxide species adjacent to the GEOR active sites. ,, The enhanced activity is then a result of either the increased hydroxide species providing a more oxidative environment, participating in the GEOR or aiding the oxidative removal of inhibiting CO ad intermediates. For the electronic effect, the addition of non-noble transition metals to the lattice of noble metals such as Pt and Pd decreases the binding energy for inhibiting species such as CO and OH, and it can increase the number of available surface electrons and lower glycerol adsorption energy; the result being easier desorption of intermediates and, therefore, increased active sites during the GEOR as well as less C–C bond cleavage.…”
Section: Resultsmentioning
confidence: 99%
“…During electrochemical oxidation, nickel forms an active redox pair Ni­(OH) 2 /NiOOH, which reduces the overpotential of the oxidation reaction . In recent years, nickel-based materials, such as NiOOH-CuO, NiFeOOH, Rh metal-modified Ni nanowires, and porous nickel electrodes are among the most prevalent. The palladium-based nanoparticles are used as one of the most among the surface modifiers because of its high activity in alcohol oxidation to its corresponding acid products. …”
Section: Mechanism For Nickel and Nickel-based Catalysts In Alkaline ...mentioning
confidence: 99%
“…This is because during the oxidation process, nickel creates an electrochemically active redox pair Ni(OH) 2 /NiOOH, for which the oxidation reaction has a reduced overpotential [ 17 ]. Currently, the main trends in this field are the synthesis of nickel-based alloy materials, such as NiOOH-CuO oxide nanostructures [ 18 ] NiFeOOH [ 19 ], metal-modified Ni nanowires precious metals such as Rh [ 20 ] and porous nickel electrodes [ 21 , 22 , 23 , 24 ]. One of the most commonly used surface modifiers are palladium-based nanoparticles due to their highest activity in the oxidation of ethanol to acetate [ 25 , 26 , 27 ].…”
Section: Introductionmentioning
confidence: 99%