2015
DOI: 10.1016/j.electacta.2015.07.073
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How do Bi-modified palladium nanoparticles work towards glycerol electrooxidation? An in situ FTIR study

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Cited by 69 publications
(75 citation statements)
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“…For potential higher than 0.9 V vs. RHE Pt suffers strong deactivation, due to the formation of an inhibiting surface oxide [10,17,18]. Glycerol oxidation on Pd lead to a selectivity towards GALD and GLA at low potentials, and then towards HPA, dicarboxylates and products derived by C-C bond cleavage (C2 and C1 compounds) at higher potentials [18,26]. It has to be denoted that the structure and morphology of the catalysts can play a role for the selectivity: GLA and TA were obtained on Pd/C, and HPA on Pd nanofoam [2].…”
Section: Pure Pt Pd and Au Catalysts And Binary Ptau And Pdau Catalystsmentioning
confidence: 99%
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“…For potential higher than 0.9 V vs. RHE Pt suffers strong deactivation, due to the formation of an inhibiting surface oxide [10,17,18]. Glycerol oxidation on Pd lead to a selectivity towards GALD and GLA at low potentials, and then towards HPA, dicarboxylates and products derived by C-C bond cleavage (C2 and C1 compounds) at higher potentials [18,26]. It has to be denoted that the structure and morphology of the catalysts can play a role for the selectivity: GLA and TA were obtained on Pd/C, and HPA on Pd nanofoam [2].…”
Section: Pure Pt Pd and Au Catalysts And Binary Ptau And Pdau Catalystsmentioning
confidence: 99%
“…The increase of the mass activity is due to the enhancement of the specific activity and/or the electrochemically active surface area. The comparison of the GOR activity of binary/ternary catalysts with that of the respective pure metal catalysts and their selectivity are reported in Table 2 [13,18,24,26,28,33,44,50,. Generally, the addition of a second/third metal improves the GOR activity, and an optimum catalyst composition is observed.…”
Section: Pt-and Pd-and Au-based Binary/ternary Catalystsmentioning
confidence: 99%
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“…Furthermore, when glycerol is used for fuel cell, the reversible energy efficiency of the cell is 0.993 at 25 °C under standard conditions when glycerol is completely oxidized, while for H 2 /O 2 fuel cell, it is 0.83. In order to avoid intermediates of glycerol electro‐oxidation, such as aldehydes, ketones, acids and carbon monoxide (CO), these would not only block the surface active sites and minish the catalytic efficiency of electrocatalyst but also greatly reduce the efficiency of energy conversion, therefore, the reasonable design of high‐performance (activity and durability) electrocatalysts to achieve 14‐electron oxidation of glycerol (i.e., CH 2 OH‐CHOH‐CH 2 OH + 20OH − → 3CO 3 2− + 14H 2 O + 14e − ) is crucial for final commercialization of direct glycerol fuel cell (DGFC).…”
Section: Introductionmentioning
confidence: 99%
“…Pd surfaces produce glyceraldehyde, glyceric acid, mesoxalic acid, and tartronic acid. Furthermore, the bimetallic mixture of Pd with Bi (PdBi), directs the reaction towards glyceraldehyde and dihydroxyacetone . The electro‐oxidation of glycerol has been investigated by combining voltammetry with HPLC online.…”
Section: Introductionmentioning
confidence: 99%