Oxophilic Sn to Promote Glucose Oxidation to Formic Acid in Ni Nanoparticles

The electrochemical glucose oxidation reaction (GOR) presents an opportunity to produce hydrogen and high-value chemical products. Herein, we investigate the effect of Sn in Ni nanoparticles for the GOR to formic acid (FA). Electrochemical results show that the maximum activity is related to the amo...

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Veröffentlicht in:ChemSusChem 2024-11, p.e202401256
Hauptverfasser: Montaña-Mora, Guillem, Mejia-Centeno, Karol V, Qi, Xueqiang, Xue, Qian, Chacón-Borrero, Jesus, Salutari, Francesco, Spadaro, Maria Chiara, Andreu, Teresa, Salazar-Alvarez, Germán, Güell, Frank, Llorca, Jordi, Arbiol, Jordi, Martinez-Alanis, Paulina R, Cabot, Andreu
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Sprache:eng
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Zusammenfassung:The electrochemical glucose oxidation reaction (GOR) presents an opportunity to produce hydrogen and high-value chemical products. Herein, we investigate the effect of Sn in Ni nanoparticles for the GOR to formic acid (FA). Electrochemical results show that the maximum activity is related to the amount of Ni, as Ni sites are responsible for catalyzing the GOR via the NiOOH/Ni(OH) pair. However, the GOR kinetics increases with the amount of Sn, associated with an enhancement of the OH supply to the catalyst surface for Ni(OH) reoxidation to NiOOH. NiSn nanoparticles supported on carbon nanotubes (NiSn/CNT) exhibit excellent current densities and direct GOR via C-C cleavage mechanism, obtaining FA with a Faradaic efficiency (FE) of 93 % at 1.45 V vs. reversible hydrogen electrode. GOR selectivity is further studied by varying the applied potential, glucose concentration, reaction time, and temperature. FE toward FA production decreases due to formic overoxidation to carbonates at low glucose concentrations and high applied potentials, while acetic and lactic acids are obtained with high selectivity at high glucose concentrations and 55 °C. Density functional theory calculations show that the SnO facilitates the adsorption of glucose on the surface of Ni and promotes the formation of the catalytic active Ni species.
ISSN:1864-5631
1864-564X
1864-564X
DOI:10.1002/cssc.202401256