甲酸
催化作用
电化学
化学
选择性
醋酸
无机化学
吸附
纳米颗粒
电催化剂
法拉第效率
氢
可逆氢电极
电极
材料科学
纳米技术
有机化学
物理化学
工作电极
作者
Guillem Montaña Mora,Karol V. Mejia‐Centeno,Xueqiang Qi,Qian Xue,Jesús Chacón‐Borrero,Francesco Salutari,Maria Chiara Spadaro,Teresa Andreu,Germán Salazar-Álvarez,Frank Güell,Jordi Llorca,Jordi Arbiol,Paulina R. Martínez‐Alanis,Andreu Cabot
标识
DOI:10.1002/cssc.202401256
摘要
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 GOR via the NiOOH/Ni(OH)2 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)2 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 SnO2 facilitates the adsorption of glucose on the surface of Ni and promotes the formation of the catalytic active Ni3+ species
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