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量身定制的基于纳米颗粒的钯镍锡催化剂作为甘油燃料电池的潜在阳极。

Tailor-designed nanoparticle-based PdNiSn catalyst as a potential anode for glycerol fuel cells.

作者信息

El-Nowihy Ghada H

机构信息

Chemical Engineering Department, Faculty of Engineering, The British University in Egypt, Cairo, 11837, Egypt.

出版信息

Sci Rep. 2023 Aug 15;13(1):13244. doi: 10.1038/s41598-023-40374-4.

Abstract

In order to effectively use glycerol as a fuel in direct glycerol fuel cells, a catalyst that can break the C-C bond and enhance the electro-oxidation of glycerol to CO is necessary. In this particular investigation, a palladium-nickel-tin nanocomposite electrodeposited on a glassy carbon electrode (PdNiSn/GC) exhibited excellent activity towards the electro-oxidation of glycerol, thanks to the synergistic effect of the catalyst composition. The PdNiSn/GC surface generated a peak current (I) that was 2.5 times higher than that obtained at a Pd/GC electrode, with a cathodic shift in the onset potential (E) of approximately 300 mV. Additionally, the current obtained at the PdNiSn/GC surface remained stable during continuous electrolysis. Capacitance measurements were used to interpret the results of the electrocatalytic activity, and high-performance liquid chromatography indicated that the products of the glycerol electro-oxidation reaction were oxalic acid and formic acid, which were subsequently oxidized to CO, as revealed by the charge calculations. The results depict that the synergy between Pd, β-Ni(OH), and SnO is crucial for boosting GEOR through enhancing the C-C bond cleavage and completely oxidize the reaction intermediates to CO.

摘要

为了在直接甘油燃料电池中有效地将甘油用作燃料,需要一种能够断裂碳-碳键并增强甘油电氧化为一氧化碳的催化剂。在这项具体研究中,沉积在玻碳电极上的钯-镍-锡纳米复合材料(PdNiSn/GC)对甘油的电氧化表现出优异的活性,这得益于催化剂成分的协同效应。PdNiSn/GC表面产生的峰值电流(I)比在Pd/GC电极上获得的电流高2.5倍,起始电位(E)发生了约300 mV的阴极偏移。此外,在连续电解过程中,PdNiSn/GC表面获得的电流保持稳定。通过电容测量来解释电催化活性的结果,高效液相色谱表明甘油电氧化反应的产物是草酸和甲酸,电荷计算结果显示它们随后被氧化为一氧化碳。结果表明,Pd、β-Ni(OH)和SnO之间的协同作用对于通过增强碳-碳键断裂并将反应中间体完全氧化为一氧化碳来促进甘油电氧化反应至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71eb/10427691/ce7c790aa3d9/41598_2023_40374_Fig1_HTML.jpg

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