Cu–N4 in copper phthalocyanine@CFC catalyst for ammonia oxidation reaction catalysis

催化作用 过电位 化学 无机化学 吸附 氨生产 电化学 光化学 物理化学 有机化学 电极
作者
Ziyi Liu,Mengxue Wu,Jinfu Ma
出处
期刊:Physical Chemistry Chemical Physics [Royal Society of Chemistry]
卷期号:25 (11): 7859-7868 被引量:2
标识
DOI:10.1039/d2cp05589a
摘要

The high oxidation overpotential in the ammonia oxidation reaction (AOR) is a key factor restricting the fields of ammonia fuel cells, hydrogen production by electrochemical decomposition of ammonia, and treatment of ammonia-containing wastewater. Copper-based catalysts have been considered hopeless for AOR; however, in this research, copper phthalocyanine (CuPc) catalysts grown on carbon fiber cloth (CFC), CuPc@CFC, were investigated firstly for AOR catalysis, and the unique Cu-N4 resulted in a peak potential of -0.29 V vs. Hg/HgO for AOR, which is superior to Pt/C. Density functional theory (DFT) calculations show that Cu-N4 is the reactive center of AOR, and the LUMO of CuPc is distributed on the Cu site, which is favorable to gain electrons from NH3 and thus adsorb NH3; in contrast, the HOMO of C10H10CuN8 is distributed on the Cu site, which tends to give electrons and is unfavorable to NH3 adsorption. However, copper azide pyridine (C10H10CuN8) was found in the samples after the AOR. Analysis of the comparison samples showed that changing the ethanol content has the effect of changing the grain size and inhibiting the generation of C10H10CuN8 after the AOR process, as well as slightly changing the Cu-N4, leading to the change of its Fermi energy level and d-orbital energy level center, thus providing new ideas for the future fabrication of catalysts in various fields of AOR.
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