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Design and synthesis of Co(II)HMTAA-14/16 macrocycles and their nano-composites for oxygen reduction electrocatalysis
The major concerns in the design of macrocycle based-ORR catalysts are: (i) understanding the macrocyclic, π-conjugation, central metal and substituent effects on ORR electrocatalysis; and (ii) the use of macrocycles on the electrode surface for the retention of ORR activity because of their poor st...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9063917/ https://www.ncbi.nlm.nih.gov/pubmed/35520816 http://dx.doi.org/10.1039/c9ra02169h |
Sumario: | The major concerns in the design of macrocycle based-ORR catalysts are: (i) understanding the macrocyclic, π-conjugation, central metal and substituent effects on ORR electrocatalysis; and (ii) the use of macrocycles on the electrode surface for the retention of ORR activity because of their poor stability. In this work, we demonstrated the aromaticity/π-electron conjugation effect on ORR activity by using the same macrocycles [HMTAA-14 and 16 (hexamethyltetraaza [14] and [16] annulenes)] with a difference in their macrocyclic cavity/π-electron conjugation. The macrocycles Co(II)HMTAA-14 and Co(II)HMTAA-16 and their nanocomposites with highly conductive carbon black were prepared by a microwave-assisted method and characterized by using multiple spectroscopy techniques. Comparative redox and oxygen reduction activity studies of Co(II)HMTAA-14 and Co(II)HMTAA-16 were undertaken by using cyclic voltammetry and linear sweep voltammetry in an alkaline medium. The composite Co(II)HMTAA-16@C showed good ORR activity compared to Co(II)HMTAA-14@C in O(2)-saturated KOH electrolyte. Since the Co(II)HMTAA-14 and Co(II)HMTAA-16 systems have a similar central atom and substituents, the shift of the ORR peak position in the +ive potential region for HMTAA-16 can be attributed to the difference in the size of the macrocyclic cavity (macrocyclic effect) and the extra stability of HMTAA-16 annulene due to its aromaticity. |
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