LAPSE:2023.2835
Published Article

LAPSE:2023.2835
Catalytic Properties of Free-Base Porphyrin Modified Graphite Electrodes for Electrochemical Water Splitting in Alkaline Medium
February 21, 2023
Abstract
Hydrogen generation via electrochemical water splitting is considered an eco-friendly pathway for obtaining this desired alternative energy source, and it has triggered an intensive search for low cost and efficient catalysts. Within this context, four free-base porphyrins were studied as heterogeneous catalysts for the oxygen and hydrogen evolution reactions (OER and HER) in alkaline aqueous solutions. TEM and STEM analyses of samples obtained by drop-casting the porphyrins from different organic solvents on TEM grids revealed a rich variety of aggregates due to the self-assembling property of the porphyrin molecules. Modified electrodes were manufactured by applying the four tetrapyrrolic macrocycles from various solvents on the surface of graphite supports, in one or more layers. Experiments performed in 0.1 M and 1 M KOH electrolyte solutions allowed the identification of the most electrocatalytically active electrodes for the OER and HER, respectively. In the first case, the electrode was manufactured by applying three layers of 5-(4-pyridyl)-10,15,20-tris(4-phenoxyphenyl)porphyrin on the graphite substrate from N,N-dimethylformamide solution was identified as overall catalytically superior. In the second case, the electrode obtained by applying one layer of 5,10,15,20-tetrakis(4-allyloxyphenyl)-porphyrin from benzonitrile solution displayed an HER overpotential value of 500 mV at i = −10 mA/cm2 and a Tafel slope of 190 mV/dec.
Hydrogen generation via electrochemical water splitting is considered an eco-friendly pathway for obtaining this desired alternative energy source, and it has triggered an intensive search for low cost and efficient catalysts. Within this context, four free-base porphyrins were studied as heterogeneous catalysts for the oxygen and hydrogen evolution reactions (OER and HER) in alkaline aqueous solutions. TEM and STEM analyses of samples obtained by drop-casting the porphyrins from different organic solvents on TEM grids revealed a rich variety of aggregates due to the self-assembling property of the porphyrin molecules. Modified electrodes were manufactured by applying the four tetrapyrrolic macrocycles from various solvents on the surface of graphite supports, in one or more layers. Experiments performed in 0.1 M and 1 M KOH electrolyte solutions allowed the identification of the most electrocatalytically active electrodes for the OER and HER, respectively. In the first case, the electrode was manufactured by applying three layers of 5-(4-pyridyl)-10,15,20-tris(4-phenoxyphenyl)porphyrin on the graphite substrate from N,N-dimethylformamide solution was identified as overall catalytically superior. In the second case, the electrode obtained by applying one layer of 5,10,15,20-tetrakis(4-allyloxyphenyl)-porphyrin from benzonitrile solution displayed an HER overpotential value of 500 mV at i = −10 mA/cm2 and a Tafel slope of 190 mV/dec.
Record ID
Keywords
aggregate, electrocatalysis, electron microscopy, porphyrin, water splitting
Subject
Suggested Citation
Taranu BO, Fagadar-Cosma E. Catalytic Properties of Free-Base Porphyrin Modified Graphite Electrodes for Electrochemical Water Splitting in Alkaline Medium. (2023). LAPSE:2023.2835
Author Affiliations
Taranu BO: National Institute for Research and Development in Electrochemistry and Condensed Matter, Dr. A. Paunescu Podeanu Street No. 144, 300569 Timisoara, Romania
Fagadar-Cosma E: Institute of Chemistry “Coriolan Dragulescu”, Mihai Viteazu Ave. 24, 300223 Timisoara, Romania [ORCID]
Fagadar-Cosma E: Institute of Chemistry “Coriolan Dragulescu”, Mihai Viteazu Ave. 24, 300223 Timisoara, Romania [ORCID]
Journal Name
Processes
Volume
10
Issue
3
First Page
611
Year
2022
Publication Date
2022-03-21
ISSN
2227-9717
Version Comments
Original Submission
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PII: pr10030611, Publication Type: Journal Article
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LAPSE:2023.2835
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https://doi.org/10.3390/pr10030611
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Feb 21, 2023
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