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Cobalt porphyrin intercalation into zirconium phosphate layers for electrochemical water oxidation

A cobalt porphyrin molecule, namely CoTcPP (TcPP = the dianion of meso -tetra(4-carboxyphenyl)porphyrin), is intercalated into zirconium phosphate (ZrP) layers as an effective way to heterogenize a porphyrin-based molecular electrocatalyst. Fourier-transform infrared (FT-IR) spectroscopy, X-ray powd...

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Bibliographic Details
Published in:Sustainable energy & fuels 2021-01, Vol.5 (2), p.43-437
Main Authors: Barraza Alvarez, Isabel, Wu, Yanyu, Sanchez, Joel, Ge, Yulu, Ramos-Garcés, Mario V, Chu, Tong, Jaramillo, Thomas F, Colón, Jorge L, Villagrán, Dino
Format: Article
Language:English
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Summary:A cobalt porphyrin molecule, namely CoTcPP (TcPP = the dianion of meso -tetra(4-carboxyphenyl)porphyrin), is intercalated into zirconium phosphate (ZrP) layers as an effective way to heterogenize a porphyrin-based molecular electrocatalyst. Fourier-transform infrared (FT-IR) spectroscopy, X-ray powder diffraction (XRPD) measurements, UV-Vis spectroscopy, elemental mapping, energy dispersive X-ray (EDX) analysis, inductively coupled plasma mass spectrometry (ICP-MS) and X-ray photoelectron spectroscopy (XPS) were utilized to determine the successful intercalation of CoTcPP into ZrP. While the CoTcPP molecule is not amendable to be used as a heterogeneous catalyst in basic environment due to the carboxylic groups, the intercalated species (CoTcPP/ZrP) is effective towards water oxidation from KOH aqueous solution when utilized as a heterogeneous electrocatalyst and shows remarkable catalytic durability. Electrochemical results show that CoTcPP/ZrP requires an overpotential of 0.467 V to achieve a current density of 10 mA cm −2 while the pristine α-ZrP shows negligible electrocatalytic OER behavior. A cobalt porphyrin molecule, namely CoTcPP (TcPP = the dianion of meso -tetra(4-carboxyphenyl)porphyrin), is intercalated into zirconium phosphate (ZrP) layers as an effective way to heterogenize a porphyrin-based molecular electrocatalyst.
ISSN:2398-4902
2398-4902
DOI:10.1039/d0se01134g