4.7 Article

Photoelectrochemical Stability under Anodic and Cathodic Conditions of Meso-Tetra-(4-Sulfonatophenyl)-Porphyrinato Cobalt (II) Immobilized in Polypyrrole Thin Films

Journal

POLYMERS
Volume 13, Issue 4, Pages -

Publisher

MDPI
DOI: 10.3390/polym13040657

Keywords

photoelectrochemistry; polypyrrole; porphyrin; stability; thin films

Funding

  1. Universidad de los Andes (Chemistry Department)
  2. CEIBA foundation
  3. Universidad de los Andes (Chemical Engineering Department)
  4. [INV-2020-96-1988]
  5. [INV-2019-84-1828]
  6. [INV-2019-68-1749]

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Cobalt porphyrins are promising catalysts for electrochemical and photoelectrochemical applications due to their excellent performance, low cost, and abundance on Earth. Immobilizing negatively charged TPPS in PPy and metallizing it with cobalt to obtain CoTPPS had different effects on the photoelectrochemical behavior towards thiosulfate oxidation and oxygen reduction. The findings are important for understanding the role of CoTPPS as a catalyst in applications like water splitting and could contribute to the design of novel photocathodes.
Cobalt porphyrins have emerged as promising catalysts for electrochemical and photoelectrochemical applications because of their good performance, low cost and the abundance of cobalt in the earth. Herein, a negatively charged porphyrin meso-tetra-(4-sulfonatophenyl)-porphin (TPPS) was immobilized in polypyrrole (PPy) during the electro-polymerization, and then it was metallized with cobalt to obtain meso-tetra-(4-sulfonatophenyl)-porphyrinato cobalt (II) (CoTPPS) as a dopant in PPy. The coatings were evaluated as photoelectrodes towards thiosulfate oxidation and oxygen reduction. For comparison purposes, the photoelectrochemical behavior of ClO4--doped polypyrrole films was also evaluated. Characterizations by chronoamperometry, UV-Vis spectroscopy and Raman spectroscopy showed that polypyrrole is stable under anodic and cathodic conditions, but CoTPPS and TPPS immobilized in PPy are degraded during the anodic process. Thus, decreases in photocurrent of up to 87% and 97% for CoTPPS-doped PPy and TPPS-doped PPy were observed after a 30-min chronoamperometry test. On the other hand, good stability of CoTPPS and TPPS immobilized in PPy was observed during photoelectrochemical oxygen reduction, which was reflected in almost constant photocurrents obtained by chronoamperometry. These findings are relevant to understanding the role of CoTPPS as a catalyst or pre-catalyst in photoelectrochemical applications such as water splitting. In addition, these results could pave the way for further research to include CoTPPS-doped PPy in the design of novel photocathodes.

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