Cobalt porphyrin immobilized on the TiO2 nanotube electrode for CO2 electroreduction in aqueous solution

Herein we report CO2 electrochemical reduction reaction (CO2 ERR) on the cobalt tetraphenylporphyrin (CoTPP) modified TiO2 nanotube (TNT) electrode. It was found the axial coordination of drop-casting solvent to CoTPP and the porphyrin structure are the major factors that have significant effects on the catalytic performance of the electrode. As confirmed by spectrophotometric titration, pyridine has a stronger coordination bond to CoTPP than DMF and THE thus leading to the highest efficiency among the dropcasting solvents tested in the study. Based on the spectrophotometric analysis, possible coordination mechanism between drop-casting solvents and CoTPP is put forward. On the other hand, introduction of -COOMe substituents in phenyl rings of CoTPP weakens the coordination bond between pyridine and CoTPP as clearly evidenced by deuterium NMR spectra, resulting in a detrimental effect on CO2 ERR. Therefore, the manipulation of the coordination environment around the metal center of immobilized catalyst is crucial in designing an efficient electrocatalytic system. (C) 2020 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.

Automated summary

In this study, the axial coordination of drop-casting solvent to CoTPP and the porphyrin structure were found to have significant effects on the catalytic performance of the CO2 ERR reaction. Pyridine demonstrated a stronger coordination bond to CoTPP compared to DMF and THE, resulting in the highest efficiency among the tested solvents. However, introducing -COOMe substituents in CoTPP weakened the coordination bond, leading to a detrimental effect on CO2 ERR. Manipulating the coordination environment around the metal center of the immobilized catalyst is crucial in designing an efficient electrocatalytic system.