Abstract <p>The catalytic performance and mechanism of the prepared iron meso-tetra (4-carboxyphenyl) porphyrin (FeTCPP) on oxygen reduction reaction in alkaline environments were studied. At high concentrations of FeTCPP, the oxygen reduction reaction followed an efficient direct 4-electron transfer mechanism instead of 2+2 electron transfer mechanism. The central iron ion in FeTCPP underwent redox reactions from Fe<sup>III</sup> to Fe<sup>II</sup>. O<sub>2</sub> molecules formed a superoxide anion coordination complex with Fe<sup>II</sup>TCCP, transferring an electron from the central iron ion. Protonation of the complex formed a superoxide hydrogen radical complex, which then acquired another electron, generating a hydroperoxide radical and completing the first 2-electron reduction. The peroxide formed a coordination complex with Fe<sup>II</sup>TCCP to produce a peroxide complex Fe<sup>III</sup>TCCP:O<sub>2</sub><sup>–</sup> with intramolecular charge transfer. And then it acquired two electrons, completing the second 2-electron reduction and being reduced to OH<sup>–</sup>. When the concentration of Fe<sup>III</sup>TCCP was high, the complex Fe<sup>III</sup>TCCP:O<sub>2</sub><sup>–</sup> could protonate without stepwise reactions, directly acquiring three electrons from the electrode surface and being reduced to OH<sup>–</sup>. The oxygen reduction reaction exhibited a 4-electron mechanism. Both the 2+2 and 4-electron pathways occurred simultaneously, with the 4-electron pathway becoming more prominent as the concentration of FeTCPP increased.</p>

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Catalytic Performance and Mechanism of Iron meso-Tetra(4-carboxyphenyl)porphine for Oxygen Reduction Reaction

  • X. Liu,
  • Q.-x. Yue,
  • Y.-h. Wang,
  • M.-d. Lei,
  • Y.-l. Zhang,
  • Y.-w. Zhang,
  • A.-l. Ji,
  • Y.-c. Zhang,
  • X.-q. Zhang,
  • R. Ding,
  • J. Liu

摘要

Abstract

The catalytic performance and mechanism of the prepared iron meso-tetra (4-carboxyphenyl) porphyrin (FeTCPP) on oxygen reduction reaction in alkaline environments were studied. At high concentrations of FeTCPP, the oxygen reduction reaction followed an efficient direct 4-electron transfer mechanism instead of 2+2 electron transfer mechanism. The central iron ion in FeTCPP underwent redox reactions from FeIII to FeII. O2 molecules formed a superoxide anion coordination complex with FeIITCCP, transferring an electron from the central iron ion. Protonation of the complex formed a superoxide hydrogen radical complex, which then acquired another electron, generating a hydroperoxide radical and completing the first 2-electron reduction. The peroxide formed a coordination complex with FeIITCCP to produce a peroxide complex FeIIITCCP:O2 with intramolecular charge transfer. And then it acquired two electrons, completing the second 2-electron reduction and being reduced to OH. When the concentration of FeIIITCCP was high, the complex FeIIITCCP:O2 could protonate without stepwise reactions, directly acquiring three electrons from the electrode surface and being reduced to OH. The oxygen reduction reaction exhibited a 4-electron mechanism. Both the 2+2 and 4-electron pathways occurred simultaneously, with the 4-electron pathway becoming more prominent as the concentration of FeTCPP increased.