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Updated: Apr 30, 2026

Solar-Driven Electrochemical Green Fuel Production from CO2 and Water Using Ti3C2Tx MXene-Supported CuZn and NiCo Catalysts
Published on: November 7, 2025
Cobalt porphyrin electrode films for electrocatalytic water oxidation
Ali Han1, Hongxing Jia, Hao Ma
1CAS Key Laboratory of Materials for Energy Conversion, Department of Materials Science and Engineering, Department of Chemistry, University of Science and Technology of China (USTC), Hefei, 230026, China. dupingwu@ustc.edu.cn.
Abstract:
Catalysts play very important roles in artificial photosynthesis for solar energy conversion. In this present study, two water-insoluble cobalt porphyrin complexes, cobalt(II) meso-tetraphenylporphyrin (CoP-1) and cobalt(II) 5,10,15,20-tetrakis-(4-bromophenyl)porphyrin (CoP-2), were synthesized and coated as thin films on the FTO working electrode. The films showed good activities for electrocatalytic water oxidation in aqueous solutions at pH 9.2. The Faradaic efficiencies of both films approached to ~100%, measured using a fluorescence-based oxygen sensor. The turnover frequencies were close to 0.50 s(−1) and 0.40 s(−1) for CoP-1 and CoP-2, respectively, under an applied anodic potential of 1.3 V (vs. Ag/AgCl) at pH 9.2. Importantly, no cobalt oxide particles were observed on the working electrode after catalysis. The stability of the catalyst films was further evaluated by UV-vis spectroscopy, inhibition measurements, mass spectrometry, scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX). The pH dependence of water oxidation on CoP-1 and CoP-2 suggested a proton-coupled electron transfer (PCET) mechanism. The catalyst films could be recycled and showed almost unchanged catalytic activities when they were reused in new electrocatalytic studies of water oxidation.
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