The two-electron water oxidation reaction (2e−-WOR) and oxygen reduction reaction (2e−-ORR) represent sustainable and promising processes for the electrochemical synthesis of hydrogen peroxide (H2O2). The main factor hampering the realization of a paired electrochemical cell for H2O2 production is finding appropriate catalysts for both 2e−-ORR and 2e−-WOR, able to work under the same experimental conditions. Herein we show that Cu(tmpa)) and Sn-TMPyP are compatible and efficient catalysts for 2e−-ORR and 2e−-WOR, respectively. They have been used to assemble a paired electrochemical cell for H2O2 production. The latter exhibits a total overpotential of 570 mV, distributed between the two electrodes. During a 3 h bulk electrolysis experiment, the cathodic Faradaic efficiency ranged from 15% to 19% with a H2O2 production rate of 1.6 µmol h−1 cm−2. Meanwhile, at the anode, the Faradaic efficiency stabilized between 40% and 50%, yielding a H2O2 production rate of 3.5 µmol h−1 cm−2. The remarkable activity of Sn-TMPyP as a catalyst for the 2e−-WOR, ranking among the highest reported for molecular catalysts, is ascribed to the selection of a carbonate buffer as the electrolyte, which enhanced catalytic performance by facilitating dissociation of H2O2 from the Sn catalyst. This work establishes a new benchmark for homogeneous dual-electrode H2O2 electrosynthesis.
A Homogeneously Catalyzed Paired Electrolytic Cell for Hydrogen Peroxide Production
Trotta, Caterina;Menendez Rodriguez, Gabriel;Macchioni, Alceo;
2026
Abstract
The two-electron water oxidation reaction (2e−-WOR) and oxygen reduction reaction (2e−-ORR) represent sustainable and promising processes for the electrochemical synthesis of hydrogen peroxide (H2O2). The main factor hampering the realization of a paired electrochemical cell for H2O2 production is finding appropriate catalysts for both 2e−-ORR and 2e−-WOR, able to work under the same experimental conditions. Herein we show that Cu(tmpa)) and Sn-TMPyP are compatible and efficient catalysts for 2e−-ORR and 2e−-WOR, respectively. They have been used to assemble a paired electrochemical cell for H2O2 production. The latter exhibits a total overpotential of 570 mV, distributed between the two electrodes. During a 3 h bulk electrolysis experiment, the cathodic Faradaic efficiency ranged from 15% to 19% with a H2O2 production rate of 1.6 µmol h−1 cm−2. Meanwhile, at the anode, the Faradaic efficiency stabilized between 40% and 50%, yielding a H2O2 production rate of 3.5 µmol h−1 cm−2. The remarkable activity of Sn-TMPyP as a catalyst for the 2e−-WOR, ranking among the highest reported for molecular catalysts, is ascribed to the selection of a carbonate buffer as the electrolyte, which enhanced catalytic performance by facilitating dissociation of H2O2 from the Sn catalyst. This work establishes a new benchmark for homogeneous dual-electrode H2O2 electrosynthesis.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


