A Homogeneously Catalyzed Paired Electrolytic Cell for Hydrogen Peroxide Production

C Caterina Trotta (Department of Chemistry Biology and Biotechnology and CIRCC University of Perugia Perugia Italy) J Jesse Orta (Leiden Institute of Chemistry Leiden University Leiden The Netherlands) H Hendrik C. de Heer (Leiden Institute of Chemistry Leiden University Leiden The Netherlands) P Pim G. J. van Duren (Leiden Institute of Chemistry Leiden University Leiden The Netherlands) M Maxime A. Siegler (Department of Chemistry) G Gabriel Menendez Rodriguez (Department of Chemistry, Biology and Biotechnology and CIRCC) A Alceo Macchioni (Department of Chemistry, Biology and Biotechnology and CIRCC) D D. G. H. Hetterscheid (Leiden Institute of Chemistry Leiden University Leiden The Netherlands)

Abstract

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 (H 2 O 2 ). The main factor hampering the realization of a paired electrochemical cell for H 2 O 2 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 H 2 O 2 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 H 2 O 2 production rate of 1.6 µmol h − 1 cm − 2 . Meanwhile, at the anode, the Faradaic efficiency stabilized between 40% and 50%, yielding a H 2 O 2 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 H 2 O 2 from the Sn catalyst. This work establishes a new benchmark for homogeneous dual‐electrode H 2 O 2 electrosynthesis.

Article Details

Volume / Issue Vol. 65, Issue 19
Published May 04, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

C

Caterina Trotta

Department of Chemistry Biology and Biotechnology and CIRCC University of Perugia Perugia Italy

J

Jesse Orta

Leiden Institute of Chemistry Leiden University Leiden The Netherlands

H

Hendrik C. de Heer

Leiden Institute of Chemistry Leiden University Leiden The Netherlands

P

Pim G. J. van Duren

Leiden Institute of Chemistry Leiden University Leiden The Netherlands

M

Maxime A. Siegler

Department of Chemistry

G

Gabriel Menendez Rodriguez

Department of Chemistry, Biology and Biotechnology and CIRCC

A

Alceo Macchioni

Department of Chemistry, Biology and Biotechnology and CIRCC

D

D. G. H. Hetterscheid

Leiden Institute of Chemistry Leiden University Leiden The Netherlands