2,2’-Dipyridylamine as Heterogeneous Organic Molecular Electrocatalyst for Two-Electron Oxygen Reduction Reaction in Acid Media

25 June 2019, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Continuous production of hydrogen peroxide (H2O2) through the two-electron oxygen reduction reaction (2e-ORR) in distributed electrochemical cells offers important advantages for point-of-use water treatment and pulp bleaching over the complex industrial anthraquinone process. A low-cost, heterogeneous 2e-ORR electrocatalyst with high activity and selectivity is key to meeting the future needs for distributed production of H2O2 with large capacity. Herein, we demonstrate high activity and selectivity of a new heterogeneous organic molecular electrocatalyst, 2,2’-dipyridylamine, with an H2O2 yield of ca. 80%, and an onset potential of ca. 0.60 V vs. RHE in acidic aqueous electrolyte. We show that this acid-compatible, inexpensive, small organic molecule can catalyze 2e-ORR as efficiently as the state-of-the-art catalysts based on mercury-precious metal alloys. We propose different mechanisms of dioxygen electroreduction based on density functional theory calculations, which correlate activity with calculated standard reduction potential of reaction intermediates.

Keywords

Two-Electron Oxygen Reduction Reaction
2,2'-dipyridylamine
Hydrogen Peroxide Production
H2O2
Heterogeneous Electrocatalysis
organic molecular electrocatalyst
Organocatalyst
Organocatalysis

Supplementary materials

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Description
Actions
Title
H2O2 ACS Catalysis SI
Description
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