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.
Supplementary materials
Title
H2O2 ACS Catalysis SI
Description
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