Novel Fully Organic Water Oxidation Electrocatalysts: A Quest for Simplicity

Despite the growing need for readily available and inexpensive catalysts for the half-reactions involved in water splitting, water oxidation and reduction electrocatalysts are still traditionally based on noble metals. One long-standing challenge has been the development of an oxygen evolution reaction catalyzed by easily available, structurally simple, and purely organic compounds. Herein, we first generalize the performance of the known <i>N</i>-ethyl-flavinium ion to a number of derivatives. Furthermore, we demonstrate an unprecedented application of different pyridinium and related salts as very simple, inexpensive water oxidation organocatalysts consisting of earth-abundant elements (C, H, O, and N) exclusively. The results establish the prospects of heterocyclic aromatics for further design of new organic electrocatalysts for this challenging oxidation reaction

Novel Fully Organic Water Oxidation Electrocatalysts: A Quest for Simplicity

Despite the growing need for readily available and inexpensive catalysts for the half-reactions involved in water splitting, water oxidation and reduction electrocatalysts are still traditionally based on noble metals. One long-standing challenge has been the development of an oxygen evolution reaction catalyzed by easily available, structurally simple, and purely organic compounds. Herein, we first generalize the performance of the known <i>N</i>-ethyl-flavinium ion to a number of derivatives. Furthermore, we demonstrate an unprecedented application of different pyridinium and related salts as very simple, inexpensive water oxidation organocatalysts consisting of earth-abundant elements (C, H, O, and N) exclusively. The results establish the prospects of heterocyclic aromatics for further design of new organic electrocatalysts for this challenging oxidation reaction