The production of renewable feedstocks through the coupled
oxygen
evolution reaction (OER) with selective organic oxidation requires
a perfect balance in the choice of a catalyst and its synthesis access,
morphology, and catalytic activity. Herein we report a rapid in-liquid plasma approach to produce a hierarchical amorphous
birnessite-type manganese oxide layer on 3D nickel foam. The as-prepared
anode exhibits an OER activity with overpotentials of 220, 250, and
270 mV for 100, 500, and 1000 mA·cm–2, respectively,
and can spontaneously be paired with chemoselective dehydrogenation
of benzylamine under both ambient and industrial (6 M KOH, 65 °C)
alkaline conditions. The in-depth ex-situ and in-situ characterization unequivocally demonstrate the intercalation
of potassium in the birnessite-type phase with prevalent MnIII states as an active structure, which displays a trade-off between
porous morphology and bulk volume catalytic activity. Further, a structure–activity
relationship is realized based on the cation size and structurally
similar manganese oxide polymorphs. The presented method is a substantial
step forward in developing a robust MnO
x
catalyst for combining effective industrial OER and value-added
organic oxidation.