• O 2 plasma enables surface-confined modification of ZIF-67 nanostructures. • Regardless initial MOF morphology/crystallinity, plasma generates Co 3 O 4 nanoclusters, undercoordinated Co 2+ sites, and partially oxidized linkers. • The alterations extent and their correlation with plasma duration depends on the initial nanostructure. • All plasma-engineered ZIF-67 materials show enhanced OER activity, however the improvements foundations depend on initial MOF features. • Stationary and rotating plasma modes selectively control Co 3 O 4 nanocluster formation. Oxygen plasma offers a rapid, sustainable, and controllable method to tailor ZIF-67, however, the link between nanostructure, plasma-induced surface modifications, and electrocatalytic performance remains unclear. Here, canonical (Z) and non-canonical (nZ) ZIF-67 materials were engineered via O 2 plasma and evaluated using the oxygen evolution reaction (OER) as a model. Plasma exposure times of 30, 45, and 60 min were explored. Three surface-confined transformations occurred in both variants: Co 3 O 4 formation, partial oxidation of 2-methylimidazole linkers, and generation of undercoordinated Co 2+ defect sites. Their extent and impact on porosity, crystallinity, and morphology strongly depended on the initial nanostructure and plasma duration, with clearer correlations for Z-derivatives. After 60 min-plasma treatment, Z-p60 and nZ-p60 reached ∼ 7.5 mA cm −2 at 1.76 V vs . RHE (LSV, without iR -compensation), corresponding to 3.1x and 3.5x higher OER current densities than Z and nZ, respectively. Improved kinetics were observed (Tafel slopes: Z-p60, 130 and 222 mV dec -1 ; nZ-p60, 133 and 204 mV dec -1 ), surpassing RuO 2 ( j 1.76 = 4.8 mA cm −2 ; TS = 221 and 427 mV dec -1 ). Remarkably, controlled Co 3 O 4 formation demonstrated that this oxide contributes significantly, although overall performance gains result from the interplay of all plasma-induced modifications.
Vismara et al. (Sun,) studied this question.