• Freire, Cristina
• Abdelkader Fernandez, Vk
• Fernandes, Dm
• Cunha Silva, L.
• Balula, Ss

Abstract

The smart assembly of Co-containing polyoxometalates (POMs) and Co-based zeolitic imidazole frameworks (ZIF-67) is a promising tool to produce active electrocatalysts for the oxygen evolution reaction (OER). The encapsulation of SiW11Co inside ZIF-67 cavitiesvia'in situ' synthesis produced two novel POM@ZIF-67 nanocomposites with low and high POM loadings-SiW11Co@ZIF-67 and SiW11Co[h]@ZIF-67, respectively. Other materials involving the analogue tri-substituted silicotungstate, SiW9Co3@ZIF-67 and SiW9Co3[h]@ZIF-67, have been prepared for comparison reasons. Regardless of the POM substitution degree, we demonstrated that the bidirectional synergistic POM-ZIF-67 interaction found for the already reported material, SiW9Co3@ZIF-67, is applicable to the other first-time prepared nanocomposites. Remarkably, this synergy is radically enhanced in the case of the two high POM loading samples, with these nanostructured materials being very active OER electrocatalysts, exhibiting 150-160 mV decreased overpotentials and much faster kinetics (similar to 35% decreased Tafel slopes) in relation to pristine ZIF-67. Moreover, they reveal intrinsic OER activities higher than those developed by the expensive commercial references (RuO(2)and IrO(2)powders) especially in the case of SiW9Co3[h]@ZIF-67. This important electrocatalytic improvement can be related to the higher POM loadings achieved, as well as to the formation of an open defect-enriched phase wrapping the 'standard' ZIF-67 framework in these nanomaterials.

Topics

• nanocomposite
• impedance spectroscopy
• phase
• Oxygen
• defect
• Co-containing