Dataset for Controlled Formation of CoOOH/Co(III) MOF Active Phase for Boosting Electrocatalytic Alkaline Water Oxidation

Surface reconstituted metal-organic frameworks (MOFs) offer appealing properties for electrocatalysis due to their unique structural and compositional advantages. In this work, a controlled potential-induced reconstruction of a two-dimensional cobalt metal-organic framework for boosting oxygen evolu...

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Detalles Bibliográficos
Autores: Márquez Escudero, Inmaculada, Gutiérrez Tarriño, Silvia, Portorreal Bottier, Arismendy Antonio, Río Rodríguez, José Luis del, Hernández Salvador, Sergio, Calvente Pacheco, Juan José, Oña Burgos, Pascual, Olloqui Sariego, José Luis
Tipo de recurso: conjunto de datos
Fecha de publicación:2025
País:España
Institución:Universidad de Sevilla (US)
Repositorio:idUS. Depósito de Investigación de la Universidad de Sevilla
OAI Identifier:oai:idus.us.es:11441/179127
Acceso en línea:https://hdl.handle.net/11441/179127
https://doi.org/10.12795/11441/179127
Access Level:acceso abierto
Palabra clave:Cobalt MOF
Controlled MOF reconstruction
In-situ Raman spectroelectrochemistry
Electrocatalysis
Oxygen evolution reaction
Descripción
Sumario:Surface reconstituted metal-organic frameworks (MOFs) offer appealing properties for electrocatalysis due to their unique structural and compositional advantages. In this work, a controlled potential-induced reconstruction of a two-dimensional cobalt metal-organic framework for boosting oxygen evolution reaction in alkaline media is reported. The current MOF is shown to undergo a partial structural transformation that generates a heterogeneous system, where the original MOF coexists with an oxyhydroxide phase. In fact, the potential-induced stabilization of Co(III) metal centers in the MOF is crucial for delaying its full degradation in alkaline media. This partial retention of the Co(III)MOF phase in the so-derived heterogeneous catalyst has been demonstrated to be decisive for boosting the alkaline electrocatalytic oxygen evolution reaction (OER), displaying superior OER activity in terms of both thermodynamic and kinetic merits compared to the benchmark IrO2 and RuO2 electrocatalysts and the prototypical cobalt (oxy)hydroxides, with a Tafel slope of 52 mV dec−1 and a turnover frequency (TOF) of 6.8 s−1 at 450 mV. Remarkably, the generated final product is stable, exhibiting high robustness and long durability for long-term OER electrolysis. This work provides new insight into the impact of the reconstruction of a MOF for alkaline OER under typical electrochemical conditions, which ultimately benefits the rational design of MOF-based catalysts with high electrocatalytic activity for oxidation reactions.