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March 12, 20267 citations

Unlocking Synergistic Ligand-Metal Interplay in Dual Redox-Active Metal-Organic Framework for High-Efficiency and Durable Overall Water Splitting.

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PMPartha Pratim MondalSRSuprobhat Singha RoyRCRudra Chand

Key Points

  • To develop an efficient bifunctional electrocatalyst for overall water splitting that operates effectively for both oxygen and hydrogen evolution reactions.
  • Designed a Co(II)-based metal-organic framework using naphthalenediimide linkers and dicarboxylate ligands.
  • Engineered the interface with conductive nickel foam to enhance electrochemical performance.
  • Evaluated the electrocatalytic activity under high current density in alkaline media.
  • Achieved a current density of 100 mA·cm^-2 with overpotentials of 313 mV (OER) and 263 mV (HER).
  • Demonstrated >95% Faradaic efficiency and low charge-transfer resistance.
  • Showed durability for over 40 hours with stable structural characteristics during water splitting.

Abstract

The development of bifunctional electrocatalysts that efficiently operate for both the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in a single electrolyte under high current density remains a critical challenge toward applied overall water splitting. Herein, we designed a robust and microporous Co(II)-based nonpenetrating metal-organic framework (MOF) via juxtaposition of redox-active naphthalenediimide linker and π-electron rich C2-symmetric dicarboxylate ligand that features in situ-generated Co2(COO)4 chain and exhibits high thermo-chemical stability. The efficient charge-mediating architecture upon interface engineering with conductive nickel foam (NF) delivers remarkable bifunctional water splitting activity in an alkaline medium (1 M KOH), achieving an industrially relevant current density of 100 mA·cm-2 with low overpotentials of 313 mV (OER) and 263 mV (HER). Importantly, rapid reaction kinetics, minimal charge-transfer resistance, and >95% Faradaic efficiency outperform the majority of contemporary as well as benchmark materials. The catalyst demonstrated excellent electrochemical durability in both water oxidation and reduction reactions for over 40 h and retains its structural and morphological attributes after prolonged chronoamperometric operation, demonstrating high-performance water splitting. Performance comparison with an isostructural Cd-MOF analogue confirms the essential contribution of ligand-metal synergism in the Co-MOF for much enhanced redox articulation and electrocatalysis. When deployed as both electrodes, the bifunctional MOF/NF system efficiently catalyzes overall water splitting with only 1.678 V cell voltage at 10 mA·cm-2, marking it among the leading MOF-based electrocatalysts. The findings highlight the pivotal role of ligand-metal cooperativity and hierarchical interface engineering in boosting the electrochemical efficacy of MOF catalysts and provide a promising strategy in designing next-generation bifunctional electrocatalysts for sustainable energy applications.

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Cite This Study

Mondal et al. (2026) studied this question.

synapsesocial.com/papers/69b25b1996eeacc4fcec9828https://doi.org/10.1021/acsami.5c23129
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