Mixed Ni/Cu-sandwich dawson polyoxotungstates: Electrochemistry and DFT insights

• Mixed Ni/Cu Dawson POMs synthesised with identical frameworks but swapped metal sites • CV and EQCM reveal distinct Cu(II)/Cu(I)/Cu(0) pathways depending on metal ordering • Ni–Cu electronic synergy modulates W(VI) redox waves and enhances Cu reducibility • XPS confirms internal vs external Cu and Ni positions in the sandwich cluster • DFT explains site-dependent redox behaviour and supports experimental assignments Given the established electrocatalytic potential of Ni(II)- and Cu(II)-containing tungsten-based POMs, the primary objective of this work was to create a unique molecular architecture combining both active metal centres in the two Dawson sandwich POMs, [(CuOH 2 ) 2 Ni 2 (As 2 W 15 O 56 ) 2 ] 16− and [(NiOH 2 ) 2 Cu 2 (As 2 W 15 O 56 ) 2 ] 16− . This aims to exploit potential synergistic effects for enhanced catalytic performance and to deepen the understanding of redox mechanisms in these mixed-metal systems. A detailed electrochemical study of the two POMs in solution, compared to their homometallic analogues containing only Ni(II) or only Cu(II) centres, was conducted using cyclic voltammetry (CV), also coupled to quartz crystal microbalance in order to monitor Cu deposition/desorption phenomena, and controlled potential coulometry, enabling unambiguous identification and differentiation. X-ray photoelectron spectroscopy (XPS) unequivocally corroborated these findings. Furthermore, density functional theory (DFT) calculations provide additional insights that are relevant to rationalise the electrochemical measurements. The molecular orbital sequence, energies and shapes provide relevant supporting information to the experimental facts. Combined evidence establishes that Na/Ni compounds maintain the W-only electrochemical fingerprint, whereas new CV features appear when Cu(II) is part of the structure, modulated by the rest of the equatorial composition. Protonation has been explored and its effects on the redox chemistry examined at the theoretical level.

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Journal
Electrochimica Acta
Published
2025-11-23
DOI
https://doi.org/10.1016/j.electacta.2025.147858
Primary Topic
Polyoxometalates: Synthesis and Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

Mixed Ni/Cu-sandwich dawson polyoxotungstates: Electrochemistry and DFT insights

Coen de Graaf, Pedro de Oliveira, Anne‐Lucie Teillout, Neus Vilà et al.
Electrochimica Acta
Polyoxometalates: Synthesis and Applications
article

Mixed Ni/Cu-sandwich dawson polyoxotungstates: Electrochemistry and DFT insights

Coen de Graaf, Pedro de Oliveira, Anne‐Lucie Teillout, Neus Vilà, Xavier López, Israël M. Mbomekallé, Khaoula Merimi, I. Stan, Anaïs Abrousse
article en

Abstract

• Mixed Ni/Cu Dawson POMs synthesised with identical frameworks but swapped metal sites • CV and EQCM reveal distinct Cu(II)/Cu(I)/Cu(0) pathways depending on metal ordering • Ni–Cu electronic synergy modulates W(VI) redox waves and enhances Cu reducibility • XPS confirms internal vs external Cu and Ni positions in the sandwich cluster • DFT explains site-dependent redox behaviour and supports experimental assignments Given the established electrocatalytic potential of Ni(II)- and Cu(II)-containing tungsten-based POMs, the primary objective of this work was to create a unique molecular architecture combining both active metal centres in the two Dawson sandwich POMs, [(CuOH 2 ) 2 Ni 2 (As 2 W 15 O 56 ) 2 ] 16− and [(NiOH 2 ) 2 Cu 2 (As 2 W 15 O 56 ) 2 ] 16− . This aims to exploit potential synergistic effects for enhanced catalytic performance and to deepen the understanding of redox mechanisms in these mixed-metal systems. A detailed electrochemical study of the two POMs in solution, compared to their homometallic analogues containing only Ni(II) or only Cu(II) centres, was conducted using cyclic voltammetry (CV), also coupled to quartz crystal microbalance in order to monitor Cu deposition/desorption phenomena, and controlled potential coulometry, enabling unambiguous identification and differentiation. X-ray photoelectron spectroscopy (XPS) unequivocally corroborated these findings. Furthermore, density functional theory (DFT) calculations provide additional insights that are relevant to rationalise the electrochemical measurements. The molecular orbital sequence, energies and shapes provide relevant supporting information to the experimental facts. Combined evidence establishes that Na/Ni compounds maintain the W-only electrochemical fingerprint, whereas new CV features appear when Cu(II) is part of the structure, modulated by the rest of the equatorial composition. Protonation has been explored and its effects on the redox chemistry examined at the theoretical level.

Electrochimica ActaVol. 548
Institució Catalana de Recerca i Estudis Avançats (ES), Universitat Autònoma de Barcelona (ES), Centre National de la Recherche Scientifique (FR), Université Paris-Saclay (FR), Laboratoire d'Electrochimie Moléculaire (FR), Laboratoire de Chimie Physique et Microbiologie pour les Matériaux et l'Environnement (FR), Universitat Rovira i Virgili (ES), Université de Lorraine (FR)
Agence Nationale de la Recherche, Generalitat de Catalunya, Centre National de la Recherche Scientifique, Université Paris-Saclay
Openalex Percentile: Top 71%
Polyoxometalates: Synthesis and Applications
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