Modulating Cu electrode microenvironments with MOF coatings: insights from molecular dynamics and electrochemical experiments of CO reduction

• MOF coatings reshape Cu electrode microenvironments during CO reduction. • MD reveals how pore size and hydrophobicity affect CO and H 2 O coordination. • ZIF-8@Cu in ACN enhances ethylene selectivity by limiting water access. • NU-901@Cu promotes HER by concentrating water near the Cu surface. • MOFs act as physical modulators of reactant delivery and solvation. Metal-organic frameworks (MOFs) present a compelling strategy for tuning electrochemical interfaces by reshaping interfacial solvent structure. In this study, we examine how MOF coatings influence the microenvironment at copper electrodes during the CO electroreduction reaction (CORR) using a combined approach of molecular dynamics (MD) simulations and electrochemical experiments. Two MOFs, NU-901 and ZIF-8, are selected to explore the impact of pore size and channel hydrophobicity on electrochemical activity and interfacial concentration in acetonitrile (ACN) and dimethyl sulfoxide (DMSO) electrolytes. Electrochemical measurements reveal that MOF@Cu electrodes exhibit lower Faradaic efficiencies for CO hydrogenation products (ethylene and methane) compared to bare copper but have dramatic impacts on the interfacial microenvironment. NU-901, with its larger pores and strong interactions with DMSO, traps DMSO molecules and enhances CO coordination in DMSO but suppresses CORR selectivity in favor of the hydrogen evolution reaction (HER). ZIF-8, with smaller pores and hydrophobic channels, limits the interfacial water concentration, and, in ACN, promotes CO coordination. The simulations provide insights into how MOFs can act as physical modulators of reactant delivery and interfacial structure to control electrochemical microenvironments. This work highlights the value of molecular dynamics in uncovering how structural features of MOFs influence interfacial phenomena, even when catalytic performance is not directly improved.

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Publication Details

Journal
Journal of Catalysis
Published
2026-01-30
DOI
https://doi.org/10.1016/j.jcat.2026.116723
Primary Topic
CO2 Reduction Techniques and Catalysts
Type
article
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article

Modulating Cu electrode microenvironments with MOF coatings: insights from molecular dynamics and electrochemical experiments of CO reduction

Matthew Neurock, Chibueze V. Amanchukwu, Manish Maurya, Joseph T. Hupp et al.
Journal of Catalysis
CO2 Reduction Techniques and Catalysts
article

Modulating Cu electrode microenvironments with MOF coatings: insights from molecular dynamics and electrochemical experiments of CO reduction

Matthew Neurock, Chibueze V. Amanchukwu, Manish Maurya, Joseph T. Hupp, Rachel B. Getman, Hannah Fejzić, Xavier Krull, Huy Nguyen
article en

Abstract

• MOF coatings reshape Cu electrode microenvironments during CO reduction. • MD reveals how pore size and hydrophobicity affect CO and H 2 O coordination. • ZIF-8@Cu in ACN enhances ethylene selectivity by limiting water access. • NU-901@Cu promotes HER by concentrating water near the Cu surface. • MOFs act as physical modulators of reactant delivery and solvation. Metal-organic frameworks (MOFs) present a compelling strategy for tuning electrochemical interfaces by reshaping interfacial solvent structure. In this study, we examine how MOF coatings influence the microenvironment at copper electrodes during the CO electroreduction reaction (CORR) using a combined approach of molecular dynamics (MD) simulations and electrochemical experiments. Two MOFs, NU-901 and ZIF-8, are selected to explore the impact of pore size and channel hydrophobicity on electrochemical activity and interfacial concentration in acetonitrile (ACN) and dimethyl sulfoxide (DMSO) electrolytes. Electrochemical measurements reveal that MOF@Cu electrodes exhibit lower Faradaic efficiencies for CO hydrogenation products (ethylene and methane) compared to bare copper but have dramatic impacts on the interfacial microenvironment. NU-901, with its larger pores and strong interactions with DMSO, traps DMSO molecules and enhances CO coordination in DMSO but suppresses CORR selectivity in favor of the hydrogen evolution reaction (HER). ZIF-8, with smaller pores and hydrophobic channels, limits the interfacial water concentration, and, in ACN, promotes CO coordination. The simulations provide insights into how MOFs can act as physical modulators of reactant delivery and interfacial structure to control electrochemical microenvironments. This work highlights the value of molecular dynamics in uncovering how structural features of MOFs influence interfacial phenomena, even when catalytic performance is not directly improved.

Journal of CatalysisVol. 456
Northwestern University (US), University of Minnesota (US), University of Chicago (US), Material Sciences (United States) (US), The Ohio State University (US)
Clean water and sanitation
Openalex Percentile: Top 73%
CO2 Reduction Techniques and Catalysts
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