Stabilization of Cu Species in UiO-66 Metal–Organic Framework for CO2-to-Methanol

Insights From Operando X-ray and Electron Microscopy Studies

Journal Article (2026)
Author(s)

Anna Liutkova (Center for Energy and Environmental Sciences)

Fabio André Peixoto Esteves (ETH Zürich, Center for Energy and Environmental Sciences)

Marianela López Romero (European Synchrotron Radiation Facility, Center for Energy and Environmental Sciences)

M.S. Baidun (TU Delft - Applied Sciences)

Anastasia Molokova (European Synchrotron Radiation Facility, LBA synchrotron)

Davide Salusso (European Synchrotron Radiation Facility)

Andrea Testino (École Polytechnique Fédérale de Lausanne, Center for Energy and Environmental Sciences)

A.A. Kolganov (TU Delft - Applied Sciences)

E.A. Pidko (TU Delft - Applied Sciences)

More Authors (External organisation)

Research Group
ChemE/Inorganic Systems Engineering
DOI related publication
https://doi.org/10.1002/smll.74210 Final published version
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Publication Year
2026
Language
English
Research Group
ChemE/Inorganic Systems Engineering
Journal title
Small
Article number
e74210
Downloads counter
11
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Abstract

UiO-66, a Zr-based metal–organic framework (MOF), provides an ordered porous environment capable of adsorbing/retaining CO2 and oxygenated intermediates relevant for methanol synthesis. Although UiO-66-based composites containing Cu and Cu-Zn species show promising performance for CO2-to-methanol conversion, the role of the MOF framework in stabilizing the active metallic species under working conditions remains insufficiently understood. Here, the stabilization of copper species by UiO-66 and the influence of Zn promotion on Cu speciation and catalytic performance during CO2 hydrogenation are investigated. Operando X-ray absorption spectroscopy at the Cu, Zn, and Zr K-edges is combined with electron microscopy and density functional theory calculations to follow the evolution of metal species and the framework during reduction, reaction, and transient switching experiments. Zn promotes the formation and stability of highly dispersed Cu under reaction conditions, while the Zr6 nodes of UiO-66 respond dynamically through reversible hydroxylation and dehydroxylation. By correlating metal speciation, framework response, and methanol productivity under continuous-flow conditions, this work provides molecular-level insight into metal stabilization in Zr-based MOFs and informs the design of MOF-based catalysts for CO2 hydrogenation.