Rare-Earth Europium Substitution Allows for More Control Over CO₂-to-Fuel Conversion
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Rare-Earth Europium Substitution Allows for More Control Over CO₂-to-Fuel Conversion

12/12/2025 Tohoku University

The electrochemical CO2 (carbon dioxide) reduction reaction takes harmful pollutants, and transforms them into valuable products like fuel. However, selectively tailoring various processes in this reaction to successfully and efficiently arrive at a particular desired outcome remains a challenge.

"We want to be able to tailor this reaction so we can accurately predict what the result will be each time - and to control what that result is," explains Hao Li (Distinguished Professor, Advanced Institute for Materials Research (WPI-AIMR)).

The team of researchers from Tohoku University found that the rare-earth element Europium (Eu) was the key to controlling the selectivity of this reaction for C1 or C2+ products. When atomic Eu was incorporated into Cu2O, it was able to shift the dominant product depending on whether Eu concentration was high or low. For example, low Eu-doped Cu2O achieves a high Faradaic efficiency of nearly 80% for C2+ products, while higher Eu doping tips the pathway toward C1 products such as CH4.

Theoretical calculations and other observations imply that the mechanism behind this involves the way Eu facilitates different reactions depending on its concentration. At low Eu concentrations, certain bonds are weakened that lead to C-C coupling and produce C2+ via the frustrated deep hydrogenation of *CHO. For high Eu concentrations, certain bonds become strengthened instead, which facilitates the deep hydrogenation of *CHO to CH4 via the C1 pathway.

This work establishes a clear, intrinsic mechanism for switching between C1 and C2+ products in electrochemical CO2 reduction by using Eu as an electronic modulator in Cu2O-based catalysts. By leveraging the reversible Eu3+/Eu2+ redox couple and its impact on the *CHO intermediate, this study shows how subtle changes in electronic structure can selectively favor either C-C coupling (toward C2+ products) or deep hydrogenation (toward CH4).

This research provides a design concept for "dialing in" desired carbon products from CO2 using earth-abundant Cu-based catalysts and rare-earth promoters. Such precise control over CO2-to-fuels conversion supports the development of electrified, CO2-based production routes for high-value chemicals and fuels. In the long term, this can contribute to carbon-neutral chemical manufacturing, more efficient use of renewable electricity, and the mitigation of greenhouse gas emissions.

The findings were published in the Journal of the American Chemical Society on December 1, 2025.

Title: Atomic Eu Substitution in Cu2O Tailors C1 and C2+ Product Selectivity by Frustrated Deep Hydrogenation in Electrochemical CO2 Reduction

Authors: Yang Liu, Xuan Wang, Zichun Mao, Jiaxiong Zhang, Meng Li, Dongmei Sun, Yawen Tang, Hao Li, Gengtao Fu

Journal: Journal of the American Chemical Society

DOI: 10.1021/jacs.5c19360
Attached files
  • Material synthesis and ex-situ structure characterizations. The design strategy and physical characterizations of LD-Eu/Cu2O and HD-Eu/Cu2O. (a) Schematic route for the synthesis of Eu/Cu2O. (b) XRD patterns of LD-Eu/Cu2O, HD-Eu/Cu2O and Cu2O. (c) Elemental mapping images of LD-Eu/Cu2O. (d) AC-HAADF-STEM image of LD-Eu/Cu2O. (e) Elemental mapping images of HD-Eu/Cu2O. (f) AC-HAADF-STEM image of HD-Eu/Cu2O. (g) EELS diagrams for LD-Eu/Cu2O and HD-Eu/Cu2O. ©Hao Li et al.
  • Electrochemical analysis of eCO2RR process in H-type cell. (a) LSV on Cu2O, LD-Eu/Cu2O and HD-Eu/Cu2O. (b-c) FE and the product distributions of LD-Eu/Cu2O and HD-Eu/Cu2O at different current densities. (d-e) Comparison of the average FE of C2+ and CH4 products on Eu/Cu2O at different Eu doping levels. (f-g) The stability of LD-Eu/Cu2O and HD-Eu/Cu2O at the current densities of -35 and -20 mA cm−2, respectively. ©Hao Li et al.
  • Electronic state analysis for adsorption mode over pathway shifting. (a-c) PDOS for *CHO of Cu2O, LD-Eu/Cu2O and HD-Eu/Cu2O, respectively. (d-f) Crystal orbital analysis for adsorption of *CHO over Cu2O, LD-Eu/Cu2O and HD-Eu/Cu2O, respectively, where yellow and cyan area represents positive and negative phase of wavefunction. (g) Mayer bond order of C=O in *CHO with HOCO diagram. (h) Crystal orbital energy level diagrams for adsorption of *CO and *CHO over LD-Eu/Cu2O. The differential charge density diagrams are also attached, where the yellow and cyan areas represent charge accumulation and depletion, respectively. The brown, cyan, red, grey and white balls represent Cu, Eu, O, C and H, respectively. The iso-surface value for the crystal orbital and differential charge density diagrams is set to be 0.007. (i) Collection of FE values of carbon products for LD-Eu/Cu2O and HD-Eu/Cu2O and the KIE values of CH4 and C2H4 for LD-Eu/Cu2O and HD-Eu/Cu2O. ©Hao Li et al.
12/12/2025 Tohoku University
Regions: Asia, Japan
Keywords: Science, Chemistry, Energy, Physics

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