Zn-Doped Ruddlesden–Popper-Type Layered Perovskite La <sub>2</sub> Fe <sub> 1– <i>x</i> </sub> Zn <sub> <i>x</i> </sub> O <sub>4</sub> as Efficient Fuel Electrodes for Enhanced CO <sub>2</sub> –CO Mutual Conversion in Reversible Solid Oxide Cells

A reversible solid oxide cell (RSOC) enables efficient interconversion between CO and CO2, and it is recognized as a highly promising device for energy storage and conversion. To enhance the kinetics of CO2 to CO conversion, B-site Zn-doped Ruddlesden–Popper (RP)-type layered perovskite fuel electrodes, specifically La2Fe1–xZnxO4 (x = 0, 0.05, and 0.1), are fabricated and deployed as the fuel electrode. The characterization results reveal that Zn doping can significantly boost the concentration of oxygen vacancies and promote the charge transfer process. When the Zn doping amount is 0.1, the current density of the single cell with this fuel electrode is 0.73 A cm–2 at 800 °C with a voltage of 1.5 V. Furthermore, the maximum power density is 123 mW cm–2 in a 50% CO–50% CO2 atmosphere. Additionally, at 800 °C and 1.5 V, a single cell composed of the La2Fe0.9Zn0.1O4 fuel electrode demonstrates a current density of 1.41 A cm–2 for CO2 electrolysis, marking an 85.5% enhancement in performance over that of the La2FeO4 fuel electrode. Consequently, Zn doping elevates the electrocatalytic performance of RP-type layered perovskite fuel electrodes, offering a novel strategy for advancing fuel electrode material development.

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Journal
Industrial & Engineering Chemistry Research
Published
2026-01-02
DOI
https://doi.org/10.1021/acs.iecr.5c04289
Primary Topic
Advancements in Solid Oxide Fuel Cells
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article
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article

Zn-Doped Ruddlesden–Popper-Type Layered Perovskite La 2 Fe 1– x Zn x O 4 as Efficient Fuel Electrodes for Enhanced CO 2 –CO Mutual Conversion in Reversible Solid Oxide Cells

Fei Yan, Xiaofeng Tong, Ligang Wang, Tiantian Zhang et al.
Industrial & Engineering Chemistry Research
Advancements in Solid Oxide Fuel Cells
article

Zn-Doped Ruddlesden–Popper-Type Layered Perovskite La 2 Fe 1– x Zn x O 4 as Efficient Fuel Electrodes for Enhanced CO 2 –CO Mutual Conversion in Reversible Solid Oxide Cells

Fei Yan, Xiaofeng Tong, Ligang Wang, Tiantian Zhang, Kuan Li, Ping Li, Chen Li
article en

Abstract

A reversible solid oxide cell (RSOC) enables efficient interconversion between CO and CO2, and it is recognized as a highly promising device for energy storage and conversion. To enhance the kinetics of CO2 to CO conversion, B-site Zn-doped Ruddlesden–Popper (RP)-type layered perovskite fuel electrodes, specifically La2Fe1–xZnxO4 (x = 0, 0.05, and 0.1), are fabricated and deployed as the fuel electrode. The characterization results reveal that Zn doping can significantly boost the concentration of oxygen vacancies and promote the charge transfer process. When the Zn doping amount is 0.1, the current density of the single cell with this fuel electrode is 0.73 A cm–2 at 800 °C with a voltage of 1.5 V. Furthermore, the maximum power density is 123 mW cm–2 in a 50% CO–50% CO2 atmosphere. Additionally, at 800 °C and 1.5 V, a single cell composed of the La2Fe0.9Zn0.1O4 fuel electrode demonstrates a current density of 1.41 A cm–2 for CO2 electrolysis, marking an 85.5% enhancement in performance over that of the La2FeO4 fuel electrode. Consequently, Zn doping elevates the electrocatalytic performance of RP-type layered perovskite fuel electrodes, offering a novel strategy for advancing fuel electrode material development.

Industrial & Engineering Chemistry ResearchVol. 65(1)
North China Electric Power University (CN), Energy Storage Systems (United States) (US), CAS Key Laboratory of Urban Pollutant Conversion (CN)
Affordable and clean energy
Openalex Percentile: Top 99%
Advancements in Solid Oxide Fuel Cells
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Zn-Doped Ruddlesden–Popper-Type Layered Perovskite La <sub>2</sub> Fe <sub> 1– <i>x</i> </sub> Zn <sub> <i>x</i> </sub> O <sub>4</sub> as Efficient Fuel Electrodes for Enhanced CO <sub>2</sub> –CO Mutual Conversion in Reversible Solid Oxide Cells — Fei Yan, Xiaofeng Tong, et al. · Industrial & Engineering Chemistry Research (2026) | TGRS Research Map | TGRS