Fluorine-Stabilized BO6 Octahedron of Host Perovskites for Robust Carbon Dioxide Electrolysis on Exsolved Catalysts

电解 钙钛矿(结构) 材料科学 催化作用 电催化剂 氧化物 析氧 无机化学 八面体 化学工程 化学 物理化学 晶体结构 电化学 电极 结晶学 电解质 冶金 生物化学 工程类
作者
Bowen Zhang,Mengnan Zhu,Min‐Rui Gao,Xiaoyu Liu,Jing Shen,Xiuan Xi,Nanqi Duan,Natalia Semagina,Hongbo Zeng,Jing‐Li Luo
出处
期刊:ACS Catalysis [American Chemical Society]
卷期号:13 (20): 13333-13343 被引量:17
标识
DOI:10.1021/acscatal.3c01897
摘要

Exsolution of nanoparticles has become a prevalent technique for enhancing the catalytic activity of perovskites for carbon dioxide (CO2) electrolysis in solid oxide electrolysis cells. However, the potential negative impact of phase evolution of the host perovskite on catalytic performance is often overlooked in light of the overall performance enhancement from exsolution. Herein, we illustrate a facile fluorine doping strategy to suppress the phase transition of Sr2Fe1.2Ni0.3Mo0.5O6–δ (SFN3M) during exsolution. The experimental characterizations combined with density functional theory calculations reveal that the incorporation of fluorine into the SFN3M lattice is beneficial for preserving the high oxidation states of B-site cations and inhibiting the lattice oxygen loss, resulting in a robust BO6 octahedron in the host perovskite. It is found that the well-preserved double perovskite structure exhibits a stronger interaction with CO2, thus enhancing the catalytic activity of F-doped exsolved SFN3M (F-SFN3M-red). Furthermore, the robust BO6 octahedron of the host perovskite significantly enhances the resistance of F-SFN3M-red to decomposition under high-voltage CO2 electrolysis, leading to the significantly increased carbon monoxide productivity over a broad voltage range. These findings highlight that the F doping strategy has great potential to aid the development of exsolved perovskites with high catalytic activity and stability for a wider range of electrocatalysis applications.
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