Fluorine-doped perovskite cathodes with boosted electrocatalytic activity for CO2 electrolysis

IF 5.5 3区 材料科学 Q1 ELECTROCHEMISTRY
Muhammad Nadeem Khan , Lingting Ye , Kui Xie
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Abstract

Global energy demands that have traditionally been satisfied by the use of fossil fuels have led to substantial emissions of CO2, an important greenhouse gas. Solid oxide electrolysis cells (SOECs) offer a practical approach for transforming CO2 into valuable fuels. Accordingly, creating stable electrocatalysts and perovskite cathodes capable of efficiently converting CO2 is a primary aim for the further development of SOECs. Although reconstructing active sites during CO2 electrolysis is significantly challenging, it is also constrained by our lack of understanding of this process. Herein, we introduce an innovative strategy that involves co-doping with Cu and F to better facilitate the exsolution reaction, which resulted in the formation of an advanced cathode composed of Cu-Fe alloy nanoparticles embedded in a fluorine-doped Sr2Fe1.5Mo0.5O6−δ (SFM) ceramic matrix. The in-situ electrochemical reconstruction of the SFM cathode through co-doping not only improves mass-transfer efficiency during CO2 electrolysis but also enhances the catalytic activity and durability of the ceramic cathode. A SOEC assembled with this material as a symmetrical electrode delivered 4.99 mL min−1 cm−2 of CO at 850 °C and an applied voltage of 1.8 V, which is 168 % higher than that of a pure SFM electrode. In addition, no carbon deposits were observed at the end of the reaction. The co-doping strategy delivered enhanced performance without degradation over 100 h of high-temperature operation, which suggests that it is a reliable cathode material for CO2 electrolysis. This study introduced an innovative method for improving the SOEC-electrode microstructure and developing efficient electrocatalysts for CO2 electrolysis.
提高二氧化碳电解电催化活性的掺氟过氧化物阴极
传统上通过使用化石燃料来满足全球能源需求的做法导致了重要温室气体二氧化碳的大量排放。固体氧化物电解池(SOEC)为将二氧化碳转化为有价值的燃料提供了一种实用方法。因此,创造能够高效转化二氧化碳的稳定电催化剂和过氧化物阴极是进一步开发 SOEC 的首要目标。尽管在二氧化碳电解过程中重建活性位点极具挑战性,但由于我们对这一过程缺乏了解,因此也受到了限制。在本文中,我们介绍了一种创新策略,即通过共同掺杂铜和氟来更好地促进外溶解反应,从而形成一种先进的阴极,该阴极由镶嵌在掺氟 Sr2Fe1.5Mo0.5O6-δ (SFM) 陶瓷基体中的铜铁合金纳米颗粒组成。通过共掺杂对 SFM 阴极进行原位电化学重构,不仅提高了二氧化碳电解过程中的传质效率,还增强了陶瓷阴极的催化活性和耐用性。用这种材料作为对称电极组装的 SOEC 在 850°C 和 1.8 V 的外加电压下可输出 4.99 mL min-1 cm-2 的 CO,比纯 SFM 电极高出 168%。此外,反应结束时未观察到碳沉积。这种共掺杂策略在 100 小时的高温运行过程中未出现性能退化,性能得到了提高,这表明它是一种可靠的二氧化碳电解阴极材料。这项研究为改进 SOEC 阴极微观结构和开发用于二氧化碳电解的高效电催化剂提供了一种创新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Electrochimica Acta
Electrochimica Acta 工程技术-电化学
CiteScore
11.30
自引率
6.10%
发文量
1634
审稿时长
41 days
期刊介绍: Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.
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