Dual-Doping Strategy for Lowering the Thermal Expansion Coefficient and Promoting the Catalytic Activity in Perovskite Cobaltate Air Electrodes for Solid Oxide Cells

IF 13 2区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Small Pub Date : 2024-12-17 DOI:10.1002/smll.202410672
Shuxiong Wang, Xiaoxin Zhang, Yu Chen, Fan Fan, Chang Jiang, Yongkang Xiang, Xiao Xiao, Yuan Fang, Abdullah N. Alodhayb, Jianhui Li, Jijie Huang, Yifei Sun, Zhou Chen
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Abstract

Lowering the thermal expansion coefficient (TEC) and promoting the catalytic activity of cobalt-based perovskite air electrodes is crucial for efficient solid oxide cells (SOCs) devices. However, the co-achievement of both merits has usually been largely compromised in most scenarios. Herein, a dual-doping strategy to manipulate the properties of perovskite cobaltate electrocatalyst is reported in which a high valence element of Ta5+ is incorporated into B-site to significantly suppress the dynamic reduction of Co4+ species and reduces the TEC value from PrBaCo2O5+δ (PBC, 17.8 × 10⁻6 K−1) to PrBaCo1.96Ta0.04O5+δ (PBCT, 12.5 × 10⁻6 K−1) and suppresses the oxygen loss in SOCs operation condition, revealing the improved structural stability. Meanwhile, the Ca2+ is doped into A-site of Ta-incorporated candidate, further decreasing the covalency of Co─O bonds and facilitating the formation of oxygen vacancies, benefiting the oxygen exchange kinetics and leading to a low polarization resistance of 0.026 Ω cm2 (800 °C) in as-prepared PrBa0.8Ca0.2Co1.96Ta0.04O5+δ (PBCCT) electrode. The cell with PBCTT demonstrates remarkable robustness during a 50 h thermal cycling test (25 cycles). Moreover, it delivers a high current density of 1.44 A cm⁻2 (1.6 V, 800 °C), as well as attractive durability over 100 h for pure CO2 electrolysis.

Abstract Image

降低钴基过氧化物空气电极的热膨胀系数(TEC)并提高其催化活性对于高效固体氧化物电池(SOC)设备至关重要。然而,在大多数情况下,要同时实现这两个优点通常会受到很大影响。本文报告了一种操纵包晶体钴酸盐电催化剂特性的双重掺杂策略,即在 B 位掺入高价元 Ta5+ 以显著抑制 Co4+ 物种的动态还原,并将 TEC 值从 PrBaCo2O5+δ (PBC, 17. 8 × 10-6 K-1) 降低到 17.8 × 10-6 K-1)降低到 PrBaCo1.96Ta0.04O5+δ(PBCT,12.5 × 10-6 K-1),抑制了 SOCs 运行条件下的氧损耗,显示出结构稳定性的提高。同时,Ca2+被掺杂到Ta-incorporated候选化合物的A位上,进一步降低了Co─O键的共价性,促进了氧空位的形成,有利于氧交换动力学,使制备的PrBa0.8Ca0.2Co1.96Ta0.04O5+δ(PBCCT)电极的极化电阻低至0.026 Ω cm2(800 ℃)。带有 PBCTT 的电池在 50 小时的热循环测试(25 次循环)中表现出卓越的稳健性。此外,它还能提供 1.44 A cm-2 的高电流密度(1.6 V,800 °C),以及 100 小时以上纯二氧化碳电解的耐久性。
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
Small
Small 工程技术-材料科学:综合
CiteScore
17.70
自引率
3.80%
发文量
1830
审稿时长
2.1 months
期刊介绍: Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments. With a remarkable 2022 Journal Impact Factor of 13.3 (Journal Citation Reports from Clarivate Analytics, 2023), Small remains among the top multidisciplinary journals, covering a wide range of topics at the interface of materials science, chemistry, physics, engineering, medicine, and biology. Small's readership includes biochemists, biologists, biomedical scientists, chemists, engineers, information technologists, materials scientists, physicists, and theoreticians alike.
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