Ru-Ce0.7Zr0.3O2-δ 作为固体氧化物燃料电池中二甲醚内部转化的阳极催化剂

Nanomaterials Pub Date : 2024-03-28 DOI:10.3390/nano14070603
Miguel Morales, M. Rezayat, S. García-González, Antonio Mateo, E. Jiménez-Piqué
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摘要

直接二甲醚(DME)固体氧化物燃料电池(SOFC)的开发存在一些缺陷,原因是传统的镍锆基阳极催化活性低且存在碳沉积。在本研究中,插入 2.0 wt.%的 Ru-Ce0.7Zr0.3O2-δ(钌锆掺杂铈,Ru-CZO)作为阳极催化剂层(ACL)被认为是一种很有前景的解决方案。为此,采用溶胶-凝胶合成法制备了 CZO 粉末,然后通过浸渍法和煅烧法合成了纳米 Ru(1.0-2.0 wt.%)。催化剂粉末采用 BET 比表面积、X 射线衍射(XRD)、场发射扫描电子显微镜与能量色散光谱探测器(FESEM-EDS)和透射电子显微镜(TEM)技术进行表征。随后,利用二甲醚部分氧化法研究了 Ru-CZO 催化剂的催化活性。最后,通过将 Ru-CZO 沉积到阳极支架上并使用退火工艺,制备了带有 Ru-CZO ACL 的按钮式阳极支撑 SOFC。在 750 °C 的二甲醚和空气混合物条件下,研究了 ACL 对电池电化学性能的影响。结果表明,Ru 在 CZO 固溶体中的分散度很高,在 750 ℃ 下可实现二甲醚的完全转化,并产生大量的 H2 和 CO。因此,2.0 wt.% Ru-CZO ACL 在 750 ℃ 时可将电池性能提高 20% 以上。对含有 ACL 的电池进行的测试后分析表明,与参考电池相比,Ru-CZO ACL 具有显著的抗碳沉积能力,这证明了 Ru-CZO 作为催化剂和 ACL 在直接二甲醚 SOFC 中的潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ru-Ce0.7Zr0.3O2−δ as an Anode Catalyst for the Internal Reforming of Dimethyl Ether in Solid Oxide Fuel Cells
The development of direct dimethyl ether (DME) solid oxide fuel cells (SOFCs) has several drawbacks, due to the low catalytic activity and carbon deposition of conventional Ni–zirconia-based anodes. In the present study, the insertion of 2.0 wt.% Ru-Ce0.7Zr0.3O2−δ (ruthenium–zirconium-doped ceria, Ru-CZO) as an anode catalyst layer (ACL) is proposed to be a promising solution. For this purpose, the CZO powder was prepared by the sol–gel synthesis method, and subsequently, nanoparticles of Ru (1.0–2.0 wt.%) were synthesized by the impregnation method and calcination. The catalyst powder was characterized by BET-specific surface area, X-ray diffraction (XRD), field emission scanning electron microscopy with an energy-dispersive spectroscopy detector (FESEM-EDS), and transmission electron microscopy (TEM) techniques. Afterward, the catalytic activity of Ru-CZO catalyst was studied using DME partial oxidation. Finally, button anode-supported SOFCs with Ru-CZO ACL were prepared, depositing Ru-CZO onto the anode support and using an annealing process. The effect of ACL on the electrochemical performance of cells was investigated under a DME and air mixture at 750 °C. The results showed a high dispersion of Ru in the CZO solid solution, which provided a complete DME conversion and high yields of H2 and CO at 750 °C. As a result, 2.0 wt.% Ru-CZO ACL enhanced the cell performance by more than 20% at 750 °C. The post-test analysis of cells with ACL proved a remarkable resistance of Ru-CZO ACL to carbon deposition compared to the reference cell, evidencing the potential application of Ru-CZO as a catalyst as well as an ACL for direct DME SOFCs.
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