Blinn Kevin S, Li Xiaxi, Liu Mingfei, Bottomley Lawrence A, Liu Meilin
Center for Innovative Fuel Cells and Battery Technologies, School of Materials Science and Engineering, Georgia Institute of Technology, GA, USA.
J Vis Exp. 2012 Sep 20(67):e50161. doi: 10.3791/50161.
Solid oxide fuel cells (SOFCs) are potentially the most efficient and cost-effective solution to utilization of a wide variety of fuels beyond hydrogen (1-7). The performance of SOFCs and the rates of many chemical and energy transformation processes in energy storage and conversion devices in general are limited primarily by charge and mass transfer along electrode surfaces and across interfaces. Unfortunately, the mechanistic understanding of these processes is still lacking, due largely to the difficulty of characterizing these processes under in situ conditions. This knowledge gap is a chief obstacle to SOFC commercialization. The development of tools for probing and mapping surface chemistries relevant to electrode reactions is vital to unraveling the mechanisms of surface processes and to achieving rational design of new electrode materials for more efficient energy storage and conversion(2). Among the relatively few in situ surface analysis methods, Raman spectroscopy can be performed even with high temperatures and harsh atmospheres, making it ideal for characterizing chemical processes relevant to SOFC anode performance and degradation(8-12). It can also be used alongside electrochemical measurements, potentially allowing direct correlation of electrochemistry to surface chemistry in an operating cell. Proper in situ Raman mapping measurements would be useful for pin-pointing important anode reaction mechanisms because of its sensitivity to the relevant species, including anode performance degradation through carbon deposition(8, 10, 13, 14) ("coking") and sulfur poisoning(11, 15) and the manner in which surface modifications stave off this degradation(16). The current work demonstrates significant progress towards this capability. In addition, the family of scanning probe microscopy (SPM) techniques provides a special approach to interrogate the electrode surface with nanoscale resolution. Besides the surface topography that is routinely collected by AFM and STM, other properties such as local electronic states, ion diffusion coefficient and surface potential can also be investigated(17-22). In this work, electrochemical measurements, Raman spectroscopy, and SPM were used in conjunction with a novel test electrode platform that consists of a Ni mesh electrode embedded in an yttria-stabilized zirconia (YSZ) electrolyte. Cell performance testing and impedance spectroscopy under fuel containing H2S was characterized, and Raman mapping was used to further elucidate the nature of sulfur poisoning. In situ Raman monitoring was used to investigate coking behavior. Finally, atomic force microscopy (AFM) and electrostatic force microscopy (EFM) were used to further visualize carbon deposition on the nanoscale. From this research, we desire to produce a more complete picture of the SOFC anode.
固体氧化物燃料电池(SOFCs)可能是利用除氢气之外的多种燃料的最有效且最具成本效益的解决方案(1 - 7)。一般来说,SOFCs的性能以及能量存储和转换装置中许多化学和能量转换过程的速率主要受沿电极表面和跨界面的电荷及质量传递限制。不幸的是,由于在原位条件下表征这些过程存在困难,目前对这些过程的机理理解仍然不足。这一知识空白是SOFC商业化的主要障碍。开发用于探测和绘制与电极反应相关的表面化学的工具,对于揭示表面过程的机制以及实现合理设计用于更高效能量存储和转换的新型电极材料至关重要(2)。在相对较少的原位表面分析方法中,拉曼光谱即使在高温和恶劣气氛下也能进行,这使其成为表征与SOFC阳极性能和降解相关的化学过程的理想选择(8 - 12)。它还可以与电化学测量一起使用,有可能在运行的电池中直接将电化学与表面化学关联起来。适当的原位拉曼映射测量对于确定重要的阳极反应机制很有用,因为它对相关物种敏感,包括通过碳沉积(8, 10, 13, 14)(“结焦”)和硫中毒(11, 15)导致的阳极性能下降,以及表面改性防止这种降解的方式(16)。当前的工作在这方面取得了重大进展。此外,扫描探针显微镜(SPM)技术家族提供了一种以纳米级分辨率探测电极表面的特殊方法。除了通过原子力显微镜(AFM)和扫描隧道显微镜(STM)常规收集的表面形貌外,还可以研究其他性质,如局部电子态、离子扩散系数和表面电位(17 - 22)。在这项工作中,电化学测量、拉曼光谱和SPM与一种新型测试电极平台结合使用,该平台由嵌入氧化钇稳定氧化锆(YSZ)电解质中的镍网电极组成。对含H2S燃料下的电池性能测试和阻抗谱进行了表征,并使用拉曼映射进一步阐明硫中毒的本质。原位拉曼监测用于研究结焦行为。最后,使用原子力显微镜(AFM)和静电力显微镜(EFM)进一步在纳米尺度上可视化碳沉积。通过这项研究,我们希望更全面地了解SOFC阳极。