Stoupin Stanislav, Chung Eun-Hyuk, Chattopadhyay Soma, Segre Carlo U, Smotkin Eugene S
Physics Division, Department of Biological, Chemical, and Physical Sciences, Illinois Institute of Technology, Chicago, 60616, USA.
J Phys Chem B. 2006 May 25;110(20):9932-8. doi: 10.1021/jp057047x.
In situ X-ray absorption spectroscopy, ex situ X-ray fluorescence, and X-ray powder diffraction enabled detailed core analysis of phase segregated nanostructured PtRu anode catalysts in an operating direct methanol fuel cell (DMFC). No change in the core structures of the phase segregated catalyst was observed as the potential traversed the current onset potential of the DMFC. The methodology was exemplified using a Johnson Matthey unsupported PtRu (1:1) anode catalyst incorporated into a DMFC membrane electrode assembly. During DMFC operation the catalyst is essentially metallic with half of the Ru incorporated into a face-centered cubic (FCC) Pt alloy lattice and the remaining half in an amorphous phase. The extended X-ray absorption fine structure (EXAFS) analysis suggests that the FCC lattice is not fully disordered. The EXAFS indicates that the Ru-O bond lengths were significantly shorter than those reported for Ru-O of ruthenium oxides, suggesting that the phases in which the Ru resides in the catalysts are not similar to oxides.
原位X射线吸收光谱、非原位X射线荧光和X射线粉末衍射技术,能够对运行中的直接甲醇燃料电池(DMFC)内相分离的纳米结构铂钌阳极催化剂进行详细的核心分析。当电位穿过DMFC的电流起始电位时,未观察到相分离催化剂的核心结构发生变化。该方法以一种纳入DMFC膜电极组件的庄信万丰无载体铂钌(1:1)阳极催化剂为例进行了说明。在DMFC运行期间,催化剂基本上呈金属态,其中一半的钌掺入面心立方(FCC)铂合金晶格,其余一半处于非晶相。扩展X射线吸收精细结构(EXAFS)分析表明,FCC晶格并未完全无序。EXAFS表明,钌 - 氧键长明显短于报道的氧化钌中钌 - 氧键长,这表明催化剂中钌所在的相与氧化物不同。