Higashi Kotaro, Takao Shinobu, Samjeské Gabor, Matsui Hirosuke, Tada Mizuki, Uruga Tomoya, Iwasawa Yasuhiro
Innovation Research Center for Fuel Cells, The University of Electro-Communications, Chofu, Tokyo 182-8585, Japan.
Phys Chem Chem Phys. 2020 Sep 14;22(34):18919-18931. doi: 10.1039/d0cp01356k. Epub 2020 Jun 16.
We developed a multi-analysis system that can measure in situ time-resolved quick XAFS (QXAFS) and in situ three-dimensional XAFS-CT spatial imaging in the same area of a cathode electrocatalyst layer in a membrane-electrode assembly (MEA) of a polymer electrolyte fuel cell (PEFC) at the BL36XU beamline of SPring-8. The multi-analysis system also achieves ex situ two-dimensional nano-XAFS/STEM-EDS same-view measurements of a sliced MEA fabricated from a given place in the XAFS-CT imaged area at high spatial resolutions under a water-vapor saturated N atmosphere using a same-view SiN membrane cell. In this study, we applied the combination method of time-resolved QXAFS/3D XAFS-CT/2D nano-XAFS/STEM-EDS for the first time for the visualization analysis of the anode-gas exchange (AGEX) (simulation of the start-up/shut-down of PEFC vehicles) degradation process of a PEFC MEA Pt/C cathode. The AGEX cycles bring about serious irreversible degradation of both Pt nanoparticles and carbon support due to a spike-like large voltage increase. We could visualize the three-dimensional distribution and two-dimensional depth map of the amount, oxidation state (valence), Pt elution, detachment, and aggregation of Pt species and the formation of carbon voids, where the change and movement of the Pt species in the cathode catalyst layer during the AGEX cycles did not proceed exceeding the 1 μm region. It is very different from the case of an ADT (an accelerated durability test between 0.6-1.0 V)-degraded MEA. We discuss the spatiotemporal behavior of the AGEX degradation process and the degradation mechanism.
我们开发了一种多分析系统,该系统能够在位于SPring-8的BL36XU光束线上的聚合物电解质燃料电池(PEFC)的膜电极组件(MEA)的阴极电催化剂层的同一区域,原位测量时间分辨快速X射线吸收精细结构(QXAFS)以及进行原位三维X射线吸收精细结构-计算机断层扫描(XAFS-CT)空间成像。该多分析系统还能在水蒸气饱和的氮气气氛下,使用同视图氮化硅膜电池,对从XAFS-CT成像区域中给定位置制备的切片MEA进行高空间分辨率的非原位二维纳米XAFS/扫描透射电子显微镜-能谱仪(STEM-EDS)同视图测量。在本研究中,我们首次将时间分辨QXAFS/三维XAFS-CT/二维纳米XAFS/STEM-EDS的组合方法应用于PEFC MEA铂/碳(Pt/C)阴极的阳极气体交换(AGEX)(模拟PEFC车辆的启动/关闭)降解过程的可视化分析。AGEX循环由于尖峰状的大幅电压升高,导致铂纳米颗粒和碳载体都发生严重的不可逆降解。我们能够可视化铂物种的数量、氧化态(化合价)、铂的洗脱、脱离和聚集以及碳空洞形成的三维分布和二维深度图,其中在AGEX循环期间阴极催化剂层中铂物种的变化和移动未超过1μm区域。这与加速耐久性测试(ADT,在0.6 - 1.0V之间)降解的MEA情况有很大不同。我们讨论了AGEX降解过程的时空行为及其降解机制。