钴
X射线光电子能谱
氧气
催化作用
吸收光谱法
化学
光化学
酞菁
吸收(声学)
光谱学
氢
X射线吸收光谱法
原位
无机化学
分析化学(期刊)
材料科学
核磁共振
有机化学
光学
物理
复合材料
量子力学
作者
Piter S. Miedema,Matti M. van Schooneveld,René Bogerd,Túlio C. R. Rocha,Michael Hävecker,Axel Knop‐Gericke,Frank M. F. de Groot
摘要
Cobalt phthalocyanine (CoPc) and iron phthalocyanine (FePc) are possible oxygen reduction catalysts in fuel cells, but the exact functioning and deactivation of these catalysts is unknown. The electronic structure of the CoPc and FePc has been studied in situ under hydrogen and oxygen atmospheres by a combination of ambient-pressure X-ray photoelectron spectroscopy and X-ray absorption spectroscopy. The results show that when oxygen is introduced, the iron changes oxidation state while the cobalt does not. The data show that oxygen binds in an end-on configuration in CoPc, while for FePc side-on binding is most likely.
科研通智能强力驱动
Strongly Powered by AbleSci AI