Observation of Transient Iron(II) Formation in Dye-Sensitized Iron Oxide Nanoparticles by Time-Resolved X-ray Spectroscopy

• Published in: The journal of physical chemistry letters Vol. 1; no. 9; pp. 1372 - 1376
• Main Authors: Katz, Jordan E., Gilbert, Benjamin, Zhang, Xiaoyi, Attenkofer, Klaus, Falcone, Roger W., Waychunas, Glenn A.
• Format: Journal Article
• Language: English
• Published: American Chemical Society 06-05-2010
• Subjects: Nanops and Nanostructures
• ISSN: 1948-7185; 1948-7185
• DOI: 10.1021/jz100296r

The reduction of ferric iron in solid phase minerals leads to the mobilization of ferrous iron in the environment and is thus a crucial component of the global iron cycle. Despite the importance of this process, a mechanistic understanding of the structural and chemical changes that are caused by this electron transfer reaction is not established because the speed of the fundamental chemical steps renders them inaccessible to conventional study. Ultrafast time-resolved X-ray spectroscopy is a technique that can overcome this limitation and measure changes in oxidation state and structure occurring during chemical reactions that can be initiated by a fast laser pulse. We use this approach with ∼100 ps resolution to monitor the speciation of Fe atoms in iron oxide nanoparticles following photoinduced electron transfer from a surface-bound photoactive dye molecule. These data represent the first direct real-time observation of the dynamics of ferrous ion formation and subsequent reoxidation in iron oxide.