1. In situ Raman studies on Mo-based mixed oxides during the partial oxidation of propene - an attempt to bridge the “materials gap” - Pablo Beato, Annette Trunschke, Robert Schlögl Department of Inorganic Chemistry, Fritz Haber Institute of the MPG, Faradayweg 4-6; DE - 14195 Berlin, Germany, http://www.fhi-berlin.mpg.de Introduction combination of surface sensitive and bulk sensitive methods prepare adequate models The partial oxidation of light alka(e)nes e.g. propa(e)ne to higher valuable chemicals e.g. acrolein and/or acrylic acid is technically performed over multi metal oxides (MMO). Although much effort has been made to understand the working mechanism of MMO’s, the complexity of such systems has prevented up to now unequivocal proofs for the existing theories. It is obvious that in situ analytical methods are indispensable to get such proofs. The main problem is that most of the research on MMO’s has only been conducted via bulk analytical techniques (XRD, EXAFS, IR, Raman, etc.) because charging effects and surface roughness of real powder catalysts make the reliable analysis by surface science methods impossible. However, a combination of surface sensitive and bulk sensitive methods are necessary to fully characterize and understand such complex systems. Our ultimate goal is therefore to prepare adequate models ranging from pure molybdenum oxides to complex mixed metal oxides which should preserve as much as possible of the chemical and structural complexity of real catalysts but at the same time stay accessible to both surface science and bulk analytic techniques. A promising strategy to meet these requirements is to deposit a thin film or nanoparticles of the metal oxide on an inert, conducting substrate, such as silicon. Our preliminary results are presented here. Mo-V-W-oxide Si/SiO 2 before after Si TTTT TTTT precursor-synthesis fundamentalunderstanding powder thin film catalysiscatalyst catalyst in situ bulk-analytics surface-analyticssynthesissynthesisreaction sol-gel,precipitation spin coating gas in gas out to PTR-MS cover plate middle plate base plate side view Laser (623 nm) confocal hole slit grating ccd Notch filter 10 mm heater sticks (up to ~800°C) thin film Si[100] powder pellet Ø = 5 mm (5-15 mg) Si[100] Mo: 68%, V: 23%, W: 9% (xrf of powder) (NH 4 ) 6 (Mo 7 O 24 ), V 2 O 5 /oxalic ac., (NH 4 ) 6 (W 12 O 41 ) (NH 4 ) 6 (Mo 7 O 24 ), V 2 O 5 /oxalic ac., (NH 4 ) 6 (W 12 O 41 ) in H 2 O spray drying thin film powder powder + gelatin gel model catalyst catalyst spin-coating 350°C/air 300°C/air Sumary & Conclusions & Outlook We believe that the concept to develop complex model systems as thin films in order to mimic real mixed oxide catalysts is promising. The prepared Mo 0.68 V 0.23 W 0.09 Ox thin film was able to directly convert propene to acrylic acid and was further activated during time on stream. This enables us to study such complex reactions on flat conducting catalysts by surface sensitive methods as could be in situ XPS. The presented micro-reactor can give valuable information on the reaction kinetics and at the same time offers the possibility to apply different types of optical in situ spectroscopies. The combination of in situ Raman spectroscopy and ex situ HRTEM gave a detailed view of the structural dynamics occurring during reaction. The possibility to directly compare thin film data and powder data has the great advantage to obtain information about bulk and surface structure under the same conditions. The observed structural changes during reaction clearly indicate, that the active phase of the investigated Mo 0.68 V 0.23 W 0.09 Ox catalysts is actually a very dynamic one and not to describe as a stiff crystal structure. For the catalyst to be active in the selective oxidation of propene there seems to be no need for a crystalline Mo 5 O 14 -type structure since the presence of small clusters containing the main structural motifs is sufficient. However, activity and selectivity seem to be enhanced when an ordered “superstructure” is present. More information about the composition of the catalytically active surface species will hopefully be gained in the near future by using the presented model for in situ XPS investigations. after before time at 298 K - after reaction Ref. Mo 5 O 14 at 673 K A. Müller et al., Current Opinion in Solid State and Materials Science 4 (1999) 141-153 after before