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  Pump-flow-probe X-ray absorption spectroscopy as a tool for studying intermediate states of photocatalytic systems.

Smolentsev, G., Guda, A., Zhang, X., Haldrup, K., Andreiadis, E. S., Chayarot-Kerlidou, M., et al. (2013). Pump-flow-probe X-ray absorption spectroscopy as a tool for studying intermediate states of photocatalytic systems. Journal of Physical Chemistry C, 117(34), 17367-17375. doi:10.1021/jp4010554.

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Smolentsev, G., Author
Guda, A., Author
Zhang, X., Author
Haldrup, K., Author
Andreiadis, E. S., Author
Chayarot-Kerlidou, M., Author
Canton, S. E.1, Author           
Nachtegaal, M., Author
Artero, V., Author
Sundstrom, V., Author
Affiliations:
1Research Group of Structural Dynamics of (Bio)Chemical Systems, MPI for Biophysical Chemistry, Max Planck Society, ou_578564              

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 Abstract: A new setup for pump-flow-probe X-ray absorption spectroscopy has been implemented at the SuperXAS beamline of the Swiss Light Source. It allows recording X-ray absorption spectra with a time resolution of tens of microseconds and high detection efficiency for samples with sub-millimolar concentrations. A continuous wave laser is used for the photoexcitation, with the distance between laser and X-ray beams and velocity of liquid flow determining the time delay, while the focusing of both beams and the flow speed profile define the time resolution. This method is compared with the alternative measurement technique that utilizes a 1 kHz repetition rate laser and multiple X-ray probe pulses. Such an experiment was performed at beamline 11ID-D of the Advanced Photon Source. Advantages, limitations, and potential for improvement of the pump-flow-probe setup are discussed by analyzing the photon statistics. Both methods with Co K-edge probing were applied to the investigation of a cobaloxime-based photocatalytic reaction. The interplay between optimizing for efficient photoexcitation and time resolution as well and the effect of sample degradation for these two setups are discussed.

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Language(s): eng - English
 Dates: 2013-07-292013-08-29
 Publication Status: Issued
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 Rev. Type: Peer
 Identifiers: DOI: 10.1021/jp4010554
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Title: Journal of Physical Chemistry C
Source Genre: Journal
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Pages: - Volume / Issue: 117 (34) Sequence Number: - Start / End Page: 17367 - 17375 Identifier: -