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Issue 21, 2010
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L-edge XANES analysis of photoexcited metal complexes in solution

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Abstract

Ultrafast X-ray absorption spectroscopy is a powerful tool to observe electronic and geometric structures of short-lived reaction intermediates. The ab initioFEFF9 code is applied to simulate the Pt L3-edge XANES spectrum of the photocatalytic diplatinum molecule [Pt2(P2O5H2)4]4− and the photo-induced changes that occur therein. The spectra are interpreted within a XAFS-like scattering theoretical framework (bound-continuum transitions) or in terms of a final-state local l-projected density of states (LDOS) (bound–bound transitions). By using a novel Bayesian fitting procedure, we show that the ground-state structures obtained independently from the XANES and EXAFS regions of the spectrum are in good agreement with each other. The semi-quantitative result obtained for the Pt–Pt contraction in the excited state is in line with recently published values. The improved theoretical treatment of inelastic losses has shown to result in more accurate peak positions in the above-continuum region of the spectrum which is an important prerequisite for obtaining quantitative structural information from (time-resolved) XANES spectra.

Graphical abstract: L-edge XANES analysis of photoexcited metal complexes in solution

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Article information


Submitted
22 Dec 2009
Accepted
17 Feb 2010
First published
17 Mar 2010

Phys. Chem. Chem. Phys., 2010,12, 5551-5561
Article type
Paper

L-edge XANES analysis of photoexcited metal complexes in solution

R. M. van der Veen, J. J. Kas, C. J. Milne, V. Pham, A. E. Nahhas, F. A. Lima, D. A. Vithanage, J. J. Rehr, R. Abela and M. Chergui, Phys. Chem. Chem. Phys., 2010, 12, 5551
DOI: 10.1039/B927033G

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