framework CPO-27-Ni by coupling resonant inelastic X-ray scattering (RIXS) and UV−vis spectroscopy, and we show that the element selectivity of RIXS is crucial to observing the full dd multiplet structure, which is not visible in UV−vis. The combination of calculations using crystal-field multiplet theory and density functional theory can reproduce the RIXS spectral features, crucially improving interpretation of the experimental data. We obtain the crystal-field splitting and magnitude of the electron−electron interactions and correct previously reported values. RIXS instruments at synchrotron radiation sources are accessible to all researchers, and the technique can be applied to a broad range of systems.

dd Excitations in CPO-27-Ni Metal–Organic Framework: Comparison between Resonant Inelastic X-ray Scattering and UV–vis Spectroscopy

Gallo, Erik;LAMBERTI, Carlo;
2013-01-01

Abstract

framework CPO-27-Ni by coupling resonant inelastic X-ray scattering (RIXS) and UV−vis spectroscopy, and we show that the element selectivity of RIXS is crucial to observing the full dd multiplet structure, which is not visible in UV−vis. The combination of calculations using crystal-field multiplet theory and density functional theory can reproduce the RIXS spectral features, crucially improving interpretation of the experimental data. We obtain the crystal-field splitting and magnitude of the electron−electron interactions and correct previously reported values. RIXS instruments at synchrotron radiation sources are accessible to all researchers, and the technique can be applied to a broad range of systems.
2013
52
10
5633
5635
http://pubs.acs.org/doi/abs/10.1021/ic400350w
CPO-27-Ni; Resonant Inelastic X-ray Scattering; RIXS; MOF; metallorganic framework; d-d transitions; UV−vis spectroscopy; multiplet theory; Ni2+; Tanabe−Sugano diagram; DFT calculations; crystal-field splitting
Erik Gallo; Carlo Lamberti; Pieter Glatzel
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/138533
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