Publication | Open Access
Probing Transient Photoinduced Charge Transfer in Prussian Blue Analogues with Time‐Resolved XANES and Optical Spectroscopy
26
Citations
63
References
2017
Year
Magnetic PropertiesOptical MaterialsEngineeringTime‐resolved XanesMagnetic ResonanceChemistryMagnetic MaterialsMagnetismHigh SpinPrussian Blue AnaloguesOptical SpectroscopyPhotophysical PropertyMaterials ScienceRbmnfe Powder SamplePhotochemistryPhysicsNanotechnologyPhysical ChemistryQuantum ChemistryMagnetic MaterialSolid-state PhysicNanophysicsFerromagnetismNanomaterialsNatural SciencesSpectroscopyApplied PhysicsCondensed Matter PhysicsThermal Equilibrium
We studied the transient electron‐transfer process in CsCoFe and RbMnFe Prussian Blue analogues by time‐resolved X‐ray absorption near‐edge structure (XANES) and by time‐resolved optical spectroscopy. We performed time‐resolved studies on CsCoFe nanocrystals dispersed in solution. The XANES results obtained at room temperature clearly evidence Co III (low spin)Fe II →Co II (high spin)Fe III electron transfer between the metal centers through opposite spectral shifts at the Fe and Co edges. We also studied the Mn III (low spin)Fe II →Mn II (high spin)Fe III process in an RbMnFe powder sample at thermal equilibrium and under laser excitation. Optical spectroscopy revealed that the process occurs on the picosecond timescale, as already reported by Raman spectroscopy, and that the lifetime of the photoinduced charge‐transfer states is in the 1–10 µs range, depending on the sample and temperature.
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