We study by femtosecond optical pump-probe spectroscopy the photoinduced charge transfer (CT) in the RbMnFe Prussian blue analogue. Previous studies evidenced the local nature of the photoinduced MnIII FeII → MnII FeIII process, occurring within less than 1 ps. Here we show experimentally that two photoswitching pathways exist, depending on the excitation pump wavelength, which is confirmed by band structure calculations. Photoexcitation of α spins corresponds to the Mn(d-d) band, which drives reverse Jahn-Teller distortion through the population of antibonding Mn-N orbitals, and induces CT within ≈190 fs. The process launches coherent lattice torsion during the self-trapping of the CT small-polaron. Photoexcitation of β spins drives intervalence Fe→Mn CT towards non-bonding states and results in a slower dynamic.
Keywords: charge transfer; electronic structure; photochemistry; spin crossover; time-resolved spectroscopy.
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