Correlation between the O 2p Orbital and Redox Reaction in LiMn_0.6Fe_0.4PO₄ Nanowires Studied by Soft X-ray Absorption

The changes in the electronic structure of LiMn_0.6Fe_0.4PO₄ nanowires during discharge processes were investigated by using ex situ soft X-ray absorption spectroscopy. The Fe L-edge X-ray absorption spectrum attributes the potential plateau at 3.45 V versus Li/Li⁺ of the discharge curve to a reduction of Fe³⁺ to Fe²⁺. The Mn L-edge X-ray absorption spectra exhibit the Mn²⁺ multiplet structure throughout the discharge process, and the crystal-field splitting was slightly enhanced upon full discharge. The configuration-interaction full-multiplet calculation for the X-ray absorption spectra reveals that the charge-transfer effect from O 2p to Mn 3d orbitals should be considerably small, unlike that from the O 2p to Fe 3d orbitals. Instead, the O K-edge X-ray absorption spectrum shows a clear spectral change during the discharge process, suggesting that the hybridization of O 2p orbitals with Fe 3d orbitals contributes essentially to the reduction.