Understanding 2p core-level excitons of late transition metals by analysis of mixed-valence copper in a metal-organic framework.
Han WangGregory M SuBrandon R BarnettWalter S DrisdellJeffrey R LongDavid PrendergastPublished in: Physical chemistry chemical physics : PCCP (2024)
The L 2,3 -edge X-ray absorption spectra of late transition metals such as Cu, Ag, and Au exhibit absorption onsets lower in energy for higher oxidation states, which is at odds with the measured spectra of earlier transition metals. Time-dependent density functional theory calculations for Cu 2+ /Cu + reveal a larger 2p core-exciton binding energy for Cu 2+ , overshadowing shifts in single-particle excitation energies with respect to Cu + . We explore this phenomenon in a Cu + metal-organic framework with ∼12% Cu 2+ defects and find that corrections with self-consistent excited-state total energy differences provide accurate XAS peak alignment.
Keyphrases
- metal organic framework
- density functional theory
- molecular dynamics
- aqueous solution
- high resolution
- health risk
- health risk assessment
- magnetic resonance
- transcription factor
- molecular dynamics simulations
- mass spectrometry
- single cell
- gold nanoparticles
- sensitive detection
- hydrogen peroxide
- heavy metals
- highly efficient
- reduced graphene oxide
- oxide nanoparticles
- electron microscopy