On possible multiple occurrences of the breakdown of the dipole and dipole-quadrupole approximations in angle-differential spectra of fullerene anions, C$_{n}^{-}$
V K Dolmatov, A Edwards, C G Lane

TL;DR
This study investigates the limitations of dipole and dipole-quadrupole approximations in describing the angle-differential photodetachment spectra of fullerene anions, revealing breakdowns at relatively low photon energies and increasing with fullerene size.
Contribution
It introduces a model-based analysis showing the potential failure of common approximations in fullerene anions' spectra at certain energies, highlighting the need for more advanced theories.
Findings
Breakdowns occur at photon energies of a few tens of eV.
Breakdowns start at lower energies for larger fullerenes.
Frequency of breakdowns increases with fullerene size.
Abstract
We provide the initial insight into the angle-differential photodetachment spectra of fullerene anions beyond the dipole approximation by utilizing a broadly used modelling of C. In the model, the C cage is approximated by a spherical attractive potential of a certain inner radius, thickness and depth which binds an external electron, thereby turning into a C anion. It is demonstrated in the framework of the utilized model, which a single-electron model in its essence, that the dipole and dipole-quadrupole approximations might get broken down in the angle-differential photodetachment spectra of fullerene anions, C, at a great number of photon energies of only a few tens of eV. Moreover, the breakdown occurrences are shown to start developing at lower photon energies, and the frequency of the occurrences grows with increasing size of C. The…
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Taxonomy
TopicsFullerene Chemistry and Applications · Atomic and Molecular Physics · Advanced Chemical Physics Studies
