Momentum-resolved non-resonant inelastic x-ray scattering study of C60
For large molecular systems such as C60, accurate ab initio calculations remain challenging, making experimental methods a more reliable alternative. In this work, we employed the non-resonant inelastic x-ray scattering technique to study the electronic excitation dynamics of C60. The measurements spanned a momentum transfer range of 0.63–5.10 a.u. at a photon energy of ∼10 keV with an energy resolution around 1.0 eV. The dynamic structure factors in the excitation energy range of 5–500 eV and the generalized oscillator strengths for the core excitations of π*←1s were determined on absolute scales. A new feature at ∼24 eV was identified. In addition, the optical oscillator strengths were obtained by extrapolating the generalized oscillator strengths to zero momentum transfer, which show good agreement with the earlier x-ray absorption results. These findings demonstrate that the non-resonant inelastic x-ray scattering is a powerful technique for probing the electronic excitation process and extracting the corresponding dynamic parameters in complex molecular systems.
Authors
- Shuoxue Jin (ORCID: https://orcid.org/0000-0002-7195-6259)
- Lin‐Fan Zhu (ORCID: https://orcid.org/0000-0002-5771-0471)
- Zhiying Guo (ORCID: https://orcid.org/0000-0001-5904-3409)
- Jin-Feng Chen (ORCID: https://orcid.org/0009-0000-4637-5121)
- Tao Xiong (ORCID: https://orcid.org/0000-0002-9484-4903)
- Yujun Zhang (ORCID: https://orcid.org/0000-0003-4892-1100)
- Qingwen Gu
- Wei Xu (ORCID: https://orcid.org/0000-0003-1950-9037)
- Rui-Qi Tang
Institutions
- University of Science and Technology of China (CN)
- Chinese Academy of Sciences (CN)
- China Spallation Neutron Source (CN)
- Institute of High Energy Physics (AT)
- Institute of High Energy Physics (CN)
Publication Details
- Journal
- The Journal of Chemical Physics
- Published
- 2026-10-01
- DOI
- https://doi.org/10.1063/5.0353785
- Primary Topic
- Fullerene Chemistry and Applications
- Type
- article
- Field-Weighted Citation Impact
- 0.00