ArticleProceedings of the National Academy of Sciences of the United States of America2013
Watching energy transfer in metalloporphyrin heterodimers using stimulated X-ray Raman spectroscopy.
Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Stimulated X-ray emission spectroscopy.Photosynthesis research · 2024Review
- Electrocatalytic oxidation of pyrrole on a quasi-reversible silver nanodumbbell particle surface for supramolecular porphyrin production.ChemistryOpen · 2024Article
- Efficient prediction of attosecond two-colour pulses from an X-ray free-electron laser with machine learning.Scientific reports · 2024Article
- Coupled Cluster Simulation of Impulsive Stimulated X-ray Raman Scattering.The journal of physical chemistry. A · 2023Article
- Manipulating valence and core electronic excitations of a transition-metal complex using UV/Vis and X-ray cavities.Chemical science · 2021Article
- The measurement of ultrafast electronic and structural dynamics with X-rays.Philosophical transactions. Series A, Mathematical, physical, and engineering sciences · 2019Article
- Time-, frequency-, and wavevector-resolved x-ray diffraction from single molecules.The Journal of chemical physics · 2014Article
- Understanding Excitation Energy Transfer in Metalloporphyrin Heterodimers with Different Linkers, Bonding Structures and Geometries through Stimulated X-Ray Raman Spectroscopy.Journal of modern optics · 2014Article
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
Understanding the excitation energy transfer mechanism in multiporphyrin arrays is key for designing artificial light-harvesting devices and other molecular electronics applications. Simulations of the stimulated X-ray Raman spectroscopy signals of a Zn/Ni porphyrin heterodimer induced by attosecond X-ray pulses show that these signals can directly reveal electron-hole pair motions. These dynamics are visualized by a natural orbital decomposition of the valence electron wavepackets.
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Registered trials
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