Ultrafast electron diffractive imaging of the dissociation of pre-excited molecules
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| Main Authors: | , , , , , , |
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| Format: | Preprint |
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2025
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| _version_ | 1866911390098259968 |
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| author | Xiong, Yanwei Zhao, Haoran Muvva, Sri Bhavya Le, Cuong Heald, Lauren F. Lederer, Jackson Centurion, Martin |
| author_facet | Xiong, Yanwei Zhao, Haoran Muvva, Sri Bhavya Le, Cuong Heald, Lauren F. Lederer, Jackson Centurion, Martin |
| contents | Gas phase ultrafast electron diffraction (GUED) has become a powerful technique to directly observe the structural dynamics of photoexcited molecules. GUED reveals information about the nuclear motions that is complementary to the information on the electronic states provided by spectroscopic measurements. GUED experiments so far have utilized a single laser pulse to excite the molecules and an electron pulse to probe the dynamics. This limits the excited states which can be studied to only those that can be reached by absorption of a photon from the ground state or in some cases simultaneous absorption of multiple photons. A broader class of experiments and dynamics can be accessed using two time-delayed laser pulses to access unexplored regions of the potential energy surfaces. As a proof-of-principle experiment using a double excitation, we studied the photodissociation of trifluoroiodomethane molecules that are pre-excited with an infrared (800 nm) femtosecond laser pulse before photo-dissociation is triggered with an ultraviolet (266 nm) femtosecond laser pulse. We have observed significant differences in the dissociation dynamics, with pre-excitation resulting in a slower dissociation process. This new capability can offer new insights on the evolution of nuclear wavepackets in regions of the excited potential energy surface which are inaccessible in single photon excitation. We present a methodology to carry out the measurement, analyze and interpret the data that could be applied to a broad class of experiments. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2511_13479 |
| institution | arXiv |
| publishDate | 2025 |
| record_format | arxiv |
| spellingShingle | Ultrafast electron diffractive imaging of the dissociation of pre-excited molecules Xiong, Yanwei Zhao, Haoran Muvva, Sri Bhavya Le, Cuong Heald, Lauren F. Lederer, Jackson Centurion, Martin Chemical Physics Gas phase ultrafast electron diffraction (GUED) has become a powerful technique to directly observe the structural dynamics of photoexcited molecules. GUED reveals information about the nuclear motions that is complementary to the information on the electronic states provided by spectroscopic measurements. GUED experiments so far have utilized a single laser pulse to excite the molecules and an electron pulse to probe the dynamics. This limits the excited states which can be studied to only those that can be reached by absorption of a photon from the ground state or in some cases simultaneous absorption of multiple photons. A broader class of experiments and dynamics can be accessed using two time-delayed laser pulses to access unexplored regions of the potential energy surfaces. As a proof-of-principle experiment using a double excitation, we studied the photodissociation of trifluoroiodomethane molecules that are pre-excited with an infrared (800 nm) femtosecond laser pulse before photo-dissociation is triggered with an ultraviolet (266 nm) femtosecond laser pulse. We have observed significant differences in the dissociation dynamics, with pre-excitation resulting in a slower dissociation process. This new capability can offer new insights on the evolution of nuclear wavepackets in regions of the excited potential energy surface which are inaccessible in single photon excitation. We present a methodology to carry out the measurement, analyze and interpret the data that could be applied to a broad class of experiments. |
| title | Ultrafast electron diffractive imaging of the dissociation of pre-excited molecules |
| topic | Chemical Physics |
| url | https://arxiv.org/abs/2511.13479 |