The effect of pump-2 laser on Autler–Townes splitting in photoelectron spectra of K2 molecule
Literature Information
Wei Guo, Xingqiang Lu, Xinlin Wang, Hongbin Yao
We theoretically investigated Autler–Townes (AT) splitting in the photoelectron spectra of a four-level ladder K2 molecule driven by pump1–pump2–probe pulses by employing the time-dependent wave packet approach. The effect of pump-2 laser intensity and wavelength on AT splitting was studied for the first time. Triple splitting with asymmetric profiles arises because of the non-resonant excitation. The triple splitting transforms to double splitting when pump-2 detuning approaches ±1/2 times of pump-1 Rabi frequency. The splitting between two side band peaks in the triplet or doublet does not change with the pump-2 laser wavelength. The three peaks shift to a lower energy with a different shift as pump-2 wavelength increases. The magnitude of AT splitting increases with increasing pump-2 laser intensity. The asymptotic behavior of AT splitting with the pump-2 laser intensity are interesting at the threshold point of the near resonant region and far-off resonant region.
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Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.











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