Controlling the mechanism of fulvene S1/S0 decay: switching off the stepwise population transfer
文献信息
David Mendive-Tapia, Benjamin Lasorne, Graham A. Worth, Michael J. Bearpark, Michael A. Robb
Direct quantum dynamics simulations were performed to model the radiationless decay of the first excited state S1 of fulvene. The full space of thirty normal mode nuclear coordinates was explicitly considered. By default, ultrafast internal conversion takes place centred on the higher-energy planar region of the S1/S0 conical intersection seam, giving the stepwise population transfer characteristic of a sloped surface crossing, and leading back to the ground state reactant. Two possible schemes for controlling whether stepwise population transfer occurs or not—either altering the initial geometry distribution or the initial momentum composition of the photo-excited wavepacket—were explored. In both cases, decay was successfully induced to occur in the lower-energy twisted/peaked region of the crossing seam, switching off the stepwise population transfer. This absence of re-crossing is a direct consequence of the change in the position on the intersection at which decay occurs (our target for control), and its consequences should provide an experimentally observable fingerprint of this system.
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Physical Chemistry Chemical Physics

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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