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Xiuyan Wang

Researcher at Dalian Institute of Chemical Physics

Publications -  25
Citations -  1136

Xiuyan Wang is an academic researcher from Dalian Institute of Chemical Physics. The author has contributed to research in topics: Reaction dynamics & Excited state. The author has an hindex of 14, co-authored 25 publications receiving 1095 citations. Previous affiliations of Xiuyan Wang include Dalian University of Technology.

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Journal ArticleDOI

Observation of Feshbach Resonances in the F+ H2 → HF +H Reaction

TL;DR: The highly sensitive H atom Rydberg tagging time-of-flight method is used to conduct a crossed molecular beam scattering study of the F + H2 → HF + H reaction with full quantum-state resolution, finding pronounced forward-scattered HF products in the v′ = 2 vibrational state.
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Breakdown of the Born-Oppenheimer approximation in the F+ o-D2 -> DF + D reaction.

TL;DR: Excellent agreement is found between multistate, quantum reactive scattering calculations and both the measured energy dependence of the F*/F reactivity ratio and the differential cross sections that confirms the fundamental understanding of the factors controlling electronic nonadiabaticity in abstraction reactions.
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Interference of quantized transition-state pathways in the H + D2 -> D + HD chemical reaction.

TL;DR: The collision-energy dependence of the state-resolved differential cross section at a specific backward-scattering angle for the reaction H + D2 → D + HD is measured with the D-atom Rydberg “tagging” time-of-flight technique.
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The extent of non-Born-Oppenheimer coupling in the reaction of Cl(2P) with para-H2.

TL;DR: This study reports molecular beam experiments, based on hydrogen-atom Rydberg tagging detection, that reveal only a minor role of Cl*, and confirms the ability to simulate accurately chemical reactions on multiple potential energy surfaces.
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Probing the resonance potential in the F atom reaction with hydrogen deuteride with spectroscopic accuracy.

TL;DR: A global potential energy surface is constructed by using the CCSD(T) method that could predict the correct resonance peak positions as well as the dynamics for both F + H2 → HF + H and F + HD →HF + D, providing an accurate resonance potential for this benchmark system with spectroscopic accuracy.