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The n-resolved single-electron capture in slow O^(6+)-Ne collisions
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作者 崔述成 邢大地 +7 位作者 朱小龙 苏茂根 高永 郭大龙 赵冬梅 张少锋 符彦飙 马新文 《Chinese Physics B》 SCIE EI CAS CSCD 2024年第7期16-20,共5页
A study of single-electron capture(SEC) in 18-240 keV O^(6+)-Ne collisions has been conducted employing a combination of experimental and theoretical methodologies.Utilizing a reaction microscope,state-selective SEC c... A study of single-electron capture(SEC) in 18-240 keV O^(6+)-Ne collisions has been conducted employing a combination of experimental and theoretical methodologies.Utilizing a reaction microscope,state-selective SEC cross sections and projectile scattering angle distributions were obtained.The translational energy spectra for SEC reveal the prevailing capture into n=3 states of the projectile ion,with a minor contribution from n=4 states.Notably,as the projectile's energy increases,the relative contribution of SEC n=4 states increases while that of SEC n=3 states diminishes.Furthermore,we computed state-selective relative cross sections and angular differential cross sections employing the classical molecular Coulomb over-the-barrier model(MCBM) and the multichannel Landau-Zener(MCLZ) model.A discernible discrepancy between the state-selective cross sections from the two theoretical models is apparent for the considered impact energies.However,regarding the angular differential cross sections,an overall agreement was attained between the current experimental results and the theoretical results from the MCLZ model. 展开更多
关键词 charge exchange state-selective cross sections angular differential cross sections COLTRIMS
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Stereodynamics of O(^3P)+H2 at Scattering Energies of 0.5, 0.75, and 1.0 eV 被引量:2
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作者 Victor Wei-keh Wu 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2010年第2期149-154,I0001,共7页
Quasiclassical trajectory calculation of the title reaction O(^3P)+H2→OH+H at three different scattering energies of 0.5, 0.75, and 1.0 eV on the lowest electronic potential energy surface 1^3A" has been done. D... Quasiclassical trajectory calculation of the title reaction O(^3P)+H2→OH+H at three different scattering energies of 0.5, 0.75, and 1.0 eV on the lowest electronic potential energy surface 1^3A" has been done. Distribution P(θr) of polar angles between the relative velocityk of the reactant and rotational angular momentum vector j' of the product, distribution P(φr) of the azimuthal as well as dihedral angles correlating k-k'-j', 3-dimensional distri-bution, and polarization-dependent differential cross sections (PDDCSs)dependent upon the scattering angle of the product molecule OH between the relative velocity k of the reactant and k' of the product at different scattering energies of 0.5, 0.75, and 1.0 eV are presented and discussed. 展开更多
关键词 Quasiclassical trajectory calculation Stereodynamics Alignment Rotational angular momentum Polarization-dependent differential cross section O+H2 reaction
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