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Electron localization of linear symmetric molecular ion H3-(2+)
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作者 Zheng-Mao Jia zhi-nan zeng Ru-Xin Li 《Chinese Physics B》 SCIE EI CAS CSCD 2017年第1期97-101,共5页
Electron localization in the dissociation of the symmetric linear molecular ion H3-(2+) is investigated. The numerical simulation shows that the electron localization distribution is dependent on the central freque... Electron localization in the dissociation of the symmetric linear molecular ion H3-(2+) is investigated. The numerical simulation shows that the electron localization distribution is dependent on the central frequency and peak electric field amplitude of the external ultrashort ultraviolet laser pulse. When the electrons of the ground state are excited onto the 2pσ-2Σu-+ by a one-photon process, most electrons of the dissociation states are localized at the protons on both sides symmetrically. Almost no electron is stabilized at the middle proton due to the odd symmetry of the wave function. With the increase of the frequency of the external ultraviolet laser pulse, the electron localization ratio of the middle proton increases, for more electrons of the ground state are excited onto the higher 3pσ-2Σu-+ ustate. 50.9% electrons of all the dissociation events can be captured by the middle Coulomb potential well through optimizing the central frequency and peak electric field amplitude of the ultraviolet laser pulse. Besides, a direct current(DC) electric field can be utilized to control the electron motions of the dissociation states after the excitation of an ultraviolet laser pulse, and 68.8% electrons of the dissociation states can be controlled into the middle proton. 展开更多
关键词 dissociation localization time-dependent Schr ¨odinger equation Coulomb potential ultraviolet laser pulse
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