Electron localization of H_2^+ in a dc electric field

A dc electric field is utilized to steer the electron motion after the molecular ion H2-＋ is excited by an ultrashort ultraviolet laser pulse. The numerical simulation shows that the electron localization distribution and the dissociation control ratio are dependent on the polarization direction and amplitude of the dc electric field. Most electrons of the dissociation state move opposite to the dc electric field and stabilize at the dressed-up potential well, for the dressed-down well is occupied by the electrons of the 1 sσg state.

Electron localization of linear symmetric molecular ion H3-(2＋)

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.

Deposition of Ag Nanoparticles on Carbon Microspheres Surface：Evaluation of Structures,Electrochemical and Optical Properties

A hybrid material of carbon microspheres（CMSs） with Ag decoration（Ag/CMSs） was developed.Poly（3-hexylthiophene）：Ag/CMSs composite film was prepared by spin-coating.Scanning electron microscopy,transmission electron microscopy,Fourier transform infrared spectrometry,X-ray diffraction,thermogravimetric analysis and cyclic voltammetry were employed to analyze the morphologies,structures,thermal properties and energy levels of Ag/CMSs.The optical property of the composite films was characterized by ultraviolet-visible spectrophotometry and fluorescent spectrometry.The results indicate that silver nanoparticles（AgNPs,d = 10-20 nm） are distributed on the surface of CMSs.LUMO and HOMO energy levels of Ag/CMSs are-3.97 and-5.52 e V,below the vacuum energy level,respectively,indicating that it is feasible to use Ag/CMSs as an electron acceptor.Ag NPs are blended into the active layer to trigger localized surface plasmon resonance,and consequently enhance light harvesting.The coupling of surface plasmons and excitons increased the probability of exciton dissociation.