In this study, the influence of a circularly polarized non-resonant high-frequency laser field radiation on the electronic structure of a hydrogen molecular ion formed by two fixed hydrogen-like donor atoms bound to an electron confined in a two-dimensional Gaussian quantum dot is carried out. The low-lying energy states of the molecular complex were calculated by using the two-dimensional diagonalization method. The results show that the stability of the molecular complex is sensitive to the non-resonant laser field intensity and the internuclear distance. We conclude that the dissociation process of the molecular ion system can be tuned by changing the distance between donor atoms and the non-resonant laser field intensity. It was also co...
A theoretical study of the effects of non-resonant intense laser field on the donor impurity binding...
The competitive mechanism between dissociation and ionization of hydrogen molecular ion in intense f...
For the first time, a full-dimensional quantum-mechanical description of excitation, dissociation an...
Using the two-dimensional (2D) diagonalisation method, the impurity-related electronic states and op...
This study reports a theoretical investigation on the electronic spectrum and the photoionization cr...
Using the two-dimensional diagonalization method and the effective mass approximation, the electroni...
For different nitrogen and indium concentrations, intense laser field (ILF) effect on donor impurity...
Using quantum mechanics calculations, we theoretically study the dissociation and ionization dynamic...
The effects of intense high-frequency laser field on photoionization cross-section and binding energ...
The influence of the internuclear distance and quantum dot size on the nonlinear optical rectificati...
In this work, we have theoretically investigated the effects of a high-frequency intense laser field...
In this work, we have performed a theoretically study on the energy spectrum, binding energy and int...
The main goal of this dissertation is to examine the role of excited states and multi-electron inter...
We present the numerical results obtained by the two dimensional diagonalisation method concerning t...
The dynamics of a two-dimensional H2+ molecule interacting with a strong laser pulse beyond the usua...
A theoretical study of the effects of non-resonant intense laser field on the donor impurity binding...
The competitive mechanism between dissociation and ionization of hydrogen molecular ion in intense f...
For the first time, a full-dimensional quantum-mechanical description of excitation, dissociation an...
Using the two-dimensional (2D) diagonalisation method, the impurity-related electronic states and op...
This study reports a theoretical investigation on the electronic spectrum and the photoionization cr...
Using the two-dimensional diagonalization method and the effective mass approximation, the electroni...
For different nitrogen and indium concentrations, intense laser field (ILF) effect on donor impurity...
Using quantum mechanics calculations, we theoretically study the dissociation and ionization dynamic...
The effects of intense high-frequency laser field on photoionization cross-section and binding energ...
The influence of the internuclear distance and quantum dot size on the nonlinear optical rectificati...
In this work, we have theoretically investigated the effects of a high-frequency intense laser field...
In this work, we have performed a theoretically study on the energy spectrum, binding energy and int...
The main goal of this dissertation is to examine the role of excited states and multi-electron inter...
We present the numerical results obtained by the two dimensional diagonalisation method concerning t...
The dynamics of a two-dimensional H2+ molecule interacting with a strong laser pulse beyond the usua...
A theoretical study of the effects of non-resonant intense laser field on the donor impurity binding...
The competitive mechanism between dissociation and ionization of hydrogen molecular ion in intense f...
For the first time, a full-dimensional quantum-mechanical description of excitation, dissociation an...