We present completely ab initio nonperturbative calculations of the integral and single differential cross sections for double photoionization of H2 for photon energies from 53.9 to 75.7 eV. The method of exterior complex scaling, implemented with B-splines, is used to solve the Schrodinger equation for a correlated continuum wave function corresponding to a single photon having been absorbed by a correlated initial state. The results are in good agreement with experimental integral cross sections
The hydride anion H- would not be bound in the absence ofelectron correlation. Electron correlation ...
We present the results of numerical calculations on the single photon double photoionization of H{su...
Calculations of fully differential cross sections for two-photon double ionization of the hydrogen m...
We present converged, completely ab initio calculations of the triple differential cross sections f...
Exterior complex scaling provides a practical path for first-principles studies of atomic and molec...
Exterior complex scaling provides a practical path forfirst-principles studies of atomic and molecul...
We have studied the process of direct (nonsequential) two-photon double ionization of molecular hydr...
Calculations of fully differential cross sections for two-photon double ionization of the hydrogen m...
The hydride anion H- would not be bound in the absence of electron correlation. Electron correlatio...
We perform time-dependent calculations of triply differential cross sections (TDCS) of two-photon do...
Calculations of absolute triple differential and single differential cross sections for helium doubl...
Calculations of absolute triple differential and single differential cross sections for helium doubl...
Calculations of absolute triple differential and single differential cross sections for helium doubl...
We present a single-center model of double photoionization (DPI) of the H2 molecule which combines a...
We have studied the process of direct (nonsequential) two-photon double ionization of molecular hydr...
The hydride anion H- would not be bound in the absence ofelectron correlation. Electron correlation ...
We present the results of numerical calculations on the single photon double photoionization of H{su...
Calculations of fully differential cross sections for two-photon double ionization of the hydrogen m...
We present converged, completely ab initio calculations of the triple differential cross sections f...
Exterior complex scaling provides a practical path for first-principles studies of atomic and molec...
Exterior complex scaling provides a practical path forfirst-principles studies of atomic and molecul...
We have studied the process of direct (nonsequential) two-photon double ionization of molecular hydr...
Calculations of fully differential cross sections for two-photon double ionization of the hydrogen m...
The hydride anion H- would not be bound in the absence of electron correlation. Electron correlatio...
We perform time-dependent calculations of triply differential cross sections (TDCS) of two-photon do...
Calculations of absolute triple differential and single differential cross sections for helium doubl...
Calculations of absolute triple differential and single differential cross sections for helium doubl...
Calculations of absolute triple differential and single differential cross sections for helium doubl...
We present a single-center model of double photoionization (DPI) of the H2 molecule which combines a...
We have studied the process of direct (nonsequential) two-photon double ionization of molecular hydr...
The hydride anion H- would not be bound in the absence ofelectron correlation. Electron correlation ...
We present the results of numerical calculations on the single photon double photoionization of H{su...
Calculations of fully differential cross sections for two-photon double ionization of the hydrogen m...