scholarly journals Machine Learning for Absorption Cross Sections

Author(s):  
Bao-Xin Xue ◽  
Mario Barbatti ◽  
Pavlo O. Dral

We present a machine learning (ML) method to accelerate the nuclear ensemble approach (NEA) for computing absorption cross sections. ML-NEA is used to calculate cross sections on vast ensembles of nuclear geometries to reduce the error due to insufficient statistical sampling. The electronic properties — excitation energies and oscillator strengths — are calculated with a reference electronic structure method only for relatively few points in the ensemble. Kernel-ridge-regression-based ML combined with the RE descriptor as implemented in MLatom is used to predict these properties for the remaining tens of thousands of points in the ensemble without incurring much of additional computational cost. We demonstrate for two examples, benzene and a 9-dicyanomethylene derivative of acridine, that ML-NEA can produce statistically converged cross sections even for very challenging cases and even with as few as several hundreds of training points.

2020 ◽  
Author(s):  
Bao-Xin Xue ◽  
Mario Barbatti ◽  
Pavlo O. Dral

We present a machine learning (ML) method to accelerate the nuclear ensemble approach (NEA) for computing absorption cross sections. ML-NEA is used to calculate cross sections on vast ensembles of nuclear geometries to reduce the error due to insufficient statistical sampling. The electronic properties — excitation energies and oscillator strengths — are calculated with a reference electronic structure method only for relatively few points in the ensemble. Kernel-ridge-regression-based ML combined with the RE descriptor as implemented in MLatom is used to predict these properties for the remaining tens of thousands of points in the ensemble without incurring much of additional computational cost. We demonstrate for two examples, benzene and a 9-dicyanomethylene derivative of acridine, that ML-NEA can produce statistically converged cross sections even for very challenging cases and even with as few as several hundreds of training points.


2020 ◽  
Author(s):  
Bao-Xin Xue ◽  
Mario Barbatti ◽  
Pavlo O. Dral

We present a machine learning (ML) method to accelerate the nuclear ensemble approach (NEA) for computing absorption cross sections. ML-NEA is used to calculate cross sections on vast ensembles of nuclear geometries to reduce the error due to insufficient statistical sampling. The electronic properties — excitation energies and oscillator strengths — are calculated with a reference electronic structure method only for relatively few points in the ensemble. Kernel-ridge-regression-based ML combined with the RE descriptor as implemented in MLatom is used to predict these properties for the remaining tens of thousands of points in the ensemble without incurring much of additional computational cost. We demonstrate for two examples, benzene and a 9-dicyanomethylene derivative of acridine, that ML-NEA can produce statistically converged cross sections even for very challenging cases and even with as few as several hundreds of training points.


1996 ◽  
Vol 14 (4) ◽  
pp. 575-586 ◽  
Author(s):  
S. Mabong ◽  
G. Maynard ◽  
K. Katsonis

Parametric electron-ion potential for fast estimation of atomic data required for “on-line” calculations in inertial confinement fusion (ICF) driven by heavy ions is presented. Comparisons of our results (outer- and inner-shell ionization energies, oscillator strengths, and logarithmic mean excitation energies) with experimental and self-consistent-field (SCF) calculation values are made. Using the wave functions generated by the previously mentioned potential, generalized oscillator strengths and integrated inelastic collision cross sections are computed within the frame of Born approximation.


Absorption cross-sections for oxygen in the region 2000 to 1750 Å, corresponding to the process O 2 X 3 Σ - g + hv → O 2 B 3 Σ - u have been measured. The oscillator strengths for the vibrational transitions have been calculated from these results. The total oscillator strength (including the continuum) is found to be 0·259. The cross-sections for intermolecular collisions causing deactivation of the upper state are found and analyzed. The (0-19) and (0-20) members of the system are observed, and the dissociation limit found to be 57140 ± 20 K .


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