Maximum entropy solution to the Stieltjes moment problem in chemical physics
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11320%2F25%3A10508635" target="_blank" >RIV/00216208:11320/25:10508635 - isvavai.cz</a>
Výsledek na webu
<a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=svKnU.vxFD" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=svKnU.vxFD</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1063/5.0310150" target="_blank" >10.1063/5.0310150</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Maximum entropy solution to the Stieltjes moment problem in chemical physics
Popis výsledku v původním jazyce
In the inverse Stieltjes moment problem, one seeks to reconstruct a non-negative distribution from its spectral moments defined on an unbounded interval < 0 , infinity . In chemical physics, this problem arises when computing continuous quantities such as photoionization cross sections or electronic decay widths using discretized approximations to the electronic continuum. While Stieltjes imaging (SI) is the established method in this context, it provides only sparse, discrete sampling of the distribution. Here, we develop a maximum entropy (ME) approach to the solution of the inverse Stieltjes moment problem in the context of Fano theory of resonances, where the sought-after quantity is the decay width function. We implement two ME variants-with polynomial and exponential asymptotic damping-and introduce an averaging procedure over spectral moment orders that addresses convergence issues and provides reliable error estimates. Benchmarking against ab initio Fano-ADC data for molecular Auger decay and interatomic Coulombic decay, we show that ME achieves comparable accuracy to SI while providing a continuous representation of the function. Our results establish ME as a valuable alternative to SI, particularly when analytical continuation or additional verification is required.
Název v anglickém jazyce
Maximum entropy solution to the Stieltjes moment problem in chemical physics
Popis výsledku anglicky
In the inverse Stieltjes moment problem, one seeks to reconstruct a non-negative distribution from its spectral moments defined on an unbounded interval < 0 , infinity . In chemical physics, this problem arises when computing continuous quantities such as photoionization cross sections or electronic decay widths using discretized approximations to the electronic continuum. While Stieltjes imaging (SI) is the established method in this context, it provides only sparse, discrete sampling of the distribution. Here, we develop a maximum entropy (ME) approach to the solution of the inverse Stieltjes moment problem in the context of Fano theory of resonances, where the sought-after quantity is the decay width function. We implement two ME variants-with polynomial and exponential asymptotic damping-and introduce an averaging procedure over spectral moment orders that addresses convergence issues and provides reliable error estimates. Benchmarking against ab initio Fano-ADC data for molecular Auger decay and interatomic Coulombic decay, we show that ME achieves comparable accuracy to SI while providing a continuous representation of the function. Our results establish ME as a valuable alternative to SI, particularly when analytical continuation or additional verification is required.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10300 - Physical sciences
Návaznosti výsledku
Projekt
<a href="/cs/project/GA22-22658S" target="_blank" >GA22-22658S: Mnoha-elektronové rozpadové procesy ve víceatomových systémech</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2025
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Journal of Chemical Physics
ISSN
0021-9606
e-ISSN
1089-7690
Svazek periodika
163
Číslo periodika v rámci svazku
24
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
10
Strana od-do
244102
Kód UT WoS článku
001650156800001
EID výsledku v databázi Scopus
2-s2.0-105025738442