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Rationale: The aim of the investigation was to understand the variation in ionization dynamics of inert gas clusters upon doping with species with lower ionization energy than the inert gas constituent. It was postulated that the use of dopant species having lower ionization energy would lead to facile ionization of doped inert gas clusters, resulting in enhancement of the charge state of atomic ions compared with those obtained for pure inert gas clusters.
Methods: Inert gas clusters (Ar(n), Kr(n) or Xe(n)) doped with iron pentacarbonyl were generated by supersonic expansion and subjected to gigawatt intensity laser pulses (266, 355, 532 and 1064 nm wavelengths) obtained from a nanosecond Nd:YAG laser. The ions generated upon laser-cluster interaction were characterized using a time-of-flight mass spectrometer.
Results: Upon interaction of the laser with the doped inert gas clusters, the charge states of the atomic ions were found to increase with the laser wavelength. However, the highest observed charge states were found to be lower for doped inert gas clusters than for pure inert gas clusters, at all laser wavelengths.
Conclusions: Wavelength-dependent generation of multiply charged atomic ions has been explained based on the three stage model, i.e. multiphoton ionization ignited-inverse bremsstrahlung heating, and electron ionization. This model explains enhancement in the charge state of atomic ions with increasing wavelength based on inverse bremsstrahlung heating of the inner ionized electron, which is a more efficient process at longer wavelengths. Inefficient coupling of laser energy in the case of doped inert gas clusters compared with pure inert gas clusters has been rationalized on the basis of accelerated disintegration of the cluster due to facile initial ionization of dopant molecules having low ionization energy. The results suggest that a longer laser wavelength and a slower rate of cluster expansion facilitate the efficient transfer of optical energy into cluster systems.
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http://dx.doi.org/10.1002/rcm.6341 | DOI Listing |
Environ Geochem Health
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Environmental Hydrology Division, National Institute of Hydrology, Roorkee, 247667, India.
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Department of Chemistry and Biochemistry, Florida State University, Tallahassee, Florida 32306-4390, USA.
We present an implementation of relativistic double ionization potential (DIP) equation-of-motion coupled cluster (EOMCC) with up to 4-hole-2-particle (4h2p) excitations that makes use of the molecular mean-field exact two-component (mmfX2C) framework. We apply mmfX2C-DIP-EOMCC to several neutral atoms and diatomic molecules to obtain the ground and first few excited states of the corresponding dication species, and we observe excellent agreement (to within 0.001 eV) between DIPs obtained from mmfX2C- and four-component DIP-EOMCC calculations that include 3-hole-1-particle (3h1p) excitations, with either the Dirac-Coulomb or Dirac-Coulomb-Gaunt Hamiltonians.
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Istituto Nazionale di Fisica Nucleare, Sez. Padova, Padova, Italy.
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Western Switzerland Center for Indoor Air Quality and Radon (croqAIR), Transform Institute, School of Engineering and Architecture of Fribourg, HES-SO University of Applied Sciences and Arts Western Switzerland, Fribourg, Switzerland.
Since the 1980s, radon has been recognized as a public health concern in Switzerland and internationally. In an effort to more accurately estimate the number of lung cancer cases attributable to radon exposure, Swiss health authorities initiated the creation of radon measurements into a centralized national database. As of 2025, this database comprises approximately 300,000 measurements from 150,000 buildings across the country.
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Jiangsu Institute for Food and Drug Control (JSIFDC), Nanjing, Jiangsu, China.
The research team established a quantitative H NMR method to determine the relative ethoxy content (EO%) in ethylcellulose using a CDCl/TFA-d solvent mixture. High-field NMR spectroscopy enabled direct measurement without the use of internal or external calibrants by integrating the methyl proton signals (δ 1.15 ppm) and the methylene/methine proton signals (δ 2.
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