2014
DOI: 10.1016/j.cplett.2014.05.087
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Cross sections for electron scattering from α-tetrahydrofurfuryl alcohol

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Cited by 19 publications
(46 citation statements)
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“…22 we previously outlined our spectral deconvolution approach, and the basis 20,22 for that approach, and so we also do not repeat that detail again here. Rather, we simply note that the various EELS were deconvoluted, using a standard least-squares fitting procedure, into contributions arising from each individual or unresolved combination of excited electronic-states.…”
Section: Experimental Details and Analysis Proceduresmentioning
confidence: 99%
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“…22 we previously outlined our spectral deconvolution approach, and the basis 20,22 for that approach, and so we also do not repeat that detail again here. Rather, we simply note that the various EELS were deconvoluted, using a standard least-squares fitting procedure, into contributions arising from each individual or unresolved combination of excited electronic-states.…”
Section: Experimental Details and Analysis Proceduresmentioning
confidence: 99%
“…The short-dashed green lines represent spectral features of individual spectral deconvolution bands (bands 1-5, respectively), while the blue longer dashes indicate the bands which are subsequently combined together (i.e., bands 1+2, band 3, and bands 4+5). 22 Also indicated are the excitation energies for the electronic spectrum of the isomers A and C of THFA as calculated by Limão-Vieira et al 20 trons, with a typical current of 1-3 nA, was incident on an orthogonal beam of THFA molecules. That molecular beam was formed by allowing vapour from a high-purity THFA sample (Sigma-Aldrich, 99% assay) to effuse through a single capillary of 0.7 mm internal diameter.…”
Section: Experimental Details and Analysis Proceduresmentioning
confidence: 99%
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“…For instance for some of the composite vibrational modes, 5,7,11 for incident electron energies between 15 and 50 eV, the angular distributions of the cross sections are quasi-isotropic, whereas at those same energies, the elastic angular distributions and the angular distributions for the optically allowed discrete-inelastic electronic states are often strongly peaked in magnitude [20][21][22][23][24][25][26][27][28][29] at the smaller scattered electron angles. That latter behaviour is understood in terms of the strong dipole polarisabilities and permanent dipole moments of the molecules in question.…”
Section: Introductionmentioning
confidence: 99%