@article {1361,
	title = {Density functional theory calculation of electron spectra of formaldehyde},
	journal = {Chemical Physics Letters},
	volume = {418},
	number = {1-3},
	year = {2006},
	note = {ISI Document Delivery No.: 005UMTimes Cited: 12Cited Reference Count: 30},
	month = {Jan},
	pages = {286-291},
	type = {Article},
	abstract = {Both ionization and excitation spectra for outer valence-shell electrons and inner-shell electrons of formaldehyde are calculated with density functional methods. In addition, both resonant and non-resonant X-ray emission spectra are also computed. For all of these calculations, we use four different basis sets: large and efficient sets, with and without diffuse functions. Choice of method for each type of electron spectroscopy is based on past experience. For excitation spectra, especially when the final states are Rydberg-like in nature, basis sets with diffuse functions are recommended. On the other hand, for ionization spectra and X-ray emission spectra, diffuse functions are apparently unnecessary. Available experimental data for formaldehyde enable us to judge the accuracy of the present density functional calculations. The average absolute deviation from experiment is generally about 0.3 eV or better, confirming the adequacy of our choice of method. (c) 2005 Elsevier B.V. All rights reserved.},
	keywords = {EMISSION SPECTRA, EXCITATION-ENERGIES, HYDROGEN, KRYPTON, MOLECULES, ORBITALS, photoabsorption, RAY-ABSORPTION SPECTRA, SLATER-TYPE, VERTICAL IONIZATION-POTENTIALS},
	isbn = {0009-2614},
	url = {<Go to ISI>://000234849500055},
	author = {Chong, D. P. and Takahata, Y.}
}
