@article {9927,
	title = {Density Functional Study of Interaction of Atomic Pt with Pristine and Stone-Wales-Defective Single-Walled Boron Nitride Nanotubes.},
	journal = {J. Phys. Chem. C},
	volume = {114},
	year = {2010},
	note = {CAPLUS AN 2010:847939(Journal)},
	pages = {12382-12388},
	publisher = {American Chemical Society},
	abstract = {<p>Interactions between at. Pt and pristine or Stone-Wales-defective (5,5) single-walled boron nitride nanotubes (BNNTs) were studied using d. functional theory (DFT-B3LYP) with truncated nanotube models. The binding energy of Pt on a pristine BNNT is about 20 kcal/mol with little dependency on the binding site. On the other hand, when the Stone-Wales (SW) defect is presented, the at. Pt is preferentially inserted between the B-B bond in the SW defect region with a large binding energy of 58 kcal/mol. On an SW-defective BNNT, the at. Pt, even placed away from the defect site, may eventually (thermodynamically) move toward the defect area until being trapped between the B-B bond, and the final adduct has decreased reactivity toward both electrophiles and nucleophiles compared with Pt adsorption to pristine BNNTs. Pt adsorption on pure or SW-defective BNNTs makes the hosting nanotube wide-gap semiconductive by introducing the valence states of the absorbed Pt into the band gap of the nanotube. In comparison, the Pt atom filling into a B or N single vacancy on a BNNT changes the electronic structure of the vacancy-defective BNNT so dramatically that the Pt-doped BNNT becomes semiconducting with improved reactivity. [on SciFinder(R)]</p>},
	keywords = {DFT platinum atom interaction boron nitride nanotube defect},
	isbn = {1932-7447},
	author = {Y. K. Chen and L. V. Liu and Y. A. Wang*}
}
