Role of Hydroxyl Groups in the NH(x) (x=1-3) Adsorption on the TiO(2) Anatase (101) Surface Determined by a First-Principles Study

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Title:	Role of Hydroxyl Groups in the NH(x) (x=1-3) Adsorption on the TiO(2) Anatase (101) Surface Determined by a First-Principles Study
Authors:	Chang, JG (Chang, Jee-Gong) Chen, HT (Chen, Hsin-Tsung) Ju, SP (Ju, Shin-Pon) Chen, HL (Chen, Hui-Lung) Hwang, CC (Hwang, Chi-Chuan)
Contributors:	化學系
Keywords:	DENSITY-FUNCTIONAL THEORY RUTILE 110 SURFACE TITANIUM-DIOXIDE VISIBLE-LIGHT INDIUM NITRIDE HYDRAZOIC ACID SOLAR-CELLS THIN-FILMS WATER NANOPARTICLES
Date:	2010-12
Issue Date:	2011-12-12 13:51:15 (UTC+8)
Abstract:	A spin-polarized density functional theory calculation was carried out to study the adsorption of NH(x) species (x = 1-3) on a TiO(2) anatase (101) surface with and without hydroxyl groups by using first-principles calculations. It was found that the present hydroxyl group has the effect of significantly enhancing the adsorption of monodentate adsorbates H(2)N-Ti(a) compared to that on a bare surface. The nature of the interaction between the adsorbate (NH(x)) and the hydroxylated or bare surface was analyzed by the Mulliken charge and density of states (DOS) calculations. This facilitation of NH(2) is caused by the donation of coadsorbed H filling the nonbonding orbital of NH(2), resulting in an electron gain in NH(2) from the bonding. In addition, the tipper valence band, which originally consisted of the mixing of O 2p and Ti 3d orbitals, has been broadened by the two adjacent H 1s and NH(2) o(y)(b) orbitals joined to the bottom of the original TiO(2) valence band. The results are important to understand the OH effect in heterogeneous catalysis.
Appears in Collections:	[Department of Chemistry & Graduate Institute of Applied Chemistry ] journal articles

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