The nitrogen-boron paramagnetic center in visible light sensitized N-B co-doped TiO2. Experimental and theoretical characterization

被引:44
作者
Czoska, A. M. [2 ,3 ]
Livraghi, S. [2 ,3 ]
Paganini, M. C. [2 ,3 ]
Giamello, E. [2 ,3 ]
Di Valentin, C. [1 ]
Pacchioni, G. [1 ]
机构
[1] Univ Milano Bicocca, Dipartimento Sci Mat, I-20125 Milan, Italy
[2] Univ Turin, Dipartimento Chim IFM, I-10125 Turin, Italy
[3] Nanostruct Interfaces & Surfaces Ctr Excellence, NIS, I-10125 Turin, Italy
关键词
PHOTOCATALYTIC ACTIVITY; TITANIUM-DIOXIDE; AB-INITIO; RESONANCE; TIO2-XNX; TRANSITION; ORIGIN; STATE;
D O I
10.1039/c0cp00143k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nitrogen boron co-doped TiO2 prepared via sol-gel synthesis and active under visible light, contains two types of paramagnetic extrinsic defects, both exhibiting a well resolved EPR spectrum. The first center is the well characterized [NiO](center dot) species (i = interstitial) also present in N-doped TiO2, while the second one involves both N and B. This latter center (labeled [NOB](center dot)) exhibits well resolved EPR spectra obtained using either 14 N or 15 N which show a high spin density in a N 2p orbital. The structure of the [NOB](center dot) species is different from that previously proposed in the literature and is actually based on the presence of interstitial N and B atoms both bound to the same lattice oxygen ion. The interstitial B is also linked to two other lattice oxygen ions reproducing the trigonal planar structure typical of boron compounds. The energy level of the [NOB](center dot) center lies near the edge of the valence band of TiO2 and, as such, does not contribute to the visible light absorption. However, [NOB](center dot) can easily trap one electron generating the [NOB](center dot) diamagnetic center which introduces a gap state at about 0.4 eV above the top of the valence band. This latter species can contribute to the visible light activity.
引用
收藏
页码:136 / 143
页数:8
相关论文
共 48 条
[1]   Enhanced photocatalytic activity of zeolite-encapsulated TiO2 clusters by complexation with organic additives and N-doping [J].
Alvaro, M ;
Carbonell, E ;
Fornés, V ;
García, H .
CHEMPHYSCHEM, 2006, 7 (01) :200-205
[2]   Visible-light photocatalysis in nitrogen-doped titanium oxides [J].
Asahi, R ;
Morikawa, T ;
Ohwaki, T ;
Aoki, K ;
Taga, Y .
SCIENCE, 2001, 293 (5528) :269-271
[3]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[4]   EPR Characterization and Reactivity of Surface-Localized Inorganic Radicals and Radical Ions [J].
Chiesa, Mario ;
Giamello, Elio ;
Che, Michel .
CHEMICAL REVIEWS, 2010, 110 (03) :1320-1347
[5]   Density functional theory and electron paramagnetic resonance study on the effect of N-F codoping of TiO2 [J].
Di Valentin, C. ;
Finazzi, E. ;
Pacchioni, G. ;
Selloni, A. ;
Livraghi, S. ;
Czoska, A. M. ;
Paganini, M. C. ;
Giamello, E. .
CHEMISTRY OF MATERIALS, 2008, 20 (11) :3706-3714
[6]   Characterization of paramagnetic species in N-doped TiO2 powders by EPR spectroscopy and DFT calculations [J].
Di Valentin, C ;
Pacchioni, G ;
Selloni, A ;
Livraghi, S ;
Giamello, E .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (23) :11414-11419
[7]   N-doped TiO2:: Theory and experiment [J].
Di Valentin, Cristiana ;
Finazzi, Emanuele ;
Pacchioni, Gianfranco ;
Selloni, Annabella ;
Livraghi, Stefano ;
Paganini, Maria Cristina ;
Giamello, Elio .
CHEMICAL PHYSICS, 2007, 339 (1-3) :44-56
[8]   Doping and functionalization of photoactive semiconducting metal oxides [J].
Di Valentin, Cristiana ;
Diebold, Ulrike ;
Selloni, Annabella .
CHEMICAL PHYSICS, 2007, 339 (1-3) :VII-VIII
[9]   Reduced and n-Type Doped TiO2: Nature of Ti3+ Species [J].
Di Valentin, Cristiana ;
Pacchioni, Gianfranco ;
Selloni, Annabella .
JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (48) :20543-20552
[10]   Photochemical activity of nitrogen-doped rutile TiO2(111) in visible light [J].
Diwald, O ;
Thompson, TL ;
Zubkov, T ;
Goralski, EG ;
Walck, SD ;
Yates, JT .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (19) :6004-6008