Understanding the high photocatalytic activity of (B, Ag)-codoped TiO2 under solar-light irradiation with XPS, solid-state NMR, and DFT calculations.
J Am Chem Soc
; 135(4): 1607-16, 2013 Jan 30.
Article
en En
| MEDLINE
| ID: mdl-23316875
ABSTRACT
The origin of the exceptionally high activity of (B, Ag)-codoped TiO(2) catalysts under solar-light irradiation has been investigated by XPS and (11)B solid-state NMR spectroscopy in conjunction with density functional theory (DFT) calculations. XPS experimental results demonstrated that a portion of the dopant Ag (Ag(3+)) ions were implanted into the crystalline lattice of (B, Ag)-codoped TiO(2) and were in close proximity to the interstitial B (B(int.)) sites, forming [B(int.)-O-Ag] structural units. In situ XPS experiments were employed to follow the evolution of the chemical states of the B and Ag dopants during UV-vis irradiation. It was found that the [B(int.)-O-Ag] units could trap the photoinduced electron to form a unique intermediate structure in the (B, Ag)-codoped TiO(2) during the irradiation, which is responsible for the photoinduced shifts of the B 1s and Ag 3d peaks observed in the in situ XPS spectra. Solid-state NMR experiments including (11)B triple-quantum and double-quantum magic angle spinning (MAS) NMR revealed that up to six different boron species were present in the catalysts and only the tricoordinated interstitial boron (T*) species was in close proximity to the substitutional Ag species, leading to formation of [T*-O-Ag] structural units. Furthermore, as demonstrated by DFT calculations, the [T*-O-Ag] structural units were responsible for trapping the photoinduced electrons, which prolongs the life of the photoinduced charge carriers and eventually leads to a remarkable enhancement in the photocatalytic activity. All these unprecedented findings are expected to be crucial for understanding the roles of B and Ag dopants and their synergistic effect in numerous titania-mediated photocatalytic reactions.
Texto completo:
1
Bases de datos:
MEDLINE
Asunto principal:
Teoría Cuántica
/
Plata
/
Titanio
/
Boro
/
Luz
Idioma:
En
Revista:
J Am Chem Soc
Año:
2013
Tipo del documento:
Article
País de afiliación:
China