Niobium pentoxide prepared by soft chemical routes: morphology, structure, defects and quantum size effect

被引:167
作者
Brayner, R [1 ]
Bozon-Verduraz, F [1 ]
机构
[1] Univ Paris 07, CNRS, Lab Chim Mat Divises & Catalyse, ITODYS,UMR 7086, F-75251 Paris 05, France
关键词
D O I
10.1039/b210055j
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
Niobium pentoxide (Nb2O5) is prepared by soft chemical routes (digestion either in ammonia or in hydrazine solutions) and is compared to a commercial sample. According to various characterization methods (XRD, HRTEM, DTA-TG, UV-visible diffuse reflectance, Raman and EPR spectroscopies), Nb2O5 shows particular bulk and surface properties. The phase transformation temperatures (amorphous --> pseudo-hexagonal, pseudo-hexagonal --> orthorhombic and orthorhombic --> monoclinic) for the synthetic Nb2O5 are about 100-150degreesC higher than for the commercial sample. The textural properties depend strongly on the preparation method. After calcination at 400degreesC, the sample prepared in ammonia has a larger pore volume (0.22 cm(3) g(-1)) and a better resistance to sintering at 600degreesC. The preparation in hydrazine gives the following advantages only if the gel is sonically redispersed in ethanol: low particle size, narrow size distribution, and higher resistance to sintering (140 m(2) g(-1) at 600degreesC). Preparation in ammonia or in hydrazine favors the formation of defects, characterized by a significant absorption in the visible range adjacent to the interband transition (3.4 eV, 360 nm). These defects, which disappear upon heating in oxygen, are identified as Nb4+ species and ionized oxygen vacancies as confirmed by EPR measurements. Finally, the nanoparticles obtained by sonication in ethanol (average particle size 4.5 nm) shows a significant band gap increase ( from 3.4 eV to 4.2 eV) which is assigned to a quantum size effect.
引用
收藏
页码:1457 / 1466
页数:10
相关论文
共 56 条
[1]  
AEGERTER MA, 1995, STRUCTURE BONDING
[2]   Infrared studies on SnO2 and Pd/SnO2 [J].
Amalric-Popescu, D ;
Bozon-Verduraz, F .
CATALYSIS TODAY, 2001, 70 (1-3) :139-154
[3]  
[Anonymous], 1995, Transition Metal Oxides: An Introduction to Their Electronic Structure and Properties
[4]   Ligand-assisted liquid crystal templating in mesoporous niobium oxide molecular sieves [J].
Antonelli, DM ;
Nakahira, A ;
Ying, JY .
INORGANIC CHEMISTRY, 1996, 35 (11) :3126-3136
[5]   PHOTOCHEMISTRY AND RADIATION-CHEMISTRY OF COLLOIDAL SEMICONDUCTORS .12. INTERMEDIATES OF THE OXIDATION OF EXTREMELY SMALL PARTICLES OF CDS, ZNS, AND CD3P2 AND SIZE QUANTIZATION EFFECTS (A PULSE-RADIOLYSIS STUDY) [J].
BARAL, S ;
FOJTIK, A ;
WELLER, H ;
HENGLEIN, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1986, 108 (03) :375-378
[6]   VIBRATIONAL-SPECTRA OF YTTRIUM NIOBATE AND TANTALATE [J].
BLASSE, G .
JOURNAL OF SOLID STATE CHEMISTRY, 1973, 7 (02) :169-171
[7]   Liquid-phase hydrogenation of hexadienes on metallic colloidal nanoparticles immobilized on supports via coordination capture by bifunctional organic molecules [J].
Brayner, R ;
Viau, G ;
Bozon-Verduraz, F .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2002, 182 (01) :227-238
[8]   Preparation and characterization of high surface area niobia, ceria-niobia and ceria-zirconia [J].
Brayner, R ;
Ciuparu, D ;
da Cruz, GM ;
Fiévet-Vincent, F ;
Bozon-Verduraz, F .
CATALYSIS TODAY, 2000, 57 (3-4) :261-266
[9]   Preparation, characterization and reactivity of Pd/Nb2O5 catalysts in hexa-1,5-diene hydrogenation [J].
Brayner, R ;
Viau, G ;
da Cruz, GM ;
Fiévet-Vincent, F ;
Fiévet, F ;
Bozon-Verduraz, F .
CATALYSIS TODAY, 2000, 57 (3-4) :187-192
[10]  
BRAYNER R, 2003, IN PRESS CATAL TODAY