TRANSITION-METAL ION DIMERS FORMED IN CEO2 - AN EPR STUDY

被引:54
作者
ABIAAD, E
BENNANI, A
BONNELLE, JP
ABOUKAIS, A
机构
[1] UNIV SCI & TECH LILLE FLANDRES ARTOIS,CATALYSE HETEROGENE & HOMOGENE LAB,CNRS,URA 402,F-59655 VILLENEUVE DASCQ,FRANCE
[2] UNIV LITTORAL,CATALYSE & ENVIRONNEMENT LAB,F-62100 CALAIS,FRANCE
[3] CNRS,URA 402,F-75700 PARIS,FRANCE
来源
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS | 1995年 / 91卷 / 01期
关键词
D O I
10.1039/ft9959100099
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
MeCeO oxides (Me = Cu2+, Mn2+, V4+, Mo5+), With an atomic ratio Me/Ce = 0.1, have been prepared by impregnation of ceria (CeO,) with the corresponding Me salt. Subsequently, the solids were oxidized or reduced at given temperatures. An EPR study evidenced the presence of dimers in the solids. A fine structure was obtained for CuCeO and MoCeO oxides. The signal at half magnetic field intensity (Delta m(s) = +/-2), characteristic of dimers, was present in all the MeCeO oxides with a hyperfine structure for Cu2+, Mn2+ or V4+ ions. From the relative intensity of the half-field and the normal-field signals characterizing the dimer spectrum, the distance between the Me ions has been calculated. For CuCeO and MoCeO oxides, monomer ions have been evidenced as precursors of the dimers. The dimer spectrum of Mo5+ ions has been observed only at 77 K and not at room temperature. In all cases, the dimers are located in oxygen Vacancies near Ce3+ ions, present in the solid before the introduction of transition-metal ions.
引用
收藏
页码:99 / 104
页数:6
相关论文
共 41 条
  • [1] PREPARATION AND CHARACTERIZATION OF CEO2 UNDER AN OXIDIZING ATMOSPHERE - THERMAL-ANALYSIS, XPS, AND EPR STUDY
    ABIAAD, E
    BECHARA, R
    GRIMBLOT, J
    ABOUKAIS, A
    [J]. CHEMISTRY OF MATERIALS, 1993, 5 (06) : 793 - 797
  • [2] HIGHLY RESOLVED ELECTRON-PARAMAGNETIC RESONANCE-SPECTRUM OF COPPER(II) ION-PAIRS IN CUCE OXIDE
    ABOUKAIS, A
    BENNANI, A
    AISSI, CF
    WROBEL, G
    GUELTON, M
    VEDRINE, JC
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1992, 88 (04): : 615 - 620
  • [3] ABOUKAIS A, 1992, J CHEM SOC FARADAY T, V88, P1321
  • [4] 12-HETEROPOLYMOLYBDATES AS CATALYSTS FOR VAPOR-PHASE OXIDATIVE DEHYDROGENATION OF ISOBUTYRIC ACID .2. GROUP-IB, GROUP-IIB, GROUP-IIIB, AND VIII-METAL SALTS
    AKIMOTO, M
    SHIMA, K
    IKEDA, H
    ECHIGOYA, E
    [J]. JOURNAL OF CATALYSIS, 1984, 86 (01) : 173 - 186
  • [5] ELECTRON-PARAMAGNETIC-RES LINESHAPES IN POLYCRYSTALLINE SAMPLES - 6S5/2 IONS IN AXIAL AND CUBIC-CRYSTAL FIELDS
    BELTRANLOPEZ, V
    CASTROTELLO, J
    [J]. JOURNAL OF MAGNETIC RESONANCE, 1980, 39 (03) : 437 - 460
  • [6] EXPLANATION OF SOME FORBIDDEN TRANSITIONS IN PARAMAGNETIC RESONANCE
    BLEANEY, B
    RUBINS, RS
    [J]. PROCEEDINGS OF THE PHYSICAL SOCIETY OF LONDON, 1961, 77 (493): : 103 - &
  • [7] EPR SPECTRA OF MN2+ IN CHLORIDE BROMIDE AND IODIDE HOST COMPOUNDS
    BREIVOGEL, FW
    SARKISSIAN, V
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1968, 48 (06) : 2442 - +
  • [8] SURFACE-STRUCTURE AND REACTIVITY OF VANADIUM-OXIDE SUPPORTED ON TITANIUM-DIOXIDE - V2O5/TIO2 (RUTILE) CATALYSTS PREPARED BY HYDROLYSIS
    CAVANI, F
    CENTI, G
    FORESTI, E
    TRIFIRO, F
    BUSCA, G
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1988, 84 : 237 - 254
  • [9] PHYSICOCHEMICAL CHARACTERIZATION OF V-SILICALITE
    CENTI, G
    PERATHONER, S
    TRIFIRO, F
    ABOUKAIS, A
    AISSI, CF
    GUELTON, M
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1992, 96 (06) : 2617 - 2629
  • [10] ELECTRON PARAMAGNETIC RESONANCE OF MN(2) COMPLEXES IN ACETONITRILE
    CHAN, SI
    FUNG, BM
    LUTJE, H
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1967, 47 (06) : 2121 - &