ULTRATHIN REACTIVE METAL-FILMS ON TIO2(110) - GROWTH, INTERFACIAL INTERACTION AND ELECTRONIC-STRUCTURE OF CHROMIUM FILMS

被引:63
作者
PAN, JM [1 ]
DIEBOLD, U [1 ]
ZHANG, LZ [1 ]
MADEY, TE [1 ]
机构
[1] RUTGERS UNIV, DEPT PHYS & ASTRON, SURFACE MODIFICAT LAB, PISCATAWAY, NJ 08855 USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/0039-6028(93)90288-U
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
A study of ultrathin Cr films on TiO2(110) surfaces is reported. The combination of low energy ion scattering (LEIS) and X-ray photoelectron spectroscopy (XPS) enables us to study quantitatively the growth of reactive metal films on metal oxides, and the chemical interactions at the interface. Ultrathin Cr films grow initially in a quasi-two-dimensional fashion at room temperature. Changes in oxidation states of both Ti and Cr during film formation suggest that strong chemical interactions at the interface are of great importance in the growth of reactive metal films. Cr ''wets'' the surface more effectively at 300 K than ultrathin films of less reactive metals, Fe and Cu. This suggests that a relation exists between the metal reactivity with oxygen and the wetting of metal films on oxides: The more reactive the metal towards oxygen, the better is the wetting ability. The chemical interaction is accompanied by charge transfer at the interface, causing a reduction of the surface work function. The interfacial interaction also causes the interfacial Cr layer to behave differently from the top metallic Cr atoms upon thermal annealing. The top layers of metallic Cr show a strong clustering tendency at 500-degrees-C, while the interfacial Cr seems to have less surface mobility and slow bulk diffusion.
引用
收藏
页码:411 / 426
页数:16
相关论文
共 53 条
[1]   A STUDY OF SMALL PT PARTICLES ON AMORPHOUS AL2O3 AND ALPHA-AL2O3[0001] SUBSTRATES USING TPD OF CO AND H21 [J].
ALTMAN, EI ;
GORTE, RJ .
JOURNAL OF CATALYSIS, 1988, 110 (01) :191-196
[2]  
BELTON DN, 1984, J PHYS CHEM-US, V88, P4172
[3]   ELASTIC AND INELASTIC ELECTRON MEAN FREE PATHS FROM X-RAY PHOTOELECTRON DIFFRACTION EXPERIMENTS [J].
BONZEL, HP ;
BREUER, U ;
KNAUFF, O .
SURFACE SCIENCE, 1990, 237 (1-3) :L398-L404
[4]   A SIMS STUDY OF NICKEL DEPOSITION ON TIO2(100) - INFLUENCE OF THE STOICHIOMETRY OF THE SUPPORT [J].
BOURGEOIS, S ;
JOMARD, F ;
PERDEREAU, M .
SURFACE SCIENCE, 1991, 249 (1-3) :194-198
[5]   MONOLAYERS OF PLATINUM AND IRON ON TIO2(001) - CHARACTERIZATION BY AUGER-ELECTRON SPECTROSCOPY, SECONDARY-ELECTRON EMISSION AND WORK FUNCTION CHANGES [J].
BRUGNIAU, D ;
PARKER, SD ;
RHEAD, GE .
THIN SOLID FILMS, 1984, 121 (03) :247-257
[6]   LOW-ENERGY ELECTRON-DIFFRACTION AND ELECTRON-SPECTROSCOPY STUDIES OF CLEAN (110) AND (100) TITANIUM-DIOXIDE (RUTILE) CRYSTAL-SURFACES [J].
CHUNG, YW ;
LO, WJ ;
SOMORJAI, GA .
SURFACE SCIENCE, 1977, 64 (02) :588-602
[7]   ELECTRICAL AND OPTICAL PROPERTIES OF RUTILE SINGLE CRYSTALS [J].
CRONEMEYER, DC .
PHYSICAL REVIEW, 1952, 87 (05) :876-886
[8]   INTERACTIONS IN THE FE/TIO2(110) SYSTEM [J].
DENG, JZ ;
WANG, DZ ;
WEI, XM ;
ZHAI, RS ;
WANG, HL .
SURFACE SCIENCE, 1991, 249 (1-3) :213-222
[9]   GROWTH MODE OF ULTRATHIN COPPER OVERLAYERS ON TIO2(110) [J].
DIEBOLD, U ;
PAN, JM ;
MADEY, TE .
PHYSICAL REVIEW B, 1993, 47 (07) :3868-3876
[10]  
DUFOUR LC, 1985, SURFACE NEAR SURFACE