Detailed scanning probe microscopy tip models determined from simultaneous atom-resolved AFM and STM studies of the TiO2(110) surface

被引:68
作者
Enevoldsen, Georg H. [1 ,2 ]
Pinto, Henry P. [3 ]
Foster, Adam S. [3 ]
Jensen, Mona C. R. [1 ,2 ]
Kuehnle, Angelika [4 ]
Reichling, Michael [4 ]
Hofer, Werner A. [5 ]
Lauritsen, Jeppe V.
Besenbacher, Flemming
机构
[1] Univ Aarhus, Interdisciplinary Nanosci Ctr iNANO, DK-8000 Aarhus, Denmark
[2] Univ Aarhus, Dept Phys & Astron, DK-8000 Aarhus, Denmark
[3] Aalto Univ, Phys Lab, FIN-02150 Espoo, Finland
[4] Univ Osnabruck, Dept Phys, D-4500 Osnabruck, Germany
[5] Univ Liverpool, Surface Sci Res Ctr, Liverpool L69 3BX, Merseyside, England
关键词
D O I
10.1103/PhysRevB.78.045416
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The atomic-scale contrast in noncontact atomic force microscopy (nc-AFM) images is determined by the geometry and exact atomic structure of the tip apex. However, the tip state is an experimentally unknown parameter, and the lack of insight into the tip apex often limits the possibilities of extracting precise quantitative and qualitative atomistic information on the surface under inspection. From an interplay between simultaneously recorded nc-AFM and scanning tunneling microscopy (STM) data, and atomistic STM simulations based on multiple scattering theory, we demonstrate how the state of the scanning probe microscopy (SPM) tip in the experiments may be determined. The analysis of a large number of experimental SPM images recorded with different tips reveals that no general correlation exists between the contrast observed in the nc-AFM and the tunneling current (I-t) images on TiO2(110) surface. The exact state of the SPM tip must, therefore, be determined for each specific case, which is normally a very difficult endeavor. However, our analysis of the AFM contrast on TiO2(110) surface allows us to considerably reduce the number of tips to be considered in a full simulation. By carefully evaluating the contrast of a handpicked library of SPM tips, we manage to determine a very accurate model of the SPM tip used in an experiment for the first time. It is envisioned that the approach presented here may eventually be used in future studies to screen for and select a SPM tip with a special functionalization prior to imaging an unknown sample, and in that way facilitate precise modeling and chemical identification of surface species.
引用
收藏
页数:19
相关论文
共 42 条
[1]  
[Anonymous], 1993, INTRO SCANNING TUNNE
[2]   MULTIPLE-BAND CONDUCTION IN N-TYPE RUTILE (TIO2) [J].
BECKER, JH ;
HOSLER, WR .
PHYSICAL REVIEW, 1965, 137 (6A) :1872-&
[3]   Direct visualization of defect-mediated dissociation of water on TiO2(110) [J].
Bikondoa, O ;
Pang, CL ;
Ithnin, R ;
Muryn, CA ;
Onishi, H ;
Thornton, G .
NATURE MATERIALS, 2006, 5 (03) :189-192
[4]  
Briggs GAD, 1999, SURF SCI REP, V33, P3
[5]   GENERALIZED MANY-CHANNEL CONDUCTANCE FORMULA WITH APPLICATION TO SMALL RINGS [J].
BUTTIKER, M ;
IMRY, Y ;
LANDAUER, R ;
PINHAS, S .
PHYSICAL REVIEW B, 1985, 31 (10) :6207-6215
[6]   ATTRACTIVE INTERATOMIC FORCE AS A TUNNELING PHENOMENON [J].
CHEN, CJ .
JOURNAL OF PHYSICS-CONDENSED MATTER, 1991, 3 (10) :1227-1245
[7]   The surface science of titanium dioxide [J].
Diebold, U .
SURFACE SCIENCE REPORTS, 2003, 48 (5-8) :53-229
[8]   Evidence for the tunneling site on transition-metal oxides: TiO2(110) [J].
Diebold, U ;
Anderson, JF ;
Ng, KO ;
Vanderbilt, D .
PHYSICAL REVIEW LETTERS, 1996, 77 (07) :1322-1325
[9]   Noncontact atomic force microscopy studies of vacancies and hydroxyls of TiO2(110):: Experiments and atomistic simulations [J].
Enevoldsen, Georg H. ;
Foster, Adam S. ;
Christensen, Mona C. ;
Lauritsen, Jeppe V. ;
Besenbacher, Flemming .
PHYSICAL REVIEW B, 2007, 76 (20)
[10]  
ENEVOLDSEN GH, 2007, THESIS U AARHUS