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Effect of dielectric coating on the positron work function of a metal PDF

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Preview Effect of dielectric coating on the positron work function of a metal

Effect of dielectric coating on the positron work function of a metal V. V. Pogosov, A. V. Babich Department of Micro- and Nanoelectronics, Zaporozhye National Technical University, Zhukovsky Str. 64, Zaporozhye 69063, Ukraine (Dated: January 28, 2011) We show that the dielectric coating of the metal surface leads to the change in the sign of the positron work function. 1 PACSnumbers: 78.70.Bj,71.60.+z 1 0 2 Positron work function is of importance for a proper keeping the same metal (or the crystal face). n description of both bulk and surface states in a metal. The effect of sign for Al Cu is illustrated in Fig. 1. a Electron work function We− for metals is always posi- For polycrystalline Zn / Zn (0001), the effect of ε does J tive (metal can be consideredas a potential box for e−). notresultinanydramaticchanges: Wp =+0.61/−2.59 7 For some metals, positronwork function We+ has a neg- and +2.01/− 1.23 eV for ε = 1 and 80, respectively. 2 ative sign [1, 2] (these metals are equivalent to the po- Similar conclusions can be drawn for Al (110) / (100) tentialbarrierforemittede+). Amongthemetalswitha [W = −4.86/−2.23; −3.39/−0.55 eV] and Cu (110) ] p l negative positron work function are cooper, aluminium, / (100) [W = −4.52/− 2.64; −3.02/ − 0.95 eV ] at l p a iron, molybdenum, nickel, chromium, and titanium. For h these metals, the value of W < 0 was obtained from - e+ s reemitted positron energy distribution relatively to the e vacuum level (see Refs. [1–3] and references therein). m Electronandpositronworkfunctionsarecontrolledby . their bulk contributionsas wellasby the surfaceelectro- t a static dipole barrier D, which enables one to distinguish m between different crystal faces: - nd We− =Web−ulk+eD, We+ =Web+ulk−eD, (1) o where e is the unit positive charge and the term Wbulk c e+ [ includes the positron band shift energy and positron- electron correlation contribution. In the present pa- 1 per, for Al, Cu, and Zn, we use the following values of FIG. 1: Thecalculated dependenceWe+(ε). v Wbulk : 3.97, 2.82 and 3.80 eV, respectively, these val- 5 e+ ues being extracted from the literature (see Ref. [2] and 8 2 references therein). ε=1; 80, respectively. 5 By assuming that the value of the electrostatic poten- Note that the positronium work function can be cal- . tialfar beyondthe metal is equalto zeroit is possible to culated from the Born cycle, 1 find the dipole barrier D =−φ¯, where φ¯<0 is the bulk 0 1 valueoftheelectrostaticpotential[4]. Owingtoinequal- WPs =We− +We+ −Ry/2. 1 ities Wbulk, D > 0, the strong competition between the e+ v: terms in Eq. (1) leads to the negative sign of We+. WPs does not depend on D(ε) but it is determined en- i InRef. [4],wereportedonthemethodtocalculateen- tirely by the bulk properties. X ergycharacteristicsofmetallicsurface(includingD)cov- To conclude, we have demonstrated that the sign of r eredbyaninsulatorcoatingasfunctions ofthe dielectric the positron work function is sensitive to the dielectric a constant ε. The calculations are performed by using the coating of the metal surface. The reported results on Kohn-Shammethodandstabilizedjelliummodel. Strong the work function sign change can be of importance for dependenceofDonεallowsonetoestablishthatthesign applicationsinpositrondiagnosticsofadsorbatesoroxide of W can be changed by changing ε of coating, while at surface and possibly in nanotechnologies. e+ [1] P. J. Schultz, K.G. Lynn,Rev.Mod. Phys.60, 3 (1988). C. Lei, Phys.Rev. B44, 12166 (1991). [2] M. J. Puska, R. M. Nieminen, Rev. Mod. Phys. 66, 841 [4] A.V.Babich,V.V.Pogosov, Surf.Sci.603, 2393(2009). (1994). [3] M.Jibaly,A.Weiss,A.R.Koymen,D.Mehl,L.Stiborek,

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