1 / 21

Lecture 3 More on Adsorption and Thin Films Monolayer adsorption Several adsorption sites

Lecture 3 More on Adsorption and Thin Films Monolayer adsorption Several adsorption sites Thin Films (S ~ constant, multilayer adsorption).

trygg
Download Presentation

Lecture 3 More on Adsorption and Thin Films Monolayer adsorption Several adsorption sites

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Lecture 3 More on Adsorption and Thin Films • Monolayer adsorption • Several adsorption sites • Thin Films (S ~ constant, multilayer adsorption) Lecture 3: More on adsorption

  2. Consider a surface in equilibrium with a gas for a given length of time. We will assume that the rate of desorption at the adsorption temperature is negligibe: Lecture 3: More on adsorption

  3. The flux of gas molecules to a surface (molecules/cm2-sec is given by: F = P[2πkTM]-1/2 So, the flux is proportional to the pressure. Putting P in Torr, M in grams, and T in Kelvin we have (see Somorjai) F = 3.51 x 1022P/(MT)1/2 Lecture 3: More on adsorption

  4. Single Adsorption Site: Monolayer adsorption: The number of molecules or atoms adsorbed on a surface, is then given as N = FtS Where t = time, and S = sticking coefficient, which typically varies with coverage: S = S(N) However, when N/Nmax = Θ << 1, we have S ~ S0 Therefore, we can expect that adsorbate coverage will vary linearly with exposure in the early stages. However, for Θ~ 1 (larger exposures) we then have S = S0(1-Θ) ~ 0, so eventually, the surface coverage does not increase. Lecture 3: More on adsorption

  5. This is certainly the case for O2 on Fe(110) at 90 K (Smentkowski and Yates) Lecture 3: More on adsorption

  6. If there is only one type of adsorption binding site, with one characteristic adsorbate binding energy, then the desorption spectra will look fairly straightforward: If desorption is 1st order, then the desorption spectrum is fairly simple: The peak is always at the same temperature, and the intensity is proportional to the number of adsorbed molecules: P Increasing initial exposure T Lecture 3: More on adsorption

  7. This is the case H2 desorption following Si2H6 adsorption on Si(100)(2x1) for adsorption at exposures of up to 2 L at 300 K. A single H2 peak is observed at ~ 800 K. Why is this first order? Adapted from Nix and Wu, Surf. Sci. 306 (1994) 59 Lecture 3: More on adsorption

  8. Substrate : fcc(100) surface with unit cell lattice vectors a1, a2 Adsorbate overlayer( 1 type of adsorption site) b1 = 2a1 b2 = 2a2 Lecture 3: More on adsorption

  9. Let’s assume that a surface as two adsorption sites for atomic H Top view, simple Cubic lattice Site 1, a-top site, desorption energy E1 X X X Site 2, 4-fold hallow site, desorption energy E2 X X X X X X Now, assume that E1 > E2 Therefore , the desorption temperature for E1 (TD1) is higher than for E2L TD1>> TD2 Lecture 3: More on adsorption

  10. Which site gets filled first? Suppose we “dose” the surface (expose it to) H2 at 300 K, then do TPD. Will both sites get filled at the same time? No! Atoms (including dissociated H2) are generally mobile on surfaces The sites with highest EB (highest TD) get filled first… Lecture 3: More on adsorption

  11. First, the sites with the highest EB are filled…. H H H H H H H H H H Then, the sites with the next highest EB are filled… Lecture 3: More on adsorption

  12. At low exposures, only Type 1 sites occupied, desorption spectrum will have only one peak (2nd order reaction shown) H2 H H H At increasing doses, 2nd order peak moves to lower desorption temperatures, finally, all the type 1 sites are saturated… PH2 T  Lecture 3: More on adsorption

  13. T2 T1 H2 H2 H H H H H H H H Lecture 3: More on adsorption

  14. Desorption of H2 from W(100), Madey and Yates, Surf. Sci. 49 (1975) 465 Lecture 3: More on adsorption

  15. This picture holds even for more complex adsorbates e.g., Si2H6 on Si(100)(2x1) Lecture 3: More on adsorption

  16. Consider H2 desorption from Si2H6/Si(100)(2x1)… 1st or 2nd order desorption? Wu and Nix, Surf. Sci. 306 (1994) 59 Lecture 3: More on adsorption

  17. If there are several occupied adsorption sites, you can desorbe from the lower energy site at the lower desorption temperature, without desorbing from the higher temperature. Lecture 3: More on adsorption

  18. Lecture 3: More on adsorption

  19. Multilayer adsorption: In this case, the sticking coefficient does not go to zero at full monolayer coverage. Instead, the sticking coefficient remains roughly constant with formation of 1st, 2nd, 3rd monolayer, etc. Examples: Deposition of a metal film on an unreactive substrate. One example is the MBE of C(111) (graphene) on Co3O4(111) (M. Zhou, et al., JPCM 24 (2012) 072201) In this case, the total number of atoms on the surface is simply given by N = FtS0A (where A = sample area). Lecture 3: More on adsorption

  20. Lecture 3: More on adsorption

  21. Summary: • Mulitple absorption sites Multiple Peaks • Sites with highest EB fill up first • Sites with smallest EB desorb at the lowest temperature • Desorption from different sites can obey different desorption kinetics • Deposition of, e.g., thin films does not obey monolayer adsorption, sticking coefficient does not go to zero. Lecture 3: More on adsorption

More Related