Electronic Structure Study of CO Adsorption on the Fe(001) Surface

Abstract

The adsorption of CO on the Fe(001) surface has been investigated by ab initio density functional methods. The surface is modeled using both an infinite periodic slab and a finite cluster which allows a detailed comparison of these two approaches. We have studied CO adsorption at three different surface locations and find that the energetically preferred site for CO adsorption corresponds to the 4-fold hollow site (R 3 ) followed by binding to the on-top (R 1 ) and 2-fold (R 2 ) positions. Our study is in good agreement with experiments, which show that the R 3 site is the preferred binding site. The theoretical value for the tilting angle in the R 3 position (54°in both slab and cluster calculations) agrees with the experimental value of 45 ( 10°, while the greatly increased theoretical CO bond length of 1.30 Å (compared to 1.11 Å in the gas phase) demonstrates the activation of the CO bond in the R 3 position and correlates well to the observed CO stretch frequency of 1200 cm -1 as opposed to the gas-phase value of 2143 cm -1 . Both the R 2 site and R 1 position are known to exist experimentally, but the precise energetic ordering of these sites has not been established unambiguously. In these sites the theoretical CO bond length increases to about 1.18-1.20 Å in correspondence to the experimentally observed vibrational features that are shifted to lower frequencies of about 2010 cm -1 . In our calculations we find that the R 1 CO is bound more strongly than the R 2 CO by 7.6 kcal/mol.

Density-functional study of the CO adsorption on ferromagnetic Co(0001) and Co(111) surfaces

“…An analogous finding was made in the first-principle calculation of Ref. [10] for CO on the Fe(0 0 1) surface. On semiquantitative level, the conclusion of the semi-empirical model [28] is thus confirmed.…”

“…These data include also CO deposition upon magnetic systems. Calculation of CO effect upon surface magnetization has been published for Fe [10,11] and Ni [12][13][14][15][16].…”

Prediction of a Highly Activated State of CO Adsorbed on an Al/Fe(100) Bimetallic Surface

“…The C-O bond length in the TH configuration is even larger than that in gaseous methanol (R(H 3 C-OH) ) 1.425 Å 60,61 ), indicating that the C-O bond order in this adsite is reduced to e1. As mentioned earlier, this TH configuration was previously found experimentally 21,59 and theoretically 48,49,62 for CO/Fe(100). However, CO on Al/Fe(100) is predicted to be tilted even more toward the surface, with a ∼300 cm -1 lower stretching frequency, and a ∼0.15 Å longer bond length than CO on Fe(100) (see Table 2).…”

Density Functional Theory Study on the Carbon-Adhering Reaction on Fe3O4(111) Surface

“…[13] The Perdew-Burke-Ernzerhof functional [14] within the generalized gradient approximation [15] was used for all calculations. The parameters used in the calculation [16][17][18][19] were listed in Table I. Fe 3 O 4 has a cubic inverse spinel structure with a lattice constant of 8.394 Å [20] (Figure 2(1)).…”