Laser Field Characteristics Investigation in The Chemisorption Process For The System Na/W

International Association of Scientific Innovation and Research (IASIR)
(An Association Unifying the Sciences, Engineering, and Applied Research)

International Journal of Emerging Technologies in Computational
and Applied Sciences (IJETCAS)
www.iasir.net
IJETCAS 14-306; 2014, IJETCAS All Rights Reserved Page 1
ISSN (Print): 2279-0047
ISSN (Online): 2279-0055
Laser Field Characteristics Investigation in the Chemisorption Process for
the System Na/W(111)
I. Q. Taha, J. M. Al-Mukh and S. I. Easa
Physics Department, Education College for Pure Science,
Basrah University, Basrah, Iraq
______________________________________________________________________________________
Abstract: Detailed theoretical treatment and model calculations for describing the interaction between species
and solid surface, in the presence of a monochromatic electromagnetic field (laser field) throughout the
chemisorption process, have been developed. Our previous work for the scattering process in the presence of
laser field and the well known Anderson model for atomic chemisorption are the basis in deriving our
theoretical treatment. The derived occupation number and the chemisorption energy are presented as a function
of laser parameters and normal distance from the surface as the adatom approaches to the surface. The model
calculation is applied to the Na/W(111) system for it's experimental and academic importance. Many important
features are explained concerning the adatom charge state and the bonding type. One can conclude that the
laser field is a controlling tool of ionization and bonding type, which is experimentally the truth.
Keywords: chemisorption process; monochromatic electromagnetic field; occupation number; chemisorption
energy;
________________________________________________________________________________________

I. Introduction
Surface chemical reactions, in which at least one of the reaching species is adsorbed on solid surface, are
important for chemical industry. It is hence of interest to investigate laser-stimulated surface processes [1] which
include surface excitation [2-4], desorption [5,6], dissociation [7,8] and catalysis [9]. Laser-stimulated surface
processes have been investigated during the past several years, due to both their academic interest and industrial
potential. Recent progress in the experimental and theoretical studies and applications of laser-stimulated surface
processes have been reported [10]. Laser excitation or desorption of adspecies have been investigated
theoretically by a variety of techniques including Morse potential models [11] and master equation approaches
[12]. Since the charge transfer is the essence of chemistry, surface catalysis would be greatly affected by this
phenomenon. With laser, chemists have begun to control chemical reaction dynamics in gas-phase reactions and
the reactions occurring at the gas-solid interface [13]. In this paper, the chemisorption of atoms on solid surfaces
in the presence of laser field is studied. The theoretical treatment in our pervious works [14-16] and the well-
known Anderson model [17,18] for atomic chemisorption are our basis in deriving the occupation numbers and
the binding energy formulas in the static case of u (atomic velocity) 0 .
In order to develop a "basis treatment", many complications must be avoided such as,
1. The variation of the screening length with laser field parameters is not taken into account.
2. The dependence of the intra-atomic Coulomb interaction on laser field parameters is not considered as well
as the correlation effect on the surface site.
3. The electronic excitations in the adatom-surface orbitals are neglected.
4. The effect of surface temperature is not considered since by including it, one must establish the heating of
the system due to laser field.
Each of these remarks may have a wide-range of researching both theoretically and experimentally, which may
be considered as future work.
II. Derivation of the Adatom Occupation Numbers
To derive a formula for the occupation number
A
n of the adatom level, we get use of the following equation
that is derived in our previous paper [15](eq. (20)),
( ) ( ) ( ) ( ) ( )
( ) ( ) ( ) ( ) ( )
}
' '
' (
' + '
'
+
'
'
+
'
'
=
'
t
t
t d t
A
C t
A
W
~
t
A
V
~

t
A
W
~
t
A
V
~

2
1
t
A
W
~
t
A
V
~

i
t
A
C t
im
i
t
A
.
C

(1)
which is treated firstly as the velocity of the atom goes to zero. This means, that the occupation number and all
the related chemisorption functions are calculated as a function of the normal distance Z from the surface. By
using the following definitions,
I. Q. Taha et al., International Journal of Emerging Technologies in Computational and Applied Sciences, 8(1), March-May, 2014, pp. 01-12
( ) ( )
( )
}
=
o
' ' c
'
'
t
t
im
t d t i
A
A
e t C t C , ( ) =
'
t
A
V
~
( ) t
A
V
'
t
A
E
E i
e
|
|
|
.
|
\
|

'

( ) =
'
t
A
W
~
( ) t
A
W
'
( ) t E E i
A
e

'

|
|
.
|
\
| e
o
+
e
o
t
L
i
e
i
e
t
L
i
e
i
e (2)
However, ( ) ( )
2
t
A
C
2
t
A
C
'
=
'
. Then we get from eq.(1),
( )
( )
( ) ( )( )
( ) ( ) ( )
t d e
e e e e t W t V e i t C
t
0
A
L L
t
0
A
t d t G t Z E E i
t
0
t i i t i i
A A
t d t G t iE
A
'
}
+ ' + '
}
=
'
'
' ' ' ' + '

' e o ' e o
' '
' '
'
}

where the function ( ) t G at certain Z is given by,
( ) ( ) ( ) ( )( ) {
( ) ( )}
t i 2 i 2 t i 2 i 2
2
A
t i i t i i
A A
2
A
L L
L L
e e 2 t W
e e t W t V 2 t V t G
e o e + o
e o e + o

+ + +
+ + t =

The first term of eq. (4) includes the adatom energy level broadening due to coupling interaction with the surface
band levels while the third one includes the adatom level broadening due to laser field coupling interaction. The
second one includes the interference between the two over mentioned coupling interactions. Then by using the
definition of the atomic level broadening [19], we can write
( ) ( ) ( )
( ) ( ) ( ) ( )

o t = A
o t = A
o t = A
E E Z W Z V Z
) E E ( ) Z ( W ) Z (
E E Z V Z
A A int
2
A L
2
A C

As our derivation works in the limit 0 u , the atomic level broadenings are written as a function of the
normal distance. So eq. (4) can be written in the wide band approximation limit as,
( ) ( ) ( )
t i 2 i 2 t i 2 i 2
L
t i i t i i
int C
L L L L
e e 2 e e 2 t G
e o e + o e o e + o
+ + A + + A + A =
with,
( ) ( )
width band / 1 , ) Z ( W ) Z ( V
, Z W , Z V
int
2
L
2
C
= t = A
t = A t = A
(7)
Then by integrating eq. (6), we get
( )
( ) ( ) ( )
( ) ( ) ( )
t i 2 i 2 t i 2 i 2
L
L t i i t i i
L
int
L C
t i 2 i 2 t i 2 i 2
L
L t i i t i i
L
int
L C
L L L L
L L L L
e e
2
i
e e
i 2
t 2
e e
2 i
e e
i
2
t 2
t d t G
e o e + o e o e + o
e o e + o e o e + o
e
A

e
A
A + A =
e
A
+
e
A
+ A + A =
' '
}

And by getting use of the definition of exponential function [20], we write,
( ) ( ) ( )
( ) ( )
( )
( ) ( ) ( ) ( ) t i 2 i 2 k t i 2 i 2 l t i i m t i i n
nmlk
k
L
L
l
L
L
m
L
int
n
L
int
t 2 t Z E E i
t Z E E i t d t G
L L L L
L C A
A
e e e e
2
i
2
i i 2 i 2
e e
e
e o e + o e o e + o
A + A

}
' '
|
|
.
|
\
|
e
A
|
|
.
|
\
|
e
A
|
|
.
|
\
|
e
A
|
|
.
|
\
|
e
A
=

By substituting eq. (9) in eq. (3) we get,
(3)
(4)
(5)
(6)
(8)
(9)
( )
( )
( )
( )
( ) ( ) ( ) | |
( ) ( ) ( )
( ) ( ) ( ) | |
( ) ( ) ( )
( ) ( ) ( ) | |
( ) ( ) ( )
A + A + + + e +
+
A + A + + + e +
+
A + A + + e +
|
|
.
|
\
|
e
A
|
|
.
|
\
|
e
A
}
=
A + A + + + e + o
A + A + + + e + o
+ e + A + A +
+ o
+ +
+
' '
'
L C L A
t 2 i k 2 l 2 m n 1 Z E E i i
A
L C L A
t 2 i k 2 l 2 m n 1 Z E E i i
A
L C L A
t k 2 l 2 m n 2 i Z E E i
A k 2 l 2 m n i
nmlk
k l
L
L
m n
L
int
l n
t d t G t iE
A
2 i k 2 l 2 m n 1 Z E E
e e W
2 i k 2 l 2 m n 1 Z E E
e e W
2 i k 2 l 2 m n Z E E
e V
e
2
i i 2
1 e i t C
L C L A
L C L A
L L C A
t
0
A
(10)
However, if the perturbation is time dependent harmonic one, then the system levels generated from ) Z ( E
A
will
be ( )
L A
n Z E e + , with
L L
e e and ,...... 2 , 1 , 0 n = . Some of these levels are thrown above Fermi
level and the others below the conduction band bottom position. So they may do not effectively take parts in the
resonance charge exchange process. Accordingly, all the terms in eq. (10) are neglected except for
1 k l m n = = = = , so eq. (10) can be written as,
( )
( ) ( )
( ) ( )
( ) ( ) ( ) ( ) ( ) ( )
A + A + e +
+
A + A + e
+
A + A +
=
e o
e + o

L C L A
t i i
A
L C L A
t i i
A
L C A
A t Z E E i
A
2 i Z E E
e W
2 i Z E E
e W
2 i Z E E
V
e t C
L L
A

The adatoms occupation level can be given by [21],
( )
}

o
t
= dE E E C
1
n
2
A
A
(12)
Substituting eq. (11) in eq. (12), we get the following expression,
( ) ( ) ( ) ( ) ( ) ( )
( ) ( ) ( )
( ) ( ) ( ) | | ( ) ( ) ( ) | |
( ) ( ) ( ) | | ( ) ( ) ( ) | |
( ) ( ) ( ) | | ( ) ( ) ( ) | |
( ) ( ) ( ) | | ( ) ( ) ( ) | |
( ) ( ) ( ) | | ( ) ( ) ( ) | |
( ) ( ) ( ) | | ( ) ( ) ( ) | |
}
}
}
}
}
}
}
} }
A + A e A + A + e +
A
t
+
A + A + e A + A e +
A
t
+
A + A e + A + A +
A
t
+
A + A + e + A + A
A
t
+
A + A + e A + A
A
t
+
A + A e A + A +
A
t
+
A + A + e +
A
t
+
A + A + e
A
t
+
A + A +
A
t
=
e o
e + o
e + o
e o
e + o
e o
L C L A L C L A
t i 2 i 2
L
L C L A L C L A
t i 2 i 2
L
L C L A L C A
t i i
int
L C L A L C A
t i i
int
L C L A L C A
t i i
int
L C L A L C A
t i i
int
2
L C
2
L A
L
2
L C
2
L A
L
2
L C
2
A
C
A
2 i Z E E 2 i Z E E
dE e 1
2 i Z E E 2 i Z E E
dE e 1
2 i Z E E 2 i Z E E
dE e 1
2 i Z E E 2 i Z E E
dE e 1
2 i Z E E 2 i Z E E
dE e 1
2 i Z E E 2 i Z E E
dE e 1
2 Z E E
dE 1
2 Z E E
dE 1
2 Z E E
dE 1
n
L
L
L
L
L
L

(13)
(11)
There are nine terms, the first three terms do not include the time-dependent exponential term while the others
six terms include it. These six terms turn to be zero due to averaging over the phase, with n is an integer
0 d e
2
1
2
0
in
= o
t
}
t
o

That leaves the occupation number time-independent term.

III. The Model Calculation
Eq. (13) is employed to calculate the occupation number of the atomic energy level which can be written as,
( ) ( ) ( )
( ) ( ) ( )
( ) ( ) ( )
}
}
}
o
o
o
A + A + e +
A + A
A + A
A
t
+
A + A + e
A + A
A + A
A
t
+
A + A +
A + A
A + A
A
t
=
F
F
F
E
u
2
L C
2
L A
L C
L C
L
E
u
2
L C
2
L A
L C
L C
L
E
u
2
L C
2
A
L C
L C
C
A
dE
2 Z E E
2
2
1
dE
2 Z E E
2
2
1
dE
2 Z E E
2
2
1
n

with
o
u and
F
E are the bottom of the band and Fermi energy respectively. Accordingly, eq. (14) can also be
written as [21],
( )
}
o
=
n
E
u
n n A
F
dE E g n (15)
with,
( )
( ) ( ) ( )
2
L C
2
L A
L C
n
2 n Z E E
2 1
E
A + A + e +
A + A
t
= (16)
L C
L
1 1
L C
C
2
g g ,
2
g
A + A
A
= =
A + A
A
=
o

Since
n
n
is the local density of states on the adatom in the presence of laser field. The spin dependence of
A
n
o
A
n and
n

o
n
is considered throughout the adatom energy level ( ) Z E
A
as well as the
chemisorption function, i.e. the broadening one. Note that, ( ) Z E
A
is written as ( ) Z E
A
o
, o + for spin up and
o for spin down atomic levels. By incorporating the repulsive electron-electron Coulomb interaction U
[22,23] on the adatom, the ( ) Z E
A
o
takes the following expression,
( ) ( ) Z Un E Z E
A A A
o o
+ =

;
i A
V E | =
(18)
| and
i
V are the metal work function and the ionization energy of the adsorbed atom respectively.
o +
A
E and
o
A
E differ by U whose value may be taken as
A i
V V

, with
i
V and
A
V are the ionization and
the affinity energies respectively. As the atom is far away from the surface then 1 n
A
=
o +
and
i A
V E | =
o +

while 0 n
A
=
o
and ( ) U V E
i A
+ | =
o
. Now as the atom approaches the surface, U decreases due to the
screening out of the electron-electron interaction and its effective value can be given by [24,25],
) Z ( 2 V V U
im A i
c = (19)
where ) Z (
im
c is the image shift [26],
( )
o
+
= c
Z Z 4
e
) Z (
2
im
with
o
Z is the screening length.
In chemisorption theory calculation, the broadening function as well as the intra-atomic electron-electron
interaction, both make the theoretical treatments achieve higher a priori accuracy in calculations of charge
(14)
(17)
fractions ( )
o
A
n . e . i . In the limit of wide band approximation,
o
A
C
and
L
A are calculated from the following
formalisms [27],
( )
Z 2
C C
C
0
e Z
o
o o
A = A ; ( )
Z 2
L L
L
0
e Z
o
A = A (20)
With,
i L
V 2 = o and
o
o
C
will be defined later.
0
C
A and
0
L
A represent the broadening at 0 Z = with
0 L
A
equal to
2
W
o
t ,
o
W is the coupling strength due to laser field. | = 4 / 1 , | 4 is the energy band width.
In order to calculate the occupation numbers and all the related functions, we firstly solved eq. (14) analytically,
|
|
.
|
\
|
A + A
e +
A + A
e +
A + A
A
t
+
|
|
.
|
\
|
A + A
e
A + A
e
A + A
A
t
+
|
|
.
|
\
|
A + A

A + A

A + A
A
t
=
o
o
o
o
o
o
o
o
o
o
o
o
o
o
o
o
o
o
o
o
L C
L A 1
L C
L A F 1
L C
L
L C
L A 1
L C
L A F 1
L C
L
L C
A 1
L C
A F 1
L C
C
A
2
E u
tan
2
E E
tan
2
1
2
E u
tan
2
E E
tan
2
1
2
E u
tan
2
E E
tan
2
1
n

Then eqs. (21) and (18) must be solved self-consistently using the following initial conditions as the species is
far away from the surface (i.e. at nm 10 Z = ), 1 n
A
=
o +
and 0 n
A
=
o
.

IV. The Chemisorption Energy
The chemisorption energy,
che
E , in general, is defined as being the difference between the final and the initial
energies of the system. According to Anderson model, the chemisorption energy is the change in the initial
ground state energy on switching on the coupling. In general, the chemisorption energy is divided into two parts.
These are the metallic part and the ionic part [28].
The metallic part of the bond energy, results from allowing the valance electron of the adatom to spread
throughout the metal and the metal electrons to spread a bit into the region of the adatom. This part is given by
[29],
( ) ( )
}
o
o o +

o
=
A A
0
A M
n n U dE E E Z E
(22)
Then, by substituting the formula of local density of states on the adatom in the presence of laser field eq.(12) in
eq. (22), we get
( ) ( )

}
o =
o o + o
=
o
1 , 0 n
A A
E
u
n n M
n n U dE E E g Z E
F
(23)
( )
( )
( ) ( )
( )
( ) ( )
( ) ( )
( ) ( )
( ) ( )
( ) ( )
( ) ( )
( ) ( )
o o
o o
o o
o o
o o
o o
o o o
o
o
o
o
o
o
o
o
o
o
o
o
o
o
o
o
o
o
o
o
(
(
A + A + e |
A + A + e A
+
A + A + e + |
A + A + e + A
+
A + A + |
A + A + A
+
)
`
A + A
e + |
A + A
e +
A + A
A
e + +
)
`
A + A
e |
A + A
e
A + A
A
e +
)
`
A + A
|
A + A

A + A
A
t
=

A A 2
L C
2
L A
2
L C
2
L A F L
2
L C
2
L A
2
L C
2
L A F L
2
L C
2
A
2
L C
2
A F C
L C
L A 1
L C
L A F 1
L C
L
L A
L C
L A 1
L C
L A F 1
L C
L
L A
L C
A 1
L C
A F 1
L C
C
A M
n n U
2 E 2
2 E E
ln
2
2 E 2
2 E E
ln
2
2 E 2
2 E E
ln
2
2
E 2
tan
2
E E
tan
2
E
2
E 2
tan
2
E E
tan
2
E
2
E 2
tan
2
E E
tan
2
E
1
Z E

(21)
(24)
Note that in eq. (24), the laser field frequency is added explicitly to the atomic energy levels positions and the
broadening due to laser field is also add to the broadening function due to coupling interaction. The ionic energy
is the energy associated with bringing a unit of charge infinitely far removed from the metal up to a distance Z
from the surface. However as the atom is brought to the surface, its sharp state broadens and overlaps a bit with
the metal conduction band such that the effective net charge on the ion is now a function of distance [29],
( )
o o
=
A A eff
n n 1 Z Z (25)
Now, the work or the change in energy to bring the charge from = ' Z to Z Z = ' is given by,
( )
( )
( )
}
o
+ '
' '
=
Z
2
2
eff
I
Z Z 4
Z d Z Z
Z E
(26)
Finally, eq. (26) is calculated numerically to get the total chemisorption energy,
( ) ( ) ( ) Z E Z E Z E
I M che
+ = (27)
The dominant energy contribution depends on
1- Whether the adatom is one of electronegative nature or electropositive one.
2- The surface electronic structure, i.e. whether the surface is clean or not.
3- The laser field parameters.

V. Results and Discussion
We apply our theoretical treatment to real systems in order to extract some physical useful conclusions
about the effects of laser field throughout the chemisorption process. The model calculation is applied to the
system of Na on W(111). The chemisorption dynamics of Na-atom ( ) eV 14 . 5 V
i
= and ( ) eV 54 . 0 V
A
=
[30] as it approaches the surface of W(111) ( ) eV 4 . 4 = | [31] is investigated. This system is of the
type
i
V < | . The screening length is fixed on nm 11635 . 0 Z =
o
, this value gives the experimental atomic
chemisorption energy which is equal to 2.35 eV [32] in the absence of laser field. The parameter | is fixed on 3
eV which works in the wide band approximation limit.
The adatom energy level broadening function that is used for this system is given by [33],
( )
( ) ( )
( )
o
+
o
o
o
o
|
|
.
|
\
|
+
+
+
= A
A i
2
q r Z 2
A i
A
i
2
A
C
e
q r Z 2
1
1 q V 2
r Z V 16
q
) Z (
(28)
where,
o o
=
A A
E 2 q , | + | = 2 V and
i
r is the atomic radius of the adatom. The
o
A
C
-laser field
parameters dependence is being throughout
o
A
E . This formula is usually used for the alkali adatoms adsorption
on transition metal surface because it gives the general physical features for their chemisorption dynamics, while
L
A is given by eq. (20).
To calculate the occupation numbers
o
A
n and all the related chemisorption functions, eqs. (21) and (18) are
solved self-consistently to determine the adatom charge state as it approaches to the surface. So the initial
conditions at large distance from the surface are,
( ) ( ) 0 n , 1 n
A A
= =
o o
(29)
The occupation numbers and the related chemisorption functions are considered as an "input-data" to
calculate the chemisorption energy and its contributions. This energy is calculated as a function of normal
distance to the surface, i.e. the potential energy surfaces. This step is an important one in the chemisorption
theory calculation. Since, the potential energy surfaces give the type of bonding at every normal distance from
surface, which is what one needs for comparison with the experimental foundings.
Figs.(1) shows our results for the chemisorption energy as a function of the normal distance Zand the laser
coupling strength
o
W at the laser field frequency . u . a 17 . 0
L
= e . It is clear that the "adsorption potential
well" minimum for . u . a 4 . 0 W >
o
at certain value of Z may considered as equilibrium distance or "the
adsorption position",
ad
Z . The distance
ad
Z can be considered as a variation in screening length
L
Z
o
A due to
laser field effect. So the total screening length will be
L
Z Z
o o
A + for . u . a 4 . 0 W >
o
. The distance
ad
Z , at
which the adsorption well is noticed [14], is of the most interesting one. This distance is used to extract a non-
linear relationship between the screening length
L
Z
o
A and the laser coupling strength
o
W and the laser field
frequency
L
e as in fig.(2), which shows that the value
ad
Z increases with
o
W and
L
e . The relationship
between
L
Z
o
A and
L
e for different values of
o
W ( . u . a 4 . 0 W >
o
) is estimated by using best fitting from
fig.(2), it takes the following non-linear expression,
2
L L L
47495 . 3 474458 . 0 040967 . 0 Z e + e = A
o
for .) u . a ( 4 . 0 W =
o

2
L L L
46112 . 3 472888 . 0 285885 . 0 Z e + e = A
o
for .) u . a ( 7 . 0 W =
o

2
L L L
42910 . 3 462996 . 0 440347 . 0 Z e + e = A
o
for .) u . a ( 1 W =
o

The coefficients in the linear terms are varied due to laser coupling variation. Fig. (3) shows the occupation
numbers as a function of
L
e for different values of laser coupling strength
o
W ( . u . a 4 . 0 W >
o
) at
( = Z
ad
Z ). It is clear that the values of ) n ( n
A A
o o +
= increase with
o
W and
L
e . The solutions are non-
magnetic (
o o
=
A A
n n ) where there is no net spin on the adatom at relatively small distance. The calculated
o
A
C

and
L
A are also presented in fig.(4) and fig.(5) as a function of
L
o
W ( . u . a 4 . 0 W >
o
) at ( = Z
ad
Z ). The values of
o
A
C
and
L
A decrease with
o
W and
L
e . In fig. (6), the
chemisorption energy and its contributions parts (the ionic and metallic parts) are presented as a function of
L
e
for different values of
o
W ( . u . a 4 . 0 W >
o
) at ( = Z
ad
Z ), where the metallic part is nearly equal to the
chemisorption energy and the ionic part has relatively very small contribution. It is well known that the Na atom
adsorbed at W surface as positive ion with ionic bond [22] but by using laser field the Na atom also adsorbed as
positive ion but with metallic bond. From this, one can conclude that the type of bond on the surface can be
controlled by laser field. This is not contracted with the experimental role of using laser field for the desorption
of atoms or ions from solid surfaces. Finally, to know more about laser effect, , E ( E
ad che
= where
ad
E the
chemisorption energy at = Z
ad
Z ) is presented as a function of
o
W and
L
e in fig.(7). It is clear that the values
of
ad
E increase with
o
W and
L
e .
VI. Conclusions
1. Our theoretical treatment and the model calculation describe and explain precisely the dynamics of the
chemisorption process in the presence of laser field throughout potential surfaces calculations.
2. One of the most interesting features in our treatment is introducing the level broadening due to the
interference between the electronic coupling and the laser field coupling interactions.
3. The laser field is a tool for controlling the charge states on the adatom and the type of bonding with solid
surface.
4. Our theoretical treatment for the chemisorption process illustrates all the reaction dynamics for the
adsorption process, which we consider as a "basis treatment" for other related surface processes such as
adatom desorption from solid surface.
0
.2
0
.4
0
.6
0
.8
1
.0
-5
-4
-3
-2
-1
0
0
2
4
6
8
1 0
E
c
h
e

(
e
V
)
Z
1
0
-1 (
n
m
)
W
O (a
.u
.)
-5.900
-5.178
-4.456
-3.735
-3.013
-2.291
-1.569
-0.8473
-0.1255
) a (

Fig. (1): a. The chemisorption energy as a function of
o
W and Z at . u . a 17 . 0
L
= e

0 . 2
0 . 4
0 . 6
0 . 8
1 . 0
-5
-4
-3
-2
-1
0
0
2
E
c
h
e

(
e
V
)
Z
1
0
- 1
( n
m
)
W
O

(
a
.
u
.
)
-5.900
-5.178
-4.456
-3.735
-3.013
-2.291
-1.569
-0.8473
-0.1255
) b (

Fig. (1): b. The figure illustrates the variation with distance at closest approach where
nm 2 . 0 0 Z = .

0
.
4
0
.
6
0
.
8
1
.
0
0
.
1
0
.
2
0
.
3
0
.
4
0
.
5
0
.
6
0
. 1
0
0
. 1
5
0
. 2
0
0 . 2 5
A

Z
O
L
1
0 -
1

(
n
m

)
e
L

(
a
.
u
.
)
W
O
(
a
.u
.)
0.02200
0.08725
0.1525
0.2178
0.2830
0.3483
0.4135
0.4788
0.5440

Fig. (2): The relationship between
L
Z
o
A ,
L
e and
o
W ( . u . a 4 . 0 W >
o
).

0.10 0.15 0.20 0.25
0.29
0.30
0.31
0.32
0.33
0.34
0.35
0.36
0.37
W
O
=0.4 a.u.
W
O
=0.7 a.u.
W
O
=1 a.u.
n
A
+
o
=

n
A
-
o
e
L
(a.u.)

Fig. (3): The values of
o
A
n as a function of
L
o
W ( . u . a 4 . 0 W >
o
) at
( = Z
ad
Z ).
0.10 0.15 0.20 0.25
0.015
0.020
0.025
0.030
0.035
0.040
0.045
0.050
0.055
0.060
0.065
0.070
0.075
W
O
=0.4 a.u.
W
O
=0.7 a.u.
W
O
=1 a.u.
A
c
+
o
=
A
c
-
o

(
e
V
)
e
L
(a.u.)

o
A
C
as a function of
L
o
W ( . u . a 4 . 0 W >
o
) at ( = Z
ad
Z ).
0.10 0.15 0.20 0.25
3.5
4.0
4.5
5.0
5.5
6.0
6.5
7.0
W
O
=0.4 a.u.
W
O
=0.7 a.u.
W
O
=1 a.u.
A
L

(
e
V
)
e
L
(a.u.)

L
A as a function of
L
o
W ( . u . a 4 . 0 W >
o
) at ( = Z
ad
Z ).
-7
-6
-5
-4
-3
-2
-1
0
0.10 0.15 0.20 0.25
W
O
=0.4 a.u.
e
L
(a.u.)
E
che
eV
E
M
eV
E
I
eV
C
h
e
m
i
s
o
r
p
t
i
o
n

e
n
e
r
g
y

(
e
V
)

Fig. (6): a
-7
-6
-5
-4
-3
-2
-1
0
0.10 0.15 0.20 0.25
W
O
=0.7 a.u.
e
L
(a.u.)
E
che
eV
E
M
eV
E
I
eV
C
h
e
m
i
s
o
r
p
t
i
o
n

e
n
e
r
g
y

(
e
V
)

Fig. (6): b

-7
-6
-5
-4
-3
-2
-1
0
0.10 0.15 0.20 0.25
W
O
=1 a.u.
e
L
(a.u.)
E
che
eV
E
M
eV
E
I
eV
C
h
e
m
i
s
o
r
p
t
i
o
n

e
n
e
r
g
y

(
e
V
)

Fig. (6): c. The chemisorption energy and its contributions (the ionic and metallic parts) as a function of
L
e for
different values of
o
W ( . u . a 4 . 0 W >
o
) at ( = Z
ad
Z ).
0
.4
0
.6
0
.8
1
.
0
5
.6
5
.7
5
.8
5.9
6.0
6.1
6.2
6.3
6.4
0
. 1
0
0
. 1
5
0
. 2
0
0
. 2
5
I
E
c
h
e
I

=

I
E
a
d
I

(
e
V
)
e
L

(
a
.
u
.
)
W
O (
a
.u
.)
5.576
5.668
5.761
5.853
5.945
6.037
6.130
6.222
6.314

Fig. (7): The chemisorption energy at ( = Z
ad
Z ) as a function of
L
e and
o
W ( . u . a 4 . 0 W >
o
).
References
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