High-Frequency Electrical Breakdown in Electronegative Gases With Fast Electron Attachment and Detachment Processes
High-Frequency Electrical Breakdown in Electronegative Gases With Fast Electron Attachment and Detachment Processes
High-Frequency Electrical Breakdown in Electronegative Gases With Fast Electron Attachment and Detachment Processes
f min
d/w
a
s max
(1)
where w
a
is the electron drift velocity in the eld E
a
,
f min
is the smallest of the frequencies of the fast processes
and
s max
is the greatest of the frequencies of the slow
processes.
The continuity equations for electrons and an arbitrary
number (k 1) of short-lived negative ion species are
n
t
=
Bn gE
a
cos t
n
1
x
+
Cn (2)
where
n =
_
_
_
_
n
1
n
2
.
.
.
n
k
_
_
_
_
g =
_
_
_
_
1
0
.
.
.
0
_
_
_
_
B =
_
_
_
_
R
1
21
. . .
k1
12
R
2
. . .
k2
.
.
.
.
.
.
.
.
.
.
.
.
1k
2k
. . . R
k
_
_
_
_
and
C =
_
_
_
_
ion
1
0 . . . 0
0
2
. . . 0
.
.
.
.
.
.
.
.
.
.
.
.
0 0 . . .
k
_
_
_
_
.
Here, n
i
is the number density of electrons (i = 1) and of
the short-lived negative ions (2 i k), is the electron
mobility,
ij
is the reaction frequency per ion (electron)
from species i to j,
R
i
=
k
j=1
j=i
ij
is the total frequency of removal of ith species through
fast processes,
ion
is the ionization frequency,
1
is the
frequency of electron attachment to molecules to form long-
lived ions and
i
is the frequency (per ion) of the reaction
which converts the short-lived negative ion of species i
into the long-lived one. In that notation, R
1
is a sum of
the frequencies of electron attachment to molecules to form
short-lived negative ions and
i1
is the frequency of electron
detachment from the short-lived negative ion of species i.
Equation (2) neglects electron diffusion and ion drift and
diffusion in comparison with the electron drift which is
directed along the x axis.
We assume that, with the exception of
ion
, the
quantities which are contained in matrices
B and
C and the
value of are time independent. This is true if
u
,
where
u
is the frequency of the electron energy relaxation.
The reverse inequality
u
is more typical for the RF
range of at atmospheric gas pressure; therefore, in this
case, the last assumption should be considered as a model
one.
It follows from (1) that on the right-hand side of
equation (2) the rst term is much greater than the second
one which in turn is much greater than the third term.
However, the third term cannot be neglected because it
determines the breakdown threshold.
In a short time of about
1
f min
, the densities of electrons
and short-lived ions reach the quasi-steady state
n
0
= n
_
_
_
_
p
1
p
2
.
.
.
p
k
_
_
_
_
(3)
where n
0
is the eigenvector of matrix
B corresponding to
the zero-eigenvalue, that is
Bn
0
= 0. (4)
Here, n
k
i=1
(i, i)
(5)
where (i, i) is the cofactor of the (i, i) element in matrix
B.
From equations (3) and (5) a proportionality between the
electron density n
1
and n
B
2
+
2
I)
1
g
n
e
x
(7)
and
b = w
a
(
B
2
+
2
I)
1
g
n
e
x
(8)
where w
a
= E
a
, n
e
= n
p
1
and
t
=
ion
n
e
+
2
x
2
D
n
e
i=1
i
n
i
(9)
where the overline denotes time averaging
(t ) =
2
T
_
t +T/2
t
() d
(T = 2/ is the eld period) and
D
=
w
2
a
2
[
B(
B
2
+
2
I)
1
]
11
. (10)
In deriving equation (9) we assumed
ion
, that is n
e
varies only slightly over the period and
ion
n
e
ion
n
e
.
The second term on the right-hand side of equation (9) is
of a diffusion nature because it can be interpreted in terms
of a divergence of the electron ux which is proportional
to the gradient of n
e
along the x axis. The coefcient D
, n
e
and n
i
which follows
from (3) on averaging and assuming n
e
(x = 0) = n
e
(x =
d) = 0 we obtain from equation (9) for a uniform-eld gap
in the one-dimensional case (MacDonald 1966, Meek and
Craggs 1978)
n
e
(t ) = n
e
(0) exp
___
(
ion
d
)p
1
i=1
i
p
i
_
t
__
(11)
where
d
=
2
d
2
D
.
This is true if the sizes of the plane electrodes are much
greater than d. The breakdown criterion is written as
ion
=
d
+
k
i=1
i
p
i
p
1
. (12)
In the absence of long-lived negative ions the breakdown
threshold corresponds to the balance between the average
ionization and the loss of electrons due to pseudo diffusion
to the electrodes, whereas electron detachment compensates
for the loss of electrons due to attachment to molecules
(Aints et al 1995). The second term on the right-hand side
of equation (12) shows that the formation of long-lived
negative ions results in the additional loss of electrons.
It is interesting to note that according to equation (11)
both ionization and attachment rates are rescaled by the
relative density of electrons, p
1
< 1. This means that the
ionization and attachment rates effectively decrease.
3. The pseudo diffusion coefcient: particular
cases
Accounting for only one sort of short-lived negative ions
(k = 2), it follows from equations (5) and (10) that
p
1
=
21
12
+
21
p
2
=
12
12
+
21
(13)
and
D
=
w
2
a
2
12
2
+(
12
+
21
)
2
. (14)
Formula (14) has been derived earlier (Aints et al 1995)
and in the limit 0 it reduces to that in the steady
electric eld E = E
a
/
m
, where is the electron mean free
path for momentum transfer. Equation (14) shows that
the pseudo diffusion coefcient D
A
2
12
at >
12
+
21
, where A = w
a
/ is the amplitude of electron
drift oscillations. The mechanism of the pseudo diffusion
process may be explained in the following way (Aints et al
1995). An electron which executes oscillatory drift motion
with amplitude A along the eld attaches to a molecule
to form a short-lived negative ion which is essentially at
rest. Then, at a random moment the electron detaches from
the ion and oscillates around the new midpoint which is
displaced by a distance of the order of A along the x
1405
Comment
axis because the electric eld is now phase shifted. If
A d the phenomenon described for this electron is
repeated many times. The direction of the displacement
along the eld direction is also random. Therefore, the
considered transport of electrons (and short-lived negative
ions) can be treated as pseudo diffusion of charged particles.
The breakdown criterion (equation (12)) in a gas
comprising one sort of short-lived negative ion and an
arbitrary number of sorts of long-lived ones reduces to
ion
=
d
+
1
+
12
2
/
21
.
That is, the loss of electrons is due to pseudo diffusion,
direct formation of long-lived ions (with the frequency
1
) and indirect formation with a frequency which is the
product of the frequency of electron attachment to form
a short-lived negative ion (
12
) and the possibility of
converting the short-lived ion into a long-lived one (
2
/
21
in the considered case when
2
21
). It should be
noted that the effect of the indirect formation of long-lived
negative ions on the breakdown in a steady eld when there
is no pseudo diffusion electron loss has been studied before
(see, for instance, Eletskii and Smirnov 1990, Wetzer and
Wen 1991).
In a gas with two species of short-lived negative ions
(k = 3), instead of equations (13) and (14) we have
p
i
= S
i
/S
and
D
=
w
2
a
2
R
1
2
+S
2
(R
3
+
23
) +S
3
(R
2
+
32
)
4
+
2
(R
2
2S) +S
2
(15)
where
S
1
= R
2
R
3
23
32
S
2
= R
3
R
1
31
13
S
3
= R
1
R
2
12
21
S = S
1
+S
2
+S
3
R = R
1
+R
2
+R
3
.
If the frequencies of reactions involving short-lived ions of
the third species are small (
13
=
31
=
23
=
32
0)
equation (15) reduces to (14). There are also other cases
when equation (15) reduces to (14). For instance, let us
assume that an electron can attach to a molecule to form the
negative ion of the second species (i = 2) which does not
participate in the electron detachment reaction, yet converts
into the negative ion of the third species (i = 3) which
is involved in the fast electron detachment reaction, i.e.
13
=
21
=
32
0. Then, from (15)
D
=
w
2
a
2
12
(
2
+
2
23
+
23
31
+
2
31
)
[
4
+
2
(
2
23
+
2
31
+
2
12
)
+(
23
31
+
12
23
+
31
12
)
2
]
1
. (16)
In the limit of fast conversion of an ion of the second
species into that of the third species (
23
31
,
12
)
equation (16) reduces to
D
=
w
2
a
2
12
2
+(
12
+
31
)
2
.
This looks like equation (14) because a large value of
23
implies that the apparent frequency of electron attachment
to form an ion of third species is
12
and the intermediate
ion of the second species can be neglected.
4. The effect of electron pseudo diffusion on RF
breakdown in real gases
We consider conditions when electron pseudo diffusion
governs RF breakdown in gases. To estimate the order
of magnitude let us take
ij
= and
i
= for any i and
j. Then, the condition that the rst term on the right-hand
side of equation (12) is much greater than the second one
reduces to
2
2
_
w
a
d
_
2
1
1 +(k/)
2
. (17)
Considering that the pseudo diffusion concept is true only
for amplitudes of electron drift oscillations which are much
less than a quarter of the distance between the electrodes
(A = w
a
/ d/4), from (17) it follows that a necessary
condition for pseudo diffusion to be important to breakdown
is
2
32
1
1 +(k/)
2
. (18)
That is, electron attachment is followed by electron
detachment almost every time without the formation of
long-lived negative ions.
Aints et al (1995) observed that the measured value of
the RF breakdown voltage in air under normal conditions
is 20% lower than that calculated from equating the
frequencies of ionization and electron attachment. This was
interpreted in terms of the total compensation for electron
attachment loss by electron detachment and, therefore, the
breakdown criterion was written as the equality between the
ionization frequency and rate of electron loss due to pseudo
diffusion. However, this approach gave a breakdown
voltage 20% lower than the measured value.
Let us analyse the effect of the electron pseudo
diffusion on RF breakdown under the conditions of the
experiment performed by Aints et al (1995). Based on the
observation of time-resolved avalanche current waveforms,
Wetzer and Wen (1991) derived the apparent rates of
electron detachment from short-lived negative ions and
conversion of short-lived negative ions into long-lived ions
in air as functions of E/N and gas pressure. These data
show that the conditions used by Aints et al correspond
to 1. A similar result ( 0.5) follows from a
study by Akishev et al (1994) of the spatial structure of a
glow discharge in atmospheric-pressure dry air; they have
shown that the O
2
and O
3
ions as long-lived ion species.
The above estimates of are inconsistent with
inequality (18); that is, the electron pseudo diffusion
has little or no effect on RF breakdown in air, but,
more importantly, the concept of pseudo diffusion fails
in air because of slow electron detachment from short-
lived negative ions. This contradicts the interpretation of
experimental data by Aints et al (1995). Our estimates
1406
Comment
show that the observations by Aints et al (1995) can be
interpreted (without pseudo diffusion) in terms of electron
detachment which partially compensates for the loss of
electrons due to attachment to molecules. This effect
is described by the second term on the right-hand side
of equation (12). Unfortunately, this approach fails to
calculate the breakdown voltage in air exactly because of
the uncertainty in the rates of ionmolecule reactions.
However, the inuence of electron pseudo diffusion
on high-frequency breakdown can become more important
as the rate of electron detachment increases. This can
be observed for repetitive breakdown in air when a
substantial number of active neutral particles such as
O atoms, radicals and electronically excited molecules
are accumulated from impulse to impulse (Kozlov and
Kudravtsev 1985). Collisions between active particles
and negative ions result in fast electron detachment in air
(Kossyi et al 1992). Another way of increasing the rate of
electron detachment in air is to heat the gas to 1000 K.
This leads to fast electron detachment from the O
2
ion
(Massey 1976, Aleksandrov 1986).
High-frequency breakdown can also be controlled by
electron pseudo diffusion in N
2
O. In this case at the
breakdown voltage electrons attach to the N
2
O molecules
due to the process (Massey 1976)
e +N
2
O O
+N
2
followed by the fast processes (Parkes 1972, Meek and
Craggs 1978, Aleksandrov and Konchakov 1992)
O
+N
2
O NO
+NO
and
NO
+N
2
O e +NO +N
2
O.
The removal of the NO
+2N
2
O N
3
O
2
+N
2
O
and
NO
+N
2
O NO
2
+N
2
.
Therefore, O
and NO
2
and NO
2
ions as long-lived ions.
Then, the criterion of high-frequency breakdown in N
2
O
can be described by equation (12) where the pseudo
diffusion coefcient is given by equation (15).
A similar effect is anticipated to take place in gas
mixtures in which the dominant electron attachment
process results in the formation of O
if the mixture
contains components (NO, CO, H
2
, SO
2
, C
2
H
4
, etc) which
effectively destroy O