Temperature effect of metastable atom desorption from solid Ne by low-energy electron impact
We study the desorption of metastable atoms induced by electronic transitions in solid Ne by low energy electron impact. Time-of-flight spectra and the angular distribution of metastable atoms desorbed from the surface of an annealed sample show increased kinetic energy, higher signal intensity, a...
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| Zitieren: | Temperature effect of metastable atom desorption from solid Ne by low-energy electron impact / H. Kato, T. Tachibana, T. Hirayama // Физика низких температур. — 2012. — Т. 38, № 8. — С. 949-952. — Бібліогр.: 9 назв. — англ. |
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Kato, H. Tachibana, T. Hirayama, T. 2017-05-23T14:58:59Z 2017-05-23T14:58:59Z 2012 Temperature effect of metastable atom desorption from solid Ne by low-energy electron impact / H. Kato, T. Tachibana, T. Hirayama // Физика низких температур. — 2012. — Т. 38, № 8. — С. 949-952. — Бібліогр.: 9 назв. — англ. 0132-6414 PACS: 79.20.La, 71.35.Gg https://nasplib.isofts.kiev.ua/handle/123456789/117430 We study the desorption of metastable atoms induced by electronic transitions in solid Ne by low energy electron impact. Time-of-flight spectra and the angular distribution of metastable atoms desorbed from the surface of an annealed sample show increased kinetic energy, higher signal intensity, and a narrower angular distribution compared with those measured using an unannealed sample. These results are explained by considering the sample’s surface conditions in the framework of the cavity ejection mechanism. Our results for annealed solid Ne show that when the sample temperature increases from 5 to 7 K, the width of the angular distribution increases by about 10%. A simple trajectory calculation qualitatively reproduces our experimental results. One of us (T.H.) is grateful to Dr. Elena V. Savchenko for her valuable discussions and comments as well as continuous encouragement since we first met in 1994. This work was partially supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology, Japan, and by the Rikkyo University Special Fund for Research (Rikkyo SFR). en Фізико-технічний інститут низьких температур ім. Б.І. Вєркіна НАН України Физика низких температур Low Temperature Spectroscopy and Radiation Effects Temperature effect of metastable atom desorption from solid Ne by low-energy electron impact Article published earlier |
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Temperature effect of metastable atom desorption from solid Ne by low-energy electron impact |
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Temperature effect of metastable atom desorption from solid Ne by low-energy electron impact Kato, H. Tachibana, T. Hirayama, T. Low Temperature Spectroscopy and Radiation Effects |
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Temperature effect of metastable atom desorption from solid Ne by low-energy electron impact |
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Temperature effect of metastable atom desorption from solid Ne by low-energy electron impact |
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Temperature effect of metastable atom desorption from solid Ne by low-energy electron impact |
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Temperature effect of metastable atom desorption from solid Ne by low-energy electron impact |
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temperature effect of metastable atom desorption from solid ne by low-energy electron impact |
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Kato, H. Tachibana, T. Hirayama, T. |
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Kato, H. Tachibana, T. Hirayama, T. |
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Low Temperature Spectroscopy and Radiation Effects |
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Low Temperature Spectroscopy and Radiation Effects |
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2012 |
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English |
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Физика низких температур |
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Фізико-технічний інститут низьких температур ім. Б.І. Вєркіна НАН України |
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Article |
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We study the desorption of metastable atoms induced by electronic transitions in solid Ne by low energy electron
impact. Time-of-flight spectra and the angular distribution of metastable atoms desorbed from the surface of
an annealed sample show increased kinetic energy, higher signal intensity, and a narrower angular distribution
compared with those measured using an unannealed sample. These results are explained by considering the sample’s
surface conditions in the framework of the cavity ejection mechanism. Our results for annealed solid Ne
show that when the sample temperature increases from 5 to 7 K, the width of the angular distribution increases
by about 10%. A simple trajectory calculation qualitatively reproduces our experimental results.
|
| issn |
0132-6414 |
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https://nasplib.isofts.kiev.ua/handle/123456789/117430 |
| citation_txt |
Temperature effect of metastable atom desorption from solid Ne by low-energy electron impact / H. Kato, T. Tachibana, T. Hirayama // Физика низких температур. — 2012. — Т. 38, № 8. — С. 949-952. — Бібліогр.: 9 назв. — англ. |
| work_keys_str_mv |
AT katoh temperatureeffectofmetastableatomdesorptionfromsolidnebylowenergyelectronimpact AT tachibanat temperatureeffectofmetastableatomdesorptionfromsolidnebylowenergyelectronimpact AT hirayamat temperatureeffectofmetastableatomdesorptionfromsolidnebylowenergyelectronimpact |
| first_indexed |
2025-11-27T04:18:14Z |
| last_indexed |
2025-11-27T04:18:14Z |
| _version_ |
1850799629869776896 |
| fulltext |
© Haruaki Kato, Takayuki Tachibana, and Takato Hirayama, 2012
Low Temperature Physics/Fizika Nizkikh Temperatur, 2012, v. 38, No. 8, pp. 949–952
Temperature effect of metastable atom desorption
from solid Ne by low-energy electron impact
Haruaki Kato1, Takayuki Tachibana2*, and Takato Hirayama1
1 Department of Physics, Rikkyo University, Nishi-Ikebukuro, Toshima-ku, Tokyo 171-8501, Japan
E-mail: hirayama@rikkyo.ac.jp
2 Department of Physics, Tokyo University of Science, Shinjuku-ku, Tokyo 162-8601, Japan
Received May 16, 2012
We study the desorption of metastable atoms induced by electronic transitions in solid Ne by low energy elec-
tron impact. Time-of-flight spectra and the angular distribution of metastable atoms desorbed from the surface of
an annealed sample show increased kinetic energy, higher signal intensity, and a narrower angular distribution
compared with those measured using an unannealed sample. These results are explained by considering the sam-
ple’s surface conditions in the framework of the cavity ejection mechanism. Our results for annealed solid Ne
show that when the sample temperature increases from 5 to 7 K, the width of the angular distribution increases
by about 10%. A simple trajectory calculation qualitatively reproduces our experimental results.
PACS: 79.20.La Photon- and electron-stimulated desorption;
71.35.Gg Exciton-mediated interactions.
Keywords: metastable atom, desorption, electronic transition, time-of-flight spectra.
1. Introduction
Desorption induced by electronic transitions (DIET) in
rare gas solids by elementary excitation has been investi-
gated over the past 20 years [1]. Cavity ejection (CE) is
one of the mechanisms that leads to excited atom desorp-
tion such that an excited atom created on the surface of the
solid by incident electrons or photons is repelled by sur-
rounding atoms in the ground state and desorbs from the
surface. When this mechanism is applicable, desorbed ex-
cited atoms are expected to show a narrow angular distri-
bution that is concentrated near the surface normal direc-
tion. In real samples, this narrow angular distribution may
become broader because of either imperfections in the
crystal or lattice vibration, or both.
Sakurai et al. [2] measured the angular distribution of
metastable atoms desorbed from the surface of solid Ne by
low energy photon irradiation. They succeeded in qualita-
tively reproducing their experimental results using a simple
trajectory calculation.
To observe the effects caused by conditions of the sam-
ple surface as well as those owing to lattice vibration, we
measured time-of-flight spectra and the angular distribu-
tion of atoms desorbed from the surfaces of unannealed
and annealed samples at various temperatures. We will
discuss the results within the framework of the CE mecha-
nism, and we also performed a simple trajectory calcula-
tion of desorbed excited Ne atoms.
2. Experimental setup
Figure 1 shows a side view of the experimental setup,
which was similar to the one we used in our previous work
[3–5], except for the addition of a low-energy electron gun
and a channel electron multiplier (CEM) for the detection
of desorbed metastable atoms. The main chamber was
evacuated by a series of turbo molecular pumps and a Ti-get-
ter pump, resulting in a pressure of approximately 3·10–8 Pa.
The sample film was prepared on a polycrystalline Cu
disk of 10 mm diameter, which was fixed to a mechanical
cryostat and cooled down to 5.0 K. The cryostat was sur-
rounded by a heat shield that was kept at about 40 K.
The cryostat can be rotated without breaking the vacuum,
which enables us to measure the angular distribution of de-
sorbed particles. The sample film was condensed on the Cu
disk by filling the chamber with gaseous Ne to a pressure
of 10–6–10–4 Pa. The film thickness was estimated from the
exposure assuming a condensation coefficient to be unity.
* Present address: Department of Physics, Rikkyo University, Nishi-Ikebukuro, Toshima-ku, Tokyo 171-8501, Japan
Haruaki Kato, Takayuki Tachibana, and Takato Hirayama
950 Low Temperature Physics/Fizika Nizkikh Temperatur, 2012, v. 38, No. 8
The temperature of the sample was controlled in the
range between 5 and 100 K by a heater mounted in the
cryostat. The temperature stability during the measure-
ments was 0.1± K. The sample temperature was measured
using a Si-diode (LakeShore, DT-670A-SD) attached to
the Cu substrate. Solid Ne was formed at a substrate tem-
perature of 5.0 K, and was annealed at 7.0 K.
An electron gun, which produces an electron beam with
an energy between 17 and 100 eV, was fixed to the heat
shield, so that the incident angle of the electron beam to
the sample surface was fixed during the measurements of
the angular distribution. For our measurements of the time-
of-flight spectra, the electron beam was pulsed by applying
a pulsed voltage to the first grid of the electron gun. The
width and frequency of the pulsed beam were approxi-
mately 10 μs and 500 Hz, respectively.
Desorbed metastable atoms were directly detected by
a CEM that was fixed to the chamber wall. The distance
between the sample and the CEM was 287 mm. The life-
times of the Ne metastable states (2p53s 3P0.2) are known to
be much longer than the flight time in the present experi-
ments (typically less than 1 ms). Desorbed ions and emit-
ted electrons were rejected by applying a positive voltage
to the grid mesh in front of the CEM and a negative volt-
age to the entrance funnel of CEM, respectively.
3. Experimental results
3.1. Time-of-flight spectra
Figure 2 shows the time-of-flight spectra of metastable
atoms desorbed from the surface of solid Ne measured at
the sample normal direction (θ = 0°). The incident electron
energy was 30 eV and the sample thickness was 300 atom-
ic layers. The strongest peak at flight time tf = 0 is caused
by the emitted VUV light from the sample. The higher
kinetic energy peak (tf ~
80 μs, Ek = 1.4 ± 0.1 eV) is owing
to metastable Ne atoms that are desorbed through the
excimer dissociation (ED) process. The peak at tf ~ 210 μs
(Ek = 0.18 ± 0.02 eV) is caused the cavity ejection (CE)
mechanism.
Figure 2 shows that the CE peak of the annealed sample
(solid line) exhibits a higher intensity. A slight increase of
the kinetic energy (~
0.6%) was also observed in the spec-
trum of the annealed sample. The kinetic energy did not
change in the spectra of the annealed sample measured at
temperatures between 5.0 and 7.0 K within the experi-
mental statistical uncertainties.
3.2. Angular distribution
The time-of-flight spectra measured at θ = 0, 10, and
20° from the sample normal direction are shown in Fig. 3.
The intensity of the CE peak significantly decreases as the
angle increases. The CE peak area as a function of obser-
vation angle (angular distribution) is plotted in Fig. 4. This
clearly shows that the sample that annealed at 7.0 K (open
circles) exhibits a narrower angular distribution than the
unannealed sample (solid circles).
The angular distribution of the CE peak area of the an-
nealed sample was measured as a function of temperature.
The temperature dependence of the full width at half max-
imum (FWHM) of the distribution is shown in Fig. 5. The
FWHM increases by approximately 10% when the sample
temperature increases from 5.0 to 7.0 K.
Fig. 1. (Color online) Schematic of the experimental setup (side
view).
Si Diode
Solid Ne/Cu
CEM
Mechanical
Cryostat
Heat Shield
30 mm Electron Gun
Fig. 2. (Color online) Time-of-flight spectra of metastable atoms
desorbed from the surface of solid Ne measured in the sample
normal direction (θ = 0°). The incident electron energy was
30 eV and the thickness of the sample was 300 atomic layers. The
solid line and dots represent the spectra from annealed and
unannealed Ne solid, respectively.
In
te
ns
ity
, a
rb
. u
ni
ts
0 100 200 300 400 500
Without annealing
With annealing at 7.0 K
Temperature effect of metastable atom desorption from solid Ne by low-energy electron impact
Low Temperature Physics/Fizika Nizkikh Temperatur, 2012, v. 38, No. 8 951
4. Annealing effect
Our results for the time-of-flight spectra and the angular
distribution indicate that
– the signal intensity detected in the sample normal di-
rection increases in the annealed sample,
– the angular distribution of the unannealed sample is
broader than that of the annealed sample, and
– the kinetic energy of the desorbed metastable atoms
increases in the annealed sample.
The motive force associated with desorption through
the CE mechanism is the repulsive force from ground state
atoms surrounding the excited atom, which should be axi-
ally symmetric around the sample normal direction. The
desorbed excited atoms should, therefore, exhibit a narrow
angular distribution towards the sample normal direction,
as observed in the present study. If the surface is rough, as
shown in Fig. 6,a, which is the case if the sample is formed
at low temperatures, atoms desorb in the direction normal
to the local surface. This results in a broadening of the
angular distribution, as seen in Fig. 4. This also explains
why the signal intensity detected in the sample normal di-
rection increases when the sample is annealed.
Cui et al. pointed out, based on molecular dynamics
calculations [6], that the kinetic energy of excited atoms
desorbed from the surface of solid Ar increases as the
number of surrounding atoms increases. It can be reasona-
bly assumed that the number of surrounding atoms in the
annealed sample — see Fig. 6,b — is larger than that in the
unannealed sample: see Fig. 6,a. Therefore we attribute the
increase in the kinetic energy in the annealed sample to the
flatness of the sample surface, i.e., the average number of
atoms surrounding the excited (desorbing) atom.
Fig. 3. (Color online) Time-of-flight spectra of metastable atoms
desorbed from the surface of annealed solid Ne measured at
θ = 0, 10 and 20°. The incident electron energy was 30 eV and
the thickness of the sample was 300 atomic layers.
θ = 0°
θ = 10°
θ = 20°
0 100 200 300 400 500
In
te
ns
ity
, a
rb
. u
ni
ts
Flight time, sμ
Fig. 4. (Color online) Angular distribution of desorbed metastable
Ne atoms through the CE mechanism. Solid and open circles are
the results measured with an unannealed sample and a sample
annealed at 7.0 K, respectively. Solid lines are the best-fitting
curves using a Gaussian fitting function.
In
te
ns
ity
, a
rb
. u
ni
ts
Angle, deg.
–40 –20 0 20 40
Without annealing
With annealing at 7.0 K
FW
H
M
, d
eg
34
33
32
31
30
29
28
Measurements
Simulation
18.4
18.2
18.0
17.8
18.6
W
id
th
, d
eg
5.0 5.5 6.0 6.5 7.0
Sample temperature, K
Fig. 5. (Color online) FWHM of the angular distribution of de-
sorbed metastable Ne atoms through the CE mechanism as a func-
tion of the sample temperature (solid circles). The solid line is the
result of our simple trajectory calculation. See text for details.
Fig. 6. (Color online) Schematic of the surface of the unannealed
(a) and the annealed (b) sample. Solid circles represent Ne atoms
and the arrows point in the direction of the desorption through the
CE mechanism. See text for details.
a b
Unannealed sample Annealed sample
Haruaki Kato, Takayuki Tachibana, and Takato Hirayama
952 Low Temperature Physics/Fizika Nizkikh Temperatur, 2012, v. 38, No. 8
5. Temperature effect
The present results show that the width of the angular
distribution becomes broader as the sample temperature
increases. Sakurai et al. [2] pointed out, based on their
simple trajectory calculation, that the angular spread can-
not be explained by the zero-point energy of the atom at
the lattice point alone, but it is essentially caused by vibra-
tional displacement of Ne atoms around the lattice point.
Therefore we attribute the broadening of the angular distri-
bution at higher sample temperatures to an increase in the
vibrational amplitude. To confirm this idea, we performed
a simple trajectory calculation, which will be discussed
below.
6. Trajectory calculation
The trajectory of desorbing excited atoms that are cre-
ated at the (111) surface of solid Ne is calculated as de-
scribed in [2]. Briefly, an excited Ne atom in the
2p53s (1P1) state is surrounded by atoms in the ground
state (1S0). The potential surface around the excited atom is
calculated by superposition of the pair potential between
the excited atom and the ground state atoms. The potential
between ground state atoms is calculated using the Len-
nard-Jones 6–12 potential, and that between Ne* (1P1) and
Ne (1S0) is calculated based on the theoretical results of
Kunsch and Coletti [7]. Ground state atoms within a dis-
tance equal to twice the lattice constant (36 atoms) are in-
cluded in the potential calculation. It is assumed that the
ground state atoms do not move during desorption of the
excited atom.
The potential thus calculated is inserted into a SIMION
potential array file [8]. The trajectory of a desorbing excit-
ed Ne atom is calculated by placing a positive ion with a
kinetic energy E0 at a distance R(T) from the lattice point.
R(T) is estimated as
3
0 22( )
( )
E kT
R T
K
+
=
and K is a constant calculated using
2
0 0
1
2
Kx E= ,
where x0 = 0.032 nm and E0 = 0.01 eV are the mean square
amplitude and the energy of the zero-point vibration in
the Ne crystal, respectively [9]. Ions are distributed along
a circle of radius R(T) at intervals of 15° and the direction
of the initial motion is towards and outwards from the cen-
ter of the circle, i.e., the lattice point.
The calculated angular spread as a function of tempera-
ture is shown as the solid line in Fig. 5. Although the cal-
culated angular spread is about 60% of the measured
FWHM, our calculation qualitatively reproduces the exper-
imental temperature dependence.
7. Summary
We have measured the time-of-flight spectra and the
angular distribution of metastable Ne atoms desorbed from
the surface of annealed and unannealed solid Ne at temper-
atures between 5.0 and 7.0 K by low energy electron im-
pact. The dependence on the sample surface conditions and
temperature found in the present work are well explained
in the framework of the CE mechanism. A simple trajecto-
ry calculation qualitatively reproduced the results obtained
here.
Acknowledgments
One of us (T.H.) is grateful to Dr. Elena V. Savchenko
for her valuable discussions and comments as well as con-
tinuous encouragement since we first met in 1994. This
work was partially supported by a Grant-in-Aid for Scien-
tific Research from the Ministry of Education, Culture,
Sports, Science and Technology, Japan, and by the Rikkyo
University Special Fund for Research (Rikkyo SFR).
1. For recent review, see T. Hirayama and I. Arakawa, J. Phys.
Cond. Matter 18, S1563 (2006) and references therein.
2. J. Sakurai, T. Nagai, M. Abo, T. Hirayama, and I. Arakawa,
J. Vac. Soc. Jpn. 38, 414 (1995).
3. S. Fujita, K. Fukai, T. Tachibana, T. Koizumi, and T. Hira-
yama, J. Phys. Conf. Ser. 163, 012083 (2009).
4. K. Fukai, S. Fujita, T. Tachibana, T. Koizumi, and T. Hira-
yama, J. Phys. Cond. Matter 22, 084007 (2010).
5. T. Tachibana, K. Fukai, T. Koizumi, and T. Hirayama, J.
Phys. Cond. Matter 22, 475002 (2010).
6. S. Cui, R.E. Johnson, and P. Cummings, Phys. Rev. B39,
9580 (1989).
7. P.L. Kunsch and F. Coletti, J. Chem. Phys. 70, 726 (1979).
8. http://simion.com/
9. H.R. Lyde, in: Rare Gas Solid, M.L. Klein, and J.A. Ven-
ables (eds.), Academic Press, London (1976), Vol. 1, p. 382.
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