Click here to load reader
Upload
y-sato
View
216
Download
1
Embed Size (px)
Citation preview
Charge fraction of 6.0 MeV/n heavy ions with a carbonfoil: Dependence on the foil thickness and projectile
atomic number
Y. Sato a,*, A. Kitagawa a, M. Muramatsu a, T. Murakami a, S. Yamada a,C. Kobayashi b, Y. Kageyama b, T. Miyoshi b, H. Ogawa b, H. Nakabushi b,
T. Fujimoto b, T. Miyata b, Y. Sano b
a National Institute of Radiological Sciences, Accelerator Physics and Engineering Division NIRS, 4-9-1 Anagawa-4-chome,
Inage-ku, Chiba-shi 263-8555, Japanb Accelerator Engineering Corporation (AEC), 2-13-1 Konakadai, 263-0043 Chiba-Inage, Japan
Received 18 September 2002; received in revised form 5 December 2002
Abstract
We measured the charge fraction of 6.0 MeV/n heavy ions (C, Ne, Si, Ar, Fe and Cu) with a carbon foil at the NIRS-
HIMAC injector. At this energy they are stripped with a carbon foil before being injected into two synchrotron rings
with a maximum energy of 800 MeV/n. In order to find the foil thickness ðDEÞ at which an equilibrium charge state
distribution occurs, and to study the dependence of the DE-values on the projectile atomic number, we measured the exit
charge fractions for foil thicknesses of between 10 and 350 lg/cm2. The results showed that the DE-values are 21.5, 62.0,
162, 346, 121, 143 lg/cm2 for C, Ne, Si, Ar, Fe, Cu, respectively. The fraction of Ar18þ ions was actually improved to
33% at 320 lg/cm2 from �15% at 100 lg/cm2. For Fe and Cu ions, the DE-values were found to be only 121 and 143 lg/cm2; there is a large gap between Ar and Fe, which is related to the differences in the ratio of the binding energy of the
K-shell electrons to an electron energy (3.26 keV) corresponding to the velocity of a 6.0 MeV/n projectile. The well-
known ‘‘two disjoint Gaussians (shell effect)’’ was also observed in the measured charge fractions of both Fe and Cu.
The results of the charge fractions were also compared with other data and to calculations of Rozet et al. [2], in which
there was a good agreement for light ions (C); however, a significant difference was observed for ion species heavier than
Ne.
� 2003 Elsevier Science B.V. All rights reserved.
1. Introduction
At the NIRS-HIMAC injector [1], we measuredthe charge fraction of heavy ions after passing
though a carbon foil at an energy of 6.0 MeV/n,
which corresponds to a velocity of 15.1 atomic
units. In this energy region, few data concerningthe charge fraction have yet been reported, par-
ticularly for ions heavier than Ne; data are neces-
sary not only to design and operate accelerators,
but also to improve model calculations for heavy-
ion beam interactions in solids. Accelerators
*Corresponding author. Fax: +81-043-251-1840.
E-mail address: [email protected] (Y. Sato).
0168-583X/03/$ - see front matter � 2003 Elsevier Science B.V. All rights reserved.
doi:10.1016/S0168-583X(02)02225-5
Nuclear Instruments and Methods in Physics Research B 201 (2003) 571–580
www.elsevier.com/locate/nimb
usually require the highest charge states (which
occur at the equilibrium charge state distribution)
with the thinnest foils, which minimize the energy
loss, and multiple scattering and energy straggling.The results were also compared with those obtained
at other facilities and calculated results using a
computer program (ETACHA), which was devel-
oped by Rozet et al. [2], based on data using the
10–80 MeV/n heavy ions at GANIL; this calcula-
tion is applicable to ions lighter than Ar. The
lifetime of the foils has been long (the order of
year) since the beginning of the HIMAC opera-tion, because the energy loss within the foil is very
small in the 6.0 MeV/n region.
Beams of 8 keV/n heavy ions are produced at
three ion sources before being accelerated up to
6.0 MeV/n by both the RFQ (8–800 keV/n) and
Alvarez (0.8–6.0 MeV/n) linacs. Regarding the
high energy of heavy ions, fully stripped ions are
desirable for synchrotrons, except for a part ofatomic physics experiments; for example, the
measurement of convoy electrons ejected from
foils through an electron-loss process of relativistic
H-like or He-like ions. Information concerning the
fraction of fully stripped ions is thus particularly
important. When designing the HIMAC 10 years
ago, or earlier, there were few data and little in-
formation concerning the stripping efficiency atsuch a high-energy region. Nevertheless, a rough
estimation was made to start the HIMAC opera-
tion, based on few data and calculations. Conse-
quently, a thickness of around 100 lg/cm2 was
found to be appropriate for light ions, such as
carbon and neon; hence, this fixed thickness has so
far been used for other ion species without any
optimization regarding the efficiency. Precise in-formation on both the exit charge fraction and its
dependence on the foil thickness has still been
important, particularly for ion species heavier than
Ne, though systematic measurements have not yet
been performed, except for light ions or at low
energies. The primary motivation in this work was
to experimentally obtain such information; an
additional motivation was to compare the ob-tained results to advanced calculations [2,3]. In
addition, the HIMAC injector can produce vari-
ous ion species having the same velocity, thus al-
lowing us to study the relation between the foil
thickness at the equilibrium charge state distribu-
tion and the projectile atomic number.
Along recent progress in research projects using
various ion species at HIMAC, another interesthas been focused on the quantitative charge state
distribution and its impact on the maximum in-
tensity, particularly for ions heavier than Fe; in
such cases, the fraction of fully stripped ions is
very small in the stripping process with foils at the
6.0 MeV/n region, and are generally not useful. It
is thus necessary to find the highest charge state
and the thinnest foil.The apparatus uses the existing beam line be-
tween the carbon stripper just downstream of the
Alvarez linac and the experimental cave with
6.0 MeV/n heavy ions. The main modification was
to develop an automatic sweeping system for all
magnets and the debuncher (DBC) in this beam
line, according to the different charge states. In the
summer of 2001, the apparatus began to worksuccessfully. The expected data for several ion
species have been obtained for a thickness range of
between 10 and 350 lg/cm2 with some new results,
which are presented and discussed in this article.
For example, an increase in the thickness from 100
to 320 lg/cm2 allowed us to improve the yield of
Ar18þ ions by a factor of 2 with no reduction in
their transmission efficiency or in the injection ef-ficiency into the synchrotron.
2. Apparatus and methods
2.1. Layout of the apparatus
Fig. 1 shows a schematic layout of the appa-
ratus. The carbon stripper foil (CSF) is attached to
a frame of 20 mm diameter, and is set just down-
stream of the Alvarez linac, where the beam spot
size is around 5 mm diameter. The momentumresolution of this beam line is 1=20; 000 at maxi-
mum, which allows us to clearly separate the iso-
topes of Xe and to adjust the linac beam energy
precisely to 6.0 MeV/n for injection into the syn-
chrotron. The beams after passing through CSF
generally have several fractions with different
charge-to-mass ðq=mÞ ratios. They are analyzed by20� pulsed switching and 70� DC analyzing mag-
572 Y. Sato et al. / Nucl. Instr. and Meth. in Phys. Res. B 201 (2003) 571–580
nets before being measured at a Faraday cup (FC-
2) regarding their peak intensity (current). Sweep-
ing of the magnetic field (B) is controlled by a Hall
detector in the 70� analyzing magnet, thus cover-
ing the various q=m values. The other elements in
the beam-transport line between CSF and FC-2,
such as the Q-magnets and steering magnets, are
also swept in the same way. Since the maximumq=m value is limited to 1/4 in this beam line, the
low-charge-state ions after stripping cannot be
measured; for example, Ar1þ–Ar9þ ions cannot be
measured for the case of Ar. However, such ions
generally have very small fractions at 6.0 MeV/n,
which are negligible at the equilibrium thickness
and are of little interest in this work.
There is a horizontal slit just upstream of FC-2,of which the width is usually set at 10 mm to
separate the adjoining charge states. Since the
beam size is of the order of a few mm, the beam
current of each charge state, when sweeping the
beam across FC-2, was measured to be a trapezoid
shape, and its flat peak value is proportional to the
product of each charge fraction and the charge
state. The charge fraction can thus be obtainedfrom both the charge state and the ratio of each
peak to the total of all peak values. Fig. 2 shows an
example of the measured charge state distribution.
A capacitive pickup-type non-destructive beam
monitor (CTN) [4], also shown in Fig. 1, monitors
the beam intensity upstream of the Alvarez linac,
and is used to normalize the measured value at
FC-2. The fluctuation of the beam current is duemainly to that of the ion sources, which is nor-
mally on the order of �10%, and cannot be easily
reduced. The amplitude of signals from this CTN
is proportional to the peak beam intensity, be-
tween 5 and 1000 elA, while the actually used
beam intensity (50–500 elA in this work) was
within the limits. The width of the pulsed beam in
the HIMAC injector is 350 ls and its repetition
rate is 1–2 Hz. Since the response time of this CTNis faster than 1 ls, the precision in normalization
with this CTN should be satisfactory regarding
both the dynamic range and the response time.
The fluctuation in the transmission efficiency of
the Alvarez linac depends on neither the ion spe-
cies nor their intensity; it is normally constant at
92%, as long as the intensity is less than 500 elA.The use of CTN allows us to measure the chargefraction within an adequate accuracy.
2.2. Transmission efficiency (g) of beams in theapparatus
The transmission efficiency ðgÞ between FC-1
and FC-2 was measured in order to know the
beam loss in this beam line. Although this effi-ciency is independent of the charge fraction, it has
been an important parameter to study the beam
quality when using CSFs with different thicknesses
Fig. 1. Layout of the apparatus.
Fig. 2. Measured charge distribution for Ar with a carbon foil
(351 lg/cm2). The signal from the non-destructive current
monitor is also indicated, which represents the fluctuation in the
beam intensity.
Y. Sato et al. / Nucl. Instr. and Meth. in Phys. Res. B 201 (2003) 571–580 573
for various ion species. g was measured to be 90%
without CSF, and 85–88% with CSF, depending
on both the ion species and the thickness. The
beam loss ðDgÞ due to CSF can thus be evaluatedto be 2–5%, which is due mainly to an emittance
growth or an increase in the momentum spread
when using CSF. This Dg does not fluctuate
among fractions for one ion species using a par-
ticular thickness under an almost constant beam
intensity. Although the emittance value of the
beams from three ion sources varies widely, it is
always defined as being 150 pmm�mrad at theRFQ; this value is quite smaller than the accep-
tance of the Alvarez linac. The emittance of the
beams should thus be nearly constant at FC-1;
hereafter, a value of 90% ðgÞ should be applicable
to every ion species.
2.3. Measurement of the thickness of carbon strip-
per foils
Table 1 summarizes the thickness of the CSFs
used in this work. These CSF frames are attached
to a remote-controlled rotating device, with which
every thickness can be quickly selected. The
thickness of CSF measured by the maker was
compared to the measured value. Our method is to
measure the difference in the magnetic field (B)values of the 70� analyzing magnet between with
and without CSFs when tuning the N6þ beam on
the center of the multi-wire type profile monitor
just upstream of FC-2. B-values are precisely
measured by using a Hall detector, which is set
inside the analyzing magnet. Since the effective
curvature ðqÞ of the beam path through this
magnet is constant, we can know the difference inthe Bq-values ðDBq=BqÞ between with and withoutCSFs.
Since the Bq-value is proportional to the mo-
mentum of the beams (P ), we can finally know the
difference in the momentum of the beam DP=P .This difference is converted once into that of en-
ergy loss (2DP=P ¼ DE=E, E ¼ 6:0 MeV/n), and
then translated into thickness by using the stop-ping power table [5]. The precision of the profile
monitor is 0.1 mm, which corresponds to a reso-
lution in energy loss of 0.6 keV/n ðDE=E ¼1=10; 000Þ and in thickness of 2.9 lg/cm2. The
maker (Israel and Arizona) evaluated the thickness
by measuring the absorption of visible light for
foils thinner than �20 lg/cm2, or the weight for
thicker than �50 lg/cm2. The difference in thethickness between the two methods was �13 �þ19% for all used CSFs. Our method was carried
out under exactly the same condition in this work,
thus including some change in thickness, which
may have been produced in the processes of both
attachment to a frame and exposure to the actual
beams in the vacuum condition. The values mea-
sured by our method seem to be more reliable andare used for discussions in this work.
Here, we consider the energy reduction ratio
ðDE=EÞ between before and after CSFs, that is the
ratio of the energy loss of incident beams within
the foil to 6.0 MeV/n. The energy loss of a 6.0
MeV nitrogen ion within the foil was evaluated to
be 72 keV/n per 350 lg/cm2, which means an en-
ergy reduction ratio ðDE=EÞ of 1.2%; the energy is6.0 MeV/n before entering the CSFs, while it de-
creases to 5.93 MeV/n after passing through a CSF
with a thickness of 350 lg/cm2. The DE=E-valuesare roughly proportional to z2eff=m, where zeff is theeffective charge and m is the mass number. The
values of DE=E per 350 lg/cm2 are thus calculated
to be on the order of 1.0–3.5% for C–Cu ions,
where the zeff -values for C and Cu were estimatedto be 6.0 and 25.5, respectively. The effects pro-
duced by such energy reduction are included in our
data, though they are not significantly large to
discuss the charge state distributions of various ion
Table 1
Thickness of carbon foils used in this work (lg/cm2)
Catalog value Measured by the
maker
Measured in this
work
10 8.9 11
20 22.6 20
30 30.9 28
40 42.9 39
50 53.2 52
100 – 89
100 98.1 115
150 – 166
200 192 206
250 – 255
300 317 329
300 322 351
574 Y. Sato et al. / Nucl. Instr. and Meth. in Phys. Res. B 201 (2003) 571–580
species having the same velocity. A similar esti-
mation was made in our previous work on electron
emission from foils [6].
At present, the overall error in the measurementof the charge fraction is dominated by the reading
error in determining each fraction at FC-2, which
is better than 1% in the maximum fraction values
observed for each ion species.
3. Results and discussion
3.1. Charge state distributions
Figs. 3–8 show the charge fraction versus
thickness of the CSFs for various beams (C, Ne,
Si, Ar, Fe and Cu) at 6.0 MeV/n. The calculations
of Rozet et al. [2] are also directly shown by the
solid lines. Table 2 summarizes the relation be-
tween the ion species and their charge fractions inthe equilibrium charge state distributions. As can
be seen from Fig. 3 (C) and Table 2, the fractions
of C6þ and C5þ reach an equilibrium state at a
thickness larger than �20 lg/cm2, and are 97.86%
and 2.10%, which agree well with both Shima�sdata of 97.67% and 2.33% at 5.983 MeV/n [7], and
the calculated values of 98.10% and 1.90% at 6.0
MeV/n.
Fig. 3. Charge fraction versus thickness of the carbon foils for
the impact of 6.0 MeV/n C2þ ions. The solid lines are from the
calculations of Rozet et al.
Fig. 4. Charge fraction versus thickness of the carbon foils for
the impact of 6.0 MeV/n Ne4þ ions. The solid lines are from the
calculations of Rozet et al.
Fig. 5. Charge fraction versus thickness of the carbon foils for
the impact of 6.0 MeV/n Si5þ ions. The solid lines are from the
calculations of Rozet et al.
Y. Sato et al. / Nucl. Instr. and Meth. in Phys. Res. B 201 (2003) 571–580 575
For Ne–Ar ð106 z6 18Þ, however, the mea-
sured equilibrium charge state fractions of fullystripped ions were significantly smaller than those
of the calculated values in brackets: 83.50%
(86.80%) for Ne, 61.26% (70.31%) for Si and
35.15% (52.26%) for Ar. The differences between
our measurements and the calculations of Rozet
et al. [2] become large as the atomic number (z) ofincident ions increases. The fractions, except for
those of fully stripped ions, are also consistentwith these results. For Ar, Baudinet-Robinet�sanalysis [8] and Baron�s data [9] are quite differentfrom our data and the calculations of Rozet et al.
Concerning the mean charge ðhqiÞ of Ar, Baudi-net-Robinet and Baron showed that it is 16.71–
16.74, though our result (17.12) is smaller than the
calculations of Rozet et al. (17.40) by only 0.28.
Taking account of the good precision (<1%) in ourexperiment, the value of 17.12 should be the most
reliable for Ar. Generally speaking, for C–Ar the
calculations of Rozet et al. [2] are not very far from
our data, and his model calculation seems basically
correct, though the precision in the cross-sections
is somewhat unsatisfactory. Actually, his calcula-
tion was in good agreement with the data of 13.6
MeV/n Ar ions accelerated at GANIL; the prob-lem seems to be only in the precision of the cross-
sections.
Fig. 6. Charge fraction versus thickness of the carbon foils for
the impact of 6.0 MeV/n Ar8þ ions. The solid lines are from the
calculations of Rozet et al.
Fig. 7. Charge fraction versus thickness of the carbon foils for
the impact of 6.0 MeV/n Fe9þ ions. The solid lines are from the
calculations of Rozet et al.
Fig. 8. Charge fraction versus thickness of the carbon foils for
the impact of 6.0 MeV/n Cu10þ ions. The solid lines are the
calculations of Rozet et al.
576 Y. Sato et al. / Nucl. Instr. and Meth. in Phys. Res. B 201 (2003) 571–580
For Fe and Cu, the calculations of Rozet et al.[2] did not agree with our results regarding the
equilibrium charge fractions. For example, the
maximum charge fraction is 47.23% for Fe24þ in
the calculation, while it is 37.53% for Fe23þ in our
data; the charge state distribution is considerably
shifted to a higher charge state in the calculation.
hqi of our data is 23.09, while the calculated value
is 23.94; there is a big difference. A similar ten-dency can also be seen for the case of Cu. The
present calculation of Rozet et al. [2] cannot be
used for such heavy atoms.
3.2. DE-values at which the equilibrium charge state
distributions occur
The DE-values were derived by fitting a simpleexponential form of Fq ¼ Aq � Bq expð�t=tqÞ,where tq is the 1=e point of the curve, Aq equals the
equilibrium charge fraction of charge q, and Bq is
the fitting constant [10]. The equilibrium thicknessvalues, DE, are defined as the thickness t at whichFq equals 95% of its equilibrium value: Fq ¼0:95Aq. The obtained results of several fractions
show a similar value; for example for C, they were
calculated to be 21.5 and 21.4 lg/cm2 for 6þ and
5þ, respectively. In this case the average of these
two values was determined as the DE-value (21.5
lg/cm2). A similar technique was applied for otherion species. The finally determined DE-values are
listed in Table 2.
Fig. 9 shows the relation between the DE-values
and the atomic number, z, in which the obtained
DE-values from our data are 21.5, 62.0, 162, 346,
121 and 143 lg/cm2 for C, Ne, Si, Ar, Fe and Cu,
respectively, while those from the calculations of
Rozet et al. [2] are 26.1, 72.8, 212, 470, 147 and 147lg/cm2. A comparison between our data and the
calculation shows two clear tendencies: the DE-
values are smaller than those obtained in the
Table 2
Relation between the ion species (C, Ne, Si, Ar, Fe, Cu) and their charge fractions in the equilibrium charge state distributions
Ion species Charge fractions (%) hqi DE
C 4þ 5þ 6þThis work 0.04 2.10 97.86 5.98 21.5� 0.1
Rozet 0 1.90 98.10 5.98 26.1� 0.1
Shima 0 2.33 97.67 5.98
Ne 8þ 9þ 10þThis work 0.95 15.55 83.50 9.83 62.0� 0.3
Rozet 0.58 12.62 86.80 9.86 72.8� 1.4
Si 11þ 12þ 13þ 14þThis work 0 4.97 33.77 61.26 13.56 162� 1
Rozet 0 3.45 26.24 70.31 13.66 212� 15
Ar 13þ 14þ 15þ 16þ 17þ 18þThis work 0 0 1.55 19.27 44.03 35.15 17.12 346� 19
Rozet 0 0 0.51 11.12 36.11 52.26 17.40 470� 40
Baudinet-Robinet
model
0 1 9 26 46 18 16.71
Baron 0 0.81 6.99 29.94 42.08 20.18 16.74 75
Fe 19þ 20þ 21þ 22þ 23þ 24þ 25þ 26þThis work 0 0.78 5.36 20.76 37.53 29.15 5.66 0.76 23.09 121� 2
Rozet 0.69 5.35 24.35 47.23 20.13 2.25 23.94 147� 18
Cu 22þ 23þ 24þ 25þ 26þ 27þ 28þ 29þThis work 0.48 3.00 13.20 31.81 35.41 15.26 0.84 0 25.48 143� 9
Rozet 0.47 8.86 32.15 50.05 8.47 26.58 147� 10
The values listed above are the results from this work, other data and the calculated results by Rozet at 6.0 MeV/n, and Shima�s data at5.983 MeV/n. The mean charge ðhqiÞ and the DE-values (lg/cm2), at which the equilibrium charge state distributions occur, are also
listed.
Y. Sato et al. / Nucl. Instr. and Meth. in Phys. Res. B 201 (2003) 571–580 577
calculation for C–Ar, though the tendency of the
curve is not very different; there is not a significant
difference for Fe and Cu. In the case of C, there is
a small, but meaningful, difference between 21.5
and 26.1 lg/cm2. Judging from both such a sig-
nificant difference and a good agreement in the
equilibrium charge state distribution, one can tell
that the ratio of cross-sections between the elec-tron loss (ionization and excitation) and capture
used in the calculation seems to be basically cor-
rect; however, their absolute values are slightly
small, thus requiring many interaction events
(large thickness) to reach equilibrium. This ten-
dency is somewhat true for Ne–Ar.
As can also be seen in Fig. 9, the DE-values
increase monotonically from 21.5 to 346 lg/cm2
with increasing the atomic number z from z ¼ 6
(C) to z ¼ 18 (Ar), while it rapidly decreases down
to 121 and 152 lg/cm2 for Fe ðz ¼ 26Þ and Cu
ðz ¼ 29Þ. In the former case ðz6 18Þ, an equilib-
rium (charge state) condition is obtained when all
electrons, including those in the K-shell, are bal-
anced regarding loss and capture; it is possible to
efficiently remove all of these electrons, due totheir small binding energies. In the latter, however,
there is little possibility to remove the K-shell
electrons due to their large binding energies. In
this case, the equilibrium condition should be de-
termined primarily by the behavior (loss/capture)
of the L- and outer-shell electrons. Since their in-teraction cross-sections are much larger than those
of the K-shell electrons in the 6.0 MeV/n region,
charge state equilibrium is obtained at a small
thickness. In the rest frame of the projectile, the
speed of a 6.0 MeV/n projectile corresponds to an
electron energy of 3.26 keV. The binding energies
of K-shell electrons are of 4.3 keV for Ar, 9.0 keV
for Fe and 11.2 keV for Cu, respectively [11]. Forthe case of Fe and Cu, the energy of 3.26 keV is
too small to effectively remove the K-shell elec-
trons. For Ar, it is comparable to 4.3 keV; there is
a significant possibility to remove the K-shell
electrons of the Ar atom by the impact of target
electrons, resulting in a 35.15% fraction of Ar18þ.
The large gap between Ar and Fe in Fig. 9
suggests that the binding energy plays an impor-tant role in the process of electron loss and cap-
ture. The binding energy of the 2s1 electron in the
L-shell of the Cu atom is 2.523 keV, which is close
to that (2.569 keV) of the 1s1 electron in the K-
shell of the Si atom [11]. Meanwhile, the DE-values
of Si and Cu are 143 and 162 lg/cm2; there is a
reasonable consistency in the relation between the
binding energy and the DE-values. Additional in-terest is focused on the information for K–Mn
ð196 z6 25Þ, though very few data have so far
been reported, as far as we know. We will try to
obtain them, though this depends strongly on the
capability of the ion sources used to produce me-
tallic ions. Fig. 10 shows the equilibrium charge
state distributions for Fe and Cu, in which the
well-known ‘‘two disjoint Gaussians’’ (shell effect)can be seen for both Fe and Cu [12–15]. The
measured charge fractions of Fe are 5.66 at q ¼ 25
and 0.76 at q ¼ 26, while those on the Gaussian
(left-side solid curve) are 9.96 and 1.49. For Cu,
the fractions are 0.84 at q ¼ 28 and 0.00 at q ¼ 29,
while those on the Gaussian (right-side) are 3.07
and 0.25, respectively. The measured charge frac-
tions of the K-shell electrons are thus significantlysmaller than those on the Gaussians obtained for
the L-shell.
As can seen in Figs. 7 and 8 (Fe and Cu), the
maximum charge fractions were found to be
Fig. 9. Projectile atomic number z versus equilibrium thickness
at 6.0 MeV/n. � indicates our data point and � the calculationsof Rozet et al.
578 Y. Sato et al. / Nucl. Instr. and Meth. in Phys. Res. B 201 (2003) 571–580
37.53% and 35.41% for 23þ and 26þ (Li-likeions), at which the DE-values were 121 and 143 lg/cm2, respectively. According to these results, Fe23þ
ions are usually used for injection into the syn-
chrotron regarding the maximum intensity. Some
experiments require as large a momentum as pos-
sible, for which Fe24þ (He-like) ions are also used,
because their fraction is not small (29.15%). In the
HIMAC accelerator system, there is only onecharge exchange stripper at 6.0 MeV/n between the
Alvarez linac and the synchrotron rings. The mo-
mentum of the synchrotron beam is proportional
to q=m, thus depending on the charge state ðqÞafter CFS. From this point of view, Cu27þ ions are
also usable, of which the fraction is 15.26%.
4. Summary
We measured the charge fraction of heavy ions
after stripping with carbon foils at a projectile
energy of 6.0 MeV/n. The measured equilibrium
fractions of fully stripped ions for Ne–Ar
ð106 z6 18Þ were significantly smaller than those
of the calculations of Rozet et al. [2]. Althoughthese differences become large as the atomic
number ðzÞ of the incident ions increases, the cal-culations of Rozet are not very far from our data,
and his model calculation seems to be basically
correct. The precision in the cross-sections, how-
ever, is somewhat unsatisfactory at a projectile
energy of 6.0 MeV/n, except for C.
For C–Ar ð66 z6 18Þ, the thickness of theequilibrium charge state increased monotonically
from 21.5 to 346 lg/cm2 with increasing atomic
number, z, while it rapidly decreased to 121 and
143 lg/cm2 for Fe and Cu (z ¼ 26 and 29). In the
latter two cases, the equilibrium condition should
be determined by the behavior of the L- and outer-
shell electrons (shell effect); there is little possibility
to remove the K-shell electrons due to their largebinding energies (9 and 11 keV), compared to the
relative energy of the target electrons (3.26 keV) in
the rest frame of the projectile.
Acknowledgements
The authors would like to thank Prof. K. Shima(Tsukuba University), Dr. F. Soga (NIRS) and the
staff in the Division of Accelerator Physics and
Engineering (NIRS) for fruitful discussions on
atomic physics. This work was part of the research
project with heavy ions at NIRS-HIMAC.
References
[1] Y. Sato, T. Honma, T. Murakami, A. Kitagawa, M.
Muramatsu, S. Yamada, H. Ogawa, T. Fukushima, C.
Kobayashi, Proc. 20th Int. Conf. on Linac, Monterey in
CA, 2000, 654.
[2] J.P. Rozet, C. Stephan, D. Vernhet, Nucl. Instr. and Meth.
B 107 (1996) 67.
[3] J.P. Rozet, A. Chetiou, P. Piquemal, D. Vernhet, K.
Wohrer, C. Stephan, L. Tassan-Got, J. Phys. B: At. Mol.
Opt. Phys. 22 (1989) 33.
[4] T. Katoh, T. Murakami, S. Yamada, J. Yoshizawa, C.
Kobayashi, Y. Honda, S. Hara, in: Proc. 11th Symp. on
Accel. Sci. and Technology, Harima in Japan, 1997, p. 249.
[5] J.F. Ziegler, Hand Book of Stopping Cross-Sections for
Energetic Ions in All Elements, NY 10598, 1980, p. 93.
Fig. 10. Equilibrium charge state distributions for Fe and Cu.
Symbols of � and � indicate the fractions of L-shell electrons,
and � and j K-shell electrons for Fe and Cu, respectively. Two
disjoint Gaussians can be seen between the L-shell and K-shell
electrons for both Fe and Cu. The measured fractions of Fe are
5.66 at q ¼ 25 and 0.76 at q ¼ 26, while those on the Gaussian
(solid curves) are 9.96 and 1.49. For Cu, the fractions are 0.84
at q ¼ 28 and 0.00 at q ¼ 29, while those on the Gaussian are
3.07 and 0.25, respectively.
Y. Sato et al. / Nucl. Instr. and Meth. in Phys. Res. B 201 (2003) 571–580 579
[6] Y. Sato, A. Higashi, D. Ohsawa, Y. Fujita, Y. Hashimoto,
S. Muto, Phys. Rev. A 61 (2000) 052901.
[7] K. Shima, N. Kuno, M. Yamanouchi, Phys. Rev. A 40
(1989) 3557.
[8] Y. Baudinet-Robinet, Phys. Rev. A 26 (1982) 62.
[9] E. Baron, IEEE Trans. Nucl. Sci. NS-19 (1972) 256.
[10] S.K. Allison, Rev. Mod. Phys. 30 (1958) 1137.
[11] T.A. Carlson, C.W. Nestor, J.N. Wasserman, J.D. McDo-
well, Atomic Data 2 (1970) 63.
[12] K. Shima, T. Mukoyama, T. Mizogawa, Y. Kanai, T.
Kambara, Y. Awaya, Nucl. Instr. and Meth. B 53 (1991)
404.
[13] H.O. Funsten, B.L. Barraclough, D.J. McComas, Nucl.
Instr. and Meth. B 80–81 (1993) 49.
[14] L. H€aagg, O. Goscinski, J. Phys. B: At. Mol. Opt. Phys. 26
(1993) 2345.
[15] L. H€aagg, O. Goscinski, J. Phys. B: At. Mol. Opt. Phys. 27
(1994) 81.
580 Y. Sato et al. / Nucl. Instr. and Meth. in Phys. Res. B 201 (2003) 571–580