In-source laser spectroscopy of isotopes far from stability (ISOLDE, CERN & IRIS, PNPI) Anatoly...
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Transcript of In-source laser spectroscopy of isotopes far from stability (ISOLDE, CERN & IRIS, PNPI) Anatoly...
In-source laser spectroscopy of isotopes far from stability
(ISOLDE, CERN & IRIS, PNPI)
Anatoly BarzakhPNPI
IS 511: Shape coexistence in the lightest Tl isotopes studied by laser
spectroscopy
IS 534:Beta-delayed fission, laser spectroscopy
and shape-coexistence studies with radioactive 85At beams
IS 534 (addendum):Laser spectroscopy
and shape-coexistence studies with radioactive 79Au beams
Shape Coexistence in the Lead Region studied by laser resonance spectroscopy
• A collaboration of ~30 atomic and nuclear physicists•12 institutions
ISOLDE
Preliminary results for At and Au isotopes!
Magnetic moments, hyperfine structure anomaly and mean squared charge radii of neutron deficient Tl isotopes
IRIS
Isotope/isomer shift1 ppm
A,Z A-1,Z
Laser beams
Experiments
Mass separation
Target Hot Cavity Extractor Ion Source
Reaction products(neutral)
IonsProtonsTarget material
60 kV
Laser Ion Source at ISOLDELaser Ion Source at ISOLDE
•Isotope shift (IS), hyperfine structure (HFS) measurements: The wavelength of the narrow-band laser is scanned across the chosen transition. The photoion current at the collector of the mass separator increases at the resonance. •Detection of photoion current by measuring FC current, or ToF spectra while scanning the frequency
Laser beams
Mass separatorprotons target
ion source
Laser Ion Source at IRISLaser Ion Source at IRIS
A substantial increase of the ionization efficiency can be achieved by decreasing of the inner diameter of the laser ion source tube with a corresponding focusing of the laser beam inside. At IRIS facility the laser spot as low as 1 mm in diameter can be provided due to a lens, placed in a distance of 2 m from the ion source
Detection: Windmill System at ISOLDEDetection: Windmill System at ISOLDE
Annular Si Si
pure 50 keV beam from RILIS+ISOLDE
Setup: Si detectors from both sides of the C-foil
• Large geometrical efficiency (up to 80%)• 2 fold fission fragment coincidences• ff-γ, γ-α, γ-γ, etc coincidences
C-foils20 mg/cm2 Si detectors
50 keV beam from ISOLDE
SiAnnular Si
ff
ff
C-foil
MINIBALL Ge cluster
A. Andreyev et al., PRL 105, 252502 (2010)
The WM technique requires waiting for the decay of the isotope (usually, α-decay). Not practical for long-lived or stable isotopes (or for β-decaying).
R. N. Wolf et al., Nucl. Instr. and Meth. A 686, 82-90 (2012), S. Kreim et al., INTC-P-299, IS 518 (2011)
Multi-reflection time-of-flight mass separator (MR-ToF MS)
Detection: MR-ToF MS at ISOLDE
~1000 revolutions, ~35 ms, m/Δm ~ 105
MR-ToF MS is not limited by decay scheme or long half-lives MR-ToF MS offers a way to separate background for direct single-ion detection using MCP (time scale: tens of ms).
Tape driving device
2(2 1) (2 1)
( )12 1
f i f fi f
i i
F F J F IS F F
F JI
JIJIJIFJIF
JJIIFFK
JIJI
JJIIKKB
KAF
FFFF iffi
,...,1|||,|,
)1()1()1(
)12()12(2
)1()1()1(75.0
2
0,
-10000 0 10000 20000 30000 40000
0
100
200
co
unt
I FC, p
A
, MHz
197Au, stable
200
600
1000
1400 179Au, T1/2
=7.1 s, E=5850 keVAmplitudes of the components:
Positions of the components:
)(1790 Au
)(1970 Au
Ji=1/2
Jf=1/2
F1=I-1/2
F2=I+1/2
F’1=I-1/2
F’2=I+1/2
0
F
QBA ,
Number of components and their relative intensities give the possibility to determine nuclear spin I
-10000 0 10000 20000 30000 40000
0
100
200
co
unt
I FC, p
A
, MHz
197Au, stable
200
600
1000
1400 179Au, T1/2
=7.1 s, E=5850 keV
IS
, ' , ' '( )
'A A A A
NMS SMS
A AF M M
A A
( / )NMS
p e
Mm m
93.0)(,2 AuKrK
Green Beams 90 W @ 532 nm
UV beam18 W @ 355 nm
10kHz rep rate6 - 8 ns pulses
RILIS upgradeRILIS upgrade
CVL to Nd:Yag
Laser ion source at ISOLDENd:YAG lasersDye lasersTi:Sa lasers
3 Ti:Sa lasers:5 GHz linewidthUp to 5 W output power680 – 1030 nm (fund.)35 ns pulse length
RILIS upgradeRILIS upgrade
Dye+Ti:Sa system
Since the two systems can be used either independently or in combination,there exists far greater flexibility for switching from one ionization scheme to another or rapidly changing the scanning step.
2 21/2 3/2
276.9 511 5786 6
nm nm nm
NBL CVLp P d D continuum
Isotope shift δ A,A’:
2, ’ , ’
- '
'A A A A
A AF r M
A A
J. A. Bounds et al., Phys. Rev. C36, 2560 (1987); R. Menges et al., Z. Phys. A341 (1992) 475; H. A. Schuessler et al., Hfi 74 (1992) 13
IS/hfs’s were previously measured for 535 nm transition with reliably established F and M for 186-207Tl:
2.4x107 2.8x107 3.2x107 3.6x107 4.0x1071.2x107
1.4x107
1.6x107
1.8x107
2.0x107
2.2x107
2.4x107
2.6x107
2.8x107
mg
m
A, A'
=A, A'
AA'/(A-A')
King plot for 535 nm and 277 nm lines in Tl
A
,205
(277
nm
)
A,205 (535 nm)
187m
203
207
191m189m
193m
190
186
188
192
194
g
Isotope shift δ A,A’:
2, ’ , ’
- '
'A A A A
A AF r M
A A
, ' , '
'
'A A A A
A A
A A
Δσ for different transitions should lie on thestraight line with a slope Fλ1/ Fλ2
F535nm, M535nm F277nm, M277nm
King plot
Electronic factor and mass shift Electronic factor and mass shift for 277 nm transition (IRIS)for 277 nm transition (IRIS)
183Tl, I=1/2, T1/2=6.9 s
184Tl, I=2, T1/2=11 s
185Tl, I=1/2, T1/2=19.5 s
185Tl, I=9/2, T1/2=1.8 s
183Tl, I=1/2, T1/2=6.9 s
184Tl, I=2, T1/2=11 s
183Tl, I=9/2, T1/2= 53 ms
184Tl, I=10, T1/2= 37 ms
180Tl, I=(4,5), T1/2=1.1 s
181Tl, I=1/2, T1/2=3.4 s
182Tl, I=(4,5), T1/2=3.1 s
179Tl, I=1/2, T1/2= 0.23 s
IRIS
IRIS & ISOLDE
ISOLDE
186Tl, I=10, T1/2= 2.9 s
195mTl, I=9/2, T1/2=3.6 s
197mTl, I=9/2, T1/2=0.54 s
Hyperfine structures observed for 184Tl with different detection modes
with frequency of the narrow-band laser fixed at the marked positions isomer selectivity is obtained and one can investigate properties of the pure isomer state
hfs of the previously unknown isomer (I=10)
ground state hfs
Isomer selectivity for Isomer selectivity for 184184Tl (ISOLDE)Tl (ISOLDE)
Shape coexistence and charge radii in Pb Shape coexistence and charge radii in Pb regionregion
?
85At?
2011: Tl isotopes: IS511 ISOLDE and IRIS (Gatchina)
Pb ISOLDE, PRL98, 112502 (2007) H. De Witte et al.
Po ISOLDE,T. Cocolios et al., PRL106, 052503 (2011)
Development and use of laser-ionized At beams at ISOLDE
• Determination of optical lines and efficient photoionization scheme. First measurement of the ionization potential of the element At
• Beta delayed fission of 194,196At
• Charge radii and electromagnetic moments measurement for At isotopes
At
Photoionization scheme for the radioactive element At
Optimal photoionization scheme.Narrow band lasers for 1st and 2nd transitions
216 nm
795 nm
532 nmIP
6p5, J=3/2
6p47s, J=3/2
6p48p(?), J=3/2 or 5/2
In collaboration with TRIUMF-ISAC radioactive ion beam facility with the TRILIS laser ion source
IP (At)=9.317510(84) eV 2 2
Mn
RIP E
n
Precise determination of the Ionization Potential for the radioactive element At
15410.9 15411.0 15411.1 15411.2 15411.3 15411.4
0
1000
2000
3000
4000
5000
6000 hfs for m.s. (I=10) hfs for g.s. (I=3)
, cm-1
N
198At15411.123pure g.s. (I=3)
15411.0 15411.1 15411.2 15411.3 15411.4 15411.5
0
200
400
600
800
1000
1200
1400
1600
1800
hfs for g.s. (I=9/2) hfs for m.s. (I=1/2)
N
, cm-1
197At15411.154pure g.s. (I=9/2)
Isomer selectivity enable ISOLTRAP team to measure masses of 197g,198gAt.Nuclear spectroscopic information for pure g.s. was obtained
IS534: Isomer selectivity for IS534: Isomer selectivity for 197,198197,198AtAt
IS534: Astatine HFS spectraIS534: Astatine HFS spectra
1st step scanning is better for Δ<r2> extraction2nd step scanning is better for hfs resolution (Q and μ determination). But to decipher these hfs’sone should know J for 58805 cm-1 level (5/2 or 3/2)
2, ’ , ’
- '
'A A A A
A AF r M
A A
216 nm
795 nm
532 nmIP
-5000 0 5000 10000 15000
0
100
200
300
400
500
600
700
800
N
, MHz
197At, I=1/2, 2nd step scan
The number of peaks (4 rather than 3) unambiguously points to J=3/2 for 58805 cm-1 atomic state in At
IS534:IS534: Additional atomic spectroscopic information Additional atomic spectroscopic information
for Astatinefor Astatine
216 nm
795 nm
532 nmIP
58805 cm-1, J=3/2 or 5/2
J=3/2
J=3/2
F1=1
Jf=5/2
F2=2
F’1=2
F’2=3
Ji=3/2
I=1/2
Jf=3/2
F1=1
F2=2
F’1=1
F’2=2
Ji=3/2
795 nm
-5.0E+07
-4.0E+07
-3.0E+07
-2.0E+07
-1.0E+07
0.0E+00
0.0E+00 2.0E+07 4.0E+07 6.0E+07
A,205(795nm) A
,20
5 (2
16
nm
)
197g
197m
207
198g198m
217
, ' , '
'
'A A A A
A A
A A
Isotope shift δ A,A’:
2, ’ , ’
- '
'A A A A
A AF r M
A A Δσ for different transitions should lie on a straight line with a slope Fλ1/ Fλ2
King plot for 216 nm and 795 nm lines King plot for 216 nm and 795 nm lines in Atin At
F216/F795(At)=-2.26(8)
compare with F256/F843(Po)=-2.241(7)for similar transitions in Po
IS534IS534 October 2012:October 2012:Charge radii of At isotopesCharge radii of At isotopes
WM
WM
MR-ToF
FC
108 110 112 114 116 118 120 122 124 126 128 130 132 134
-0.6
-0.4
-0.2
0.0
0.2
0.4
0.6
0.8
1.0
Po At At isomers
<r2 >
N,1
26, f
m2
N
Astatine seems to follow Polonium δ<r2> trend — i.e. there is the same early onset of deformation after N=113. Data for lighter isotopes are necessary to verify this conclusion
October 2012:October 2012:IS534 experiment at ISOLDE – Au IS534 experiment at ISOLDE – Au
isotopesisotopes
•Are the light Au isotopes deformed?
•What are the spins of ground and isomeric states?
267.7 nm
306.6 nm
674.1 nmIP
autoionizing state
Au ionization scheme
Au hfs spectraAu hfs spectra
F1=0
Jf=1/2
F2=1
F’1=0
F’2=1
Ji=1/2
I=1/2
0—>0 transition is forbidden!
Only 3 rather than usual 4 peaks will be seen in the hfs spectra of isotopes with I=1/2 (for I=3/2 — 4 peaks)
F’2
F’1
F1
F2
Is it possible to discriminate between I=1/2 Is it possible to discriminate between I=1/2 and I=3/2 for Au isotopes by hfs spectra?and I=3/2 for Au isotopes by hfs spectra?
IS534: Hyperfine Structure Scans for 177,179Au
179Au (WM)
179Au 3/2+ calculated179Au 1/2+ calculated
177Au (WM)
Number of peaks and their intensities ratiofix ground state spins of 177,179Au: I=1/2
Why is 1/2+1/2+ 181Tl177Au decay hindered?
Plot from A.Andreyev et al., PRC 80, 024302 (2009)
1/2+
1/2+
~1.6N , pure sph. 3s1/2, (as in the heavier Tl’s)
~1.1N , (preliminary) mixed/def/triaxial 3s1/2,/d3/2
HF>3 I=3/2
Summary: Charge Radii in Pb regionSummary: Charge Radii in Pb region
• At seems to follow Po unusual δ<r2> trend• “Back to sphericity” in the lightest Au isotopes• Magnetic/quadrupole moments will be deduced• Large amount of by-product nuclear spectroscopic information on At and Au and their daughter products
1. IS’s and hfs’s for 10 At isotopes (isomers) were measured for two transitions, 216 nm and 795 nm, The fast switching between these modes of scanning provides much more flexibility to experiment and gives more reliable and complementary data for analysis (especially for atoms without known spectroscopic information).
2. MR-ToF mass separator was used for photo-ions detection for the first time. This method seems to be indispensable for measurements with great surface ionized background and for long lived isotopes with great yield and/or absence of alpha decay mode.
3. Using WM installation for photo-ions detection gives the possibility to obtain wealth of additional nuclear spectroscopic information (decay schemes, spin and parity assignment etc.) without supplementary time requirement.
4. Coordinated (ISOLDE&IRIS) program for Tl isotopes investigation enabled us to use both installation more efficiently.
5. Very interesting results for At and Au isotopes by IS/hfs measurements were obtained: “inverse jump of deformation”, unexpected spin assignments, shape isomers etc. The study of shape coexistence in the lead region will be continued: to go further for Au’s, to fill the gaps and go further for At’s (ISOLDE), to investigate Bi isotopes (IRIS), etc.
Conclusions
5000
10000
15000
0
400
800
1200
0400800
1200
0200400600
1000
2000
3000
-12000 -9000 -6000 -3000 0 3000 6000 9000 120000
50010001500
A=191m, I=9/2E= 265, 326 keV
T1/2= 313 s
A=193m, I=9/2E= 365 keV
T1/2=127 s
A=195m, I=9/2E=384 keV
T1/2=3.6 s
(MHz)
coun
tsco
unts
coun
tsco
unts
IS
A=197m, I=9/2E=386 keV
T1/2=0.54 s
coun
tsI FC
, arb
. uni
ts
A=205, I=1/2Faraday cupstable isotope
A=189m, I=9/2E= 216 keV
T1/2= 84 s
Hyperfine structure anomaly for Au isotopesHyperfine structure anomaly for Au isotopes
,22
11
2211 , Aln
AlnA
lnln a
a )()(1 2211
,
, 2121
2
2211
1
221122
2
11
1lnln AAAA
Alnln
Alnlnln
AlnA
)1()(
)(0
00
0
Anl
A
A
A
A
AAA nla
nla
I
I
IRIS: 30 new 189Hg γ-lines from 189mTl decay are unambiguously identified by hfs patternand their relative intensities are determined
Additional nuclear spectroscopic information Additional nuclear spectroscopic information from Tl isotopes decayfrom Tl isotopes decay
ISOLDE: decay schemes for some Tl isotopesare determined
183Tl, I=1/2, T1/2=6.9 s
184Tl, I=2, T1/2=11 s
185Tl, I=1/2, T1/2=19.5 s
185Tl, I=9/2, T1/2=1.8 s
186Tl, I=10, T1/2=2.9 s
195Tl, I=9/2, T1/2=3.6 s
197Tl, I=9/2, T1/2=0.54 s
…
186Tl, I=7, T1/2=27.5 s
187Tl, I=9/2, T1/2=15.6 s
188Tl, I=7, T1/2=71 s
190Tl, I=7, T1/2=3.7 m
189Tl, I=9/2, T1/2=84 s
190Tl, I=2, T1/2=2.6 m
191Tl, I=9/2, T1/2=5.2 m
192Tl, I=7, T1/2=10.8 m
192Tl, I=2, T1/2=9.6 m
194Tl, I=7, T1/2=32.8 m
193Tl, I=9/2, T1/2=2.1 m
194Tl, I=2, T1/2=33 m
203Tl, I=1/2, stable
207Tl, I=1/2, T1/2=4.77 m
repeated for another atomic transition
(276.9 nm)
for King-plot calibration
21/26p P 2
3/26d Dpreviously measured for
23/26p P 2
1/27s S
transition (535.2 nm)