HAL Id: jpa-00227471
https://hal.archives-ouvertes.fr/jpa-00227471
Submitted on 1 Jan 1988
HAL is a multi-disciplinary open access archive for the deposit and dissemination of sci- entific research documents, whether they are pub- lished or not. The documents may come from teaching and research institutions in France or abroad, or from public or private research centers.
L’archive ouverte pluridisciplinaire HAL, est destinée au dépôt et à la diffusion de documents scientifiques de niveau recherche, publiés ou non, émanant des établissements d’enseignement et de recherche français ou étrangers, des laboratoires publics ou privés.
ULTRAVIOLET ABSORPTION OF REFRACTORY ELEMENTS BY A DUAL LASER PLASMA METHOD
J. Costello, W. Lynam, P. Carroll
To cite this version:
J. Costello, W. Lynam, P. Carroll. ULTRAVIOLET ABSORPTION OF REFRACTORY ELE-
MENTS BY A DUAL LASER PLASMA METHOD. Journal de Physique Colloques, 1988, 49 (C1),
pp.C1-243-C1-246. �10.1051/jphyscol:1988151�. �jpa-00227471�
JOURNAL DE PHYSIQUE
Colloque C1, SupplQment au n 0 3 , Tome 49, Mars 1988
ULTRAVIOLET ABSORPTION OF REFRACTORY ELEMENTS B Y A DUAL LASER PLASMA METHOD
J.T. COSTELLO, W.G. LYNAM* and P.K. CARROLL*
School of Physical Sciences, NIHED., Dublin 9, Republic of Irel and
'physics Department, University College, Dublin 4, Republic of Irel and
A b s t r a c t
-
The dual laser-produced plasma technique f o r t h e study o f i o n i c absorption spectra has been developed by t h e use o f two Q- switched ruby 1 asers t o enable independent generation o f t h e absorbing and b a c k - l i g h t i n g plasmas. O p t i c a l p u l s e handling i s used i n t h e c o u p l i n g c i c u i t s t o enable r e p r o d u c i b l e p u l s e delays from 250 nsec. t o 10 msec. t o be achieved. A t delay times > 700 nsec. spectra o f e s s e n t i a l l y pure n e u t r a l species a r e observed. The technique i s valuable, n o t o n l y f o r o b t a i n i n g t h e n e u t r a l spectra o f h i g h l y r e f r a c t o r y and/or c o r r o s i v e m a t e r i a l s b u t a l s o f o r studying behaviour o f i o n i c species as a f u n c t i o n o f time. Typical spectra a r e shown i n Fig. 1.I
-
INTRODUCTIONThe f i r s t experiment i n which a laser-produced continuum was used t o study t h e absorption spectra o f i o n s generated i n a second laser-produced plasma was c a r q e d o u t by C a r r o l l and Kennedy ( 1 ) i n 2 1977 t o r e c o r d t h e spectrum of L i
.
I n t h i s work t h e a u t o i o n i z i n g I s-
2snp resonances ( t h e analogue o f the Madden-Cod1 i ng s e r i e s o f he1 i urn) were observed and t h e i r p o s i t i o n and p r o f i l e s compared w i t h theory ( 2 ) . The success o f t h e technique depended on the a v a i l a b i l i t y o f c l e a n laser-produced c o n t i n u a ( 3 ) and on t h e s u i t a b i l i t y o f t h e pulsed source f o r synchronized o r time r e s o l v e d s t u d i e s (4). I n t h e o r i g i n a l experiment t h e o u t p u t o f a s i n g l e ruby l a s e r was d i v i d e d by a beam s p l i t t e r t o produce b o t h b a c k l i g h t i n g and absorbing plasma. A l i m i t e d degree o f t i m e r e s o l u t i o n was achieved by v a r y i n g t h e o p t i c a l path l e n g t h s and some c o n t r o l o f t h e absorbing species, i.e. i o n stage, by a d j u s t i n g t h e focus o f t h e beam generating t h e absorbing plasma+. The technique has since been a p p l i e d s u c c e s s f u l l y t o t h e spectrum o f Be where by t h e use o f r e l a t i v e l y l o n g p a t h l e n g t h s time delays up t o 70 nsec. were a t t a i n e d (5).I 1
-
TWO LASER SYSTEMI n s t e a d o f using a s i n g l e l a s e r and beam s p l i t t e r we have r e c e n t l y developed a two l a s e r system ( 6 ) which has t h e advantages o f ( a ) d e l i v e r i n g enhanced l a s e r power on each t a r g e t and ( b ) p r o v i d i n g a g r e a t e r range i n time r e s o l u t i o n . With the system i t i s p o s s i b l e n o t o n l y t o study v a r i o u s i o n stages b u t also, by u s i n g s u f i c i e n t l y l o n g time delays, t o observe absorption spectra o f n e u t r a l species f r e e from i o n i c c o n t a d n a t i o n . This i s p a r t i c u l a r l y u s e f y l i n studying r e f r a c t o r y o r c o r r o s i v e elements which are d i f f i c u l t o r impossible t o o b t a i n i n v a p o u r by more conventional methods. As an example we show i n Fig. 2 t h e 5 d - 5 , ~ f g i a n t resonance o f UI ( 7 ) together w i t h t h e t h e o r e t i c a l p r o f i l e as c a l c u l a t e d by Wendin (8).
S i m i l a r r e s u l t s were obtained f o r t h e analogous spectrum o f atomic t h o r i um which was observed i n absorption f o r t h e f i r s t time w i t h t h e new technique (6).
Article published online by EDP Sciences and available at http://dx.doi.org/10.1051/jphyscol:1988151
Fig 1. TIME-RESOLVED XUV ABSORPTION SPECTRA OF BERYLLIUM.BORON,SILlCON AND STRONTIUM PLASMAS. 1s-2p,3p Transitions.
60 65
2s2np ('PIMA)
Bell ls22s (2S)-l~2~~p (2~)1I
(1) 2CW/cm1,750ns. (b) Boron. Time Delay:500ns. (2) 2CW/cn-?,4OOnsI
2p-ns,nd Transitions.1 100 110
I120
I
85 90
(c)Silicon. Time Delay:250ns.A(A)
(d) Strontium.Time Delay:425ns.MA)
The experimental l a s e r system i s shown schematically in Fig 3. The two ruby l a s e r s ( n o t i d e n t i c a l ) a r e triggered so t h a t the pumping pulses peak simultaneously, (they may be o f f s e t i f delays
>1000 nsec. a r e required).
Part of the Q-switched output pulse of the l a s e r which generates the absorbing plasma i s passed through a variable time delay c i r c u i t and used to a c t i v a t e the Pockels c e l l u n i t of the second l a s e r . The output from both l a s e r s i s %1.5J i n 25 nsec. and the repetition r a t e of the system a s a whole i s limited by the performance of the slower l a s e r
(Q 1ppm). Inter- plasma delay times,
A t ,range from 250 nsec (our present minimum delay) t o 10 msec. For the l a r g e r
A tvalues
( >1000 nsec.) an appropriate delay i s introduced in the pumping pulses t o ensure t h a t maximum output i s available a t time of observation.
Theory F i g . 2. Absorption o f atomic
.
.
. . ..
. ..
U Atomic uranium i n the v i c i n i t yo f t h e 5d t h r e s h o l d .
Photon Energy (ev).
To improve the r e l i a b i l i t y of the original two l a s e r system ( 6 ) the timing electronics have been redesigned t o secure noise immunity. The current system uses a simp1 i f i e d trigger-pul s e delay generator, f i b r e optic coupling f o r the flash-tube t r i g g e r pulses and a high speed optical t r i g g e r u n i t t o a c t i v a t e the Pockels c e l l of the second l a s e r . As a r e s u l t a 100%
reproducibility in shot t o shot time delays has been achieved.
In Fig.
1we show spectra, some new, t o i l l u s t r a t e the c a p a b i l i t y of t h e system. In, t h e case of beryllium, a t a time delay of 400 nsec.
absorption of Be appears with our i n t e n s i t y comparable t o t h a t of the neutral [Fig. l a
(2,311whereas a t at
=750 nsec. [Fig. l a (111 i t i s absent except f o r a t r a c e of the 1s-2p t r a n s i t i o n which completely disappears a t s t i l l longer delays. In early work
(1)when only short time delays were available lower ion stages were favoured by defocusing the beam generating the .absorbing plasma but
w i t hthe new system t i g h t focusing [Fig.
1
(31, ~t
=400 nsec.1 may s t i l l be used; the crucial f a c t o r in reaching lower ion stages
i sthe a v a i l a b i l i t y of longer time delays.
F i g . 3 . Schematic diagram o f t h e t w i n - l a s e r system.
? MP-master t r i g g e r p u l s e ; G - t r i g g e r p u l s e d e l a y
FI[
..,B generator- T1 /T2 f l a s h t u b e t r i g g e r p u l s e s ; C1 /C2- R
1 - - ,
PI
p. ' h i g h v o l t a g e charge1Tri gger c i r c u i t s ; F1 /FZ-
flashlamps; Rl/RZ-ruby rods; Pl/P2-Pockels c e l l ;
PU1 /PU2-Pockel s c e l l d r i v e u n i t s ; '&beam s p l i t t e r ; L / A - f i b r e - o p t i c a l l y coupled t r i g g e r u n i t ; D-delay
C2 u n i t - 01 102-9-swi tched l a s e r p u l s e s .
In Fig. 1
( b )we show the 1s-2p,3p absorption of neutral boron, the 2s
absorption of which had previously been observed in the normal incidence
region
(9).Fig 1 ( c ) shows the Zp-ns,nd t r a n s i t i o n s of s i l i c o n . The
spectrum, here recorded f o r the f i r s t time, i s of some theoretical i n t e r e s t
because of the predictions of Daum and Kelly (10). Although analysis has
not y e t been carried out t h e dominant l i n e s a r e believed t o be due t o Si I
and 11. In Fig.
1( d l we show the spectrum of strontium a t a delay of
425nsec. The longer wavelength group of l i n e s corresponds t o the 3d-5p,6p
t r a n s i t i o n s previously observed by Mansfield and Connerade (11) and those a t
shorter wavelength comprise t h e 3d t r a n s i t i o n s of S r I I , which a r e
isoelectronic with the known 3d spectrum of
Rbl(12).
C1-246 JOURNAL
DE
PHYSIQUEI 1 1
-
CONCLUSIONThe two l a s e r technique i s n o t o n l y e f f e c t i v e i n c o n t r o l l i n g t h e i o n stages observed i n dual plasma a b s o r p t i o n b u t a t s u f f i c i e n t l y l o n g t i m e delays enables pure n e u t r a l absorption t o be studied. I n p a r t i c u l a r r e f r a c t o r y and c o r r o s i v e m a t e r i a l s , whose atomic spectra have i n some cases n o t y e t been observed, are now r e a d i l y accessible t o study. It should a1 so prove u s e f u l i n the case o f o t h e r elements such as sulphur o r phosphorus whose vapour phase tends t o be dominated by molecular species.
This work was sllpported by NBST ( I r e l a n d ) Research Grant SC/131/86.
REFERENCES
P.K. C a r r o l l and E.T. Kennedy, Phys. Rev. L e t t . 38, 1068, (1977) G.W.F. Drake and A. Dalgarno, Proc. Roy. Soc. A T O , 549, (1971) P.K. C a r r o l l , E.T. Kennedy and G. O ' S u l l i v a n , 0pt.Lett. 2, 72, (1978) P.K. C a r r o l l , E.T. Kennedy and G. 0 ' S u l l ivan, Appl
.
Opt.E,
1454,(1980)
P.K. C a r r o l l , E,T. Kennedy and G. O ' S u l l i v a n , IEEE J. Quantum Electron.
QE19, 12 (1983).
E. J a n n i t t i , M. M u z o n i , P. N i c o l o s i , G. Tondello and Wang Yongchang, J. Opt. Soc. Am, 28, 1078, (1985)
P.K. C a r r o l l and
m.
C o s t e l l o , Phys. Rev. L e t t s . 57, 1581 (1986) P.K. C a r r o l l and J.T. C o s t e l l o , J. Phys. B. At. M O T Phys.g,
L201, (1987)G. Wendin, Phys. Rev. L e t t 53, 724, (1984);
A. Zangwill, At. Phys.
8,
3 3 , (1983)J.M. Esteva, G. Mehlmen-Balloffet and J. Rromand, J. Quant. Spec. Rad.
Transfer. 12, 1291 (1972);
R.A. Roig and G. Tondello, J. Phys. B. At. Mol. Phys.
2,
2373, (1976) G.R. Daum and H. K e l l y , Phys. Rev. 13A, 715 (1976)M.W.D. M a n s f i e l d and J.P. C o n n e r a d e 3 r o c . Roy. Soc. A342, 421 (1975) M.W.D. M a n s f i e l d and J.P. Connerade, Proc. Roy. Soc.