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Adam P. Hitchcock

Canada Research Chair

in Materials Research
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McMaster University
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PHYSICS in CANADA  55 (1999) 191-198 (September/October, 1999)

Applications of synchrotron light to physics and chemistry

Adam P. Hitchcock

Dept. of Chemistry, & Brockhouse Institute for Materials Research

McMaster University, Hamilton, ON Canada L8S 4M1

John J. Neville

Dept. of Chemistry, University of New Brunswick,

Box #45222, Fredericton, NB Canada E3B 6E2

Abstract

Synchrotron light is an accelerator based light source that covers the complete electromagnetic spectrum from infrared to hard X-ray. It is intense, bright, fully tunable, highly polarized, and has a time structure useful for many types of dynamics experiments. Aside from the visible, near-IR and near-UV where lasers are generally superior, the properties of synchrotron light far surpass those of available lab sources. The ~50 facilities world wide are used by up to 20,000 scientists annually, from many disciplines, but researchers from physics and chemistry are the most prevalent. This article describes some Canadian research in this area using mainly examples from our research. It also describes the Canadian Light source, a proposed 2.9 GeV facility that will enable Canadian scientists to contribute more effectively in this arena. The future of synchrotron research in Canada is bright indeed!
 
 

1. What is synchrotron light ?

2. Research in chemistry and physics using synchrotron light

2.A Spectroscopy & Dynamics

Synchrotron light is virtually unique in its ability to tune photon energy with continuous coverage over wide ranges and with excellent intensity. This leads to many different types of applications in spectroscopy - mapping the quantized energy levels of a gas, liquid or solid target and using these results to learn about the electronic and geometric structure of the sample. Much of the spectroscopy with synchrotron light deals with inner-shell or core levels for which energies above 50 eV are required. Mike Bancroft (Western) has spent much of his career working on systematic investigations of the X-ray photoelectron and X-ray photoabsorption spectroscopy of inorganic compounds with the Canadian Synchrotron Radiation Facility, several beamlines at the Synchrotron Radiation Centre (Madison, WI ) [4,5] High resolution spectroscopy of various types is an important field of chemical physics, one in which Canada is very active. Synchrotron spectroscopy studies are continuing this tradition. For example. John Hepburn (Waterloo) is carrying out high resolution spectroscopy [6] and photoionization dynamics measurements in the vacuum ultraviolet range at the Advanced Light Source (Berkeley, CA).

Photoionization dynamics investigates the time evolution of specific states of atoms, molecules or solids. Photoionization, and related processes such as X-ray or Auger decay of core holes, provide a powerful tool to study dynamics, either directly through combined laser-synchrotron pump-probe approaches - such as are being carried out by Larzillière (Laval) at Super-ACO, Paris - or indirectly, using the characteristic time-scale of the core hole decay as a 'femto-second clock'. An example of the latter is the phenomena of ultra-fast decay whereby a bond in a molecule is broken in the core excited state and dissociation occurs before the Auger process refills the core hole. Aksela, Bancroft and coworkers [7] were one of the first to document the ultra-fast decay process in the dissociative (Cl2p-1,s *) state of HCl. Recently X-ray emission using fully resolved incident and outgoing photons has been shown to be an extremely powerful way to study photoionization dynamics. At the deepest level one needs to make a unified description of the excited state creation, its time evolution, and its subsequent decay. This new understanding has implications for photochemical control - for example, it has been shown that tuning the incident photon energy away from a core excitation resonance can change the nature of the core-valence coupling and thus the pathway of the decay [8].

We are using time-of-flight mass spectrometry and multi-stop coincidence techniques at the CSRF beamlines at SRC to investigate the core-excitation spectroscopy and dynamics of core state decay of small molecules. Fig, 4 shows a spectroscopy example from a recent study of SPF3 [9] in which the symmetry of core excited states is determined directly from the angular distribution of ionic fragmentation processes which lead to pairs (or triplets) of energetic ions. Basically, if bond breaking in an energetic ionic fragmentation occurs before the molecular orientation has had a chance to randomize by rotation, then the direction of preferential ion emission is closely related to the symmetry of the excitation. In this case, when the time-of-flight detector is aligned perpendicular to the electric vector of the light the P 1s ® 9e* transition dominates the S+ partial ion yield spectrum, whereas when the time-of-flight detector is rotated 90o to place the time-of-flight detector parallel to the electric vector, the P 1s ® 14a1* transition becomes strongest. By comparison, the total ion yield spectra and partial yield spectra of thermal ions from P 1s excited SPF3 show negligible angular anisotropy. Fig 4 also includes sketches of the molecular orbitals involved in these core excitations. The diagrams are derived from ab initio calculations of core excited states. Parallel experimental and computational studies are an integral part of synchrotron science, as in almost all other areas of chemistry and physics.

Auger decay of inner-shell excited and ionized states is an efficient source of multiply charged ions. The charge separation and fragmentation of these species, studied by photoelectron-photoion-photoion coincidence (also called charge separation mass spectrometry [10]) gives insights into bonding and electronic structure. In molecules, the dependence of the fragmentation process on the X-ray energy can reveal cases of site and/or state selective fragmentation. The identification of potential candidates for selective X-ray photochemistry is an ongoing goal of our research program. In addition to being an aspect of photoionization dynamics, state-selective photochemistry in either gas or condensed phases can be used to control chemical reactions in a way that may be useful for making new materials or devices. Comparison of the different core edge signals in SPF3 reveals that this molecule is one with a high degree of site-selective fragmentation [11] - see Figs. 5 and Fig. 6. Thus loss of all 3 fluorine atoms to produce SP+ occurs predominantly with P 2p excitation, and not at all with S 2p excitation or ionization. In contrast, the S=P bond is much more readily broken with S 2p excitation, as evidenced by the production of PF3+, PF3++ and the (S+,PF3+) ion pair signals only following S 2p excitation. Even complete dissociation of the molecule into ionized atoms appears to have site selectivity since the (F+,S+/P+) atomic ion pair signal is exclusively generated by P 2p/2s excitation and ionization [11].

 

Similar investigations of photoionization dynamics of core states are being carried out by a number of groups with Canadian participation, including studies by Chris Brion (UBC) and Tong Leung (Waterloo). Recently Leung, in collaboration with Lindle and coworkers [12] have discovered that neutral hydrogen is generated in high yield in Cl 1s excited HCl and S 1s excited H2S. While the origin is not fully understood, one possibility is ultrafast decay - bond breaking prior to core hole decay. If correct, this would require very fast neutral separation since the core hole lifetime is extremely short for such a high energy state.

 

Analysis of the peak shapes from multi-ion coincidence signals can provide detailed information about energetics, angular distributions, and thus fragmentation mechanisms. Fig. 7 shows the line shape of the three ion pair signals - (F+,PF2+), (F+,PF+) and (F+,P+) - produced from P 2p ionization of PF3. The peak at the upper left of the lower two contour plots arises from events in which the lighter ion (F+) flies directly towards the time-of-flight detector and the heavier ion (PFx+, x= 0-2) flies directly away, while the peak to the lower right corresponds to the opposite process. The width of the (F+,PF2+) signal or the peak separation is determined by the kinetic energy released. The average kinetic energy, along with the shape and alignment of the coincidence signal on the TOF-1 versus TOF-2 plot, gives useful insights into fragmentation mechanisms. In this case the (F+,PF2+) signal is aligned exactly along the -1 diagonal (as is required for a two body dissociation [12]), with a size indicating an average kinetic energy release of 9.0 eV, consistent with the 9.2 eV energy of Coulomb repulsion of two ions separated by the P-F bond length. The undetected neutral or ion partners generated in events leading to (F+,PF+) and (F+,P+) pair signals can take away energy and momentum and thus it is possible these signals are associated with fragmentation processes with mechanisms very different from a simple two-body concerted dissociation. Surprisingly, the orientation (slopes close to -1) and line shape of the (F+,PF+) and (F+,P+) ion pair signals are consistent with these ion pairs being produced in concerted dissociative processes, with most of the kinetic energy taken by these two ions. However, for (F+,P+) the average kinetic energy release (14.4 eV) is significantly higher than the 9.2 eV Coulomb repulsion value. Even if the other two F atoms formed F2 this would provide only 1.6 eV, much less than the excess 5.2 eV. From this it appears a significant portion of the (F+,P+) pair signal may arise from triple ionization processes in which a second F+ is generated but not detected since its flight time would be nearly identical to that of the detected F+ ion.
 
 

2.B Materials Science

Many of the applications of synchrotron light are in the area of high performance analysis of new materials. There is an old saying, 'you can't control what you can't see'. By pushing the frontiers of what can be analyzed - lowering spatial, temporal, precision, and detection limits - synchrotron light is contributing in diverse and significant ways to new material and new device development. By the year 2003 it is widely expected that semiconductor devices requiring the finest features - particularly microprocessors and high capacity memory chips - will use X-ray lithography based on synchrotron light in part of their manufacture. Total reflection X-ray fluorescence analysis - a photon in - photon out technique - is being developed as a key technique to monitor contamination of semiconductor surfaces, an issue which becomes increasingly critical as device dimensions shrink.

In the area of analytical sciences, synchrotron light is greatly enhancing the capabilities of well-established techniques such as X-ray photoelectron spectroscopy, and also leading to the development of new techniques, such as resonant inelastic X-ray scattering [13], zone-plate based X-ray spectromicroscopy [14], and extended X-ray absorption fine structure (XAFS) [2,15]. Some of our recent work in zone plate microscopy is described below to illustrate only one aspect of the exciting new materials science enabled by synchrotron light.

2.B.1 Microscopy

Fig. 8 shows a schematic of a scanning transmission X-ray microscope (STXM) [14]. It uses a small X-ray spot created by focussing monochromatized x-rays with a Bragg-Fresnel zone plate, which is a circular transmission diffraction grating with a variable line spacing. The zone plate uses only the spatially coherent component of the X-rays with which it is illuminated so the high brightness and partial coherence of third generation undulator light is critical to their performance. In addition, the fabrication of soft X-ray zone plates pushes the limits of modern electron beam mask generation and lithographic techniques so the spatial resolution is closely related to how fine and precise the zone plate structure can be made. Images are produced pixel by pixel by raster scanning the sample through the beam while recording a suitable signal such as transmitted flux (STXM), fluorescent X-rays, luminescence, or photo-ejected electrons (SPEM) In STXM the sample is located in an atmospheric pressure helium enclosure, a vacuum, or in a liquid contained within X-ray transparent windows. Imaging with the photon energy tuned to chemically-specific spectral features provides chemical maps. Alternatively, the photon energy can be scanned to acquire a Near Edge X-ray Absorption Fine Structure (NEXAFS) spectrum from a small area. Recently procedures to acquire sequences of full images at many photon energies have been implemented (see core-shell particles, toner particles, protein-on-polymers, or jacobsen web site for examples). The acquisition of an image sequence is an extremely powerful way of studying samples which has already provided many interesting surprises, revealing aspects of sample chemistry that would not have been discovered by other means.

So what is new ? - what does X-ray spectromicroscopy offer, that can't be provided by other techniques such as high performance optical or electron microscopy? Even the best optical techniques have an order of magnitude lower spatial resolution (~0.5 m m versus 50 nm) and, unless some intrusive chemistry is employed, such as species-specific fluorescent labeling, optical techniques have much less chemical sensitivity. Electron microscopy has better spatial resolution (as good as 0.1 nm), but there are severe limitations associated with radiation damage when studying sensitive polymer or biological samples. We have demonstrated [16] that NEXAFS microscopy has an advantage of about three orders of magnitude over the corresponding electron microscopy technique in being able to spectroscopically analyze and image small sample areas of radiation sensitive materials such as polymers. In addition, x-ray linear dichroism microscopy can determine orientation of chemical moieties at high spatial resolution [17]. These inherent advantages of x-ray microscopy have opened up new avenues for the characterization of polymers.

 
  In collaboration with John Dutcher (Physics, Guelph) we are using X-ray microscopy to investigate mechanisms of polymer "self-organization". Patterning of thin polymer films is attracting increasing interest, both from a fundamental point of view, and on account of potential technological applications. Normally polymer films are deposited on a flat substrate such as a silicon wafer. However the thermal stability of deposited films can be a limitation on account of hole formation caused by dispersion forces which amplify structural instabilities at the film surface. Mechanical confinement of polymer films offers the possibility to control this instability which raises possibilities for unique self-assemblies of polymers on surfaces patterned on submicron length scales. We have used STXM to study very thin (~50 nm prior to annealing) polystyrene films confined between thin continuous layers of silicon suboxide (see Fig. 9). The SiOx layers prevent hole formation. However aggressive annealing above the glass transition temperature (Tg) generates a novel structure driven not by phase segregation, but by the attractive dispersion force between the SiOx-air surface [18]. These structures offer an attractive test-bed for understanding and developing control mechanisms for one of the fundamental forces governing self-assembly of polymer structures. In order to fully model the mechanisms for this spontaneously generated lateral morphology, it is important to know the thickness of the trapped polymer film throughout the structure. STXM readily provides this information. Prior to these measurements it had been assumed that there was almost complete exclusion of the polystyrene from the dark, non-continuous regions. However, STXM indicated ~30% residual polystyrene in those areas (see Fig. 9). In the near future we plan to investigate trapped thin film polymers of materials with different strengths of interaction with SiOx.


 
  A second example is from recent STXM studies of novel latex particles with internal structure produced by Harald Stöver's group (BIMR, Chemistry, McMaster). These latex spheres are attractive for a number of applications, including coatings, adhesives, chemical delivery etc. In order to optimize these structures for particular applications (e.g. pheromone delivery for environmentally benign, controlled release pest control) it is important to be able to determine the origin of their internal structure. In particular, while electron microscopy of cross-sections of latex spheres readily reveals the presence or absence of internal structure of micron sized latex particles, the limited chemical sensitivity of electron microscopy means that one cannot be sure if the observed structure arises from a genuine chemical difference in the various regions (e.g. core versus shell) or whether it is a consequence of a density and/or thickness variation (perhaps driven by some underlying chemical difference).

  Comparison of STXM images at several photon energies provide a means to quantify the relative contributions of chemical versus density/thickness contrast. Fig 10 shows examples of a recent study of acrylate-polystyrene latex particles which have been synthesized in a two-step process to intentionally segregate all of the poly-acrylate component to the shell region. The exquisite sensitivity of NEXAFS microscopy to this structure is clear. Quantitative chemical compositions of the shell can be derived from the intensities of specific features of the NEXAFS spectra of the shell region (see Fig. 10). More challenging has been a study of a 'tree-ring' morphology in latex particles formed from a blend of styrene and chlorostyrene (Fig 11). The 'tree-ring' morphology is observed only at specific photon energies. This clearly points to a chemical compositional origin rather than a thickness or density origin of this morphology. In turn, this suggests the tree-ring morphology is generated by heterogeneous chemical oscillations in the one-step synthesis.
 
 

3. Canadian Light Source

In 1990 many scientists in Canada grouped together to form the Canadian Institute for Synchrotron Radiation (CISR), an umbrella organization dedicated to education, co-ordination, and facilitation of synchrotron light research. There are currently about 350 faculty level members, more than half of whom are directing research programs at off-shore facilities. In part through CISR initiatives, there is now formal Canadian participation in one or more beam line projects at ALS (Berkeley), APS (Argonne), and SRC (Madison).

Until the start of the CLS project, Canada was virtually the only developed nation without a synchrotron light facility. In 1994 a committee of NSERC identified the need for a light source in Canada. This led to an open competition, in which groups from Eastern Canada and Western Canada competed with site specific project proposals. In 1996 a peer review committee, administered by NSERC and chaired by Dr. Alex McAuley (Victoria) re-affirmed the need for a light source and recommended that Saskatoon be the site. NSERC council accepted the recommendations of the McAuley committee in Nov 1996. In 1999, with the award of a Canada Foundation for Innovation grant for $54 M, the Canadian Light Source project was launched. The toal project budget is ovr $140 M in new funds (and over $170 M if the value of the infrastructure inherited from the SAL faiclity is included). The first scientific experiments with CLS generated synchrotron light will occur in 2004.

CLS will be a full service national synchrotron light facility. The 2.9 GeV, low emittance CLS design is fully competitive third generation technology, with high current (500 mA in 2008). It will have a brightness comparable to existing third generation facilities (see Table 1). When equipped with a small gap undulator, the CLS will even be competitive with wigglers at the Advanced Photon Source. Relative to other third generation facilities the CLS design is characterized as having the highest beam energy and the highest brightness per unit accelerator length. Thus there are novel aspects of the machine design and the research program that will make CLS truly unique. The CLS team is confident that CLS can be built on time and on budget.

Table 1. Comparison of the ring energy and emittance parameters (critical to brightness of the light) for ALS, CLS and APS

In developing plans for the CLS the Canadian synchrotron light community identified user communities and a documentable need for 12 light points (3 undulator, 2 wiggler, and 7 bending magnet lines) with a total of 15 end stations. The CLS has an ultimate capacity for up to 48 bending magnet lines and 10 insertion device lines, allowing more than 50 different experiments to be carried out simultaneously. Matching funds for approximately half of the cost of each of the initial lines have been committed by the federal and Saskatchewan provincial governments. User groups for each research area are in the process of identifying sources, such as other provincial capital development funds or industrial partners, of the remaining funds needed to complete the first phase CLS beam lines.

4. How can you learn more about synchrotron light research ?

If you are interested in a specific topic discussed in this article contact one of the authors or the principal investigator identified in the text. Web sites which provide further information of specific organizations or synchrotron light facilities are listed in table 2.

Table 2. Institutions and contact information
 
Institute/facility location Web site
CISR - Canadian Institute for Synchrotron Radiation UWO, London, ON Saskatoon, SK www.cisr.ca
CLS - Canadian Light Source Saskatoon, SK cls-ccrs.usask.ca
ALS - Advanced Light Source Berkeley, CA www-als.lbl.gov
APS - Advanced Photon Source Argonne, IL www.aps.anl.gov
NSLS - National Synchrotron Light Source Brookhaven, NY www.nsls.bnl.gov
SRC - Synchrotron Radiation Centre Madison, WI www.src.wisc.edu

 

Acknowledgements

This article has touched on the work of only a few of the more than 100 groups in Canada who are using synchrotron light. We apologize in advance for our restricted selection of examples. We would especially like to thank our colleagues, Dr. Tolek Tyliszczak and Dr. Stephen Urquhart, and numerous collaborators, who have played a major role in the synchrotron chemical physics research described herein.
 
 

References

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