research papers
Performance upgrade in the JAEA actinide science beamline BL23SU at SPring-8 with a new twin-helical undulator
aQuantum Beam Science Directorate, Japan Atomic Energy Agency, 1-1-1 Kouto, Sayo, Hyogo 679-5148, Japan, bDepartment of Physics, Kyoto Sangyo University, Kyoto 603-8555, Japan, cJapan Synchrotron Radiation Research Institute, 1-1-1 Kouto, Sayo, Hyogo 679-5198, Japan, and dRIKEN Harima Institute, 1-1-1 Kouto, Sayo, Hyogo 679-5148, Japan
*Correspondence e-mail: ysaitoh@spring8.or.jp
The soft X-ray beamline BL23SU at SPring-8 has undergone an upgrade with a twin-helical undulator of in-vacuum type to enhance the experimental capabilities of the endstations. The new light source with a fast helicity-switching operation allows not only the data throughput but also the sensitivity in X-ray β-US2 measured with a 10 T superconducting magnet.
(XMCD) to be improved. The operational performance and potential are described by presenting XMCD results of paramagneticKeywords: twin-helical undulator; helicity switching; soft X-ray beamline; X-ray magnetic circular dichroism; uranium compounds.
1. Introduction
The JAEA actinide science beamline, BL23SU, built and operated by Japan Atomic Energy Agency (JAEA), is a soft X-ray beamline at the SPring-8 synchrotron facility with its first light being received in 1998 (Saitoh et al., 2001). The primary aim of BL23SU is to investigate the electronic structures of uranium-based compounds and related materials using soft X-ray photoemission (SX-PES) and (XMCD) spectroscopies with a focus on superconductivity and magnetism. The uranium compounds display a variety of intriguing phenomena, which is considered to be due to complex many-body interactions between the valence-electron states. Recently, superconductivity has been discovered in heavy-fermion such as UGe2, URhGe, UCoGe and UIr [for a recent review see, for example, Pfleiderer (2009)], and therefore XMCD as well as SX-PES studies are required for a comprehensive understanding of the nature of the 5f electrons. With the availability of synchrotron radiation sources, XMCD has been developing as a probe of local (element- and angular-momentum-specific) spin and orbital magnetic moments (Funk et al., 2005).
The BL23SU beamline was initially commissioned with an APPLE-2-type undulator with flexible polarization properties (Sasaki, 1994), in which the four rows of periodic magnets are arranged with two rows above and two rows below the stored electron orbit plane. The length (L) of the undulator was 2 m and located at the upstream half of a 5.7 m straight section. The periodic length (λu) of the undulator was 12 cm and the number of periods (Np) was 16. It covered the energy range down to 240 eV in circular polarization mode with a minimum gap of 25 mm (see Fig. 1). In this device, photon helicity was switched by the longitudinal mechanical shift of the magnetic arrays (i.e. changing the magnetic row phase), and the helicity switching at each photon energy of an XMCD spectrum was an important technical approach for high-accuracy XMCD experiments (Agui et al., 2001). A local feed-forward correction system for the orbit distortion at the switching time up to around 2.5 s between opposite helical polarizations (the phase parameter in its pure helical mode was roughly proportional to the gap) has been developed (Nakatani et al., 2005). This system allowed us to perform efficient XMCD measurements using a superconducting magnet under fixed sample conditions (Okamoto et al., 2004). This superconducting magnet requires a long-field reversing time and therefore point-by-point field reversal was impractical. The frequent mechanical motion of the magnet arrays, however, resulted in a high percentage of beamline downtime caused by component failures, thus creating some problems with maintenance and parts replacement. With regard to the SX-PES experiments, a clear advantage of the circular polarization mode over the linear polarization mode was the higher stability in photon energy and intensity, reflecting the much lower heat load on optical components (Kincaid, 1977).
Meanwhile, the twin-helical undulator of BL25SU (Hara et al., 1998), ID25, pioneered at SPring-8, has provided reliable and productive operations for helicity-switching dichroism experiments (Muro et al., 2005; Nakamura et al., 2005; Hayashi et al., 2011) with almost complete circular polarization (Pc) and full polarization reversal (Hirono et al., 2005) for a switching frequency up to 10 Hz (Shirasawa et al., 2004). The twin-helical undulator consists of two in-line helical undulators and five kicker magnets. In these helical undulators the six rows of periodic magnets are arranged with three rows above and three rows below the electron orbit plane. Each of the helical undulators is an out-of-vacuum device (λu = 12 cm, Np = 12) with a minimum gap of 20 mm to cover the energy range down to 120 eV. In helicity-switching mode, the kicker magnets alternately separate the photon beams horizontally by 0.3 mrad in order to minimize the overlap between the cones of fundamental radiation with opposite helicities from the two devices. Coordinated scanning of the undulator gaps and the monochromator has also been successfully demonstrated in this mode. The angular aperture for the central radiation cones along the beamline axis is defined by front-end XY slits (Oura et al., 1998). A detailed description of the helicity switching in the twin-helical undulator has been given previously (Hara et al., 2003).
This type of undulator was adopted for BL23SU using in-vacuum helical undulators, each with Np = 17, of λu = 7.52 cm in order to enhance the above the N 1s Fig. 1 shows a comparison of the and in circular polarization mode between the replaced APPLE-2 undulator (L = 2 m) and the single new undulator (L = 1.3 m) calculated using the program SPECTRA (Tanaka & Kitamura, 2001). Unlike ID25, the central row of the magnetic array, namely the phase of the magnetic field, is fixed in ID23 because of the difficulty of having linear guide systems in an UHV environment. Thus the polarization of the soft X-ray radiation was restricted to be circular. The two undulator gaps of the new ID23 can be independently adjusted down to 8 mm at present, covering photon energies down to 370 eV. Small gaps of the in-vacuum undulator allow us to reduce λu, thereby increasing Np, being proportional to the output.
The maximum frequency of helicity switching is 10 Hz, which is limited by the diagnostics of the electron beam orbit. To maintain coexistence with other beamlines, the variation of the electron beam orbit owing to helicity switching is required to be less than ±1 µm r.m.s. Since the operation of the kicker magnets is independent of the undulator gaps, a simple feed-forward correction scheme is employed for the orbit correction. The twin-helical undulator of ID23 can also be applied to XMCD experiments at much higher switching frequency by using a fast mechanical chopper and angularly separated dual photon beams, in which the kicker magnets generate a stationary orbit bump (Sawhney et al., 1997).
The use of an electromagnetic undulator (Freeland et al., 2002) has an important advantage over the twin-helical undulator for an identical source point of both helicities. However, a fast orbit correction feed-back, which is currently not adopted in the SPring-8 storage ring, is necessary, otherwise feed-forward tables should be made for each electromagnet current and the orbit correction becomes too complicated and less accurate (Oura et al., 2007). Therefore it was not considered as a new ID23.
Soft X-ray magnetic linear dichroism (XMLD) spectroscopy measurements were not included in the scientific case of BL23SU because both the experiment and interpretation were considered to be more challenging than for XMCD. For this reason, no XMLD experiments had been conducted with the APPLE-2 device.
Recently, the helicity switching capability at a frequency of 1 Hz has reached operational status as a first step. In this operation each of the two polarized beams is alternately supplied to the beamline for a period of 0.3 s with a transient time of 0.2 s. We report here its performance for XMCD experiments as well as some recent upgrades of BL23SU.
2. Beamline description
A schematic overview of the main beamline components of BL23SU is shown in Fig. 2. The undulator radiation is transported by the front-end within the storage-ring shield wall to the downstream optics. In order to stop the off-axis beam deflected by the kicker magnets, some of the front-end components upstream of the XY slits, including heat-absorbing photon masks, have been replaced by ones with wider acceptances.
The optical system of BL23SU, as detailed elsewhere (Saitoh et al., 2001), consists of prefocusing mirrors (Mv and Mh) and a varied-line-spacing plane-grating monochromator (VLSPGM, from S1 to S2) equipped with an entrance slit and refocusing mirrors (M3a,b, M3.5, M4a,b). This undulator replacement did not need the modification of a hutch enclosure housing the prefocusing mirrors. The VLSPGM was designed to provide an operational range from 0.2 to at least 1.5 keV with mechanically ruled blazed gratings and achieved a in excess of 1 × 104 at the nitrogen K-edge in full aperture operation for the circular polarization mode of the APPLE-2 undulator (Saitoh et al., 2001). However, the available turned out to be insufficient for soft X-ray angle-resolved photoemission spectroscopy (SX-ARPES) successfully demonstrated at the BL25SU beamline (Suga et al., 2004). Recent SX-ARPES measurements at BL23SU with energy resolutions down to 0.1 eV (Fujimori et al., 2007) have been facilitated by the substitution of a holographic ruled grating with a central groove density of 600 lines mm−1 into the VLSPGM, which resulted in practically four-fold improvement in throughput while providing a better than 1 × 104 up to 1 keV.
After the installation of the new twin-helical undulator, the optical components were slightly adjusted to accommodate a change in the source centers by 1 m by maximizing the transmitted 12 photons s−1 (0.01% bandwidth)−1 at 700 eV (see Fig. 3). The enhanced is quite useful, not only for SX-ARPES measurements (Kawasaki et al., 2011) but also for surface reaction analyses at the SC station (Teraoka & Yoshigoe, 2001) and biological spectroscopies at the BS1–BS3 stations (Fujii et al., 2009; Yokoya & Akamatsu, 2001; Ukai et al., 2009).
at the highest resolution of the VLSPGM using both undulator beams. In this case, monochromatic was almost twice that of the APPLE-2 device, as expected, achieving ∼1 × 10More recently, the SX-ARPES analyzer of a Scienta SES 2002 has been calibrated by modifying the voltage tables in a collaborative research with the Osaka University group of Sekiyama, Kiss et al. This calibration provided its original specification in angular resolution and effective angular window, which is accompanied by an enhancement in transmission and by a factor of at least six, thereby reducing data collection times and increasing throughput (Sekiyama et al., 2012).
The XMCD endstation terminates BL23SU at approximately 120 m from the light source. The experimental UHV chamber is equipped with the superconducting magnet and a sample holder attached to a liquid-He cryostat reaching a sample temperature of 4.5 K. This magnet provides a variable field parallel to the photon beam direction in the range of ±10 T with a sweeping rate up to 1 T min−1. XMCD spectra are obtained in total electron yield mode by measuring the sample drain current (I) normalized by incident (I0) monitored with a Au-coated SiO2 refocusing toroidal mirror, M4a, or a Au-coated mesh between the M4a mirror and the XMCD station. Each of the signals I0 and I is converted by a current amplifier into a voltage which is subsequently converted to a frequency. These signals are fed into separate counters for individual polarization. In the helicity-switching mode the signals are integrated during time periods determined by gating TTL (transistor–transistor logic) signals from the undulator control system. In addition to this, without the reconnection of signal cables, on-the-fly scanning mode (constant velocity motion of the VLSPG and either undulator gap) with a typical rate of 40 eV min−1 has been implemented (Takeda et al., 2008). This scanning mode was not effective for the APPLE-2 undulator, because the gap scan had been limited to a phase parameter of 0 mm, corresponding to the horizontal linear polarization mode.
3. Experimental observations
Fig. 3 shows the measured at the XMCD endstation during the 1 Hz-switching mode for a photon energy (hν) of 700 eV along with the received gating TTL signals for left- and right-handed circularly polarized (LCP and RCP) light. The beam-defining aperture, located at approximately 29 m from the center of the light source, was unchanged from 2.5 mm × 2 mm (horizontally × vertically) that had been determined for SX-ARPES experiments. Both of the helical undulators were set to the same gap to maximize the During the switching transients, both of the beams with opposite helicities pass through the beamline. The change in intensity of approximately 10% for each helicity, which was measured to be fairly independent of the first-harmonic photon energies, is ascribed to the difference in angular acceptance of the beam-defining aperture owing to the positional difference of 2 m between the two undulator centers. This is because the calculated transmitted through the aperture using the SPECTRA program adequately accounts for these behaviors.
Fig. 4 shows the intensity profiles of the focused beam spots at the XMCD station obtained at hν = 700 eV while varying either vertical or horizontal knife-edge position. The focus spots are produced by the refocusing toroidal M4a mirror which imaged the light source (exit slit width) in the horizontal (vertical) direction with a nominal demagnification of about 6 (1/3). The width of the VLSPGM exit slit was set to 20 µm. These measurements were conducted with the same beam intensity by detuning the downstream LCP undulator gap slightly. The LCP and RCP beams are focused on almost a common spot without additional optical alignment. The subtle difference has virtually no influence on dichroic experiments as shown below.
The XMCD performance was tested on a polycrystalline Fe (purity 99.99%) sample at room temperature. Fig. 5 shows the photon-flux-normalized Fe L2,3 (μL + μR) and XCD (μL − μR) spectra measured with an energy resolution of 70 meV for a fixed magnetic field of 6 T, in which both helicities in one cycle were used for every energy point. Here, μL (μR) is the X-ray absorption for LCP (RCP) light. The L3 intensity from the pre-edge background is normalized to unity for ease of comparison with the results obtained by Chen et al. (1995) as described below. The noise level of the measured XMCD spectrum is approximately ±0.03% of the intensity, corresponding to an order of magnitude improvement in sensitivity in our beamline. This sensitivity permits the XMCD onset to be observed at about 18 eV below the L3 edge.
A closer look at the XMCD data by use of the APPLE-2 device shows that the XMCD sensitivity was generally limited by uneven signals taken immediately following the helicity switching performed at every two measurement points (Agui et al., 2001). In conventional measurements without helicity switching, the noise level was suppressed to ±0.02% or less of the averaged intensity. The signal variations in the previous XMCD spectra were most likely due to a significant increase in heat load on the optical components caused by the linear polarization mode during the helicity switching.
The inset in Fig. 5 shows the XMCD asymmetry [(μL − μR)/(μL + μR)] recorded at the L3 (708.1 eV) and L2 (721.3 eV) edges while sweeping the applied magnetic field. No correction has been made to the curves. The XMCD asymmetry is known to be proportional to the element-specific magnetization projected along the incident photon wavevector (Chen et al., 1993). In addition, switching the field direction is equivalent to reversing the helicity of the incoming beam for ferromagnetic Fe. The magnetization curves indicate the same circular polarization rate (|Pc|) of the two beams as well as the full saturation of the Fe moment at 6 T, because the XMCD signals for each helicity on reversing magnetization are the same.
The measured XMCD effect is consistent with the previous results of transmission experiments for magnetically saturated Fe films with a correction for the incomplete Pc (Chen et al., 1995). In addition, the XMCD asymmetry at 1.4 T is precisely equal to that obtained at BL25SU (Muro et al., 2005). The spectroscopy results clearly show that the helicity-switching operation of the twin-helical undulator is well suited for high-precision XMCD studies.
When the effective source point for LCP and RCP light is slightly different, this can transform into an energy difference even for a given monochromator setting. The energy shift was examined by the measurement of the Ti 2p3/2–3d (L3–t2g) absorption spectra of a non-magnetic SrTiO3 sample as shown in Fig. 6. These spectra were taken at room temperature without applying a magnetic field for an energy resolution of 40 meV, in which both helicities in one cycle were used at every energy point. In the difference spectrum, no evidence of dichroic behavior is observed within the An energy difference between the two beams will yield a derivative-shaped contribution to the difference spectrum. The energy difference is estimated to be not more than 2 meV from the Voigt fit to the μL,R spectra.
4. Application to a uranium compound
As an example of investigations that were previously unapproachable, the N4,5 edges in a paramagnetic β-US2 single crystal measured along the 〈010〉 direction at 20 K in an applied field of 10 T are shown in Fig. 7 (sample provided by Advanced Science Research Center, JAEA). These spectra prove U 5f states through the dipole allowed 4d5/2 → 5f5/2,7/2 (N5) and 4d3/2 → 5f5/2 (N4) transitions. β-US2 is a semiconductor and the U4+ (5f 2) ionic scheme provides a good qualitative description of its magnetic behavior (Ikeda et al., 2009). So far, no detailed XMCD investigations of U compounds with formally 5f2 ground state have been reported. The uranium projected along the photon wavevector is of the order of 0.1 μB under the experimental conditions, resulting in an XMCD variation of only 0.15% of the intensity at the N5 edge. In order to eliminate any experimental artifacts arising from system errors, the XMCD spectrum was measured for opposite orientations of the applied magnetic field and the resulting spectra were averaged. Each of the spectra was acquired in two cycles of the helicity switching at every energy point with an energy resolution of ∼125 meV.
and XMCD spectra at the UApplication of the well known sum rules to the XMCD spectrum (Thole et al., 1992; Carra et al., 1993) provides valuable information on the 5f magnetic moments. The sum rules relate the integrals of the XMCD signal over the N5 edge (p) and over both N5 and N4 edges (q) to ground-state magnetic properties as
where 〈Lz〉, 〈Sz〉 and 〈Tz〉 are the expectation values of the orbital angular momentum, spin angular momentum and the magnetic dipole term in the magnetization direction, respectively. 〈Se〉 is referred to as the effective spin. The ratio 〈Se〉/〈Lz〉 is instructive for the analysis of data on magnetically unsaturated samples and is independent of Pc. From the measured XMCD spectrum, we derive 〈Se〉/〈Lz〉 = −0.63 ± 0.02, which is in agreement with an atomic 5f 2 value of −0.66 calculated in intermediate coupling mechanisms for the angular momenta much better than that for LS coupling of −0.46 (Collins et al., 1995; van der Laan & Thole, 1996). Here we ignored in this analysis the so-called saturation effects in the total electron yield detection (Nakajima et al., 1999), which have not been investigated for U N4,5 edges both experimentally and theoretically. Hence, the transmission XMCD experiments of the samples in thin-film form are required. Such experiments, however, are virtually impossible in the BL23SU beamline, because the vaporization of uranium materials is not permitted in the SPring-8 facility.
The sum-rule analysis uses only the integrated MCD intensities and ignores the information contained in the spectral shape. In Fig. 7, atomic calculations adopting the intermediate coupling scheme for the U 5f 2 ground state (van der Laan & Thole, 1996) are compared. Although the experimental and theoretical curves possess the same qualitative features, there are some discrepancies in the XMCD structure at the N5 edge. The apparent discrepancies are attributable to additional solid-state effects. In metallic uranium compounds, XMCD spectra at the N5 and M5 edges display a significant variation in shape (Antonov et al., 2008). Further analysis is currently under way (Takeda et al., 2012).
5. Summary
The new twin-helical undulator, with the capability of switching the photon helicity, installed in BL23SU at SPring-8 is now operational. This device has improved the XMCD sensitivity by an order of magnitude. The experiments performed on paramagnetic β-US2 demonstrate the usefulness and promise of this technique. XMCD spectroscopy using lock-in detection methods is planned to allow more detailed studies. The new light source combined with on-going upgrades will elevate this beamline to an advanced instrumentation level and therefore greatly expand the scientific scope.
Acknowledgements
The authors are grateful for the continuous encouragement and support of Dr J. Mizuki and Dr K. Aoki (JAEA, Japan). We thank Dr S. Ikeda (University of Hyogo, Japan) and Dr Y. Haga (JAEA, Japan) for permission to include the data on β-US2. The XMCD measurements on β-US2 were performed under the approval of BL23SU at SPring-8 (Proposal No. 2011A3835) with the assistance of Dr T. Okane (JAEA, Japan). This work was financially supported in part by a Grant-in-Aid for Scientific Research on Innovative Areas `Heavy Electrons' (No. 20102003) from the Ministry of Education, Culture, Sports, Science and Technology, Japan.
References
Agui, A., Yoshigoe, A., Nakatani, T., Matsushita, T., Saitoh, Y., Yokoya, A., Tanaka, H., Miyahara, Y., Shimada, T., Takeuchi, M., Bizen, T., Sasaki, S., Takao, M., Aoyagi, H., Kudo, T. P., Satoh, K., Wu, S., Hiramatsu, Y. & Ohkuma, H. (2001). Rev. Sci. Instrum. 72, 3191–3197. Web of Science CrossRef CAS Google Scholar
Antonov, V. N., Shpak, A. P. & Yaresko, A. N. (2008). Low Temp. Phys. 34, 79–111. Web of Science CrossRef CAS Google Scholar
Carra, P., Thole, B. T., Altarelli, M. & Wang, X. (1993). Phys. Rev. Lett. 70, 694–697. CrossRef PubMed CAS Web of Science Google Scholar
Chen, C. T., Idzerda, Y. U., Lin, H.-J., Meigs, G., Chaiken, A. & Prinz, G. A. (1993). Phys. Rev. B, 48, 642–645. CrossRef CAS Web of Science Google Scholar
Chen, C. T., Idzerda, Y. U., Lin, H., Smith, N. V., Meigs, G., Chaban, E., Ho, G. H., Pellegrin, E. & Sette, F. (1995). Phys. Rev. Lett. 75, 152–155. CrossRef PubMed CAS Web of Science Google Scholar
Collins, S. P., Laundy, D., Tang, C. C. & van der Laan, G. (1995). J. Phys. Condens. Matter, 7, 9325–9341. CrossRef CAS Web of Science Google Scholar
Freeland, J. W., Lang, J. C. Srajer, G., Winarski, R. Shu, D. & Mills, D. M. (2002). Rev. Sci. Instrum. 73, 1408–1410. Web of Science CrossRef CAS Google Scholar
Fujii, K., Shikazono, N. & Yokoya, A. (2009). J. Phys. Chem. B, 113, 16007–16015. Web of Science CrossRef PubMed CAS Google Scholar
Fujimori, S.-I., Saitoh, Y., Okane, T., Fujimori, A., Yamagami, H., Haga, Y., Yamamoto, E. & Ōnuki, Y. (2007). Nat. Phys. 3, 618–622. Web of Science CrossRef CAS Google Scholar
Funk, T., Deb, A., George, S. J., Wang, H. X. & Cramer, S. P. (2005). Coord. Chem. Rev. 249, 3–30. Web of Science CrossRef CAS Google Scholar
Hara, T., Shirasawa, K., Takeuchi, M., Seike, T., Saitoh, Y., Muro, T. & Kitamura, H. (2003). Nucl. Instrum. Methods Phys. Res. A, 498, 496–502. Web of Science CrossRef CAS Google Scholar
Hara, T., Tanaka, T., Tanabe, T., Mare´chal, X.-M., Kumagai, K. & Kitamura, H. (1998). J. Synchrotron Rad. 5, 426–427. Web of Science CrossRef CAS IUCr Journals Google Scholar
Hayashi, M., Narumi, Y., Nojiri, H., Nakamura, T., Hirono, T., Kinoshita, T., Kodama, K. & Kindo, K. (2011). J. Electron Spectrosc. Relat. Phenom. 184, 338–341. Web of Science CrossRef CAS Google Scholar
Hirono, T., Kimura, H., Muro, T., Saitoh, Y. & Ishikawa, T. (2005). J. Electron Spectrosc. Relat. Phenom. 144–147, 1097–1099. Web of Science CrossRef CAS Google Scholar
Ikeda, S., Sakai, H., Tateiwa, N., Matsuda, T. D., Aoki, D., Homma, Y., Yamamoto, E., Nakamura, A., Shiokawa, Y., Ota, Y., Sugiyama, K., Hagiwara, M., Kindo, K., Matsubayashi, K., Hedo, M., Uwatoko, Y., Haga, Y. & Ōnuki, Y. (2009). J. Phys. Soc. Jpn, 78, 114704. Web of Science CrossRef Google Scholar
Kawasaki, I., Fujimori, S.-I., Takeda, Y., Okane, T., Yasui, A., Saitoh, Y., Yamagami, H., Haga, Y., Yamamoto, E. & Ōnuki, Y. (2011). Phys. Rev. B, 83, 235121. Web of Science CrossRef Google Scholar
Kincaid, B. M. (1977). J. Appl. Phys. 48, 2684–2691. CrossRef Web of Science Google Scholar
Laan, G. van der & Thole, B. T. (1996). Phys. Rev. B, 53, 14458–14469. Google Scholar
Muro, T., Nakamura, T., Matsushita, T., Kimura, H., Nakatani, T., Hirono, T., Kudo, T., Kobayashi, K., Saito, Y., Takeuchi, M., Hara, T., Shirasawa, K. & Kitamura, H. (2005). J. Electron Spectrosc. Relat. Phenom. 144–147, 1101–1103. Web of Science CrossRef CAS Google Scholar
Nakajima, R., Stöhr, J. & Idzerda, Y. U. (1999). Phys. Rev. B, 59, 6421–6429. Web of Science CrossRef CAS Google Scholar
Nakamura, T., Muro, T., Guo, F. Z., Matsushita, T., Wakita, T., Hirono, T., Takeuchi, Y. & Kobayashi, K. (2005). J. Electron Spectrosc. Relat. Phenom. 144–147, 1035–1038. Web of Science CrossRef CAS Google Scholar
Nakatani, T., Agui, A., Aoyagi, H., Matsushita, T., Takao, M., Takeuchi, M., Yoshigoe, A. & Tanaka, H. (2005). Rev. Sci. Instrum. 76, 055105. Web of Science CrossRef Google Scholar
Okamoto, J., Mamiya, K., Fujimori, S.-I., Okane, T., Saitoh, Y., Muramatsu, Y., Fujimori, A., Ishikawa, S. & Takano, M. (2004). AIP Conf. Proc. 705, 1110–1113. CrossRef CAS Google Scholar
Oura, M., Nakamura, T., Takeuchi, T., Senba, Y., Ohashi, H., Shirasawa, K., Tanaka, T., Takeuchi, M., Furukawa, Y., Hirono, T., Ohata, T., Kitamura, H. & Shin, S. (2007). J. Synchrotron Rad. 14, 483–486. Web of Science CrossRef CAS IUCr Journals Google Scholar
Oura, M., Sakurai, Y. & Kitamura, H. (1998). J. Synchrotron Rad. 5, 606–608. Web of Science CrossRef CAS IUCr Journals Google Scholar
Pfleiderer, C. (2009). Rev. Mod. Phys. 81, 1551–1624. Web of Science CrossRef CAS Google Scholar
Saitoh, Y., Nakatani, T., Matsushita, T., Agui, A., Yoshigoe, A., Teraoka, Y. & Yokoya, A. (2001). Nucl. Instrum. Methods Phys. Res. A, 474, 253–258. Web of Science CrossRef CAS Google Scholar
Sasaki, S. (1994). Nucl. Instrum. Methods Phys. Res. A, 347, 83–86. CrossRef Web of Science Google Scholar
Sawhney, K. J. S., Senf, F., Scheer, M., Schiifers, F., Bahrdt, J., Gaupp, A. & Gudat, W. (1997). Nucl. Instrum. Methods Phys. Res. A, 390, 395–402. CrossRef CAS Web of Science Google Scholar
Sekiyama, A., et al. (2012). In preparation. Google Scholar
Shirasawa, K., Hara, T., Takeuchi, M., Hiraya, A. & Kitamura, H. (2004). AIP Conf. Proc. 705, 191–194. CrossRef Google Scholar
Suga, S., Shigemoto, A., Sekiyama, A., Imada, S., Yamasaki, A., Irizawa, A., Kasai, S., Saitoh, Y., Muro, T., Tomita, N., Nasu, K., Eisaki, H. & Ueda, Y. (2004). Phys. Rev. B, 70, 155106. Web of Science CrossRef Google Scholar
Takeda, Y., et al. (2012). In preparation. Google Scholar
Takeda, Y., Kobayashi, M., Okane, T., Ohkochi, T., Okamoto, J., Saitoh, Y., Kobayashi, K., Yamagami, H., Fujimori, A., Tanaka, A., Okabayashi, J., Oshima, M., Ohya, S., Hai, P. N. & Tanaka, M. (2008). Phys. Rev. Lett. 100, 247202. Web of Science CrossRef PubMed Google Scholar
Tanaka, T. & Kitamura, H. (2001). J. Synchrotron Rad. 8, 1221–1228. Web of Science CrossRef CAS IUCr Journals Google Scholar
Teraoka, Y. & Yoshigoe, A. (2001). Appl. Surf. Sci. 169–170, 738–741. Web of Science CrossRef CAS Google Scholar
Thole, B. T., Carra, P., Sette, F. & van der Laan, G. (1992). Phys. Rev. Lett. 70, 1943–1946. CrossRef Web of Science Google Scholar
Ukai, M., Yokoya, A., Nonaka, Y., Fujii, K. & Saitoh, Y. (2009). Radiat. Phys. Chem. 78, 1202–1206. Web of Science CrossRef CAS Google Scholar
Yokoya, A. & Akamatsu, K. (2001). Nucl. Instrum. Methods Phys. Res. A, 467–468, 1333–1337. Web of Science CrossRef CAS Google Scholar
This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.