A versatile experimental system for tracking ultrafast chemical reactions with X-ray free-electron lasers

An experimental system, SPINETT (SACLA Pump-probe INstrumEnt for Tracking Transient dynamics), dedicated for ultrafast pump-probe experiments using X-ray free-electron lasers has been developed. SPINETT consists of a chamber operated under 1 atm helium pressure, two Von Hamos spectrometers, and a large two-dimensional detector having a short work distance. This platform covers complementary X-ray techniques; one can perform time-resolved X-ray absorption spectroscopy, time-resolved X-ray emission spectroscopy, and time-resolved X-ray diffuse scattering. Two types of liquid injectors have been prepared for low-viscosity chemical solutions and for protein microcrystals embedded in a matrix. We performed a test experiment at SPring-8 Angstrom Compact free-electron LAser and demonstrated the capability of SPINETT to obtain the local electronic structure and geometrical information simultaneously.


I. INTRODUCTION
X-ray free-electron lasers (XFELs), 1-5 generating unprecedentedly brilliant coherent X-ray pulses with an ultrashort duration ($10 fs), have boosted femtochemistry research activities. Beyond the optical-domain observables, XFELs offer exciting opportunities to observe structural and local electronic changes of matter in ultrafast pump-probe experiments. To date, time-resolved X-ray spectroscopic or scattering measurements using XFELs have revealed various fundamental phenomena such as a covalent bond formation, 6,7 photocarrier generation, and trapping inside semiconductor nanoparticles, 8-10 a ligand dissociation 11 or exchange 12 of transition metal complexes, and coherent molecular vibrations associated with the nuclear wavepacket dynamics. [13][14][15][16] A combination of complementary X-ray techniques in ultrafast experiments is useful for disentangling the complexity of excited-state processes and allows a comprehensive understanding of the nonequilibrium reaction dynamics. For example, time-resolved X-ray absorption spectroscopy (TR-XAS) can probe both the unoccupied electronic states and local nuclear structure around an absorbing atom, while time-resolved X-ray emission spectroscopy (TR-XES) provides information about the occupied density of states projected on the absorbing atom. Time-resolved X-ray diffuse scattering (TR-XDS) is an important tool to obtain structural insights from an interference pattern of elastically scattered photons. The usefulness of these combinations is well illustrated in the work by Canton and co-workers, 17 who exploited TR-XES and TR-XDS to investigate a bimetallic donor-acceptor complex and determined the time scales of the intramolecular charge transfer and the subsequent structural change.
At BL3 of SPring-8 Angstrom Compact free-electron LAser (SACLA), 1 we have developed advanced X-ray optics and beamline components for accommodating these applications. The most widely used system is an arrival-timing monitor based on a beam-splitting scheme. 18,19 With this diagnostics, one is able to measure shot-to-shot timing fluctuations between the optical pump and X-ray probe pulses during the experiments, to compensate for them with postprocess analysis, and to improve the time resolution to the $20 fs level. 20 Later, we also implemented a double channel-cut crystal monochromator (DCCM) and compound refractive lenses (CRLs), 21 which are compatible with the arrival-timing diagnostics and facilitate to tailor the XFEL beam conditions, i.e., bandwidth and beam size. These fundamental beamline components are working reliably.
For an efficient operation of ultrafast XFEL experiments at SACLA, we have also developed a robust measurement system, SPINETT (SACLA Pump-probe INstrumEnt for Tracking Transient dynamics), covering complementary X-ray techniques. This experimental platform allows one to carry out TR-XAS, TR-XES, and TR-XDS measurements of various molecular and protein samples. In this paper, we describe the design concept and functionality of SPINETT. A test experiment was performed to demonstrate instrumental capabilities. In the conclusion, we briefly discuss future perspectives.
II. DESIGN A. Overview Figure 1(a) shows a schematic layout of SPINETT, consisting of a chamber with a size of 528 Â 468 Â 395 mm 3 , two Von Hamos spectrometers, and a multiport charge-coupled device (MPCCD) detector 22 with a short working distance (SWD). The chamber is separated from the beamline by a polyimide film and can be filled with helium gas at a pressure of 1 atm to suppress the scattering and absorption of the incident X-ray beam by air. Statistics of SPINETT are summarized in Table I.

B. Optical laser path
Optical pulses are introduced into the chamber through a 1-mmthick quartz window attached to a sidewall and are delivered to the interaction point with a collinear geometry via a prism mirror. The incident angle difference between optical pump and X-ray probe pulses is $4 . The optical beam is focused by a lens located upstream of the prism mirror. The lens position is adjustable to control the optical beam size at the interaction point.  23 or cellulose. 24 To rapidly achieve a spatial overlap between XFEL and optical laser pulses, we replace these injectors with a tungsten pinhole having a diameter of 50 lm [ Fig. 2(d)], move its center hole to the XFEL beam, and align the optical beam with a motorized steering mirror. The surface of the pinhole is coated with phosphor (Gd 2 O 2 S:Tb, P43) powder via a heterogeneous precipitation method and emits visible light when XFEL

D. Intensity monitors
TR-XAS can be measured with a total fluorescence detection method using monochromatic XFELs, whose intensity fluctuates stochastically owing to the self-amplified spontaneous emission (SASE) process. Consequently, the data quality strongly depends on the precision with which the incoming and fluorescence X-ray intensities (I 0 and I) are measured. In order to achieve a high signal-to-noise (S/N) ratio in TR-XAS, I 0 and I intensity monitors are installed inside the chamber. The I 0 transmissive intensity monitor consists of an X-ray scatterer (a polyimide or CVD film) and two Si photodiodes (Hamamatsu, S3590-09) as shown in Fig. 3(a). These photodiodes produce charge pulses upon X-ray irradiation, which are processed by the charge-sensitive and shaping amplifiers. The output signals from the amplifiers are evaluated by a waveform fitting procedure and the I 0 intensity can be measured with a relative accuracy of $10 À3 , as described in Ref. 25. The I 0 intensity fluctuation can be defined as the standard deviation over the average I 0 intensity (r I0 =I 0 ), which was measured to be $50% at 8.985 keV [ Fig. 3(b)]. Despite such large intensity fluctuations of monochromatic XFELs, the normalization can be achieved by using another Si photodiode to measure the fluorescence intensity, which is placed at $10 mm from the interaction point so as to cover a large solid angle ($0.81 sr). Figure 3(c) shows shot-to-shot fluorescence intensity plotted against the I 0 intensity, which corroborates an excellent linear correlation between them. This is also confirmed by the residual error after the linear fitting, as shown in Fig. 3(d).

E. Von Hamos spectrometers
The two Von Hamos spectrometers consist of 6 cylindrically bent crystals (Fig. 4). The crystals are each 25 mm Â 100 mm Â 150 lm (in the dispersive direction, the focusing direction, and the thickness, respectively), which is glued onto the cylindrical glass lens with a radius of curvature of 250 mm. The shape errors of the crystal surfaces were measured with an optical interferometer (Zygo Verifire TM ATZ) and were kept within $0.4 lm in root mean square over 90% of the surface area. The available crystals are Si(531) and Si(111). In the future, we plan to fabricate analyzer crystals with different Miller indices or materials, such as Si(220), Ge(111), and Ge(220). The Bragg angle range covered by these spectrometers is from 60 to 75 . One of the spectrometers is positioned at 90 with respect to the incident X-ray beam [horizontal-scattering geometry; Fig. 4(a)], while the other has a back-scattering geometry [ Fig. 4(b)]. Owing to these two spectrometers, multiple signals can be measured simultaneously, for example, Ka and Kb emissions of 3d transition metals. Two MPCCD detectors, which have an area of 25.6 mm Â 51.2 mm with a pixel size of 50 lm, are used for XES measurements. These detectors are positioned at the top and at the side of the interaction point, depending on the reflection geometry.

F. MPCCD SWD detector
The MPCCD SWD detector shown in Fig. 5(a) is composed of eight sensor modules and constitutes a square sensor area of 110 mm Â 110 mm with a square aperture of 3 mm Â 3 mm at the center. This detector is mounted downstream of the chamber and allows measuring XDS or X-ray diffraction (XRD) from the sample. The working distance between the sample and the sensor surface is adjustable in the range of 55 mm-1400 mm, while we usually set it at the minimum of 55 mm in order to reach a high scattering angle (2h) of 45 [ Fig. 5(b)]. In the experiment, we block the incident XFEL beam with a 3mm-diameter beam stopper equipped inside the chamber to prevent damage to the detector. Figure 5(c) shows the averaged XDS image measured for the [Co II (bpy) 3 ] 2þ (bpy ¼ bipyridine) complex dissolved in water with a concentration of 10 mM. The solution was flowed as a liquid jet through the injector [ Fig. 2(b)] with an inner diameter of 100 lm in a closed circulating system. An intense ring in Fig. 5(c) arises from the solvent scattering.

III. PERFORMANCE TEST
The data quality of TR-XAS measured using SPINETT can be found in Refs. 8-11 and 16. In this work, we report a test experiment investigating the electronic ground structures of Fe atoms by XES. The samples were 50 mM [Fe II (phen) 3 ] 2þ (phen ¼ phenanthroline) aqueous solution and photosystem II (PSII) microcrystals. The PSII preparation procedure is described elsewhere. [26][27][28][29] A 100 ll PSII suspension was mixed with a 3 ml grease matrix 23  Structural Dynamics ARTICLE scitation.org/journal/sdy microcrystal size ranging from 10 lm to 100 lm. We employed injectors with inner diameters of 100 lm for the [Fe II (phen) 3 ] 2þ solution and 150 lm for the PSII microcrystals. In the XES measurement of PSII, XRD was collected simultaneously. Diffraction images were filtered by the program of Cheetah, 30,31 which allows us to extract the events when the XFEL pulses are diffracted by the microcrystals. The experiment was performed at BL2 of SACLA. We used the pink XFEL beam with an average pulse energy of 470 lJ and a central photon energy of 8 keV. At the interaction point, the beam was focused to a full-width at half-maximum (FWHM) spot size of 1.5 lm Â 1.5 lm by Kirkpatrick-Baez mirrors. 32 Fe Kb spectra were recorded with the Si(531) reflection (Bragg angle ¼ 73.14 ) using the horizontal-scattering geometry, while Fe Ka spectra were measured with the Si(333) reflection (Bragg angle ¼ 67.89 ) using the backscattering geometry. The elastic peaks of the monochromatic beam through the Si(111) monochromator gave 1.1 eV (1.0 eV) FWHMs for the Kb (Ka) region. After deconvoluting the monochromator contribution, the energy resolutions were evaluated to be $0.5 eV for Kb and $0.6 eV for Ka, which are mainly due to the geometrical contribution 33,34 and the misalignment in overlapping analyzer crystals ($0.3 eV). The geometrical contribution DE G can be described as . Although the Ka and Kb spectra do not directly probe valence electrons, their spectral shape is sensitive to the number of unpaired 3d electrons (the spin moment) reflecting the magnitude of the 3p(2p)-3d intra-atomic exchange interaction, hence providing information about the oxidation state. Previous studies showed that the increase in unpaired 3d electrons leads to the broadening of the Ka line and the blue shift of the Kb 1,3 peak. 37,38 This indicates that the Fe spin moment of PSII is higher than that of [Fe II (phen) 3 ] 2þ . Indeed, the PSII dimer has three Fe atoms; one is a nonheme ferrous ion (Fe 2þ ) and the other two are ferric ions (Fe 3þ ) in the heme groups. The ferric ions contain unpaired 3d electrons and therefore, the average Fe spin state of PSII is larger than zero (S > 0). On the other hand, the [Fe II (phen) 3 ] 2þ complex has only one Fe 2þ ion in the low-spin configuration (S ¼ 0). 39 Figure 7 shows a typical diffraction image of PSII. The Bragg spots are observable only in a low-q region and the diffraction quality is poor. Although this problem was not addressed in this test experiment, the optimized sample preparation including the postcrystallization treatment will drastically improve the achievable resolution in XRD. The combination of XES and XRD (XDS) will be a powerful tool to gain detailed insights into the reaction mechanism when combined with the pump-probe scheme.

IV. CONCLUSIONS
We have developed the measurement system for ultrafast experiments, SPINETT, at SACLA. It is designed to cover complementary X-ray techniques and successfully applied to simultaneous measurements of XES and XRD. Combined with an optical laser, SPINETT allows one to track the electronic and structural changes of matter with an ångstr€ om and femtosecond spatiotemporal resolution. In future, we plan to fabricate different types of analyzer crystals for XES, which will enable the simultaneous measurement of spectra of different elements, such as Cu, Fe, and Mn, using two Von Hamos spectrometers. This capability is particularly important for

ARTICLE
scitation.org/journal/sdy understanding the electron transfer processes inside polymetallic complexes or proteins.

ACKNOWLEDGMENTS
We greatly thank the staff of SACLA for their support and contribution. This research was performed with the approval of Japan Synchrotron Radiation Research Institute (JASRI; Proposal No. 2018B8062). JSPS KAKENHI Grant Nos. JP19H04407, JP19H05782, JP17H06438, and JP17H06141 supported this work.

APPENDIX: DATA AVAILABILITY
The data used for Figs. 3(b)-3(d), 5(c), 6, and 7 are available from the corresponding author upon request. All raw data are saved in the SACLA storage system or database. 40 Figures can be extracted from the "run," an experimental unit to bundle the consecutive shot-to-shot data.