Lithium-ion battery (LIB) technology is the most attractive technology for energy storage systems in today’s market. However, further improvements and optimizations are still required to solve challenges such as energy density, cycle life, and safety. Addressing these challenges in LIBs requires a fundamental understanding of the reaction mechanisms in various physical/chemical processes during LIB operation. Advanced in situ/operando synchrotron-based X-ray characterization techniques are powerful tools for providing valuable information about the complicated reaction mechanisms in LIBs. In this review, several state-of-the-art in situ/operando synchrotron-based X-ray techniques and their combination with other characterization tools for battery research are introduced. Various in situ cell configurations and practical operating tips for cell design and experimental set-ups are also discussed.
Lithium-ion batteries (LIBs) are the most widely used electrochemical storage devices for portable electronics, and are considered the best candidates for the power systems of electrical vehicles1. Although extensive efforts have been made to develop LIBs, further improvement and optimization are still required, especially for energy density, cycle life, and safety characteristics.
Therefore, an in-depth understanding of the scientific aspects relating to LIBs, such as charge storage mechanisms, performance degradation mechanisms, and reactions at the electrode/electrolyte interfaces, is critically important. The synchrotron-based X-ray techniques provide powerful tools for studying and monitoring the changes of crystal structure, electronic structure, chemical composition, and morphology of electrode materials in electrochemical cells during operation, and the results are very valuable to improve the performance of existing systems and to design new battery materials.
Over the past few decades, significant developments in synchrotron-based X-ray techniques have provided substantial opportunities to study the working mechanisms of battery materials. When used in combination with other scattering, spectroscopy, and imaging techniques, comprehensive studies have been carried out to understand the complicated issues that arise during LIB operation with different physical/chemical aspects and at multiple length scales (Fig. 1 and Table 1). More importantly, high-brilliance synchrotron X-ray sources offer opportunities to perform in situ/operando experiments with various techniques to study dynamic properties and time-dependent reaction process.
The significant advantages of in situ/operando approaches over ex situ characterization are as follows: (1) In situ measurements instantly probe the reaction taking place at the specific interested location of a sample, providing better reliability and higher precision for the data analysis; (2) in operando measurements continuously monitor electrochemical, physical, or chemical processes on a single sample or a device under operating conditions, eliminating the preparation of multiple samples for ex situ measurements and providing closer to real-time operation information; (3) this method allows the investigation of the non-equilibrium or fast-transient process during electrochemical or chemical reactions. The non-equilibrium or short-lived intermediate states or species, which cannot be captured by ex situ characterizations, can be detected2,3,4,5. (4) In situ approaches remove the possibility for contamination, relaxation, or irreversible changes of highly reactive charged/discharged samples when preparing, handling, and transferring them for ex situ measurements (e.g., the reaction with organic solvent during sample washing, the reaction with moisture and oxygen during sample transfer, etc.)3, and the true reaction products can be more reliably identified. Indeed, the most recent results from advanced in situ/operando synchrotron-based experiments play a critical role in providing deeper insight into the complicated reaction mechanisms in LIBs 6,7,8,9,10.
Considering the importance of advanced in situ/operando characterization techniques in battery studies, this review presents an overview of state-of-the-art in situ/operando synchrotron-based X-ray techniques for LIB research, providing some basic guidelines for researchers in the battery field. In situ/operando techniques including X-ray diffraction (XRD), X-ray pair distribution function (PDF) analysis, X-ray absorption spectroscopy (XAS), and X-ray imaging techniques will be discussed, and some practical tips for electrochemical cell design will be given.
Designing in situ/operando X-ray characterization
Combination of multiple in situ/operando X-ray techniques
The electrochemical reactions of electrode materials usually involve complex, dynamic, and inhomogeneous processes, such as charge transfer, ion diffusion, formation and breakage of chemical bonding, phase transformation, and surface reconstruction. Due to the complex nature of the physical/chemical phenomena occurring during LIB operation, a combination of multiple complementary characterization techniques needs to be considered in order to provide more reliable information for understanding how these physical/chemical properties are related to the electrochemical performance of the batteries. Because each technique provides certain information about the different aspects of physical/chemical changes within the samples at different length scales, the choice and combination of appropriate techniques is quite important.
Since synchrotron beamtime is precious and difficult to get, in situ/operando experiments should be well planned and should focus only on dynamic processes for which ex situ measurements are inadequate. Therefore, ex situ measurements are still highly recommended prior to in situ/operando measurements. Ex situ results would provide some important information for designing more efficient in situ experiments. In particular, ex situ results can also be used as good references for in situ data analysis.
In situ electrochemical cell design
To conduct in situ experiments successfully, design of the in situ cell is the first important step. A poorly designed in situ cell could introduce artifacts into the data, and signals from inactive parts of the cell interfere with signals of interest. Therefore, the in situ cell needs to be designed carefully. In most cases, in situ cell should be designed to fit the specific experimental technique. Fortunately, many in situ cell designs for characterizing LIBs using various X-ray techniques have recently been reported in the literature. As shown in Fig. 2, several different kinds of in situ/operando cells, such as modified coin cells, modified pouch cells, Argonne’s multipurpose in situ X-ray (AMPIX) electrochemical cell11, radially accessible tubular in situ X-ray (RATIX) cell12, soft XAS cells13, and capillary type cells14 have been reported for different types of in situ/operando experiments.
It is worthwhile to give some tips for designing in situ/operando electrochemical cells as well as for the experimental design to make these cells function properly for both electrochemical processes and X-ray optics.
The in situ/operando electrochemical cell should be designed to be easy to assemble/disassemble at synchrotron facilities. The cell should be highly reproducible for electrochemical testing. In addition, the cells should be able to be incorporated into the existing beamline setup and should fit properly in X-ray optics. For example, for in situ/operando experiments with X-ray signal detection in reflection mode, an in situ/operando cell with a wide solid angle window for X-ray collection is often required. For in situ/operando X-ray tomography measurements, the sample needs to rotate in a wide range of angles to obtain a series of 2D images for the reconstruction of a 3D image. In this case, a cylindrical geometry and cell case made from low X-ray absorption materials are preferred to avoid blockage of outgoing X-rays 11,12,13,15,16,17,18,19.
To allow X-rays to reach the sample region and the detector, one hole for reflection mode and two holes for transmission mode are covered with X-ray transparent materials (e.g., Kapton film, beryllium, or aluminum foil, etc.) and are usually made on in situ/operando cells as windows, except for experiments using very high energy X-rays, which can penetrate the entire cell body20. An ideal window material should be as follows: (a) chemically and electrochemically stable in the cell during operation. In other words, the window materials should not react with cell components, such as electrode and electrolyte, and should resist oxidation and reduction during charge and discharge; (b) impermeable to oxygen and moisture; (c) stiff to apply uniform pressure to ensure a uniform electrochemical reaction. Because of the penetration power of the beam is proportional to the X-ray energy, it is relatively easier to do in situ/operando experiments using hard X-rays due to more options for window materials. In general, polyimide (Kapton) film is a widely used window material for hard X-ray experiments not only because of its versatile performance, but also because it is very easy to handle. However, a thin Kapton film is too soft to apply constant pressure, causing the sample area underneath the window to react abnormally sometimes (e.g., no reaction, delay of the reaction, etc.). Beryllium should always be avoided due to safety hazards, and because it is easily oxidized during battery charging, though it is ideal for X-ray transmission. In the tender X-ray region, a very thin window with materials composed of light elements, such as thin polyester (Mylar) film, should be used21. Because ultra-high vacuum (UHV) environments are necessary for soft X-ray absorption spectroscopy (sXAS) measurements, an ultrathin silicon nitride window or solid-state electrolyte is frequently used for in situ sXAS experiments 22.
Interference from inactive cell components to outgoing X-ray signals should be avoided, especially for X-ray detection in transmission mode when the X-ray beam has to penetrate the entire cell. Therefore, cell components or materials in the X-ray beam path have to be carefully selected and constructed. For example, a Cu current collector, which is a conventionally used anode current collector, will cause attenuation of the X-rays and result in a poor signal-to-noise ratio (S/N) of the X-ray signal detected when doing XAS experiments on low-Z elements (e.g., V, Cr, etc.). This could cause many problems when acquiring high-quality XAS data. Ti can be used to replace Cu as an anode current collector in such circumstances to improve the quantity of data. Interaction of the X-rays with cell components often generates background signals, which come together with X-ray signals from the real sample interested. For some measurements, such background signals need to be precisely removed afterwards from the total signals detected for quantitative data analysis. For example, data analysis of high-quality PDF requires both the Bragg scattering and diffuse scattering signals from only the sample. However, the background signals from other cell components, such as window materials, the separator, the current collector, the electrolyte, etc., collected and mixed together with the useful diffuse scattering signals from the sample need to be carefully removed. The background signals from an empty cell without the active sample need to be precisely measured and extracted during data collection and analysis. Therefore, the in situ/operando cells for PDF should be highly reproducible (e.g., exactly the same window materials, current collector, separator, same amount of electrolyte being used, etc.). An AMPIX cell (Fig. 2c) is capable of precisely measuring background signals and enabling reliable electrochemical performance 11.
Beam damage should also be considered. Unless continuous data collection is needed, intermittent sample probing (e.g., using beam shutter or moving the sample region off the beam, etc.) is recommended to reduce the total amount of X-ray radiation during the entire measurement.
Synchrotron-based X-ray techniques for battery research
In situ X-ray diffraction (XRD)
The crystal structures of electrode materials are closely related to the properties of the battery cells including the power and energy density, cyclic life, and rate capability. In-depth understanding of these relationships is valuable to optimize the current electrode systems as well as develop new electrode materials with better electrochemical performance. Therefore, it is very important to study the structural changes of the electrode materials during the electrochemical process, including changes in the lattice parameters, phase transition, and atomic occupancy. In situ XRD has been proved as a very powerful technique for providing information about the crystal structural and phase transformation of crystalline electrode materials during cycling.
As a good example of in situ XRD studies, Zhou et al.29 investigated the structural evolution of a Li2MoO3 cathode material using in situ XRD, and proposed the “abnormal” unit cell breathing mechanism of Li2MoO3 during the charge-discharge process. As shown in Fig. 3a and c, all the peaks in the XRD pattern of pristine and charged Li2MoO3 can be indexed based on a layered structure with the R\(\bar 3\)m space group. The in situ XRD patterns (Fig. 3b) of a Li2MoO3 electrode during the charge process demonstrated that the solid solution reaction occurs in the region of 0<x<0.5 and all the main peaks shifted to lower angles, indicating an increase in d-spacing for phase I. Furthermore, a new phase (phase II), which has the same layered structure as phase I but larger lattice parameters formed during the charge process, suggests that a two-phase reaction occurred in region of 0.5<x<1. Both lattice parameters a (b) and c of phase II were larger than those of phase I and increased continuously. In the x>1 region, phase I disappeared, and a solid solution reaction of phase II was observed. For widely used LiMO2 (M = Co, Ni, Mn), lattice parameters, a and b, contract during charging. However, for Li2MoO3, such changes are in opposite directions. Metal–metal bonding is used to explain such “abnormal” behavior and a generalized hypothesis is developed. The expansion of the M–M bond becomes the controlling factor for a(b) evolution during charge, which is in contrast to the shrinking M–O bond as the controlling factor in “normal” materials.
Time-resolved X-ray diffraction (TR-XRD) techniques have also been developed to investigate the dynamic properties of electrodes during fast charge/discharge process. Taking advantages of the ultrafast data collection capability of TR-XRD using synchrotron X-ray beams. Zhou et al.15 also investigated the charge-rate dependent phase transition process of layered LiNi1/3Mn1/3Co1/3O2 by using fast in situ TR-XRD. As shown in Fig. 3e, the charging process at current rates of 0.1 and 1 C show two regions of solid solution reactions with two hexagonal phases of H1 to H2 and the two-phase coexistence region of H1 + H2 in the middle stage of the charging process. Interestingly, when the charging rate is increased to 10 C a new intermediate phase was observed in between the two solid solution reaction regions, and the peaks representing this new phase become more and more pronounced at higher rates of 30 and 60 C. Furthermore, an abnormal Li-poor region with tetrahedral Li occupation and a normal Li-rich region with octahedral Li occupation was observed in the half-charged sample using scanning transmission electron microscopy (STEM). It is suggested that the intermediate phase can act as a buffer between the Li-rich and Li-poor phase and can reduce the local stress and strain produced by inhomogeneity during charging.
Like in the case of the above examples, modified coin cells (Fig. 2a) are used for in situ XRD measurements. However, other cases, flexible Kapton tape windows cannot provide a sufficiently airtight seal and cannot keep out moisture for a long time. The potential for leakage of electrolyte from the cell is a large problem. In addition, the cell casing with holes (windows) can cause uneven pressure and windows using insulating materials can reduce the electrical connection with the electrode. To overcome these drawbacks of the coin cell, an AMPIX cell (Fig. 2c) with a conductive glassy carbon window was designed by Borkiewicz et al.11 This cell has been proved as compatible with various synchrotron-based X-ray scattering and spectroscopy measurements without the undesired delays in the electrochemical reactions near the window area and shows improved long-term cycle stability. Liu et al.16 investigated the dynamic process of the LiFePO4 electrode material by using TR-XRD with an AMPIX cell and detected the metastable intermediate phase. At lower current rates of 5 and 10 C, all diffraction peaks observed from the in situ XRD of the initial 5 cycles can be indexed to either the Li-rich Li1-αFePO4 or Li-poor LiβFePO4 phase. Surprisingly, a new phase with lattice parameters smaller than those of LiFePO4 but larger than those of FePO4 under equilibrium was observed at a fast rate of 20 C. The individual diffraction patterns during the first cycle at various rates of 5, 10, and 20 C were also compared. The results, as shown in Fig. 4a–c, demonstrated that the phase transformation in LiFePO4 at a high rate continues by changing the structure rather than through distinct relocation of the phase boundary between LiFePO4 and FePO4. This kind of structural change avoids a major structural rearrangement across a moving interface, which helps to explain the good high-rate performance of LiFePO4 despite a large Li miscibility gap between LiFePO4 and FePO4 at room temperature. This work also reconfirmed that investigation of the equilibrium system (e.g., ex situ measurement) is insufficient to elucidate the operation mechanism of electrode materials operated at high rates.
Most in situ cells including coin cells, pouch cells, and AMPIX cells are designed for an X-ray geometry, so the incident beam is along the electrode stacking direction. In this measurement geometry, the incident beam penetrates all the cell components such as the cathode, anode, separator, and electrolytes, and the diffracted signals from these components are collected by the detector. The advantages of this geometry is the easy construction and alignment of the in situ cell, but a disadvantage is the inability to distinguish the signals coming from different parts of the electrode sample along the beam path. In other words, if structural changes are inhomogeneous among the parts near the current collector and closer to the separator, they will not be individually detected. As we know, inhomogeneous electrochemical reactions should be considered for cathode materials, especially when thick electrodes are used. Thicker electrodes can increase the energy density of the cell, but may cause more serious inhomogeneous reactions, especially at high cycling rates. To investigate the rate dependent inhomogeneous reactions in parts near current collector to those close to the separator, a RATIX cell (Fig. 2d) for spatially resolved in operando X-ray scattering and spectroscopic studies was developed with advantages of the high intensity and micron focused X-ray source from the Advanced Photon Source (APS) beamline. Liu et al.12 conducted a “depth profile” measurement of the LiFePO4 electrode and provided insight into the relationship between the inhomogeneity of the structural changes and the electrochemical performance of the cell by using the RATIX cell. The important conclusion is that the electrode parts near the separator showed a more advanced reaction than those near the current collector under the same charge (discharge) state.
In situ pair distribution function (PDF)
Although XRD techniques can provide important structural information about crystalline materials, it is not easy to perform characterization studies using conventional powder diffraction on materials without long-range order, such as amorphous materials or materials with nano-sized crystals. For instance, it is hard to investigate the reaction mechanism of conversion-type electrode materials using XRD due to nano-sized and highly disordered particles that form during the conversion-type electrochemical process. For this kind of study, the pair distribution function (PDF) is a good choice. While XRD covers only Bragg scattering and provides long-range average structural information, the PDF techniques utilize the total scattering (Bragg and diffuse scattering), which can be used to investigate the materials with short-range ordering, and provides local information especially the atomic pair distribution relating to chemical, structural, and morphological transformations that occur during electrochemical reactions.
Mixed-anion iron oxyfluoride (i.e., FeOF) material is a typical conversion-type electrode with a good rate capability and relatively good reversibility. Wiaderek et al.30 investigated the electrochemical reaction mechanism of an FeOF electrode using in operando PDF combined with Li nuclear magnetic resonance (NMR) NMR spectroscopy. For better background subtraction, an AMPIX cell was used in this in situ PDF experiment, and the results are shown in Fig. 5a. The PDF data collected during the initial discharge process show smooth changes in local structural features and bond lengths, indicating the conversion of FeOF to metallic Fe. Rietveld refinement results show the transformation from FeOF to Fe via a rock-salt-type intermediate phase. More interestingly, the structure of the re-charged electrode is completely different from the initial single-phase electrode, although the recharge capacity is almost fully reversible for the discharge capacity. By analyzing the bond length, oxidation state, and coordination numbers of the positions and the intensities of the peaks representing the Fe–O/F and Fe–Fe pairs, the charge capacity should be attributed to the formation of a nanoscale composite of the rock-salt phase, which is oxide-rich, and the rutile phase, which is fluoride-rich. Similarly, Hua et al.31 investigated the reaction mechanism of a conversion-type CuF2 electrode using PDF and NMR measurements, and provided the results of the local structure information during the first discharge process. As shown in Fig. 5b, the PDF peaks of equatorial and axial Cu–F bonds in the pristine electrode indicate Jahn-Teller distortion of Cu2+. Variations in the peak position and intensity during the discharge process suggest the transformation from CuF2 to metallic Cu.
PDF is also utilized for the depth profile measurement to investigate inhomogeneous structural changes at the electrode level. Unfortunately, few reports using in situ/operando PDF to do depth profile studies have been conducted, and we believe such studies will provide more in-depth understanding of the inhomogeneity of electrochemical reactions in the near future. Borkiewicz et al.32 designed an ex situ experiment to investigate the distribution of the charge/discharge states perpendicular to the electrode surface by using spatially resolved hard X-ray PDF. A free-standing pellet of nanoscale α-Fe2O3 was used as an electrode, and was discharged to the midpoint of the fully discharged state during conversion of the rock-salt phase to the Fe nanoparticle phase. PDF data collected as a function of distance from the surface of the partially discharged electrode are shown in Fig. 5c. The features associated with Fe (Fe–Fe ~ 2.5 Å) are most pronounced near the surface, while the features associated with the rock-salt phase (Fe1-xO, Fm3m, a = 4.2 Å) are most pronounced near the current collector. Phase fraction analysis (Fig. 5d) suggested that the reaction is most advanced close to the separator, and the rate is limited by Li diffusion rather than electronic conductivity. In this case, a higher current rate may exacerbate the formation of a phase fraction gradient.
In situ X-ray absorption spectroscopy (XAS)
XAS is a technique that measures the X-ray absorption coefficient of a sample as a function of the X-ray photon energy below and above the absorption edge of a certain element. According to the energy range (wavelength) of the probing X-ray source, XAS can be divided into soft (<1 keV), tender (1–5 keV), and hard XAS (>5 keV)33.
An XAS spectrum is typically divided into two regions by the relative energy range to the absorption edge: (1) the X-ray absorption near-edge structure (XANES), which covers from a few eV below the absorption edge to approximately 50 eV above the edge, and (2) the extended X-ray absorption fine-structure (EXAFS), which extends from approximately 50 eV above the edge to as much as 1000 eV34. The XANES data collected on the cathode samples cycled to different states of charge provide useful quantitative or qualitative information about the changes in the oxidation states of the elements being probed, their site symmetries, and the covalent bond strengths. EXAFS can be used to study short-range local structures and obtain coordination numbers, bond distances, and the chemical identity of the nearest neighbors through data fitting. In general, for soft XAS, the EXAFS part is not considered, and the typical data are collected on the K-edges of low-Z elements (e.g., C, N, O) and L-edges of 3d transition metals (3d-TM). XANES in soft XAS is also called near-edge X-ray absorption fine-structure (NEXAFS) spectroscopy35.
A great advantage of XAS over other techniques is the elemental selectivity, which enables us to study the local chemical environment surrounding certain elemental atoms. Due to its elemental selectivity and high chemical sensitivity, in situ XAS has been used as a key characterization tool to study the charge compensation mechanisms of LIB electrode materials. In situ XAS can provide information about the chemical environment and oxidation state of each individual element in a material containing multiple elements, helping us to determine the main contributing element of a redox processes at a certain charge/discharge state.
A good example of this is the work of Yu et al.36, which studied different contributions of three transition metals to the electrochemical charge/discharge reactions in Li1. 2Ni0.15Co0.1Mn0.55O2. As shown in Fig. 6a, Li1.2Ni0.15Co0.1Mn0.55O2 exhibits a high-charge capacity of 300 mAh g−1, with a high average operating voltage (>3.5 V vs. Li/Li+). Ni, Co, and Mn K-edge XANES (Fig. 6b) shows that major charge compensation at the metal site during charging is achieved by the oxidation of Ni2+ ions, as reflected by the rigid edge shift of Ni, while the K-edge positions of Mn and Co ions remain mostly unchanged near the Mn4+ and Co3+ edge positions. Since the K-edge XANES energy position changes can only be used to track the contribution from Ni but not from Mn and Co, other spectral parameters are needed to correlate the structural changes with the charge capacity contribution of Mn and Co during the charging process. EXAFS analysis was performed to correlate the charge capacity with changes in the intensity of the Mn–O and Co–O first shell peaks obtained by Fourier transformed EXAFS spectra (Fig. 6c). Semi-quantitative analysis of Ni K-edge XANES with energy position changes and the Debye-Waller factors of Mn-O and Co-O derived from EXAFS fitting during cycling were also performed, as presented in Fig. 6d and e. The σMn-O values show a continuous increase in the whole voltage range up to 4.8 V during the initial charge process. Changes in these values before the voltage plateau (approximately 4.5 V) could be caused by local structural changes induced by lithium extraction from the LiMO2 structure. The σCo–O values show a significant increase in the first voltage slope region (3–4.5 V). Upon further charging in the voltage plateau region, the σMn–O values continue to increase, reaching the maximum value at the end of the first charge, while the σCo–O and σNi–O values reveal only a slight change, indicating that the lithium extraction-induced local structural changes mainly occur in the area surrounding the Mn sites, thus providing more information about the contribution of Mn.
The dispersive XAS instrumentation enables time-resolved XAS (TR-XAS) experiments on a time scale as short as milliseconds37,38, making it possible to investigate the dynamic process of battery materials under high-rate operating conditions. Unlike conventional in situ XAS experiments performed at slow charge/discharge rates (e.g., C/20 and C/5) for several hours, Zhou et al.15 reported results collected in a time frame as short as several minutes at very high charge-discharge rates utilizing the TR-XAS technique. Figure 7a–c shows the Ni, Co, and Mn K-edge XANES spectra of LiNi1/3Mn1/3Co1/3O2 during 30 C charging (charged in 2 min). To avoid potential problems that could be caused by soft Kapton windows, the modified coin cell using glassy carbon windows was used to enhance the pressure of the window region. The K-edge of Ni shifts continuously to higher energy, indicating oxidation of Ni ions from Ni2+ to Ni4+ during the charging process. In contrast, the K-edges of Co and Mn show almost no energy shift. Only changes to the shape of the Co and Mn K-edge features occur, indicating that the local environment changes around the Co and Mn ions. However, Co and Mn contribute very little to the capacity. The edge shift of Ni K-edge XANES as a function of the state-of-charge (amount of delithiated Li+) at different C rates (Fig. 7d) demonstrates that oxidation of Ni accelerates with increasing charging rate, and the Ni4+ state can be reached at the end of charging even at a high 30 C rate. These results show the good kinetic properties of Ni, indicating that the high Ni content in NMC aids in achieving a high rate capability. Another good example of TR-XAS studies is the work of Yu et al.36, which aimed to better understand the rate-limiting element in Li1.2Ni0.15Co0.1Mn0.55O2. Yu et al. applied a constant voltage of 5 V on a Li1.2Ni0.15Co0.1Mn0.55O2 cathode to oxidize Ni, Co, and Mn ions simultaneously. The comparative Fourier transformed magnitude of the corresponding Ni, Co, Mn K-edge EXAFS spectra shown in Fig. 7e demonstrated the different kinetic behaviors of the three metal elements. The results clearly showed that oxidation of Mn is much slower than oxidation of Ni and Co in Li1.2Ni0.15Co0.1Mn0.05O2 cathode materials, and nano-domains of Li2MnO3 are the major rate-limiting factors.
Compared with hard XAS, sXAS is a more direct and efficient tool to probe the electronic states through excitation of core-level electrons to unoccupied states above the Fermi level. In particular, for LIB research, 3d electron states of 3d-TM and the p electron states of anions can be directly studied using sXAS. In addition, sXAS can be used to study samples with various probing depths (from surface to bulk), by using different signal detection modes (as shown in Fig. 1). Due to the different penetration lengths of the photo electrons and fluorescence photons, the electron yield (EY) mode signal mainly provides information about the surface (1–10 nm), while the fluorescence yield (FY) mode signal is mainly from the bulk. Therefore, sXAS is considered a powerful tool to study surface/interface related issues such as a solid electrolyte interphase (SEI) or a cathode-electrolyte interface (CEI). Combining hXAS and sXAS at multiple probing depths will provide valuable information to understand complicated and inhomogeneous reactions during LIBs operation. The poor penetration power of soft X-rays requires UHV conditions, causing difficulty in performing in situ sXAS experiments, especially for liquid electrolyte cells.
It is quite interesting to note that significant progress has been made recently on designing and applying in situ/operando cells for sXAS experiments under UHV conditions. For example, Liu et al.13 developed an in situ sXAS cell with a modified current collector and polymer electrolyte, as shown Fig. 2e. Interestingly, the strong relaxation effect and a state-of-charge (SOC) gradient were observed in the LiFePO4 electrode, shown in Fig. 8. In contrast, the sXAS results of the LiCo1/3Ni1/3Mn1/3O2 electrodes show uniform SOC across whole electrodes. The cooperation of the electronic and ionic conductivity, the phase transformation mechanism and the mesoscale morphology lead to an observed difference in the charge dynamics of NMC and LiFePO4. It is revealed that electron transportation is the determining factor for LiFePO4 during electrochemical cycling, while the open-circuit relaxation time is governed by ionic conductivity. This comparative study demonstrates the power of in situ sXAS for studying charge dynamics in battery electrodes.
As discussed before in the XRD section, the investigation of the depth profile is also considered with XAS. Considering the working principle of XAS, the depth of beam penetration in XAS measurements is highly dependent on the energy level of the incident beam. Unfortunately, the K-edge energy of most of elements used in LIBs (i.e., 3d-TM) is below 10 keV, which requires a relatively thin sample thickness (~few hundred µm). Furthermore, other cell components in the beam pathway, such as window materials or electrolyte, will absorb the beam, and therefore, the cell configuration and materials greatly restricted compared to those in XRD. A RATIX cell might be applicable in some energy ranges, but the thickness of a tubular cell needs to be very thin in a lower energy range. The micro-size beam with high flux is also required. Regardless of such technical difficulties, some efforts have been made to obtain a depth profile for ex situ studies. Orikasa et al.39 demonstrated cross-sectional 2D mapping of the absorption energy at the Fe K-edge in LiFePO4 composite electrodes (Fig. 9). Fe K-edge XAS spectra were collected in transmission mode using a CMOS detector with spatial resolution of 10 µm. 2D Fe K-edge XAS mapping reveals that more significant inhomogeneity of the electrochemical reaction occurred in lower porosity electrodes, which have lower ionic conductivities. This work could further motivate other researchers to develop new cells for in situ depth profile XAS measurements in the future.
In situ X-ray imaging
Imaging methods provide opportunities for the direct visualization of battery materials and components, and therefore offer straightforward information about the microstructure, morphology, and chemical composition. X-ray microscopy allows for the direct visualization of battery materials and components in a non-invasive manner under in operando conditions. In general, X-ray imaging techniques can be classified into real-space imaging methods and reciprocal space imaging methods depending on the setup of the imaging systems. The reciprocal image methods can achieve a relatively higher spatial resolution because no X-ray optics are needed between the sample and the recorder, removing the optical limits of the spatial resolution of the imaging systems40. Based on the data acquisition method, X-ray imaging techniques can also be categorized as full-field X-ray imaging methods and scanning X-ray imaging methods.
Real-space full-field imaging methods are usually superior in terms of the data acquisition speed. The typical exposure time of a single image can be completed in a time frame as short as a few tens of milliseconds at synchrotron light sources, which favors in situ/operando and time-resolved studies. Absorption contrast and phase contrast are the most commonly used mechanisms for full-field X-ray imaging methods. The power of real-space full-field imaging methods to visualize battery materials in real-time operation has been demonstrated by various recent works20,41,42,43,44,45,46,47,48,49. Combined with spectroscopic measurements, full-field X-ray imaging becomes even more powerful for obtaining chemical information in addition to the morphological information. For example, Yang et al.50 reported the chemical phase, oxidation state and morphology changes of Li1.2Mn0.525Ni0.175Co0.1O2 after multiple cycles; Lin et al.51 revealed transition metal segregation at the subparticle level in LiNi0.4Mn0.4Co0.2O2 cathode material; Xu et al.52 investigated the evolution of chemical and morphological changes of Li-rich Li2Ru0.5Mn0.5O3 cathode materials at the nanoscale upon electrochemical cycling.
Unlike the full-field imaging method, scanning X-ray imaging experiments are performed by using well-focused X-rays to illuminate the sample, which is raster-scanned in the focal plane. Different types of signals (e.g., transmission, fluorescence, diffraction, etc.) can be recorded at each data collecting position to construct the full X-ray images. The major drawback of the scanning method is the relative slower data acquisition speed, which has been greatly improved with the development of more brilliant synchrotron light sources. Scanning imaging techniques for LIB studies have been widely employed in recent years44,53,54,55,56. One example is the investigation of the spatiotemporal evolution of the Li composition and insertion rates in LiFePO4 in primary particles by using soft X-ray scanning transmission X-ray microscopy (STXM) (Fig. 10). Soft X-ray transition metal (TM) L-edge spectra are very sensitive to the valence of 3d TM ions57. Lim et al.44 designed a soft X-ray in situ liquid cell (with a Si3N4 thin film as a window), which can be used in a vacuum chamber during measurement. The dynamics of the nanoscale spatial variation of the Fe valence associated with the lithium composition (LixFePO4) at different lithiation/delithiation rates was mapped. The results indicate that the nanoscale intraparticle electrochemical reaction inhomogeneity in the phase and composition is rate dependent, and the lithiation and delithiation behavior is remarkably different in LiFePO4. The reaction heterogeneities and compositional non-uniformity at the particle or subparticle scales can be probed and well visualized by in situ/operando X-ray imaging.
Most of the in situ/operando X-ray imaging experiments have been focused on the first or first several charge-discharge cycles only. However, studies of the degradation mechanisms of battery materials inevitably require tracking the electrochemical reaction of the batteries for long-term cycling. Since synchrotron beamtime not often granted for prolonged experiments, continuous monitoring of the electrochemical reaction during long-term cycling at synchrotron facilities is not economically feasible. Recently, Xu and co-workers41 developed an in situ setup that is capable of tracking the same particle of a sample after dismounting and remounting it over multiple charge-discharge cycles by intermittent sampling. As seen in Fig. 11, the in situ apparatus is made of a pouch cell attached to a cell holder. The cell holder is mounted on the sample stage with recordable absolute coordinates. As long as the sample is mounted with the same absolute position on the sample stage as the previous measurement, the same sample particle can be relocated. This kind of setup also has the advantage of reducing radiation damage caused by long-term X-ray beam illumination during cycling. Taking advantages of this kind of setup, electrochemical cycling can be done offline (out of the X-ray beam) until the specific cycling state of interest is reached. Under this arrangement, data can be collected as a function of the SOC and/or the number of cycles. As an example, the reaction heterogeneity of LiCoO2 on the sub-micro-scale for a particle at different charge-discharge states and cycle numbers is clearly observed. Inactive domains were observed and redistributed within the particle upon long-term cycling and is directly linked to the degradation behavior of LiCoO2 material. This study also demonstrates that X-ray imaging is capable of investigating the degradation mechanism of battery materials over prolonged cycles.
When the X-ray tomography technique is used, a series of X-ray images at different angles are recorded (the sample is rotated along an axis that is perpendicular to the incident X-rays) and then reconstructed by computer to produce the 3D images58. This X-ray tomography technique using synchrotron X-ray sources has been applied to the in situ/operando studies on dynamic 3D morphological changes during electrochemical reactions. Electrode materials that store lithium through conversion or alloying reactions face the major problem of volume changes during lithium insertion and extraction42,59,60. The in operando study of dynamic changes in the sample morphology in 3D provides valuable information for the fundamental understanding of the lithium (or other alkali ions) storage mechanisms of these materials, as well as insightful information for material design. Several good examples of using in situ/operando X-ray tomography for battery material studies are shown in the work of Villevieille et al.49 regarding the influence of particle morphology on the alloying phase transformation process of an Sb/TiSb2 electrode, and in the work of Wang et al.14 regarding three-dimensional structural/chemical evolution of a tin anode electrode material for sodium-ion batteries. A more detailed study using a tomographic technique for an in operando experiment was reported by Ebner et al.42 as shown in (Fig. 12). They used X-ray tomography to visualize the morphological changes in a conversion/alloying-type SnO anode during battery operation, and discussed the origins of electrochemical and mechanical degradation associated with such volume changes. The chemical reaction of SnO during lithium insertion (discharge) and extraction (charge) can be tracked by monitoring the attenuation coefficient of the electrode. The tomographic analysis provided 3D chemical and morphological information within a sample particle. The phase transformation, crack creation and growth, and electrode deformation can be clearly observed, offering direct visualization associated with the degradation of battery performance. The application of X-ray tomography can be extended to lithium metal anode research; although, it is well known that lithium is difficult to characterize by using X-ray-based techniques due to the weak interaction between lithium and the X-ray photons. A recent publication by Guillaume et al. shows promising results proving that X-ray tomography is useful for investigating the morphology and structural changes of lithium metal anodes61. Overall, X-ray tomography enables the investigation of dynamic changes in a sample in real batteries and, therefore, opens a new avenue for the rational design of battery materials.
Significant progress toward developing in situ/operando techniques using an advanced synchrotron X-ray source has been made, and various in situ cell designs for LIB studies have been reported recently. The studies of in situ/operando XRD, PDF, XAS, and imaging techniques highlighted in this review can be used as good references to guide future development of in situ/operando experiments, and suitable in situ electrochemical cells for such experiments as well as the selection of appropriate X-ray techniques for certain research purposes.
The combination of different characterization techniques is important to obtain a more complete picture and more comprehensive information about the structural changes in LIB materials. For example, although synchrotron-based X-ray imaging techniques can provide morphological and chemical information at wide length scales, from tens of nm to the mm scale, imaging at the atomic-length scale (sub or few nm) still requires transmission electron microscopy (TEM) techniques. Nuclear magnetic resonance (NMR) and mass spectrometry (MS) can also provide important complementary information to the X-ray techniques. For further development of in situ/operando X-ray techniques, high-speed data collection and the automated analysis of large amount of data (data mining) are quite important, and we hope this review is helpful for these aspects.
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The work at Brookhaven National Lab was supported by the U.S. Department of Energy, the Assistant Secretary for Energy Efficiency and Renewable Energy, Vehicle Technologies Office (BMR project including the VTO Battery 500) under Contract Number DE-SC0012704. The work at the Institute of Physics, Chinese Academy of Sciences was supported by funding from the National Key R&D Program of China (Grants No. 2017YFB0102004) and “Thousand Talents Program for Young Scientists”.
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Bak, SM., Shadike, Z., Lin, R. et al. In situ/operando synchrotron-based X-ray techniques for lithium-ion battery research. NPG Asia Mater 10, 563–580 (2018). https://doi.org/10.1038/s41427-018-0056-z
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