Design Strategies of Spinel Oxide Frameworks Enabling Reversible Mg-Ion Intercalation.

ConspectusReversible Mg2+ intercalation in metal oxide frameworks is a key enabler for an operational Mg-ion battery with high energy density needed for the next generation of energy storage technologies. While functional Mg-ion batteries have been achieved in structures with soft anions (e.g., S2- and Se2-), they do not meet energy density requirements to compete with the current rechargeable lithium-ion batteries due to their low insertion potentials. It emphasizes the necessity of finding an oxide-based cathode that operates at high potentials. A leading hypothesis to explain the limited availability of oxide Mg-ion cathodes is the belief that Mg2+ has sluggish diffusion kinetics in oxides due to strong electrostatic interactions between the Mg2+ ions and oxide anions in the lattice. From this assessment, it can be hypothesized that such rate limiting kinetic shortcomings can be mitigated by tailoring an oxide framework through creating less stable Mg2+-O2- coordination.Based on theoretical calculations and preliminary experimental data, oxide spinels have been identified as promising cathode candidates with storage capacity, insertion potential, and cation mobility that meet the requirements for a secondary Mg-ion battery. However, spinels with a single redox metal, such as MgCr2O4 or MgMn2O4, were not found to demonstrate sufficiently reversible Mg-ion intercalation at high redox potentials when coupled with nonaqueous Mg-electrolytes. Therefore, a materials development effort was initiated to design, synthesize, and evaluate a new class of solid-solution oxide spinels that can satisfy the required properties needed to create a sustainable Mg-ion cathode. These were designed by bringing together electrochemically active metals with stable redox potentials and charged states against the electrolyte, for instance, Mn3+, in combination with a structural stabilization component, typically Cr3+. Furthermore, common spinel structural defects that degrade performance, i.e., antisite inversion, were controlled to see correlation between structures and electrochemical overpotentials, thus controlling overall hysteresis. The designed materials were characterized by both short- and long-range structure in both ex situ and in situ modes to confirm the nature of solid-solution and to correlate structural changes and redox activity to electrochemical performance. Consistent and reproducible results were observed for facile bulk Mg2+-ion activity without phase transformations, leading to enhanced energy storage capability based on reversible intercalation of Mg2+, enabled by understanding the variables that control the electrochemical performance of the spinel oxide. Based on these observations, with proper materials design, it is possible to develop an oxide cathode material that has many of the desired properties of a Li-ion intercalation cathode, representing a significant mile marker in the quest for high energy density Mg-ion batteries.This Account describes strategies for the design and development of new spinel oxide intercalation materials for high-energy Mg-ion battery cathodes through a combination of theoretical and experimental approaches. We will review the key factors that govern the kinetics of Mg2+ diffusion in spinel oxides and illustrate how material complexity correlates with the electrochemical Mg2+ activity in oxides and is supported by secondary characterization. The understanding gained from the fundamental studies of cation diffusion in oxide cathodes will be beneficial for chemists and materials scientists who are developing rechargeable batteries.

Investigation of Ca Insertion into α-MoO3 Nanoparticles for High Capacity Ca-Ion Cathodes.

Calcium-ion batteries (CIBs) are a promising alternative to lithium-ion batteries (LIBs) due to the low redox potential of calcium metal and high abundance of calcium compounds. Due to its layered structure, α-MoO3 is regarded as a promising cathode host lattice. While studies have reported that α-MoO3 can reversibly intercalate Ca ions, limited electrochemical activity has been noted, and its reaction mechanism remains unclear. Here, we re-examine Ca insertion into α-MoO3 nanoparticles with a goal to improve reaction kinetics and clarify the storage mechanism. The α-MoO3 electrodes demonstrated a specific capacity of 165 mA h g-1 centered near 2.7 V vs Ca2+/Ca, stable long-term cycling, and good rate performance at room temperature. This work demonstrates that, under the correct conditions, layered oxides can be a promising host material for CIBs and renews prospects for CIBs.

Reciprocal space imaging of ionic correlations in intercalation compounds.

The intercalation of alkali ions into layered materials has played an essential role in battery technology since the development of the first lithium-ion electrodes. Coulomb repulsion between the intercalants leads to ordering of the intercalant sublattice, which hinders ionic diffusion and impacts battery performance. While conventional diffraction can identify the long-range order that can occur at discrete intercalant concentrations during the charging cycle, it cannot determine short-range order at other concentrations that also disrupt ionic mobility. In this Article, we show that the use of real-space transforms of single-crystal diffuse scattering, measured with high-energy synchrotron X-rays, allows a model-independent measurement of the temperature dependence of the length scale of ionic correlations along each of the crystallographic axes in sodium-intercalated V2O5. The techniques described here provide a new way of probing the evolution of structural ordering in crystalline materials.

Author Correction: Reciprocal space imaging of ionic correlations in intercalation compounds.

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Synthesis and Characterization of MgCr2S4 Thiospinel as a Potential Magnesium Cathode.

Magnesium-ion batteries are a promising energy storage technology because of their higher theoretical energy density and lower cost of raw materials. Among the major challenges has been the identification of cathode materials that demonstrate capacities and voltages similar to lithium-ion systems. Thiospinels represent an attractive choice for new Mg-ion cathode materials owing to their interconnected diffusion pathways and demonstrated high cation mobility in numerous systems. Reported magnesium thiospinels, however, contain redox inactive metals such as scandium or indium, or have low voltages, such as MgTi2S4. This article describes the direct synthesis and structural and electrochemical characterization of MgCr2S4, a new thiospinel containing the redox active metal chromium and discusses its physical properties and potential as a magnesium battery cathode. However, as chromium(III) is quite stable against oxidation in sulfides, removing magnesium from the material remains a significant challenge. Early attempts at both chemical and electrochemical demagnesiation are discussed.

Degradation Mechanisms of Magnesium Metal Anodes in Electrolytes Based on (CF3SO2)2N- at High Current Densities.

The energy density of rechargeable batteries utilizing metals as anodes surpasses that of Li ion batteries, which employ carbon instead. Among possible metals, magnesium represents a potential alternative to the conventional choice, lithium, in terms of storage density, safety, stability, and cost. However, a major obstacle for metal-based batteries is the identification of electrolytes that show reversible deposition/dissolution of the metal anode and support reversible intercalation of ions into a cathode. Traditional Grignard-based Mg electrolytes are excellent with respect to the reversible deposition of Mg, but their limited anodic stability and compatibility with oxide cathodes hinder their applicability in Mg batteries with higher voltage. Non-Grignard electrolytes, which consist of ethereal solutions of magnesium(II) bis(trifluoromethanesulfonyl)imide (Mg(TFSI)2), remain fairly stable near the potential of Mg deposition. The slight reactivity of these electrolytes toward Mg metal can be remedied by the addition of surface-protecting agents, such as MgCl2. Hence, ethereal solutions of Mg(TFSI)2 salt with MgCl2 as an additive have been suggested as a representative non-Grignard Mg electrolyte. In this work, the degradation mechanisms of a Mg metal anode in the TFSI-based electrolyte were studied using a current density of 1 mA cm-2 and an areal capacity of ∼0.4 mAh cm-2, which is close to those used in practical applications. The degradation mechanisms identified include the corrosion of Mg metal, which causes the loss of electronic pathways and mechanical integrity, the nonuniform deposition of Mg, and the decomposition of TFSI- anions. This study not only represents an assessment of the behavior of Mg metal anodes at practical current density and areal capacity but also details the outcomes of interfacial passivation, which was detected by simple cyclic voltammetry experiments. This study also points out the absolute absence of any passivation at the electrode-electrolyte interface for the premise of developing electrolytes compatible with a metal anode.

Binary Cation Matrix Electrolyte and Its Effect on Solid Electrolyte Interphase Suppression and Evolution of Si Anode.

An unstable solid electrolyte interphase (SEI) has been recognized as one of the biggest challenges to commercializing silicon (Si) anodes for high-energy-density batteries. This work thoroughly investigates a binary cation matrix of Mg2++Li+ electrolyte and its role in SEI development, suppression, and evolution of a Si anode. Findings demonstrate that introducing Mg ions dramatically reduces the SEI growth before lithiation occurs, primarily due to the suppression of solvent reduction, particularly ethylene carbonate (EC) reduction. The Mg2+ alters the Li+ cation solvation environment as EC preferably participates in the oxophyllic Mg2+ solvation sheath, thereby altering the solvent reduction process, resulting in a distinct SEI formation mechanism. The initial SEI formation before lithiation is reduced by 70% in the electrolyte with the presence of Mg2+ cations. While the SEI continues to develop in the postlithiation, the inclusion of Mg ions results in an approximately 80% reduction in the postlithiation SEI growth. Continuous electrochemical cycling reveals that Mg2+ plays a crucial role in stabilizing the deep-lithiated Si phases, which effectively mitigates side reactions, resulting in controlled SEI growth and stable interphase while eliminating complex LixSiy formation. Mg ions promote the development of a notably more rigid and homogeneous SEI, characterized by a reduced dissipation (ΔD) in the Mg2++Li+ ion matrix compared to the solely Li+ system. This report reveals how the Mg2++Li+ ion matrix affects the SEI evolution, viscoelastic properties, and electrochemical behavior at the Si interface in real time, laying the groundwork for devising strategies to enhance the performance and longevity of Si-based next-generation battery systems.

AgNa(VO2F2)2: a trioxovanadium fluoride with unconventional electrochemical properties.

We present structural and electrochemical analyses of a new double-wolframite compound: AgNa(VO2F2)2 or SSVOF. SSVOF is fully ordered and displays electrochemical characteristics that give insight into electrode design for energy storage beyond lithium-ion chemistries. The compound contains trioxovanadium fluoride octahedra that combine to form one-dimensional chain-like basic building units, characteristic of wolframite (NaWO4). The 1D chains are stacked to create 2D layers; the cations Ag(+) and Na(+) lie between these layers. The vanadium oxide-fluoride octahedra are ordered by the use of cations (Ag(+), Na(+)) that differ in polarizability. In the case of sodium-ion batteries, thermodynamically, the use of a sodium anode introduces a 300 mV loss in overall cell voltage as compared to a lithium anode; however, this can be counter-balanced by introduction of fluoride into the framework to raise the reduction potentials via an inductive effect. This allows sodium-ion batteries to have comparable voltages to lithium systems. With SSVOF as a baseline compound, we have identified new materials design rules for emerging sodium-ion systems that do not apply to lithium-ion systems. These strategies can be applied broadly to provide materials of interest for fundamental structural chemistry and appreciable voltages for sodium-ion electrochemistry.

Expanding the Ambient-Pressure Phase Space of CaFe2O4-Type Sodium Postspinel Host-Guest Compounds.

CaFe2O4-type sodium postspinels (Na-CFs), with Na+ occupying tunnel sites, are of interest as prospective battery electrodes. While many compounds of this structure type require high-pressure synthesis, several compounds are known to form at ambient pressure. Here we report a large expansion of the known Na-CF phase space at ambient pressure, having successfully synthesized NaCrTiO4, NaRhTiO4, NaCrSnO4, NaInSnO4, NaMg0.5Ti1.5O4, NaFe0.5Ti1.5O4, NaMg0.5Sn1.5O4, NaMn0.5Sn1.5O4, NaFe0.5Sn1.5O4, NaCo0.5Sn1.5O4, NaNi0.5Sn1.5O4, NaCu0.5Sn1.5O4, NaZn0.5Sn1.5O4, NaCd0.5Sn1.5O4, NaSc1.5Sb0.5O4, Na1.16In1.18Sb0.66O4, and several solid solutions. In contrast to earlier reports, even cations that are strongly Jahn-Teller active (e.g., Mn3+ and Cu2+) can form Na-CFs at ambient pressure when combined with Sn4+ rather than with the smaller Ti4+. Order and disorder are probed at the average and local length-scales with synchrotron powder X-ray diffraction and solid-state NMR spectroscopy. Strong ordering of framework cations between the two framework sites is not observed, except in the case of Na1.16In1.18Sb0.66O4. This compound is the first example of an Na-CF that contains Na+ in both the tunnel and framework sites, reminiscent of Li-rich spinels. Trends in the thermodynamic stability of the new compounds are explained on the basis of crystal-chemistry and density functional theory (DFT). Further DFT calculations examine the relative stability of the CF versus spinel structures at various degrees of sodium extraction in the context of electrochemical battery reactions.

Probing the Reactivity of the Active Material of a Li-Ion Silicon Anode with Common Battery Solvents.

Calculations and modeling have shown that replacing the traditional graphite anode with silicon can greatly improve the energy density of lithium-ion batteries. However, the large volume change of silicon particles and high reactivity of lithiated silicon when in contact with the electrolyte lead to rapid capacity fading during charging/discharging processes. In this report, we use specific lithium silicides (LS) as model compounds to systematically study the reaction between lithiated Si and different electrolyte solvents, which provides a powerful platform to deconvolute and evaluate the degradation of various organic solvents in contact with the active lithiated Si-electrode surface after lithiation. Nuclear Magnetic Resonance (NMR) characterization results show that a cyclic carbonate such as ethylene carbonate is chemically less stable than a linear carbonate such as ethylmethyl carbonate, fluoroethylene carbonate, and triglyme as they are found to be more stable when mixed with LS model compounds. Guided by the experimental results, two ethylene carbonate (EC)-free electrolytes are studied, and the electrochemical results show improvements with graphite-free Si electrodes relative to the traditional ethylene-carbonate-based electrolytes. More importantly, the study contributes to our understanding of the significant fundamental chemical and electrochemical stability differences between silicon and traditional graphite lithium-ion battery (LIB) anodes and suggests a focused development of electrolytes with specific chemical stability vs lithiated silicon which can passivate the surface more effectively.

A Simple Halogen-Free Magnesium Electrolyte for Reversible Magnesium Deposition through Cosolvent Assistance.

Rechargeable Mg batteries are one of the most investigated polyvalent-metal storage batteries owing to the increased safety associated with the nondendritic nature of Mg electrodeposition, high volumetric capacity, and low cost. To realize the commercial applications of Mg batteries, there are still a number of challenges remaining unsolved, in particular, the lack of halogen-free Mg electrolytes, as the use of the halogens remains a major limiting factor to achieving high voltage cathodes. Work presented here introduces an innovative approach to prepare a halogen-free Mg-based electrolyte in a simple, nonsynthetic method that can plate and strip Mg reversibly. Results suggest that by introducing a secondary amine cosolvent the magnesium bis(trifluoromethanesulfonyl)imide (Mg(TFSI)2) salt can be easily dissolved into a wide array of polar but aprotic ether solvents. A systematic structural investigation of a representative Mg(TFSI)2 electrolyte in the cosolvent systems with the secondary amine was performed using pair distribution function (PDF) analysis, single crystal diffraction analysis, and NMR. The experimental atomic scale understanding reveals an ion pair structure of Mg2+ coordinated with six oxygen donors from the bis(trifluoromethanesulfonyl)imide (TFSI) anions and the THF solvent located in the first solvation shell. The as-formed neutral ion pair structure acts as the active component for reversible Mg deposition. We believe this new route of preparing Mg electrolytes can extend the current understanding of Mg electrolyte functionality for rechargeable Mg batteries and offers more guidance for the future electrolyte design.

Using Mixed Salt Electrolytes to Stabilize Silicon Anodes for Lithium-Ion Batteries via in Situ Formation of Li-M-Si Ternaries (M = Mg, Zn, Al, Ca).

Replacing traditional graphite anode by Si anode can greatly improve the energy density of lithium-ion batteries. However, the large volume expansion and the formation of highly reactive lithium silicides during charging cause the continuous lithium and electrolyte consumption as well as the fast decay of Si anodes. In this work, by adding 0.1 M M(TFSI)x (M = Mg, Zn, Al and Ca) as a second salt into the electrolyte, we stabilize the anode chemistry through the in situ formation of Li-M-Si ternary phases during the charging process. First, lithium silicides and magnesium lithium silicides were synthesized as model compounds to investigate the influence of metal doping on the reactivity of lithiated Si. Using solid-state nuclear magnetic resonance spectroscopy, we show that Mg doping can dramatically suppress the chemical reactions between the lithium silicide compounds and common electrolyte solvents. New mixed salt electrolytes were prepared containing M(TFSI)x as a second salt to LiPF6 and tested in commercially relevant electrodes, which show higher capacity, superior cyclability, and higher Coulombic efficiencies in both half-cell and full-cell configurations (except for Zn) when compared with standard electrolytes. Post-electrochemistry characterizations demonstrate that adding M salts leads to the co-insertion of M cations along with Li into Si during the lithiation process, stabilizing silicon anions by forming more stable Li-M-Si ternaries, which fundamentally changes the traditional Li-Si binary chemistry while minimally affecting silicon electrochemical profiles and theoretical capacities. This study opens a new and simple way to stabilize silicon anodes to enable widespread application of Si anodes for lithium-ion batteries.

From Coating to Dopant: How the Transition Metal Composition Affects Alumina Coatings on Ni-Rich Cathodes.

Surface alumina coatings have been shown to be an effective way to improve the stability and cyclability of cathode materials. However, a detailed understanding of the relationship between the surface coatings and the bulk layered oxides is needed to better define the critical cathode-electrolyte interface. In this paper, we systematically studied the effect of the composition of Ni-rich LiNixMnyCo1-x-yO2 (NMC) on the surface alumina coatings. Changing cathode composition from LiNi0.5Mn0.3Co0.2O2 (NMC532) to LiNi0.6Mn0.2Co0.2O2 (NMC622) and LiNi0.8Mn0.1Co0.1O2 (NMC811) was found to facilitate the diffusion of surface alumina into the bulk after high-temperature annealing. By use of a variety of spectroscopic techniques, Al was seen to have a high bulk compatibility with higher Ni/Co content, and low bulk compatibility was associated with Mn in the transition metal layer. It was also noted that the cathode composition affected the observed morphology and surface chemistry of the coated material, which has an effect on electrochemical cycling. The presence of a high surface Li concentration and strong alumina diffusion into the bulk led to a smoother surface coating on NMC811 with no excess alumina aggregated on the surface. Structural characterization of pristine NMC particles also suggests surface Co segregation, which may act to mediate the diffusion of the Al from the surface to the bulk. The diffusion of Al into the bulk was found to be detrimental to the protection function of surface coatings leading to poor overall cyclability, indicating the importance of compatibility between surface coatings and bulk oxides on the electrochemical performance of coated cathode materials. These results are important in developing a better coating method for synthesis of next-generation cathode materials for lithium-ion batteries.

Understanding the Role of Temperature and Cathode Composition on Interface and Bulk: Optimizing Aluminum Oxide Coatings for Li-Ion Cathodes.

Surface coating of cathode materials with Al2O3 has been shown to be a promising method for cathode stabilization and improved cycling performance at high operating voltages. However, a detailed understanding on how coating process and cathode composition change the chemical composition, morphology, and distribution of coating within the cathode interface and bulk lattice is still missing. In this study, we use a wet-chemical method to synthesize a series of Al2O3-coated LiNi0.5Co0.2Mn0.3O2 and LiCoO2 cathodes treated under various annealing temperatures and a combination of structural characterization techniques to understand the composition, homogeneity, and morphology of the coating layer and the bulk cathode. Nuclear magnetic resonance and electron microscopy results reveal that the nature of the interface is highly dependent on the annealing temperature and cathode composition. For Al2O3-coated LiNi0.5Co0.2Mn0.3O2, higher annealing temperature leads to more homogeneous and more closely attached coating on cathode materials, corresponding to better electrochemical performance. Lower Al2O3 coating content is found to be helpful to further improve the initial capacity and cyclability, which can greatly outperform the pristine cathode material. For Al2O3-coated LiCoO2, the incorporation of Al into the cathode lattice is observed after annealing at high temperatures, implying the transformation from "surface coatings" to "dopants", which is not observed for LiNi0.5Co0.2Mn0.3O2. As a result, Al2O3-coated LiCoO2 annealed at higher temperature shows similar initial capacity but lower retention compared to that annealed at a lower temperature, due to the intercalation of surface alumina into the bulk layered structure forming a solid solution.

Direct Observation of Lattice Aluminum Environments in Li Ion Cathodes LiNi1-y-zCoyAlzO2 and Al-Doped LiNixMnyCozO2 via (27)Al MAS NMR Spectroscopy.

Direct observations of local lattice aluminum environments have been a major challenge for aluminum-bearing Li ion battery materials, such as LiNi1-y-zCoyAlzO2 (NCA) and aluminum-doped LiNixMnyCozO2 (NMC). (27)Al magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectroscopy is the only structural probe currently available that can qualitatively and quantitatively characterize lattice and nonlattice (i.e., surface, coatings, segregation, secondary phase etc.) aluminum coordination and provide information that helps discern its effect in the lattice. In the present study, we use NMR to gain new insights into transition metal (TM)-O-Al coordination and evolution of lattice aluminum sites upon cycling. With the aid of first-principles DFT calculations, we show direct evidence of lattice Al sites, nonpreferential Ni/Co-O-Al ordering in NCA, and the lack of bulk lattice aluminum in aluminum-"doped" NMC. Aluminum coordination of the paramagnetic (lattice) and diamagnetic (nonlattice) nature is investigated for Al-doped NMC and NCA. For the latter, the evolution of the lattice site(s) upon cycling is also studied. A clear reordering of lattice aluminum environments due to nickel migration is observed in NCA upon extended cycling.

Advanced hybrid battery with a magnesium metal anode and a spinel LiMn2O4 cathode.

Two Mg-Li dual salt hybrid electrolytes are developed, which exhibit excellent oxidative stability up to around 3.8 V (vs. Mg/Mg(2+)) on an aluminum current collector, enabling the successful coupling of several state-of-the-art lithium-ion intercalation cathodes (LiMn2O4, LiCoO2 and LiNi1/3Mn1/3Co1/3O2) with magnesium metal anodes. The Mg-LiMn2O4 battery delivers an initial discharge capacity of about 106 mA h g(-1) with a working voltage of around 2.8 V (vs. Mg/Mg(2+)), highlighting the highest working voltage of rechargeable batteries with magnesium metal anodes to date.

The Role of MgCl2 as a Lewis Base in ROMgCl-MgCl2 Electrolytes for Magnesium-Ion Batteries.

A series of strong Lewis acid-free alkoxide/siloxide-based Mg electrolytes were deliberately developed with remarkable oxidative stability up to 3.5 V (vs. Mg/Mg(2+)). Despite the perception of ROMgCl (R=alkyl, silyl) as a strong base, ROMgCl acts like Lewis acid, whereas the role of MgCl2 in was unambiguously demonstrated as a Lewis base through the identification of the key intermediate using single crystal X-ray crystallography. This Lewis-acid-free strategy should provide a prototype system for further investigation of Mg-ion batteries.

Role of Chloride for a Simple, Non-Grignard Mg Electrolyte in Ether-Based Solvents.

Mg battery operates with Chevrel phase (Mo6S8, ∼1.1 V vs Mg) cathodes that apply Grignard-based or derived electrolytes, which allow etching of the passivating oxide coating forms at the magnesium metal anode. Majority of Mg electrolytes studied to date are focused on developing new synthetic strategies to achieve a better reversible Mg deposition. While most of these electrolytes contain chloride as a component, and there is a lack of literature which investigates the fundamental role of chloride in Mg electrolytes. Further, ease of preparation and potential safety benefits have made simple design of magnesium electrolytes an attractive alternative to traditional air sensitive Grignard reagents-based electrolytes. Work presented here describes simple, non-Grignard magnesium electrolytes composed of magnesium bis(trifluoromethane sulfonyl)imide mixed with magnesium chloride (Mg(TFSI)2-MgCl2) in tetrahydrofuran (THF) and diglyme (G2) that can reversibly plate and strip magnesium. Based on this discovery, the effect of chloride in the electrolyte complex was investigated. Electrochemical properties at different initial mixing ratios of Mg(TFSI)2 and MgCl2 showed an increase of both current density and columbic efficiency for reversible Mg deposition as the fraction content of MgCl2 increased. A decrease in overpotential was observed for rechargeable Mg batteries with electrolytes with increasing MgCl2 concentration, evidenced by the coin cell performance. In this work, the fundamental understanding of the operation mechanisms of rechargeable Mg batteries with the role of chloride content from electrolyte could potentially bring rational design of simple Mg electrolytes for practical Mg battery.

A Lewis acid-free and phenolate-based magnesium electrolyte for rechargeable magnesium batteries.

A novel Lewis acid-free and phenolate-based magnesium electrolyte has been established. The excellent reversibility and stability of this electrolyte in battery cycling render this novel Lewis acid-free synthetic approach as a highly promising alternative for the development of highly anodically stable magnesium electrolytes for rechargeable magnesium batteries.

Full-field synchrotron tomography of nongraphitic foam and laminate anodes for lithium-ion batteries.

Nondestructive methods that allow researchers to gather high-resolution quantitative information on a material's physical properties from inside a working device are increasingly in demand from the scientific community. Synchrotron-based microcomputed X-ray tomography, which enables the fast, full-field interrogation of materials in functional, real-world environments, was used to observe the physical changes of next-generation lithium-ion battery anode materials and architectures. High capacity, nongraphitic anodes were chosen for study because they represent the future direction of the field and one of their recognized limitations is their large volume expansion and contraction upon cycling, which is responsible for their generally poor electrochemical performance. In this work, Cu6Sn5 coated on a three-dimensional copper foam was used to model a high power electrode while laminated silicon particles were used to model a high energy electrode. The electrodes were illuminated in situ and ex situ, respectively, at Sector 2-BM of the Advanced Photon Source. The changes in electrode porosity and surface area were measured and show large differences based on the electrode architecture. This work is one of the first reports of full-field synchrotron tomography on high-capacity battery materials under operating conditions.