Formation of an Anti-Core–Shell Structure in Layered Oxide Cathodes for Li-Ion Batteries

The layered → rock-salt phase transformation in the layered dioxide cathodes for Li-ion batteries is believed to result in a “core–shell” structure of the primary particles, in which the core region remains as the layered phase while the surface region undergoes a phase transformation to the rock-salt phase. Using transmission electron microscopy, here we demonstrate the formation of an “anti-core–shell” structure in cycled primary particles with a formula of LiNi_0.80Co_0.15Al_0.05O₂, in which the surface and subsurface regions remain as the layered structure while the rock-salt phase forms as domains in the bulk with a thin layer of the spinel phase between the rock-salt core and the skin of the layered phase. Formation of this anti-core–shell structure is attributed to oxygen loss at the surface that drives the migration of oxygen from the bulk to the surface, thereby resulting in localized areas of significantly reduced oxygen levels in the bulk of the particle, which subsequently undergoes phase transformation to the rock-salt domains. The formation of the anti-core–shell rock-salt domains is responsible for the reduced capacity, discharge voltage, and ionic conductivity in cycled cathodes

Formation of an Anti-Core–Shell Structure in Layered Oxide Cathodes for Li-Ion Batteries

The layered → rock-salt phase transformation in the layered dioxide cathodes for Li-ion batteries is believed to result in a “core–shell” structure of the primary particles, in which the core region remains as the layered phase while the surface region undergoes a phase transformation to the rock-salt phase. Using transmission electron microscopy, here we demonstrate the formation of an “anti-core–shell” structure in cycled primary particles with a formula of LiNi_0.80Co_0.15Al_0.05O₂, in which the surface and subsurface regions remain as the layered structure while the rock-salt phase forms as domains in the bulk with a thin layer of the spinel phase between the rock-salt core and the skin of the layered phase. Formation of this anti-core–shell structure is attributed to oxygen loss at the surface that drives the migration of oxygen from the bulk to the surface, thereby resulting in localized areas of significantly reduced oxygen levels in the bulk of the particle, which subsequently undergoes phase transformation to the rock-salt domains. The formation of the anti-core–shell rock-salt domains is responsible for the reduced capacity, discharge voltage, and ionic conductivity in cycled cathodes

An Organic Coprecipitation Route to Synthesize High Voltage LiNi_0.5Mn_1.5O₄

High-voltage cathode material LiNi_0.5Mn_1.5O₄ has been prepared with a novel organic coprecipitation route. The as-prepared sample was compared with samples produced through traditional solid state method and hydroxide coprecipitation method. The morphology was observed by scanning electron microscopy, and the spinel structures were characterized by X-ray diffraction and Fourier transform infrared spectroscopy. Besides the ordered/disordered distribution of Ni/Mn on octahedral sites, the confusion between Li and transition metal is pointed out to be another important factor responsible for the corresponding performance, which is worthy further investigation. Galvanostatic cycles, cyclic voltammetry, and electrochemical impedance spectroscopy are employed to characterize the electrochemical properties. The organic coprecipitation route produced sample shows superior rate capability and stable structure during cycling

Atomic Insight into the Layered/Spinel Phase Transformation in Charged LiNi_0.80Co_0.15Al_0.05O₂ Cathode Particles

Layered LiNi_0.80Co_0.15Al_0.05O₂ (NCA) holds great promise as a potential cathode material for high energy density lithium ion batteries. However, its high capacity is heavily dependent on the stability of its layered structure, which suffers from a severe structure degradation resulting from a not fully understood layered → spinel phase transformation. Using high-resolution transmission electron microscopy and electron diffraction, we probe the atomic structure evolution induced by the layered → spinel phase transformation in the NCA cathode. We show that the phase transformation results in the development of a particle structure with the formation of complete spinel, spinel domains, and intermediate spinel from the surface to the subsurface region. The lattice planes of the complete and intermediate spinel phases are highly interwoven in the subsurface region. The layered → spinel transformation occurs via the migration of transition metal (TM) atoms from the TM layer into the lithium layer. Incomplete migration leads to the formation of the intermediate spinel phase, which is featured by tetrahedral occupancy of TM cations in the lithium layer. The crystallographic structure of the intermediate spinel is discussed and verified by the simulation of electron diffraction patterns

Rock-Salt Growth-Induced (003) Cracking in a Layered Positive Electrode for Li-Ion Batteries

For the first time, (003) cracking is observed and determined to be the major cracking mechanism for the primary particles of Ni-rich layered dioxides as the positive electrode for Li-ion batteries. Using transmission electron microscopy techniques, here we show that the propagation and fracturing of platelet-like rock-salt phase along the (003) plane of the layered oxide are the leading cause for the cracking of primary particles. The fracturing of the rock-salt platelet is induced by the stress discontinuity between the parent layered oxide and the rock-salt phase. The high nickel content is considered to be the key factor for the formation of the rock-salt platelet and thus the (003) cracking. The (003)-type cracking can be a major factor for the structural degradation and associated capacity fade of the layered positive electrode

Tuning the Activity of Oxygen in LiNi_0.8Co_0.15Al_0.05O₂ Battery Electrodes

Layered transition metal oxides such as LiNi_0.8Co _0.15Al_0.05O₂ (NCA) are highly desirable battery electrodes. However, these materials suffer from thermal runaway caused by deleterious oxygen loss and surface phase transitions when in highly overcharged and overheated conditions, prompting serious safety concerns. Using in situ environmental transmission electron microscopy techniques, we demonstrate that surface oxygen loss and structural changes in the highly overcharged NCA particles are suppressed by exposing them to an oxygen-rich environment. The onset temperature for the loss of oxygen from the electrode particle is delayed to 350 °C at oxygen gas overpressure of 400 mTorr. Similar heating of the particles in a reducing hydrogen gas demonstrated a quick onset of oxygen loss at 150 °C and rapid surface degradation of the particles. The results reported here illustrate the fundamental mechanism governing the failure processes of electrode particles and highlight possible strategies to circumvent such issues

Structure and Electrochemistry of Vanadium-Modified LiFePO₄

Doping LiFePO₄ with vanadium has proven to enhance electrochemical performance, but the underlying reasons for this improvement are not well understood. To better comprehend the relationships between the electrochemical performance, crystal structure, and surface carbon layer, we prepared vanadium-modified LiFePO₄ by three different methods. The electrochemical performance of each sample was determined via a series of cycling studies, the detailed crystal structures of the doped samples were identified by X-ray diffraction and absorption spectroscopy, and the surface carbon coating was examined by high resolution transmission electron microscopy. In V-modified LiFePO₄ prepared by a modified solid-state reaction, the vanadium is present in an impurity phase at the surface, which improves conductivity but has only a slight improvement in the electrochemical properties. The V-modified LiFePO₄ samples prepared by the conventional solid-state reaction method and a solution method revealed that the vanadium was substituted into the lattice occupying iron sites in the FeO₆ octahedron. This structural modification improves the cycling rate performance by increasing the Li⁺ effective cross-sectional area of the LiO₆ octahedral face and thereby reducing the bottleneck for Li⁺ migration. In addition, analysis of the carbon coating revealed that the material prepared by the solution method forms a uniform carbon coating with a thin, well-ordered interface between the LiFePO₄ and the carbon. The surface properties improve the electronic and ionic conductivities (with respect to the other samples), resulting in a high rate capability (87 mAh g^–1 at 50 C)

Li₃Mo₄P₅O₂₄: A Two-Electron Cathode for Lithium-Ion Batteries with Three-Dimensional Diffusion Pathways

The structure of the novel compound Li₃Mo₄P₅O₂₄ has been solved from single crystal X-ray diffraction data. The Mo cations in Li₃Mo₄P₅O₂₄ are present in four distinct types of MoO₆ octahedra, each of which has one open vertex at the corner participating in a MoO double bond and whose other five corners are shared with PO₄ tetrahedra. On the basis of a bond valence sum difference map (BVS-DM) analysis, this framework is predicted to support the facile diffusion of Li⁺ ions, a hypothesis that is confirmed by electrochemical testing data, which show that Li₃Mo₄P₅O₂₄ can be utilized as a rechargeable battery cathode material. It is found that Li can both be removed from and inserted into Li₃Mo₄P₅O₂₄. The involvement of multiple redox processes occurring at the same Mo site is reflected in electrochemical plateaus around 3.8 V associated with the Mo⁶⁺/Mo⁵⁺ redox couple and 2.2 V associated with the Mo⁵⁺/Mo⁴⁺ redox couple. The two-electron redox properties of Mo cations in this structure lead to a theoretical capacity of 198 mAh/g. When cycled between 2.0 and 4.3 V versus Li⁺/Li, an initial capacity of 113 mAh/g is observed with 80% of this capacity retained over the first 20 cycles. This compound therefore represents a rare example of a solid state cathode able to support two-electron redox capacity and provides important general insights about pathways for designing next-generation cathodes with enhanced specific capacities

Single-Phase Lithiation and Delithiation of Simferite Compounds Li(Mg,Mn,Fe)PO₄

Understanding the phase transformation behavior of electrode materials for lithium ion batteries is critical in determining the electrode kinetics and battery performance. Here, we demonstrate the lithiation/delithiation mechanism and electrochemical behavior of the simferite compound, LiMg_0.5Fe_0.3Mn_0.2PO₄. In contrast to the equilibrium two-phase nature of LiFePO₄, LiMg_0.5Fe_0.3Mn_0.2PO₄ undergoes a one-phase reaction mechanism as confirmed by ex situ X-ray diffraction at different states of delithiation and electrochemical measurements. The equilibrium voltage measurement by galvanostatic intermittent titration technique shows a continuous change in voltage at Mn³⁺/Mn²⁺ redox couple with addition of Mg²⁺ in LiMn_0.4Fe_0.6PO₄ olivine structure. There is, however, no significant change in the Fe³⁺/Fe²⁺ redox potential

Composition-Structure Relationships in the Li-Ion Battery Electrode Material LiNi_0.5Mn_1.5O₄

A study of the correlations between the stoichiometry, secondary phases, and transition metal ordering of LiNi_0.5Mn_1.5O₄ was undertaken by characterizing samples synthesized at different temperatures. Insight into the composition of the samples was obtained by electron microscopy, neutron diffraction, and X-ray absorption spectroscopy. In turn, analysis of cationic ordering was performed by combining neutron diffraction with Li MAS NMR spectroscopy. Under the conditions chosen for the synthesis, all samples systematically showed an excess of Mn, which was compensated by the formation of a secondary rock-salt phase and not via the creation of oxygen vacancies. Local deviations from the ideal 3:1 Mn:Ni ordering were found, even for samples that show the superlattice ordering by diffraction, with different disordered schemes also being possible. The magnetic behavior of the samples was correlated with the deviations from this ideal ordering arrangement. The in-depth crystal-chemical knowledge generated was employed to evaluate the influence of these parameters on the electrochemical behavior of the materials