The lithium metal battery is strongly considered to be one of the most promising candidates for high-energy-density energy storage devices in our modern and technology-based society. However, uncontrollable lithium dendrite growth induces poor cycling efficiency and severe safety concerns, dragging lithium metal batteries out of practical applications. This review presents a comprehensive overview of the lithium metal anode and its dendritic lithium growth. First, the working principles and technical challenges of a lithium metal anode are underscored. Specific attention is paid to the mechanistic understandings and quantitative models for solid electrolyte interphase (SEI) formation, lithium dendrite nucleation, and growth. On the basis of previous theoretical understanding and analysis, recently proposed strategies to suppress dendrite growth of lithium metal anode and some other metal anodes are reviewed. A section dedicated to the potential of full-cell lithium metal batteries for practical applicatio...

Toward Safe Lithium Metal Anode in Rechargeable Batteries: A Review.

Metal Oxides and Oxysalts as Anode Materials for Li Ion Batteries

Recent developments in cathode materials for lithium ion batteries

Nanostructured materials have shown extraordinary promise for electrochemical energy storage but are usually limited to electrodes with rather low mass loading (~1 milligram per square centimeter) because of the increasing ion diffusion limitations in thicker electrodes. We report the design of a three-dimensional (3D) holey-graphene/niobia (Nb2O5) composite for ultrahigh-rate energy storage at practical levels of mass loading (>10 milligrams per square centimeter). The highly interconnected graphene network in the 3D architecture provides excellent electron transport properties, and its hierarchical porous structure facilitates rapid ion transport. By systematically tailoring the porosity in the holey graphene backbone, charge transport in the composite architecture is optimized to deliver high areal capacity and high-rate capability at high mass loading, which represents a critical step forward toward practical applications.

Three-dimensional holey-graphene/niobia composite architectures for ultrahigh-rate energy storage

Three-Dimensional Holey-Graphene/Niobia Composite Architectures for Ultrahigh-Rate Energy Storage

Theoretical and Experimental Analysis of Porous Electrodes for Lithium-Ion Batteries by Electrochemical Impedance Spectroscopy Using a Symmetric Cell

I. Analysis by Electrochemical and Spectroscopic Examination Tsuyoshi Sasaki,* Takamasa Nonaka, Hideaki Oka, Chikaaki Okuda, Yuichi Itou, Yasuhito Kondo, Yoji Takeuchi, Yoshio Ukyo,* Kazuyoshi Tatsumi, and Shunsuke Muto* Toyota Central Research and Development Laboratories, Incorporated, Nagoakute 480-1192, Japan Department of Materials, Physics and Energy Engineering, Graduate School of Engineering, Nagoya University, Chikusa-ku, Nagoya 464-8603, Japan

Capacity-Fading Mechanisms of LiNiO2-Based Lithium-Ion Batteries I. Analysis by Electrochemical and Spectroscopic Examination

Effects of Mg-substitution in Li(Ni,Co,Al)O2 positive electrode materials on the crystal structure and battery performance

Factors affecting the cycling life of cylindrical lithium-ion batteries of LiNi0.8Co0.15Al0.05O2 (NCA) with graphite were examined in terms of the rechargeable capacity and polarization of NCA derivatives of LizNi0.8Co0.15Al0.05O2−δ (0.8 ≤ z ≤ 1.05). NCA derivatives with rock-salt domains in the structure were prepared by a co-precipitation method and the structures of [Li1−yNiy]3(b)[Ni,Co,Al]3(a)O26(c) based on a space group of Rm were refined by a Rietveld method of the XRD patterns. The electrochemical reactivity of the NCA derivatives with rock-salt domains was examined in non-aqueous lithium cells, and it was found that the rechargeable capacities (Q) of the samples decrease linearly as the amount of rock-salt domain (y) increases. An empirical relation is obtained to be Q = 181.4 − 725.5y in which Q reaches zero at y = 0.25, which is derived from not only the capacity loss owing to inactive rock-salt domains but also the polarization increase. The galvanostatic intermittent titration technique (GITT) measurement told us that polarization of NCA derivatives increases when the amount of rock-salt domains is above 2%, i.e., y > 0.02, and such a relation is remarkable in the lithium insertion direction into the structure, which is ascribed to slow lithium ion mobility due to nickel ions in the lithium layers. The NCA derivatives with increased rock-salt domains of above 2% deteriorate rapidly in non-aqueous lithium cells upon charge and discharge cycles, which is ascribed to the cumulative increase in polarization during charge and discharge. An extended cycling test for cylindrical lithium-ion batteries of the NCA derivatives with a graphite negative electrode at elevated temperature was performed and the quantitative relation is discussed thereof.

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Chikaaki Okuda

Papers

Theoretical and Experimental Analysis of Porous Electrodes for Lithium-Ion Batteries by Electrochemical Impedance Spectroscopy Using a Symmetric Cell

Capacity-Fading Mechanisms of LiNiO2-Based Lithium-Ion Batteries I. Analysis by Electrochemical and Spectroscopic Examination

Effects of Mg-substitution in Li(Ni,Co,Al)O2 positive electrode materials on the crystal structure and battery performance

Factors affecting cycling life of LiNi0.8Co0.15Al0.05O2 for lithium-ion batteries

Numerical simulation of thermal behavior of lithium-ion secondary batteries using the enhanced single particle model