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Lithium metal, with ultrahigh theoretical specific capacity, is considered as an ideal anode material for the lithium‐ion batteries. However, its practical application is severely plagued by the uncontrolled formation of dendritic Li. Here, a cation‐loaded porous Mg2+‐Zeolite layer is proposed to enable the dendrite‐free deposition on the surface of Li metal anode. The skeleton channels of zeolite provide the low coordinated Li+‐solvation groups, leading to the faster desolvation process at the interface. Meanwhile, anions‐involved solvation sheath induces a stable, inorganic‐rich SEI, contributing to the uniform Li+ flux through the interface. Furthermore, the co‐deposition of sustained release Mg2+ realizes a new faster migration pathway, which proactively facilitates the uniform diffusion of Li on the lithium substrate. The synergistic modulation of these kinetic processes facilitates the homogeneous Li plating/stripping behavior. Based on this synergistic mechanism, the high‐efficiency deposition with cyclic longevity exceeding 2100 h is observed in the symmetric Li/Li cell with Mg2+‐Zeolite modified anode at 1 mA cm−2. The pouch cell matched with LiFePO4 cathode fulfills a capacity retention of 88.4% after 100 cycles at a severe current density of 1 C charge/discharge. This synergistic protective mechanism can give new guidance for realizing the safe and high‐performance Li metal batteries. [ABSTRACT FROM AUTHOR]

Doping of Ru has been used to enhance the performance of LiNi0.5Mn1.5O4 cathode materials. However, the effects of Ru doping on the two types of LiNi0.5Mn1.5O4 are rarely studied. In this study, Ru4+ with a stoichiometric ratio of 0.05 is introduced into LiNi0.5Mn1.5O4 with different space groups (Fd 3 ¯ m, P4332). The influence of Ru doping on the properties of LiNi0.5Mn1.5O4 (Fd 3 ¯ m, P4332) is comprehensively studied using multiple techniques such as XRD, Raman, and SEM methods. Electrochemical tests show that Ru4+-doped LiNi0.5Mn1.5O4 (P4332) delivers the optimal electrochemical performance. Its initial specific capacity reaches 132.8 mAh g−1, and 97.7% of this is retained after 300 cycles at a 1 C rate at room temperature. Even at a rate of 10 C, the capacity of Ru4+-LiNi0.5Mn1.5O4 (P4332) is still 100.7 mAh g−1. Raman spectroscopy shows that the Ni/Mn arrangement of Ru4+-LiNi0.5Mn1.5O4 (Fd 3 ¯ m) is not significantly affected by Ru4+ doping. However, LiNi0.5Mn1.5O4 (P4332) is transformed to semi-ordered LiNi0.5Mn1.5O4 after the incorporation of Ru4+. Ru4+ doping hinders the ordering process of Ni/Mn during the heat treatment process, to an extent. [ABSTRACT FROM AUTHOR]

In this paper, using four carbonates as raw materials, the cathode material LiNi0.5Co0.2Mn0.3O2 was prepared with the "ball milling-calcining" solid-phase synthesis method. The specific reaction process, which consists of the decomposition of the raw materials and the generation of target products, was investigated thoroughly using the TG-DSC technique. XRD, SEM and charge/discharge test methods were utilized to explore the influence of different sintering temperatures on the structure, morphology and electrochemical performance of the LiNi0.5Co0.2Mn0.3O2 cathode. The results show that 900~1000 °C is the appropriate synthesis temperature range. LiNi0.5Co0.2Mn0.3O2 synthesized at 1000 °C delivers optimal cycling stability at 0.5 C. Meanwhile, its initial discharge specific capacity and coulomb efficiency reached 167.2 mAh g−1 and 97.89%, respectively. In addition, the high-rate performance of the cathode sample prepared at 900 °C is particularly noteworthy. Cycling at 0.5 C, 1 C, 1.5 C and 2 C, the corresponding discharge specific capacity of the sample exhibited 148.1 mAh g−1, 143.1 mAh g−1, 140 mAh g−1 and 138.9 mAh g−1, respectively. [ABSTRACT FROM AUTHOR]