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Layered oxides, particularly including Li[NixCoyMnz]O2 (NCMxyz) materials, such as NCM523, are the most promising cathode materials for high‐energy lithium‐ion batteries (LIBs). One major strategy to increase the energy density of LIBs is to expand the cell voltage (>4.3 V). However, high‐voltage NCM∥ graphite full cells typically suffer from drastic capacity fading, often referred to as “rollover” failure. In this study, the underlying degradation mechanisms responsible for failure of NCM523∥ graphite full cells operated at 4.5 V are unraveled by a comprehensive study including the variation of different electrode and cell parameters. It is found that the “rollover” failure after around 50 cycles can be attributed to severe solid electrolyte interphase growth, owing to formation of thick deposits at the graphite anode surface through deposition of transition metals migrating from the cathode to the anode. These deposits induce the formation of Li metal dendrites, which, in the worst cases, result in a “rollover” failure owing to the generation of (micro‐) short circuits. Finally, approaches to overcome this dramatic failure mechanism are presented, for example, by use of single‐crystal NCM523 materials, showing no “rollover” failure even after 200 cycles. The suppression of cross‐talk phenomena in high‐voltage LIB cells is of utmost importance for achieving high cycling stability.

Solid‐state lithium–sulfur battery (SSLSB) is attractive due to its potential for providing high energy density. However, the cell chemistry of SSLSB still faces challenges such as sluggish electrochemical kinetics and prominent “chemomechanical” failure. Herein, a high‐performance SSLSB is demonstrated by using the thio‐LiSICON/polymer composite electrolyte in combination with sulfurized polyacrylonitrile (S/PAN) cathode. Thio‐LiSICON/polymer composite electrolyte, which processes high ionic conductivity and wettability, is fabricated to enhance the interfacial contact and the performance of lithium metal anodes. S/PAN is utilized due to its unique electrochemical characteristics: electrochemical and structural studies combined with nuclear magnetic resonance spectroscopy and electron paramagnetic resonance characterizations reveal the charge/discharge mechanism of S/PAN, which is the radical‐mediated redox reaction within the sulfur grafted conjugated polymer framework. This characteristic of S/PAN can support alleviating the volume change in the cathode and maintaining fast redox kinetics. The assembled SSLSB full cell exhibits excellent rate performance with 1183 mAh g−1 at 0.2 C and 719 mAh g−1 at 0.5 C, respectively, and can accomplish 50 cycles at 0.1 C with the capacity retention of 588 mAh g−1. The superior performance of the SSLSB cell rationalizes the construction concept and leads to considerations for the innovative design of SSLSB.

Because of its high specific capacity, silicon is regarded as the most promising candidate to be incrementally added to graphite‐based negative electrodes in lithium‐ion batteries. However, silicon suffers from significant volume changes upon (de‐)lithiation leading to continuous re‐formation of the solid electrolyte interphase (SEI) and ongoing active lithium losses. One prominent approach to compensate for active lithium losses is pre‐lithiation. Here, the “contact pre‐lithiation” of silicon/graphite (Si/Gr) negative electrodes in direct contact with passivated Li metal powder (PLMP) is studied, focusing on the pre‐lithiation mechanism in “dry state” and after electrolyte addition. PLMP is pressed onto the electrode surface to precisely adjust the degree of pre‐lithiation (25%, 50%, and 75%). By in situ XRD and ex situ 7Li NMR studies, it is proven that significant lithiation of Si/Gr electrodes occurs by direct contact to Li metal, that is, without electrolyte. After electrolyte addition, de‐lithiation of silicon and graphite is confirmed, resulting in SEI formation. The amount of Li metal highly impacts the presence and durability of the LixC and LixSi phases. Finally, the challenges for homogeneous pre‐lithiation and SEI formation are identified, and the impact of electrolyte addition is assessed by analysis of the lateral and in‐depth lithium distribution within the Si/Gr electrode.

The incorporation of inorganic lithium superionic conductors in polymer/ceramic composite electrolytes has been frequently proposed since this approach is expected to take advantage of the high ionic conductivities of the lithium superionic conductors and the elasticity of the polymer constituents of the composites. Nevertheless, the properties and mechanisms of polymer/ceramic composite electrolytes are yet to be comprehensively investigated. In this work, we systematically study sulfidebased polymer/ceramic composites from the aspects of composition dependence, electrochemical performance, and chemical stability. The composition-dependent Li-ion conduction mechanism and electrochemical behavior have been revealed for polyethylene oxide/Li 10 GeP 2 S 12 composite electrolytes, highlighting the rational selection of compositions of polymer/ ceramic composites toward desired functions. Furthermore, the chemical stability of the sulfide electrolyte in diverse solvent media as well as the potential internal reactions between the components of the composite electrolyte have been investigated, which underline the chemical stability consideration in the design and fabrication of the composite electrolyte. Thus, this work aims at contributing to the design and fabrication of sulfide-based polymer/ceramic composite electrolytes that enable high-performance lithium metal batteries.

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Dual-graphite batteries have emerged as promising candidate for sustainable energy storage due to their potentially low costs and absence of toxic materials. However, the mechanism of anion intercalation and the structures of the resulting graphite intercalation compounds (GICs) are still not well understood. Here, we systematically evaluate the anion intercalation characteristics into graphite for three highly concentrated electrolytes containing LiPF6, LiTFSI and their equimolar binary mixture. The binary mixture exhibits a significantly enhanced capacity retention and improved intercalation kinetics compared to the single-salt electrolytes in graphite ∣∣ Li metal cells. In situ X-ray diffraction studies prove the formation of stage 1-GICs and a homogeneous distribution of anions within graphite. From ex situ solid-state 19F magic-angle spinning (MAS) nuclear magnetic resonance (NMR) measurements, GICs can be identified at various states-of-charge (SOCs). The 19F chemical shifts of intercalated anions indicate no significant charge transfer between anion and graphite. The observed narrow 19F linewidths of the GIC-signals are most likely caused by a high translational and/or rotational mobility of the intercalates. Furthermore, the 19F MAS NMR studies allow the identification of the molar ratios for PF6 − and TFSI− anions intercalated into graphite, suggesting a preferred intercalation of PF6 − anions, especially at lower SOCs.