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Rational carbonate electrolyte chemistry is critical for the development of high-voltage lithium metal batteries (LMBs). However, the implementation of traditional carbonate electrolyte is greatly hindered by the generation of an unstable electrode interphase and corrosive by-product (HF). Herein, we propose a triple-function eutectic solvent additive of N-methylacetamide (NmAc) with LiNO 3 to enhance the stability and compatibility of carbonate electrolyte. Firstly, the addition of NmAc significantly improves the solubility of LiNO 3 in carbonate electrolyte by forming an eutectic pair, which regulates the Li + solvation structure and leads to dense and homogenous Li plating. Secondly, the hydrolysis of acidic PF 5 is effectively alleviated due to the strong complexation of NmAc with PF 5 , thus reducing the generation of corrosive HF. In addition, the optimized cathode electrolyte interphase layer decreases the structural degradation and transition metal dissolution. Consequently, Li||LiNi 0.6 Co 0.2 Mn 0.2 O 2 (NCM622) cells with the designed electrolyte deliver superior long-term cycle reversibility and excellent rate capability. This study unveils the rationale for incorporating eutectic solvent additives within carbonate electrolytes, which significantly contribute to the advancement of their practical application for high-voltage LMBs., (Copyright © 2024 Science China Press. Published by Elsevier B.V. All rights reserved.)

The renewable energy industry demands rechargeable batteries that can be manufactured at low cost using abundant resources while offering high energy density, good safety, wide operating temperature windows, and long lifespans. Utilizing fluorine chemistry to redesign battery configurations/components is considered a critical strategy to fulfill these requirements due to the natural abundance, robust bond strength, and extraordinary electronegativity of fluorine and the high free energy of fluoride formation, which enables the fluorinated components with cost effectiveness, nonflammability, and intrinsic stability. In particular, fluorinated materials and electrode|electrolyte interphases have been demonstrated to significantly affect reaction reversibility/kinetics, safety, and temperature tolerance of rechargeable batteries. However, the underlining principles governing material design and the mechanistic insights of interphases at the atomic level have been largely overlooked. This review covers a wide range of topics from the exploration of fluorine-containing electrodes, fluorinated electrolyte constituents, and other fluorinated battery components for metal-ion shuttle batteries to constructing fluoride-ion batteries, dual-ion batteries, and other new chemistries. In doing so, this review aims to provide a comprehensive understanding of the structure-property interactions, the features of fluorinated interphases, and cutting-edge techniques for elucidating the role of fluorine chemistry in rechargeable batteries. Further, we present current challenges and promising strategies for employing fluorine chemistry, aiming to advance the electrochemical performance, wide temperature operation, and safety attributes of rechargeable batteries.

The carbonate electrolyte chemistry is a primary determinant for the development of high-voltage lithium metal batteries (LMBs). Unfortunately, their implementation is greatly plagued by sluggish electrode interfacial dynamics and insufficient electrolyte thermodynamic stability. Herein, lithium trifluoroacetate-lithium nitrate (LiTFA-LiNO 3 ) dual-salt additive-reinforced carbonate electrolyte (LTFAN) is proposed for stabilizing high-voltage LMBs. We reveal that 1) the in situ generated inorganic-rich electrode-electrolyte interphase (EEI) enables rapid interfacial dynamics, 2) TFA - preferentially interacts with moisture over PF 6 - to strengthen the moisture tolerance of designed electrolyte, and 3) NO 3 - is found to be noticeably enriched at the cathode interface on charging, thus constructing Li + -enriched, solvent-coordinated, thermodynamically favorable electric double layer (EDL). The superior moisture tolerance of LTFAN and the thermodynamically stable EDL constructed at cathode interface play a decisive role in upgrading the compatibility of carbonate electrolyte with high-voltage cathode. The LMBs with LTFAN realize 4.3 V-NCM523/4.4 V-NCM622 superior cycling reversibility and excellent rate capability, which is the leading level of documented records for carbonate electrode., (© 2024 Wiley-VCH GmbH.)

The high specific capacity and relatively low volume expansion of silicon suboxide (SiO x ) highlight its potential as one of the most promising anode materials for lithium-ion batteries. Nevertheless, the traditional binder of polyacrylic acid (PAA) still cannot adapt to enormous stress during the repeated volume expansion/contraction owing to its intrinsic rigid backbone. Inspired by the "soft and hard composite body armor", we herein design a double-wrapped binder consisting of PAA with a high internal Young's modulus (hard part) and polyurethane (DOU) with a low external Young's modulus (soft part). When the SiO x particle expands during lithiation, the rigid PAA firstly accommodates the volume change to dissipate most of the inner stress, and the elastic DOU with triple dynamic bonds serves as a buffer layer to absorb the residual stress via the breakage/formation of dynamic bonds. By optimizing the PAA/DOU ratio, the SiO x anode can maintain the integrity during long-term cycling and deliver a relatively high reversible capacity of 1064.1 mAh g -1 with a preeminent capacity retention of 83.7% at 0.5C after 300 cycles. Such a double-wrapped binder can provide a novel design strategy for multicomponent functional polymer binders toward high-performance SiO x anodes.

Li metal is the ultimate anode material for next-generation high-energy-density rechargeable batteries. However, the uncontrollable growth of Li dendrites and low Coulombic efficiency (CE) prevent it from practical applications in Li metal batteries (LMBs). Here, a facile and low-cost strategy is developed to decorate a Cu current collector with a self-assembled γ-aminopropyltrimethoxysilane (γ-APS) film. The thin polymer film with nanopores promotes the formation of cobblestone-like Li deposition and suppresses Li-dendrite formation due to its low surface energy. The protecting layer not only increases the lithiophilicity of the Cu current collector but also alleviates the ambient corrosion and galvanic corrosion in practical use. Owing to these advantages, the half cell using γ-APS-Cu collectors exhibits a high average CE value of 99.2% for 100 cycles. The symmetric cell of γ-APS-Cu@Li shows an improved lifespan of 1400 h with a small voltage hysteresis of 12 mV at 0.5 mA cm -2 . The full cell assembled with LiFePO 4 (LFP) cathodes and γ-APS-Cu@Li anodes delivers a high capacity of 136 mAh g -1 after 600 cycles at 0.5C.

Recycling spent lithium-ion batteries (LIBs) is an urgent task in view of the resource shortage and environmental concerns. Here, a facile ternary molten salt approach is presented for efficiently regenerating the LiNi 0.5 Co 0.2 Mn 0.3 O 2 (NCM523) cathode of spent LIBs. Such an approach involves the treatment of spent cathode powder in the ternary molten salt at a moderate temperature (400 °C) and subsequent annealing in oxygen. The Li loss and degraded phases in spent NCM that cause the capacity decay can be fully remedied after the regeneration process. As a result, the regenerated cathode delivers a reversible capacity of 160 mAh g -1 at 0.5 C with retention of 93.7% after 100 cycles and maintains a high capacity of 132 mAh g -1 at a high rate of 5 C. The electrochemical performance of regenerated NCM cathode is compared favorably to the fresh NCM cathode, which demonstrates the feasibility of the molten salt approach to directly regenerate spent NCM cathode., (© 2022 Wiley-VCH GmbH.)

Flocculation or restacking of different kinds of two-dimensional (2D) nanosheets into heterostructure nanocomposites is of interest for the development of high-performance electrode materials and catalysts. However, lacking a molecular-scale control on the layer sequence hinders enhancement of electrochemical activity. Herein, we conducted electrostatic layer-by-layer (LbL) assembly, employing oxide nanosheets (e.g., MnO 2 , RuO 2.1 , reduced graphene oxide (rGO)) and layered double hydroxide (LDH) nanosheets (e.g., NiFe-based LDH) to explore a series of mono- and bilayer films with various combinations of nanosheets and sequences toward oxygen evolution reaction (OER). The highest OER activity was attained in bilayer films of electrically conductive RuO 2.1 nanosheets underlying catalytically active NiFe LDH nanosheets with mixed octahedral/tetrahedral coordination (NiFe LDH Td/Oh ). At an overpotential of 300 mV, the RuO 2.1 /NiFe LDH Td/Oh film exhibited an electrochemical surface area (ECSA) normalized current density of 2.51 mA cm -2 ECSA and a mass activity of 3610 A g -1 , which was, respectively, 2 and 5 times higher than that of flocculated RuO 2.1 /NiFe LDH Td/Oh aggregates with a random appearance of a surface layer. First-principles density functional theory calculations and COMSOL Multiphysics simulations further revealed that the improved catalytic performance was ascribed to a substantial electronic coupling effect in the heterostructure, in which electrons are transferred from exposed NiFe LDH Td/Oh nanosheets to underneath RuO 2.1 . The study provides insight into the rational control and manipulation of redox-active surface layers and conductive underlying layers in heteroassembled nanosheet films at molecular-scale precision for efficient electrocatalysis.