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Abstract Achieving durable lithium (Li) metal anodes in liquid electrolytes remains challenging, primarily due to the instability of the formed solid‐electrolyte interphases (SEIs). Modulating the Li‐ion solvation structures is pivotal in forming a stable SEI for stabilizing Li metal anodes. Here a strategy is developed to fine‐tune the Li‐ion solvation structures through enhanced dipole–dipole interactions between the Li‐ion‐coordinated solvent and the non‐Li‐ion‐coordinating diluent, for creating a stable SEI in the developed binary salt electrolyte. The enhanced dipole–dipole interactions weaken the coordination between Li‐ions and the solvents while strengthening the interaction between Li‐ions and dual anions, thereby facilitating the Li‐ion transport and a robust anion‐derived SEI with a distinct bilayer structure. Consequently, the developed electrolyte exhibited exceptional electrochemical performance in high energy‐density Li||LiNi_0.8Mn_0.1Co_0.1O₂ (NMC811) cells, with long calendar life, stable cyclability at 1 C, and reliable operation between 25 and −20 °C, and it also demonstrat remarkable cycling stability for a Li||NMC811 pouch cell with projected energy density of 402 Wh kg⁻¹, maintaining 80% capacity retention over 606 cycles under practical conditions. 

Metallic anodes (lithium, sodium, and zinc) are attractive for rechargeable battery technologies but are plagued by an unfavorable metal–electrolyte interface that leads to nonuniform metal deposition and an unstable solid–electrolyte interphase (SEI). Here we report the use of electrochemically labile molecules to regulate the electrochemical interface and guide even lithium deposition and a stable SEI. The molecule, benzenesulfonyl fluoride, was bonded to the surface of a reduced graphene oxide aerogel. During metal deposition, this labile molecule not only generates a metal-coordinating benzenesulfonate anion that guides homogeneous metal deposition but also contributes lithium fluoride to the SEI to improve Li surface passivation. Consequently, high-efficiency lithium deposition with a low nucleation overpotential was achieved at a high current density of 6.0 mA cm⁻². A Li|LiCoO₂cell had a capacity retention of 85.3% after 400 cycles, and the cell also tolerated low-temperature (−10 °C) operation without additional capacity fading. This strategy was applied to sodium and zinc anodes as well. 

Molybdenum disulfide (MoS 2 ) may be a promising alternative for lithium ion batteries (LIBs) because it offers a unique layered crystal structure with a large and tunable distance between layers. This enables the anticipated excellent rate and cycling stability because they can promote the reversible lithium ion intercalation and de-intercalation without huge volume change which consequently prevents the pulverization of active materials during repeated charge and discharge processes. Herein, we prepared hierarchical MoS 2 –carbon (MoS 2 –C) microspheres via a continuous and scalable ultrasonic nebulization assisted route. The structure, composition, and electrochemical properties are investigated in detail. The MoS 2 –C microspheres consist of few-layer MoS 2 nanosheets bridged by carbon, which separates the exfoliated MoS 2 layers and prevents their aggregation and restacking, thus leading to improved kinetic, enhanced conductivity and structural integrity. The novel architecture offers additional merits such as overall large size and high packing density, which promotes their practical applications. The MoS 2 –C microspheres have been demonstrated with excellent electrochemical performances in terms of low resistance, high capacity even at large current density, stable cycling performance, etc. The electrodes exhibited 800 mA h g −1 at 1000 mA g −1 over 170 cycles. At a higher current density of 3200 mA g −1 , a capacity of 730 mA h g −1 can be also maintained. The MoS 2 –C microspheres are practically applicable not only because of the continuous and large scale synthesis via the current strategy, but also the possess a robust and integrated architecture which ensures the excellent electrochemical properties.