To realize high-energy-density Li metal batteries at low temperatures, a new electrolyte is needed to solve the high-voltage compatibility and fast lithium-ion de-solvation process. A gel polymer electrolyte with a small-molecular-weight polymer is widely investigated by combining the merits of a solid polymer electrolyte (SPE) and liquid electrolyte (LE). Herein, we present a new gel polymer electrolyte (P-DOL) by the lithium difluoro(oxalate)borate (LiDFOB)-initiated polymerization process using 1,3-dioxolane (DOL) as a monomer solvent. The P-DOL presents excellent ionic conductivity (1.12 × 10 S cm) at -20 °C, with an oxidation potential of 4.8 V. The Li‖LiCoO cell stably cycled at 4.3 V under room temperature, with a discharge capacity of 130 mAh g at 0.5 C and a capacity retention rate of 86.4% after 50 cycles. Moreover, a high-Ni-content LiNiCoMnO (NCM811) cell can steadily run for 120 cycles at -20 °C, with a capacity retention of 88.4%. The underlying mechanism of high-voltage compatibility originates from the dense and robust B- and F-rich cathode interface layer (CEI) formed at the cathode interface. Our report will shed light on the real application of Li metal batteries under all-climate conditions in the future.
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http://dx.doi.org/10.3390/molecules29112454 | DOI Listing |
Nano Lett
January 2025
The Institute for Advanced Studies, Wuhan University, Wuhan 430072, China.
Robust interfaces in anodes play a crucial role in boosting sodium-ion battery (SIB) performance. However, the fragile interfaces constructed by a two-step synthesis or artificial stack are prone to be destroyed during the charging/discharging processes, which significantly reduces the lifetime of SIBs. Here, a facile construction strategy is developed to produce robust interfaces in hollow sphere-like CoSe/nitrogen-doped carbon (HS-CoSe/NC) using intrinsic Co, N, C in metal-organic framework as precursors, which enhance the electron/ion diffusion kinetics.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
State Key Laboratory for Manufacturing System Engineering, School of Mechanical Engineering, Xi'an Jiaotong University, Xi'an 710049, China.
Lithium dendrites are widely acknowledged as the main culprit of the degradation of performance in various Li-based batteries. Studying the mechanism of lithium dendrite formation is challenging because of the high reactivity of lithium metal. In this work, a phase field model and in situ observation experiments were used to study the growth kinetics and morphologies of lithium dendrites in terms of anisotropy, temperature, and potential difference.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Department of Chemistry, Sardar Patel University, Vallabh Vidyanagar 388120, Gujarat, India.
The development of devices capable of storing energy harnessed from photons is on the rise, owing to the increasing global energy demand for smart systems. The majority of reports in this field cover the use of integrated type devices, which houses a separate photovoltaic module and supercapacitor or battery. Herein, we are reporting a photocapacitor with a simple two-electrode design, capable of operating without a conventional electrolyte or metal ions.
View Article and Find Full Text PDFNat Nanotechnol
January 2025
Department of Chemical and Biomolecular Engineering, University of Maryland, College Park, MD, USA.
Room-temperature non-aqueous sodium metal batteries are viable candidates for cost-effective and safe electrochemical energy storage. However, they show low specific energy and poor cycle life as the use of conventional organic-based non-aqueous electrolyte solutions enables the formation of interphases that cannot prevent degradations at the positive and negative electrodes. Here, to promote the formation of inorganic NaF-rich interphases on both negative and positive electrodes, we propose the salt-in-presalt (SIPS) electrolyte formulation strategy.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
Nanoyang Group, Tianjin Key Laboratory of Advanced Carbon and Electrochemical Energy Storage, School of Chemical Engineering and Technology, National Industry-Education Integration Platform of Energy Storage, and Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin University, Tianjin 300072, China.
In situ polymerization strategies hold great promise for enhancing the physical interfacial stability in solid-state batteries, yet (electro)chemical degradation of polymerized interfaces, especially at high voltages, remains a critical challenge. Herein, we find interphase engineering is crucial for the polymerization process and polymer stability and pioneer an in situ polymerization-fluorination (Poly-FR) strategy to create durable interfaces with excellent physical and (electro)chemical stabilities, achieved by designing a bifunctional initiator for both polymerization and on-surface lithium donor reactions. The integrated in situ fluorination converts LiCO impurities on LiNiCoMnO (NCM811) surfaces into LiF-rich interphases, effectively inhibiting the aggressive (de)lithiation intermediates and protecting the interface from underlying chemical degradation, thereby surpassing the stability limitations of polymerization alone.
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