Lithium-rich manganese oxide (LRMO) is a promising high-energy-density material for high-voltage lithium-ion batteries, but its performance is hindered by interfacial side reactions, transition metal dissolution, and oxygen release. To address these issues, we propose a high-voltage electrolyte strategy that utilizes cosolvent and additive synergy to create stable dual interphases at both the cathode and anode. Specifically, lithium difluoro(oxalato)borate (LiDFOB) additive sacrificially decomposes to form a uniform yet stable cathode-electrolyte interphase (CEI) layer, while cosolvent of bis(2,2,2-trifluoroethyl) carbonate (BTFEC) effectively adjusts the solvation structure and synergistically stabilizes the solid-electrolyte interphase (SEI) on the anode, ultimately achieving ultrahigh cycle stability and fast-charging feasibility. The presence of B-F, LiBO species derived from LiDFOB exceptionally stabilizes the fast-ion-transfer CEI layer, while the F-rich robust SEI layer inhibits the irregular growth of lithium dendrites. Our electrolyte enables Li||LRMO cells to maintain 95% capacity after 200 cycles at 4.8 V, with a specific capacity of 238 mAh g after 350 cycles at 3C. Importantly, a 5 Ah graphite||LRMO pouch cell achieves a high energy density of 323 Wh kg with 80.4% capacity retention after 150 cycles, demonstrating its practical application potential.
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http://dx.doi.org/10.1021/acsami.4c23006 | DOI Listing |
ACS Appl Mater Interfaces
March 2025
State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.
Lithium-rich manganese oxide (LRMO) is a promising high-energy-density material for high-voltage lithium-ion batteries, but its performance is hindered by interfacial side reactions, transition metal dissolution, and oxygen release. To address these issues, we propose a high-voltage electrolyte strategy that utilizes cosolvent and additive synergy to create stable dual interphases at both the cathode and anode. Specifically, lithium difluoro(oxalato)borate (LiDFOB) additive sacrificially decomposes to form a uniform yet stable cathode-electrolyte interphase (CEI) layer, while cosolvent of bis(2,2,2-trifluoroethyl) carbonate (BTFEC) effectively adjusts the solvation structure and synergistically stabilizes the solid-electrolyte interphase (SEI) on the anode, ultimately achieving ultrahigh cycle stability and fast-charging feasibility.
View Article and Find Full Text PDFEnviron Technol
March 2025
Institute of Environmental, Chemical and Pharmaceutical Sciences, Universidade Federal de São Paulo, São Paulo, Brazil.
The processing of coffee consists on the separation of the grains from other parts of the fruit, then roasted and extracted to obtain the beverage that is so appreciated worldwide. Several studies have dedicated efforts to treat the residue from coffee processing, while recovering lignols of industrial interest. Given this scenario, the nutrients in the coffee husk can enhance microbial growth, providing optimal conditions for the microorganisms to produce metabolites that may have medicinal properties.
View Article and Find Full Text PDFJ Am Chem Soc
March 2025
Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Nishikyo-ku, Kyoto 615-8510, Japan.
Helical poly(quinoxaline-2,3-diyl)s (PQX) containing chiral carboxylic acid side chains derived from natural l-lactic acid were synthesized. The newly synthesized helical polycarboxylated polymer was soluble in basic pure water by forming polycarboxylate and adopted the -helical conformation (right-handed), whereas the -helical conformation is predominant under weakly acidic aqueous conditions. The water-soluble PQX containing additional monomer units bearing a 2-(diarylphosphino)phenyl group was employed in the asymmetric Suzuki-Miyaura coupling reaction in pure water in the absence of organic cosolvents.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
February 2025
State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science, Institute of Fiber Materials and Devices, Research Center of AI for Polymer Science, Collaborative Innovation Center of Chemistry for Energy Materials, Fudan University, Shanghai, 200433, China.
K-ion batteries face significant challenges due to a severe shortage of active K ions, with cathode materials typically containing less than 70% K ions and first-cycle irreversible reactions consuming up to 20% more. Conventional K-ion compensation methods fail to supply sufficient K ions without compromising cell integrity. To address this, we introduce potassium sulfocyanate (KSCN) as an electrolyte additive capable of delivering up to 100% active K ions.
View Article and Find Full Text PDFSmall Methods
February 2025
Beijing National Laboratory for Molecular Science, CAS Key Laboratory of Green Printing, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.
Metal halide perovskite solar cells (PSCs) are emerging as promising candidates for next-generation photovoltaics aimed at green energy production. However, during solution-processed film deposition, the distinct rheological behaviors of blade coating, compared to spin coating, result in less controlled crystallization, leading to inferior film quality and limiting the power conversion efficiency (PCE) of blade-coated photovoltaics. In this work, ethylene glycol (EG) is introduced as an inert co-solvent in perovskite precursor solutions to achieve high-quality perovskite films via blade coating.
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