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Ultrahigh-voltage potassium-ion batteries (PIBs) with cost competitiveness represent a viable route towards high energy battery systems. Nevertheless, rapid capacity decay with poor Coulombic efficiencies remains intractable, mainly attributed to interfacial instability from aggressive potassium metal anodes and cathodes. Additionally, high reactivity of K metal and flammable electrolytes pose severe safety hazards. Herein, a weakly solvating fluorinated electrolyte with intrinsically nonflammable feature is successfully developed to enable an ultrahigh-voltage (up to 5.5 V) operation. Through breaking the anionic solvation barrier, synergistic interfacial modulation can be achieved by the formation of robust anion-derived inorganic-rich electrode-electrolyte interfaces on both the cathode and anode. As proof of concept, a representative KVPOF cathode can sustain 1600 cycles with 84.4 % of capacity retention at a high cutoff voltage of 4.95 V. Meanwhile, K plating/stripping process in our designed electrolyte also demonstrates optimized electrochemical reversibility and stability with effectively inhibited potassium dendrites. These findings underscore the critical impact of anion-dominated solvation configuration on synergistic interfacial modulation and electrochemical properties. This work provides new insights into rational design of ultrahigh-voltage and safe electrolyte for advanced PIBs.
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http://dx.doi.org/10.1002/anie.202423044 | DOI Listing |
Nanoscale Horiz
September 2025
Departamento de Ciencias del Ambiente, Facultad de Química y Biología, Universidad de Santiago de Chile (USACH), Av. Libertador Bernardo O'Higgins 3363, Estación Central, Santiago, 9170022, Chile.
The functional electronic and spectro-electrochemical properties of two structural pyridinium isomers, Py_Down-BF and Py_Up-BF, were studied at the single-molecule level using the STM-BJ technique. These isomers differ in the position of the redox-active pyridinium core. The aim was to identify the role of core's position in promoting reversible switching between electromers (redox isomers) in solution and at the gold-pyridinium-gold junction circuit.
View Article and Find Full Text PDFAdv Healthc Mater
September 2025
Huiya Hospital of The First Affiliated Hospital of Sun Yat-sen University, National and Local United Engineering Lab of Druggability and New Drugs Evaluation, School of Pharmaceutical Sciences, Sun Yat-sen University, Huizhou, 516081, P. R. China.
Heart failure (HF) is a global public health challenge closely associated with oxidative stress and immune dysregulation. However, current therapeutic strategies for HF generally lack specific targeting to cardiac tissue, and the high perfusion rate of the heart further exacerbates insufficient drug accumulation at lesion sites, thus compromising therapeutic efficacy. Inspired by the barb-hook of Xanthium strumarium, FeO@UiO-66 is functionalized with tannic acid (TA) to obtain a dual-target nanocatalyst, termed FUTA.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Faculty of Materials Science and Engineering, South China University of Technology, Guangzhou 510640, China.
Compared with the conventionally used strong acid/electrophile initiators, carboxylic acids are much more compatible with other functional groups but are incapable of initiating cationic polymerization for the one-step synthesis of end-functionalized polymers. Using lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) as a catalyst, we realized carboxylic acid-initiated cationic ring-opening polymerization (CROP) of 2-ethyl-2-oxazoline (EtOx). The dynamic exchange between carboxylate and TFSI anions, driven by Li-carboxylate interaction, significantly enhances the activity of oxazolinium propagating species and ensures uniform chain growth, as shown by both experiments and calculations.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
State Key Laboratory of Electroanalytic Chemistry, Jilin Province Key Laboratory of Low Carbon Chemistry Power, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun, 130022, China.
The sustainable and widespread developments of fuel cells require material innovation toward the sluggish oxygen reduction reaction (ORR). Although iron and nitrogen co-doped carbon material (Fe-N-C) is a promising alternative to scarce and expensive platinum-based electrocatalysts, the linear scaling relationships among the intermediates' adsorption energy limit maximum performance. Herein, we propose a coordination-adaptive catalyst design to bypass the intrinsic scaling relations through incorporating quasi-covalent Fe─F bond.
View Article and Find Full Text PDFJ Food Sci
September 2025
College of Light Industry and Food Technology, Zhongkai University of Agriculture and Engineering, Guangzhou, China.
To address post-harvest issues of litchi, including browning, water loss, and nutrient degradation, a moisture microenvironment-regulating electro spun membrane was prepared by incorporating hydrophobic carnauba wax (CW)@nano silica (SiO) composite powder into a polyethylene terephthalate (PET) matrix via electro spinning. The dynamic water penetration equilibrium was evaluated by monitoring the water vapor absorption of the electrospun membrane within 12 h, while the effects of CW@SiO on the micro-structure, mechanical properties, hydrophobicity, and thermal stability were investigated. Results showed that the tensile strength of the PET-2.
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