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Ultrathick battery electrodes are appealing as they reduce the fraction of inactive battery parts such as current collectors and separators. However, thick electrodes are difficult to dry and tend to crack or flake during production. Moreover, the electrochemical performance of thick electrodes is constrained by ion and electron transport as well as fast capacity degradation. Here, we report a thermally induced phase separation (TIPS) process for fabricating thick Li-ion battery electrodes, which incorporates the electrolyte directly in the electrode and alleviates the need to dry the electrode. The proposed TIPS process creates a bicontinuous electrolyte and electrode network with excellent ion and electron transport, respectively, and consequently achieves better rate performance. Using this process, electrodes with areal capacities of more than 30 mAh/cm are demonstrated. Capacity retentions of 87% are attained over 500 cycles in full cells with 1-mm-thick anodes and cathodes. Finally, we verified the scalability of the TIPS process by coating thick electrodes continuously on a pilot-scale roll-to-roll coating tool.
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http://dx.doi.org/10.1073/pnas.2007250117 | DOI Listing |
Angew Chem Int Ed Engl
September 2025
School of Integrated Circuits, State Key Laboratory of New Textile Materials and Advanced Processing, Key Laboratory of Material Chemistry for Energy Conversion and Storage (Ministry of Education), Huazhong University of Science and Technology, Wuhan, 430074, China.
Low-temperature rechargeable batteries face great challenges due to the sluggish reaction kinetics. Redox covalent organic frameworks (COFs) with porous structures provide a viable solution to accelerate the ionic diffusion and reaction kinetics at low temperatures. However, the applications of COFs in low-temperature batteries are still at their infancy stage.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
State Key Laboratory of Electrical Insulation and Power Equipment, Xi'an Jiaotong University, Xi'an 710049, China.
Economically viable and biologically compatible amino acids demonstrate significant potential as electrolyte microstructure modifiers in aqueous zinc-ion batteries (AZIBs). Compared to polar amino acids, nonpolar amino acids simultaneously own zincophilicity and hydrophobicity, showing great potential in the industrial application of AZIBs. However, nonpolar amino acids have been comparatively understudied in existing research investigations.
View Article and Find Full Text PDFLangmuir
September 2025
College of Textile and Clothing Engineering, Soochow University, Suzhou 215123, PR China.
Sodium-ion batteries are promising candidates for large-scale energy storage due to their low cost and resource abundance. However, their cathode materials suffer from poor conductivity and limited cycling stability. Here, we report a Prussian blue (PB)-based cathode hybridized with carboxyl-functionalized carbon nanotubes (CNTs) via a glutamic acid-assisted in situ coordination route.
View Article and Find Full Text PDFSmall
September 2025
Institute of Chemistry, Academia Sinica, Taipei, 115201, Taiwan.
Achieving high capacitance while maintaining rapid charge transport and structural stability remains a major challenge in the design of battery-type supercapacitor electrodes. Herein, a molecularly engineered strategy is presented for constructing hierarchical hybrid electrodes by integrating petal-like NiCu-LDH nanosheets onto 3D HBC-x (x = H, F, OMe)-functionalized CNT paper via a one-step hydrothermal process. The incorporation of HBC effectively mitigates CNT agglomeration and constructs an interconnected conductive framework that enhances charge transport, shortens ion diffusion paths, and reduces internal resistance.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Anhui Province Key Laboratory for Control and Applications of Optoelectronic Information Materials, Key Laboratory of Functional Molecular Solids Ministry of Education, and Department of Physics, Anhui Normal University, Wuhu, Anhui 241000, China.
Dual-ion batteries (such as alkali metal ion-hexafluorophosphate anion systems) have demonstrated an excellent performance; however, identifying suitable cathode materials with superior electrochemical properties remains a major challenge impeding their advancement. In this work, the feasibility of biphenylite as a dual-ion battery cathode material is investigated systematically by first-principles calculations. The calculated result indicates that biphenylite has an ultrahigh cathode specific capacity for PF anions (107.
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