98%
921
2 minutes
20
The growing demand for high-energy-density, safe, and sustainable lithium-ion batteries (LIBs) necessitates the development of innovative electrolytes. Herein, we present a facile in situ preparation strategy for fabricating a high-performance single-ion conductor (SC). This SC is based on hydroxypropyl cellulose (HPC) integrated with polyethylene glycol diacrylate cross-linker, in combination with sodium styrene sulfonate (NaSS) as a functional monomer. The introduction of NaSS is crucial, as it introduces sulfonate groups that are immobilized within the polymer network, enabling selective lithium-ion transport. This approach offers a significant advancement over conventional polyether-based gel polymer electrolytes (GPEs), which usually suffer from limited oxidative stability and require the use of separators, particularly in high-voltage battery applications. The in situ polymerization method presented here eliminates the need for a separator and offers several key advantages: rapid processability, excellent scalability, and the formation of a stable solid electrolyte interface. The result is a robust, separator-free GPE. Our HPC-based single-ion conductor (MHPC SC) exhibits a high lithium transference number of 0.89 and an ionic conductivity of 2.4 mS cm at room temperature. These properties are attributed to efficient lithium-ion transport through its synergistic effect of the polyanionic conductor and HPC matrix. The mechanically robust and highly conformal polymer network effectively suppresses detrimental interfacial reactions and mitigates dendrite growth, resulting in an enhanced cycling stability. Notably, the MHPC SC enables stable operation with high-voltage cathodes up to 4.3 V, achieving 94% capacity retention over 100 cycles. These findings highlight the potential of cellulose-based GPEs as a sustainable and high-performance electrolyte that significantly enhances both the safety and performance of advanced LIBs.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acsami.5c07304 | DOI Listing |
Dalton Trans
September 2025
Sun Yat-Sen University, MOE Laboratory of Polymeric Composite and Functional Materials, School of Materials Science and Engineering, Guangzhou 510275, China.
The main bottleneck faced by traditional hydrogen production technology through water electrolysis lies in the high energy consumption of the anodic oxygen evolution reaction (OER). Combining the thermodynamically favorable ethanol oxidation reaction (EOR) with the hydrogen evolution reaction provides a promising route to reduce the energy consumption of hydrogen production and generate high value-added products. In this study, a facile method was developed for nickel oxyhydroxide (NiOOH) fabrication.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
Key Laboratory of Automobile Materials, Ministry of Education and School of Materials Science and Engineering, Jilin University, Changchun 130022, China. Electronic address:
Neither single electrolyte design nor solid electrolyte interface (SEI) engineering alone can effectively resolve the dual challenges of sluggish reaction kinetics and unstable interfaces in polymer-based lithium metal batteries (LMBs). Herein, a rational integrated design strategy is adopted to simultaneously fabricate poly(trifluoroethyl methacrylate-co-4-oxo-5,8,11-trioxa-3-azatridec-12-en-1-yl acrylate)-based gel polymer electrolyte (PTDA-GPE) and stable composite SEI during the thermal-induced in situ polymerization process. The resulting PTDA-GPE demonstrates superior Li transport kinetics (1.
View Article and Find Full Text PDFBiomaterials
August 2025
Department of Prosthodontics, School and Hospital of Stomatology, Cheeloo College of Medicine, Shandong University & Shandong Key Laboratory of Oral Tissue Regeneration & Shandong Engineering Research Center of Dental Materials and Oral Tissue Regeneration & Shandong Provincial Clinical Research Cen
Dental tissue regeneration is often challenged by the hostile inflammatory microenvironment and the dysfunction of reparative cells due to oxidative stress. This study presents a reactive oxygen species (ROS)-scavenging nanozyme induced by ligand-to-metal charge transfer, engineered as a multifunctional capping material through the in situ growth of copper-gallate (CuGA) on hydroxyapatite nanofibers (HAFs). The obtained CuGA@HAF demonstrates superior ROS-scavenging capacity through its multi-enzyme mimetic activity, effectively rescuing the function of dental pulp stem cells (DPSCs) under oxidative stress by restoring mitochondrial homeostasis.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
State Key Laboratory of Heavy Oil Processing, China University of Petroleum, Chang Ping, Beijing 102249, China.
The dynamic structural evolution of heterogeneous catalysts is a ubiquitous phenomenon that has attracted a lot of interest. Catalyst reconstruction can occur after appropriate pretreatment, resulting in more efficient active catalysts, which is an attractive but challenging issue. Here, we reveal a CO activation strategy that controls the microenvironment of the Co sites in the high-silica Co-ZSM-5 catalyst (denoted as 0.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
School of Biomedical Engineering (Suzhou), Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei 230026, P. R. China.
Quantifying and monitoring glutathione (GSH) in living cells is of great significance for understanding GSH-related oxidative stress disorders and neoplastic conditions. In this work, we developed nitrogen/sulfur/boron codoped MXene quantum dots (NSB-MQDs) through a facile single-pot hydrothermal synthesis strategy for fluorescence/colorimetric detection and imaging of GSH. The fluorescence "Turn-On" sensing signal was generated by the electron or energy transfer process between GSH and NSB-MQDs, which exhibited a fluorescence quenching phenomenon with the increase of GSH.
View Article and Find Full Text PDF