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Author

Geyuan Jiang

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Review Jul 2026

Cellulosic Composites in Lithium Metal Batteries.

Lithium metal batteries (LMBs) hold great promise for next-generation high-energy-density energy storage, yet their practical deployment is severely hindered by lithium dendrite growth, unstable solid electrolyte interphase (SEI), infinite volume expansion of lithium anodes, and poor thermal safety. As an abundant, renewable, biodegradable, and low-cost biomass polymer, cellulose and its derivatives feature outstanding mechanical robustness, tunable flexibility, rich surface hydroxyl groups, and designable hierarchical micro/nanostructures, which endow them with unique advantages in addressing critical bottlenecks of LMBs. This review focuses on the multifunctional roles and underlying mechanisms of cellulose-based composites in boosting the electrochemical and safety performance of LMBs. By virtue of polar functional groups and rigid-flexible integrated structures, cellulose can effectively homogenize Li+ flux, guide uniform lithium deposition, suppress dendrite nucleation and propagation, and alleviate volume fluctuation during cycling. Meanwhile, cellulose-based matrices significantly enhance the mechanical strength, thermal stability, flame retardancy, and ionic conductivity of polymer electrolytes and separators. Seven types of functional cellulose composites are highlighted regarding their applications in electrolytes, separators, 3D anode hosts, artificial interphase layers, and interface regulators. Finally, the future development of cellulose materials toward high-performance LMBs is prospected from the aspects of precise molecular modification, biomimetic ordered ion transport, and scalable green fabrication. This review provides systematic insights into the performance enhancement mechanisms and application strategies of cellulose for high-safety and long-lifespan lithium metal batteries.

Jun Guan, Minxin Wang, Zihao Zheng et al. · 1 citation
Open access Aug 2026

Supramolecular polymers with water-triggered dense domains enabling mechanical robustness programmability and weather resistance

Polymers play a crucial role in our daily lives; however, achieving a balance among mechanical performance, resistance to high and low temperatures, and mild shaping remains challenging. Here, we report a water-triggered supramolecular polymer composed of cellulose and polymethyl methacrylate. Following water-induced transformation of a stretchable supramolecular network into a densified cross-linked domain, the resulting polymer exhibits a remarkable increase in tensile strength from 2.7 MPa to 61.7 MPa, representing more than a 22-fold enhancement, and a flexural strength of 97 MPa, while maintaining structural integrity across a temperature range of −196 °C to 200 °C. In addition, the polymer enables scalable water-mediated shaping and reinforcement even in seawater, surfactant wastewater, and dye wastewater, while retaining high mechanical performance. Economic analysis and recycling assessment demonstrate that this polymer is amenable to scalable production and has considerable market potential. This study provides a biomimetic formulation for the fabrication of high-performance supramolecular polymers and broadens their potential applications across diverse fields. 'Water-enhanced materials usually exhibit tensile strengths of only a few to several tens of megapascals and limited water-induced reinforcement. Here the authors report a water triggered supramolecular polymer composed of cellulose and polymethyl methacrylate that achieves more than a 22-fold improvement in mechanical properties.'

Chang-Hong Lin, Geyuan Jiang, Min-Xin Wang et al. · 0 citations

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