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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
Aug 2026

Structural Water-Enabled Helicity Emergence From an Asymmetric Achiral Molecule.

Helical supramolecular architectures are ubiquitous in nature yet remain challenging to construct from asymmetric achiral molecules. Here, we demonstrate that structural water acts as a symmetry-breaking and frustration-generating element in artificial self-assembly. Using an asymmetric achiral naphthalene derivative (N1) as a model system, we show that trace water fundamentally redirects its assembly pathway. In the presence of structural water, N1 forms racemic P/M helical fibers, whereas only non-helical aggregates are obtained under anhydrous conditions or with control molecules lacking sufficient hydrogen-bonding capability. Single-crystal x-ray analysis reveals that each water molecule functions as a tetravalent hydrogen-bonding node, bridging four N1 molecules into a nonplanar C2-symmetric tetramer. This water-centered motif introduces geometric incompatibility with optimal π-π stacking, generating packing frustration that is relieved through hierarchical helical twisting. The hydrogen-bonding network can be reversibly modulated by acid-base stimuli, enabling interconversion between helical and non-helical morphologies. Moreover, the resulting helices can be biased into homochiral states by chiral aromatic amino acids, revealing a water-gated chirality transfer mechanism that is absent under anhydrous conditions. This work extends design principles for supramolecular helicity beyond conventional symmetric monomers and highlights the role of structural water in controlling complex self-assembly pathways.

Hao Kong, Zhen Wu, Bijun Wang et al. · 0 citations

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