The microscale is challenging to probe, inherently heterogeneous, and fundamentally important. Lithium-metal batteries are widely regarded as one of the most promising candidates for next-generation energy storage systems^[1]. However, the uncontrolled growth of lithium dendrites has long remained a critical obstacle, leading to internal short circuits, electrolyte decomposition, safety hazards, and rapid capacity decay. For decades, the field has been guided by a central assumption: bulk lithium is a soft and ductile metal, and therefore rigid solid electrolytes with sufficiently high shear modulus can physically suppress dendrite penetration. Yet, extensive studies have demonstrated that even stiff inorganic solid electrolytes, such as garnet-type lithium lanthanum zirconate^[2,3], fail to prevent dendrite propagation. This key contradiction has puzzled researchers worldwide. Recently, Ai et al. reported a study that directly quantifies the nanomechanical properties of individual lithium dendrites^[4]. Their findings reveal that lithium dendrites exhibit unexpectedly high strength and pronounced brittleness at the microscale, fundamentally reshaping the mechanical understanding of dendrite behavior and resolving this long-standing paradox.

Ai et al.^[4] employed advanced micro-and nanoscale experimental techniques, including custom-designed air-free transfer systems, in situ scanning electron microscope (SEM) nanomanipulators, icro-electro-mechanical systems (MEMS)-based micro-mechanical testing chips, and Pt e-beam deposition [Figure 1A]. The e-beam in SEM enables direct observation of dendrite fracture during tensile testing. Interestingly, however, the e-beam itself can influence the measurement results [Figure 1B]. Beam irradiation may alter the physical properties of the sample, thereby affecting the measured fracture stress. Moreover, the thermal effects induced by e-beam exposure can even lead to partial recovery of fractured lithium dendrites [Figure 1C]. Therefore, this comparative result (highlighting the irradiation-induced artifacts and identifying the true modulus) serves as the primary support for central claims and conclusions. These findings highlight an important consideration: while direct characterization techniques provide intuitive observation of experimental phenomena, it is essential to carefully evaluate whether the probing method perturbs the intrinsic properties of the material^[5]. This raises broader questions regarding in situ characterization techniques based on high-energy radiation. In contrast, certain indirect characterization approaches may better reflect realistic battery operating conditions^[6]. Bulk lithium behaves as a soft and highly ductile polycrystalline metal. In contrast, body-centered cubic metals (such as Fe, Cr, and W) typically exhibit high strength and hardness. This difference originates from their intrinsic lattice resistance: for example, Fe possesses a relatively high Peierls stress^[7], which imposes significant resistance to dislocation motion. In contrast, lithium, due to its weak metallic bonding, low atomic mass, large interplanar spacing, and high stacking fault energy, allows dislocations to remain compact and glide readily. However, in the study by Ai et al., the fracture stress of a single lithium dendrite exceeds ~150 MPa, which is nearly 250 times higher than the yield strength of bulk lithium (~0.6 MPa) [Figure 1D and E]. More importantly, bulk lithium undergoes substantial plastic deformation and necking prior to failure [Figure 1F], whereas lithium dendrites exhibit fully brittle fracture with almost no observable plastic flow. This finding overturns the conventional perception of lithium dendrites as soft and deformable structures. Instead, they behave more like hard and sharp wedges, capable of penetrating rigid solid electrolytes by initiating and propagating cracks, thereby challenging the Monroe-Newman criterion that has guided electrolyte design for nearly two decades^[8].

Through cryogenic transmission electron microscopy (cryo-TEM) and multiscale mechanical modeling, the authors uncover the structural origin of this anomalous mechanical behavior. Lithium dendrites exhibit a unique core-shell architecture, consisting of a nanoscale single-crystalline lithium core surrounded by a ~15 nm thick solid electrolyte interphase (SEI) layer. Two synergistic mechanisms give rise to their high strength and brittleness. First, the ultrasmall size of the lithium core significantly reduces the availability of dislocation sources, suppressing plastic deformation at room temperature^[9]. Second, the rigid SEI shell imposes strong surface constraints, inhibiting dislocation nucleation and emission. Meanwhile, dislocation pile-up at the Li-SEI interface generates back stress, further increasing the effective yield strength. Together, these effects transform intrinsically ductile lithium into a high-strength, brittle material at the nanoscale. The authors propose the use of lithium alloy anodes, such as lithium-indium alloys, to introduce abundant dislocation sources, thereby restoring ductility and reducing brittle fracture and dead lithium formation. For solid electrolytes, they suggest shifting away from the singular pursuit of ultrahigh modulus and instead focusing on microstructural design strategies that enhance resistance to crack propagation. The differences in the mechanical behavior between bulk lithium and lithium dendrites are summarized in Table 1.

In the experiments by Ai et al.^[4], tensile loading was applied to lithium dendrites, which effectively reflects their intrinsic mechanical properties. However, in practical battery systems, dendrite formation is more likely governed by compressive stresses and bending during electrochemical deposition. Therefore, incorporating additional loading modes, such as compression and bending, may provide a more comprehensive understanding of the mechanical behavior of lithium dendrites. Preventing dislocation in lithium dendrites requires the shell to possess sufficient strength. Therefore, this study indirectly demonstrates that the SEI layer itself has relatively high stiffness and mechanical strength, enabling it to effectively act as a grain-boundary-like barrier, thereby suppressing dislocation activity. Furthermore, the work involves SEI formed in liquid electrolytes as well as passivation layers formed at solid-state electrolyte interfaces. Previous studies have shown that these two types of interphases differ significantly in structure, indicating the need for further investigation into their respective microscale mechanical properties.

In summary, this landmark study by Ai et al. redefines the mechanical behavior of lithium dendrites in batteries. It not only provides a fundamental resolution to a long-standing contradiction in the field but also opens up new research directions and prompts deeper reflection on the relationship between characterization methods and intrinsic material behavior.