Strong and brittle lithium dendrites
The growth and penetration of lithium dendrites through electrolytes and separators remain key challenges to realizing high-energy density lithium-metal batteries. Using mechanically strong electrolytes and separators has been considered a promising strategy based on the commonly believed softness of lithium. However, dendrite formation persists in stiff solid electrolytes, suggesting distinct mechanical behaviors. We measured the mechanical properties of individual lithium dendrites using an air-free protocol. We found that lithium dendrites are unexpectedly strong and brittle, with fracture stress greater than ~150 megapascals, unlike the ductile bulk metal. Cryo-transmission electron microscopy and mechanical modeling showed that this behavior arises from solid electrolyte interface constraints and nanoscale strengthening. These findings provide alternative mechanisms for dendrite penetration and dead lithium formation as well as guidance for design strategies for lithium-metal batteries.
Authors
- Huajian Gao (ORCID: https://orcid.org/0000-0002-8656-846X)
- Xiaoyin Tian
- Xuan Zhao (ORCID: https://orcid.org/0000-0002-4669-5149)
- Youtian Zhang
- Lihong Zhao
- B. Zhang
- Qiyi Fang (ORCID: https://orcid.org/0000-0001-8435-636X)
- Hao Guo (ORCID: https://orcid.org/0000-0001-6232-6901)
- Yifan Zhu (ORCID: https://orcid.org/0000-0001-8359-6492)
- Qing Ai (ORCID: https://orcid.org/0000-0002-6872-9848)
- Xintong Weng
- Tianshu Zhai
- Yimo Han
- Doug Steinbach
- Jun Lou
- Ming Tang
- Bongki Shin
- Wenhua Guo
- Yan Yao
- Ting Zhu
- Fan Wang
- Xing Liu
- Yifeng Liu
- Guanhui Gao
Institutions
- Agency for Science, Technology and Research (SG)
- New Jersey Institute of Technology (US)
- Georgia Institute of Technology (US)
- Nanyang Technological University (SG)
- Institute of High Performance Computing (SG)
- University of Houston (US)
- Rice University (US)
Publication Details
- Journal
- Science
- Published
- 2026-03-12
- DOI
- https://doi.org/10.1126/science.adu9988
- Primary Topic
- Advanced Battery Materials and Technologies
- Type
- article
- Field-Weighted Citation Impact
- 0.00