1.同济大学,机械工程博士后流动站&汽车与能源学院,上海 201804
2.(同济大学,汽车与能源学院&新能源汽车工程中心 上海 201804) (,上海 201804)
3.同济大学,上海济鼎实业有限公司,上海 201804
E-mail: nijie@tongji.edu.cn
收稿:2026-01-21,
录用:2026-03-04,
网络首发:2026-04-07,
移动端阅览
倪洁, 沈伟, 张存满. 光聚合制备刚柔并济的锂负极界面保护层及其电化学性能. 高分子学报, doi: 10.11777/j.issn1000-3304.2026.26014.
Ni, J; Shen, W; Zhang, C M. Fabrication of a rigid-flexible lithium anode interfacial protection layer via photopolymerization and electrochemical performance. Acta Polymerica Sinica (in Chinese), doi: 10.11777/j.issn1000-3304.2026.26014.
倪洁, 沈伟, 张存满. 光聚合制备刚柔并济的锂负极界面保护层及其电化学性能. 高分子学报, doi: 10.11777/j.issn1000-3304.2026.26014. DOI: CSTR: 32057.14.GFZXB.2026.7575.
Ni, J; Shen, W; Zhang, C M. Fabrication of a rigid-flexible lithium anode interfacial protection layer via photopolymerization and electrochemical performance. Acta Polymerica Sinica (in Chinese), doi: 10.11777/j.issn1000-3304.2026.26014. DOI: CSTR: 32057.14.GFZXB.2026.7575.
针对锂电池负极界面副反应问题,通过光聚合法在锂负极表面构筑了“刚柔并济”的无机-有机复合界面层. 该层具有优异的锂离子传输能力及力学性能,能引导锂离子均化沉积、抑制锂枝晶生长并适应锂负极体积变化,有效提升电池循环稳定性.
Lithium metal anodes
with their ultrahigh theoretical specific capacity
are regarded as ideal candidates for next-generation high-energy-density batteries. However
its practical application is hindered by uncontrolled dendrite growth
severe interfacial side reactions
and significant volume change. The low lithium-ion transference number of conventional liquid electrolytes exacerbates the ionic concentration gradients at the elect
rode surface
further aggravating these issues. This study proposes and validates a facile photopolymerization strategy for constructing a rigid-yet-flexible ion-organic composite layer (IOL) on a lithium metal surface. This IOL is composed of inorganic cubic-phase garnet (Al/Nb-LLZO) particles with high ionic conductivity and mechanical rigidity
compounded with an elastic organic matrix of bisphenol A-glycerolate dimethacrylate (Bis-GMA). Systematic characterization confirmed that the composite IOL exhibited an ionic conductivity of 2.3×10
-5
S/cm and a high Li
+
transference number of 0.82
which homogenized the Li
+
flux and accelerated interfacial transport. Meanwhile
its synergistic rigid-flexible structure physically suppresses dendrite growth while accommodating volume changes during cycling and maintaining intimate interfacial contact. Electrochemical performance tests demonstrated that the IOL-modified symmetric cell exhibited ultralow and stable polarization (about 0.15 V) for over 3000 h. When paired with an NCM811 cathode
the full cell with a limited lithium source exhibited significantly enhanced cycling stability. Post-mortem microscopic analysis further revealed that the IOL guided the lithium metal to deposit in a dense and planar morphology
effectively suppressing "dead Li" formation and parasitic reactions. This study provides an efficient and scalable solution for concurrently addressing the kinetic
mechanical
and chemical stability challenges of lithium metal anodes from an interfacial engineering perspective
offering crucial insights for advancing the practical application of high-energy-density lithium metal batteries.
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