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Updated: Jun 3, 2026

In Situ Neutron Powder Diffraction Using Custom-made Lithium-ion Batteries
Published on: November 10, 2014
Dopaje heterogéneo a través de recubrimiento a nanoescala impacta la mecánica de la intrusión de litio en
Xin Xu1,2,3, Teng Cui4, Geoff McConohy5,6
1Department of Materials Science and Engineering, Stanford University, Stanford, CA, USA. xxu@asu.edu.
Abstract:
Lithium dendrite intrusion in solid-state batteries limits fast charging and causes short-circuiting, yet the underlying regulating mechanisms are not well-understood. Here we discover that heterogeneous Ag+ doping dramatically affects lithium intrusion into Li6.6La3Zr1.6Ta0.4O12 (LLZO), a brittle solid electrolyte. Nanoscale Ag+ doping is achieved by thermally annealing a 3-nm-thick metallic coating on LLZO, inducing Ag-Li ion exchange and Ag diffusion into grains and grain boundaries. Density functional theory calculations and experimental characterization show negligible impact on the electronic properties and surface wettability from Ag+ incorporation. Mechanically, nanoindentation experiments show a fivefold increase in the mechanical force required to fracture the surface Ag+-doped LLZO, indicating substantial doping-induced surface toughening. Operando microprobe scanning electron microscopy experiments show that the Ag+-doped LLZO surface exhibits improved lithium plating at >250 mA cm-2 and an electroplating diameter that is expanded by over fourfold, even under an extreme indentation stress of 3 GPa. This demonstrates enhanced defect tolerance in LLZO, rather than electronic or adhesion effects. Our study reveals a chemo-mechanical mechanism via surface heterogeneous doping, complementing present bulk design rules to minimize mechanical failures in solid-state batteries.
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