Lithiation-induced phase transitions in alloying anodes for thin film lithium-ion batteries

As a result of the ever-increasing demands for miniaturized autonomous devices, high-performance batteries compatible with micro-systems have been attracting researchers' attention. Amorphous silicon (a-Si) and germanium (a-Ge), which store lithium through alloying processes rather than through intercalation, are among the top candidates as anodes for thin film Li-ion batteries. This thesis explores different types of lithiation-induced phase transitions and develops corresponding kinetic models in amorphous Si and Ge films using a framework consisting of electrochemical, structural and analytic approaches. The first section of this thesis covers the initial lithiation process of a-Si. Potentiostatic techniques reveal a kink feature in the temporal evolution of current, indicating an interface propagation mechanism for the irreversible phase transition. The rate-limiting step for propagation of the interface between unlithiated Si and the lithiated alloy is further determined to be the diffusion of Li through the lithiated phase, based on quantitative analyses of film-thickness dependence in potentiostatic tests. The second section deals with the reversible lithiation of a-Si beyond the first cycle, often assumed to be governed by simple diffusion into single-phase a-Si. We show that reversible lithiation proceeds through phase transitions between amorphous phases with different stoichiometries. Using a two-step potentiostatic technique and the Johnson-Mehl-Avrami-Kolmogorov model, it is shown that these amorphous-to-amorphous transitions occur through three-dimensional nucleation and growth processes. This conclusion is supported by TEM observations for which phase contrast is achieved through preferential high-energy electron-beam induced sputtering of Li. Instead of a complete transition at fixed voltage, reversible phase transitions in a-Si occur in a step-by-step nucleation fashion. The last section focuses on phase transitions during reversible lithiation of a-Ge using similar techniques to those used for the studies of a-Si. The only crystalline phase, Li₁₅Ge₄, is found to coexist with two amorphous alloy phases over a wide voltage range during lithiation. The formation of this crystalline phase turns is found to be highly constrained by kinetic barriers, and is very sensitive to structural evolutions such as cracking in the early cycles.

Name thesis:degree_name

Doctoral

Department dc:contributor.department

Massachusetts Institute of Technology. Department of Materials Science and Engineering

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2020

Author dc:creator

• Miao, Jinghui, author.

Advisor dc:contributor.advisor

• Carl V. Thompson.

• Materials Science and Engineering.

Statement dc:rights

• MIT theses may be protected by copyright. Please reuse MIT thesis content according to the MIT Libraries Permissions Policy, which is available through the URL provided.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

https://hdl.handle.net/1721.1/150464

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/150464