Show simple item record

dc.contributor.advisorMartin Z. Bazant.en_US
dc.contributor.authorBurch, Damianen_US
dc.contributor.otherMassachusetts Institute of Technology. Dept. of Mathematics.en_US
dc.date.accessioned2010-04-26T19:41:17Z
dc.date.available2010-04-26T19:41:17Z
dc.date.copyright2009en_US
dc.date.issued2009en_US
dc.identifier.urihttp://hdl.handle.net/1721.1/54233
dc.descriptionThesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Mathematics, 2009.en_US
dc.descriptionThis electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.en_US
dc.descriptionCataloged from student-submitted PDF version of thesis.en_US
dc.descriptionIncludes bibliographical references (p. 153-160).en_US
dc.description.abstractA new continuum model has been proposed by Singh, Ceder, and Bazant for the ion intercalation dynamics in a single crystal of rechargeable-battery electrode materials. It is based on the Cahn-Hilliard equation coupled to reaction rate laws as boundary conditions to handle the transfer of ions between the crystal and the electrolyte. In this thesis, I carefully derive a second set of boundary conditions--necessary to close the original PDE system--via a variational analysis of the free energy functional; I include a thermodynamically-consistent treatment of the reaction rates; I develop a semi-discrete finite volume method for numerical simulations; and I include a careful asymptotic treatment of the dynamical regimes found in different limits of the governing equations. Further, I will present several new findings relevant to batteries: Defect Interactions: When applied to strongly phase-separating, highly anisotropic materials such as LiFePO4, this model predicts phase-transformation waves between the lithiated and unlithiated portions of a crystal. This work extends the analysis of the wave dynamics, and describes a new mechanism for current capacity fade through the interactions of these waves with defects in the particle. Size-Dependent Spinodal and Miscibility Gaps: This work demonstrates that the model is powerful enough to predict that the spinodal and miscibility gaps shrink as the particle size decreases. It is also shown that boundary reactions are another general mechanism for the suppression of phase separation.en_US
dc.description.abstract(cont.) Multi-Particle Interactions: This work presents the results of parallel simulations of several nearby crystals linked together via common parameters in the boundary conditions. The results demonstrate the so-called "mosaic effect": the particles tend to fill one at a time, so much so that the particle being filled actually draws lithium out of the other ones. Moreover, it is shown that the smaller particles tend to phase separate first, a phenomenon seen in experiments but difficult to explain with any other theoretical model.en_US
dc.description.statementofresponsibilityby Damian Burch.en_US
dc.format.extent160 p.en_US
dc.language.isoengen_US
dc.publisherMassachusetts Institute of Technologyen_US
dc.rightsM.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.en_US
dc.rights.urihttp://dspace.mit.edu/handle/1721.1/7582en_US
dc.subjectMathematics.en_US
dc.titleIntercalation dynamics in lithium-ion batteriesen_US
dc.typeThesisen_US
dc.description.degreePh.D.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mathematics
dc.identifier.oclc606912795en_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record