MIT Libraries logoDSpace@MIT

MIT
View Item 
  • DSpace@MIT Home
  • MIT Libraries
  • MIT Theses
  • Doctoral Theses
  • View Item
  • DSpace@MIT Home
  • MIT Libraries
  • MIT Theses
  • Doctoral Theses
  • View Item
JavaScript is disabled for your browser. Some features of this site may not work without it.

Non-equilibrium thermodynamics in porous media : battery degradation, and sorption and transport in porous materials

Author(s)
Pinson, Matthew Bede
Thumbnail
DownloadFull printable version (5.418Mb)
Alternative title
Battery degradation, and sorption and transport in porous materials
Other Contributors
Massachusetts Institute of Technology. Department of Physics.
Advisor
Martin Z. Bazant and Mehran Kardar.
Terms of use
M.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. http://dspace.mit.edu/handle/1721.1/7582
Metadata
Show full item record
Abstract
Porous media offer many interesting problems in physics and engineering due to the interaction of phase transitions, surface effects and transport. In this thesis I examine two such problems: the degradation of lithium-ion batteries, and sorption and transport of fluids in porous materials. The dominant capacity fade mechanism in many lithium-ion batteries is the loss of cyclable lithium to a solid-electrolyte interphase layer on the surface of the negative electrode. I develop a single-particle model of this fade mechanism, based on diffusion of the reacting species through the growing layer and reaction at the surface of the active material. This analytical model is justified by comparison with a computational porous electrode model. Temperature is identified as the most important variable influencing the capacity fade rate, and the model is able to make predictions for accelerated aging tests as well as the effect of mismatched internal resistances in battery packs. The quantity of a fluid taken up by a porous material as a function of the partial pressure of the fluid relative to saturation can be used to measure the pore size distribution of the material. However, hysteresis between the wetting and drying paths complicates the interpretation of experimental results. I present a unified model of hysteresis that accounts for both single-pore and network effects, enabling the calculation of not only the pore size distribution but also a parameter measuring the connectivity between large and small pores. I then use the ideas of the model to examine drying shrinkage in hardened cement paste, demonstrating that the hysteresis in this shrinkage is primarily due to water inserted between molecular layers in calcium-silicate-hydrate. Finally, I outline a model of transport of a sorbing fluid with hysteresis, and suggest possible extensions to allow quantitative comparison with experimental results.
Description
Thesis: Ph. D., Massachusetts Institute of Technology, Department of Physics, 2015.
 
This electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.
 
Cataloged from student-submitted PDF version of thesis.
 
Includes bibliographical references (pages 111-126).
 
Date issued
2015
URI
http://hdl.handle.net/1721.1/99250
Department
Massachusetts Institute of Technology. Department of Physics
Publisher
Massachusetts Institute of Technology
Keywords
Physics.

Collections
  • Doctoral Theses

Browse

All of DSpaceCommunities & CollectionsBy Issue DateAuthorsTitlesSubjectsThis CollectionBy Issue DateAuthorsTitlesSubjects

My Account

Login

Statistics

OA StatisticsStatistics by CountryStatistics by Department
MIT Libraries
PrivacyPermissionsAccessibilityContact us
MIT
Content created by the MIT Libraries, CC BY-NC unless otherwise noted. Notify us about copyright concerns.