Toward commercializable microphase-separating copolymer electrolytes for rechargeable lithium batteries
Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2003.
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Format: | Thesis |
Language: | eng |
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Massachusetts Institute of Technology
2005
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Online Access: | http://hdl.handle.net/1721.1/7967 |
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author | Trapa, Patrick E. (Patrick Ervin), 1976- |
author2 | Anne M. Mayes and Donald R. Sadoway. |
author_facet | Anne M. Mayes and Donald R. Sadoway. Trapa, Patrick E. (Patrick Ervin), 1976- |
author_sort | Trapa, Patrick E. (Patrick Ervin), 1976- |
collection | MIT |
description | Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2003. |
first_indexed | 2024-09-23T11:22:15Z |
format | Thesis |
id | mit-1721.1/7967 |
institution | Massachusetts Institute of Technology |
language | eng |
last_indexed | 2024-09-23T11:22:15Z |
publishDate | 2005 |
publisher | Massachusetts Institute of Technology |
record_format | dspace |
spelling | mit-1721.1/79672019-04-11T01:51:37Z Toward commercializable microphase-separating copolymer electrolytes for rechargeable lithium batteries Trapa, Patrick E. (Patrick Ervin), 1976- Anne M. Mayes and Donald R. Sadoway. Massachusetts Institute of Technology. Dept. of Materials Science and Engineering. Massachusetts Institute of Technology. Dept. of Materials Science and Engineering. Materials Science and Engineering. Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Materials Science and Engineering, 2003. Includes bibliographical references (p. 106-113). Microphase-separating copolymers have been shown to possess the electrical properties of a polymer liquid and the mechanical properties of a solid. In the past, these materials had to be produced via anionic methods that are not easily scalable. To circumvent this problem, two approaches were adopted. In one, atom transfer radical polymerization (ATRP) was used to create the block copolymer, poly(oligo(oxyethylene) methacrylate)-b-poly(butyl methacrylate) [POEM-b-PBMA], which when doped with LiCF₃SO₃ (lithium triflate) exhibited good conductivity at room temperature ([sigma] [approximately] 3 x 10⁻⁶ S/cm at 23CÌ). The other approach used free radical techniques to prepare the graft copolymer, POEM-g-PDMS, starting with commercially available high molecular weight poly(dimethyl siloxane) [PDMS] monomethacrylate-terminated macromonomer. When doped with lithium triflate this material exhibited a conductivity of [sigma] [approximately] 8 x 10⁻⁶ S/cm at 23° C.This material was found to be stable up to [approximately] 300° C and flow resistant below an applied pressure of [approximately] 60 psi. In an effort to achieve single-ion conduction by Li⁺, the anionic charge was incorporated into the polymer backbone as a carboxylate. To prevent undesirable ion-pairing interactions two approaches were adopted: (1) tethering the anionic charge outside the conducting block of a block copolymer; (2) reacting the Lewis acid BF3 with the carboxylate to delocalize the negative charge. Both approaches produced materials with T[sub]Li⁺ = 1 while retaining conductivity ([sigma] <[or equal to] 7 x 10⁻⁶ S/cm) nearly identical to that observed in salt-doped systems. The self-doped electrolytes, however, demonstrated the ability to deliver stable currents at high drain rates, suggesting that immobilizing the anion improves rate capability. 100% solid-state cells consisting of lithium anodes, thin-film, fully-dense, vanadium oxide cathodes and microphase-separating copolymer electrolytes were operated for hundreds of cycles at discharge rates as high as [approximately] 1.5 C. Such batteries are conservatively projected to possess energy densities of 173 Wh/kg or 337 Wh/L. A design exercise optimizing a multilayer, thin-film battery configuration with the materials studied in this investigation speculated that specific energies exceeding 400 Wh/kg or 700 Wh/L may be attainable. The use of inexpensive materials and scalable processes in a simple design is expected to keep the cost of production low. by Patrick E. Trapa. Ph.D. 2005-08-24T23:20:44Z 2005-08-24T23:20:44Z 2003 2003 Thesis http://hdl.handle.net/1721.1/7967 54768641 eng 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 113 p. 9074637 bytes 9074390 bytes application/pdf application/pdf application/pdf Massachusetts Institute of Technology |
spellingShingle | Materials Science and Engineering. Trapa, Patrick E. (Patrick Ervin), 1976- Toward commercializable microphase-separating copolymer electrolytes for rechargeable lithium batteries |
title | Toward commercializable microphase-separating copolymer electrolytes for rechargeable lithium batteries |
title_full | Toward commercializable microphase-separating copolymer electrolytes for rechargeable lithium batteries |
title_fullStr | Toward commercializable microphase-separating copolymer electrolytes for rechargeable lithium batteries |
title_full_unstemmed | Toward commercializable microphase-separating copolymer electrolytes for rechargeable lithium batteries |
title_short | Toward commercializable microphase-separating copolymer electrolytes for rechargeable lithium batteries |
title_sort | toward commercializable microphase separating copolymer electrolytes for rechargeable lithium batteries |
topic | Materials Science and Engineering. |
url | http://hdl.handle.net/1721.1/7967 |
work_keys_str_mv | AT trapapatrickepatrickervin1976 towardcommercializablemicrophaseseparatingcopolymerelectrolytesforrechargeablelithiumbatteries |