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Changes in the cation ordering of layered O3 Lix̳Ni₀.₅Mn₀.₅O₂ during electrochemical cycling to high voltages

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dc.contributor.advisor Yang Shao-Horn. en_US
dc.contributor.author Li, Hayley Han en_US
dc.contributor.other Massachusetts Institute of Technology. Dept. of Mechanical Engineering. en_US
dc.date.accessioned 2007-08-29T20:47:17Z
dc.date.available 2007-08-29T20:47:17Z
dc.date.copyright 2007 en_US
dc.date.issued 2007 en_US
dc.identifier.uri http://hdl.handle.net/1721.1/38706
dc.description Thesis (S.M.)--Massachusetts Institute of Technology, Dept. of Mechanical Engineering, 2007. en_US
dc.description Pages 124-125 blank. In title on t.p., double-underscored "x" appears as subscript. en_US
dc.description Includes bibliographical references (p. 95-98). en_US
dc.description.abstract Selected area electron diffraction patterns were collected from a pristine LiNi₀.₅Mn₀.₅O₂ sample and cycled Lix̳Ni₀.₅Mn₀.₅O₂ samples to 4.5 V and 5.3 V in the charged and discharged states. In the pristine sample, the single-crystal diffraction patterns clearly revealed superlattice reflections consistent with a ... supercell that is characteristic of cation ordering in the transition metal layer. Furthermore, these superlattice reflections were found to have considerably weakened or completely disappeared in the charged samples. Comparing the 4.5 V and 5.3 V charged samples, fewer crystals in the 5.3 V charged sample were found to exhibit these superlattice reflections. Another difference is that additional superlattice reflections consistent with the 01 phase with hexagonal-close-packed oxygen array were detected in the 5.3 V but not in the 4.5 V charged sample. Therefore, electron diffraction evidence was found to support the concept of Ni migration from the Li to the transition metal layer, and to confirm the increased Ni occupancy in the transition metal layer upon charging. In addition, electron diffraction data showed that Ni migration was in part reversible upon discharge as demonstrated by the increase in the fractions of crystals exhibiting the ... superlattice reflections from the charged to the discharged samples. en_US
dc.description.abstract (cont.) The excellent electrochemical activity and reversibility of LiNi₀.₅Mn₀.₅O₂ having Ni in the Li layer may be attributed to the mobility of Ni ions upon electrochemical cycling. It has been found that high voltage exposure has resulted in higher discharge capacity and better rate capability. In the cycled samples, a new type of superlattice reflections was observed in addition to the ... superlattice reflections. These superlattice reflections are similar for both the charged and the discharged samples, but their origins were believed to differ. For the charged samples, it was proposed that Li, Ni, and vacancies are partially ordered in the tetrahedral sites in a ... supercell with the space group ... Such ordering may improve the stability of the 03 layered structure upon charging to high voltages. For the discharged samples, Li, Ni, and vacancies order mostly in the octahedral sites in an ... cell with the space group P2/m. It was believed that this arrangement may facilitate Li diffusion in the interlayer slab space upon discharge. en_US
dc.description.statementofresponsibility by Hayley Han Li. en_US
dc.format.extent 125 p. en_US
dc.language.iso eng en_US
dc.publisher Massachusetts Institute of Technology en_US
dc.rights 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. en_US
dc.rights.uri http://dspace.mit.edu/handle/1721.1/7582
dc.subject Mechanical Engineering. en_US
dc.title Changes in the cation ordering of layered O3 Lix̳Ni₀.₅Mn₀.₅O₂ during electrochemical cycling to high voltages en_US
dc.type Thesis en_US
dc.description.degree S.M. en_US
dc.contributor.department Massachusetts Institute of Technology. Dept. of Mechanical Engineering. en_US
dc.identifier.oclc 166143683 en_US


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