Design of novel lithium storage materials with a polyanionic framework

Lithium ion batteries for large-scale applications demand a strict safety standard from a cathode material during operating cycles. Lithium manganese borate (LiMnBO₃) that crystallizes into a hexagonal or monoclinic framework is one prominent polyanionic compound to cope with such requirement since it can possess high safety and high energy density simultaneously, without trading one for the other, theoretically. However, the hexagonal phase was nothing but a disregarded composition due to its negligible Li intercalation capacity. In contrast, the monoclinic LiMnBO₃ compound exhibited much more electrochemical activity than the hexagonal polymorph. In this thesis work, the discharge capacity of 100 mAh g 1 with acceptable capacity retention was achieved by simple optimization. The different electrochemical behaviors between them were understood in relation to their structural difference as it affects the Li migration barrier, structural stability of Li-deficient states, and even particle morphology. However, although promising, monoclinic LiMnBO₃ needed further improvement in terms of the achievable capacity and cyclability. Electrochemical analysis showed that the limited capacity of LiMnBO₃ mostly originated from transport limitation, a hindered Li migration through the one-dimensional diffusion channel. It also struggled from the phase decomposition and Mn dissolution due to the instability of the delithiated state, which led to gradual capacity fading in prolonged cycles. As an effective materials design strategy to overcome such limitations, systematic substitution of transition metal elements was proposed. To increase achievable capacity, Mn was partially substituted by Fe. Also, to fortify the structural integrity, Mg replaced Mn. In order to obtain both improved capacity and cyclability, Fe and Mg are co-doping led to an optimized composition. Prepared by cold-isostatic pressing, LiMg₀.₁Mn₀.₅Fe₀.₄4BO₃ showed near theoretical capacity of 200 mAh g-¹ with much improved capacity retention. These newly established materials outperformed most of the polyanionic cathode compounds. Therefore, it can be concluded a new promising candidate as a Li storage material has been developed through this thesis research.

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

2014

Author dc:creator

• Kim, Jae Chul, Ph. D. Massachusetts Institute of Technology

Advisor dc:contributor.advisor

• Gerbrand Ceder.

• Materials Science and Engineering.

Statement 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.

Licence dc:rights.uri

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

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/88373

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/88373