Microwave-assisted synthesis and local analyses of positive insertion electrodes for Li-ion batteries

Ashton, Thomas E. (2016) Microwave-assisted synthesis and local analyses of positive insertion electrodes for Li-ion batteries. PhD thesis, University of Glasgow.

Full text available as:
Download (77MB) | Preview
Printed Thesis Information: https://eleanor.lib.gla.ac.uk/record=b3261333


Efficient energy storage holds the key to reducing waste energy and enabling the use of advanced handheld electronic devices, hydrid electric vehicles and residential energy storage. Recently, Li-ion batteries have been identified and employed as energy storage devices due to their high gravimetric and volumetric energy densities, in comparison to previous technologies. However, more research is required to enhance the efficiency of Li-ion batteries by discovering electrodes with larger electrochemical discharge capacities, while maintaining electrochemical stability. The aims of this study are to develop new microwave-assisted synthesis routes to nanostructured insertion cathodes, which harbor a greater affinity for lithium extraction and insertion than bulk materials. Subsequent to this, state-of-the-art synchrotron based techniques have been employed to understand structural and dynamic behaviour of nanostructured cathode materials during battery cell operation. In this study, microwave-assisted routes to a-LiFePO4, VO2(B), V3O7, H2V3O8 and V4O6(OH)4 have all been developed. Muon spin relaxation has shown that the presence of b-LiFePO4 has a detrimental effect on the lithium diffusion properties of a-LiFePO4, in agreement with first principles calculations. For the first time, a-LiFePO4 nanostructures have been obtained by
employing a deep eutectic solvent reaction media showing near theoretical capacity (162
mAh g–1). Studies on VO2(B) have shown that the discharge capacity obtained is linked to
the synthesis method. Electrochemical studies of H2V3O8 nanowires have shown outstanding discharge capacities (323 mAh g–1 at 100 mA g–1) and rate capability (180 mAh g–1 at 1 A g–1). The electrochemcial properties of V4O6(OH)4 have been investigated for the first time and show a promising discharge capacity of (180 mAh g–1). Lastly, in situ X-ray
absorption spectroscopy has been utilised to track the evolution of the oxidation states in
a-LiFePO4, VO2(B) and H2V3O8, and has shown these can all be observed dynamically.

Item Type: Thesis (PhD)
Qualification Level: Doctoral
Subjects: Q Science > Q Science (General)
Q Science > QD Chemistry
Colleges/Schools: College of Science and Engineering > School of Chemistry
Supervisor's Name: Corr, Dr Serena Ann
Date of Award: 2016
Depositing User: Dr Thomas E Ashton
Unique ID: glathesis:2016-7856
Copyright: Copyright of this thesis is held by the author.
Date Deposited: 10 Jan 2017 09:08
Last Modified: 25 Apr 2017 08:54
URI: http://theses.gla.ac.uk/id/eprint/7856

Actions (login required)

View Item View Item


Downloads per month over past year