Efficient energy storage and conversion of renewable energy is in great demand due to the
population growth, increased energy consumption, global warming, and depletion of petroleum
resources. However, the intermittence and unpredictability make the practical utilization of
renewable energy such as wind and solar energy inefficient. Advanced electrochemical energy
storage and conversion devices such as fuel cells, lithium-ion batteries, electrolyzers, and metal-air
batteries are expected to help resolve these critical issues. In this thesis, the focus is on
surface/interface of complex oxides for potential applications in electrochemical energy
conversion (alkaline fuel cells) and storage (lithium-ion batteries) devices.
In the first part, the surface of La
0.8Sr
0.2MnO
3(LSMO) is...[
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Efficient energy storage and conversion of renewable energy is in great demand due to the
population growth, increased energy consumption, global warming, and depletion of petroleum
resources. However, the intermittence and unpredictability make the practical utilization of
renewable energy such as wind and solar energy inefficient. Advanced electrochemical energy
storage and conversion devices such as fuel cells, lithium-ion batteries, electrolyzers, and metal-air
batteries are expected to help resolve these critical issues. In this thesis, the focus is on
surface/interface of complex oxides for potential applications in electrochemical energy
conversion (alkaline fuel cells) and storage (lithium-ion batteries) devices.
In the first part, the surface of La
0.8Sr
0.2MnO
3(LSMO) is treated with diluted HNO
3. This
process leads to the preferential formation of MnO
x/LSMO on the surface, leading to the
exposure of Mn cations at the surface of LSMO. The electrocatalytic activity of the
MnO
x/LSMO heterostructure towards oxygen reduction reaction (ORR) is shown to increase
when compared to the untreated LSMO. Thanks to the formation of MnO
x at the surface, the
resulting MnO
x/LSMO possesses i) a relatively high specific surface area and a mesoporous
structure; ii) a higher coverage of Mn
4+/Mn
3+ cations at the surface; and iii) a high concentration
of highly oxidative oxygen species. This work develops a facile strategy (i.e., HNO
3 treatment)
for improving the ORR-activity of perovskite oxides in alkaline solution at room temperature.
In the second part, we develop a LLZTO and PVDF solid-state composite membrane
characterized by high conductivity, tensile strength, and flexibility as well as low impedance
when interfacially modified by a minute amount of liquid electrolyte. A corresponding solid-state
lithium-ion battery with LiFePO
4 and Li as electrodes delivers excellent rate capability and
cycling stability at room temperature. In particular, the battery shows an initial discharge
capacity of 155 mAh g
-1 and, after 100 cycles at 1C, of 145 mAh g
-1. Even at 4C, the discharge
capacity is 96 mAh g
-1. Our study suggests that the interfacially modified LLZTO-PVDF
membrane is a promising electrolyte for solid-state lithium-ion batteries.
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