Graphene composites for energy storage applications
Flexible energy storage devices are one of the many emerging technologies which have been highly sought after. This is particularly due to the anticipated release of flexible electronics by manufacturing giants such as Samsung and Apple, as well as wearable electronic products such as light...
Saved in:
Main Author: | |
---|---|
Other Authors: | |
Format: | Theses and Dissertations |
Language: | English |
Published: |
2015
|
Subjects: | |
Online Access: | http://hdl.handle.net/10356/65086 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
id |
sg-ntu-dr.10356-65086 |
---|---|
record_format |
dspace |
spelling |
sg-ntu-dr.10356-650862023-03-04T16:32:31Z Graphene composites for energy storage applications Foo, Ce Yao Lee Pooi See School of Materials Science & Engineering DRNTU::Engineering::Materials::Energy materials Flexible energy storage devices are one of the many emerging technologies which have been highly sought after. This is particularly due to the anticipated release of flexible electronics by manufacturing giants such as Samsung and Apple, as well as wearable electronic products such as light-emitting shirts. All these products require power sources which are not only able to generate enough power, but must also display a certain degree of flexibility and mechanical robustness. In our work, highly flexible and free-standing graphene-based composite electrodes have been fabricated. These composite electrodes do not require current collectors as it is by itself an electrode which comprises entirely of the active materials for energy storage. This effectively removes the need for additives such as binders, which unnecessarily adds to the resistance and weight of the electrode. Furthermore, by encompassing materials which exhibit both pseudocapacitive and electrical double-layer capacitive (EDLC) behvarior, we are able to fully harness the potential of the composite electrode and improve the overall charge storage capability. Graphene-based derivatives such as reduced graphene oxide (rGO) and electrochemically exfoliated graphene (EEG) which exhibits high conductivity were prepared and used as a free-standing electrode. Incorporation of materials such as YzOs, Mn02 and polypyrrole were included to introduce the pseudocapacitive aspect of charge generation. The abundant oxygen functional groups in GO acts as anchoring sites for the growth of metal oxides.[ll Growth of these materials on graphene which exhibits high surface area is especially beneficial as these accessible areas allow easier penetration of electrolyte ions, enhancing electrochemical interactions. The addition of graphene also alleviates the conductivity issues of metal oxides, making it possible to achieve higher mass loadings, better cycling stability and improved reversibility. Addition of a carbon-based support was also shown to further improve the mechanical properties. OH-rich nanocellulose (NC) fibers possess great chemical affinity with rGO which have abundant oxygen functional groups, this holds the graphene sheets together and improve their interaction, giving rise to improved mechanical properties such as Youngs' modulus and tensile strength. To show the scalability of our methodology, we emphasize the importance of fabricating high mass electrodes which are more realistic to the requirements of practical applications. High capacitive performance will never be achievable during scalability if the active material mass is very low. We also demonstrate the ability of our free-standing electrodes to power up commercially available products such as LED decorative lights by fabricating it into a device, signifying the feasibility of our work to be used in commercial applications. The device also demonstrated excellent capacitive behavior in the bent state as well, showing the excellent mechanical stability of our electrodes. Master of Engineering (MSE) 2015-06-15T01:24:14Z 2015-06-15T01:24:14Z 2014 2014 Thesis http://hdl.handle.net/10356/65086 en 75 p. application/pdf |
institution |
Nanyang Technological University |
building |
NTU Library |
continent |
Asia |
country |
Singapore Singapore |
content_provider |
NTU Library |
collection |
DR-NTU |
language |
English |
topic |
DRNTU::Engineering::Materials::Energy materials |
spellingShingle |
DRNTU::Engineering::Materials::Energy materials Foo, Ce Yao Graphene composites for energy storage applications |
description |
Flexible energy storage devices are one of the many emerging technologies which have
been highly sought after. This is particularly due to the anticipated release of flexible
electronics by manufacturing giants such as Samsung and Apple, as well as wearable
electronic products such as light-emitting shirts. All these products require power sources
which are not only able to generate enough power, but must also display a certain degree
of flexibility and mechanical robustness. In our work, highly flexible and free-standing
graphene-based composite electrodes have been fabricated. These composite electrodes
do not require current collectors as it is by itself an electrode which comprises entirely of
the active materials for energy storage. This effectively removes the need for additives
such as binders, which unnecessarily adds to the resistance and weight of the electrode.
Furthermore, by encompassing materials which exhibit both pseudocapacitive and
electrical double-layer capacitive (EDLC) behvarior, we are able to fully harness the
potential of the composite electrode and improve the overall charge storage capability.
Graphene-based derivatives such as reduced graphene oxide (rGO) and electrochemically
exfoliated graphene (EEG) which exhibits high conductivity were prepared and used as a
free-standing electrode. Incorporation of materials such as YzOs, Mn02 and polypyrrole
were included to introduce the pseudocapacitive aspect of charge generation. The
abundant oxygen functional groups in GO acts as anchoring sites for the growth of metal
oxides.[ll Growth of these materials on graphene which exhibits high surface area is
especially beneficial as these accessible areas allow easier penetration of electrolyte ions, enhancing electrochemical interactions. The addition of graphene also alleviates the
conductivity issues of metal oxides, making it possible to achieve higher mass loadings,
better cycling stability and improved reversibility. Addition of a carbon-based support
was also shown to further improve the mechanical properties. OH-rich nanocellulose
(NC) fibers possess great chemical affinity with rGO which have abundant oxygen
functional groups, this holds the graphene sheets together and improve their interaction,
giving rise to improved mechanical properties such as Youngs' modulus and tensile
strength.
To show the scalability of our methodology, we emphasize the importance of fabricating
high mass electrodes which are more realistic to the requirements of practical
applications. High capacitive performance will never be achievable during scalability if
the active material mass is very low. We also demonstrate the ability of our free-standing
electrodes to power up commercially available products such as LED decorative lights by
fabricating it into a device, signifying the feasibility of our work to be used in commercial
applications. The device also demonstrated excellent capacitive behavior in the bent state
as well, showing the excellent mechanical stability of our electrodes. |
author2 |
Lee Pooi See |
author_facet |
Lee Pooi See Foo, Ce Yao |
format |
Theses and Dissertations |
author |
Foo, Ce Yao |
author_sort |
Foo, Ce Yao |
title |
Graphene composites for energy storage applications |
title_short |
Graphene composites for energy storage applications |
title_full |
Graphene composites for energy storage applications |
title_fullStr |
Graphene composites for energy storage applications |
title_full_unstemmed |
Graphene composites for energy storage applications |
title_sort |
graphene composites for energy storage applications |
publishDate |
2015 |
url |
http://hdl.handle.net/10356/65086 |
_version_ |
1759855722486562816 |