dc.contributor.author |
Azeem, Muhammad |
|
dc.date.accessioned |
2023-08-10T06:02:03Z |
|
dc.date.available |
2023-08-10T06:02:03Z |
|
dc.date.issued |
2019 |
|
dc.identifier.other |
00000118195 |
|
dc.identifier.uri |
http://10.250.8.41:8080/xmlui/handle/123456789/36180 |
|
dc.description |
Supervisor: Dr. Saif Ullah Awan |
en_US |
dc.description.abstract |
Graphene oxide is a promising alternative to Graphene. Its low cost large scale production
method make it favorable for semiconductor energy storage applications. But the optical
bandgap of Graphene oxide is far greater than it is require to operate as a semiconductor in
electronic devices. In this thesis we have designed and performed three different schemes to
tailor the optical bandgap of Graphene oxide to make it usable in electronic industry. Firstly
we have tried to control the oxidation of Graphene oxide during its synthesis. Reason behind
this was to control the sp2/sp3 hybridization ratio of carbon. This was achieved with the help
of reduced amount of Oxidizing agent during its synthesis. Absorption spectrophotometry
shows the reduction in optical bandgap of the resultant material as the amount of oxidant is
decreased. This decrease in sp2
/sp3
hybridization ratio was further confirmed with the help of
Raman spectroscopy but this oxidation process is not even throughout the basil plane of
graphene oxide flake. X-ray diffraction (XRD) analysis reveals the presence of un-oxidized
graphitic domains all over the graphene oxide flake which in turn effects the exfoliation
efficiency and hydrophilic properties of the resultant material. Limited range of optical band
gap reduction and the reduced exfoliation efficiency caused by the un-oxidized graphitic
domains rules out the feasibility of this process. To achieve better range in optical bandgap
control another technique is opted that used 𝛼-Fe2O3 - Graphene oxide nanocomposite. XRD
analysis reveals the in situ reduction of graphene oxide which drastically degrades the
crystallinity of graphene oxide by introduction the lattice defects. To overcome this problem a
novel synthesis process for Iron oxide-Graphene oxide nanocomposites named as “Wet
impregnation method” is devised that uses pre-synthesized Iron oxide nanoparticles. XRD
analysis of synthesized nanocomposites rules out the possibility off in situ reduction of
graphene oxide. Optical bandgap measured with the help of absorption spectrophotometry
reveals the linear decrease in optical bandgap as the loading of Iron oxide nanoparticles is
increased from 0.25% to 7%. Morphology of these nanoparticles is probed with scanning
electron microscopy (SEM) that rules out all the possibilities of agglomeration of iron oxide
nanoparticles and coagulation of Graphene oxide sheets. EDX analysis and Elemental mapping
shows the even distribution of iron oxide nanoparticles throughout the Graphene oxide sheets.
In the last Raman and Photoluminescence spectroscopy is used to understand the electronic
interaction among the constituents of the synthesized nanocomposites. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
College of Electrical & Mechanical Engineering (CEME), NUST |
en_US |
dc.title |
Graphene oxide based nanocomposite systems for Optical device applications |
en_US |
dc.type |
Thesis |
en_US |