Show/Hide Menu
Hide/Show Apps
Logout
Türkçe
Türkçe
Search
Search
Login
Login
OpenMETU
OpenMETU
About
About
Open Science Policy
Open Science Policy
Open Access Guideline
Open Access Guideline
Postgraduate Thesis Guideline
Postgraduate Thesis Guideline
Communities & Collections
Communities & Collections
Help
Help
Frequently Asked Questions
Frequently Asked Questions
Guides
Guides
Thesis submission
Thesis submission
MS without thesis term project submission
MS without thesis term project submission
Publication submission with DOI
Publication submission with DOI
Publication submission
Publication submission
Supporting Information
Supporting Information
General Information
General Information
Copyright, Embargo and License
Copyright, Embargo and License
Contact us
Contact us
THIENOTHIOPHENE Π-BRIDGE MODIFIED QUINOXALINE BASED CONJUGATED POLYMERS FOR ORGANIC SOLAR CELLS
Download
Gizem Arslan Ünver Thesis.pdf
chem gizem a. unver (1).pdf
Date
2025-6-25
Author
Arslan Ünver, Gizem
Metadata
Show full item record
This work is licensed under a
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
.
Item Usage Stats
126
views
0
downloads
Cite This
In this study, novel thienothiophene π-bridged three different quinoxaline based monomeric acceptor units and two different benzodithiophene based monomeric donor units were polymerized via Stille Cross-Coupling reactions to synthesize six different conjugated donor polymers (P1, P2, P3, P4, P5, and P6). These polymers were used in the active layer of organic solar cell by bulk heterojunction type mixture with non-fullerene type acceptors. Moreover, the effect of different halogen and side chain substitutions to the polymers on optical, electrochemical, and photovoltaic properties were investigated. According to the UV-Vis spectrometry, the optical band gaps of P1, P2, P3, P4, P5, and P6 were calculated as 1.70, 1.75, 1.95, 1.64, 1.71, and 1.89, respectively. Based on the DPV results that are similar to the CV results, the HOMO/LUMO energy levels of the polymers were found as -5.55/-3.67, -5.49/-3.72, -5.94/-3.74, -5.79/-3.73, -5.60/-3.68, and -5.96/-3.74 for P1, P2, P3, P4, P5, and P6, respectively. The conventional type organic solar cell devices were fabricated with the structure of ITO/PEDOT:PSS/Donor:Acceptor/PDINN/Ag. Using a solar simulation system with AM 1.5 G light, current-voltage characteristics of the constructed devices were investigated. According to the calculated power conversion efficiencies of the devices, the best device performances were found as 2.87% for P1, 3.78% for P2, 3.58% for P3, 4.00% for P4, 5.98% for P5, and 1.39% for P6.
Subject Keywords
Quinoxaline
,
Benzodithiophene
,
Halogen Effect
,
Conjugated Polymer
,
Organic Solar Cell
URI
https://hdl.handle.net/11511/115179
Collections
Graduate School of Natural and Applied Sciences, Thesis
Citation Formats
IEEE
ACM
APA
CHICAGO
MLA
BibTeX
G. Arslan Ünver, “THIENOTHIOPHENE Π-BRIDGE MODIFIED QUINOXALINE BASED CONJUGATED POLYMERS FOR ORGANIC SOLAR CELLS,” M.S. - Master of Science, Middle East Technical University, 2025.