Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

Tailoring of Energy Levels in D-pi-A Organic Dyes via Fluorination of Acceptor Units for Efficient Dye-Sensitized Solar Cells

Authors
Lee, Min-WooKim, Jae-YupSon, Hae JungKim, Jin YoungKim, BongSooKim, HonggonLee, Doh-KwonKim, KyungkonLee, Duck-HyungKo, Min Jae
Issue Date
16-1월-2015
Publisher
NATURE PUBLISHING GROUP
Citation
SCIENTIFIC REPORTS, v.5
Indexed
SCIE
SCOPUS
Journal Title
SCIENTIFIC REPORTS
Volume
5
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/94630
DOI
10.1038/srep07711
ISSN
2045-2322
Abstract
A molecular design is presented for tailoring the energy levels in D-pi-A organic dyes through fluorination of their acceptor units, which is aimed at achieving efficient dye-sensitized solar cells (DSSCs). This is achieved by exploiting the chemical structure of common D-pi-A organic dyes and incorporating one or two fluorine atoms at the ortho-positions of the cyanoacetic acid as additional acceptor units. As the number of incorporated fluorine atoms increases, the LUMO energy level of the organic dye is gradually lowered due to the electron-withdrawing effect of fluorine, which ultimately results in a gradual reduction of the HOMO-LUMO energy gap and an improvement in the spectral response. Systematic investigation of the effects of incorporating fluorine on the photovoltaic properties of DSSCs reveals an upshift in the conduction-band potential of the TiO2 electrode during impedance analysis; however, the incorporation of fluorine also results in an increased electron recombination rate, leading to a decrease in the open-circuit voltage (V-oc). Despite this limitation, the conversion efficiency is gradually enhanced as the number of incorporated fluorine atoms is increased, which is attributed to the highly improved spectral response and photocurrent.
Files in This Item
There are no files associated with this item.
Appears in
Collections
ETC > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetrics

Total Views & Downloads

BROWSE