TY - JOUR
T1 - Effects of phenylalkanoic acids as co-adsorbents on the performance of dye-sensitized solar cells
AU - Nath, Narayan Chandra Deb
AU - Lee, Ho Joon
AU - Choi, Won Youl
AU - Lee, Jae Joon
PY - 2013/12
Y1 - 2013/12
N2 - The photoelectrochemical effects of a series of phenylalkanoic acids as co-adsorbents along with a ruthenium sensitizer, cis-diisothiocyanato-bis(2,2)-bipyridyl-4,4-dicarboxylato) ruthenium(II) bistetrabutylammonium dye (N719), were investigated in dye-sensitized solar cells (DSSCs). All the co-adsorbents used in this study enhanced the short circuit current density (Jsc) resulting from the increased electron injection efficiency due to the significant reduction of dye-aggregation, and this enhancement increased with increasing chain-length of their hydrophobic alkyl groups. They suppressed interfacial back electron transfer rate from the conduction band of TiO2 to triiodide (I? 3) in electrolyte without shifting the quasi-Fermi level of the TiO2 in general, and induced a longer recombination lifetime This corresponded to the enhancement of the open circuit voltage (Voc) of the cells by up to ca. 20 mV compared to that with no co-adsorbents. On the contrary, the photovoltage decreased by ca. 10 mV when 2-phenylethanoic acid was used as a co-adsorbent, which was attributed to the negative shift of the quasi-Fermi level of the TiO2 nanoparticles.
AB - The photoelectrochemical effects of a series of phenylalkanoic acids as co-adsorbents along with a ruthenium sensitizer, cis-diisothiocyanato-bis(2,2)-bipyridyl-4,4-dicarboxylato) ruthenium(II) bistetrabutylammonium dye (N719), were investigated in dye-sensitized solar cells (DSSCs). All the co-adsorbents used in this study enhanced the short circuit current density (Jsc) resulting from the increased electron injection efficiency due to the significant reduction of dye-aggregation, and this enhancement increased with increasing chain-length of their hydrophobic alkyl groups. They suppressed interfacial back electron transfer rate from the conduction band of TiO2 to triiodide (I? 3) in electrolyte without shifting the quasi-Fermi level of the TiO2 in general, and induced a longer recombination lifetime This corresponded to the enhancement of the open circuit voltage (Voc) of the cells by up to ca. 20 mV compared to that with no co-adsorbents. On the contrary, the photovoltage decreased by ca. 10 mV when 2-phenylethanoic acid was used as a co-adsorbent, which was attributed to the negative shift of the quasi-Fermi level of the TiO2 nanoparticles.
KW - Back Electron Transfer Rate
KW - Co-Adsorbents
KW - Dye-Sensitized Solar Cell
KW - Phenylalkanoic Acids
KW - Quasi-Fermi Level
UR - http://www.scopus.com/inward/record.url?scp=84886941957&partnerID=8YFLogxK
U2 - 10.1166/jnn.2013.8117
DO - 10.1166/jnn.2013.8117
M3 - Article
AN - SCOPUS:84886941957
SN - 1533-4880
VL - 13
SP - 7880
EP - 7885
JO - Journal of Nanoscience and Nanotechnology
JF - Journal of Nanoscience and Nanotechnology
IS - 12
ER -