TY - JOUR
T1 - Designing Squaraines to Control Charge Injection and Recombination Processes in NiO-based Dye-Sensitized Solar Cells
AU - Langmar, Oliver
AU - Saccone, Davide
AU - Amat, Anna
AU - Fantacci, Simona
AU - Viscardi, Guido
AU - Barolo, Claudia
AU - Costa, Rubén D.
AU - Guldi, Dirk M.
N1 - Publisher Copyright:
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2017/6/9
Y1 - 2017/6/9
N2 - Herein, the synthesis of a new family of squaraines (SQs) and their application in p-type dye-sensitized solar cells (DSSCs) is presented. In particular, two sets of SQs were designed featuring either two or four anchoring carboxylic groups combined with either oxygen or dicyanovinyl central groups. The SQs were characterized by using a joint theoretical, photophysical, and electrochemical approach. Importantly, the presence of different central groups forces a frozen cis (dicyanovinyl group) or a trans (oxygen group) SQ conformation. Based on the latter, the current work enables a direct comparison between cis and trans isomers as well as the impact of a different number of anchors. Considering their electron-accepting and light-harvesting character, they were tested in NiO-based DSSCs. Photocurrent–voltage, incident photon-to-current conversion efficiency (IPCE), and electrochemical impedance spectroscopy measurements were performed. By virtue of their different symmetry, stereochemistry, and number of carboxylic groups, altered adsorption behavior onto NiO electrodes as well as diverse charge injection and charge recombination dynamics were noted under operation conditions. SQs with four linkers in a frozen cis isomerism show the best charge collection properties among the investigated SQs, providing a valuable guideline for the molecular design of future SQs for p-type DSSCs. In addition, we assembled tandem DSSCs featuring SQ/NiO photocathodes and N719/TiO2 photoanodes. The IPCE of the resulting tandem DSSCs implies light harvesting throughout most of the visible part of the solar spectrum owing to the complementary absorption features of SQ and N719.
AB - Herein, the synthesis of a new family of squaraines (SQs) and their application in p-type dye-sensitized solar cells (DSSCs) is presented. In particular, two sets of SQs were designed featuring either two or four anchoring carboxylic groups combined with either oxygen or dicyanovinyl central groups. The SQs were characterized by using a joint theoretical, photophysical, and electrochemical approach. Importantly, the presence of different central groups forces a frozen cis (dicyanovinyl group) or a trans (oxygen group) SQ conformation. Based on the latter, the current work enables a direct comparison between cis and trans isomers as well as the impact of a different number of anchors. Considering their electron-accepting and light-harvesting character, they were tested in NiO-based DSSCs. Photocurrent–voltage, incident photon-to-current conversion efficiency (IPCE), and electrochemical impedance spectroscopy measurements were performed. By virtue of their different symmetry, stereochemistry, and number of carboxylic groups, altered adsorption behavior onto NiO electrodes as well as diverse charge injection and charge recombination dynamics were noted under operation conditions. SQs with four linkers in a frozen cis isomerism show the best charge collection properties among the investigated SQs, providing a valuable guideline for the molecular design of future SQs for p-type DSSCs. In addition, we assembled tandem DSSCs featuring SQ/NiO photocathodes and N719/TiO2 photoanodes. The IPCE of the resulting tandem DSSCs implies light harvesting throughout most of the visible part of the solar spectrum owing to the complementary absorption features of SQ and N719.
KW - dye-sensitized solar cells
KW - electrochemical impedance spectroscopy
KW - squaraines
KW - symmetry
KW - tandem
UR - http://www.scopus.com/inward/record.url?scp=85017567326&partnerID=8YFLogxK
U2 - 10.1002/cssc.201700152
DO - 10.1002/cssc.201700152
M3 - Article
C2 - 28318143
AN - SCOPUS:85017567326
SN - 1864-5631
VL - 10
SP - 2385
EP - 2393
JO - ChemSusChem
JF - ChemSusChem
IS - 11
ER -