532
Y. Ooyama
Kim JY, Lee K, Coates NE, Moses D, Nguyen T-Q, Dante M, Heeger AJ (2007) Efficient tandem
polymer solar cells fabricated by all-solution processing. Science 317:222–225
Kim C, Choi H, Kim S, Baik C, Song K, Kang M-S, Kang SO, Ko J (2008a) Molecular engineering
of organic sensitizers containing p-phenylene vinylene unit for dye-sensitized solar cells. J Org
Chem 73:7072–7079
Kim S, Kim D, Choi H, Kang M-S, Song K, Kang SO, Ko J (2008b) Enhanced photovoltaic
performance and long-term stability of quasi-solid-state dye-sensitized solar cellsvia molecular
engineering. Chem Commun 4951–4953
Kim D, Kang M-S, Song K, Kang SO, Ko J (2008c) Molecular engineering of organic sensitizers
containing indole moiety for dye-sensitized solar cells. Tetrahedron 64:10417–10424
Kimura M, Nomoto H, Masaki N, Mori S (2012) Dye molecules for simple co-sensitization process:
fabrication of mixed-dye-sensitized solar cells. Angew Chem 124:4447–4450 (2012); Angew
Chem Int Ed 51:4371–4374
Kolemen S, Cakmak Y, Erten-Ela S, Altay Y, Brendel J, Thelakkat M, Akkaya EU (2010) Solidstate dye-sensitized solar cells using red and near-IR absorbing bodipy sensitizers. Org Lett
12:3812–3815
Kolemen S, Bozdemir OA, Cakmak Y, Barin G, Erten-Ela S, Marszalek M, Yum J-H, Zakeeruddin
SM, Nazeeruddin MK, Grätzel M, Akkaya EU (2011) Optimization of distyryl-Bodipy chromophores for efficient panchromatic sensitization in dye sensitized solar cells. Chem Sci
2:949–954
Koumura N, Wang Z-S, Mori S, Miyashita M, Suzuki E, Hara K (2006) Alkyl-functionalized organic
dyes for efficient molecular photovoltaics. J Am Chem Soc 128:14256–14257
Kuang D, Uchida S, Humphry-Baker R, Zakeeruddin SK, Grätzel M (2008) Organic dye-sensitized
ionic liquid based solar cells: remarkable enhancement in performance through molecular design
of indoline sensitizers. Angew Chem 120:1949–1953 (2008); Angew Chem Int Ed 47:1923–1927
Kubo Y, Eguchi D, Matsumoto A, Nishiyabu R, Yakushiji H, Shigaki K, Kaneko M (2014) Boron–
dibenzopyrromethene-based organic dyes for application in dye-sensitized solar cells. J Mater
Chem A 2:5204–5211
Kumara GRA, Kaneko S, Okuya M, Onwona-Agyeman B, Konno A, Tennakone K (2006) Shiso
leaf pigments for dye-sensitized solid-state solar cell. Sol Energy Mater Sol Cells 90:1220–1226
Kumaresan D, Thummel RP, Bura T, Ulrich G, Ziessel R (2009) Color tuning in new metal-free
organic sensitizers (bodipys) for dye-sensitized solar cells. Chem Eur J 15:6335–6339
Kuster S, Sauvage F, Nazeeruddin MK, Grätzel M, Nüesh FA, Geiger T (2010) Unsymmetrical
squaraine dimer with an extended π-electron framework: An approach in harvesting near infra-red
photons for energy conversion. Dyes Pigm 87:30–38
Ladomenou K, Kitsopoulos TN, Sharma GD, Coutsolelos AG (2014) The importance of various
anchoring groups attached on porphyrins as potential dyes for DSSC applications. RSC Adv
4:21379–21404
Le Pleux L, Chavillon B, Pellegrin Y, Blart E, Cario L, Jobic S, Odobel F (2009) Simple and
reproducible procedure to prepare self-nanostructured NiO films for the fabrication of p-type
dye-sensitized solar cells. Inorg Chem 48:8245–8250
Le Pleux L, Smeigh AL, Gibson E, Pellegrin Y, Blart E, Boschloo G, Hagfeldt A, Hammarstrcm
L, Odobel F (2011) Synthesis, photophysical and photovoltaic investigations of acceptorfunctionalized perylene monoimide dyes for nickel oxide p-type dye-sensitized solar cells. Energy
Environ Sci 4:2075–2084
Lee C-W, Lu H-P, Lan C-M, Huang Y-L, Liang Y-R, Yen W-N, Liu Y-C, Lin Y-S, Diau EW-G, Yeh
C-Y (2009) Novel zinc porphyrin sensitizers for dye-sensitized solar cells: synthesis and spectral,
electrochemical, and photovoltaic properties. Chem Eur J 15:1403–1412
Lee C-P, Lin RY-Y, Lin L-Y, Li C-T, Chu T-C, Sun S-S, Lin JT, Ho K-C (2015) Recent progress in
organic sensitizers for dye-sensitized solar cells. RSC Adv 5:23810–23825
Li L-L, Diau EW-G (2013) Porphyrin-sensitized solar cells. Chem Soc Rev 42:291–304
Li C, Wang W, Wang X, Zhang B, Cao Y (2005) Molecular design of squaraine dyes for efficient
far-red and near-IR sensitization of solar cells. Chem Lett 34:554–555
Y. Ooyama
Kim JY, Lee K, Coates NE, Moses D, Nguyen T-Q, Dante M, Heeger AJ (2007) Efficient tandem
polymer solar cells fabricated by all-solution processing. Science 317:222–225
Kim C, Choi H, Kim S, Baik C, Song K, Kang M-S, Kang SO, Ko J (2008a) Molecular engineering
of organic sensitizers containing p-phenylene vinylene unit for dye-sensitized solar cells. J Org
Chem 73:7072–7079
Kim S, Kim D, Choi H, Kang M-S, Song K, Kang SO, Ko J (2008b) Enhanced photovoltaic
performance and long-term stability of quasi-solid-state dye-sensitized solar cellsvia molecular
engineering. Chem Commun 4951–4953
Kim D, Kang M-S, Song K, Kang SO, Ko J (2008c) Molecular engineering of organic sensitizers
containing indole moiety for dye-sensitized solar cells. Tetrahedron 64:10417–10424
Kimura M, Nomoto H, Masaki N, Mori S (2012) Dye molecules for simple co-sensitization process:
fabrication of mixed-dye-sensitized solar cells. Angew Chem 124:4447–4450 (2012); Angew
Chem Int Ed 51:4371–4374
Kolemen S, Cakmak Y, Erten-Ela S, Altay Y, Brendel J, Thelakkat M, Akkaya EU (2010) Solidstate dye-sensitized solar cells using red and near-IR absorbing bodipy sensitizers. Org Lett
12:3812–3815
Kolemen S, Bozdemir OA, Cakmak Y, Barin G, Erten-Ela S, Marszalek M, Yum J-H, Zakeeruddin
SM, Nazeeruddin MK, Grätzel M, Akkaya EU (2011) Optimization of distyryl-Bodipy chromophores for efficient panchromatic sensitization in dye sensitized solar cells. Chem Sci
2:949–954
Koumura N, Wang Z-S, Mori S, Miyashita M, Suzuki E, Hara K (2006) Alkyl-functionalized organic
dyes for efficient molecular photovoltaics. J Am Chem Soc 128:14256–14257
Kuang D, Uchida S, Humphry-Baker R, Zakeeruddin SK, Grätzel M (2008) Organic dye-sensitized
ionic liquid based solar cells: remarkable enhancement in performance through molecular design
of indoline sensitizers. Angew Chem 120:1949–1953 (2008); Angew Chem Int Ed 47:1923–1927
Kubo Y, Eguchi D, Matsumoto A, Nishiyabu R, Yakushiji H, Shigaki K, Kaneko M (2014) Boron–
dibenzopyrromethene-based organic dyes for application in dye-sensitized solar cells. J Mater
Chem A 2:5204–5211
Kumara GRA, Kaneko S, Okuya M, Onwona-Agyeman B, Konno A, Tennakone K (2006) Shiso
leaf pigments for dye-sensitized solid-state solar cell. Sol Energy Mater Sol Cells 90:1220–1226
Kumaresan D, Thummel RP, Bura T, Ulrich G, Ziessel R (2009) Color tuning in new metal-free
organic sensitizers (bodipys) for dye-sensitized solar cells. Chem Eur J 15:6335–6339
Kuster S, Sauvage F, Nazeeruddin MK, Grätzel M, Nüesh FA, Geiger T (2010) Unsymmetrical
squaraine dimer with an extended π-electron framework: An approach in harvesting near infra-red
photons for energy conversion. Dyes Pigm 87:30–38
Ladomenou K, Kitsopoulos TN, Sharma GD, Coutsolelos AG (2014) The importance of various
anchoring groups attached on porphyrins as potential dyes for DSSC applications. RSC Adv
4:21379–21404
Le Pleux L, Chavillon B, Pellegrin Y, Blart E, Cario L, Jobic S, Odobel F (2009) Simple and
reproducible procedure to prepare self-nanostructured NiO films for the fabrication of p-type
dye-sensitized solar cells. Inorg Chem 48:8245–8250
Le Pleux L, Smeigh AL, Gibson E, Pellegrin Y, Blart E, Boschloo G, Hagfeldt A, Hammarstrcm
L, Odobel F (2011) Synthesis, photophysical and photovoltaic investigations of acceptorfunctionalized perylene monoimide dyes for nickel oxide p-type dye-sensitized solar cells. Energy
Environ Sci 4:2075–2084
Lee C-W, Lu H-P, Lan C-M, Huang Y-L, Liang Y-R, Yen W-N, Liu Y-C, Lin Y-S, Diau EW-G, Yeh
C-Y (2009) Novel zinc porphyrin sensitizers for dye-sensitized solar cells: synthesis and spectral,
electrochemical, and photovoltaic properties. Chem Eur J 15:1403–1412
Lee C-P, Lin RY-Y, Lin L-Y, Li C-T, Chu T-C, Sun S-S, Lin JT, Ho K-C (2015) Recent progress in
organic sensitizers for dye-sensitized solar cells. RSC Adv 5:23810–23825
Li L-L, Diau EW-G (2013) Porphyrin-sensitized solar cells. Chem Soc Rev 42:291–304
Li C, Wang W, Wang X, Zhang B, Cao Y (2005) Molecular design of squaraine dyes for efficient
far-red and near-IR sensitization of solar cells. Chem Lett 34:554–555