-
2
-
-
80555157669
-
Porphyrin-sensitized solar cells with cobalt (II/III)-based redox electrolyte exceed 12 percent efficiency
-
Yella A., Lee H.-W., Nok Tsao H., Yi C., Chandiran A.K., Nazeeruddin Md.K., et al. Porphyrin-sensitized solar cells with cobalt (II/III)-based redox electrolyte exceed 12 percent efficiency. Science 2011, 334:629-634.
-
(2011)
Science
, vol.334
, pp. 629-634
-
-
Yella, A.1
Lee, H.-W.2
Nok Tsao, H.3
Yi, C.4
Chandiran, A.K.5
Nazeeruddin, M.6
-
3
-
-
28844470918
-
Combined experimental and DFT-TDDFT computational study of photoelectrochemical cell ruthenium sensitizers
-
Nazeeruddin Md.K., De Angelis F., Fantacci S., Selloni A., Viscardi G., Liska P., et al. Combined experimental and DFT-TDDFT computational study of photoelectrochemical cell ruthenium sensitizers. JAm Chem Soc 2005, 127:16835-16847.
-
(2005)
JAm Chem Soc
, vol.127
, pp. 16835-16847
-
-
Nazeeruddin, M.K.1
De Angelis, F.2
Fantacci, S.3
Selloni, A.4
Viscardi, G.5
Liska, P.6
-
4
-
-
79959241889
-
Effect of sensitizer adsorption temperature on the performance of dye-sensitized solar cells
-
Sauvage F., Decoppet J.D., Zhang M., Zakeeruddin S.M., Comte P., Nazeeruddin Md.K., et al. Effect of sensitizer adsorption temperature on the performance of dye-sensitized solar cells. JAm Chem Soc 2011, 133:9304-9310.
-
(2011)
JAm Chem Soc
, vol.133
, pp. 9304-9310
-
-
Sauvage, F.1
Decoppet, J.D.2
Zhang, M.3
Zakeeruddin, S.M.4
Comte, P.5
Nazeeruddin, M.K.6
-
5
-
-
49449091340
-
2 film with high molar extinction coefficient ruthenium sensitizers for high performance dye-sensitized solar cells
-
2 film with high molar extinction coefficient ruthenium sensitizers for high performance dye-sensitized solar cells. JAm Chem Soc 2008, 130:10720-10728.
-
(2008)
JAm Chem Soc
, vol.130
, pp. 10720-10728
-
-
Gao, F.1
Wang, Y.2
Shi, D.3
Zhang, J.4
Wang, M.5
Jing, X.6
-
6
-
-
84876473048
-
Near-infrared sensitization in dye-sensitized solar cells
-
Park J., Viscardi G., Barolo C., Barbero N. Near-infrared sensitization in dye-sensitized solar cells. Chimia 2013, 67:129-135.
-
(2013)
Chimia
, vol.67
, pp. 129-135
-
-
Park, J.1
Viscardi, G.2
Barolo, C.3
Barbero, N.4
-
7
-
-
79952366745
-
Panchromatic engineering for dye-sensitized solar cells
-
Yum J.-H., Baranoff E., Wenger S., Nazeeruddin Md.K., Grätzel M. Panchromatic engineering for dye-sensitized solar cells. Energy Environ Sci 2011, 4:842-857.
-
(2011)
Energy Environ Sci
, vol.4
, pp. 842-857
-
-
Yum, J.-H.1
Baranoff, E.2
Wenger, S.3
Nazeeruddin, M.K.4
Grätzel, M.5
-
9
-
-
77950214390
-
Enhancement of incident photon-to-current conversion efficiency for phthalocyanine-sensitized solar cells by 3D molecular structuralization
-
Mori S., Nagata M., Nakahata Y., Yasuta K., Goto R., Kimura M., et al. Enhancement of incident photon-to-current conversion efficiency for phthalocyanine-sensitized solar cells by 3D molecular structuralization. JAm Chem Soc 2010, 132:4054-4055.
-
(2010)
JAm Chem Soc
, vol.132
, pp. 4054-4055
-
-
Mori, S.1
Nagata, M.2
Nakahata, Y.3
Yasuta, K.4
Goto, R.5
Kimura, M.6
-
10
-
-
79960175077
-
Perylene anhydride fused porphyrins as near-infrared sensitizers for dye-sensitized solar cells
-
Jiao C., Zu N., Huang K.-W., Wang P., Wu J. Perylene anhydride fused porphyrins as near-infrared sensitizers for dye-sensitized solar cells. Org Lett 2011, 13:3652-3655.
-
(2011)
Org Lett
, vol.13
, pp. 3652-3655
-
-
Jiao, C.1
Zu, N.2
Huang, K.-W.3
Wang, P.4
Wu, J.5
-
11
-
-
39149116019
-
Harvesting infrared photons with croconate dyes
-
Takechi K., Kamat P.V., Avirah R.R., Jyothish K., Ramaiah D. Harvesting infrared photons with croconate dyes. Chem Mater 2008, 20:265-272.
-
(2008)
Chem Mater
, vol.20
, pp. 265-272
-
-
Takechi, K.1
Kamat, P.V.2
Avirah, R.R.3
Jyothish, K.4
Ramaiah, D.5
-
12
-
-
70349784869
-
Metal-free organic dyes for dye-sensitized solar cells: from structure: property relationship to design rules
-
Mishra A., Fischer M.K.R., Bäuerle P. Metal-free organic dyes for dye-sensitized solar cells: from structure: property relationship to design rules. Angew Chem Int Ed 2009, 48:2474-2499.
-
(2009)
Angew Chem Int Ed
, vol.48
, pp. 2474-2499
-
-
Mishra, A.1
Fischer, M.K.R.2
Bäuerle, P.3
-
13
-
-
66749163106
-
Molecular designs and syntheses of organic dyes for dye-sensitized solar cells
-
Ooyama Y., Harima Y. Molecular designs and syntheses of organic dyes for dye-sensitized solar cells. Eur J Org Chem 2009, 2903-2934.
-
(2009)
Eur J Org Chem
, pp. 2903-2934
-
-
Ooyama, Y.1
Harima, Y.2
-
14
-
-
79960835810
-
Areview of NIR dyes in cancer targeting and imaging
-
Luo S., Zhang E., Su Y., Cheng T.n, Shi C. Areview of NIR dyes in cancer targeting and imaging. Biomaterials 2011, 32:7127-7138.
-
(2011)
Biomaterials
, vol.32
, pp. 7127-7138
-
-
Luo, S.1
Zhang, E.2
Su, Y.3
Cheng, T.4
Shi, C.5
-
15
-
-
84856747406
-
Squaraine dyes in PDT: from basic design to invivo demonstration
-
Avirah R.R., Jayaram D.T., Adarsh N., Ramaiah D. Squaraine dyes in PDT: from basic design to invivo demonstration. Org Biomol Chem 2012, 10:911-920.
-
(2012)
Org Biomol Chem
, vol.10
, pp. 911-920
-
-
Avirah, R.R.1
Jayaram, D.T.2
Adarsh, N.3
Ramaiah, D.4
-
16
-
-
77149167298
-
Squaraine compounds: tailored design and synthesis towards a variety of material science applications
-
Beverina L., Salice P. Squaraine compounds: tailored design and synthesis towards a variety of material science applications. Eur J Org Chem 2010, 1207-1225.
-
(2010)
Eur J Org Chem
, pp. 1207-1225
-
-
Beverina, L.1
Salice, P.2
-
18
-
-
79951916381
-
Efficient and stable panchromatic squaraine dyes for dye-sensitized solar cells
-
Paek S., Choi H., Kim C., Cho N., So S., Song K., et al. Efficient and stable panchromatic squaraine dyes for dye-sensitized solar cells. Chem Commun 2011, 47:2874-2876.
-
(2011)
Chem Commun
, vol.47
, pp. 2874-2876
-
-
Paek, S.1
Choi, H.2
Kim, C.3
Cho, N.4
So, S.5
Song, K.6
-
19
-
-
84887614685
-
Asimple synthetic route to obtain pure trans-ruthenium(II) complexes for dye sensitized solar cell applications
-
Barolo C., Yum J., Artuso E., Barbero N., Di Censo D., Lobello M.G., et al. Asimple synthetic route to obtain pure trans-ruthenium(II) complexes for dye sensitized solar cell applications. Chem Sus Chem 2013, 10.1002/cssc.201200973.
-
(2013)
Chem Sus Chem
-
-
Barolo, C.1
Yum, J.2
Artuso, E.3
Barbero, N.4
Di Censo, D.5
Lobello, M.G.6
-
20
-
-
78650144258
-
Panchromatic ruthenium sensitizer based on electron-rich heteroarylvinylene π-conjugated quaterpyridine for dye-sensitized solar cells
-
Abbotto A., Sauvage F., Barolo C., De Angelis F., Fantacci S., Grätzel M., et al. Panchromatic ruthenium sensitizer based on electron-rich heteroarylvinylene π-conjugated quaterpyridine for dye-sensitized solar cells. Dalton Trans 2011, 40:234-242.
-
(2011)
Dalton Trans
, vol.40
, pp. 234-242
-
-
Abbotto, A.1
Sauvage, F.2
Barolo, C.3
De Angelis, F.4
Fantacci, S.5
Grätzel, M.6
-
21
-
-
33745610034
-
Synthesis, characterization, and DFT-TDDFT computational study of a ruthenium complex containing a functionalized tetradentate ligand
-
Barolo C., Nazeeruddin Md.K., Fantacci S., Di Censo D., Comte P., Liska P., et al. Synthesis, characterization, and DFT-TDDFT computational study of a ruthenium complex containing a functionalized tetradentate ligand. Inorg Chem 2006, 45:4642-4653.
-
(2006)
Inorg Chem
, vol.45
, pp. 4642-4653
-
-
Barolo, C.1
Nazeeruddin, M.K.2
Fantacci, S.3
Di Censo, D.4
Comte, P.5
Liska, P.6
-
23
-
-
80052823228
-
Syntheses and characterization of several nickel bis(dithiolene) complexes with strong and broad near-IR absorption
-
Miao Q., Gao J., Wang Z., Yu H., Luo Yi, Ma T. Syntheses and characterization of several nickel bis(dithiolene) complexes with strong and broad near-IR absorption. Inorg Chim Acta 2011, 376:619-627.
-
(2011)
Inorg Chim Acta
, vol.376
, pp. 619-627
-
-
Miao, Q.1
Gao, J.2
Wang, Z.3
Yu, H.4
Luo, Y.5
Ma, T.6
-
24
-
-
77952711378
-
NIR absorbing poly(thieno[3,4b]thiophene2carboxylic acid) as a polymer dye for dyesensitized solar cells
-
Saji V.S., Zong K., Pyo M. NIR absorbing poly(thieno[3,4b]thiophene2carboxylic acid) as a polymer dye for dyesensitized solar cells. JPhotochem Photobiol A: Chem 2010, 212:81-87.
-
(2010)
JPhotochem Photobiol A: Chem
, vol.212
, pp. 81-87
-
-
Saji, V.S.1
Zong, K.2
Pyo, M.3
-
25
-
-
67349095754
-
Study on dye-sensitized solar cell using novel infrared dye
-
Ono T., Yamaguchi T., Arakawa H. Study on dye-sensitized solar cell using novel infrared dye. Sol Energy Mater Sol Cells 2009, 93:831-835.
-
(2009)
Sol Energy Mater Sol Cells
, vol.93
, pp. 831-835
-
-
Ono, T.1
Yamaguchi, T.2
Arakawa, H.3
-
26
-
-
0036121217
-
New low band gap polymers: control of optical and electronic properties in near infrared absorbing π-conjugated polysquaraines
-
Eldo J., Ajayaghosh A. New low band gap polymers: control of optical and electronic properties in near infrared absorbing π-conjugated polysquaraines. Chem Mater 2002, 14:410-418.
-
(2002)
Chem Mater
, vol.14
, pp. 410-418
-
-
Eldo, J.1
Ajayaghosh, A.2
-
27
-
-
54749131828
-
Anear-infrared squaraine dye as a latent ratiometric fluorophore for the detection of aminothiol content in blood plasma
-
Sreejith S., Divya K.P., Ajayaghosh A. Anear-infrared squaraine dye as a latent ratiometric fluorophore for the detection of aminothiol content in blood plasma. Angew Chem Int Ed 2008, 47:7883-7887.
-
(2008)
Angew Chem Int Ed
, vol.47
, pp. 7883-7887
-
-
Sreejith, S.1
Divya, K.P.2
Ajayaghosh, A.3
-
28
-
-
43049153277
-
Water-soluble NIR fluorescent probes based on squaraine and their application for protein labeling
-
Umezawa K., Citterio D., Suzuki K. Water-soluble NIR fluorescent probes based on squaraine and their application for protein labeling. Anal Sci 2008, 24:213-217.
-
(2008)
Anal Sci
, vol.24
, pp. 213-217
-
-
Umezawa, K.1
Citterio, D.2
Suzuki, K.3
-
29
-
-
84962381168
-
Design and synthesis of squaraine based near infrared fluorescent probes
-
Basheer M.C., Santhosh U., Alex S., Thomas K.G., Suresh C.H., Das S. Design and synthesis of squaraine based near infrared fluorescent probes. Tetrahedron 2007, 63:1617-1623.
-
(2007)
Tetrahedron
, vol.63
, pp. 1617-1623
-
-
Basheer, M.C.1
Santhosh, U.2
Alex, S.3
Thomas, K.G.4
Suresh, C.H.5
Das, S.6
-
30
-
-
47249142376
-
Fluorescent probes and labels for biomedical applications
-
Patsenker L., Tatarets A., Kosolova O., Obukhova O., Povrozin Y., Fedyunyayeva I., et al. fluorescent probes and labels for biomedical applications. Ann N.Y Acad Sci 2008, 1130:179-187.
-
(2008)
Ann N.Y Acad Sci
, vol.1130
, pp. 179-187
-
-
Patsenker, L.1
Tatarets, A.2
Kosolova, O.3
Obukhova, O.4
Povrozin, Y.5
Fedyunyayeva, I.6
-
32
-
-
39049127163
-
Assessment of water-soluble π-extended squaraines as one and two-photon singlet oxygen photosensitizers: design, synthesis, and characterization
-
Beverina L., Crippa M., Landenna M., Ruffo R., Salice P., Silvestri F., et al. Assessment of water-soluble π-extended squaraines as one and two-photon singlet oxygen photosensitizers: design, synthesis, and characterization. JAm Chem Soc 2008, 130:1894-1902.
-
(2008)
JAm Chem Soc
, vol.130
, pp. 1894-1902
-
-
Beverina, L.1
Crippa, M.2
Landenna, M.3
Ruffo, R.4
Salice, P.5
Silvestri, F.6
-
33
-
-
0031084460
-
Near-infrared reagents for fibre-optic ammonia sensors
-
Šimon P., Sekretár S., MacCraith B.D., Kvasnik F. Near-infrared reagents for fibre-optic ammonia sensors. Sens Actuator B-chem 1997, 39:252-255.
-
(1997)
Sens Actuator B-chem
, vol.39
, pp. 252-255
-
-
Šimon, P.1
Sekretár, S.2
MacCraith, B.D.3
Kvasnik, F.4
-
34
-
-
3042523900
-
NIR absorbing squaraines by extension of the conjugation with (aminothiazolyl)ethenyl groups
-
Meier H., Petermann R. NIR absorbing squaraines by extension of the conjugation with (aminothiazolyl)ethenyl groups. Helv Chim Acta 2004, 87:1109-1118.
-
(2004)
Helv Chim Acta
, vol.87
, pp. 1109-1118
-
-
Meier, H.1
Petermann, R.2
-
35
-
-
79951814178
-
Synthesis and near-infrared absorption properties of linearly π-extended squarylium oligomers
-
Yagi S., Nakasaku Y., Maeda T., Nakazumi H., Sakurai Y. Synthesis and near-infrared absorption properties of linearly π-extended squarylium oligomers. Dyes Pigment 2011, 90:211-218.
-
(2011)
Dyes Pigment
, vol.90
, pp. 211-218
-
-
Yagi, S.1
Nakasaku, Y.2
Maeda, T.3
Nakazumi, H.4
Sakurai, Y.5
-
36
-
-
77951665957
-
Unsymmetrical squaraine dimer with an extended π-electron framework: an approach in harvesting near infra-red photons for energy conversion
-
Kuster S., Sauvage F., Nazeeruddin Md.K., Grätzel M., Nüesch F.A., Geiger T. Unsymmetrical squaraine dimer with an extended π-electron framework: an approach in harvesting near infra-red photons for energy conversion. Dyes Pigment 2010, 87:30-38.
-
(2010)
Dyes Pigment
, vol.87
, pp. 30-38
-
-
Kuster, S.1
Sauvage, F.2
Nazeeruddin, M.K.3
Grätzel, M.4
Nüesch, F.A.5
Geiger, T.6
-
37
-
-
80955122716
-
Near-infrared absorbing squarylium dyes with linearly extended π-conjugated structure for dye-sensitized solar cell applications
-
Maeda T., Hamamura Y., Miyanaga K., Shima N., Yagi S., Nakazumi H. Near-infrared absorbing squarylium dyes with linearly extended π-conjugated structure for dye-sensitized solar cell applications. Org Lett 2011, 13:5994-5997.
-
(2011)
Org Lett
, vol.13
, pp. 5994-5997
-
-
Maeda, T.1
Hamamura, Y.2
Miyanaga, K.3
Shima, N.4
Yagi, S.5
Nakazumi, H.6
-
38
-
-
66049105891
-
The design, synthesis and characterization of a novel acceptor for real time polymerase chain reaction using both computational and experimental approaches
-
Benzi C., Bertolino C.A., Miletto I., Ponzio P., Barolo C., Viscardi G., et al. The design, synthesis and characterization of a novel acceptor for real time polymerase chain reaction using both computational and experimental approaches. Dyes Pigment 2009, 83:111-120.
-
(2009)
Dyes Pigment
, vol.83
, pp. 111-120
-
-
Benzi, C.1
Bertolino, C.A.2
Miletto, I.3
Ponzio, P.4
Barolo, C.5
Viscardi, G.6
-
39
-
-
84857098514
-
New insight into the regeneration kinetics of organic dye sensitised solar Cells
-
Martiniani S., Anderson A.Y., Law C., O'Regan B.C., Barolo C. New insight into the regeneration kinetics of organic dye sensitised solar Cells. Chem Commun 2012, 48:2406-2408.
-
(2012)
Chem Commun
, vol.48
, pp. 2406-2408
-
-
Martiniani, S.1
Anderson, A.Y.2
Law, C.3
O'Regan, B.C.4
Barolo, C.5
-
40
-
-
80055096351
-
Unsymmetrical squarylium dyes with π-extended heterocyclic components and their application to organic dye-sensitized solar cells
-
Maeda T., Shima N., Tsukamoto T., Yagi S., Nakazumi H. Unsymmetrical squarylium dyes with π-extended heterocyclic components and their application to organic dye-sensitized solar cells. Synth Met 2011, 161:2481-2487.
-
(2011)
Synth Met
, vol.161
, pp. 2481-2487
-
-
Maeda, T.1
Shima, N.2
Tsukamoto, T.3
Yagi, S.4
Nakazumi, H.5
-
41
-
-
84863115186
-
Symmetric vs asymmetric squaraines as photosensitisers in mesoscopic injection solar cells: a structure-property relationship study
-
Park J., Barolo C., Sauvage F., Barbero N., Benzi C., Quagliotto P., et al. Symmetric vs asymmetric squaraines as photosensitisers in mesoscopic injection solar cells: a structure-property relationship study. Chem Commun 2012, 48:2782-2784.
-
(2012)
Chem Commun
, vol.48
, pp. 2782-2784
-
-
Park, J.1
Barolo, C.2
Sauvage, F.3
Barbero, N.4
Benzi, C.5
Quagliotto, P.6
-
42
-
-
0034696029
-
Synthesis of novel unsymmetrical squarylium dyes absorbing in the near-infrared region
-
Yagi S., Hyodo Y., Matsumoto S., Takahashi N., Kono H., Nakazumi H. Synthesis of novel unsymmetrical squarylium dyes absorbing in the near-infrared region. JChem Soc Perkin Trans 2000, 1:599-603.
-
(2000)
JChem Soc Perkin Trans
, vol.1
, pp. 599-603
-
-
Yagi, S.1
Hyodo, Y.2
Matsumoto, S.3
Takahashi, N.4
Kono, H.5
Nakazumi, H.6
-
44
-
-
0030570285
-
Treatment of electronic excitations within the adiabatic approximation of time dependent density functional theory
-
Bauernshmitt R., Ahlrichs R. Treatment of electronic excitations within the adiabatic approximation of time dependent density functional theory. Chem Phys Lett 1996, 256:454-464.
-
(1996)
Chem Phys Lett
, vol.256
, pp. 454-464
-
-
Bauernshmitt, R.1
Ahlrichs, R.2
-
45
-
-
0032533083
-
An efficient implementation of time dependent density-functional theory for the calculation of excitation energies of large molecules
-
Stratmann R.E., Scuseria G.E., Frisch M.J. An efficient implementation of time dependent density-functional theory for the calculation of excitation energies of large molecules. JChem Phys 1998, 109:8218-8224.
-
(1998)
JChem Phys
, vol.109
, pp. 8218-8224
-
-
Stratmann, R.E.1
Scuseria, G.E.2
Frisch, M.J.3
-
46
-
-
0000189651
-
Density-functional thermochemistry. III. The role of exact exchange
-
Becke A.D. Density-functional thermochemistry. III. The role of exact exchange. JChem Phys 1993, 98:5648-5652.
-
(1993)
JChem Phys
, vol.98
, pp. 5648-5652
-
-
Becke, A.D.1
-
47
-
-
3142771297
-
Anew hybrid exchange-correlation functional using the Coulomb-attenuating method (CAM-B3LYP)
-
Yanai T., Tew D., Handy N. Anew hybrid exchange-correlation functional using the Coulomb-attenuating method (CAM-B3LYP). Chem Phys Lett 2004, 393:51-57.
-
(2004)
Chem Phys Lett
, vol.393
, pp. 51-57
-
-
Yanai, T.1
Tew, D.2
Handy, N.3
-
48
-
-
70450206724
-
-
Gaussian, Inc., Wallingford CT
-
Frisch M.J., Trucks G.W., Schlegel H.B., Scuseria G.E., Robb M.A., Cheeseman J.R., et al. Gaussian 09 2009, Gaussian, Inc., Wallingford CT.
-
(2009)
Gaussian 09
-
-
Frisch, M.J.1
Trucks, G.W.2
Schlegel, H.B.3
Scuseria, G.E.4
Robb, M.A.5
Cheeseman, J.R.6
-
49
-
-
37049054022
-
The reactivity of the alkylthio-group in nitrogen ring compounds. Part III. 2-Methylthiobenz[cd]indole and its methiodide
-
Ficken G.E., Kendall J.D. The reactivity of the alkylthio-group in nitrogen ring compounds. Part III. 2-Methylthiobenz[cd]indole and its methiodide. JChem Soc 1960, 1537-1541.
-
(1960)
JChem Soc
, pp. 1537-1541
-
-
Ficken, G.E.1
Kendall, J.D.2
-
50
-
-
0041018402
-
Thioanhydrides. 3. Synthesis, properties and Diels-Alder reactions of sulfur analogs of 1,8-naphthalic anhydride
-
Lakshmikantham M.V., Chen W., Cava M.P. Thioanhydrides. 3. Synthesis, properties and Diels-Alder reactions of sulfur analogs of 1,8-naphthalic anhydride. JOrg Chem 1989, 54:4746-4750.
-
(1989)
JOrg Chem
, vol.54
, pp. 4746-4750
-
-
Lakshmikantham, M.V.1
Chen, W.2
Cava, M.P.3
-
51
-
-
0019589565
-
2-Methylbenz[c, d]indole and its derivatives
-
Vasilenko N.P., Mikhailenko F.A., Rozhinsky J.I. 2-Methylbenz[c, d]indole and its derivatives. Dyes Pigment 1981, 2:231-237.
-
(1981)
Dyes Pigment
, vol.2
, pp. 231-237
-
-
Vasilenko, N.P.1
Mikhailenko, F.A.2
Rozhinsky, J.I.3
-
52
-
-
0032762850
-
Photochromic properties of cationic merocyanine dyes. thermal stability of the spiropyran form produced by irradiation with visible light
-
Yagi S., Maeda K., Nakazumi H. Photochromic properties of cationic merocyanine dyes. thermal stability of the spiropyran form produced by irradiation with visible light. JMater Chem 1999, 9:2991-2997.
-
(1999)
JMater Chem
, vol.9
, pp. 2991-2997
-
-
Yagi, S.1
Maeda, K.2
Nakazumi, H.3
-
54
-
-
34948837898
-
2 films in dye-sensitized solar cells. 2. Charge density, band edge shifts, and Quantification of recombination Losses at short circuit
-
2 films in dye-sensitized solar cells. 2. Charge density, band edge shifts, and Quantification of recombination Losses at short circuit. JPhys Chem C 2007, 111:14001-14010.
-
(2007)
JPhys Chem C
, vol.111
, pp. 14001-14010
-
-
O'Regan, B.C.1
Durrant, J.R.2
Sommeling, P.M.3
Bakker, N.J.4
-
55
-
-
0008611612
-
Photophysical and aggregation properties of a long-chain squarylium indocyanine dye
-
Tatikolov A.S., Costa S.M.B. Photophysical and aggregation properties of a long-chain squarylium indocyanine dye. JPhotochem Photobiol A 2001, 140:147-156.
-
(2001)
JPhotochem Photobiol A
, vol.140
, pp. 147-156
-
-
Tatikolov, A.S.1
Costa, S.M.B.2
-
56
-
-
0034246282
-
Radiative and nonradiative excited state relaxation channels in squaric acid derivatives bearing differently sized donor substituents: a comparison of experiment and theory
-
Gude C., Rettig W. Radiative and nonradiative excited state relaxation channels in squaric acid derivatives bearing differently sized donor substituents: a comparison of experiment and theory. JPhys Chem A 2000, 104:8050-8057.
-
(2000)
JPhys Chem A
, vol.104
, pp. 8050-8057
-
-
Gude, C.1
Rettig, W.2
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