36. Jun HK, Careem MA, Arof AK (2013) Quantum dot-sensitized solar cells—perspective and
recent developments: a review of Cd chalcogenide quantum dots as sensitizers. Renew Sust
Energ Rev 22:148–167
37. Jeltsch KF, Schädel M, Bonekamp J-B, Niyamakom P, Rauscher F, Lademann HWA,
Dumsch I, Allard S, Scherf U, Meerholz K (2012) Efficiency enhanced hybrid solar cells
using a blend of quantum dots and nanorods. Adv Funct Mater 22:397–404
38. Ma J, Chen J-Y, Idowu M, Nyokong T (2008) Generation of singlet oxygen via the
composites of water-soluble thiol-capped CdTe quantum dots-sulfonated aluminum
phthalocyanines. J Phys Chem B 112:4465–4469
39. Biadasz A, Bursa B, Barszcz B, Bogucki A, Laskowska B, Graja A, Wróbel D (2011)
Thermodynamics and in-situ absorption of Langmuir monolayers of selected copper
phthalocyanine substituted with different peripheral groups. Dyes Pigm 89:86–92
40. Martynenko IV, Orlova AO, Maslov VG, Fedorov AV, Berwick K, Baranov AV (2016) The
influence of phthalocyanine aggregation in complexes with CdSe/ZnS quantum dots on the
photophysical properties of the complexes. Beilstein J Nanotechnol 7:1018–1027
41. Fortage J, Boixel J, Blart E, Hammarström L, Becker HC, Odobel F (2008) Single-step
electron transfer on the nanometer scale: ultra-fast charge shift in strongly coupled zinc
porphyrin-gold porphyrin dyads. Chemistry 14:3467–3480
42. Leng H, Loy J, Amin V, Weiss EA, Pelton M (2016) Electron transfer from single
semiconductor nanocrystals to individual acceptor molecules. ACS Energy Lett 1:9–15
43. Claessens CG, Hahn U, Torres T (2008) Phthalocyanines: From outstanding electronic
properties to emerging applications. Chem Rec 8:75–97
44. Bae WK, Char K, Hur H, Lee S (2008) Single-step synthesis of quantum dots with chemical
composition gradients. Chem Mater 20:531–539
45. Toyoda T, Yindeesuk W, Kamiyama K, Katayama K, Kobayashi H, Hayase S, Shen Q
(2016) The electronic structure and photoinduced electron transfer rate of CdSe quantum
dots on single crystal rutile TiO 2 : dependence on the crystal orientation of the substrate.
J Phys Chem C 120:2047–2057
46. Aviv I, Gross Z (2007) Corrole-based applications. Chem Commun 20:1987–1999
47. Flamigni L, Gryko DT (2009) Photoactive corrole-based arrays. Chem Soc Rev 38:1635–
1646
48. Gryko DT (2008) Adventures in the synthesis of meso-substituted corroles. Porphyrins
Phthalocyanines 12:906
49. Harris RLN, Johnson AW, Kay IT (1966) The synthesis of porphins and related
macrocycles. Q Rev Chem Soc 20:211–244
50. Roberts JD, Streitwieser A, Regan CM (1952) Small-ring compounds. X. Molecular orbital
calculations of properties of some small-ring hydrocarbons and free radicals. J Am Chem
Soc 18:4579–4582
51. Ventura B, Esposti AD, Koszarna B, Gryko DT, Flamigni L (2005) Photophysical
characterization of free-base corroles, promising chromophores for light energy conversion
and singlet oxygen generation. New J Chem 29:1559–1566
52. Kadish KM, Shen J, Frémond L, Chen P, El Ojaimi M, Chkounda M, Gros CP, Barbe J-M,
Ohkubo K, Fukuzumi S, Guilard R (2008) Clarification of the oxidation state of cobalt
corroles in heterogeneous and homogeneous catalytic reduction of dioxygen. Inorg Chem 47
(15):6726–6737
53. Palmer JH (2011) Transition metal corrole coordination chemistry. In: Mingos D, Day P,
Dahl J (eds) Molecular electronic structures of transition metal complexes I. structure and
bonding, vol 142. Springer, Berlin, Heidelberg
54. Gouterman M, Wagnière GH, Snyder LC (1963) Spectra of porphyrins: Part II. Four orbital
model. J Mol Spectrosc 11:108–127
55. Lei H, Han A, Li F, Zhang M, Han Y, Du P, Lai W, Cao R (2014) Electrochemical,
spectroscopic and theoretical studies of a simple bifunctional cobalt corrole catalyst for
oxygen evolution and hydrogen production. Phys Chem Chem Phys 16:1883–1893
3 Quantum Dot and Fullerene with Organic Chromophores as …
119
recent developments: a review of Cd chalcogenide quantum dots as sensitizers. Renew Sust
Energ Rev 22:148–167
37. Jeltsch KF, Schädel M, Bonekamp J-B, Niyamakom P, Rauscher F, Lademann HWA,
Dumsch I, Allard S, Scherf U, Meerholz K (2012) Efficiency enhanced hybrid solar cells
using a blend of quantum dots and nanorods. Adv Funct Mater 22:397–404
38. Ma J, Chen J-Y, Idowu M, Nyokong T (2008) Generation of singlet oxygen via the
composites of water-soluble thiol-capped CdTe quantum dots-sulfonated aluminum
phthalocyanines. J Phys Chem B 112:4465–4469
39. Biadasz A, Bursa B, Barszcz B, Bogucki A, Laskowska B, Graja A, Wróbel D (2011)
Thermodynamics and in-situ absorption of Langmuir monolayers of selected copper
phthalocyanine substituted with different peripheral groups. Dyes Pigm 89:86–92
40. Martynenko IV, Orlova AO, Maslov VG, Fedorov AV, Berwick K, Baranov AV (2016) The
influence of phthalocyanine aggregation in complexes with CdSe/ZnS quantum dots on the
photophysical properties of the complexes. Beilstein J Nanotechnol 7:1018–1027
41. Fortage J, Boixel J, Blart E, Hammarström L, Becker HC, Odobel F (2008) Single-step
electron transfer on the nanometer scale: ultra-fast charge shift in strongly coupled zinc
porphyrin-gold porphyrin dyads. Chemistry 14:3467–3480
42. Leng H, Loy J, Amin V, Weiss EA, Pelton M (2016) Electron transfer from single
semiconductor nanocrystals to individual acceptor molecules. ACS Energy Lett 1:9–15
43. Claessens CG, Hahn U, Torres T (2008) Phthalocyanines: From outstanding electronic
properties to emerging applications. Chem Rec 8:75–97
44. Bae WK, Char K, Hur H, Lee S (2008) Single-step synthesis of quantum dots with chemical
composition gradients. Chem Mater 20:531–539
45. Toyoda T, Yindeesuk W, Kamiyama K, Katayama K, Kobayashi H, Hayase S, Shen Q
(2016) The electronic structure and photoinduced electron transfer rate of CdSe quantum
dots on single crystal rutile TiO 2 : dependence on the crystal orientation of the substrate.
J Phys Chem C 120:2047–2057
46. Aviv I, Gross Z (2007) Corrole-based applications. Chem Commun 20:1987–1999
47. Flamigni L, Gryko DT (2009) Photoactive corrole-based arrays. Chem Soc Rev 38:1635–
1646
48. Gryko DT (2008) Adventures in the synthesis of meso-substituted corroles. Porphyrins
Phthalocyanines 12:906
49. Harris RLN, Johnson AW, Kay IT (1966) The synthesis of porphins and related
macrocycles. Q Rev Chem Soc 20:211–244
50. Roberts JD, Streitwieser A, Regan CM (1952) Small-ring compounds. X. Molecular orbital
calculations of properties of some small-ring hydrocarbons and free radicals. J Am Chem
Soc 18:4579–4582
51. Ventura B, Esposti AD, Koszarna B, Gryko DT, Flamigni L (2005) Photophysical
characterization of free-base corroles, promising chromophores for light energy conversion
and singlet oxygen generation. New J Chem 29:1559–1566
52. Kadish KM, Shen J, Frémond L, Chen P, El Ojaimi M, Chkounda M, Gros CP, Barbe J-M,
Ohkubo K, Fukuzumi S, Guilard R (2008) Clarification of the oxidation state of cobalt
corroles in heterogeneous and homogeneous catalytic reduction of dioxygen. Inorg Chem 47
(15):6726–6737
53. Palmer JH (2011) Transition metal corrole coordination chemistry. In: Mingos D, Day P,
Dahl J (eds) Molecular electronic structures of transition metal complexes I. structure and
bonding, vol 142. Springer, Berlin, Heidelberg
54. Gouterman M, Wagnière GH, Snyder LC (1963) Spectra of porphyrins: Part II. Four orbital
model. J Mol Spectrosc 11:108–127
55. Lei H, Han A, Li F, Zhang M, Han Y, Du P, Lai W, Cao R (2014) Electrochemical,
spectroscopic and theoretical studies of a simple bifunctional cobalt corrole catalyst for
oxygen evolution and hydrogen production. Phys Chem Chem Phys 16:1883–1893
3 Quantum Dot and Fullerene with Organic Chromophores as …
119