In this study, using ultrasonic method, nanoparticles of a new phosphoramide compound and its cobalt nitrate and cadmium nitrate complexes with formula (4-NO2-C6H4NH)P(O)Cl(NH-C5H4N-2) = L (1), Co(NO3)2(L)(CH3OH) (2), Cd(NO3)2(L)(CH3OH) (3) were synthesized and characterized by 31P, 1H, 13C NMR, fourier transform infrared (FT-IR), ultraviolet–visible (UV-Vis), fluorescence spectroscopy, and elemental analysis as well as field-emission scanning electron microscopy (FE-SEM), transmission electron microsopy (TEM), and XRD techniques. The FE-SEM and high-resolution TEM (HR-TEM) analyses showed that particle sizes of the compounds 1–3 are about 20–50 nm. The compounds 1–3 were utilized as dyes for adsorption of light in dye sensitized solar cells (DSSCs) and the efficiencies of the cells were obtained equal to 0.42%, 0.49%, 0.54%, respectively. The analysis of band gap with density functional theory (DFT) calculations revealed that it decreases in the order 1 > 2 > 3, which is in consistent with the band gaps measured from fluorescence spectra. Comparing the conversion efficiencies of the three dyes illustrated that compound 3 with the smallest band gap yields the greatest efficiency.

References

1.
Vougioukalakis
,
G. C.
,
Philippopoulos
,
A. I.
,
Stergiopoulos
,
T.
, and
Falaras
,
P.
,
2011
, “
Contributions to the Development of Ruthenium-Based Sensitizers for Dye-Sensitized Solar Cells
,”
Coord. Chem. Rev.
,
255
, pp.
2602
2621
.10.1016/j.ccr.2010.11.006
2.
Chen
,
C.-H.
,
Hsu
,
Y.-C.
,
Chou
,
H.-H.
,
Thomas
,
K. R. J.
,
Lin
,
J. T.
, and
Hsu
,
C.-P.
,
2010
, “
Dipolar Compounds Containing Fluorene and a Heteroaromatic Ring as the Conjugating Bridge for High-Performance Dye-Sensitized Solar Cells
,”
Chem. Eur. J.
,
16
, pp.
3184
3193
.10.1002/chem.200903151
3.
O'Regan
,
B.
, and
Gratzel
,
M.
,
1991
, “
A Low-Cost, High-Efficiency Solar Cell Based on Dyesensitized Colloidal TiO2 Films
,”
Nature
,
353
, pp.
737
740
.10.1038/353737a0
4.
Saga
,
T.
,
2010
, “
Advances in Crystalline Silicon Solar Cell Technology for Industrial Mass Production
,”
NPG Asia Mater.
,
2
, pp.
96
102
.10.1038/asiamat.2010.82
5.
Mishra
,
A.
,
Fischer
,
M. K. R.
, and
Bäuerle
,
P.
,
2009
, “
Metal-Free Organic Dyes for Dye-Sensitized Solar Cells: From Structure: Property Relationships to Design Rules
,”
Angew. Chem. Int. Ed.
,
48
, pp.
2474
2499
.10.1002/anie.200804709
6.
Grätzel
,
M.
,
2005
, “
Solar Energy Conversion by Dye-Sensitized Photovoltaic Cells
,”
Inorg. Chem.
,
44
, pp.
6841
6851
.10.1021/ic0508371
7.
Hagfeldt
,
A.
,
Boschloo
,
G.
,
Sun
,
L.
,
Kloo
,
L.
, and
Pettersson
,
H.
,
2010
, “
Dye-Sensitized Solar Cells
,”
Chem. Rev.
,
110
, pp.
6595
6663
.10.1021/cr900356p
8.
Wang
,
H.
,
Zhang
,
X.
,
Gong
,
F.
,
Zhou
,
G.
, and
Wang
,
Z.-S.
,
2012
, “
Novel Ester-Functionalized Solidstate Electrolyte for Highly Efficient All-Solid-State Dye-Sensitized Solar Cells
,”
Adv. Mater.
,
24
, pp.
121
124
.10.1002/adma.201103785
9.
Kimura
,
M.
,
Nomoto
,
H.
,
Masaki
,
N.
, and
Mori
,
S.
,
2012
, “
Dye Molecules for Simple Cosensitization Process: Fabrication of Mixed-Dye-Sensitized Solar Cells
,”
Angew. Chem. Int. Ed.
,
51
, pp.
4371
4374
.10.1002/anie.201108610
10.
Wu
,
K.-L.
,
Li
,
C.-H.
,
Chi
,
Y.
,
Clifford
,
J. N.
,
Cabau
,
L.
,
Palomares
,
E.
,
Cheng
,
Y.-M.
,
Pan
,
H.-A.
, and
Chou
,
P.-T.
,
2012
, “
Dye Molecular Structure Device Open-Circuit Voltage Correlation in Ru(II) Sensitizers With Heteroleptic Tridentate Chelates for Dye-Sensitized Solar Cells
,”
J. Am. Chem. Soc.
,
134
, pp.
7488
7496
.10.1021/ja300828f
11.
Grätzel
,
M.
,
2001
, “
Photoelectrochemical Cells
,”
Nature
,
414
, pp.
338
344
.10.1038/35104607
12.
Grätzel
,
M.
,
2005
, “
Mesoscopic Solar Cells for Electricity and Hydrogen Production From Sunlight
,”
Chem. Lett.
,
34
, pp.
8
13
.10.1246/cl.2005.8
13.
Robertson
,
N.
,
2008
, “
Catching the Rainbow: Light Harvesting in Dye-Sensitized Solar Cells
,”
Angew. Chem. Int. Ed.
,
47
, pp.
1012
1014
.10.1002/anie.200704538
14.
Ardo
,
S.
, and
Meyer
,
G. J.
,
2009
, “
Photodriven Heterogeneous Charge Transfer With Transition-Metal Compounds Anchored to TiO2 Semiconductor Surfaces
,”
Chem. Soc. Rev.
,
38
, pp.
115
164
.10.1039/b804321n
15.
Argazzi
,
R.
,
Bignozzi
,
C. A.
,
Heimer
,
T. A.
, and
Meyer
,
G. J.
,
1997
, “
Remote Interfacial Electron Transfer From Supramolecular Sensitizers
,”
Inorg. Chem.
,
36
, pp.
2
3
.10.1021/ic960717g
16.
Robertson
,
N.
,
2006
, “
Optimizing Dyes for Dye-Sensitized Solar Cells
,”
Angew. Chem. Int. Ed.
,
45
, pp.
2338
2345
.10.1002/anie.200503083
17.
Green
,
M. A.
,
Emery
,
K.
,
Hishikawa
,
Y.
, and
Warta
,
W.
,
2010
, “
Solar Cell Efficiency Tables (version 35)
,”
Prog. Photovoltaics
,
18
, pp.
144
150
.10.1002/pip.974
18.
Funaki
,
T.
,
Yanagida
,
M.
,
Onozawa-Komatsuzaki
,
N.
,
Kasuga
,
K.
,
Kawanishi
,
Y.
,
Kurashige
,
M.
,
Sayama
,
K.
, and
Sugihara
,
H.
,
2009
, “
Synthesis of a New Class of Cyclometallated Ruthenium(II) Complexes and Their Application in Dye-Sensitized Solar Cells
,”
Inorg. Chem. Commun.
,
12
, pp.
842
845
.10.1016/j.inoche.2009.06.030
19.
Nazeeruddin
,
Md. K.
,
Klein
,
C.
,
Liska
,
P.
, and
Grätzel
,
M.
,
2005
, “
Synthesis of Novel Ruthenium Sensitizers and Their Application in Dye-Sensitized Solar Cells
,”
Coord. Chem. Rev.
,
249
, pp.
1460
1467
.10.1016/j.ccr.2005.03.025
20.
Anandana
,
S.
,
Madhavan
,
J.
,
Maruthamuthu
,
P.
,
Raghukumar
,
V.
, and
Ramakrishnan
,
V. T.
,
2004
, “
Synthesis and Characterization of Naphthyridine and Acridinedione Ligands Coordinated Ruthenium(II) Complexes and Their Applications in Dye-Sensitized Solar Cells
,”
Sol. Energy Mater. Sol. Cells
,
81
, pp.
419
428
.10.1016/j.solmat.2003.11.026
21.
Vougioukalakis
,
G. C.
,
Stergiopoulos
,
T.
,
Kantonis
,
G.
,
Kontos
,
A. G.
,
Papadopoulos
,
K.
,
Stublla
,
A.
,
Potvin
,
P. G.
, and
Falaras
,
P.
,
2010
, “
Terpyridine- and 2,6-Dipyrazinylpyridine-Coordinated Ruthenium(II) Complexes: Synthesis, Characterization and Application in TiO2-Based Dye-Sensitized Solar Cells
,”
J. Photochem. Photobiol., A
,
214
, pp.
22
32
.10.1016/j.jphotochem.2010.06.001
22.
Yum
,
J.-H.
,
Moon
,
S.-J.
,
Karthikeyan
,
C. S.
,
Wietasch
,
H.
,
Thelakkat
,
M.
,
Zakeeruddin
,
S. M.
,
Nazeeruddin
,
Md. K.
, and
Grätzel
,
M.
,
2012
, “
Heteroleptic Ruthenium Complex Containing Substituted Triphenylamine Hole-Transport Unit as Sensitizer for Stable Dye-Sensitized Solar Cell
,”
Nano Energy
,
1
, pp.
6
12
.10.1016/j.nanoen.2011.08.004
23.
Onozawa-Komatsuzaki
,
N.
,
Yanagida
,
M.
,
Funaki
,
T.
,
Kasuga
,
K.
,
Sayama
,
K.
, and
Sugihara
,
H.
,
2011
, “
Near-IR Dye-Sensitized Solar Cells Using a New Type of Ruthenium Complexes Having 2,6-Bis(Quinolin-2-yl)Pyridine Derivatives
,”
Sol. Energy Mater Sol. Cells
,
95
, pp.
310
314
.10.1016/j.solmat.2010.05.003
24.
Funaki
,
T.
,
Yanagida
,
M.
,
Onozawa-Komatsuzaki
,
N.
,
Kawanishi
,
Y.
,
Kasuga
,
K.
, and
Sugihara
,
H.
,
2009
, “
Ruthenium(II) Complexes With π Expanded Ligand Having Phenylene–Ethynylene Moiety as Sensitizers for Dye-Sensitized Solar Cells
,”
Sol. Energy Mater. Sol. Cells
,
93
, pp.
729
732
.10.1016/j.solmat.2008.09.011
25.
Li
,
C.-Y.
,
Su
,
C.
,
Wang
,
H.-H.
,
Kumaresan
,
P.
,
Hsu
,
C.-H.
,
Lee
,
I.-T.
,
Chang
,
W.-C.
,
Tingare
,
Y. S.
,
Li
,
T.-Y.
,
Lin
,
C.-F.
, and
Li
,
W.-R.
,
2014
, “
Design and Development of Cyclometalated Ruthenium Complexes Containing Thiophenyl-Pyridine Ligand for Dye-Sensitized Solar Cells
,”
Dyes Pigm.
,
100
, pp.
57
65
.10.1016/j.dyepig.2013.07.014
26.
Song
,
H.-K.
,
Park
,
Y. H.
,
Han
,
C.-H.
, and
Jee
,
J.-G.
,
2009
, “
Synthesis of Ruthenium Complex and Its Application in Dye-Sensitized Solar Cells
,”
J. Ind. Eng. Chem.
,
15
, pp.
62
65
.10.1016/j.jiec.2008.08.011
27.
Dai
,
F.-R.
,
Chen
,
Y.-C.
,
Lai
,
L.-F.
,
Wu
,
W.-J.
,
Cui
,
C.-H.
,
Tan
,
G.-P.
,
Wang
,
X.-Z.
,
Suen Lin
,
J.-T.
,
Tian
,
H.
, and
Wong
,
W.-Y.
,
2012
, “
Unsymmetric Platinum(II) Bis(Aryleneethynylene) Complexes as Photosensitizers for Dye-Sensitized Solar Cells
,”
Chem. Asian J.
,
7
, pp.
1426
1434
.10.1002/asia.201200027
28.
Wu
,
W.
,
Xu
,
X.
,
Yang
,
H.
,
Hua
,
J.
,
Zhang
,
X.
,
Zhang
,
L.
, and
Long
,
Y.
,
2011
, “
D-π-M-π-A Structured Platinum Acetylide Sensitizer for Dye Sensitized Solar Cells
,”
J. Mater. Chem.
,
21
, pp.
10666
10671
.10.1039/c1jm10942a
29.
Zhang
,
G.
,
Bala
,
H.
,
Cheng
,
Y.
,
Shi
,
D.
,
Lv
,
X.
,
Yu
,
Q.
, and
Wang
,
P.
,
2009
, “
High Efficiency and Stable Dye-Sensitized Solar Cells With an Organic Chromophore Featuring a Binary π-Conjugated Spacer
,”
Chem. Commun.
,
16
, pp.
2198
2200
.10.1039/b822325d
30.
Kim
,
S. H.
,
Kim
,
H. W.
,
Sakong
,
C.
,
Namgoong
,
J.
,
Park
,
S. W.
,
Ko
,
M. J.
,
Lee
,
C. H.
,
Lee
,
W. I.
, and
Kim
,
J. P.
,
2011
, “
Effect of Five-Membered Heteroaromatic Linkers to the Performance of Phenothiazine-Based Dye-Sensitized Solar Cells
,”
Org. Lett.
,
13
, pp.
5784
5787
.10.1021/ol2023517
31.
Panda
,
M. K.
,
Sharma
,
G. D.
,
Thomas
,
K. R. J.
, and
Coutsolelos
,
A. G.
,
2012
, “
A New Family of A2B2 Type Porphyrin Derivatives: Synthesis, Physicochemical Characterization and Their Application in Dye-Sensitized Solar Cells
,”
J. Mater. Chem.
,
22
, pp.
8092
8102
.10.1039/c2jm15420j
32.
He
,
J.
,
Benko
,
G.
,
Korodi
,
F.
,
Polivka
,
T.
,
Lomoth
,
R.
,
Akermark
,
B.
,
Sun
,
L.
,
Hagfeldt
,
A.
, and
Sundström
,
V.
,
2002
, “
Modified Phthalocyanines for Efficient Near-IR Sensitization of Nanostructured TiO2 Electrode
,”
J. Am. Chem. Soc.
,
124
, pp.
4922
4932
.10.1021/ja0178012
33.
Zhang
,
W.
,
Jin
,
X.
,
Yu
,
X.
,
Zhou
,
J.
,
Tang
,
G.
,
Peng
,
D.
,
Hu
,
J.
, and
Zhong
,
C.
,
2014
, “
Novel Dye Sensitizers of Main Chain Polymeric Metal Complexes Based on Complexes of Diaminomaleonitrile With Cd(II), Ni(II): Synthesis, Characterization, and Photovoltaic Performance for Dye-Sensitized Solar Cells
,”
J. Organomet. Chem.
,
749
, pp.
26
33
.10.1016/j.jorganchem.2013.09.006
34.
Shinpuku
,
Y.
,
Inui
,
F.
,
Nakai
,
M.
, and
Nakabayashi
,
Y.
,
2011
, “
Synthesis and Characterization of Novel Cyclometalated Iridium(III) Complexes for Nanocrystalline TiO2-Based Dye-Sensitized Solar Cells
,”
J. Photochem. Photobiol., A
,
222
, pp.
203
209
.10.1016/j.jphotochem.2011.05.023
35.
Xiang
,
N.
,
Zhou
,
W.
,
Jiang
,
Sh.
,
Deng
,
L.
,
Liu
,
Y.
,
Tan
,
Z.
,
Zhao
,
B.
,
Shen
,
P.
, and
Tan
,
S.
,
2011
, “
Synthesis and Characterization of Trivalent Metal Porphyrin With NCS Ligand for Application in Dye-Sensitized Solar Cells
,”
Sol. Energy Mat. Sol. Cells
,
95
, pp.
1174
1181
.10.1016/j.solmat.2010.12.051
36.
Kim
,
Y.
,
Jeong
,
J. H.
, and
Kang
,
M.
,
2011
, “
Synthesis of Bis (2,2′-bipyridine) Nitratocopper(II) Nitrate Using a Hydrothermal Method and its Application to Dye-Sensitized Solar Cells
,”
Inorg. Chim. Acta
,
365
, pp.
400
407
.10.1016/j.ica.2010.09.041
37.
Linfoot
,
C. L.
,
Richardson
,
P.
,
McCall
,
K. L.
,
Durrant
,
J. R.
,
Morandeira
,
A.
, and
Robertson
,
N.
,
2011
, “
A Nickel-Complex Sensitiser for Dye-Sensitised Solar Cells
,”
Sol. Energy
,
85
, pp.
1195
1203
.10.1016/j.solener.2011.02.023
38.
Liu
,
X.
,
Li
,
C.
,
Peng
,
X.
,
Zhou
,
Y.
,
Zeng
,
Z.
,
Li
,
Y.
,
Zhang
,
T.
,
Zhang
,
B.
,
Dong
,
Y.
,
Sun
,
D.
,
Cheng
,
P.
, and
Feng
,
Y.
,
2013
, “
Performance of Four Artificial Chlorine-Type Sensitizers With Different Stereostructures in Dye-Sensitized Solar Cells
,”
Dyes Pigm.
,
98
, pp.
181
189
.10.1016/j.dyepig.2013.01.013
39.
Seo
,
K. D.
,
Lee
,
M. J.
,
Song
,
H. M.
,
Kang
,
H. S.
, and
Kim
,
H. K.
,
2012
, “
Novel D-π-A System Based on Zinc Porphyrin dyes for Dye-Sensitized Solar Cells: Synthesis, Electrochemical, and Photovoltaic Properties
,”
Dyes Pigm.
,
94
, pp.
143
149
.10.1016/j.dyepig.2011.12.006
40.
Guo
,
L.
,
Deng
,
J.
,
Zhang
,
L.
,
Xiu
,
Q.
,
Wen
,
G.
, and
Zhong
,
C.
,
2012
, “
Synthesis and Applications of 3,6-Carbazole-Based Conjugated Side-Chain Copolymers Containing Complexes of 1,10-Phenanthroline With Zn(II), Cd(II), and Ni(II) for Dye-Sensitized Solar Cells
,”
Dyes Pigm.
,
92
, pp.
1062
1068
.10.1016/j.dyepig.2011.07.007
41.
Shariatinia
,
Z.
,
Mirhosseini Mousavi
,
H. S.
,
Bereciartua
,
P. J.
, and
Dusek
,
M.
,
2013
, “
Structures of a Novel Phosphoric Triamide and its Organotin(IV) Complex
,”
J. Organomet. Chem.
,
745–746
, pp.
432
438
.10.1016/j.jorganchem.2013.08.003
42.
Shariatinia
,
Z.
,
Asadi
,
E.
,
Yousefi
,
M.
, and
Sohrabi
,
M.
,
2012
, “
Novel Organotin(IV) Complexes of Organophosphorus Ligands; Synthesis, Spectroscopic, Structural Study and DFT Calculations
,”
J. Organomet. Chem.
,
715
, pp.
82
92
.10.1016/j.jorganchem.2012.05.025
43.
Shariatinia
,
Z.
,
Asadi
,
E.
,
Tavasolinasab
,
V.
, and
Gholivand
,
K.
,
2013
, “
Nanoparticles of Novel Organotin (IV) Complexes Bearing Phosphoric Triamide Ligands
,”
Beilstein J. Nanotechnol.
,
4
, pp.
94
102
.10.3762/bjnano.4.11
44.
Shariatinia
,
Z.
,
Védova
,
C. O. D.
,
Erben
,
M. F.
,
Tavasolinasab
,
V.
, and
Gholivand
,
K.
,
2012
, “
Synthesis, Conformational and NQR Analysis of Phosphoric Triamides Containing the P(O)[N]3 Skeletons
,”
J. Mol. Struct.
,
1023
, pp.
18
24
.10.1016/j.molstruc.2012.03.045
45.
Shariatinia
,
Z.
,
Sohrabi
,
M.
,
Yousefi
,
M.
,
Koval
,
T.
, and
Dusek
,
M.
,
2012
, “
X-Ray Crystallography of a New Phosphoramidate; Synthesis and Spectroscopic Investigation
,”
Heteroat. Chem.
,
23
, pp.
478
485
.10.1002/hc.21040
46.
Shariatinia
,
Z.
,
Sheykhpour
,
A.
, and
Yousefi
,
M.
,
2011
, “
New Phosphoramidates: Spectroscopic Study and Ab Initio Computations
,”
Phosphorus, Sulfur, Silicon Relat. Elem.
,
186
, pp.
1768
1781
.10.1080/10426507.2010.532840
47.
Gholivand
,
K.
,
Shariatinia
,
Z.
,
Ahmadian
,
T. Z.
, and
Tadjarodi
,
A.
,
2006
, “
Syntheses and Spectroscopic Investigation of Some Cyclophosphazanes: Analysis of Pseudo-Triplet Splitting
,”
Heteroat. Chem.
,
17
, pp.
337
343
.10.1002/hc.20229
48.
Frisch
,
M. J.
,
Trucks
,
G. W.
,
Schlegel
,
H. B.
,
Scuseria
,
G. E.
,
Robb
,
M. A.
,
Cheeseman
,
J. R.
,
Scalmani
,
G.
,
Barone
,
V.
,
Mennucci
,
B.
,
Petersson
,
G. A.
,
Nakatsuji
,
H.
,
Caricato
,
M.
,
Li
,
X.
,
Hratchian
,
H. P.
,
Izmaylov
,
A. F.
,
Bloino
,
J.
,
Zheng
,
G.
,
Sonnenberg
,
J. L.
,
Hada
,
M.
,
Ehara
,
M.
,
Toyota
,
K.
,
Fukuda
,
R.
,
Hasegawa
,
J.
,
Ishida
,
M.
,
Nakajima
,
T.
,
Honda
,
Y.
,
Kitao
,
O.
,
Nakai
,
H.
,
Vreven
,
T.
,
Montgomery
,
J. A.
, Jr.
,
Peralta
,
J. E.
,
Ogliaro
,
F.
,
Bearpark
,
M.
,
Heyd
,
J. J.
,
Brothers
,
E.
,
Kudin
,
K. N.
,
Staroverov
,
V. N.
,
Kobayashi
,
R.
,
Normand
,
J.
,
Raghavachari
,
K.
,
Rendell
,
A.
,
Burant
,
J. C.
,
Iyengar
,
S. S.
,
Tomasi
,
J.
,
Cossi
,
M.
,
Rega
,
N.
,
Millam
,
J. M.
,
Klene
,
M.
,
Knox
,
J. E.
,
Cross
,
J. B.
,
Bakken
,
V.
,
Adamo
,
C.
,
Jaramillo
,
J.
,
Gomperts
,
R.
,
Stratmann
,
R. E.
,
Yazyev
,
O.
,
Austin
,
A. J.
,
Cammi
,
R.
,
Pomelli
,
C.
,
Ochterski
,
J. W.
,
Martin
,
R. L.
,
Morokuma
,
K.
,
Zakrzewski
,
V. G.
,
Voth
,
G. A.
,
Salvador
,
P.
,
Dannenberg
,
J. J.
,
Dapprich
,
S.
,
Daniels
,
A. D.
,
Farkas
,
O.
,
Foresman
,
J. B.
,
Ortiz
,
J. V.
,
Cioslowski
,
J.
, and
Fox
,
D. J.
,
2009
, Gaussian, Inc., Wallingford CT, Gaussian 09.
49.
Lai
,
L.-F.
,
Qin
,
C.
,
Chui
,
C.-H.
,
Islam
,
A.
,
Han
,
L.
,
Ho
,
C.-L.
, and
Wong
,
W.-Y.
,
2013
, “
New Fluorenone-Containing Organic Photosensitizers for Dye-Sensitized Solar Cells
,”
Dyes Pigm.
,
98
, pp.
428
436
.10.1016/j.dyepig.2013.03.007
50.
Verbitskiy
,
E. V.
,
Cheprakova
,
E. M.
,
Subbotina
,
J. O.
,
Schepochkin
,
A. V.
,
Slepukhin
,
P. A.
,
Rusinov
,
G. L.
,
Charushin
,
V. N.
,
Chupakhin
,
O. N.
,
Makarova
,
N. I.
,
Metelitsa
,
A. V.
, and
Minkin
,
V. I.
,
2014
, “
Synthesis, Spectral and Electrochemical Properties of Pyrimidine Containing dyes as Photosensitizers for Dye-Sensitized Solar Cells
,”
Dyes Pigm.
,
100
, pp.
201
214
.10.1016/j.dyepig.2013.09.006
51.
Guo
,
L.
,
Deng
,
J.
,
Zhang
,
L.
,
Xiu
,
Q.
,
Wen
,
G.
, and
Zhong
,
C.
,
2012
, “
Synthesis and Applications of 3,6-Carbazole-Based Conjugated Side-Chain Copolymers Containing Complexes of 1,10-Phenanthroline With Zn(II), Cd(II), and Ni(II) for Dye-Sensitized Solar Cells
,”
Dyes Pigm.
,
92
, pp.
1062
1068
.10.1016/j.dyepig.2011.07.007
52.
Fu
,
Q.
,
2003
, “
Radiation (Solar)
,”
Encyclopedia of Atmospheric Sciences
,” Vol.
5
[Rad - S],
J. R.
Holton
, ed.,
Academic
,
Amsterdam
, pp.
1859
1863
.
53.
Patterson
,
A.
,
1939
, “
The Scherrer Formula for X-Ray Particle Size Determination
,”
Phys. Rev.
,
56
, pp.
978
982
.10.1103/PhysRev.56.978
54.
Corbridge
,
D. E. C.
,
1995
,
Phosphorus, an Outline of its Chemistry, Biochemistry and Technology
, 5th ed.,
Elsevier
,
The Netherlands
.
You do not currently have access to this content.