Professional Documents
Culture Documents
S1
Advanced Materials for solar energy conversion
Invited Papers
hard coatings,
transparent electrodes
tefan Antohe1,2
University of Bucharest, Faculty of Physics, P.O.Box: MG-11, Bucharest-Magurele, 077125 ROMANIA, E-mail:
santohe@solid.fizica.unibuc.ro , 2Academy of Romanian Scientists-Physics
In the last decades the second and third generations of photovoltaic cells based organic thin films have attracted a
great deal of interest among scientists involved in the research efforts to produce efficient and low-cost solar cells.
More recently, the biological materials were tested successfully in electronic and optoelectronic applications. Among
the organic semiconductors envisaged to be used in such structures, small molecules like metal-doped phthalocyanines
(MePc, with Me=Cu, Mg, Zn, etc.) and polymers are the most studied, due to their peculiar optical properties. As
biologic semiconductor, the Chlorophyll-a is a potential candidate for photovoltaic structures. For these materials, the
optical absorption in the visible range of the solar spectrum is strong, but based on an excitonic mechanism. A typical
value for the diffusion length of the exciton in organic semiconductors is of 30-80 nm, while in order to achieve the
required efficiency in light absorption, the absorber layer has to be at least 100 nm thick. This inconvenient could be
avoid, by the preparation of the multilayered structures containing different organic and biologic absorbers, or creating
a large number of Donor/Acceptor Interfaces, spread in the whole volume of the composite absorber, leading to so call
,,Bulkheterojunctioncells.
In this work are summarized the electrical and photoelectrical properties of the photovoltaic cells based on the
organic (small molecules and polymers) and biologic thin films. In the case of second generation of photovoltaic cells,
first the single-layer structures (ITO/CuPc/Al and ITO/TPyP/Al) were been prepared and characterized. The doublelayer photovoltaic structures based on the p-n heterojunction present at the interface between two organic layers, like,
ITO/CuPc/TPyP/Al and ITO/Chl a/TPyP/Al, exhibits stronger spectral sensitivity and better spectral matching to a solar
spectrum than Schottky cells using either CuPc or TPyP layer, having a power conversion efficiency with about two
orders of magnitude, higher than those of single-layer structures. Three-layered organic solar cells with an interlayer of
co-deposited dyes of p-type CuPc and n-type TPyP, between the respective dye layers were also prepared and
characterized, showing an increased power conversion efficiency, with respect of doublelayer structures.
In the case of third generation of solar cells, the polymeric photovoltaic cells were produced by spin-coating
technique. The structures based on the P3HT: PCBM (1:1) blend and the hybrid structures of Chl/:P3HT:PCBM(1:1)
shows a promising photovoltaic response, with a power conversion efficiency increased of about two order of degree,
with respect of those measured in the case of structures based on single P3HT and PCBM or Chl-a thin films. Different
design of structures were prepared and characterized trying permanently to improve the performances and the stability
of the photovoltaic cells.
Keywords: organic thin films, chlorophyll-a, Bulkheterojunction photovoltaic cells
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Oral Presentations
The understanding of degradation processes and related defect states represents important factor for further
improvement of organic solar cells (OSC). The charge capture and recombination at these states result in carrier
mobility decrease, photocurrent loss, and consequently, in the drop of power conversion efficiency. Most of previous
studies performed with various optical and electrical methods have focused on such a high degree of the organic film
degradation which was far behind OSC functionality and could not be correlated with OSC electrical parameters.
Here we present experiments which correlate defect states in OSC active layer and the degradation of OSC electrical
parameters. We investigated the defect states induced by ambient air, humid air, and UV/Vis irradiation. The purpose is
to identify the impact of these degradation agents on particular photovoltaic process. In order to find this correlation we
used charge deep-level transient spectroscopy (Q-DLTS) which was directly applied to OSC samples. The activation
energy, frequency factor, and the concentration of defect states were investigated with Q-DLTS via temperature and
isothermal scans. The basic electrical parameters of OSC including photocurrent, ideality factor, reverse saturation
current, shunt and series resistances as well as the exciton generation rate and its dissociation probability were
determined from dark and light I-V measurements.
We observed the formation of oxygen-related defect states with energy about 0.1 eV above HOMO of P3HT during
OSC degradation. Our preliminary results suggest that the oxygen-related defect states have a dominant impact on
exciton recombination leading mainly to photocurrent loss. The correlation of these states with OSC electrical
parameters indicates two stages of OSC degradation. The obtained results are discussed and compared with other
relevant published data.
15
S. Iftimie1, M.E. Barbinta-Patrascu1, A. Radu1, B. Bita1,2, N. Vasile1, N. Korganci1, L. Ion1 and S. Antohe1,3
University of Bucharest, Faculty of Physics, 405 Atomistilor, P.O. Box: MG-11, 077125, Magurele, Ilfov, Romania,
2
National Institute for Research and Development in Microtechnology IMT Bucharest, P.O. Box:38-160, 023573,
Bucharest, Romania, 3Academy of Romanian Scientists, 54 Splaiul Independentei, 050094, Bucharest, Romania
Photovoltaic cells based on biologic (Chlorophyll-a, Chl-a) and polymeric (poly(3-hexylthiophene-2,5-diyl), P3HT)
and ([6,6]-phenyl-C61 butyric acid methyl ester, PCBM) thin films were fabricated and characterized. Two types of
structures were obtained, either a bi-layer Chl-a/P3HT:PCBM (1:1, wt. %) or a single layer Chl-a:P3HT:PCBM (10:1:1,
wt. %) architecture. The spin-coating technique was used for the deposition of the biologic and polymeric thin films on
the ITO glasses, used as substrate and thermal vacuum evaporation technique was used to prepare the aluminum (Al)
thin film as back contact . The optical and photovoltaic properties of the prepared photovoltaic cells, were analyzed and
compared with those for P3HT:PCBM (1:1, wt. %) structures. Similar values were registered for fill factor and open
circuit voltage, but the spectral response was enlarged for those cells containing Chl-a. For the moment, the short-circuit
current values for the non optimized cells Chl-a/P3HT:PCBM (1:1, wt.%) and Chl-a:P3HT:PCBM (10:1:1, wt.%) were
smaller than for P3HT:PCBM (1:1, wt.%) cells, but the future optimized structures (by a very good control of the film
thickness and design) will have improved performances.
Keywords: polymeric thin films, Chl-a, photovoltaic cells
TOWARDS OFFSETTING UP AN INTERMEDIATE BAND SOLAR CELL BASED ON TITANIUM OXIDES
SOL-GELS
S. Bechu1*, A. Goullet1, L. Cattin-Guenadez1, D. Duche2, J-J. Simon2, M. Girtan3, L. Brohan1, M. Richard-Plouet1
1. IMN-Universit de Nantes, Nantes, 2. IM2NP, Marseille, 3. LPHIA, Angers, * corresponding author :
solene.bechu@cnrs-imn.fr
Third generation solar cells aims at increasing efficiency to overtake the 31% theoretical efficiency of simple
junction photovoltaic cells established by Shockley and Queisser [1] in 1961. According to Marti and Luque [2],
intermediate band cell concept could increase the photocurrent via the absorption of sub-bandgap photons without
degrading the voltage.
In this perspective, we developed hybrid photosensitive sols-gels based on titanium clusters with specific optical and
electronic properties [3]. Once illuminated under UV light, an intermediate band appears in the band structure so the
absorption spreads over visible to near infrared due to reduction of Ti(IV) in Ti(III). Thanks to this absorption range
increase, these sols-gels can be used as active layers in solar cell.
In order to optimize light absorption properties of the sol-gel layer, shaping optimisation and optical properties
studies were carried out. Thin films were obtained with an accurate control over thickness in the range from 150 nm to
10 m. Ellipsometry and XPS studies were respectively undertaken to determine optimal thickness and electronic
structure evolution under UV illumination.
This layer with original properties could be implemented as active layers in new hybrid solar cells.
[1] Shockley, W., Queisser, H.J., Journal of Applied Physics, 32, 510 (1961)
[2] Luque, A., Marti, A., Physical Review Letters, 28, 78, (1997)
[3] Cottineau T., Brohan L., Pregelj M., Cevc P., Richard-Plouet M., Aron D., Advanced Functional Materials, 18,
2602 (2008)
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Cadmium sulfide (CdS)/ cadmium telluride (CdTe) heterojunction based photovoltaic cells were fabricated onto
optical glass substrates covered with a thin indium tin oxide (ITO) layer, in superstrate configuration. In order to
minimize the induced deposition defects, the window layer, cadmium sulfide, was deposited by rf-magnetron
sputtering; the substrate was purposely unheated. CdTe layers were deposited on top of cadmium sulfide by thermal
vacuum evaporation (TVE). To complete the photovoltaic structure a copper:gold (Cu:Au) back electrode was
deposited by TVE, too. With high absorption coefficients, suitable band gaps and reduced masses as thin films,
cadmium sulfide and cadmium telluride are candidates for terrestrial and space applications. Our fabricated structures
were irradiated with protons and alpha particles with 500 keV energies and 1011 particles/cm2 fluencies, respectively.
These values are similar with those hitting artificial satellites orbiting the Earth. Electrical and photo-electrical
measurements were performed in dark and AM 1.5, at room temperature. Monte-Carlo numerical simulations showed a
detailed image of interaction between our samples and protons and alpha particles. Determined external quantum
efficiencies values (EQE) decreased after irradiation with protons and alpha particles but the peaks attributed to
fundamental absorption thresholds for CdS and CdTe kept their as grown positions in the case of irradiation with
protons and were slightly shifted in the case of irradiation with alpha particles. Parameters characterizing a photovoltaic
cell, short-circuit current, open circuit voltage and fill factor, were determined and compared for as grown and
irradiated PV cells.
Keywords: cadmium sulfide, cadmium telluride, ionizing radiations, protons, alpha particles
ON THE STRUCTURAL AND OPTICAL PROPERTIES OF HYBRID PEROVSKITE THIN FILMS
Aurelian Catalin Galca, Andrei Gabriel Tomulescu, and Ioana Pintilie
National Institute of Materials Physics, Atomistilor 105 bis, 077125 Magurele, Ilfov, Romania, corresponding author:
ac_galca@infim.ro
Perovskite-based solar cells have been proposed as novel photovoltaic devices with relatively good conversion
efficiency [1-3]. Most of the reported studies are focused only on presenting the solar cells parameters (e.g. quantum
efficiency, spectral response, fill factor), while the pure optical and structural properties of each layer are roughly
presented and discussed.
In this work we report the exhaustive optical and microstructural properties of thin films of the active hybrid
perovskite. The thin films are obtained by using a complex recipe which includes a special cleaning of the amorphous
silicon oxide substrates and a careful mixing and treatment of the precursors, and by using afterwards the spin-coating
technique.
The hybrid perovskite with the chemical formula CH3NH3PbI3-xClx results from the combination of CH3NH3I and
PbI2/PbCl2 solutions. Depending on the preparation conditions the secondary phase of inorganic halide (PbI 2/PbCl2) is
more or less present.
The authors acknowledge funding from EEA Financial Mechanism Office through the project no 8SEE/30.06.2014:
Perovskites for Photovoltaic Efficient Conversion Technology.
References
1. M. M. Lee et al., Science 338 (2012) 643.
2. B. Conings et al. , Adv. Mater. 26 (2014) 2041.
3. H. Zhou et al. , Science 345 (2014) 542.
17
EFFICIENT PEROVSKITE SOLAR CELLS PREPARED BY SOLUTION PROCESSED VIA TWO STEP
DEPOSITION
Viorica Stancu, Marian Sima, Cristina Besleaga, Andrei Tomulescu, Mariana Sima, George Stan, Lucian Pintilie, Ioana
Pintilie
National Institute of Materials Physics,105bis Atomistilor, 077125 Magurele, Ilfov, Romania, stancu@infim.ro
Perovskite solar cells are the newest technology of photovoltaic systems. They are attractive due to their properties:
high conversion efficiency, offers significantly higher voltages and their fabrication techniques are simple. The essential
component of these solar cells is a light absorbing semiconductor material with a perovskite polycrystalline structure,
CH3NH3PbX3 (X= Cl, Br, I). In this work, we fabricate perovskite solar cells with high power conversion efficiency
(average value efficience 16.6%) using a two step deposition process of CH 3NH3PbI3-xClx perovskite film. The
preparation process of the perovskite film was completed using a solvent annealing technique, where solvent vapor is
introduced during the crystallization of the perovskite film to increase the crystallinity and grain size. Our perovskite
solar cell structure contains a glass/FTO substrate covered with a compact layer of TiO 2 semiconductor. Over that is
deposit a mesoporous scaffold from the same semiconductor which is in a close contact with a perovskite film.
Perovskite film which can work effectively as both absorber and an electron transporter is covered with a Li doped spiro
OMeTAD film (hole transporter). A metallic contact (Mo and Ag) is deposited on the spiro OMeTAD film.
INVESTIGATION OF NEW ABSORBERS MATERIALS FOR EFFICIENT PHOTOVOLTAIC SOLAR
CELLS
P. Wahnona, P. Palaciosa, E. Menendez-Proupinb, E. Castellanosa, Lucenac, JC Conesac
Instituto de Energa Solar, Universidad Politcnica de Madrid, Ciudad Universitaria, 28040 Madrid, Spain;
b
Departamento de Fsica, Facultad de Ciencias, Universidad de Chile, Santiago, Chile; cInstituto de Catlisis y
Petroleoqumica, CSIC, 28049 Madrid, Spain; perla@etsit.upm.es
a
One of the challenges of materials science today is to find new technologies that will be able to make the most of
renewable energies. An example of new proposals in this field is the intermediate-band (IB) materials, which promise
higher efficiencies in photovoltaic applications.
We present in this work several materials actively studied as good absorbers for photovoltaic applications. The first
alternative consists in the introduction of a properly chosen transition metal at high concentration in an octahedral
semiconductor which gives in-gap delocalized and partially occupied levels, required by the Intermediate Band concept.
The new intermediate band allows the absorption of low energy photon increasing the photo-current but maintaining the
photo-voltage. We have verified with accurate density functional theory (DFT) calculations and beyond, that
semiconductors as In2S3 and layered SnS2 can provide this situation when an octahedral cation in their structure is
partially substituted by an element such as vanadium. For layered semiconductors, the van der Waals cleavage plane
(0001) is characterized by hexagonal arrays of close packed chalcogenide ions which are covalently bound within X-MX sandwiches. These materials are ideal substrates to study fundamental aspects of the metal/semiconductor interaction.
Experimental work made via wet chemistry methods verifies that new absorption features appear in the optical
absorption spectrum which matches the predicted DFT-based theoretical absorption results. On the other hand, a
photocatalytic process (photooxidation of an organic compound in an aqueous suspension irradiated with wavelengthselected light) is used to experimentally assess, even on polycrystalline powder materials, the ability of subbandgap
photons to produce electron-hole pairs that can be extracted at the materials interface with scarce efficiency degradation
by recombination effects. The spectral responses show that these materials have the appropriate characteristics for
building photovoltaic devices of boosted efficiency using the whole range of the visible light spectrum.
Nowadays other actively studied as novel photovoltaic material is the methyl-ammonium lead iodide perovskite
(CH3NH3PbI3). We have computed its electronic structure and relevant properties of the othorhombic phase with
accurate DFT. The crystal structure, optimized using a van der Waals functional, reproduces closely the unit cell
volume. By combining spin-orbit effects, with hybrid functionals the experimental bandgap is also reproduced. The
computed binding energy of the unrelaxed exciton agrees with recently reported experimental data, and the values
found imply an easy exciton dissociation at room temperature. Fast dynamics and large diffusion lengths of the current
carriers are key for the high photovoltaic efficiencies shown by these materials.
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Poster Presentations
GaSb-based semiconductor alloys have potential in cutting-edge applications for mid-infrared optoelectronics (Eg~
0.73 eV at 273 K) and thermophotovoltaics. It is stated [1] that the performance and reliability of GaSb devices largely
depend on surface preparation techniques (e.g. n-GaSb (100)) and requires a significant reduction of high levels of
reverse current and surface instabilities. GaSb surface is much more reactive than that of GaAs or InP and quickly
oxidizes under atmospheric conditions [2]. This work presents an XPS (X-ray Photoelectron Spectroscopy) of the native
oxides on n-GaSb (Te doped ) where the irreversible nature of the reaction is related to the fact that the oxygen atoms
are involved in chemical bonds. The evolution of Ga2O3 and Sb2O3 with temperature is presented in high vacuum
heating. Low temperature action can produce on GaSb a non-equilibrium Ga2O3-Sb2O3 surface oxide layer in wet
thermal oxidation process putted into evidence by XPS analysis. There are discussed the evolution of Sb2O3 and Ga 2O3
in four oxidation processes, namely: dry thermal oxidation in furnace (p=1 atm, T (150-200)0C ); wet thermal oxidation
(water vapors T~(90-100)0C, N2 flux ); dry thermal oxidation at low temperatures (T~550C ) and anodic oxidation. The
quality of surface oxide was also examined by Spectroscopic Ellipsometry technique. Due to the fact that the only stable
phases that can exist in thermodynamic equilibrium with GaSb are Ga2O3 and elementary Sb, the problem of developing
a stable oxide layer on GaSb surface to be used further for device processing is vital in GaSb technology. This work is
devoted to the study of a viable route in the technology of a Schottky photosensitive device on n-GaSb (100).
References
[1] M.Perotin et al, Journal of Electronic Materials, Vol.23, No.1, pp.7-12 (1994).
[2] E Papis-Polakowska , Electron Technology-Internet Journal 37/38, 4, pp.1-34 (2005/2006).
Acknowledgements:
The financial and encouragement support provided by the Ministry of Educations of the Romania-UEFISCDI,
Project No. 68/2014
21
The main subject of this work was synthesis of Carbon Nano-Onions (CNOs) and NiO composites which were
prepared by loading of Ni(OH)2 in different mass ratio on the carbon structures in the presence of 4-DMAP ((4dimethylamino)pyridine), followed by calcination to obtain CNO/NiO. CNOs consist of 6-8 carbon shells (5-6 nm in
diameter) and they can be also referred as multi-shelled fullerenes. The interest in carbon nano-onions is driven by their
unusual physico-chemical properties as well as by promising applications in electronics, optics, biosensors, and in
energy conversion and storage. CNOs/NiO were characterized by TEM, SEM, XRD, TGA-DTG-DTA, AFM, Raman,
FT-IR spectroscopy, and the cyclic voltammetric and impedimetric measurements.
Carbon-based composites are currently being investigated as supercapacitor electrodes because of the synergistic
properties arising from the carbon materials (high power density) and from the pseudocapacitive nanomaterials (high
energy density). Therefore, NiO/4-DMAP could act as an efficient hole-transport layer (HTL) in polymer solar cells
(PSCs) which are very promising organic-based devices for low-cost solar energy conversion. Nevertheless, one of the
greatest drawback of PSCs is their poor stability in ambient conditions. One of well-known HTL is PEDOT:PSS that is
strongly acidic in nature and lead degradation of the devices and limit their life. Therefore, the alternative is a
substitution of PEDOT:PSS by NiO. The hybrid material characterizes excellent stability, charge transport properties,
charge selectivity and hole collection in PSCs.
We gratefully acknowledge the financial support of the National Science Centre, Poland, grant:
#2012/05/E/ST5/03800 to M.E.P.-B. L.E. thanks the Robert A. Welch Foundation for an endowed chair, grant #AH0033 and the US NSF, grants: CHE-1110967 and CHE-1124075.
HYBRID PEROVSKITE SOLAR CELLS: AGING EFFECTS AND RELIABILITY
C. Besleaga1, V. Stancu1, A.G. Tomulescu1, M. Sima1, L.M. Trinca1, G.E. Stan1, A.C. Galca1, L. Pintilie1, I. Pintilie1,
A. Radu2, S. Iftimie2, L. Ion2, S. Antohe2, A. Nemnes2, C. Goehry3 and A. Manolescu3
1
National Institute of Materials Physics, Atomistilor 105 bis, 077125 Magurele, Ilfov, Romania, 2Faculty of Physics,
University of Bucharest, Atomistilor 405, 077125 Magurele, Ilfov, Romania, 3School of Science and Engineering,
Reykjavik University, Menntavegur 1, IS-101 Reykjavik, Iceland
Perovskite-based solar cells have attracted the interest of the photovoltaics community due to their low fabrication
costs and very good conversion. Up to now, external efficiencies measured on this type of structures surpass 10% [1,2]
with a best of 19% reported by Zhou et al. in 2014 [3]. In this work we report studies on high-performance solar cells
based on CH3NH3PbI3-xClx with PCEs up to 16% on fresh devices. The hybrid perovskite thin film is obtained by spin
coating, as well as the anatase (TiO2) and the spiro-OMeTAD, which play the roles of the blocking layer and the hole
transport material (HTM), respectively. Degradation in time of the prepared devices was observed. The source of this
instability is still under debate, being frequently suggested in literature that the aging of spiro-OMeTAD layer degrades
the cell and its efficiency [4]. The stability in time of the obtained photovoltaic devices, with and without spiroOMeTAD, was assessed and discussed, in the search for performance enhancement paths. The effect of the HTM on the
efficiency was also evaluated with numerical simulations. The research leading to these results has received funding
from EEA Financial Mecanism 2009 - 2014 under the project contract no 8SEE/30.06.2014.
References
1. M. M. Lee et al., Science 338 (2012) 643.
2. B. Conings et al. , Adv. Mater. 26 (2014) 2041.
3. H. Zhou et al. , Science 345 (2014) 542.
4. Anyi Mei et al. , Science 345 (2014) 295-298.
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National Institute of Material Physics,105 bis Atomistilor Street, 077125, Bucharest-Magurele, Romania, University
of Bucharest, Faculty of Physics, 405 Atomistilor Street, 077125, Bucharest-Magurele, Romania, 3National Institute for
Lasers, Plasma and Radiation Physics, 409 Atomistilor Street, 077125, Bucharest-Magurele, Romania, 4Laboratoire de
Photonique d'Angers, Universit dAngers, 2, Bd. Lavoisier, 49045, Angers, France, marcela.socol@infim.ro
Organic heterostructures based on metal (Zn and Mg) phthalocyanes (p types semiconductors) and 5,10,15,20tetra(4-pyrydil)21H,23H-porphyne (n type semiconductor) were prepare by Matrix-Assisted Pulsed Laser Evaporation
(MAPLE) tehnique on ITO flexible substrates. Structural, morphological, and optical properties of the bilayer and bulk
heterojunctions were investigated by UV-VIS, Photoluminescence (PL) and FTIR spectroscopy as well as Atomic Force
Microscopy (AFM) and Scanning Electron Microscopy (SEM). The layers preserved the properties of the initial
materials and exhibited a large absorption in the visible range of the solar spectrum. The morphology was characteristic
to the MAPLE organic films with large grains. I-V characteristics of (Al/ZnPc(MgPc)/TPyP/ITO and
Al/ZnPc(MgPc):TPyP/ITO) structures were recorded in dark and under the illumination with an solar simulator
(AM1.5). In the bulk heterojunctions, the current value were found to be improved (at least one order of magnitude)
compared to the value obtained in the bilayer heterojunction in the both case of the structures made with ZnPc or MgPc.
23
In this work, Au nanoparticles (NPs) were prepared by pulsed laser ablation in liquid (PLAL) technique using NdYag laser with three different energies per pulse (600, 700, and 800 mJ). The gold NPs have been added to Ru based
dye (N719) in order to form a plasmonic dye. After the adding of Au NPs colloidal to N719, the absorbance of the
plasmonic dye has increased significantly compared with the pure dye as revealed by UV-VIS spectroscopic analysis in
the figure below. In order to prepare the photo-electrode of the dye sensitized solar cell (DSSC), titanium dioxide film
of thickness about 10 m was deposited on a FTO glass and then immersed in the plasmonic dyes for 30 min. The TiO2
coatings were sintered in air at 500 C for 30 min. The XRD analysis for the sintered TiO 2 pastes showed the usual
peaks observed in TiO2 powders. However, the spectral Responsivity calculations demonstrated enhance photocurrent
in the range from 500-580 nm. IV characteristics of the DSSC under AM1 illumination showed enhanced Isc and Voc
by 19 % and 17% respectively.
References
[1] Guowei Yang, Laser Ablation in Liquids: Principles and Applications in the Preparation of Nanomaterials, 2012
Pan Stanford Publishing Pte. Ltd.
[2] M. D. Brown, T. Suteewong, R. Kumar, V. DInnocenzo, A. Petrozza, M. M. Lee, U. Wiesner, and H. J.
Snaith, Plasmonic Dye-Sensitized Solar Cells Using Core-Shell Metal-Insulator Nanoparticles. Nano Lett. 2011, 11,
438445.
STRUCTURAL AND OPTICAL PROPERTIES OF RF SPUTTERED ZnO:Ga THIN FILMS
Fawzy. A. Mahmoud1,2*, Mohammed Rasheed3, Ahmed F. Mabied1, M.Girtan3
Solid State Physics Dept., National Research Centre, P.O. 12311, Dokki, Giza, Egypt, 2Renewable Energy Group,
Center of Excellence for Advanced Sciences, National Research Centre, P.O.12311, Dokki, Giza, Egypt, 3Angers
University, Photonics Laboratory, Angers, France
ZnO:Ga films were deposited on quartz substrates by RF magnetron sputtering using ZnO:Ga target. Four types of
samples were prepared with various RF magnetron powers of 100, 150, 200 and 300Watt. The properties of these films
were investigated using X-ray diffraction (XRD), optical transmittance and reflectance, FESEM, and spectroscopic
ellipsometry in the spectral region of 200 to 1200 nm. The structural and optical properties of the prepared films were
affected by RF power. Relationships between structure of sputtered ZnO:Ga films and the optical constants were
investigated with varying RF power. The refractive and extinction coefficients were calculated by ellipsometry and the
data were correlated with the spectrophotometry measurements. Also the optical band gap was calculated from both
spectrophotometry and ellipsometry measurements, and very good correlations were founded.
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NORMAL AND INVERTED ORGANIC SOLAR CELLS BASED ON SMALL MOLECULE COMPOUNDS
M. Socol1, O. Rasoga1, C. Breazu1, 2, N. Preda1, F. Stanculescu2, A. Stanculescu1, G. Socol3, M Girtan4
1
National Institute of Material Physics, 105 bis Atomistilor Street, 077125, Bucharest-Magurele, Romania, University
of Bucharest, Faculty of Physics, 405 Atomistilor Street, 077125, Bucharest-Magurele, Romania, 3National Institute for
Lasers, Plasma and Radiation Physics, 409 Atomistilor Street, 077125, Bucharest-Magurele, Romania, 4Laboratoire de
Photonique d'Angers, Universit dAngers, 2, Bd. Lavoisier, 49045, Angers, France, marcela.socol@infim.ro and
oana.rasoga@infim.ro
In order to improve the electrical properties of the normal and inverted solar cell structures based on a zinc
phthalocyanine (ZnPc) and an 1,4,5,8-naphthalene-tetracarboxylic dianhydride (NTCDA) donor, respectively acceptor
layer, we study the effect of a fullerene aditional layer inserted between them. Indium tin oxide (ITO) was used as
transparent conductive electrod coated with a poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS)
layer in order to increase the charge conduction. The final structures are: glass/ITO/PEDOT:PSS/ZnPc
/fullerene/NTCDA/Al and: glass/Al/NTCDA/fullerene/ZnPc/PEDOT:PSS/ITO for the inverted one. The metods used
for the realization of the organic thin film structures were thermal vacuum evaporation for the small molecule
compounds and spin-coating for fullerene and PEDOT-PSS layers. Because a determinant role in the electrical
properties is played by the morphology of the layers, atomic force microscopy (AFM) and scanning electron
microscopy (SEM) were used to investigate the surface of the thin films. Optical properties of the coatings have been
investigated by UV-VIS, photoluminescence (PL) and FTIR spectroscopy. I-V characteristics of the realized structures
were recorded in dark and under the illumination with a solar simulator (AM1.5). An improvment in the electrical
properties was observed for the inverted structures.
STRUCTURAL PROPERTIES OF CIGS THIN FILMS DEPOSITED BY MAGNETRON SPUTTERING
TECHNIQUE
a
Copper indium gallium selenide (CIGS) thin films with various thicknesses (750 1200 nm) were deposited by RF
magnetron sputtering method. To simplify this procedure for deposition of chalcopyrite-type thin films, only a single
CIGS sintered target was used.
Deposition conditions for this study were: Ar pressure p = 4 10-4 4.3 10-4 Torr, deposition rate rd = 1.6 1.7
/s, 100 mm diameter target (CIGS circular disk of 99.99% purity).
The CIGS layer deposited on Mo coated glass substrate, with a thickness of 500 nm. Next, a CdS layer of 60 nm
was deposited by thermal vacuum evaporation technique. The top transparent contact electrode, ITO, was subsequently
deposited by RF magnetron sputtering method. Atomic force microscopy (AFM) and scanning electron microscopy
(SEM) investigations showed that the surface morphology changes depending on the deposition techniques and it is
influenced by the increase in thicknesses of the layers..
Profilometry measurements showed evidence of changes in the step of the deposited layers, due to the interdiffusion
from the level of each deposited layer or that will be deposited. From X-ray diffraction (XRD) measurements it was
found that all films were polycrystalline. CIGS films have a tetragonal structure with (112) plane parallel with the
surface of the substrate, and the grain size is influenced by thickness. The influence of thickness on the samples
electrical and optical properties was also studied by quantum efficiency measurements.
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DEGRADATION CHARACTERISTICS OF ZnO:B TREATED H/Ar FOR THIN FILM SOLAR CELL BY
DAMP HEAT
1,3
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Mihaela E. Trandafir1, Simona omcescu2, Jose Calderon-Moreno2, Petre Osiceanu2, Mihaela Florea1
University of Bucharest, Faculty of Chemistry, Bucharest, Romania, 2Ilie Murgulescu Institute of Physical
Chemistry, Romanian Academy, Spl. Independentei 202, 060021, Bucharest, Romania
Solid oxide fuel cells (SOFC) offer a promising way of converting chemical energy into electrical energy with great
efficiency. SOFC devices need to possess simultaneously an ionic conductivity induced by the presence of oxygen
vacancies and an electronic conductivity induced by the added metal together with a high porosity allowing the fuel
transport through the anodic layer. Our goal is to develop a synthesis method that favors uniformity of the crystalline
network and an improvement of the ionic and electronic conductivity as well as of the catalytic activity. The selfassembling method using Triton X100 as template was used for synthesis of Ni0.2Ti0.1Y0.16Zr0.54O2- (NTYZ) and
Cu0.2Ti0.1Y0.16Zr0.54O2- (CTYZ).
The XRD pattern of sample CTYZ corresponds to a fluorite type (Fm3m) cubic stabilized zirconia phase with lattice
parameter c= 5.112 . The cubic structure is stable at room temperature due to the incorporation of the yttrium,
titanium and copper cations in the zirconia-based lattice and the formation of quaternary oxide solid solution
nanocrystals, with crystal size around 6 nm. The XRD pattern of sample NTYZ corresponds also to a fluorite type
(Fm3m) cubic stabilized zirconia phase with lattice parameter c= 5.131 , with crystal size around 3.4 nm with the
present of bunsenite as minor phase. After calcination at 900 oC, the XRD pattern of sample shows a very significant
growth of the crystallite size of the zirconia phase to about 17 nm, as well as a very small increase in the lattice
parameter, c= 5.134 .e structure (less than 5 vol.%), and crystal size of about 28 nm. The new composites show high
methane conversion and CO selectivity in the catalytic partial oxidation of methane. Conductivity results showed a
predominately n-type behaviour, highlighting a promising IT-SOFC anode.
This work was supported by a grant of Partnerships in priority S&T domains Program (PNII), MEN UEFISCDI,
project number 26/2012.
MODELING THE ELECTRON TRANSFER IN DYE-ELECTROLITE SYSTEMS FOR DYE-SENSITIZED
SOLAR CELLS
Anamaria Trandafir1,2,*, Corneliu I. Oprea1, and Mihai A. Girtu1
Ovidius University of Constana, Department of Physics, 900527 Constana, Romania, 2University of Bucharest,
Faculty of Physics, 077125 Magurele-Ilfov, Romania, *Email: anamaria.trandafir@yahoo.ro
Dye-sensitized solar cells have gained widespread attention in the past few years due to low cost fabrication. Since
the conversion efficiency of these photovoltaic systems highly depends on the electron transfer at the dye-electrolyte
interface, we studied the dye regeneration of various dye-electrolyte systems for dye-sensitized solar cells. These
systems are formed of various dyes (L0, D35 and Y123) and Co-based electrolytes. Using density functional theory
(DFT) we determined the potential energy surfaces for the singlet, triplet and quintet states. We applied Marcus theory
to determine the electron transfer rate and reorganization energy for these systems. Optical characterization was
obtained using time dependent DFT for the dyes and electrolytes. Computations were made using the Gaussian03
package.
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