scholarly journals Modeling of optical characteristics of organic solar cells based on poly (3,4-ethylene dioxythiophene): polystyrene sulfonate with incorporated silver nanoparticles

Surface ◽  
2021 ◽  
Vol 13(28) ◽  
pp. 57-65
Author(s):  
A. A. Biliuk ◽  
◽  
O. Yu. Semchuk ◽  
O. O. Havryliuk ◽  
A. I. Biliuk ◽  
...  
Keyword(s):  
Silver Nanoparticles ◽  
Organic Solar Cells ◽  
Organic Solar Cell ◽  
Particle Diameter ◽  
Acid Methyl Ester ◽  
Optical Characteristics ◽  
Localized Surface Plasmon ◽  
Polystyrene Sulfonate ◽  
Exciton Dissociation ◽  
Acid Methyl

Changing the geometric parameters of the elements of the organic solar cell (OSC) and its components, changes in its optical characteristics such as reflection, absorption and transmission of light were studied. In the simulation, the main elements influencing the change in the characteristics of the OSC were poly (3,4-ethylenedioxythiophene): polystyrene sulfonate (PEDOT: PSS), poly (3-hexylthiophene): [6,6] phenyl-C61butyric acid methyl ester (P3HT: PCBM) on silver nanoparticles. The dimensions of silver nanoparticles coincide with the thickness of the PEDOT layer (50 nm) in which they are located, the particle diameter is 45 nm, the thickness of the P3HT: PCBM layer has always remained equal to 100 nm. The peak at a wavelength of about 726 nm, when there are silver particles in the OSC, indicates the presence of localized surface plasmon resonance (LPPR), which causes a local amplification of the electromagnetic field near the surface of metal nanoparticles. LPPR induced by silver nanoparticles not only increases the degree of light absorption, but also enhances the degree of exciton dissociation. As a result, photocurrent and overall OSC efficiency can be significantly improved due to LPPR.

Optical Absorption Enhancement in Polymer BHJ thin Film Using Ag Nanostructures: A Simulation Study

2020 ◽  
Vol 16 (4) ◽  
pp. 556-567
Author(s):  
Asma Khalil ◽  
Zubair Ahmad ◽  
Farid Touati ◽  
Mohamed Masmoudi
Keyword(s):  
Absorption Spectrum ◽  
Solar Cell ◽  
Methyl Ester ◽  
Butyric Acid ◽  
Organic Solar Cell ◽  
Short Circuit ◽  
Acid Methyl Ester ◽  
Short Circuit Current ◽  
Acid Methyl ◽  
Butyric Acid Methyl Ester

Background: The photo-absorption and light trapping through the different layers of the organic solar cell structures are a growing concern now-a-days as it affects dramatically the overall efficiency of the cells. In fact, selecting the right material combination is a key factor in increasing the efficiency in the layers. In addition to good absorption properties, insertion of nanostructures has been proved in recent researches to affect significantly the light trapping inside the organic solar cell. All these factors are determined to expand the absorption spectrum and tailor it to a wider spectrum. Objective: The purpose of this investigation is to explore the consequence of the incorporation of the Ag nanostructures, with different sizes and structures, on the photo absorption of the organic BHJ thin films. Methods: Through a three-dimensional Maxwell solver software, Lumerical FDTD, a simulation and comparison of the optical absorption of the three famous organic materials blends poly(3- hexylthiophene): phenyl C71 butyric acid methyl ester (P3HT:PCBM), poly[N-9″-heptadecanyl-2,7- carbazole-alt-5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadiazole)]: phenyl C71 butyric acid methyl ester (PCDTBT:PCBM) and poly[2,6-(4,4-bis-(2-ethylhexyl)-4H-cyclopenta[2,1-b;3,4-b′]dithiophene)-alt- 4,7-(2,1,3-benzothiadiazole)]: phenyl C71 butyric acid methyl ester (PCDPDTBT:PCBM) has been conducted. Furthermore, FDTD simulation study of the incorporation of nanoparticles structures with different sizes, in different locations and concentrations through a bulk heterojunction organic solar cell structure has also been performed. Results: It has been demonstrated that embedding nanostructures in different locations of the cell, specifically in the active layer and the hole transporting layer had a considerable effect of widening the absorption spectrum and increasing the short circuit current. The effect of incorporation the nanostructures in the active layer has been proved to be greater than in the HTL. Furthermore, the comparison results showed that, PCDTBT:PCBM is no more advantageous over P3HT:PCBM and PCPDTBT:PCBM, and P3HT:PCBM took the lead and showed better performance in terms of absorption spectrum and short circuit current value. Conclusion: This work revealed the significant effect of size, location and concentration of the Ag nanostructures while incorporated in the organic solar cell. In fact, embedding nanostructures in the solar cell widen the absorption spectrum and increases the short circuit current, this result has been proven to be significant only when the nanostructures are inserted in the active layer following specific dimensions and structures.

scholarly journals A comparative approach to enhance the electrical performance of PEDOT:PSS as transparent electrode for organic solar cells

2019 ◽  
Vol 28 (1) ◽  
pp. 66-73
Author(s):  
Ismail Borazan ◽  
Ayşe Celik Bedeloğlu ◽  
Ali Demir
Keyword(s):  
Solar Cells ◽  
Organic Solar Cells ◽  
Isopropyl Alcohol ◽  
Power Conversion ◽  
Acid Methyl Ester ◽  
Transparent Electrode ◽  
Electrical Performance ◽  
Comparative Approach ◽  
Acid Methyl ◽  
Butyric Acid Methyl Ester

In this article, the improvement in electrical performance of poly(3,4-ethylenedioxythiophene)–poly(styrenesulfonate) (PEDOT:PSS) as the transparent electrode doped with different additives (ethylene glycol (EG), isopropyl alcohol) or treatment of sulfuric acid was enhanced that organic solar cells (OSCs) were produced by using poly(3-hexylthiophene-2,5-diyl):[6,6]-phenyl C61 butyric acid methyl ester. OSCs were fabricated by the doped or treated PEDOT:PSS films as transparent electrodes. The photoelectrical measurements were carried out and the effects of doping or treatment were compared. As a result, EG-added PEDOT:PSS electrode showed the best power conversion efficiency value of 1.87% among the PEDOT:PSS anodes.

scholarly journals Polyethylenimine-Ethoxylated Interfacial Layer for Efficient Electron Collection in SnO2-Based Inverted Organic Solar Cells

Crystals ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 731
Author(s):  
Ikram Anefnaf ◽  
Safae Aazou ◽  
Guy Schmerber ◽  
Siham Refki ◽  
Nicolas Zimmermann ◽  
...  
Keyword(s):  
Solar Cells ◽  
Organic Solar Cells ◽  
Tin Dioxide ◽  
Bulk Heterojunction ◽  
Acid Methyl Ester ◽  
Cathode Layer ◽  
Acid Methyl ◽  
Electron Collection ◽  
Cathode Buffer Layer ◽  
20 Nm

In this work, we studied inverted organic solar cells based on bulk heterojunction using poly(3-hexylthiophene-2,5-diyl):[6,6]-phenyl-C71-butyric acid methyl ester (P3HT:PCBM) as an active layer and a novel cathode buffer bilayer consisting of tin dioxide (SnO2) combined with polyethylenimine-ethoxylated (PEIE) to overcome the limitations of the single cathode buffer layer. The combination of SnO2 with PEIE is a promising approach that improves the charge carrier collection and reduces the recombination. The efficient device, which is prepared with a cathode buffer bilayer of 20 nm SnO2 combined with 10 nm PEIE, achieved Jsc = 7.86 mA/cm2, Voc = 574 mV and PCE = 2.84%. The obtained results exceed the performances of reference solar cell using only a single cathode layer of either SnO2 or PEIE.

A mono(carboxy)porphyrin-triazine-(bodipy)2triad as a donor for bulk heterojunction organic solar cells

2015 ◽  
Vol 3 (24) ◽  
pp. 6209-6217 ◽  
Author(s):  
Ganesh D. Sharma ◽  
S. A. Siddiqui ◽  
Agapi Nikiforou ◽  
Galateia E. Zervaki ◽  
Irene Georgakaki ◽  
...  
Keyword(s):  
Solar Cells ◽  
Methyl Ester ◽  
Butyric Acid ◽  
Organic Solar Cells ◽  
Bulk Heterojunction ◽  
Acid Methyl Ester ◽  
Solution Processed ◽  
Acid Methyl ◽  
Butyric Acid Methyl Ester

A mono(carboxy)porphyrin-triazine-(bodipy)2triad(PorCOOH)(BDP)2has been used as a donor with ([6,6]-phenyl C71butyric acid methyl ester) (PC71BM) as an acceptor, in BHJ - solution processed organic solar cells.

Tuning of optoelectronic properties of triphenylamines-based donor materials for organic solar cells

2019 ◽  
Vol 18 (07) ◽  
pp. 1950036
Author(s):  
Maria Naeem ◽  
Sobia Jabeen ◽  
Rasheed Ahmad Khera ◽  
Usama Mubashar ◽  
Javed Iqbal
Keyword(s):  
Solar Cells ◽  
Acrylic Acid ◽  
Organic Solar Cells ◽  
Density Functional ◽  
Acid Methyl Ester ◽  
Reorganization Energy ◽  
Optoelectronic Properties ◽  
Functional Theory ◽  
Acid Methyl ◽  
Donor Moiety

In the present study, four molecules have been designed by substituting various acceptor moieties around the triphenylamine donor moiety like 2-cyano acrylic acid (R), 2-methylene malonitrile (M1), 2-cyano acrylic acid methyl ester(M2), 2-(2-methylene-3-oxo-indan-1-ylidene)-malonitrile (M3), 2-(6,7-difluoro-2-methylene-3-oxo-indan-1-ylidene)-malonitrile (M4), respectively. CAM-B3LYP/6-31G (d, p) level of theory by using density functional theory (DFT) has been used for the investigation of optoelectronic properties of four new triphenylamine (TPA)-based donor materials (M1–M4) for organic solar cells. In comparison with the recently reported reference molecule, the optoelectronic properties of designed molecules were evaluated. M4 showed absorption maxima at 520[Formula: see text]nm due to extended conjugation with bridged thiophene group. Results of reorganization energy calculations also favor M4 exhibiting highest transfer rate of hole as depicted from its low reorganization energy of hole ([Formula: see text].

scholarly journals Ultrafast Charge Generation Enhancement in Nanoscale Polymer Solar Cells with DIO Additive

Nanomaterials ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 2174
Author(s):  
Tongchao Shi ◽  
Zeyu Zhang ◽  
Xia Guo ◽  
Zhengzheng Liu ◽  
Chunwei Wang ◽  
...  
Keyword(s):  
Solar Cells ◽  
Vibrational Relaxation ◽  
Transient Absorption ◽  
Polymer Solar Cells ◽  
Acid Methyl Ester ◽  
Free Charge ◽  
Exciton Dissociation ◽  
Charge Generation ◽  
Carrier Generation ◽  
Acid Methyl

We study the ultrafast photoexcitation dynamics in PBDTTT-C-T (P51, poly(4,8-bis(5-(2-ethylhexyl)-thiophene-2-yl)-benzo[1,2-b:4,5-b′]dithiophene-alt-alkylcarbonyl-thieno[3,4-b]thiophene)) film (~100 nm thickness) and PBDTTT-C-T:PC71BM (P51:PC71BM, phenyl-C71-butyric-acid-methyl ester) nanostructured blend (∼100 nm thickness) with/without DIO(1,8-diiodooctane) additives with sub-10 fs transient absorption (TA). It is revealed that hot-exciton dissociation and vibrational relaxation could occur in P51 with a lifetime of ~160 fs and was hardly affected by DIO. However, the introduction of DIO in P51 brings a longer lifetime of polaron pairs, which could make a contribution to photocarrier generation. In P51:PC71BM nanostructured blends, DIO could promote the Charge Transfer (CT) excitons and free charges generation with a ~5% increasement in ~100 fs. Moreover, the dissociation of CT excitons is faster with DIO, showing a ~5% growth within 1 ps. The promotion of CT excitons and free charge generation by DIO additive is closely related with active layer nanomorphology, accounting for Jsc enhancement. These results reveal the effect of DIO on carrier generation and separation, providing an effective route to improve the efficiency of nanoscale polymer solar cells.

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