FDTD Analysis of Nanowire Based InP/Ge Tandem Solar Cell for Enhanced Power Conversion Efficiency

Author(s):  
Suneet Kumar Agnihotri ◽  
D. V. Prashant ◽  
Dip Prakash Samajdar
2019 ◽  
Vol 33 (17) ◽  
pp. 199-205 ◽  
Author(s):  
Patrick M. Boland ◽  
Kurniawan Foe ◽  
Diefeng Gu ◽  
Helmut Baumgart ◽  
Keejoo Lee ◽  
...  

Energies ◽  
2021 ◽  
Vol 14 (12) ◽  
pp. 3383
Author(s):  
Khaoula Amri ◽  
Rabeb Belghouthi ◽  
Michel Aillerie ◽  
Rached Gharbi

In this work, simulations were performed to optimize the parameters of a lead-free perovskite/silicon tandem solar cell for the improved efficiency and stability of commercial devices. The top sub-cell is based on a lead-free perovskite with a large bandgap of 1.8 eV, an electron transport layer of SnO2/PCBM, which is known for its anti-hysteresis effect, and a hole transport layer of NiO to improve stability, whereas the bottom sub-cell is based on n-type silicon to increase the efficiency of the whole cell. First, the two sub-cells were simulated under standalone conditions for calibration purposes. Then, the current matching condition was obtained by optimizing the thicknesses of the absorber layers of both sub-cells and the doping concentration of the back surface field (BSF) layer of the silicon sub-cell. As a result of this optimization phase, thicknesses of 380 nm and 20 µm for the top and bottom sub-cells, respectively, and a doping concentration of 1022 cm–3 were used in the configuration of the tandem cell, yielding a large open-circuit voltage of 1.76 V and a power conversion efficiency of 24.4% for the whole cell. Finally, the effect of the working temperature was evaluated, and the results reveal that the high performance of lead-free perovskite sub-cells is less affected by an increase in temperature compared to lead-based solar cells, such as those based on CH3NH3PbI3 perovskite.


2013 ◽  
Vol 4 (1) ◽  
Author(s):  
Jingbi You ◽  
Letian Dou ◽  
Ken Yoshimura ◽  
Takehito Kato ◽  
Kenichiro Ohya ◽  
...  

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
S. Wageh ◽  
Mahfoudh Raïssi ◽  
Thomas Berthelot ◽  
Matthieu Laurent ◽  
Didier Rousseau ◽  
...  

AbstractPoly(3,4-ethylenedioxythiophene) polystyrene sulfonate (PEDOT:PSS) mixed with single-wall nanotubes (SWNTs) (10:1) and doped with (0.1 M) perchloric acid (HClO4) in a solution-processed film, working as an excellent thin transparent conducting film (TCF) in organic solar cells, was investigated. This new electrode structure can be an outstanding substitute for conventional indium tin oxide (ITO) for applications in flexible solar cells due to the potential of attaining high transparency with enhanced conductivity, good flexibility, and good durability via a low-cost process over a large area. In addition, solution-processed vanadium oxide (VOx) doped with a small amount of PEDOT-PSS(PH1000) can be applied as a hole transport layer (HTL) for achieving high efficiency and stability. From these viewpoints, we investigate the benefit of using printed SWNTs-PEDOT-PSS doped with HClO4 as a transparent conducting electrode in a flexible organic solar cell. Additionally, we applied a VOx-PEDOT-PSS thin film as a hole transporting layer and a blend of PTB7 (polythieno[3,4-b] thiophene/benzodithiophene): PC71BM (phenyl-C71-butyric acid methyl ester) as an active layer in devices. Zinc oxide (ZnO) nanoparticles were applied as an electron transport layer and Ag was used as the top electrode. The proposed solar cell structure showed an enhancement in short-circuit current, power conversion efficiency, and stability relative to a conventional cell based on ITO. This result suggests a great carrier injection throughout the interfacial layer, high conductivity and transparency, as well as firm adherence for the new electrode.


2015 ◽  
Vol 19 (01-03) ◽  
pp. 175-191 ◽  
Author(s):  
Ganesh D. Sharma ◽  
Galateia E. Zervaki ◽  
Kalliopi Ladomenou ◽  
Emmanuel N. Koukaras ◽  
Panagiotis P. Angaridis ◽  
...  

Two porphyrin dyads with the donor-π-acceptor molecular architecture, namely ( ZnP )-[triazine-gly]-( H 2 PCOOH ) and ( ZnP )-[triazine-Npip]-( H 2 PCOOH ), which consist of a zinc-metalated porphyrin unit and a free-base porphyrin unit covalently linked at their peripheries to a central triazine group, substituted either by a glycine in the former or a N-piperidine group in the latter, have been synthesized via consecutive amination substitution reactions of cyanuric chloride. The UV-vis absorption spectra and cyclic-voltammetry measurements of the two dyads, as well as theoretical calculations based on Density Functional Theory, suggest that they have suitable frontier orbital energy levels for use as sensitizers in dye-sensitized solar cells. Dye-sensitized solar cells based on ( ZnP )-[triazine-gly]-( H 2 PCOOH ) and ( ZnP )-[triazine-Npip]-( H 2 PCOOH ) have been fabricated, and they were found to exhibit power conversion efficiency values of 5.44 and 4.15%, respectively. Photovoltaic measurements (J–V curves) and incident photon to current conversion efficiency spectra of the two solar cells suggest that the higher power conversion efficiency value of the former solar cell is a result of its enhanced short circuit current, open circuit voltage, and fill factor values, as well as higher dye loading. This is ascribed to the existence of two carboxylic acid anchoring groups in ( ZnP )-[triazine-gly]-( H 2 PCOOH ), compared to one carboxylic acid group in ( ZnP )-[triazine-Npip]-( H 2 PCOOH ), which leads to a more effective binding onto the TiO 2 photoanode. Electrochemical impedance spectra show evidence that the ( ZnP )-[triazine-gly]-( H 2 PCOOH ) based solar cell exhibits a longer electron lifetime and more effective suppression of charge recombination reactions between the injected electrons and electrolyte.


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