نتایج جستجو برای: Quantum dot solar cell
تعداد نتایج: 2079047 فیلتر نتایج به سال:
With attention to the thin film structure of colloidal quantum dot solar cells, in this paper in order to improvement of active layer absorption of them, we have proposed the use of nanostructure pattern for enhancement of their performance. For this purpose we have presented suitable nano hemisphare patterns in colloidal quantum dot solar cells for light trapping in absorption layer. Then with...
The relatively low power conversion efficiency (PCE) of quantum dot sensitized solar cells (QDSSCs) is attributed to charge recombination at the interfaces. Charge recombination process could be suppressed by coating the QD layer with a wide band gap semiconductor such as ZnS, which acts as a blocking layer between the QDs and hole transport material (HTM). In present study, to improve PCE of P...
Quantum dot solar cells, as a promising candidate for the next generation solar cell technology, have received tremendous attention in the last 10 years. Some recent developments in epitaxy growth and device structures have opened up new avenues for practical quantum dot solar cells. Unfortunately, the performance of quantum dot solar cells is often plagued by marginal photon absorption. In thi...
In this research, CdS and PbS quantum dots were applied as the light sensitizers in TiO2 based nanostructured solar cells. The PbS quantum dots could absorb a wide range of the sunlight spectrum on earth due to their low bandgap energy. As a result, the cell sensitization is more effective by application of both CdS and PbS quantum dots sensitizers. The TiO2 nanocrystals were synthesized throug...
colloidal quantum dots offer broad tuning of semiconductor band structure via the quantum size effect. in this paper, we present a detailed investigation on the influence of the thickness of colloidal lead sulfide (pbs) nanocrystals (active layer) to the photovoltaic performance of colloidal quantum dot solar cells. the pbs nanocrystals (qds) were synthesized in a non-coordinating solvent, 1-oc...
CdSe quantum dots were in situ deposited on various structures of TiO2 photoanode by successive ionic layer adsorption and reaction (SILAR). Various sensitized TiO2 structures were integrated as a photoanode in order to make quantum dot sensitized solar cells. High power conversion efficiency was obtained; 2.89 % (Voc=524 mV, Jsc=9.78 mA/cm2, FF=0.56) for the cells that sensitized by SILAR meth...
Related Articles Overcoming the bandgap limitation on solar cell materials Appl. Phys. Lett. 100, 083901 (2012) Energy transfer in CaYAlO4: Ce3+, Pr3+ for sensitization of quantum-cutting with the Pr3+-Yb3+ couple J. Appl. Phys. 111, 043104 (2012) GaAs/GaInNAs quantum well and superlattice solar cell Appl. Phys. Lett. 100, 073508 (2012) Understanding the operation of quantum dot intermediate ba...
Quantum dot (QD) solar cells have the potential to increase the maximum attainable thermodynamic conversion efficiency of solar photon conversion up to about 66% by utilizing hot photogenerated carriers to produce higher photovoltages or higher photocurrents. Three quantum dot solar cell configurations are described.
A flexible hybrid heterojunction PbS colloidal quantum dot solar cell, where the photoactive layers are deposited using a solution processed fabrication approach under ambient condition and at room temperature is presented. The bending stability of the obtained solar cell is evaluated. The results show that the solar cell exhibits high bending stability and even under the bent state the cell al...
In this work Silvaco TCAD have been used to model quantum dot solar cell. It was found that the addition of InAs QD(quantum dot) in the intrinsic layer of hetero-structure InGaP/GaAs p-i-n solar cell extends the absorption range of the solar cell, thereby giving rise to efficiency enhancement of the QD solar cell by 3.8851 % it was also observed that the fill factor increases from 83.2724% to 8...
نمودار تعداد نتایج جستجو در هر سال
با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید