The authors have demonstrated an approach to sensitized-type solar cells, based on inverse opal and the use of CdSe quantum dots (QDs) as sensitizers. CdSe QDs were grown in situ on inverse opal electrodes, utilizing a chemical bath deposition method. All of the photovoltaic performances, including short circuit photocurrent density, open circuit voltage, fill factor, and efficiency, were significantly improved by surface modification with ZnS and fluoride ions. A power conversion efficiency of about 2.7% has been attained, under solar illumination of . This value is relatively high for metal oxide solar cells, sensitized with semiconductor QDs.
Zinc oxide (ZnO) has been considered as one of the potential materials in solar cell applications, owing to its relatively high conductivity, electron mobility, stability against photo-corrosion and availability at low-cost.
Solar cells based on a mesoporous structure of TiO2 and the polysulfide redox electrolyte were prepared by direct adsorption of colloidal CdSe quantum dot light absorbers onto the oxide without any particular linker. Several factors cooperate to improve the performance of quantum-dot-sensitized solar cells: an open structure of the wide bandgap electron collector, which facilitates a higher covering of the internal surface with the sensitizer, a surface passivation of TiO2 to reduce recombination and improved counter electrode materials. As a result, solar cells of 1.83% efficiency under full 1 sun illumination intensity have been obtained. Despite a relatively large short circuit current (J(sc) = 7.13 mA cm(-2)) and open circuit voltage (V(oc) = 0.53 V), the colloidal quantum dot solar cell performance is still limited by a low fill factor of 0.50, which is believed to arise from charge transfer of photogenerated electrons to the aqueous electrolyte.
CdSe quantum dots (QDs) were adsorbed onto nanostructured films for different times by using a chemical bath deposition method in order to produce QD-sensitized solar cells (QDSSCs). Surface modification was done by coating ZnS onto the CdSe QDs. The optical absorption and current-voltage characteristics of these devices were studied. The size of the CdSe QDs increased with increasing adsorption time, and there was an optimum CdSe adsorption time for achieving the best photovoltaic conversion efficiency. The photovoltaic properties of short-circuit current density, open-circuit voltage, and photovoltaic conversion efficiency were significantly improved after modifying the surface with ZnS. Under a solar illumination of , an efficiency as high as 2.02% was achieved for the CdSe QDSSCs that were made by using this method.
Hybrid organic–inorganic perovskite (HOIP) photovoltaics have emerged as a promising new technology for the next generation of photovoltaics since their first development 10 years ago, and show a high-power conversion efficiency (PCE) of about 29.3%. The power-conversion efficiency of these perovskite photovoltaics depends on the base materials used in their development, and methylammonium lead iodide is generally used as the main component. Perovskite materials have been further explored to increase their efficiency, as they are cheaper and easier to fabricate than silicon photovoltaics, which will lead to better commercialization. Even with these advantages, perovskite photovoltaics have a few drawbacks, such as their stability when in contact with heat and humidity, which pales in comparison to the 25-year stability of silicon, even with improvements are made when exploring new materials. To expand the benefits and address the drawbacks of perovskite photovoltaics, perovskite–silicon tandem photovoltaics have been suggested as a solution in the commercialization of perovskite photovoltaics. This tandem photovoltaic results in an increased PCE value by presenting a better total absorption wavelength for both perovskite and silicon photovoltaics. In this work, we summarized the advances in HOIP photovoltaics in the contact of new material developments, enhanced device fabrication, and innovative approaches to the commercialization of large-scale devices.
1 September 2007 in Materials Science and Engineering: C