Water/alcohol-soluble conjugated polymers (WSCPs) and small molecules (WSCSs) are materials that can be processed from water or other polar solvents. They provide good opportunities to fabricate multilayer organic optoelectronic devices without interface mixing by solution processing, and exhibit a promising interface modification ability for metal or metal oxide electrodes to greatly enhance the device performance of solar cells. Moreover, owing to their intriguing processability, WSCPs and WSCSs have great potential for applying environmentally friendly processing technologies to fabricate solar cells. In this review, the authors give an overview of recent developments in WSCPs and WSCSs, including their molecular design, material synthesis, functional principles and application as interface modification layers and photoactive components in emerging photovoltaic technologies such as organic/polymer solar cells, organic-inorganic hybrid solar cells and dye-sensitised solar cells.
Bulk-heterojunction polymer solar cells have emerged as an attractive type of cost-effective solar energy-electrical power transforming device. Recently, great progress in the development of new photo-harvesting materials and device optimizations have been achieved in this field, resulting in the significant improvement of the power conversion efficiencies of polymer solar cells from around 1% to higher than 8.0%. The rational design and fine tailoring of the molecular structures of donor polymers significantly contributed to these prominent advances. Among all kinds of donor polymers, push-pull conjugated polymers, which consist of alternating electron-rich and electron-deficient units have been most extensively developed and have dominated the library of donor materials for polymer solar cells, because their intrinsic optical and electronic properties can be readily tuned to the desired situation by controlling the intramolecular charge transfer from donor unit to acceptor unit. This review provides a brief overview of the recent development of push-pull conjugated polymers and their application in solar cells. The relationships between the materials' chemical structures and properties, such as absorption spectra, energy levels, mobilities and photovoltaic behaviors, were also discussed.
Organic light-emitting diodes (OLEDs) have been successfully developed and have now entered the commercial marketplace. Besides the impressive performance as displays, one of the key advantages of OLEDs is that they can potentially be made entirely by solution process and thus are more suitable for low cost, large area flexible displays and white lighting panels. To realize this, many efforts have been devoted on the development of solution processable light-emitting materials and charge transporting materials as well as electrode materials, which have resulted in the successful demonstration of high performance fully solution processed OLEDs and have opened a way to achieve all printable roll-to-roll organic optoelectronic devices.
The effects of Au nanoparticles (NPs) incorporated into the active layer of polymer solar cells (PSCs) with a newly synthesized donor polymer are investigated in detail. Our work shows that localized surface plasmonic resonance (LSPR) introduced by the metallic NPs can experimentally and theoretically enhance the light absorption in the active layer of PSCs because the strong LSPR near field mainly distributes laterally along the active layer. The understanding can be applied to other metallic NPs incorporated organic solar cells. Meanwhile, our results show that electrical properties can counter-diminish the optical enhancement from LSPR and thus reduces the overall performance improvement. It is important that both optical and electrical properties need to be studied and optimized simultaneously for achieving improved power conversion efficiency. The study contributes to better understanding on the uses of Au NPs for enhancing PSC performances.
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