ABSTRACT
Recently, polymeric carbon nitride (g-C3 N4 ) as a proficient photo-catalyst has been effectively employed in photocatalysis for energy conversion, storage, and pollutants degradation due to its low cost, robustness, and environmentally friendly nature. The critical review summarized the recent development, fundamentals, nanostructures design, advantages, and challenges of g-C3 N4 (CN), as potential future photoactive material. The review also discusses the latest information on the improvement of CN-based heterojunctions including Type-II, Z-scheme, metal/CN Schottky junctions, noble metal@CN, graphene@CN, carbon nanotubes (CNTs)@CN, metal-organic frameworks (MOFs)/CN, layered double hydroxides (LDH)/CN heterojunctions and CN-based heterostructures for H2 production from H2 O, CO2 conversion and pollutants degradation in detail. The optical absorption, electronic behavior, charge separation and transfer, and bandgap alignment of CN-based heterojunctions are discussed elaborately. The correlations between CN-based heterostructures and photocatalytic activities are described excessively. Besides, the prospects of CN-based heterostructures for energy production, storage, and pollutants degradation are discussed.
ABSTRACT
Perovskite solar cells have attracted significant attention due to their high efficiency and low cost. In the research on methylammonium lead-iodide (CH3NH3PbI3), a lot of work has been devoted to optimize the film morphology and crystallinity resulting in an enhancement of the power conversion efficiency (PCE). A good surface coverage and uniform perovskite films are highly desirable along with a smooth and pinhole-free contact between the hole and electron extraction layers. Overall, this affects the charge transport and collection, and reduces charge recombination. Herein, we demonstrate a facile route to control perovskite crystallization by inserting an optimal amount of insulating polystyrene in the perovskite precursor solutions. The incorporation of a small amount of polystyrene results in much better surface coverage, and a smoother and uniform perovskite thin film leading to improved crystallization and larger grain size. Via careful optimization, and easy and low temperature solution-based processing, below 100 °C, we realize a device with PCE exceeding 13% along with significantly reduced leakage current.
ABSTRACT
Hybrid halide perovskite solar cells were first demonstrated in 2009 with cell efficiency quickly soaring from below 10% to more than 23% in a few years. Halide perovskites have the desirable processing simplicity but are very fragile when exposed to water and heat. This fragility represents a great challenge for the achievement of their full practical potential in photovoltaic technologies. To address this problem, here we review the recent development of the mixed-dimensional perovskites, whereby the trade-off between power conversion efficiency and stability of the material can be finely tuned using organic amine cations with different sizes and functionalities.
ABSTRACT
The development of transition metal complexes for application in light-emitting devices is currently attracting significant research interest. Among phosphorescent emitters, those involving iridium (III) complexes have proven to be exceedingly useful due to their relatively short triplet lifetime and high phosphorescence quantum yields. The emission wavelength of iridium (III) complexes significantly depends on the ligands, and changing the electronic nature and the position of the ligand substituents can control the properties of the ligands. In this chapter, we discuss recent developments of phosphorescent transition metal complexes for organic light-emitting diode applications focusing solely on the development of iridium metal complexes.
Subject(s)
Fluorescent Dyes/chemistry , Iridium/chemistry , Light , Organometallic Compounds/chemistry , Luminescent MeasurementsABSTRACT
Solution processed zirconium acetylacetonate (Zr(acac)) is successfully employed as an electron extraction layer, replacing conventional titanium oxide, in planar CH3NH3PbI3 perovskite solar cells. The as-prepared Zr(acac) film possesses high transparency, high conductivity, a smooth morphology, high wettability, compatibility with PbI2 DMF solution, and an energy level matching that of CH3NH3PbI3 perovskite material. An average power conversion efficiency of about 11.93%, along with a high fill factor of 74.36%, an open circuit voltage of 1.03 V, and a short-circuit current density of 15.58 mA cm(-2) is achieved. The overall performance of the devices is slight better than that of cells using ruthenium acetylacetonate (Ru(acac)). The differences between solar cells with different electron extraction layers in charge recombination, charge transport and transfer and lifetime are further explored and it is demonstrate that Zr(acac) is a more effective and promising electron extraction layer. This work provides a simple, and cost effective route for the preparation of an effective hole extraction layer.
