Quality Index for Stereoscopic Images by Separately Evaluating Adding and Subtracting

The human visual system (HVS) plays an important role in stereo image quality perception. Therefore, it has aroused many people’s interest in how to take advantage of the knowledge of the visual perception in image quality assessment models. This paper proposes a full-reference metric for quality assessment of stereoscopic images based on the binocular difference channel and binocular summation channel. For a stereo pair, the binocular summation map and binocular difference map are computed first by adding and subtracting the left image and right image. Then the binocular summation is decoupled into two parts, namely additive impairments and detail losses. The quality of binocular summation is obtained as the adaptive combination of the quality of detail losses and additive impairments. The quality of binocular summation is computed by using the Contrast Sensitivity Function (CSF) and weighted multi-scale (MS-SSIM). Finally, the quality of binocular summation and binocular difference is integrated into an overall quality index. The experimental results indicate that compared with existing metrics, the proposed metric is highly consistent with the subjective quality assessment and is a robust measure. The result have also indirectly proved hypothesis of the existence of binocular summation and binocular difference channels

Self-assembly of CdTe tetrapods into network monolayers at the air/water interface

Cadmium telluride (CdTe) tetrapods are synthesized with varying aspect ratios through multiple injections of the Te precursor, which provides an excellent means of controlling and tailoring the optical properties of the tetrapods. The self-assembly of CdTe tetrapods at the air/water interface is explored using the Langmuir-Blodgett (LB) technique due to potential use in solar cells arising from the intriguing tetrapod shape that improves charge transport and the optimum band gap energy of CdTe that enhances light absorption. Interestingly, the Langmuir isotherm shows two pressure plateau regions: one at ∼10 mN/m with the other at the high surface pressure of ∼39 mN/m. LB deposition at various pressures allows the discernment of the unique two-dimensional packing alluded in the isotherm. By placing CdTe at the air/water interface, it is revealed in the deposition that the tetrapods experienced a dewetting phenomenon, forming a ribbon structure at the onset of surface pressure with a height corresponding to the length of one tetrapod arm. With the increase of surface pressure, the ribbons widen to an eventual large-scale percolated network pattern. The packing density of tetrapods is successfully manipulated by controlling the surface pressure, which may find promising applications in optoelectronic devices

Optimization of molecular organization and nanoscale morphology for high performance low bandgap polymer solar cells

Air Force Office of Scientific Research [FA9550-13-1-0101]; National Science Foundation [ECCS-1305087]; Minjiang Scholar Program; Chinese Scholarship Council (CSC)Rational design and synthesis of low bandgap (LBG) polymers with judiciously tailored HOMO and LUMO levels have emerged as a viable route to high performance polymer solar cells with power conversion efficiencies (PCEs) exceeding 10%. In addition to engineering the energy-level of LBG polymers, the photovoltaic performance of LBG polymer-based solar cells also relies on the device architecture, in particular the fine morphology of the photoactive layer. The nanoscale interpenetrating networks composed of nanostructured donor and acceptor phases are the key to providing a large donor-acceptor interfacial area for maximizing the exciton dissociation and offering a continuous pathway for charge transport. In this Review Article, we summarize recent strategies for tuning the molecular organization and nanoscale morphology toward an enhanced photovoltaic performance of LBG polymer-based solar cells

Organic−Inorganic Nanocomposites via Directly Grafting Conjugated Polymers onto Quantum Dots

Nanocomposites of poly(3-hexylthiophene)−cadmium selenide (P3HT−CdSe) were synthesized by directly grafting vinyl-terminated P3HT onto [(4-bromophenyl)methyl]dioctylphosphine oxide (DOPO-Br)-functionalized CdSe quantum dot (QD) surfaces via a mild palladium-catalyzed Heck coupling, thereby dispensing with the need for ligand exchange chemistry. The resulting P3HT−CdSe nanocomposites possess a well-defined interface, thus significantly promoting the dispersion of CdSe within the P3HT matrix and facilitating the electronic interaction between these two components. The photophysical properties of nanocomposites were found to differ from the conventional composites in which P3HT and CdSe QDs were physically mixed. Solid-state emission spectra of nanocomposites suggested the charge transfer from P3HT to CdSe QDs, while the energy transfer from 3.5 nm CdSe QD to P3HT was implicated in the P3HT/CdSe composites. A faster decay in lifetime further confirmed the occurrence of charge transfer in P3HT−CdSe nanocomposites

High efficiency perovskite solar cells: from complex nanostructure to planar heterojunction

Air Force Office of Scientific Research [FA9550-13-1-0101]Perovskite solar cells have garnered great attention in recent years as promising high performance next-generation solar cells with long-term stability at low cost. Since the seminal work of Miyasaka and others in 2009, the power conversion efficiency (PCE) of perovskite-based dye-sensitized solar cells (DSSCs) has rapidly increased from 3.8% to 15% over the past four years, exceeding the highest efficiency of conventional organic dye-sensitized DSSCs. Recently, the perovskite has been demonstrated to act successfully as an active layer in simple planar-heterojunction solar cells with no need of complex nanostructured DSSC architectures, leading to an attractively high PCE of 15.4% at a competitive low manufacturing cost. In this Feature Article, we aim to review the recent impressive development in perovskite solar cells, and discuss the prognosis for future progress in exploiting perovskite materials for high efficiency solar cells

Garden-like perovskite superstructures with enhanced photocatalytic activity

Chinese Scholarship Council; National Natural Science Foundation of China [51072170, 21021002]; National Basic Research Program of China [2012CB932900]; Minjiang Scholar Program and Georgia Institute of TechnologyBy subjecting amorphous flower-like TiO2 to a facile hydrothermal synthesis in the presence of Sr2+, garden-like perovskite SrTiO3 superstructures were achieved. The amorphous TiO2 was preformed using ZnO flowers as templates. Different three-dimensional SrTiO3 architectures were coexisted in the garden, including SrTiO3 flowers composed of several hollow sword-shaped petals, many sheet-shaped petals or numerous flake-shaped petals, and SrTiO3 grass consisting of a number of long blades. These SrTiO3 superstructures were simultaneously grown on fluorine-doped tin oxide (FTO) substrates. On the basis of a comprehensive study on the effects of growth time, temperature, initial concentrations of precursor, and pH, the formation of these various hierarchical architectures was attributed primarily to the dissolution of amorphous TiO2 and precipitation of perovskite crystals, followed by the Ostwald ripening process of perovskite nanocrystals and self-organization of perovskite building blocks. Interestingly, this approach can be readily extended to create other perovskite structures, including dendritic BaTiO3 and nest-like CaTiO3, as well as PbTiO3 transformed from plate-like pyrochlore Pb2Ti2O6 after post-thermal treatment. Garden-like SrTiO3 superstructures showed a superior photocatalytic performance when compared to other as-prepared semiconductors and perovskite materials (i.e., ZnO, TiO2, BaTiO3, CaTiO3 and PbTiO3), probably due to their intrinsic photocatalytic activity and special garden-like features with a coexistence of various structures that significantly facilitated the adsorption and diffusion of methyl blue (MB) molecules and oxygen species in the photochemical reaction of MB degradation

Semiconductor hierarchically structured flower-like clusters for dye-sensitized solar cells with nearly 100% charge collection efficiency

Georgia Institute of TechnologyBy combining the ease of producing ZnO nanoflowers with the advantageous chemical stability of TiO2, hierarchically structured hollow TiO2 flower-like clusters were yielded via chemical bath deposition (CBD) of ZnO nanoflowers, followed by their conversion into TiO2 flower-like clusters in the presence of TiO2 precursors. The effects of ZnO precursor concentration, precursor amount, and reaction time on the formation of ZnO nanoflowers were systematically explored. Dye-sensitized solar cells fabricated by utilizing these hierarchically structured ZnO and TiO2 flower clusters exhibited a power conversion efficiency of 1.16% and 2.73%, respectively, under 100 mW cm(-2) illumination. The intensity modulated photocurrent/photovoltage spectroscopy (IMPS/IMVS) studies suggested that flower-like structures had a fast electron transit time and their charge collection efficiency was nearly 100%

p-n Heterojunction photoelectrodes composed of Cu2O-loaded TiO2 nanotube arrays with enhanced photoelectrochemical and photoelectrocatalytic activities

National Natural Science Foundation of China [51072170, 21021002]; Natural Science Foundation of Fujian Province of China [2011J01057]; Georgia Institute of TechnologyCu2O/TiO2 p-n heterojunction photoelectrodes were prepared by depositing different amounts of p-type Cu2O nanoparticles on n-type TiO2 nanotube arrays (i.e., forming Cu2O/TiO2 composite nanotubes) via an ultrasonication-assisted sequential chemical bath deposition. The success of deposition of Cu2O nanoparticles was corroborated by structural and composition characterizations. The enhanced absorption in the visible light region was observed in Cu2O/TiO2 composite nanotubes. The largely improved separation of photogenerated electrons and holes was revealed by photocurrent measurements. Consequently, Cu2O/TiO2 heterojunction photoelectrodes exhibited a more effective photoconversion capability than TiO2 nanotubes alone in photoelectrochemical measurements. Furthermore, Cu2O/TiO2 composite photoelectrodes also possessed superior photoelectrocatalytic activity and stability in the degradation of Rhodamine B. Intriguingly, by selecting an appropriate bias potential, a synergistic effect between electricity and visible light irradiation can be achieved

Block copolymer/ferroelectric nanoparticle nanocomposites

Nanocomposites composed of diblock copolymer/ferroelectric nanoparticles were formed by selectively constraining ferroelectric nanoparticles (NPs) within diblock copolymer nanodomains via judicious surface modification of ferroelectric NPs. Ferroelectric barium titanate (BaTiO3) NPs with different sizes that are permanently capped with polystyrene chains (i.e., PS-functionalized BaTiO3NPs) were first synthesized by exploiting amphiphilic unimolecular star-like poly(acrylic acid)-block-polystyrene (PAA-b- PS) diblock copolymers as nanoreactors. Subsequently, PS-functionalized BaTiO3 NPs were preferentially sequestered within PS nanocylinders in the linear cylinder-forming polystyrene-block-poly(methyl methacrylate) (PS-b-PMMA) diblock copolymer upon mixing the BaTiO3 NPs with PS-b-PMMA. The use of PS-b-PMMA diblock copolymers, rather than traditional homopolymers, offers the opportunity for controlling the spatial organization of PS-functionalized BaTiO3 NPs in the PS-b-PMMA/BaTiO3 NP nanocomposites. Selective solvent vapor annealing was utilized to control the nanodomain orientation in the nanocomposites. Vertically oriented PS nanocylinders containing PS-functionalized BaTiO3 NPs were yielded after exposing the PS-b-PMMA/BaTiO3 NP nanocomposite thin film to acetone vapor, which is a selective solvent for PMMA block. The dielectric properties of nanocomposites in the microwave frequency range were investigated. The molecular weight of PS-b-PMMA and the size of BaTiO3 NPs were found to exert an apparent influence on the dielectric properties of the resulting nanocomposites