A multilayer of CdSe quantum dots (QDs) was prepared on the mesoporous surface of a nanoparticulate TiO(2) film by a layer-by-layer (LBL) assembly using the electrostatic interaction of the oppositely charged QD surface for application as a sensitizer in QD-sensitized TiO(2) solar cells. To maximize the absorption of incident light and the generation of excitons by CdSe QDs within a fixed thickness of TiO(2) film, the experimental conditions of QD deposition were optimized by controlling the concentration of salt added into the QD-dissolved solutions and repeating the LBL deposition a few times. A proper concentration of salt was found to be critical in providing a deep penetration of QDs into the mesopore, thus leading to a dense and uniform distribution throughout the whole TiO(2) matrix while anchoring the oppositely charged QDs alternately in a controllable way. A series of post-treatments with (1) CdCl(2), (2) thermal annealing, and (3) ZnS-coating was found to be very critical in improving the overall photovoltaic properties, presumably through a better connection between QDs, effective passivation of QD's surface, and a high impedance of recombination, which were proved by transmission electron microscopy (TEM) and electrochemical impedance spectroscopy (EIS) experiments. With a proper post-treatment of multilayered QDs as a sensitizer, the overall power conversion efficiency in the CdSe QD-sensitized TiO(2) solar cells could reach 1.9% under standard illumination condition of simulated AM 1.5G (100 mW/cm(2)).

The ability to image pressure distribution over complex three-dimensional surfaces would significantly augment the potential applications of electronic skin. However, existing methods show poor spatial and temporal fidelity due to their limited pixel density, low sensitivity, or low conformability. Here, we report an ultraflexible and transparent electroluminescent skin that autonomously displays super-resolution images of pressure distribution in real time. The device comprises a transparent pressure-sensing film with a solution-processable cellulose/ nanowire nanohybrid network featuring ultrahigh sensor sensitivity (>5000 kPa −1 ) and a fast response time (<1 ms), and a quantum dot-based electroluminescent film. The two ultrathin films conform to each contact object and transduce spatial pressure into conductivity distribution in a continuous domain, resulting in super-resolution (>1000 dpi) pressure imaging without the need for pixel structures. Our approach provides a new framework for visualizing accurate stimulus distribution with potential applications in skin prosthesis, robotics, and advanced human-machine interfaces.

Two different quantum dots (QDs) with an identical optical band gap were prepared: one without the inorganic shell and short surface ligands (BQD) and the other with thick inorganic shells and long surface ligands (OQD). They were surface-derivatized to be positively or negatively charged and were used for layer-by-layer assemblies on TiO2. By sandwiching BQD between OQD and TiO2, OQD photoluminescence showed seven times faster decay, which is attributed to the combined effect of the efficient energy transfer from OQD to BQD with the FRET efficiency of 86% and fast electron transfer from BQD to TiO2 with the rate of 1.2 × 10(9) s(-1). The QD bilayer configuration was further applied to solar cells, and showed 3.6 times larger photocurrent and 3.8 times larger photoconversion efficiency than those of the device with the OQD being sandwiched by BQD and TiO2. This showcases the importance of sophisticated control of QD layer assembly for the design of efficient QD solar cells.

The reversible resistance switching (RS) effect of the Al/TiOx/TiO2/Al heterostructure is investigated in this study. This RS was attributed to space-charge-limited conduction (SCLC) as controlled by localized traps in the TiOx layer. The preexisting SCLC theory was extended to describe the abrupt resistance transition. An analytical model was developed with consideration of the ratio of free and trapped carrier density, which was extracted from the experimental data to show exponentially distributed traps in energy. The proposed model can be applicable to RS phenomena induced by interface-type traps in other material system.

Three inorganic capping ligands (ICLs) for quantum dots (QDs), SnS4(4-), SbS4(3-) and AsS3(3-), were synthesized and the energy levels determined. Proximity between the ICL LUMO and QD conduction level governed the electronic couplings such as absorption shift upon ligand exchange, and electron transfer rate to TiO2. QD-sensitized solar cells were fabricated, using the ICL-QDs and also using QD multilayers layer-by-layer assembled by bridging coordinations, and studied as a function of the ICL ligand and the number of QD layers.

In this work, we report on blue organic light emitting devices (OLEDs), which have multilayered graphene as its anode. Our graphene films have been grown catalytically and transferred to the support. The fabricated blue OLEDs with graphene anode showed outstanding external quantum efficiency of 15.6% and power efficiency of 24.1 lm/W at 1000 cd/m2. Weak oxygen plasma treatments on graphene film surfaces improved the injection property between the anode and hole injection layer.

We demonstrate independently and simultaneously controlled color-tunable organic light-emitting diodes (OLEDs) with vertically stacked blue, green, and red elements. The blue, green, and red elements were placed at the bottom, middle, and top positions, respectively, forming color-tunable OLEDs. The independently driven blue, green, and red elements in the color-tunable OLEDs exhibited low driving voltages of 5.3 V, 3.0 V, and 4.6 V, as well as high external quantum efficiencies of 11.1%, 10.9%, and 9.6%, respectively, at approximately 1000 cd/m. Each element in the color-tunable OLEDs showed high-purity blue, green, and red colors with little parasitic emission owing to the delicately designed device structure resultant from optical simulations. The color-tunable OLEDs could produce any colors inside the triangle formed with blue (0.136, 0.261), green (0.246, 0.697), and red (0.614, 0.386) Commission Internationale de l'éclairage (CIE) 1931 color coordinates. In addition, the correlated color temperatures (CCTs) of white colors in the color-tunable OLED can be easily changed from the warm white to the cool white by controlling the red, green, and blue emissions simultaneously. The white colors in the color-tunable OLED have the CIE 1931 color coordinate of (0.304, 0.351), with a CCT of 6289 K and (0.504, 0.440), with a CCT of 2407K at the driving voltage of 5 V (blue), 2.8 V (green), 4.4 V (red), and 4.6 V (blue), 3 V (green), 5 V (red), respectively. Furthermore, the white color in the color-tunable OLED exhibited a high color rendering index (~88.7) due to vertically stacked three color system. Moreover, we successfully fabricated a large-sized, 14 × 12 pixel array of the color-tunable OLEDs to demonstrate lighting and display applications, respectively.

Photoswitching or modulation of quantum dots (QDs) can be promising for many fields that include display, memory, and super-resolution imaging. However, such modulations have mostly relied on photomodulations of conjugated molecules in QD vicinity, which typically require high power of high energy photons at UV. We report a visible light-induced facile modulation route for QD-dye conjugates. QD crystal violets conjugates (QD-CVs) were prepared and the crystal violet (CV) molecules on QD quenched the fluorescence efficiently. The fluorescence of QD-CVs showed a single cycle of emission burst as they go through three stages of (i) initially quenched "off" to (ii) photoactivated "on" as the result of chemical change of CVs induced by photoelectrons from QD and (iii) back to photodarkened "off" by radical-associated reactions. Multicolor on-demand photopatterning was demonstrated using QD-CV solid films. QD-CVs were introduced into cells, and excitation with visible light yielded photomodulation from "off" to "on" and "off" by nearly ten fold. Individual photoluminescence dynamics of QD-CVs was investigated using fluorescence correlation spectroscopy and single QD emission analysis, which revealed temporally stochastic photoactivations and photodarkenings. Exploiting the stochastic fluorescence burst of QD-CVs, simultaneous multicolor super-resolution localizations were demonstrated.