Dustin Chen

Intrinsically stretchable and transparent thin-film transistors based on printable silver nanowires, carbon nanotubes and an elastomeric dielectric

Thin-film field-effect transistor is a fundamental component behind various mordern electronics. The development of stretchable electronics poses fundamental challenges in developing new electronic materials for stretchable thin-film transistors that are mechanically compliant and solution processable. Here we report the fabrication of transparent thin-film transistors that behave like an elastomer film. The entire fabrication is carried out by solution-based techniques, and the resulting devices exhibit a mobility of ∼30 cm2 V−1 s−1, on/off ratio of 103–104, switching current >100 μA, transconductance >50 μS and relative low operating voltages. The devices can be stretched by up to 50% strain and subjected to 500 cycles of repeated stretching to 20% strain without significant loss in electrical property. The thin-film transistors are also used to drive organic light-emitting diodes. The approach and results represent an important progress toward the development of stretchable active-matrix displays.

Electronic Muscles and Skins: A Review of Soft Sensors and Actuators

This article reviews several classes of compliant materials that can be utilized to fabricate electronic muscles and skins. Different classes of materials range from compliant conductors, semiconductors, to dielectrics, all of which play a vital and cohesive role in the development of next generation electronics. This paper covers recent advances in the development of new materials, as well as the engineering of well-characterized materials for the repurposing in applications of flexible and stretchable electronics. In addition to compliant materials, this article further discusses the use of these materials for integrated systems to develop soft sensors and actuators. These new materials and new devices pave the way for a new generation of electronics that will change the way we see and interact with our devices for decades to come.

Flexible and stretchable electrodes for next generation polymer electronics: a review

Transparent conductive electrodes play a significant role in the fabrication and development of optoelectronic devices. As next generation optoelectronic devices tend towards mobile and wearable devices, the added attribute of flexibility or stretchability for these electrodes becomes increasingly important. However, mechanical requirements aside, transparent conductive electrodes must still retain high transparency and conductivity, with the metrics for these parameters being compared to the standard, indium tin oxide. In the search to replace indium tin oxide, two materials that have risen to the forefront are carbon nanotubes and silver nanowires due to their high transparency, conductivity, mechanical compliance, and ease of fabrication. This review highlights recent innovations made by our group in electrodes utilizing carbon nanotubes and silver nanowires, in addition to the use of these electrodes in discrete devices and integrated systems.

Highly flexible organometal halide perovskite quantum dot based light-emitting diodes on a silver nanowire–polymer composite electrode

Organometal halide perovskite light-emitting diodes (LEDs) have witnessed rapid development in a short time span due to the promising electronic and optical properties of perovskite materials, which showed great potential in flexible display devices due to their ease of integration in fabrication process flows. However, simply integrating perovskite films with flexible electrodes for highly flexible LEDs has encountered obstacles, as traditionally used perovskite films show unrecoverable micrometer-sized cracks after bending. Herein, we report on highly flexible LEDs by utilizing silver nanowire based polymer electrodes as anodes, and CH3NH3PbBr3 quantum dots as the emissive layer. The resulting devices are highly flexible and mechanically robust, capable of being bent to a 2.5 mm radius and capable of undergoing 1000 cycles of repeated bending and unbending to a radius of 4 mm without discernible performance degradation. Moreover, these flexible LEDs also exhibit high performance metrics, due in part to efficient charge balance through hole-injection enhancement, with a current efficiency of 10.4 cd A−1, a luminous efficacy of 8.1 lm W−1, and an external quantum efficiency of 2.6% at a brightness of 1000 cd m−2.

Spatial exciton allocation strategy with reduced energy loss for high-efficiency fluorescent/phosphorescent hybrid white organic light-emitting diodes

Due to the poor operational lifetime of blue phosphorescent dopants and blue thermally activated delayed fluorescent (TADF) materials, hybrid white organic light-emitting diodes (WOLEDs) with conventional blue fluorescent emitters are still preferred for commercial applications in general lighting. However, the improvement in the overall efficiency of hybrid WOLEDs has been limited due to energy losses during the energy transfer process and exciton quenching after the spatial separation of the singlet and triplet excitons. Here we demonstrate the development of a Spatial Exciton Allocation Strategy (SEAS) to achieve close to 100% internal quantum efficiency (IQE) in blue-yellow complementary color hybrid WOLEDs. The employed blue fluorophore not only has a resonant triplet level with the yellow phosphor to reduce energy loss during energy transfer processes and triplet–triplet annihilation (TTA), but also has a resonant singlet level with the electron transport layer to extend singlet exciton distribution and enhance both singlet and triplet exciton utilization. The resulting hybrid WOLEDs exhibited 104 lm W−1 efficacy at 100 cd m−2 and 74 lm W−1 at 1000 cd m−2 with CIE coordinates of (0.42, 0.44) which is warm white and suitable for indoor lighting.

Efficient One-Pot Synthesis of Colloidal Zirconium Oxide Nanoparticles for High-Refractive-Index Nanocomposites

Zirconium oxide nanoparticles are promising candidates for optical engineering, photocatalysis, and high-κ dielectrics. However, reported synthetic methods for the colloidal zirconium oxide nanoparticles use unstable alkoxide precursors and have various other drawbacks, limiting their wide application. Here, we report a facile one-pot method for the synthesis of colloidally stable zirconium oxide nanoparticles. Using a simple solution of zirconium trifluoroacetate in oleylamine, highly stable zirconium oxide nanoparticles have been synthesized with high yield, following a proposed amidization-assisted sol-gel mechanism. The nanoparticles can be readily dispersed in nonpolar solvents, forming a long-term stable transparent solution, which can be further used to fabricate high-refractive-index nanocomposites in both monolith and thin-film forms. In addition, the same method has also been extended to the synthesis of titanium oxide nanoparticles, demonstrating its general applicability to all group IVB metal oxide nanoparticles.

A new bistable electroactive polymer for prolonged cycle lifetime of refreshable Braille displays

ABSTRACT: Bistable electroactive polymers (BSEP) amalgamating electrically induced large-strain actuation and shape memory effect present a unique opportunity for refreshable Braille displays. A new BSEP material with long-chain crosslinkers to achieve prolonged cycle lifetime of refreshable Braille displays is reported here. The modulus of the BSEP material decreases by more than three orders of magnitude from a rigid, plastic state to a rubbery state when heated above the polymer’s glass transition temperature. In its rubbery state, the polymer film can be electrically actuated to buckle convexly when a high voltage is applied across a circular active area. Modifying the concentration of long-chain crosslinkers in the polymer allows not only for fine-tuning of the polymer’s glass transition temperature and elasticity in the rubbery state, but also enhancement of the actuation stability. For a raised height of 0.4 mm by a Braille dot with a 1.3 mm diameter, actuation can be repeated over 2000 cycles at 70°C in the rubbery state. The actuated dome shape can be fixed by cooling the polymer below the glass transition temperature. This refreshable rigid-to-rigid actuation simultaneously provides large-strain actuation and large force support. Devices capable of displaying Braille characters over a page-size area consisting of 324 Braille cells have been fabricated.

Transparent Ultra-High-Loading Quantum Dot/Polymer Nanocomposite Monolith for Gamma Scintillation

Spectroscopic gamma-photon detection has widespread applications for research, defense, and medical purposes. However, current commercial detectors are either prohibitively expensive for wide deployment or incapable of producing the characteristic gamma photopeak. Here we report the synthesis of transparent, ultra-high-loading (up to 60 wt %) CdxZn1-xS/ZnS core/shell quantum dot/polymer nanocomposite monoliths for gamma scintillation by in situ copolymerization of the partially methacrylate-functionalized quantum dots in a monomer solution. The efficient Förster resonance energy transfer of the high-atomic-number quantum dots to lower-band-gap organic dyes enables the extraction of quantum-dot-borne excitons for photon production, resolving the problem of severe light yield deterioration found in previous nanoparticle-loaded scintillators. As a result, the nanocomposite scintillator exhibited simultaneous improvements in both light yield (visible photons produced per MeV of gamma-photon energy) and gamma attenuation. With these enhancements, a 662 keV Cs-137 gamma photopeak with 9.8% resolution has been detected using a 60 wt % quantum-dot nanocomposite scintillator, demonstrating the potential of such a nanocomposite system in the development of high-performance low-cost spectroscopic gamma detectors.

Multi-Colored Light-Emitting Electrochemical Cells Based on Thermal Activated Delayed Fluorescence Host

Light-emitting electrochemical cells (LECs) with the thermally activated delayed fluorescence(TADF) host and phosphorescent guests were fabricated using solution process. It is demonstrated for the first time that TADF, a well-known phenomenon that helps to increase electroluminescence efficiency by harvesting excitons from triplet states, is used as a host in LECs. Devices with green, yellow, red and warm white emissions were fabricated, with the best devices showing more than 7000 cd/m2 stable emission and a peak efficiency over 7 cd/A. Under high voltage stress, a burst of extremely high luminance of over 30,000 cd/m2 was observed. All these LEC devices are extremely simple with only one active layer. Thus, our results could pave way to produce low- cost light source with high luminance, using TADF molecules.

Electrolyte-Gated Red, Green, and Blue Organic Light-Emitting Diodes

We report vertical electrolyte-gated red, green, and blue phosphorescent small-molecule organic light-emitting diodes (OLED), in which light emission was modified by tuning the electron injection via electrochemical doping of the electron injection layer 4,4-bis(N-carbazolyl)-1,1-biphenyl (CBP) under the assistance of a polymer electrolyte. These devices comprise an electrolyte capacitor on the top of a conventional OLED, with the interfacial contact between the electrolyte and electron injection layer CBP of OLEDs achieved through a porous cathode. These phosphorescent OLEDs exhibit the tunable luminance between 0.1 and 10 000 cd m-2, controlled by an applied bias at the gate electrode. This simple device architecture with gate-modulated luminance provides an innovative way for full-color OLED displays.