Publications by authors named "Wan-Ki Bae"

The limited operational lifetime of quantum-dot light-emitting diodes (QLEDs) poses a critical obstacle that must be addressed before their practical application. Specifically, cadmium-free InP-based QLEDs, which are environmentally benign, experience significant operational degradation due to challenges in charge-carrier confinement stemming from the composition of InP quantum dots (QDs). This study investigates the operational degradation of InP QLEDs and provides direct evidence of the degradation process.

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Quantum-dot (QD) light-emitting diodes (QLEDs) are garnering significant attention owing to their superb optoelectrical properties, but the overinjection of electrons compared to holes into the emissive layer (EML) is still a critical obstacle to be resolved. Current approaches, such as inserting a charge-balancing interlayer and mixing p-type organic additives into the EML, face issues of process complexity and poor miscibility. In this work, we demonstrate efficient InP QLEDs by simply embedding NiO nanoparticles (NPs) into the EML which forms a homogeneous QD-metal oxide hybrid EML.

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Article Synopsis
  • Positive aging significantly improves the electroluminescence characteristics of quantum-dot light-emitting diodes (QLEDs) by enhancing electron transport and reducing exciton quenching at the interfaces.
  • The use of ultraviolet-curable resin in encapsulation helps delay harmful reactions at the aluminum and zinc magnesium oxide interface, leading to better device performance over time.
  • The study revealed that after 120 hours, the external quantum efficiency of indium phosphide (InP) QLEDs increased from 3.16% to 12.04%, showcasing the positive aging effect and providing insights into the operating mechanisms of aging agents in QLEDs.
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Quantum dots (QDs) exhibit size-tunable optical properties, making them suitable for efficient light-sensing and light-emitting devices. Tandem devices that can convert near-infrared (NIR) to visible (Vis) signals can be fabricated by integrating an NIR-sensing QD device with a Vis electroluminescence (EL) QD device. However, these devices require delicate control of the QD layer during processing to prevent damage to the predeposited QD layers in tandem devices during the subsequent deposition of other functional layers.

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In colloidal quantum dot light-emitting diodes (QD-LEDs), replacing organic hole transport layers (HTLs) with their inorganic counterparts is expected to yield distinct advantages due to their inherent material robustness. However, despite the promising characteristics of all-inorganic QD-LEDs, some challenges persist in achieving stable operation; for example, the electron overflow toward the inorganic HTL and charge accumulation within working devices return a temporal inconsistency in device characteristics. To address these challenges, we propose an operational approach that employs an alternating-current (AC) in all-inorganic QD-LEDs.

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Structural deformation modifies the bandgap, exciton fine structure and phonon energy of semiconductors, providing an additional knob to control their optical properties. The impact can be exploited in colloidal semiconductor quantum dots (QDs), wherein structural stresses can be imposed in three dimensions while defect formation is suppressed by controlling surface growth kinetics. Yet, the control over the structural deformation of QDs free from optically active defects has not been reached.

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Gallium ion incorporation into silver indium gallium sulfide nanocrystals is investigated by various methods, including photoluminescence (PL) and X-ray photoelectron spectroscopy. The ZnS shell-growth enhances a PL quantum yield of up to 16%, with which the quantum dot light-emitting diode was successfully fabricated.

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Quantum dots (QDs) have garnered a significant amount of attention as promising memristive materials owing to their size-dependent tunable bandgap, structural stability, and high level of applicability for neuromorphic computing. Despite these advantageous properties, the development of QD-based memristors has been hindered by challenges in understanding and adjusting the resistive switching (RS) behavior of QDs. Herein, we propose three types of InP/ZnSe/ZnS QD-based memristors to elucidate the RS mechanism, employing a thin poly(methyl methacrylate) layer.

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Article Synopsis
  • - The shape and structure of heterostructured semiconductor nanocrystals (h-NCs) are crucial for determining how effectively they can transport charge and how they behave in photonic applications.
  • - There has been a challenge in managing the structure of III-V/II-VI h-NCs made of non-toxic materials, but this research focuses on controlling the growth of ZnSe layers on Indium Phosphide (InP) nanocrystals as a case study.
  • - By manipulating the growth rates of ZnSe on different surfaces of InP, the study achieves a desirable morphology that enhances the light-emitting properties of InP/ZnSe h-NCs, allowing them to be more adaptable for various applications in optics
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Active matrix (AM) quantum-dot light-emitting diodes (QLEDs) driven by thin-film transistors (TFTs) have attracted significant attention for use in next-generation displays. Several challenges remain for the realisation of AM-QLEDs, such as device design, fabrication process, and integration between QLEDs and TFTs, depending on their device structures and configurations. Herein, efficient and stable AM-QLEDs are demonstrated using conventional and inverted structured QLEDs (C- and I-QLEDs, respectively) combined with facile type-convertible (p- and n-type) single-walled carbon nanotube (SWNT)-based TFTs.

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Colloidal semiconductor nanomaterials present broadband, with large cross-section, two-photon absorption (2PA) spectra, which turn them into an important platform for applications that benefit from a high nonlinear optical response. Despite that, to date, the only means to control the magnitude of the 2PA cross-section is by changing the nanoparticle volume, as it follows a universal volume scale, independent of the material composition. As the emission spectrum is connected utterly to the nanomaterial dimensions, for a given material, the magnitude of the nonlinear optical response is also coupled to the emission spectra.

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Article Synopsis
  • Colloidal Ag(In,Ga)S nanocrystals (AIGS NCs) have gained significant interest due to their adjustable band gap based on size and composition, suitable for various photonic applications.
  • Despite their advantages, AIGS NCs previously exhibited low photoluminescence quantum yield (PL QY), but recent advancements in heteroepitaxy have led to AIGS-AgGaS core-shell NCs with near-unity PL QYs and improved stability.
  • This new structure effectively confines charge carriers through a Type I heterojunction, resulting in enhanced optical properties, making them promising candidates for practical uses in displays and luminescent solar concentrators.
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Semiconductor nanocrystals with an anisotropic morphology exhibit unique properties, most notably their linear polarization. The colloidal growth of semiconductor nanorods with core dots inside, also referred to as dot-in-rod (DIR) structure, has enabled the synthesis of anisotropic nanocrystals with better stability and controllable fluorescence polarization. In this study, we synthesize CdSe/CdS DIR nanocrystals, in which the position of the CdSe core particle can be controlled by using different ligand compositions during the CdS growth.

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One of the key phenomena that determine the fluorescence of nanocrystals is the nonradiative Auger-Meitner recombination of excitons. This nonradiative rate affects the nanocrystals' fluorescence intensity, excited state lifetime, and quantum yield. Whereas most of the above properties can be directly measured, the quantum yield is the most difficult to assess.

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Article Synopsis
  • * This paper introduces a new light extraction structure called the randomly disassembled nanostructure (RaDiNa), which enhances light output by applying a special film on top of TE-QLEDs, resulting in improved brightness and efficiency.
  • * The RaDiNa-attached TE-QLED displays a 60% increase in external quantum efficiency and demonstrates effective light extraction, paving the way for future commercialization and advancement of TE-QLED technology.
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Heteroepitaxy on colloidal semiconductor nanocrystals is an essential strategy for manipulating their optoelectronic functionalities. However, their practical synthesis typically leads to scattered and unexpected outcomes due to the intervention of multiple reaction pathways associated with complicated side products of reactants. Here, the heteroepitaxy mechanism of zinc chalcogenide initiated on indium phosphide (InP) colloidal nanocrystals is elucidated using the precursors, zinc carboxylate and trialkylphosphine selenide.

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Article Synopsis
  • ZnSeTe nanocrystals (NCs) exhibit tunable photon emission from violet to orange and high quantum yields, but face challenges like broad emission line widths and complex decay dynamics.
  • The study investigates the excitonic states in ZnSeTe NCs, revealing that local hole states created by differing electronegativity between Se and Te lead to spatially separated excitons.
  • Findings indicate that these excitonic characteristics result in both inhomogeneous and homogeneous line width broadening, highlighting the potential for future research and applications in photonics.
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  • Electroluminescence from quantum dots (QDs) can enhance future displays with vibrant, custom shapes and colors, but a new technique is needed to pattern these small structures nondestructively.* -
  • A novel approach using branched light-driven ligand crosslinkers (LiXers) allows for the creation of multicolored QD patterns on a micrometer scale without damaging the QDs' key properties.* -
  • This method preserves the photoluminescence and electroluminescence of QDs, extends their device lifespan, and is suitable for industrial application, potentially revolutionizing display technology with environmentally friendly materials.*
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Colloidal quantum dots (QDs) stand at the forefront of a variety of photonic applications given their narrow spectral bandwidth and near-unity luminescence efficiency. However, integrating luminescent QD films into photonic devices without compromising their optical or transport characteristics remains challenging. Here we devise a dual-ligand passivation system comprising photocrosslinkable ligands and dispersing ligands to enable QDs to be universally compatible with solution-based patterning techniques.

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Nanophotonics relies on precise control of refractive index (RI) which can be designed with metamaterials. Plasmonic superstructures of nanoparticles (NPs) can suggest a versatile way of tuning RI. However, the plasmonic effects in the superstructures demand 1 nm-level exquisite control over the interparticle gap, which is challenging in a sub-wavelength NPs.

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Article Synopsis
  • Interest in quantum dot light-emitting diodes (QLEDs) is growing due to their potential in improving display devices and light sources.
  • This study analyzes transient electroluminescence (TREL) signals from dichromatic QLEDs, which have two different color-emitting QD layers, to understand charge injection and exciton recombination.
  • The research also measures electron mobility and explores energy transfer and exciton quenching effects, aiming to enhance the understanding and performance of QLEDs.
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The state-of-the-art quantum dot (QD) based light-emitting diodes (QD-LEDs) reach near-unity internal quantum efficiency thanks to organic materials used for efficient hole transportation within the devices. However, toward high-current-density LEDs, such as augmented reality, virtual reality, and head-up display, thermal vulnerability of organic components often results in device instability or breakdown. The adoption of a thermally robust inorganic hole transport layer (HTL), such as NiO, becomes a promising alternative, but the large energy offset between the NiO HTL and the QD emissive layer impedes the efficient operation of QD-LEDs.

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Article Synopsis
  • * The study proposes a method to control the potential profile of these nanocrystals by manipulating dipole densities at their interface, which affects the vacuum-level shift and enhances their optical and electrical characteristics.
  • * Precise synthesis of h-NCs enables a direct correlation between interfacial dipole moments and the nanocrystals' stability and performance in photochemical and optoelectronic applications.
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Quantum dot light-emitting diodes (QLEDs) are one of the most promising candidates for next-generation displays and lighting sources, but they are barely used because vulnerability to electrical and thermal stresses precludes high brightness, efficiency, and stability at high current density (J) regimes. Here, bright and stable QLEDs on a Si substrate are demonstrated, expanding their potential application boundary over the present art. First, a tailored interface is granted to the quantum dots, maximizing the quantum yield and mitigating nonradiative Auger decay of the multiexcitons generated at high-J regimes.

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