Interfacial Exciton Research Articles

Long-Range Charge Transport Facilitated by Electron Delocalization in MoS2 and Carbon Nanotube Heterostructures.

Controlling charge transport at the interfaces of nanostructures is crucial for their successful use in optoelectronic and solar energy applications. Mixed-dimensional heterostructures based on single-walled carbon nanotubes (SWCNTs) and transition metal dichalcogenides (TMDCs) have demonstrated exceptionally long-lived charge-separated states. However, the factors that control the charge transport at these interfaces remain unclear. In this study, we directly image charge transport at the interfaces of single- and multilayered MoS2 and (6,5) SWCNT heterostructures using transient absorption microscopy. We find that charge recombination becomes slower as the layer thickness of MoS2 increases. This behavior can be explained by electron delocalization in multilayers and reduced orbital overlap with the SWCNTs, as suggested by nonadiabatic (NA) molecular dynamics (MD) simulations. Dipolar repulsion of interfacial excitons results in rapid density-dependent transport within the first 100 ps. Stronger repulsion and longer-range charge transport are observed in heterostructures with thicker MoS2 layers, driven by electron delocalization and larger interfacial dipole moments. These findings are consistent with the results from NAMD simulations. Our results suggest that heterostructures with multilayer MoS2 can facilitate long-lived charge separation and transport, which is promising for applications in photovoltaics and photocatalysis.

Plasmon-Exciton Strong Coupling in Single-Molecule Junction Electroluminescence.

Single molecules bridging two metallic electrodes can emit light through electroluminescence when subjected to a bias voltage. Typically, light emission in such devices results from transitions between molecular states, although in the presence of light-matter coupling, the emission can result from a transition between hybrid light-matter states. Here, we create single metal-molecule-metal junctions and simultaneously collect conductance and electroluminescence data using a scanning tunneling microscope (STM) equipped with a custom spectrometer. Through experimental analysis and electronic structure calculations, we provide evidence for a molecule-electrode interfacial exciton coupled to a junction cavity plasmon. Importantly, we find that close to resonant transport conditions, the molecular junction functions as a single emitter that is strongly coupled to the junction cavity mode, leading to characteristic Rabi splitting of the emission spectrum and providing the first example of an electroluminescence-driven single-molecule system in the regime of strong light-matter coupling.

(Invited) Exciton Dissociation in Mixed-Dimensionality SWCNT-Based Heterojunctions

Quantum-confined semiconductors provide highly tunable optical and electrical properties for a wide variety of emerging applications. Semiconducting single-walled carbon nanotubes (s-SWCNTs) have shown tremendous potential in applications ranging from digital logic, biological imaging, quantum information processing, photovoltaics, and thermoelectric energy harvesting. Energy harvesting applications rely critically upon the creation of tailored interfaces that enable the movement of energetic species (excitons, electrons, holes) in specified directions. In this talk, I will discuss the use of a variety of rationally designed “mixed-dimensionality” heterojunctions between s-SWCNTs and transition metal dichalcogenide (TMDC) monolayers to harvest visible/near-infrared photons and convert these excitations into long-lived charge-separated states. Type-II heterojunctions between s-SWCNTs and TMDCs enable rapid exciton dissociation and microsecond charge-separated state lifetimes. We have developed new TMDC/SWCNT/TMDC trilayer architectures that enable charge transfer cascades for improving charge separation yield and lifetime. These trilayer architectures allow us to probe out-of-plane carrier diffusion in the nanotube layer and the degree to which bound interfacial excitons impact the photophysics in these mixed-dimensionality heterostructures. I will also discuss the methodology by which we attempt to quantify the photoinduced exciton dissociation quantum yields in these nanoscale heterostructures. Using several heterostructure results, we are attempting to narrow in on appropriate ways to quantify the local dielectric constant and exciton size in both the SWCNT and TMDC components, each of which impact the estimated charge carrier yields. Taken together, these studies provide fundamental insights into the links between ground-state thermodynamics and excited-state dynamics for model nanoscale heterojunctions used to harvest solar energy and produce long-lived charge-separated states.

Tailoring Niox/Perovskite Interface via a Multifunctional Self‐Assembled Molecule for High‐Performance Blue Perovskite Light‐Emitting Diodes

Nickel oxide (NiOx) serves as one of the most promising hole transport materials for perovskite light‐emitting diodes (PeLEDs). However, only moderate PeLED performances have been reported on the pristine NiOx layer due to insufficient hole injection, interfacial exciton quenching, and poor perovskite quality. Herein, a multifunctional molecule of 3‐mercapto‐1‐propanesulfonate (MPS) is demonstrated to successfully tailor the NiOx–perovskite heterogenous interface by addressing the above issues. In detail, the large binding energy between mercapto sulfur and nickel induces preferential self‐assembly of the mercapto group on the NiOx surface, which simultaneously enlarges the NiOx work function by the formation of interfacial dipole and suppresses the trap‐assisted exciton quenching by the passivation of the oxygen vacancies. Meanwhile, the self‐assembled MPS on NiOx also favors high‐quality perovskite films with good morphology, high crystallinity, and reduced defects for efficient carrier radiative recombination. As a result, blue PeLEDs show a remarkable efficiency of 10.4%, representing one of the highest efficiencies for NiOx‐based blue PeLEDs, as well as a very low turn‐on voltage of 2.8 V. Consequently, this work contributes to an efficient approach to tailor the NiOx–perovskite interface for highly efficient blue PeLEDs.

Enhanced visible light harvesting in dye-sensitized solar cells through incorporation of solution-processable silver plasmons and anthracite-derived graphene quantum dots

The major setback for the enhanced performance of DSSC is the narrow absorption window and the interfacial exciton recombination. Therefore, in this work, the photovoltaic performance of dye-sensitized solar cells has been improved by the synergistic effect of anthracite-derived graphene quantum dots and silver plasmons. GQD and Ag coupled photoanodes were fabricated by a facile solution processable process under room temperature. The as-fabricated DSSC TiO2/Ag/GQD (TAG) exhibited an enhanced power conversion efficiency of 10.5 % with a current density of 22.40 mAcm−2 measured under solar irradiation of 100 mWcm−2 with AM 1.5G. An enhancement surpassing 30.5 % was obtained for the champion cell when compared to the pristine TiO2 based DSSC. Furthermore, this study emphasizes developing a cutting-edge approach for the high-quality use of fossil fuel-derived graphene quantum dots in energy conversion systems, thereby encouraging the green conversion of fossil fuels and broadening the potential of anthracite coal's utilization in energy conversion applications.

Shelf-Stable Green and Blue Quantum Dot Light-Emitting Diodes with High Efficiencies.

Quantum dot light-emitting diodes (QLEDs) are promising electroluminescent devices for next-generation display and solid-state lighting technologies. Achieving shelf-stable and high-performance QLEDs is crucial for their practical applications. However, the successful demonstration of shelf-stable QLEDs with high efficiencies is limited to red devices. Here, we developed a solution-based amine ligand exchange strategy to passivate the surfaces of optical ZnO (O-ZnO) nanocrystals, leading to suppressed exciton quenching at the green and blue QD/oxide interface. Furthermore, we designed new bilayered oxide electron-transporting layers consisting of amine-modified O-ZnO/conductive ZnO. This design simultaneously offers suppressed interfacial exciton quenching and sufficient electron transport in the green and blue QLEDs, resulting in shelf-stable green and blue devices with high efficiencies. Our devices exhibit neglectable changes in external quantum efficiencies (maximum external quantum efficiencies of 22.4% for green and 14.3% for blue) after storage for 270 days. Our work represents a step forward in the practical applications of QLED technology.

Charge Transfer in Graphene-MoS2 Vertical Heterostructures Tuned by Stacking Order and Substrate-Introduced Electric Field.

Vertical van der Waals heterostructures composed of graphene (Gr) and transition metal dichalcogenides (TMDs) have created a fascinating platform for exploring optical and electronic properties in the two-dimensional limit. Numerous studies have focused on Gr/TMDs heterostructures to elucidate the underlying mechanisms of charge-energy transfer, quasiparticle formation, and relaxation following optical excitation. Nevertheless, a comprehensive understanding of interfacial charge separation and subsequent dynamics in graphene-based heterostructures remains elusive. Here, we have investigated the carrier dynamics of Gr-MoS2 heterostructures (including Gr/MoS2 and MoS2/Gr stacking sequences) grown on a fused silica substrate under varying photoexcitation energies by comprehensive ultrafast means, including time-resolved terahertz (THz) spectroscopy, THz emission spectroscopy, and transient absorption spectroscopy. Our findings highlight the impact of the substrate electric field on the efficiency of modulating the interfacial charge transfer (CT). Specifically, the optical excitation in Gr/MoS2 generates thermal electron injection from the graphene layer into the MoS2 layer with photon energy well below A-exciton of MoS2, whereas the interfacial CT in the MoS2/Gr is blocked by the electric field of the substrate. In turn, photoexcitation of the A exciton above leads to hole transfer from MoS2 to graphene, which occurs for both Gr-MoS2 heterostructures with opposite stacking orders, resulting in the opposite orientations of the interfacial photocurrent, as directly demonstrated by the out-of-phase THz emission. Moreover, we demonstrate that the recombination time of interfacial exciton is approximately ∼18 ps, whereas the defect-assisted interfacial recombination occurs on a time scale of ∼ns. This study provides valuable insights into the interplay between interfacial CT, substrate effects, and defect engineering in Gr-TMDs heterostructures, thereby facilitating the development of next-generation optoelectronic devices.

Stable pure-green organic light-emitting diodes toward Rec.2020 standard

Manipulating dynamic behaviours of charge carriers and excitons in organic light-emitting diodes (OLEDs) is essential to simultaneously achieve high colour purity and superior operational lifetime. In this work, a comprehensive transient electroluminescence investigation reveals that incorporating a thermally activated delayed fluorescence assistant molecule with a deep lowest unoccupied molecular orbital into a bipolar host matrix effectively traps the injected electrons. Meanwhile, the behaviours of hole injection and transport are still dominantly governed by host molecules. Thus, the recombination zone notably shifts toward the interface between the emissive layer (EML) and the electron-transporting layer (ETL). To mitigate the interfacial carrier accumulation and exciton quenching, this bipolar host matrix could serve as a non-barrier functional spacer between EML/ETL, enabling the distribution of recombination zone away from this interface. Consequently, the optimized OLED exhibits a low driving voltage, promising device stability (95% of the initial luminance of 1000 cd m−2, LT95 > 430 h), and a high Commission Internationale de L’Éclairage y coordinate of 0.69. This indicates that managing the excitons through rational energy level alignment holds the potential for simultaneously satisfying Rec.2020 standard and achieving commercial-level stability.

Photoinduced carrier transfer dynamics in a monolayer MoS2/PbS quantum dots heterostructure

Two-dimensional molybdenum disulfide (MoS2) has been proven to be a candidate in photodetectors, and MoS2/lead sulfide (PbS) quantum dots (QDs) heterostructure has been used to expand the optical response wavelength of MoS2. Time-resolved pump-probe transient absorption measurements are performed to clarify the carrier transfer dynamics in the MoS2/PbS heterostructure. By comparing the carrier dynamics in MoS2 and MoS2/PbS under different pump wavelengths, we found that the excited electrons in PbS QDs can transfer rapidly (<100 fs) to MoS2, inducing its optical response in the near-infrared region, although the pump light energy is lower than the bandgap of MoS2. Besides, interfacial excitons can be formed in the heterostructure, prolonging the lifetime of the excited carriers, which could be beneficial for the extraction of the carriers in devices.

Lignite-derived nanocarbon as surface passivator and cosensitizer in dye-sensitized solar cell

Interfacial exciton recombination and narrow absorption region are two bottlenecks that limit the performance of a dye-sensitized solar cell (DSSC). The present study focuses on improving the solar cell's efficiency by utilizing a lignite-derived nanocarbon that behaves as a surface passivator and cosensitizer. Incorporating nanocarbon enhanced the spectral absorption region of the N719 dye with a bathochromic shift and played the role of a cosensitizer. In addition, the quenched photoluminescence spectra revealed that nanocarbon also aids in the swift transfer of electrons to the conduction band of TiO2 by reducing the exciton recombination and acting as a surface passivator. On measuring the fabricated DSSC under AM 1.5G irradiation with the intensity of 100 mW/cm2, the nanocarbon-based device exhibited an efficiency (ŋ) of 9.02% with a photocurrent density of 20.45 mA/cm2, outperforming the pristine device (ŋ = 6.21%). An enhancement of 45% in the power conversion efficiency was achieved. Thus, the results unveiled that nanocarbons derived from pollution-causing fuel synergistically aided in enhancing the performance of DSSC.

Hig‐Performance Green Quasi‐2D Perovskite Light‐Emitting Diodes via Passivated Defects

AbstractIn next generation semiconductors, metal halide perovskite materials would replace traditional light‐emitting materials since their exceptional photoelectronic characteristics. The future development of perovskite light‐emitting diodes have generated challenges such as abundant surface or interfacial defects and exciton quenching. To overcome these challenges, the light‐emitting layer is modified utilizing benzimidazole/phosphine oxide hybrid 1,3,5‐tris(1‐(4‐(diphenylphenylphosphoryl)phenyl)‐1H‐benzo[d]imidazol‐2‐yl)benzene (TPOB) and 1,3,5‐tris(diphenylphosphoryl)benzene (TPO) with high triple energy state. It is demonstrated by X‐ray photoelectron spectroscopy results that the oxygen atoms in the P = O functional group of TPOB and TPO provided lone electron pairs coordinate to the unsaturated Pb2+ in turn led to a decrease in the electron cloud density of Pb2+ and Br‐, which can suppress defects. Additionally, this technique improved the morphology of film, reduced surface roughness, and facilitated carrier transport, all of which are crucial for achieving high‐emission efficiency. As a result, the optimal devices has EQEs of 16.20 (TPOB) and 20.48% (TPO), respectively. Furthermore, the devices demonstrated excellent reproducibility. Excitingly, the champion EQE value for the optimal device is 22.64%. Simultaneously, it can increase the stability of the devices and the lifetimes are increased from 1231 s (Pristine) to 5421 (TPOB) and 5631 s (TPO).

Facile fabrication of B-rGO/ZnFe2O4 p-n heterojunction-based S-scheme exciton engineering for photocatalytic Cr(vi) reduction: kinetics, influencing parameters and detailed mechanism.

The fabrication of p-n heterostructures was found to be an effective strategy to stimulate the interfacial exciton shipment and photocatalytic reactions. Herein, we report a p-n junction synthesized by combining p-type boron-doped reduced graphene oxide (B-rGO) with an n-type ZnFe2O4 semiconducting material for Cr(vi) reduction under LED light irradiation. The band structures of ZnFe2O4 and B-rGO were evaluated using UV-vis spectroscopy, Mott-Schottky (M-S) plots and photocurrent studies. The results indicated that ZnFe2O4 and B-rGO exhibit a conventional type-II charge transfer, and the Fermi-level (E F) of ZnFe2O4 was found to be much lower than that of the B-rGO material. Based on these investigations, an S-scheme charge-migration pathway was suggested and demonstrated by the photocatalytic activity and nitroblue tetrazolium (NBT) chloride experiments. The optimal 2 wt% B-rGO/ZnFe2O4 heterojunction exhibits the highest photocatalytic performance, i.e. 84% of Cr(vi) reduction in 90 min under 20 W LED light irradiation with a rate constant of 0.0207 min-1, which was 4.6- and 2.15-fold greater than that of ZnFe2O4 (ZnF) and B-rGO, respectively. The intimate interfacial contact, excellent photon-harvesting properties, effective exciton segregation and availability of active electrons are some factors responsible for enhanced photocatalytic Cr(vi) reduction. In order to fulfill the demand of applied waste-water management, the influences of various photocatalyst amounts, pH values and co-exiting ions on photocatalytic activities were evaluated. Finally, this work provides a way to fabricate S-scheme-based p-n-heterostructures for photocatalytic wastewater treatment.

Ultrafast photoinduced carrier transfer dynamics in monolayer MoS2/graphene heterostructure

Two-dimensional molybdenum disulfide (MoS2) has been proved to be a good candidate in photodetectors, and MoS2/graphene (MoS2/G) heterostructure has been widely used to expand the optical response wavelength of MoS2. To clarify the carrier transfer dynamics in the MoS2/G heterostructure, time-resolved transient absorption and two-color pump–probe measurements are performed. By comparing the carrier dynamics in MoS2 and MoS2/G under different pump wavelengths, we find that interfacial excitons are formed in the heterostructure, and fast hot carriers transfer (<200 fs) from graphene to MoS2 are observed. The results indicate that the formed heterostructure with graphene can not only expand the optical response wavelength of MoS2 but also improve the response time of the device in the near-infrared region.

Enumeration of Moiré patterns of a hexagonal twisted bilayer: Applications to intercalated transition metals

A real-space method using generating integers is used to determine possible commensurate lattice Moiré patterns for a bilayer of two equal hexagonal lattices, which can in principle be extended to lattice mismatched bilayers. These Moiré patterns can be classified by a pair of relatively prime integers (n,m), wherein a rotation θ(n,m) of the top hexagonal lattice maps its lattice vector (n,m) to (m,n) of the bottom lattice. Within this formulation, the area of the commensurate supercell is proportional to (n2+m2+nm) and the number of coincident lattice sites per supercell is given by (n−m)2. Taking bilayer boron nitride (BN) as an example, we present how to systematically generate Moiré patterns and explore the differences in local chemistry in the interstitial region by impurity intercalation. Systematic calculations of the properties of intercalated 3d transition metals were performed in an h-BN (4,3) bilayer, corresponding to a rotation of 9.43 degrees. These calculations reveal that local symmetry in the intercalated region significantly affect the energetics and magnetization of the intercalated species. These results highlight that Moiré pattern physics is not limited to optoelectronic/electronic phenomena, such as interfacial exciton formation or magic angle superconductivity, but it also produces chemical and magnetic atomic site selectivity, which may play important roles in adsorption, catalysis, or quantum information.

Interfacial Molecule Control Enables Efficient Perovskite Light‐Emitting Diodes

AbstractPerovskite light‐emitting diodes (PeLEDs) are emerging as promising candidates for new‐generation high‐definition displays with excellent color purity and low power consumption. Nevertheless, the massive defects at grain boundaries and severe interfacial exciton quenching are critical challenges that hinder the commercialization process of PeLEDs. Herein, a novel and feasible strategy of interfacial molecule control is demonstrated by employing a bifunctional material with abundant phosphine oxide groups to induce strong interaction and exciton management between the perovskite and electron‐transport layers (ETLs). This modification layer is capable of passivating the surface crystal defects and blocking the interfacial exciton transfer simultaneously, contributing to minimized energy loss at the interface. Consequently, the modified PeLEDs with green (at 513 nm), blue (at 488 nm), and red (at 666 nm) emissions achieve maximum external quantum efficiencies of 18.8%, 12.6%, and 12.3%, respectively. This study reveals the importance of interfacial molecule control for reducing the energy loss in PeLEDs.

Strong Dipolar Repulsion of One-Dimensional Interfacial Excitons in Monolayer Lateral Heterojunctions.

Repulsive and long-range exciton-exciton interactions are crucial for the exploration of one-dimensional (1D) correlated quantum phases in the solid state. However, the experimental realization of nanoscale confinement of a 1D dipolar exciton has thus far been limited. Here, we demonstrate atomically precise lateral heterojunctions based at transitional-metal dichalcogenides (TMDCs) as a platform for 1D dipolar excitons. The dynamics and transport of the interfacial charge transfer excitons in a type II WSe2-WS1.16Se0.84 lateral heterostructure were spatially and temporally imaged using ultrafast transient reflection microscopy. The expansion of the exciton cloud driven by dipolar repulsion was found to be strongly density dependent and highly anisotropic. The interaction strength between the 1D excitons was determined to be ∼3.9 × 10-14 eV cm-2, corresponding to a dipolar length of 310 nm, which is a factor of 2-3 larger than the interlayer excitons at two-dimensional van der Waals vertical interfaces. These results suggest 1D dipolar excitons with large static in-plane dipole moments in lateral TMDC heterojunctions as an exciting system for investigating quantum many-body physics.

Manipulation of Charge Delocalization in a Bulk Heterojunction Material Using a Mid-Infrared Push Pulse.

In organic bulk heterojunction materials, charge delocalization has been proposed to play a vital role in the generation of free carriers by effectively reducing the Coulomb attraction via an interfacial charge transfer exciton (CTX). Pump-push-probe (PPP) experiments produced evidence that the excess energy given by a push pulse enhances delocalization, thereby increasing photocurrent. However, previous studies have employed near-infrared push pulses in the range ∼0.4-0.6 eV, which is larger than the binding energy of a typical CTX. This raises the doubt that the push pulse may directly promote dissociation without involving delocalized states. Here, we perform PPP experiments with mid-infrared push pulses at energies that are well below the binding energy of a CTX state (0.12-0.25 eV). We identify three types of CTXs: delocalized, localized, and trapped. The excitation resides over multiple polymer chains in delocalized CTXs, while it is restricted to a single chain (albeit maintaining a degree of intrachain delocalization) in localized CTXs. Trapped CTXs are instead completely localized. The pump pulse generates a "hot" delocalized CTX, which promptly relaxes to a localized CTX and eventually to trapped states. We find that photo-exciting localized CTXs with push pulses resonant to the mid-infrared charge transfer absorption can promote delocalization and, in turn, contribute to the formation of long-lived charge separated states. On the other hand, we found that trapped CTXs are non-responsive to the push pulses. We hypothesize that delocalized states identified in prior studies are only accessible in systems where there is significant interchain electronic coupling or regioregularity that supports either inter- or intrachain polaron delocalization. This, in turn, emphasizes the importance of engineering the micromorphology and energetics of the donor-acceptor interface to exploit the full potential of a material for photovoltaic applications.

Spatially indirect interfacial excitons in n+-ZnO/p-GaN heterostructures

Electroluminescence properties of epitaxially grown n+-ZnO/p-GaN pn+-heterojunctions are investigated as functions of applied bias and temperature. This study reveals the existence of indirect interfacial excitons at sufficiently low temperatures. Electroluminescence feature associated with these excitons redshifts with increasing forward bias. It has been found that the binding energy of these entities can be controlled through applied forward bias and can even be made higher than that of the excitons in ZnO bulk (60 meV). However, the formation of these excitons becomes unsustainable when either the applied bias or the temperature crosses a threshold. This has been explained in terms of leakage and thermal escape of electrons (holes) into the GaN (ZnO) side. Calculations for the band diagram and the binding energy of these spatially indirect electron–hole coulomb-coupled entities are carried out. Theoretical results are found to explain the experimental findings quite well.

Heteroatom‐ and Bonded Z‐Scheme Channels‐Modulated Ultrafast Carrier Dynamics and Exciton Dissociation in Covalent Triazine Frameworks for Efficient Photocatalytic Hydrogen Evolution

AbstractCovalent triazine frameworks (CTF) offer a tunable platform for photocatalytic H2 generation due to their diverse structures, low costs, and precisely tunable electronic structures. However, high exciton binding energy and short lifetimes of photogenerated carriers restrict their application in photocatalytic hydrogen evolution. Herein, a novel phosphorus‐incorporated CTF is introduced to construct a chemically bonded PCTF/WO3 (PCTFW) heterostructure with a precise interface electron transfer channel. The phosphorus incorporation is found to dominantly reduce the exciton binding energy and promote the dissociation of singlet and triplet excitons into free charge carriers due to the regulation of electronic structures. High‐quality interfacial WN bonds improve the interfacial transfer of photogenerated electrons, thus prolonging the lifetime of photogenerated electrons. Femtosecond transient absorption spectroscopy characterizations and DFT calculations further confirm both phosphorus incorporation and Z‐scheme heterojunctions can synergistically boost the in‐built electric field and accelerate the migration and separation of photogenerated electrons. The optimized photocatalytic H2‐evolution rate of resultant PCTFW is 134.84 µmol h−1 (67.42 mmol h−1g−1), with an apparent quantum efficiency of 37.63% at 420 nm, surpassing many reported CTF‐based photocatalysts so far. This work highlights the significance of atom‐level interfacial exciton dissociation, and charge transfer and separation in improving photocatalysis.

ZnO/silica quasi core/shell nanoparticles as electron transport materials for high-performance quantum-dot light-emitting diodes

Quantum dot light-emitting diodes (QLEDs) are considered as the ideal candidate for next-generation displays, solid-state lighting, and optical communication applications. Although the efficiency of QLEDs has been significantly improved to the level comparable to that of organic light-emitting diodes in recent years, simultaneously achieving high efficiency and high brightness still remains challenging for QLEDs. In this work, we report a facile and effective electron-transport-layer interface control strategy of incorporating 3-aminopropyl triethoxysilane (APTES) into a ZnO nanocrystal-solution to enhance charge injection balance and suppress interfacial exciton quenching via in-situ formation of ZnO/organic silica (hereinafter referred to as ZnO/SiO2) quasi core/shell nanoparticles in the solution, enabling red QLEDs to exhibit a maximum luminance intensity of 261,700 cd m−2, a peak external quantum efficiency (EQE) of 19.0%, and low efficiency roll-off at high luminance (an EQE up to 16.8% remained at a brightness of 200, 000 cd m−2). Our results demonstrate that substituting quasi core/shell-structured ZnO/SiO2 nanoparticles for traditional ZnO nanocrystals as electron transport materials is a simple and effective means of fabricating QLEDs with both high efficiency and high luminance, which is expected to facilitate the development of QLED technology toward practical applications in lighting, displays and optical communication.