Metal halides perovskites, such as hybrid organic–inorganic CH3NH3PbI3, are newcomer optoelectronic materials that have attracted enormous attention as solution-deposited absorbing layers in solar cells with power conversion efficiencies reaching 20%. Herein we demonstrate a new avenue for halide perovskites by designing highly luminescent perovskite-based colloidal quantum dot materials. We have synthesized monodisperse colloidal nanocubes (4–15 nm edge lengths) of fully inorganic cesium lead halide perovskites (CsPbX3, X = Cl, Br, and I or mixed halide systems Cl/Br and Br/I) using inexpensive commercial precursors. Through compositional modulations and quantum size-effects, the bandgap energies and emission spectra are readily tunable over the entire visible spectral region of 410–700 nm. The photoluminescence of CsPbX3 nanocrystals is characterized by narrow emission line-widths of 12–42 nm, wide color gamut covering up to 140% of the NTSC color standard, high quantum yields of up to 90%, and radiativ...

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Nanocrystals of Cesium Lead Halide Perovskites (CsPbX3, X = Cl, Br, and I): Novel Optoelectronic Materials Showing Bright Emission with Wide Color Gamut

Colloidal core/shell nanocrystals contain at least two semiconductor materials in an onionlike structure. The possibility to tune the basic optical properties of the core nanocrystals, for example, their fluorescence wavelength, quantum yield, and lifetime, by growing an epitaxial-type shell of another semiconductor has fueled significant progress on the chemical synthesis of these systems. In such core/shell nanocrystals, the shell provides a physical barrier between the optically active core and the surrounding medium, thus making the nanocrystals less sensitive to environmental changes, surface chemistry, and photo-oxidation. The shell further provides an efficient passivation of the surface trap states, giving rise to a strongly enhanced fluorescence quantum yield. This effect is a fundamental prerequisite for the use of nanocrystals in applications such as biological labeling and light-emitting devices, which rely on their emission properties. Focusing on recent advances, this Review discusses the fundamental properties and synthesis methods of core/shell and core/multiple shell structures of II-VI, IV-VI, and III-V semiconductors.

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Core/Shell semiconductor nanocrystals.

Organometal halide perovskites are inexpensive materials with desirable characteristics of color-tunable and narrow-band emissions for lighting and display technology, but they suffer from low photoluminescence quantum yields at low excitation fluencies. Here we developed a ligand-assisted reprecipitation strategy to fabricate brightly luminescent and color-tunable colloidal CH3NH3PbX3 (X = Br, I, Cl) quantum dots with absolute quantum yield up to 70% at room temperature and low excitation fluencies. To illustrate the photoluminescence enhancements in these quantum dots, we conducted comprehensive composition and surface characterizations and determined the time- and temperature-dependent photoluminescence spectra. Comparisons between small-sized CH3NH3PbBr3 quantum dots (average diameter 3.3 nm) and corresponding micrometer-sized bulk particles (2–8 μm) suggest that the intense increased photoluminescence quantum yield originates from the increase of exciton binding energy due to size reduction as well a...

Brightly Luminescent and Color-Tunable Colloidal CH3NH3PbX3 (X = Br, I, Cl) Quantum Dots: Potential Alternatives for Display Technology.

Glucose-derived water-soluble crystalline graphene quantum dots (GQDs) with an average diameter as small as 1.65 nm (∼5 layers) were prepared by a facile microwave-assisted hydrothermal method. The GQDs exhibits deep ultraviolet (DUV) emission of 4.1 eV, which is the shortest emission wavelength among all the solution-based QDs. The GQDs exhibit typical excitation wavelength-dependent properties as expected in carbon-based quantum dots. However, the emission wavelength is independent of the size of the GQDs. The unique optical properties of the GQDs are attributed to the self-passivated layer on the surface of the GQDs as revealed by electron energy loss spectroscopy. The photoluminescence quantum yields of the GQDs were determined to be 7–11%. The GQDs are capable of converting blue light into white light when the GQDs are coated onto a blue light emitting diode.

Deep ultraviolet photoluminescence of water-soluble self-passivated graphene quantum dots

High particle uniformity, high photoluminescence quantum yields, narrow and symmetric emission spectral lineshapes and minimal single-dot emission intermittency (known as blinking) have been recognized as universal requirements for the successful use of colloidal quantum dots in nearly all optical applications. However, synthesizing samples that simultaneously meet all these four criteria has proven challenging. Here, we report the synthesis of such high-quality CdSe-CdS core-shell quantum dots in an optimized process that maintains a slow growth rate of the shell through the use of octanethiol and cadmium oleate as precursors. In contrast with previous observations, single-dot blinking is significantly suppressed with only a relatively thin shell. Furthermore, we demonstrate the elimination of the ensemble luminescence photodarkening that is an intrinsic consequence of quantum dot blinking statistical ageing. Furthermore, the small size and high photoluminescence quantum yields of these novel quantum dots render them superior in vivo imaging agents compared with conventional quantum dots. We anticipate these quantum dots will also result in significant improvement in the performance of quantum dots in other applications such as solid-state lighting and illumination.

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Compact high-quality CdSe–CdS core–shell nanocrystals with narrow emission linewidths and suppressed blinking

Quantum dots (QDs) have attracted great attention as good candidate for the next generation displays due to their narrow emission, and high luminescence efficiency, and tunable emission covering all visible range. However, QDs easily lost their initial optical properties during the process for a device fabrication and practical operation. We synthesized well passivated green and red light emitting QDs that show almost 100% of QE. When the highly luminescent green and red light emitting QDs were applied as color converters in InGaN blue LEDs, resulting cool white QD-LEDs showed 41lm/W and more than 100% of color reproducibility compared to NTSC standard in CIE1931 and maintained their optical properties for a long time operation. We also demonstrated a 46-inch LCD panel using the white QDLED backlight was successfully demonstrated (Figure).

White‐Light‐Emitting Diodes with Quantum Dot Color Converters for Display Backlights

A highly luminescent and photostable quantum dot–silica monolith (QD–SM) substance was prepared by preliminary surface exchange of the QDs and base-catalyzed sol–gel condensation of silica. The SM was heavily doped with 6-mercaptohexanol exchanged QDs up to 12 vol % (26 wt %) without particle aggregation. Propylamine catalyst was important in maintaining the original luminescence of the QDs in the SM during sol–gel condensation. The silica layer was a good barrier against oxygen and moisture, so that the QD–SM maintained its initial luminescence after high-power UV radiation (∼1 W) for 200 h and through the 150 °C LED encapsulant curing process. Green and red light-emitting QD–SMs were applied as color-converting layers on blue LEDs, and the external quantum efficiency reached up to 89% for the green QD–SM and 63% for the red one. A white LED made with a mixture of green and red QDs in the SM, in which the color coordinate was adjusted at (0.23, 0.21) in CIE1931 color space for a backlight application, sh...

Highly luminescent and photostable quantum dot-silica monolith and its application to light-emitting diodes

Preparation of Highly Luminescent Nanocrystals and Their Application to Light-Emitting Diodes†

High quality CdSeS nanocrystals synthesized by facile single injection process and their electroluminescence

Color conversion: a quantum dot (QD) structure consisting of an alloy core (CdSe//ZnS) and multishells (CdSZnS) was prepared. The photoluminescence of the QDs could be tuned especially in the green-light region by controlling the thickness of the inner CdS shell. The alloy core/multishell (AC/MS) QDs showed a quantum efficiency of 100 % and a narrow spectrum width.

Shinae Jun

Papers

White‐Light‐Emitting Diodes with Quantum Dot Color Converters for Display Backlights

Highly luminescent and photostable quantum dot-silica monolith and its application to light-emitting diodes

Preparation of Highly Luminescent Nanocrystals and Their Application to Light-Emitting Diodes†

High quality CdSeS nanocrystals synthesized by facile single injection process and their electroluminescence

Bright and Stable Alloy Core/Multishell Quantum Dots