We report a full series of blue, green and red quantum-dot-based light-emitting devices (QD-LEDs), all with high external quantum efficiencies over 10%. We show that the fine nanostructure of quantum dots-especially the composition of the graded intermediate shell and the thickness of the outer shell-plays a very important role in determining QD-LED device performance due to its effects on charge injection, transport and recombination. These simple devices have maximum current and external quantum efficiencies of 63 cd A −1 and 14.5% for green QD-LEDs, 15 cd A −1 and 12.0% for red devices, and 4.4 cd A −1 and 10.7% for blue devices, all of which are well maintained over a wide range of luminances from 10 2 to 10 4 cd m −2 . All the QD-LEDs are solution-processed for ease of mass production, and have low turn-on voltages and saturated pure colours. The green and red devices exhibit lifetimes of more than 90,000 and 300,000 h, respectively. Since their inception about three decades ago 1-3 , semiconductor quantum dots have been intensively investigated because of their unique optical properties, including size-controlled tunable emission wavelength (known as the 'quantum confinement effect'), narrow emission spectra, high luminescent efficiency and colloidal-based synthesis process 4-7 . All these attractive characteristics make quantum dots excellent candidates for the development of next-generation display technologies. Quantum dot-based lightemitting diodes (QD-LEDs) have been demonstrated recently, and may offer many advantages over conventional LED and organic LED (OLEDs) technologies in terms of colour purity, stability and production cost, while still achieving similar levels of efficiency. To date, however, the electroluminescence efficiencies of QD-LEDs have remained significantly below those of OLEDs, despite steady progress in recent years [8][9][10][11][12][13][14][15][16][17] . Recently, an efficient deep-blue QD-LED has been reported that makes use of solutionprocessed poly(3,4-ethylenedioxythiophene):polystyrene sulphonate (PEDOT:PSS) and poly(N-vinyl carbazole) (PVK) as its hole injection and transport layers (HIL and HTL), respectively, and ZnO nanoparticles as its electron transport layer (ETL), and achieves a maximum external quantum efficiency (η EQE ) of 7.1% (ref. 15). The same device structure was also used to achieve a green QD-LED with an η EQE of 12.6% (ref. 17). Highly efficient red QD-LEDs with η EQE = 18-20% have been realized using an inverted device structure containing a vacuum-deposited HIL and HTL 16 , and also in another arrangement using a thin insulating layer to obtain an enhanced charge balance 18 . These are the first times that the performances of QD-LEDs have been comparable to those of state-of-the-art phosphorescent OLEDs 19-21 .It is noted that although high efficiencies have been achieved with blue (B), green (G) and red (R) QD-LEDs, these singlecolour QD-LEDs, developed by different research groups, commonly involve very different quantum dot preparation procedures (fo...

For the state-of-the-art quantum dot light-emitting diodes, while the ZnO nanoparticle layers can provide effective electron injections into quantum dots layers, the hole transporting materials usually cannot guarantee sufficient hole injection owing to the deep valence band of quantum dots. Developing proper hole transporting materials to match energy levels with quantum dots remains a great challenge to further improve the device efficiency and operation lifetime. Here we demonstrate high-performance quantum dot light-emitting diodes with much extended operation lifetime using quantum dots with tailored energy band structures that are favorable for hole injections. These devices show a T95 operation lifetime of more than 2300 h with an initial brightness of 1000 cd m−2, and an equivalent T50 lifetime at 100 cd m−2 of more than 2,200,000 h, which meets the industrial requirement for display applications.

The operating lifetime of blue quantum-dot light-emitting diodes (QLED) is currently a short slab for this emerging display technology. To pinpoint the origin of device degradation, here we apply multiple techniques to monitor the electric-field distribution and space-charge accumulation across the multilayered structure before and after lifetime tests. Evident by charge-modulated electro-absorption and capacitance-voltage characteristics, the excited electrons in blue quantum dots (QD) are prone to cross the type II junction between the QD emission layer and the electron-transporting layer (ETL) due to the offset of conduction band minimum, leading to space-charge accumulation and operating-voltage rise in the ETL. Therefore, unlike those very stable red devices, of which the lifetime is primarily limited by the slow degradation of hole-transporting layer, the poor lifetime of blue QLED originates from the fast degradation at the QD-ETL junction. Materials engineering for efficient electron injection is prerequisite for the boost of operating lifetime.

A family of π-extended platinum(II) porphyrins has been synthesized and incorporated into solution processed polymer light emitting diodes (PLEDs) and vapor deposited multilayer organic light emitting diodes (OLEDs), giving rise to devices with peak emission ranging from 771 to 1005 nm. The longest wavelength emitter, platinum(II)-5,10,15,20-(3,5di-tert-butylphenyl)tetraanthroporphyrin (Pt-Ar 4 TAP), shows an emission maximum at 1005 nm, an external quantum efficiency (EQE) of 0.12%, and a maximum radiant emittance (R max ) of 0.23 mW/cm 2 in single layer PLED architectures, which is enhanced to an EQE of 0.20% with an R max of 0.57 mW/cm 2 upon vapor deposition of an electron transport layer. In an effort to understand substituent effects and enhance the performance of π-extended Pt-porphyrins in PLEDs and OLEDs, a family of Pt-tetrabenzoporphyrins (Pt-TBPs) with varying functionality was investigated. The luminescent lifetimes of the Pt-TBPs in solution and in films were measured, and a strong correlation was demonstrated between the film lifetimes and the PLED and OLED efficiencies. An improvement in external quantum efficiency (EQE) from 2.07 to 2.49% for PLEDs and from 8.0 to 9.2% for OLEDs was observed between the less substituted Pt-tetraphenyltetrabenzoporphyrin and the more substituted 10,15,tetrabenzoporphyrin. The PLED EQEs were further enhanced to 3.02% with the disubstituted Pt-5,15-(3,5-di-tert-butylphenyl)tetrabenzoporphyrin; however, this increase was not observed for the OLEDs where an EQE of 7.8% was measured.

World record efficiency for solution-processed CIGS solar cells has been demonstrated.