Efficient and stable hybrid perovskite-organic light-emitting diodes with external quantum efficiency exceeding 40 per cent.

Light-emitting diodes (LEDs) based on perovskite semiconductor materials with tunable emission wavelength in visible light range as well as narrow linewidth are potential competitors among current light-emitting display technologies, but still suffer from severe instability driven by electric field. Here, we develop a stable, efficient and high-color purity hybrid LED with a tandem structure by combining the perovskite LED and the commercial organic LED technologies to accelerate the practical application of perovskites. Perovskite LED and organic LED with close photoluminescence peak are selected to maximize photon emission without photon reabsorption and to achieve the narrowed emission spectra. By designing an efficient interconnecting layer with p-type interface doping that provides good opto-electric coupling and reduces Joule heating, the resulting green emitting hybrid LED shows a narrow linewidth of around 30 nm, a peak luminance of over 176,000 cd m-2, a maximum external quantum efficiency of over 40%, and an operational half-lifetime of over 42,000 h.

Phosphorescent-Dye-Sensitized Quantum-Dot Light-Emitting Diodes with 37% External Quantum Efficiency.

Exciton harvesting is of paramount importance for quantum-dot light-emitting diodes (QLEDs). Direct exciton harvesting by the quantum dots (QDs) emitting layer suffers from poor hole injection due to the low conduction bands and valence bands of QDs, leading to unbalanced electron-hole injection and recombination. To address this issue, here, an exciton sensitizing approach is reported, where excitons form on a phosphorescent-dye-doped layer, which then transfer their energies to adjacent QDs layer for photon emission. Due to the very efficient exciton formation and energy-transfer processes, higher device performance can be achieved. To demonstrate the above strategy, red QLEDs with a phosphorescent dye, iridium (III) bis(2-methyldibenzo-[f,h]quinoxaline) (acetylacetonate), Ir(MDQ)2 (acac), doped hole-transporting layer are fabricated and studied. At a doping concentration of 10 wt%, the best device achieves record high current efficiency, power efficiency, and external quantum efficiency (EQE) of 37.3 cd A-1 , 41 lm W-1 , and 37%, respectively. Simultaneously, the efficiency roll-off characteristic is greatly improved, in that 35% EQE can be well retained at a high luminance level of 450 000 cd m-2 . Moreover, the devices also exhibit good stability and reproducibility.

Efficient Tandem Quantum-Dot LEDs Enabled by An Inorganic Semiconductor-Metal-Dielectric Interconnecting Layer Stack.

Light-emitting diodes (LEDs) in a tandem configuration offer a strategy to realize high-performance, multicolor devices. Until now, though, the efficiency of tandem colloidal quantum dot LEDs (QLEDs) has been limited due to unpassivated interfaces and solvent damage originating from the materials processing requirements of interconnecting layers (ICLs). Here an ICL is reported consisting of a semiconductor-metal-dielectric stack that provides facile fabrication, materials stability, and good optoelectronic coupling. It is investigated experimentally how the ICL enables charge balance, suppresses current leakage, and prevents solvent damage to the underlying layers. As a result record efficiencies are reported for double-junction tandem QLEDs, whose emission wavelengths cover from blue to red light; i.e., external quantum efficiencies (EQEs) of 40% (average 37+/-2%) for red, 49% (average 45+/-2%) for yellow, 50% (average 46+/-2%) for green, and 24% (average 21+/-2%) for blue are achieved.

Activated Electron-Transport Layers for Infrared Quantum Dot Optoelectronics.

Photovoltaic (PV) materials such as perovskites and silicon are generally unabsorptive at wavelengths longer than 1100 nm, leaving a significant portion of the IR solar spectrum unharvested. Small-bandgap colloidal quantum dots (CQDs) are a promising platform to offer tandem complementary IR PV solutions. Today, the best performing CQD PVs use zinc oxide (ZnO) as an electron-transport layer. However, these electrodes require ultraviolet (UV)-light activation to overcome the low carrier density of ZnO, precluding the realization of CQD tandem photovoltaics. Here, a new sol-gel UV-free electrode based on Al/Cl hybrid doping of ZnO (CAZO) is developed. Al heterovalent doping provides a strong n-type character while Cl surface passivation leads to a more favorable band alignment for electron extraction. CAZO CQD IR solar cell devices exhibit, at wavelengths beyond the Si bandgap, an external quantum efficiency of 73%, leading to an additional 0.92% IR power conversion efficiency without UV activation. Conventional ZnO devices, on the other hand, add fewer than 0.01 power points at these operating conditions.

Organic semiconductor heterojunctions: electrode-independent charge injectors for high-performance organic light-emitting diodes.

Organic light-emitting diodes (OLEDs) are driven by injected charges from an anode and a cathode. The low and high work function metals are necessary for the effective injection of electrons and holes, respectively. Here, we introduce a fully novel design concept using organic semiconductor heterojunctions (OSHJs) as the charge injectors for achieving highly efficient OLEDs, regardless of the work functions of the electrodes. In contrast to traditional injected charges from the electrodes, the injected charges originate from the OSHJs. The device performance was shown to be significantly improved in efficiency and stability compared to conventional OLEDs. Attractively, the OLEDs based on OSHJs as charge injectors still exhibited an impressive performance when the low work function Al was replaced by air- and chemistry-stable high work function metals, such as Au, Ag, and Cu, as the cathode contact, which has been suggested to be difficult in conventional OLEDs. This concept challenges the conventional design approach for the injection of charges and allows for the realization of practical applications of OLEDs with respect to high efficiency, selectable electrodes, and a long lifetime.

Simultaneous efficiency enhancement and self-cleaning effect of white organic light-emitting devices by flexible antireflective films.

In this Letter, we report the improved light outcoupling efficiency of conventional white organic light-emitting devices (OLEDs) by a kind of multifunctional film with both antireflective and superhydrophobic ability. This film consisted of regular polydimethylsiloxane (PDMS) nanopillar arrays, which were readily batch produced by low-cost imprint lithography. The nanopillar arrays could effectively eliminate the light total reflection and enhance the device efficiency of OLEDs by producing the gradual refractive index due to the decreasing material density from glass to air. Moreover, owing to its superhydrophobicity (contact angle ∼151°), the antireflective film exhibited self-cleaning ability, which was beneficial for keeping the OLEDs substrate clean and ensure the high efficiency of OLEDs. This method is simple, cost-effective, and reproducible. The OLEDs showed an efficiency enhancement of 25% with the multifunctional film.