Ligand exchange with octylphosphonate enhances PLQY and LED efficiency.

In this progress report, recent improvements to the room temperaturesyntheses of lead halide perovskite nanocrystals (APbX3, X = Cl, Br, I) are assessed, focusing on various aspects which influence the commercial viability of the technology. Perovskite nanocrystals can be prepared easily from low‐cost precursors under ambient conditions, yet they have displayed near‐unity photoluminescence quantum yield with narrow, highly tunable emission peaks. In addition to their impressive ambipolar charge carrier mobilities, these properties make lead halide perovskite nanocrystals very attractive for light‐emitting diode (LED) applications. However, there are still many practical hurdles preventing commercialization. Recent developments in room temperature synthesis and purification protocols are reviewed, closely evaluating the suitability of particular techniques for industry. This is followed by an assessment of the wide range of ligands deployed on perovskite nanocrystal surfaces, analyzing their impact on colloidal stability, as well as LED efficiency. Based on these observations, a perspective on important future research directions that can expedite the industrial adoption of perovskite nanocrystals is provided.

Room-temperature perovskite nanocrystal syntheses have previously lacked the size tunability attainable through high-temperature methods. Herein, we outline a scalable approach whereby the nucleation and growth of CsPbBr 3 nanocrystals (NCs) can be decoupled and controlled at room temperature by utilizing different ligands. We employed octylphosphonic acid (OPA) ligands to regulate the critical radius and the NC growth rate. The subsequent addition of a bulkier didodecyldimethylammonium bromide ligand quenches the NC growth, defining the reaction duration. Management of these three variables enables precise tuning of the NC diameter between 6.8 and 13.6 nm. The photoluminescence quantum yield of the NCs remains above 80% for all sizes even after thorough antisolvent purification. The use of hydrogen-bonding OPA ligands enhances quantum confinement effects, characterized by strong, well-resolved absorption peaks. Solution and solid-state nuclear magnetic resonance spectra confirmed the effective removal of unbound ligands during purification and the presence of a hydrogen-bonded network of OPA ligands on the surface of the purified NCs. Overall, this approach has the potential to facilitate a broad range of future endeavors from studies of hot carrier dynamics to both optically and electrically driven device applications.

Novel Cs-containing triple cation perovskite nanocrystals produce high-performance LEDs as a result of improved surface passivation and environmental stability.

Inorganic cesium lead halide perovskite nanocrystals are promising materials for optoelectronic applications as they exhibit high thermal stability alongside precise colour tunability and high colour purity; however, their optical properties are degraded by surface defects. This work demonstrates a room temperature synthesis of CsPbBr3 nanocrystals facilitating in-situ surface passivation via the incorporation of Zn 2+ cations. The facile incorporation ZnBr2 into the precursor solution facilitates Zn 2+ substitution into the nanocrystal surface/sub-surface layers to induce passivation of existing Pb 2+ and Brvacancies and increase the photoluminescence quantum yield

This investigation has characterised the structure and surface chemistry of CsPbBr3 nanocrystals with controlled diameters between 6.4 to 12.8 nm. The nanocrystals were investigated via a thorough 133Cs solid state...

For the first time in perovskite solar cells, phenothiazine has been introduced as a low cost substituent to replace the commonly-used dimethoxydiphenylamine, which constitutes almost 90% of the final cost of hole transport materials.

Halide perovskite nanocrystals are a promising candidate for lighting applications. However, the production of white light emitting diodes (LEDs) is still a major challenge due to halide ion segregation. In this work, it is demonstrated that reducing the thickness of the perovskite layer in an LED stack can modulate the recombination zone, such that a tunable emission can be obtained. This comprises of an orange electromer emission from a hole‐transport layer (HTL), green electroluminescence from the perovskite active layer, and a blue monomer emission from the same HTL. Overall, a pure white emission can be achieved after successful device optimization, which is particularly challenging for LEDs in which the emission originates solely from perovskite layer. It is anticipated that this methodology could be employed on any type of green‐emitting nanocrystals to fabricate white LEDs.