All-inorganic perovskite nanocrystals (NCs) have emerged as a new generation of low-cost semiconducting luminescent system for optoelectronic applications. The room-temperature photoluminescence quantum yields (PLQYs) of these NCs in the green and red spectral range approach unity. However, their PLQYs in the violet are much lower, and an insightful understanding of such poor performance remains missing. We report a general strategy for the synthesis of all-inorganic violet-emitting perovskite NCs with near-unity PLQYs through engineering local order of the lattice by nickel ion doping. A broad range of experimental characterizations, including steady-state and time-resolved luminescence spectroscopy, X-ray absorption spectra, and magic angle spinning nuclear magnetic resonance spectra, reveal that the low PLQY in undoped NCs is associated with short-range disorder of the lattice induced by intrinsic defects such as halide vacancies and that Ni doping can substantially eliminate these defects and result in increased short-range order of the lattice. Density functional theory calculations reveal that Ni doping of perovskites causes an increase of defect formation energy and does not introduce deep trap states in the band gap, which is suggested to be the main reason for the improved local structural order and near-unity PLQY. Our ability to obtain violet-emitting perovskite NCs with near-perfect properties opens the door for a range of applications in violet-emitting perovskite-based devices such as light-emitting diodes, single-photon sources, lasers, and beyond.
All-inorganic perovskites have emerged as a new class of phosphor materials owing to their outstanding optical properties. Zero-dimensional inorganic perovskites, in particular the CsPbBr-related systems, are inspiring intensive research owing to the high photoluminescence quantum yield (PLQY) and good stability. However, synthesizing such perovskites with high PLQYs through an environment-friendly, cost-effective, scalable, and high-yield approach remains challenging, and their luminescence mechanisms has been elusive. Here, we report a simple, scalable, room-temperature self-assembly strategy for the synthesis of CsPbBr/CsPbBr perovskite composites with near-unity PLQY (95%), high product yield (71%), and good stability using low-cost, low-toxicity chemicals as precursors. A broad range of experimental and theoretical characterizations suggest that the high-efficiency PL originates from CsPbBr nanocrystals well passivated by the zero-dimensional CsPbBr matrix that forms based on a dissolution-crystallization process. These findings underscore the importance in accurately identifying the phase purity of zero-dimensional perovskites by synchrotron X-ray technique to gain deep insights into the structure-property relationship. Additionally, we demonstrate that green-emitting CsPbBr/CsPbBr, combined with red-emitting KSiF:Mn, can be used for the construction of WLEDs. Our work may pave the way for the use of such composite perovskites as highly luminescent emitters in various applications such as lighting, displays, and other optoelectronic and photonic devices.
Cesium
lead halide perovskite nanocrystals (NCs) have emerged as
promising luminescent materials for a range of applications. However,
the creation of highly luminescent violet-emitting CsPbCl3 NCs mostly relies on doping of a limited number of small-sized metal
ions or post-synthetic surface treatment of NCs. Alkaline-earth (AE)
metals (e.g., Ca2+, Sr2+, and Ba2+) have been proposed to be able to substitute Pb2+ in
halide perovskites, yet it remains incompletely understood whether
AE metal ions can be incorporated into the perovskite lattice or can
be merely situated at the surface. Here, we explore the possibility
of using AE metal ions for the suppression of the formation of trap
centers, which leads us to develop a one-pot synthetic passivation
strategy to boost the violet-emitting efficiency of CsPbCl3 NCs through the creation of a Ca2+/Sr2+ involved
passivation layer. The photoluminescence quantum yield of violet emission
reaches 77.1% by incorporating an optimal amount of Ca2+. A wide range of optical and structural characterizations, coupled
with first-principles calculations, aid in clarifying the underlying
mechanism for the AE-metal-dependent passivation of CsPbCl3 NCs. Specifically, based on the experimental and theoretical results,
a model is proposed for the observed abnormal incorporation phenomenon
of AE2+ ions in NCs (i.e., Ba2+ can be incorporated
into the core of NCs, Ca2+/Sr2+ can only be
at/near the surface, while Mg2+ can neither be in the core
nor at the surface). We believe that the knowledge gained here may
not only offer a new perspective to obtain high-efficiency violet-emitting
perovskite NCs through a one-pot synthetic passivation but can also
help elucidate the functions that AE2+ ions play in the
optimization of perovskite optoelectronic devices.
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