Lead halide perovskites (LHPs) in the form of nanometre-sized colloidal crystals, or nanocrystals (NCs), have attracted the attention of diverse materials scientists due to their unique optical versatility, high photoluminescence quantum yields and facile synthesis. LHP NCs have a 'soft' and predominantly ionic lattice, and their optical and electronic properties are highly tolerant to structural defects and surface states. Therefore, they cannot be approached with the same experimental mindset and theoretical framework as conventional semiconductor NCs. In this Review, we discuss LHP NCs historical and current research pursuits, challenges in applications, and the related present and future mitigation strategies explored.

Nanostructured semiconductors emit light from electronic states known as excitons. For organic materials, Hund's rules state that the lowest-energy exciton is a poorly emitting triplet state. For inorganic semiconductors, similar rules predict an analogue of this triplet state known as the 'dark exciton'. Because dark excitons release photons slowly, hindering emission from inorganic nanostructures, materials that disobey these rules have been sought. However, despite considerable experimental and theoretical efforts, no inorganic semiconductors have been identified in which the lowest exciton is bright. Here we show that the lowest exciton in caesium lead halide perovskites (CsPbX, with X = Cl, Br or I) involves a highly emissive triplet state. We first use an effective-mass model and group theory to demonstrate the possibility of such a state existing, which can occur when the strong spin-orbit coupling in the conduction band of a perovskite is combined with the Rashba effect. We then apply our model to CsPbX nanocrystals, and measure size- and composition-dependent fluorescence at the single-nanocrystal level. The bright triplet character of the lowest exciton explains the anomalous photon-emission rates of these materials, which emit about 20 and 1,000 times faster than any other semiconductor nanocrystal at room and cryogenic temperatures, respectively. The existence of this bright triplet exciton is further confirmed by analysis of the fine structure in low-temperature fluorescence spectra. For semiconductor nanocrystals, which are already used in lighting, lasers and displays, these excitons could lead to materials with brighter emission. More generally, our results provide criteria for identifying other semiconductors that exhibit bright excitons, with potential implications for optoelectronic devices.

An ensemble of emitters can behave very differently from its individual constituents when they interact coherently via a common light field. After excitation of such an ensemble, collective coupling can give rise to a many-body quantum phenomenon that results in short, intense bursts of light-so-called superfluorescence 1. Because this phenomenon requires a fine balance of interactions between the emitters and their decoupling from the environment, together with close identity of the individual emitters, superfluorescence has thus far been observed only in a limited number of systems, such as certain atomic and molecular gases and a few solid-state systems 2-7. The generation of superfluorescent light in colloidal nanocrystals (which are bright photonic sources practically suited for optoelectronics 8,9) has been precluded by inhomogeneous emission broadening, low oscillator strength, and fast exciton dephasing. Here we show that caesium lead halide (CsPbX 3 , X = Cl, Br) perovskite nanocrystals 10-13 that are self-organized into highly ordered three-dimensional superlattices exhibit key signatures of superfluorescence. These are dynamically red-shifted emission with more than 20-fold accelerated radiative decay, extension of the first-order coherence time by more than a factor of four, photon bunching, and delayed emission pulses with Burnham-Chiao ringing behaviour 14 at high excitation density. These mesoscopically extended coherent states could be used to boost the performance of opto-electronic devices 15 and enable entangled multi-photon quantum light sources 16,17. Spontaneous emission of photons-such as happens in the process of fluorescence that is commonly used in displays and lighting-occurs because of coupling between excited two-level systems (TLS) and the vacuum modes of the electromagnetic field, effectively stimulated by its zero-point fluctuations. In 1954, Dicke predicted 18 that an ensemble of N identical TLS confined in a volume smaller than about λ 3 (where λ is the corresponding emission wavelength of the TLS) can exhibit coherent and cooperative spontaneous emission. This so-called superradiant emission results from the coherent coupling between individual TLS through the common vacuum modes, effectively leading to a single giant emitting dipole from all participating TLS. Superradiant emission has been observed in distinctly different physical systems, such as molecular aggregates and crystals 19 , nitrogen vacancy centres in diamond 20 and epitaxially grown quantum dots 21 (QDs). In the case when the excited TLS are initially fully uncorrelated, the coherence can be established only through spontaneously triggered correlations due to quantum fluctuations rather than by coherent excitation. When this occurs, a so-called superfluorescence (SF) pulse is emitted 1 (Fig. 1, illustrated for the present study). Both superradiant emission and coherent SF bursts are characterized by an accelerated radiative decay time τ SF ∝ τ SE /N, where the exponential decay time τ SE of spontaneous emission fr...

Metal-halide semiconductors with perovskite crystal structure are attractive due to their facile solution processability, and have recently been harnessed very successfully for high-efficiency photovoltaics and bright light sources. Here, we show that at low temperature single colloidal cesium lead halide (CsPbX3, where X = Cl/Br) nanocrystals exhibit stable, narrow-band emission with suppressed blinking and small spectral diffusion. Photon antibunching demonstrates unambiguously nonclassical single-photon emission with radiative decay on the order of 250 ps, representing a significant acceleration compared to other common quantum emitters. High-resolution spectroscopy provides insight into the complex nature of the emission process such as the fine structure and charged exciton dynamics.

The spatial localization of charge carriers to promote the formation of bound excitons and concomitantly enhance radiative recombination has long been a goal for luminescent semiconductors. Zero‐dimensional materials structurally impose carrier localization and result in the formation of localized Frenkel excitons. Now the fully inorganic, perovskite‐derived zero‐dimensional SnII material Cs4SnBr6 is presented that exhibits room‐temperature broad‐band photoluminescence centered at 540 nm with a quantum yield (QY) of 15±5 %. A series of analogous compositions following the general formula Cs4−xAxSn(Br1−yIy)6 (A=Rb, K; x≤1, y≤1) can be prepared. The emission of these materials ranges from 500 nm to 620 nm with the possibility to compositionally tune the Stokes shift and the self‐trapped exciton emission bands.

For over 80 years, tailored molecular assemblies (e.g., H-and J-aggregates) have been of interest for the emergence of collective phenomena in their optical spectra 1 , coherent long-range energy transport 2,3 and their conceptual similarity with natural light-harvesting complexes 4,5 . Another highly versatile platform for creating controlled, aggregated states exhibiting collective phenomena arises from the organization of colloidal semiconductor nanocrystals (NCs) into long-range ordered superlattices (SLs) 6 . Cesium lead halide perovskite NCs 7-9 have recently emerged as highly appealing building blocks, owing to their high oscillator strength 10 , slow dephasing (long coherence times of up to 80 ps) 11,12 , minimal inhomogeneous broadening of emission lines, and a bright triplet exciton character with orthogonal dipole orientation 10 , potentially enabling an efficient omnidirectional coupling. Here we present perovskite-type (ABO3) binary and ternary NC SLs by a shapedirected co-assembly of steric-stabilized, highly luminescent cuboid-shaped CsPbBr3 NCs (occupying B-and/or O-sites) with spherical Fe3O4 or NaGdF4 NCs (A-sites) and truncated-cuboid PbS NCs (B-site). Such ABO3 SLs, as well as other newly obtained SL structures (binary NaCl-and AlB2-types), exhibit a high degree of orientational ordering of CsPbBr3 nanocubes. These novel perovskite mesostructures exhibit superfluorescence (SF) -a collective emission resulting in a burst of photons. SF is characterized, at high excitation density, by emission pulses with ultrafast (22 ps) radiative decay and Burnham-Chiao ringing behaviour with a strongly accelerated build-up time.

Colloidal lead halide perovskite (LHP) nanocrystals are of interest as photoluminescent quantum dots (QDs) whose properties depend on the size and shape. They are normally synthesized on subsecond time scales through hard-to-control ionic metathesis reactions. We report a room-temperature synthesis of monodisperse, isolable spheroidal APbBr 3 QDs (A=Cs, formamidinium, methylammonium) that are size-tunable from 3 to over 13 nanometers. The kinetics of both nucleation and growth are temporally separated and drastically slowed down by the intricate equilibrium between the precursor (PbBr 2 ) and the A[PbBr 3 ] solute, with the latter serving as a monomer. QDs of all these compositions exhibit up to four excitonic transitions in their linear absorption spectra, and we demonstrate that the size-dependent confinement energy for all transitions is independent of the A-site cation.

Colloidal semiconductor quantum structures allow controlling the strong confinement of charge carriers through material composition and geometry. Besides being a unique platform to study fundamental effects, these materials attracted considerable interest due to their potential in opto-electronic and quantum communication applications. Heteronanostructures like CdSe/CdS offer new prospects to tailor their optical properties as they take advantage of a small conduction band offset allowing tunability of the electron delocalization from type-I toward quasi-type-II. Here, we report on a detailed study of the exciton recombination dynamics in CdSe/CdS heterorods. We observed a clear size-dependent radiative lifetime, which can be linked to the different degree of electron wave function (de)localization. Moreover, by increasing the temperature from 70 to 300 K, we observed a considerable increase of the radiative lifetime, clearly demonstrating a reduction of the conduction band offset at higher temperatures. Understanding and controlling electron delocalization in such heterostructures will be pivotal for realizing efficient and low-cost photonic devices.