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...

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Colloidal nanoplatelets (NPLs) are atomically flat, quasi-two-dimensional particles of a semiconductor. Despite intense interest in their optical properties, several observations concerning the emission of CdSe NPLs remain puzzling. While their ensemble photoluminescence spectrum consists of a single narrow peak at room temperature, two distinct emission features appear at temperatures below ~160 K. Several competing explanations for the origin of this two-color emission have been proposed. Here, we present temperature-and time-dependent experiments demonstrating that the two emission colors are due to two subpopulations of uncharged and charged NPLs. We study dilute films of isolated NPLs, thus excluding any explanation relying on collective effects due to NPL stacking. Temperature-dependent measurements explain that trion emission from charged NPLs is bright at cryogenic temperatures, while temperature activation of nonradiative Auger recombination quenches the trion emission above 160 K. Our findings clarify many of the questions surrounding the photoluminescence of CdSe NPLs.