Enhanced robustness and dimensional crossover of superradiance in cuboidal nanocrystal superlattices

Cooperative emission of coherent radiation from multiple emitters (known as superradiance) has been predicted and observed in various physical systems, most recently in CsPbBr$_3$ nanocrystal superlattices. Superradiant emission is coherent and occurs on timescales faster than the emission from isolated nanocrystals. Theory predicts cooperative emission being faster by a factor of up to the number of nanocrystals ($N$). However, superradiance is strongly suppressed due to the presence of energetic disorder, stemming from nanocrystal size variations and thermal decoherence. Here, we analyze superradiance from superlattices of different dimensionalities (1D, 2D and 3D) with variable nanocrystal aspect ratios. We predict as much as a thirty-fold enhancement in robustness against realistic values of energetic disorder in three-dimensional (3D) superlattices composed of cuboid-shaped, as opposed to cube-shaped, nanocrystals. Superradiance from small $(N\lesssim 10^3)$ two-dimensional (2D) superlattices is up to 10 times more robust to static disorder and up to twice as robust to thermal decoherence than three-dimensional (3D) superlattices with the same $N$. As the number of $N$ increases, a crossover in the robustness of superradiance occurs from 2D to 3D superlattices. For large $N\ (> 10^3)$, the robustness in 3D superlattices increases with $N$, showing cooperative robustness to disorder. This opens the possibility of observing superradiance even at room temperature in large 3D superlattices, if nanocrystal size fluctuations can be kept small

Heterogeneous Fluorescence Intermittency in Single Layer Reduced Graphene Oxide

We provide, for the first time, direct experimental evidence for heterogeneous blinking in reduced graphene oxide (rGO) during photolysis. The spatially resolved intermittency originates from regions within individual rGO sheets and shows 1/f-like power spectral density. We describe the evolution of rGO blinking using the multiple recombination center (MRC) model that captures common features of nanoscale blinking. Our results illustrate the universal nature of blinking and suggest a common microscopic origin for the effect

Resonant multiple-phonon absorption causes efficient anti-Stokes photoluminescence in CsPbBr3_3 nanocrystals

Lead-halide perovskite nanocrystals such as CsPbBr$_3$, exhibit efficient photoluminescence (PL) up-conversion, also referred to as anti-Stokes photoluminescence (ASPL). This is a phenomenon where irradiating nanocrystals up to 100 meV below gap results in higher energy band edge emission. Most surprising is that ASPL efficiencies approach unity and involve single photon interactions with multiple phonons. This is unexpected given the statistically disfavored nature of multiple-phonon absorption. Here, we report and rationalize near-unity anti-Stokes photoluminescence efficiencies in CsPbBr$_3$ nanocrystals and attribute it to resonant multiple-phonon absorption by polarons. The theory explains paradoxically large efficiencies for intrinsically disfavored, multiple-phonon-assisted ASPL in nanocrystals. Moreover, the developed microscopic mechanism has immediate and important implications for applications of ASPL towards condensed phase optical refrigeration

Universal emission intermittency in quantum dots, nanorods, and nanowires

Virtually all known fluorophores, including semiconductor nanoparticles, nanorods and nanowires exhibit unexplainable episodes of intermittent emission blinking. A most remarkable feature of the fluorescence intermittency is a universal power law distribution of on- and off-times. For nanoparticles the resulting power law extends over an extraordinarily wide dynamic range: nine orders of magnitude in probability density and five to six orders of magnitude in time. The exponents hover about the ubiquitous value of -3/2. Dark states routinely last for tens of seconds, which are practically forever on quantum mechanical time scales. Despite such infinite states of darkness, the dots miraculously recover and start emitting again. Although the underlying mechanism responsible for this phenomenon remains an enduring mystery and many questions remain, we argue that substantial theoretical progress has been made.Comment: 9 pages, 2 figures, Accepted versio

The Origin and Genetic Variation of Domestic Chickens with Special Reference to Junglefowls Gallus g. gallus and G. varius

It is postulated that chickens (Gallus gallus domesticus) became domesticated from wild junglefowls in Southeast Asia nearly 10,000 years ago. Based on 19 individual samples covering various chicken breeds, red junglefowl (G. g. gallus), and green junglefowl (G. varius), we address the origin of domestic chickens, the relative roles of ancestral polymorphisms and introgression, and the effects of artificial selection on the domestic chicken genome. DNA sequences from 30 introns at 25 nuclear loci are determined for both diploid chromosomes from a majority of samples. The phylogenetic analysis shows that the DNA sequences of chickens, red and green junglefowls formed reciprocally monophyletic clusters. The Markov chain Monte Carlo simulation further reveals that domestic chickens diverged from red junglefowl 58,000±16,000 years ago, well before the archeological dating of domestication, and that their common ancestor in turn diverged from green junglefowl 3.6 million years ago. Several shared haplotypes nonetheless found between green junglefowl and chickens are attributed to recent unidirectional introgression of chickens into green junglefowl. Shared haplotypes are more frequently found between red junglefowl and chickens, which are attributed to both introgression and ancestral polymorphisms. Within each chicken breed, there is an excess of homozygosity, but there is no significant reduction in the nucleotide diversity. Phenotypic modifications of chicken breeds as a result of artificial selection appear to stem from ancestral polymorphisms at a limited number of genetic loci

Subcortical brain volume, regional cortical thickness, and cortical surface area across disorders: findings from the ENIGMA ADHD, ASD, and OCD Working Groups

Objective Attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder (ASD), and obsessive-compulsive disorder (OCD) are common neurodevelopmental disorders that frequently co-occur. We aimed to directly compare all three disorders. The ENIGMA consortium is ideally positioned to investigate structural brain alterations across these disorders. Methods Structural T1-weighted whole-brain MRI of controls (n=5,827) and patients with ADHD (n=2,271), ASD (n=1,777), and OCD (n=2,323) from 151 cohorts worldwide were analyzed using standardized processing protocols. We examined subcortical volume, cortical thickness and surface area differences within a mega-analytical framework, pooling measures extracted from each cohort. Analyses were performed separately for children, adolescents, and adults using linear mixed-effects models adjusting for age, sex and site (and ICV for subcortical and surface area measures). Results We found no shared alterations among all three disorders, while shared alterations between any two disorders did not survive multiple comparisons correction. Children with ADHD compared to those with OCD had smaller hippocampal volumes, possibly influenced by IQ. Children and adolescents with ADHD also had smaller ICV than controls and those with OCD or ASD. Adults with ASD showed thicker frontal cortices compared to adult controls and other clinical groups. No OCD-specific alterations across different age-groups and surface area alterations among all disorders in childhood and adulthood were observed. Conclusion Our findings suggest robust but subtle alterations across different age-groups among ADHD, ASD, and OCD. ADHD-specific ICV and hippocampal alterations in children and adolescents, and ASD-specific cortical thickness alterations in the frontal cortex in adults support previous work emphasizing neurodevelopmental alterations in these disorders

Band edge spectroscopy of CdSe quantum dots

Thesis (Ph.D.)--Massachusetts Institute of Technology, Dept. of Chemistry, 1998.Includes bibliographical references (p. 373-381) and index.In this thesis, I describe work done to understand the band edge exciton fine structure of CdSe quantum dots (QDs). These QDs or nanocrystallites are the result of recent synthetic efforts in the Bawendi group to produce nearly monodisperse nanocrystalline materials. The QDs are roughly spherical in shape and range in size from 10 to 50 A in radius. A number of optical experiments have been conducted on the material to understand its optical properties, particularly, the absorption and luminescence. However, several longstanding questions remain. Among them is the origin of the material's band edge luminescence. The emission is unusual because it displays long ([mu]s) lifetimes and exhibits a characteristic, size dependent, Stokes shift. As a consequence, many past studies have implicated the surface as the origin of the emission. In this respect, the surface localization of photogenerated carriers qualitatively explains both the long lifetimes and redshift of the luminescence. Recent theoretical and experimental studies, however, have suggested that the emission arises from an intrinsic core state analogous to a triplet state in small molecules. We describe the theoretical modeling of the QD electronic structure in.eluding the effects of shape, crystal field and the electron-hole exchange interaction. When all symmetry breaking effects are considered, we predict the presence of five fine structure states underlying the hand edge exciton rather than an eightfold degenerate exciton ground state. Following this, we intentionally modify the surface of the nanocrystallites to see the effect this has on the luminescence. Our results suggest that, to a large extent, the surface plays little role in the energetics of the emission. For QDs passivated with different organic and inorganic ligands we find little or no change in values of the "resonant" and "non-resonant" Stokes shift. This strongly supports the above mentioned fine structure model. Subsequent chapters take the proposed theory a step further, using it to explain the unusual behavior of the nanocrystallites subjected to an external magnetic field. The last two chapters pose the question of what happens when the QDs are intentionally doped with a paramagnetic impurity such as manganese? We expected that spin interactions between host and dopant will result in interesting optical phenomena such as the activation of dark excitons as well as shifts in fine structure energies due to an exchange induced mixing of states.by Masaru Kenneth Kuno.Ph.D