Federica Bertolotti

Monodisperse Formamidinium Lead Bromide Nanocrystals with Bright and Stable Green Photoluminescence

Bright green emitters with adjustable photoluminescence (PL) maxima in the range of 530–535 nm and full-width at half-maxima (fwhm) of <25 nm are particularly desirable for applications in television displays and related technologies. Toward this goal, we have developed a facile synthesis of highly monodisperse, cubic-shaped formamidinium lead bromide nanocrystals (FAPbBr3 NCs) with perovskite crystal structure, tunable PL in the range of 470–540 nm by adjusting the nanocrystal size (5–12 nm), high quantum yield (QY) of up to 85% and PL fwhm of <22 nm. High QYs are also retained in films of FAPbBr3 NCs. In addition, these films exhibit low thresholds of 14 ± 2 μJ cm–2 for amplified spontaneous emission.

Dismantling the “Red Wall” of Colloidal Perovskites: Highly Luminescent Formamidinium and Formamidinium–Cesium Lead Iodide Nanocrystals

Colloidal nanocrystals (NCs) of APbX3-type lead halide perovskites [A = Cs+, CH3NH3+ (methylammonium or MA+) or CH(NH2)2+ (formamidinium or FA+); X = Cl–, Br–, I–] have recently emerged as highly versatile photonic sources for applications ranging from simple photoluminescence down-conversion (e.g., for display backlighting) to light-emitting diodes. From the perspective of spectral coverage, a formidable challenge facing the use of these materials is how to obtain stable emissions in the red and infrared spectral regions covered by the iodide-based compositions. So far, red-emissive CsPbI3 NCs have been shown to suffer from a delayed phase transformation into a nonluminescent, wide-band-gap 1D polymorph, and MAPbI3 exhibits very limited chemical durability. In this work, we report a facile colloidal synthesis method for obtaining FAPbI3 and FA-doped CsPbI3 NCs that are uniform in size (10–15 nm) and nearly cubic in shape and exhibit drastically higher robustness than their MA- or Cs-only cousins with similar sizes and morphologies. Detailed structural analysis indicated that the FAPbI3 NCs had a cubic crystal structure, while the FA0.1Cs0.9PbI3 NCs had a 3D orthorhombic structure that was isostructural to the structure of CsPbBr3 NCs. Bright photoluminescence (PL) with high quantum yield (QY > 70%) spanning red (690 nm, FA0.1Cs0.9PbI3 NCs) and near-infrared (near-IR, ca. 780 nm, FAPbI3 NCs) regions was sustained for several months or more in both the colloidal state and in films. The peak PL wavelengths can be fine-tuned by using postsynthetic cation- and anion-exchange reactions. Amplified spontaneous emissions with low thresholds of 28 and 7.5 μJ cm–2 were obtained from the films deposited from FA0.1Cs0.9PbI3 and FAPbI3 NCs, respectively. Furthermore, light-emitting diodes with a high external quantum efficiency of 2.3% were obtained by using FAPbI3 NCs.

Coherent Nanotwins and Dynamic Disorder in Cesium Lead Halide Perovskite Nanocrystals

Crystal defects in highy luminescent colloidal nanocrystals (NCs) of CsPbX3 perovskites (X = Cl, Br, I) are investigated. Here, using X-ray total scattering techniques and the Debye scattering equation (DSE), we provide evidence that the local structure of these NCs always exhibits orthorhombic tilting of PbX6 octahedra within locally ordered subdomains. These subdomains are hinged through a two-/three-dimensional (2D/3D) network of twin boundaries through which the coherent arrangement of the Pb ions throughout the whole NC is preserved. The density of these twin boundaries determines the size of the subdomains and results in an apparent higher-symmetry structure on average in the high-temperature modification. Dynamic cooperative rotations of PbX6 octahedra are likely at work at the twin boundaries, causing the rearrangement of the 2D or 3D network, particularly effective in the pseudocubic phases. An orthorhombic, 3D γ-phase, isostructural to that of CsPbBr3 is found here in as-synthesized CsPbI3 NCs.

Crystal symmetry breaking and vacancies in colloidal lead chalcogenide quantum dots

Size and shape tunability and low-cost solution processability make colloidal lead chalcogenide quantum dots (QDs) an emerging class of building blocks for innovative photovoltaic, thermoelectric and optoelectronic devices. Lead chalcogenide QDs are known to crystallize in the rock-salt structure, although with very different atomic order and stoichiometry in the core and surface regions; however, there exists no convincing prior identification of how extreme downsizing and surface-induced ligand effects influence structural distortion. Using forefront X-ray scattering techniques and density functional theory calculations, here we have identified that, at sizes below 8 nm, PbS and PbSe QDs undergo a lattice distortion with displacement of the Pb sublattice, driven by ligand-induced tensile strain. The resulting permanent electric dipoles may have implications on the oriented attachment of these QDs. Evidence is found for a Pb-deficient core and, in the as-synthesized QDs, for a rhombic dodecahedral shape with nonpolar {110} facets. On varying the nature of the surface ligands, differences in lattice strains are found.

DEBUSSY 2.0: the new release of a Debye user system for nanocrystalline and/or disordered materials

The new release of DEBUSSY is introduced, a free open-source package devoted to the application of the Debye function analysis of powder diffraction data from nanocrystalline, defective and/or nonperiodic materials. The general strategy of the suite remains unchanged, following a two-step approach managed by the CLAUDE and DEBUSSY programs, respectively. The first step essentially consists in generating a database where structural, size and shape information on a nanocrystal population is stored; the second step consists in the calculation, through the Debye scattering equation, of the total diffraction pattern using the previously generated database and a set of model parameters provided by the user and then optimized by the program. The novelties lie in the computational, modelling and graphical levels, and several new programs and features have been added. Among these are a new general comprehensive input file format (.ddb) for the database generation, the automatic management of the space-group symmetry and .cif file, new nanocrystal shapes, size-dependent site occupancy factors and thermal parameters for each atomic species, new lattice expansion functions, and a newly developed algorithm for calculating the standard errors of the optimized parameters. The CLAUDE suite also includes a program for calculation of the pair distribution function. Last but not least, a graphical user interface, which makes it easier to edit input files, execute the programs of the suite in a chain-like way, and plot the results in an automatic or custom manner, is provided.

A total scattering Debye function analysis study of faulted Pt nanocrystals embedded in a porous matrix.

Faulted face-centred cubic platinum nanocrystals, grown within a nanoporous silica matrix, have been extensively characterized by the Debye function analysis method applied to wide-angle synchrotron X-ray total scattering data. A method for building databases of sampled interatomic distances of weakly faulted materials is proposed, maintaining statistical significance and allowing complete populations of differently sized and shaped nanocrystals to be used within the DEBUSSY approach. This study suggests that anisotropic Pt nanoclusters are formed in the presence of a shape-directing (templating) agent, and tentatively describes the effects of post-synthetic temperature treatments on fault probability, size, shape and dispersion of the nanocrystal populations. Surface relaxation effects are also observed in the smallest particles.

C–halogen…O supramolecular synthons:in situcryocrystallisation of 1,2-dihalotetrafluoroethane/HMPA adducts

The in situ cryocrystallisation technique has been used to obtain four adducts between hexamethylphosphortriamide and 1,2-dihalotetrafluoroethanes having iodine, bromine and chlorine as halogen-bonding donor atoms. These systems allowed for a precise comparison of different C–X…O synthons. The effectiveness and reliability of the pharmacologically important C–Cl…O synthons are proven.

The synergic role of collagen and citrate in stabilizing amorphous calcium phosphate precursors with platy morphology.

Bioinspired in vitro collagen mineralization experiments have been performed in the presence of citrate and the combined role of the two bone organic matrix components in controlling mineral formation was investigated for the first time. Mineralized and non-mineralized collagen fibrils have been in depth characterized by combining small- and wide-angle X-ray scattering (SAXS/WAXS) techniques with Atomic Force Microscopy (AFM) imaging. A synergic effect of collagen and citrate in driving the formation of long-term stable amorphous calcium phosphate (ACP) nanoparticles with platy morphology was found. AFM images on mineralized collagen fibrils revealed that some of the ACP nanoparticles were deposited on the intramolecular nanoscopic holes of collagen fibrils. STATEMENT OF SIGNIFICANCE Citrate is an important component of the bone organic matrix but its specific role in bone mineralization is presently unclear. In this work, bioinspired in vitro collagen mineralization experiments in the presence of citrate have been carried out and the combined role of collagen and citrate in controlling mineral formation has been addressed for the first time. Through X-ray scattering and Atomic Force Microscopy characterizations on mineralized and non-mineralized collagen fibrils, we have found that citrate in synergy with collagen stabilizes an amorphous calcium phosphate (ACP) phase with platy morphology over one week and controls its deposition on collagen fibrils.

Insight into non-linearly shaped superconducting whiskers via a synchrotron nanoprobe

We were successful in synthesizing non-linear YBa2Cu3Ox whiskers, i.e. half loops or kinked shapes, which are promising candidates for solid-state devices based on the intrinsic Josephson effect and with improved electrical connections. We report on a complete characterization of their structural properties via a synchrotron nanoprobe as well as laboratory single-crystal diffraction techniques. This investigation allowed us to fully disclose the growth mechanism, which leads to the formation of curved whiskers. The superconducting properties are evaluated in comparison with their straight counterpart, revealing a strong functional analogy and confirming their potential applicability in superconducting electronic devices.

A comprehensive structural and microstructural investigation of a new iron–telluride nano phase

A nanocrystalline iron-rich telluride, Fe5Te4, was prepared mechanochemically using ball milling procedures in an inert atmosphere, starting from FexTe powder mixtures with x = 1.0, 1.25 and 1.5, with x = 1.25 leading to the pure phase. Its crystal structure has a tetragonal (I4/m) symmetry and shows an anomalously short Fe–Fe interaction of 2.52 A. The microstructure of the nanocrystalline material was deeply studied by synchrotron X-ray total scattering techniques and the Debye scattering equation (DSE) method. A DSE-based microstrain model, integrated with structure, size and morphology information, indicates the presence of highly strained nanoparticles, with strain more preferentially accumulated in the ab-plane than along the c-axis of the tetragonal structure. Magnetic and Mossbauer spectroscopic characterization indicates that the samples present a spin glass state below the freezing temperature (ca. 150 K) and a magnetic behavior dependent on the applied field, showing ferromagnetic-like loops and a superparamagnetic-like increase of magnetization up to the maximum applied field of 90 kOe.