In situ functionalization of nanoparticles by surfactants is a versatile strategy to stabilize bicontinuous interfacially jammed emulsion gels (bijels). However, the dynamic and composition-dependent nature of surfactant adsorption complicates the reproducibility of kinetically determined formation. While prior research has primarily correlated the precursor composition with the final bijel morphology, the underlying formation dynamics have not yet been fully elucidated. This paper investigates the formation of bijels fabricated via solvent transfer-induced phase separation (STrIPS). To explore how surfactants can affect the formation kinetics, we investigated the combination of silica nanoparticles functionalized with cetyltrimethylammonium bromide (CTAB). Using in situ (ultra)small-angle X-ray scattering and ex situ confocal microscopy, we show that higher CTAB concentrations accelerate both liquid-liquid phase separation and nanoparticle self-assembly, shortening the bijel formation time from 600 to 250 ms. Moreover, we find that initially self-assembled particles can rearrange or disassemble during phase separation depending on the CTAB concentration. Analysis of the particle interactions in precursor mixtures, supported by theoretical modeling, proposes a correlation between interparticle forces and the final bijel morphology. These findings highlight the importance of understanding the formation dynamics to control the bijel structure and enhance their reproducibility. The obtained insights into phase separation and particle assembly are important to advance biosynthesis in applications like catalysis and energy storage.

This review explores different colloidal systems and their crystals as well as their special case namely-mesocrystals. First, we highlight recent advances in fabrication methods of colloidal crystals (mesocrystals) and then describe small-angle and ultra-small-angle x-ray scattering from colloidal assemblies organized from particles of different shape. Here, we already introduce different types of defects that are present in colloidal crystals. Next, we go to a modern description of angular x-ray cross-correlation analysis and its applications on colloidal and mesocrystalline materials. After that we discuss phase retrieval techniques, namely coherent x-ray diffraction imaging and ptychography, as emerging tools for structural characterization of colloidal crystals and mesocrystals. We conclude with perspectives on the opportunities that will be provided by the 4th generation synchrotron sources for studying colloidal crystals and mesocrystals.

Nanostructured materials formed via kinetically controlled self-assembly processes gather more interest nowadays. In particular, bicontinuous emulsion gels stabilized by colloidal particles, called bijels, are attractive materials as they combine bulk properties of two immiscible liquids into an interwoven network structure. The limited understanding of the complex formation phenomena of bijels restricts the control over the synthesis, and so its applicability. In this work, in situ (ultra-) small-angle X-ray scattering is applied to gain insight into the phase separation and self-assembly kinetics of bijels formed via solvent transfer induced phase separation. An X-ray compatible microfluidic setup allows accessing the kinetics of the extrusion process with a millisecond resolution. The formation of such bijels out of a liquid precursor mixture is shown to occur via three consecutive steps. The first 7 ms of the extrusion are dominated by fluid dynamics. Then, the precursor mixture remains in an induction phase for 50 ms where nanoparticles start to self-assemble without structural development on the (sub)micron scale. From 50 ms on, an inward propagation of a liquid-liquid phase separation front occurs, besides the proceeding nanoparticle self-assembly obtaining (sub)micron-sized structures. This time-resolved monitoring technique offers valuable insights into the structural evolution of kinetically controlled materials and enhances our understanding of the formation of bicontinuous emulsion gels.

Exploring Temperature- and Pressure-Dependent Elastic Properties of Halide Perovskites and ElpasolitesLoreta Muscarella a, Huygen J. Jöbsis b, Bettina Baumgartner b, P. Tim Prins b, D. Nicolette Maaskant b, Andrei V. Petukhov b, Dmitry Chernyshov c, Charles J McMonagle c, Eline M. Hutter ba Department of Physics and Astronomy, Faculty of Sciences, Vrije Universiteit Amsterdamb Utrecht University, Inorganic Chemistry and Catalysis, Debye Institute for Nanomaterials Science, Netherlandsc ESRF, The European Synchrotron, 71 Avenue des Martyrs, CS40220, 38043 Grenoble Cedex 9, FranceInternational Conference on Hybrid and Organic PhotovoltaicsProceedings of International Conference on Hybrid and Organic Photovoltaics (HOPV24)València, Spain, 2024 May 12th - 15thOrganizer: Bruno EhrlerOral, Loreta Muscarella, presentation 173DOI: https://doi.org/10.29363/nanoge.hopv.2024.173Publication date: 6th February 2024Halide perovskites and elpasolites are key for optoelectronic applications due to their exceptional performance and adaptability. However, understanding their crucial elastic properties for synthesis and device operation remains limited. We performed temperature- and pressure-dependent synchrotron-based powder X-ray diffraction at low pressures (ambient to 0.06 GPa) to investigate their elastic properties in their ambient-pressure crystal structure. We found common trends in bulk modulus and thermal expansivity, with an increased halide ionic radius (Cl to Br to I) resulting in greater softness, higher compressibility and thermal expansivity in both class of materials. For non-cubic systems, in which the elastic properties are anisotropic, we obtained axis-dependent compressibility. The A cation has a minor effect, and mixed-halide compositions show intermediate properties. Notably, thermal phase transitions in MAPbI3 and CsPbCl3 induced lattice softening and negative expansivity for specific crystal axes, even at temperatures far from the transition point. These results emphasize the significance of considering temperature-dependent elastic properties, which can significantly impact device stability and performance during manufacturing or temperature sweeps. © FUNDACIO DE LA COMUNITAT VALENCIANA SCITOnanoGe is a prestigious brand of successful science conferences that are developed along the year in different areas of the world since 2009. Our worldwide conferences cover cutting-edge materials topics like perovskite solar cells, photovoltaics, optoelectronics, solar fuel conversion, surface science, catalysis and two-dimensional materials, among many others.MATSUSPreviously nanoGe Spring Meeting (NSM) and nanoGe Fall Meeting (NFM), MATSUS is a multiple symposia conference focused on a broad set of topics of advanced materials preparation, their fundamental properties, and their applications, in fields such as renewable energy, photovoltaics, lighting, semiconductor quantum dots, 2-D materials synthesis, charge carriers dynamics, microscopy and spectroscopy semiconductors fundamentals, etc.International Conference on Hybrid and Organic PhotovoltaicsInternational Conference on Hybrid and Organic Photovoltaics (HOPV) is celebrated yearly in May. The main topics are the development, function and modeling of materials and devices for hybrid and organic solar cells. The field is now dominated by perovskite solar cells but also other hybrid technologies, as organic solar cells, quantum dot solar cells, and dye-sensitized solar cells and their integration into devices for photoelectrochemical solar fuel production.Asia-Pacific International Conference on Perovskite, Organic Photovoltaics and OptoelectronicsThe main topics of the Asia-Pacific International Conference on Perovskite, Organic Photovoltaics and Optoelectronics (IPEROP) are discussed every year in Asia-Pacific for gathering the recent advances in the fields of material preparation, modeling and fabrication of perovskite and hybrid and organic materials. Photovoltaic devices are analyzed from fundamental physics and materials properties to a broad set of applications. The conference also covers the developments of perovskite optoelectronics, including light-emitting diodes, lasers, optical devices, nanophotonics, nonlinear optical properties, colloidal nanostructures, photophysics and light-matter coupling.International Conference on Perovskite Thin Film Photovoltaics Perovskite Photonics and OptoelectronicsThe International Conference on Perovskite Thin Film Photovoltaics Perovskite Photonics and Optoelectronics (NIPHO) is the best place to hear the latest developments in perovskite solar cells as well as on recent advances in the fields of perovskite light-emitting diodes, lasers, optical devices, nanophotonics, nonlinear optical properties, colloidal nanostructures, photophysics and light-matter coupling.

Hypothesis. Multi-walled tubular aggregates formed by hierarchical self-assembly of beta-cyclodextrin (β-CD) and sodium dodecylsulfate (SDS) hold a great potential as microcarriers. However, the underlying mechanism for this self-assembly is not well understood. To advance the application of these structures, it is essential to fine-tune the cavity size and comprehensively elucidate the energetic balance driving their formation: the bending modulus versus the microscopic line tension.Experiments. We investigated temperature-induced changes in the hierarchical tubular aggregates using synchrotron small-angle X-ray scattering across a broad concentration range. Detailed analysis of the scattering patterns enabled us to determine the structural parameters of the microtubes and to construct a phase diagram of the system.Findings. The microtubes grow from the outside in and melt from the inside out. We relate derived structural parameters to enthalpic changes driving the self-assembly process on the molecular level in terms of their bending modulus and microscopic line tension. We find that the conformation of the crystalline bilayer affects the saturation concentration, providing an example of a phenomenon we call conformational freezing point depression. Inspired by the colligative phenomenon of freezing point depression, well known from undergraduate physics, we model this system by including the membrane conformation, which can describe the energetics of this hierarchical system and give access to microscopic properties without free parameters.

β-NaYF4 nanocrystals are a popular class of optical materials. They can be doped with optically active lanthanide ions and shaped into core-multi-shell geometries with controlled dopant distributions. Here, we follow the synthesis of β-NaYF4 nanocrystals from α-NaYF4 precursor particles using in situ small-angle and wide-angle X-ray scattering and ex situ electron microscopy. We observe an evolution from a unimodal particle size distribution to bimodal, and eventually back to unimodal. The final size distribution is narrower in absolute numbers than the initial distribution. These peculiar growth dynamics happen in large part before the α-to-β phase transformation. We propose that the splitting of the size distribution is caused by variations in the reactivity of α-NaYF4 precursor particles, potentially due to inter-particle differences in stoichiometry. Rate equation modeling confirms that a continuous distribution of reactivities can result in the observed particle growth dynamics.

Halide perovskites and elpasolites are key for optoelectronic applications due to their exceptional performance and adaptability. However, understanding their crucial elastic properties for synthesis and device operation remains limited. We performed temperature- and pressure-dependent synchrotron-based powder X-ray diffraction at low pressures (ambient to 0.06 GPa) to investigate their elastic properties in their ambient-pressure crystal structure. We found common trends in bulk modulus and thermal expansivity, with an increased halide ionic radius (Cl to Br to I) resulting in greater softness, higher compressibility, and thermal expansivity in both materials. The A cation has a minor effect, and mixed-halide compositions show intermediate properties. Notably, thermal phase transitions in MAPbI3 and CsPbCl3 induced lattice softening and negative expansivity for specific crystal axes, even at temperatures far from the transition point. These results emphasize the significance of considering temperature-dependent elastic properties, which can significantly impact device stability and performance during manufacturing or temperature sweeps.

An application of angular X-ray cross-correlation analysis (AXCCA) to the scattered intensity distribution measured in 3D reciprocal space from a single-crystalline sample is proposed in this work. Contrary to the conventional application of AXCCA, when averaging over many 2D diffraction patterns collected from different randomly oriented samples is required, the proposed approach provides an insight into the structure of a single specimen. This is particularly useful in studies of defect-rich samples that are unlikely to have the same structure. The application of the method is shown on an example of a qualitative structure determination of a colloidal crystal from simulated as well as experimentally measured 3D scattered intensity distributions.

Understanding the relationship between colloidal building block shape and self-assembled material structure is important for the development of novel materials by self-assembly. In this regard, colloidal superballs are unique building blocks because their shape can smoothly transition between spherical and cubic. Assembly of colloidal superballs under spherical confinement results in macroscopic clusters with ordered internal structure. By utilizing Small Angle X-Ray Scattering (SAXS), we probe the internal structure of colloidal superball dispersion droplets during confinement. We observe and identify four distinct drying regimes that arise during compression via evaporating droplets, and we track the development of the assembled macrostructure. As the superballs assemble, we found that they arrange into the predicted paracrystalline, rhombohedral C1-lattice that varies by the constituent superballs’ shape. This provides insights in the behavior between confinement and particle shape that can be applied in the development of new functional materials.

An anisotropic colloidal shape in combination with an externally tunable interaction potential results in a plethora of self-assembled structures with potential applications toward the fabrication of smart materials. Here we present our investigation on the influence of an external magnetic field on the self-assembly of hematite-silica core-shell prolate colloids for two aspect ratios ρ = 2.9 and 3.69. Our study shows a rather counterintuitive but interesting phenomenon, where prolate colloids self-assemble into oblate liquid crystalline (LC) phases. With increasing concentration, particles with smaller ρ reveal a sequence of LC phases involving para-nematic, nematic, smectic, and oriented glass phases. The occurrence of a smectic phase for colloidal ellipsoids has been neither predicted nor reported before. Quantitative shape analysis of the particles together with extensive computer simulations indicate that in addition to ρ, a subtle deviation from the ideal ellipsoidal shape dictates the formation of this unusual sequence of field-induced structures. Particles with ρ = 2.9 exhibit a hybrid shape containing features from both spherocylinders and ellipsoids, which make their self-assembly behavior richer than that observed for either of the "pure" shapes. The shape of the particles with higher ρ matches closely with the ideal ellipsoids, as a result their phase behavior follows the one expected for a "pure" ellipsoidal shape. Using anisotropic building blocks and external fields, our study demonstrates the ramifications of the subtle changes in the particle shape on the field-directed self-assembled structures with externally tunable properties.

We study the crystallization of colloidal dispersions under capillary-action-induced shear as the dispersion is drawn into flat walled capillaries. Using confocal microscopy and small angle x-ray scattering, we find that the shear near the capillary walls influences the crystallization to result in large random hexagonal close-packed (RHCP) crystals with long-range orientational order over tens of thousands of colloidal particles. We investigate the crystallization mechanism and find partial crystallization under shear, initiating with hexagonal planes at the capillary walls, where shear is highest, followed by epitaxial crystal growth from these hexagonal layers after the shear is stopped. We then characterize the three-dimensional crystal structure finding that the shear-induced crystallization leads to larger particle separations parallel to the shear and vorticity directions as compared to the equilibrium RHCP structure. Confocal microscopy reveals that competing shear directions, where the capillary walls meet at a corner, create differently oriented hexagonal planes of particles. The single-orientation RHCP colloidal crystals remain stable after formation and are produced without the need of complex shear cell arrangements.

The growth of two-dimensional platelets of the CdX family (X = S, Se, or Te) in an organic solvent requires the presence of both long- and short-chain ligands. This results in nanoplatelets of atomically precise thickness and long-chain ligand-stabilized Cd top and bottom surfaces. The platelets show a bright and spectrally pure luminescence. Despite the enormous interest in CdX platelets for optoelectronics, the growth mechanism is not fully understood. Riedinger et al. studied the reaction without a solvent and showed the favorable role for short-chain carboxylates for growth in two dimensions. Their model, based on the total energy of island nucleation, shows favored side facet growth versus growth on the top and bottom surfaces. However, several aspects of the synthesis under realistic conditions are not yet understood: Why are both short- and long-chain ligands required to obtain platelets? Why does the synthesis result in both isotropic nanocrystals and platelets? At which stage of the reaction is there bifurcation between isotropic and 2D growth? Here, we report an in situ study of the CdSe nanoplatelet reaction under practical synthesis conditions. We show that without short-chain ligands, both isotropic and mini-nanoplatelets form in the early stage of the process. However, most remaining precursors are consumed in isotropic growth. Addition of acetate induces a dramatic shift toward nearly exclusive 2D growth of already existing mini-nanoplatelets. Hence, although myristate stabilizes mini-nanoplatelets, mature nanoplatelets only grow by a subtle interplay between myristate and acetate, the latter catalyzes fast lateral growth of the side facets of the mini-nanoplatelets.

The characterization of periodic order in assemblies of colloidal particles can be complicated by the coincidence of Bragg diffraction peaks of the structure and minima in the form factor of the particles. Here, we demonstrate a general strategy to overcome this problem that is applicable to all low-dimensional structures. This approach is demonstrated in the application of small-angle X-ray scattering (SAXS) for the characterization of monolayers of colloidal silica superballs prepared using the unidirectional rubbing method. In this method, the ordering of the colloidal superballs is achieved by mechanically rubbing them onto a polydimethylsiloxane (PDMS)-coated surface. Using three differently shaped superballs, ranging from spherical to almost cubic, we show that certain Bragg peaks may not appear in the diffraction patterns due to the presence of minima in the form factor. We show that these missing Bragg peaks can be visualized by imaging the colloidal monolayers at various orientations. Moreover, we argue that the same strategy can be applied to other techniques, such as neutron scattering.

Sarah N. Schyck*,1 Janne-Mieke Meijer*,2 Lucia Baldauf,3, 4 Peter Schall,3 Andrei V. Petukhov,5, 6 and Laura Rossi1, * Delft University of Technology,Department of Chemical Engineering, 2629 HZ Delft, The Netherlands Eindhoven University of Technology, Department of Applied Physics and Insitute for Complex Molecular Systems, Eindhoven, The Netherlands University of Amsterdam, Institute of Physics, Science Park 904, Amsterdam, The Netherlands Present address: Delft University of Technology,Department of Bionanoscience, Kavli Institute of Nanoscience, Delft 2629 HZ Delft, The Netherlands Utrecht University, Debye Institute for Nanomaterials Science, Utrecht, the Netherlands Eindhoven University of Technology, Department of Chemical Engineering and Chemistry, Eindhoven, the Netherlands (Dated: August 16, 2021)

The hot injection synthesis of colloidal semiconductor nanocrystals is renowned for producing nanocolloids with superb size dispersions. Burst nucleation and diffusion-controlled size focusing during growth have been invoked to rationalize this characteristic, yet experimental evidence supporting the pertinence of these concepts is scant. Using a well-established CdSe synthesis followed with in situ X-ray scattering, we show that nucleation is an extended event that overlaps with growth and can last for 15-20% of the reaction time. Moreover, we find that size focusing outpaces predictions of diffusion-limited growth. This observation supports the conclusion that nanocrystal growth is dictated by the surface reactivity, which drops sharply for larger nanocrystals. Kinetic reaction simulations demonstrate this so-called superfocusing can lengthen the nucleation period and promote size-focusing. The finding that narrow size dispersions can emerge from the counteracting effects of extended nucleation and reaction-limited size focusing ushers in an evidence-based perspective that turns hot injection into a rational scheme to produce monodisperse nanocolloids.

Experimental evidence is presented for the spontaneous formation of chiral configurations in bulk dispersions of magnetized colloids that interact by a combination of anisotropic dipolar interactions and isotropic depletion attractions. The colloids are superparamagnetic silica spheres, magnetized and aligned by a carefully tuned uniform external magnetic field; isotropic attractions are induced by using poly(ethylene oxide) polymers as depleting agents. At specific polymer concentrations, sphere chains wind around each other to form helical structures–of the type that previously have only been observed in simulations on small sets of unconfined dipolar spheres with additional isotropic interactions.

Correction for 'Block copolymer hierarchical structures from the interplay of multiple assembly pathways' by Alessandro Ianiro et al., Polym. Chem., 2020, DOI: 10.1039/d0py00081g.

With the rapid development of short-pulse intense laser sources, studies of matter under extreme irradiation conditions enter further unexplored regimes. In addition, an application of X-ray Free-Electron Lasers (XFELs) delivering intense femtosecond X-ray pulses, allows to investigate sample evolution in IR pump - X-ray probe experiments with an unprecedented time resolution. Here we present a detailed study of the periodic plasma created from the colloidal crystal. Both experimental data and theory modeling show that the periodicity in the sample survives to a large extent the extreme excitation and shock wave propagation inside the colloidal crystal. This feature enables probing the excited crystal, using the powerful Bragg peak analysis, in contrast to the conventional studies of dense plasma created from bulk samples for which probing with Bragg diffraction technique is not possible. X-ray diffraction measurements of excited colloidal crystals may then lead towards a better understanding of matter phase transitions under extreme irradiation conditions.

We have quantified the structure of the colloidal gas-liquid interface using synchrotron X-ray reflectivity measurements on a model colloid-polymer mixture. The interfacial width shows mean-field scaling with the colloid density difference, and the density profiles appear to be monotonic. Furthermore, our measurements allow us to distinguish between different theoretical polymer descriptions commonly used to model colloid-polymer mixtures. Our results highlight the importance of capturing the correct polymer physics in obtaining a quantitative theoretical description of the colloidal gas-liquid interface.

Structurally complex hierarchical block copolymer assemblies can be formed in solution by controlling the interplay of phase separation, crystallization and block segregation with temperature.