Tuning Magnetic and Photophysical Properties of Luminomagnetic Metal-Organic Framework Composites in an Inverse Core-Satellite Structure.

Luminomagnetic composites have been synthesized that allow for an individual tuning of luminescence intensity, chromaticity and magnetization by combination of superparamagnetic, citrate-stabilized iron oxide nanoparticles with the luminescent MOFs 3 ∞ [Ln2 (BDC)3 (H2 O)4 ] (Ln=Eu, Tb; BDC2- =terephthalate). The components are arranged to a concept of inverse structuring compared to previous luminomagnetic composites with MOF@magnetic particle (shell@core) composition so that the luminescent MOF now acts as core and is covered by magnetic nanoparticles forming the satellite shell. Thereby, the magnetic and photophysical properties are individually tuneable between high emission intensity (1.2 ⋅ 106  cps mg-1 ) plus low saturation magnetization (6 emu g-1 ) and the direct opposite (0.09 ⋅ 106  cps mg-1 ; 42 emu g-1 ) by adjusting the particle coverage of the MOF. This is not achievable with a core-shell structure having a magnetic core and a dense MOF shell. The composition of the composites and the influence of different synthesis conditions on their properties were investigated by SEM/EDX, PXRD, magnetization measurements and photoluminescence spectroscopy.

A code with a twist: supraparticle microrod composites with direction dependent optical properties as anti-counterfeit labels.

Superparamagnetic iron oxide nanoparticles can be assembled to form anisotropic microrod supraparticles with the assistance of a magnetic field during synthesis. Optionally, these iron oxide microrods can furthermore be coated with a thin silica shell. Due to their anisotropic structure, both microrod types can be aligned in a magnetic field while being dispersed in a matrix material which can be cured during the alignment of the microrods. In this way, an anisotropic magnetic composite is obtained. Interestingly, it was observed that the optical extinction properties for visible light in such a composite are direction dependent, which can be explained by using appropriate models based on Maxwell equations. Based on the understanding of this principle, a clever approach for a hidden code could be proposed which is obtained from mixing pure iron oxide and silica coated microrod supraparticles in such an anisotropic composite. The hidden code, which comes down to obtaining a single value eventually, can only be revealed when knowing that the system needs to be measured with a certain "twist".

Supraparticles: Functionality from Uniform Structural Motifs.

Under the right process conditions, nanoparticles can cluster together to form defined, dispersed structures, which can be termed supraparticles. Controlling the size, shape, and morphology of such entities is a central step in various fields of science and technology, ranging from colloid chemistry and soft matter physics to powder technology and pharmaceutical and food sciences. These diverse scientific communities have been investigating formation processes and structure/property relations of such supraparticles under completely different boundary conditions. On the fundamental side, the field is driven by the desire to gain maximum control of the assembly structures using very defined and tailored colloidal building blocks, whereas more applied disciplines focus on optimizing the functional properties from rather ill-defined starting materials. With this review article, we aim to provide a connecting perspective by outlining fundamental principles that govern the formation and functionality of supraparticles. We discuss the formation of supraparticles as a result of colloidal properties interplaying with external process parameters. We then outline how the structure of the supraparticles gives rise to diverse functional properties. They can be a result of the structure itself (emergent properties), of the colocalization of different, functional building blocks, or of coupling between individual particles in close proximity. Taken together, we aim to establish structure-property and process-structure relationships that provide unifying guidelines for the rational design of functional supraparticles with optimized properties. Finally, we aspire to connect the different disciplines by providing a categorized overview of the existing, diverging nomenclature of seemingly similar supraparticle structures.

Smart Optical Composite Materials: Dispersions of Metal-Organic Framework@Superparamagnetic Microrods for Switchable Isotropic-Anisotropic Optical Properties.

A smart optical composite material with dynamic isotropic and anisotropic optical properties by combination of luminescence and high reflectivity was developed. This combination enables switching between luminescence and angle-dependent reflectivity by changing the applied wavelength of light. The composite is formed as anisotropic core/shell particles by coating superparamagnetic iron oxide-silica microrods with a layer of the luminescent metal-organic framework (MOF) 3∞[Eu2(BDC)3]·2DMF·2H2O (BDC2- = 1,4-benzenedicarboxylate). The composite particles can be rotated by an external magnet. Their anisotropic shape causes changes in the reflectivity and diffraction of light depending on the orientation of the composite particle. These rotation-dependent optical properties are complemented by an isotropic luminescence resulting from the MOF shell. If illuminated by UV light, the particles exhibit isotropic luminescence while the same sample shows anisotropic optical properties when illuminated with visible light. In addition to direct switching, the optical properties can be tailored continuously between isotropic red emission and anisotropic reflection of light if the illuminating light is tuned through fractions of both UV and visible light. The integration and control of light emission modes within a homogeneous particle dispersion marks a smart optical material, addressing fundamental directions for research on switchable multifunctional materials. The material can function as an optic compass or could be used as an optic shutter that can be switched by a magnetic field, e.g., for an intensity control for waveguides in the visible range.

Hollow Superparamagnetic Microballoons from Lifelike, Self-Directed Pickering Emulsions Based on Patchy Nanoparticles.

Herein, the formation of hollow microballoons derived from superparamagnetic iron oxide nanoparticles with silica patches is reported. Depending on the experimental conditions, single- or multishelled superparamagnetic microballoons as well as multivesicular structures were obtained. We show how such structural changes follow a lifelike process that is based on self-directing Pickering emulsions. We further demonstrate that the key toward the formation of such complex architectures is the patchy nature of the nanoparticles. Interestingly, no well-defined ordering of patches on the particles surface is required, unlike what theorists formerly predicted. The resultant hollow microballoons may be turned into hollow carbonaceous magnetic microspheres by simple pyrolysis. This opens the way to additional potential applications for such ultralightweight (density: 0.16 g·cm-3) materials.

Pushing up the magnetisation values for iron oxide nanoparticles via zinc doping: X-ray studies on the particle's sub-nano structure of different synthesis routes.

The maximum magnetisation (saturation magnetisation) obtainable for iron oxide nanoparticles can be increased by doping the nanocrystals with non-magnetic elements such as zinc. Herein, we closely study how only slightly different synthesis approaches towards such doped nanoparticles strongly influence the resulting sub-nano/atomic structure. We compare two co-precipitation approaches, where we only vary the base (NaOH versus NH3), and a thermal decomposition route. These methods are the most commonly applied ones for synthesising doped iron oxide nanoparticles. The measurable magnetisation change upon zinc doping is about the same for all systems. However, the sub-nano structure, which we studied with Mössbauer and X-ray absorption near edge spectroscopy, differs tremendously. We found evidence that a much more complex picture has to be drawn regarding what happens upon Zn doping compared to what textbooks tell us about the mechanism. Our work demonstrates that it is crucial to study the obtained structures very precisely when "playing" with the atomic order in iron oxide nanocrystals.