Tuning Mesopore Accessibility of Ce0.18Zr0.64Y0.15La0.03O2-δ by Hydrothermal Post-treatment─A Case Study for Ceria-Based Oxidation Storage Materials.

The connectivity and thermal stability of pores in heterogeneous, mesoporous metal oxide catalysts are key properties controlling their (long-term) efficacy. In this study, we investigate the influence of pH and temperature during a common hydrothermal aftertreatment step in the synthesis of mesoporous CexZr1-x-y-zYyLazO2-δ oxides obtained from molecular precursors via hydrothermal synthesis. This study has a strong focus on the methodological approach, elucidating whether and how even the smallest changes in morphology and connectivity may be unraveled and related to the underlying chemical processes to uncover key parameters for the ongoing improvement of material properties. Deep insights into the mesopore space were obtained by state-of-the-art physisorption (including hysteresis scanning), electron tomography, and small-angle X-ray scattering (SAXS) analysis. We also provide a simple tool to simulate SAXS curves from electron tomography data that allow direct comparison to experimentally obtained SAXS curves. Furthermore, the impact on surface-bound nitrate groups and the development during calcination were studied in detail by thermogravimetric analysis coupled with mass spectrometry. The key observations indicate a significant increase in thermal stability at temperatures as high as 1050 °C and improved mesopore accessibility with an increase in pH of the aftertreatment solution. The combined observations from the employed methods suggest a pH-dependent removal of surface-bound nitrate groups as well as a dissolution and reprecipitation-based fusing of the primary particles that constitute the mesopore skeleton. This transformation yields a mechanically and thermally stronger mesopore space with the capability to endure high temperatures.

Sol-Gel-Derived Ordered Mesoporous High Entropy Spinel Ferrites and Assessment of Their Photoelectrochemical and Electrocatalytic Water Splitting Performance.

The novel material class of high entropy oxides with their unique and unexpected physicochemical properties is a candidate for energy applications. Herein, it is reported for the first time about the physico- and (photo-) electrochemical properties of ordered mesoporous (CoNiCuZnMg)Fe2 O4 thin films synthesized by a soft-templating and dip-coating approach. The A-site high entropy ferrites (HEF) are composed of periodically ordered mesopores building a highly accessible inorganic nanoarchitecture with large specific surface areas. The mesoporous spinel HEF thin films are found to be phase-pure and crack-free on the meso- and macroscale. The formation of the spinel structure hosting six distinct cations is verified by X-ray-based characterization techniques. Photoelectron spectroscopy gives insight into the chemical state of the implemented transition metals supporting the structural characterization data. Applied as photoanode for photoelectrochemical water splitting, the HEFs are photostable over several hours but show only low photoconductivity owing to fast surface recombination, as evidenced by intensity-modulated photocurrent spectroscopy. When applied as oxygen evolution reaction electrocatalyst, the HEF thin films possess overpotentials of 420 mV at 10 mA cm-2 in 1 m KOH. The results imply that the increase of the compositional disorder enhances the electronic transport properties, which are beneficial for both energy applications.

Effects of Hydrothermal Treatment on Mesopore Structure and Connectivity in Doped Ceria-Zirconia Mixed Oxides.

Pore size and pore connectivity control diffusion-based transport in mesopores, a crucial property governing the performance of heterogeneous catalysts. In many cases, transition-metal oxide catalyst materials are prepared from molecular precursors involving hydrothermal treatment followed by heat treatment. Here, we investigate the effects of such a hydrothermal aftertreatment step, using an aqueous ammonia solution, on the disordered mesopore network of CexZr1-x-y-zYyLazO2-δ mixed oxides. This procedure is a common synthesis step in the preparation of such ceria-based oxygen storage materials applied in three-way catalysis, employed to improve the materials' thermal stability. We perform state-of-the-art Ar-physisorption analysis, especially advanced hysteresis scanning, to paint a detailed picture of the alterations in mesopore space caused by the hydrothermal aftertreatment and subsequent aging at 1050 °C. Furthermore, we investigate the network characteristics by electron tomography in combination with suitable statistical analysis, enabling a consistent interpretation of the desorption scans (physisorption). The results indicate that the hydrothermal aftertreatment enhances the mesopore connectivity of the continuous 3D network by widening pores and especially necks, hence facilitating accessibility to the particles' internal surface area and the ability to better withstand high temperatures.

Lignin-Derived Mesoporous Carbon for Sodium-Ion Batteries: Block Copolymer Soft Templating and Carbon Microstructure Analysis.

The demand for versatile and sustainable energy materials is on the rise, given the importance of developing novel clean technologies for transition to a net zero economy. Here, we present the synthesis, characterization, and application of lignin-derived ordered mesoporous carbons with various pore sizes (from 5 to approximately 50 nm) as anodes in sodium-ion batteries. We have varied the pore size using self-synthesized PEOn-b-PHAm block copolymers with different PEO and PHA chain lengths, applying the "soft templating" approach to introduce isolated spherical pores of 20 to 50 nm in diameters. The pore structure was evaluated by transmission electron microscopy (TEM), nitrogen physisorption, and small-angle X-ray scattering (SAXS). We report the microstructure analysis of such mesoporous lignin-based carbons using Raman spectroscopy and wide-angle X-ray scattering (WAXS). In comparison with nontemplated carbon and carbons templated employing commercial Pluronic F-127 and PIB50-b-PEO45, which created accessible channels and spherical pores up to approximately 10 nm in diameter, the carbon microstructure analysis revealed that templating with all applied polymers significantly impedes graphitization upon thermal treatment. Furthermore, the gained knowledge of similar carbon microstructures regardless of the type of template allowed the investigation of the influence of different pore morphologies in carbon applied as an anode material in sodium-ion batteries, supporting the previous theories in the literature that closed pores are beneficial for sodium storage while providing insights into the importance of pore size.

Determining Mechanical Moduli of Disordered Materials with Hierarchical Porosity on Different Structural Levels.

The impact of synthesis parameters and structural properties, respectively, on mechanical properties of porous materials on different structural levels provides valuable information for designing materials for specific applications. Within this study, we apply two nonstandard approaches for determining the mechanical properties of the mesoporous backbone phase in a series of disordered SiO2-based monolithic materials possessing hierarchical meso-macroporosity, that is, deformation upon mercury porosimetry and in situ dilatometry during nitrogen adsorption analysis. By using ordered porous model materials, the latter method has been recently proven to provide reliable mechanical moduli. This concept was now applied to a SiO2 monolith developed for high-performance liquid chromatography exhibiting disordered hierarchical meso- and macroporosity, as well as a series of analogue phenyl-modified meso-macroporous SiO2 monoliths with up to 36.1 at% organic modification. The phenyl group was introduced by adding phenyltrimethoxysilane to the sol-gel mixture. The study aimed at investigating in detail the impact of the organic modification on the morphology of the porous solid and the resulting mechanical properties. The study shows that both Hg porosimetry and in situ dilatometry performed during N2 adsorption at 77 K provide similar and reasonable moduli of compression for the mesoporous backbone of the silica materials investigated. These data were compared with moduli of the macroscopic sample as determined from sound velocity measurements by describing the fully connected macroporous backbone with a foam model. The comparison reveals an otherwise overseen side effect of the organic modification of the silica framework: in contrast to the pure reference SiO2 meso-macroporous monoliths, the hybrid material is composed of a more particulate morphology on the mesoscale, that is, mesoporous particles and corresponding necks between them are formed, which results in significant softening of the porous solid on the macroscale.

Development of Pore Morphology During Nitrate Group Removal by Calcination of Mesoporous CexZr1-x-y-zYyLazO2-δ Powders.

Here, we present a study of the development of the micro- and mesoporosity of a CexZr1-x-y-zYyLazO2-δ oxygen storage material upon treatment at temperatures up to 1050 °C. The investigated powder, obtained from nitrate-based metal oxide precursors in a specially developed hydrothermal synthesis, is highly crystalline, features a high surface area and does not show phase segregation at high temperatures. By employing an advanced methodology, consisting of state-of-the-art argon physisorption, thermogravimetric analysis coupled with mass spectrometry (TG-MS) and X-ray powder diffraction (XRD) along with Raman spectroscopy, we correlate the stability of the mesopore system to the presence of surface-bound nitrate groups introduced during synthesis, which prevent sintering up to a temperature of 600 °C. In addition, the connectivity of mesopores was further studied by hysteresis scanning within the argon physisorption measurements. These advanced physisorption experiments suggest a three-dimensionally interconnected pore system and, in turn, a 3D network of the material itself on the nanometer scale which appears to be beneficial to endow the mesopore space with enhanced stability against sintering and mesopore collapse once the removal of nitrate groups is completed.

Ionic Liquid-Based Low-Temperature Synthesis of Crystalline Ti(OH)OF·0.66H2O: Elucidating the Molecular Reaction Steps by NMR Spectroscopy and Theoretical Studies.

We present an in-depth mechanistic study of the first steps of the solution-based synthesis of the peculiar hexagonal tungsten bronze-type Ti(OH)OF·0.66H2O solid, using NMR analyses (1H, 13C, 19F, and 11B) as well as modeling based on density functional theory (DFT) and ab initio molecular dynamics (AIMD) simulation. The reaction uses an imidazolium-based ionic liquid (IL, e.g., C x mim BF4) as a solvent and reaction partner. It is puzzling, as the fluorine-rich crystalline solid is obtained in a "beaker chemistry" procedure, starting from simple compounds forming a stable solution (BF4 --containing IL, TiCl4, H2O) at room temperature, and a remarkably low reaction temperature (95 °C) is sufficient. Building on NMR experiments and modeling, we are able to provide a consistent explanation of the peculiar features of the synthesis: evidently, the hydrolysis of the IL anion BF4 - is a crucial step since the latter provides fluoride anions, which are incorporated into the crystal structure. Contrary to expectations, BF4 - does not hydrolyze in water at room temperature but interacts with TiCl4, possibly forming a TiCl4 complex with one or two coordinated BF4 - units. This interaction also prevents the heavy hydrolysis reaction of TiCl4 with H2O but-on the other side-spurs the hydrolysis of BF4 - already at room temperature, releasing fluoride and building F-containing Ti(OH) x Cl4-x F y complexes. The possible complexes formed were analyzed using DFT calculations with suitable functionals and basis sets. We show in addition that these complexes are also formed using other titanium precursors. As a further major finding, the heating step (95 °C) is only needed for the condensation of the Ti(OH) x Cl4-x F y complexes to form the desired solid product but not for the hydrolysis of BF4 -. Our study provides ample justification to state a "special IL effect", as the liquid state, together with a stable solution, the ionic nature, and the resulting deactivation of H2O are key requirements for this synthesis.

H2 S Dosimetry by CuO: Towards Stable Sensors by Unravelling the Underlying Solid-State Chemistry.

The precise detection of the toxic gas H2 S requires reliable sensitivity and specificity of sensors even at minute concentrations of as low as 10 ppm, the value corresponding to typical exposure limits. CuO can be used for H2 S dosimetry, based on the formation of conductive CuS and the concomitant significant increase in conductance. In theory, at elevated temperature the reaction is reversed and CuO is formed, ideally enabling repeated and long-term use of one sensor. Yet, the performance of CuO tends to drop upon cycling. Utilizing defined CuO nanorods we thoroughly elucidated the associated detrimental chemical changes directly on the sensors, by Raman and electron microscopy analysis of each step during sensing (CuO→CuS) and regeneration (CuS→CuO) cycles. We find the decrease in the sensing performance is mainly caused by the irreversible formation of CuSO4 during regeneration. The findings allowed us to develop strategies to reduce CuSO4 formation and thus to substantially maintain the sensing stability even for repeated cycles. We achieved CuO-based dosimeters possessing a response time of a few minutes only, even for 10 ppm H2 S, and prolonged life-time.

Synthesis of Ti(OH)OF ⋠0.66 H2 O in Imidazolium-based Ionic Liquids.

The influence of the cation of imidazolium-derived ionic liquids (ILs) on a low-temperature solution-based synthesis of hexagonal tungsten bronze (HTB) type Ti(OH)OF ⋅ 0.66 H2 O and bronze-type TiO2 (B) is investigated. The IL (Cx mim BF4 ) acts as solvent and also as reaction partner with respect to the decomposition of [BF4 ]- , releasing F- . In the present study, the chain length of the alkyl chain side groups attached to the imidazolium ring was varied (C2 mim BF4 to C10 mim BF4 ), and the obtained solids were analyzed by Powder X-Ray diffraction (PXRD) followed by Rietveld refinement. As a main finding these analyses indicate a transformation of Ti(OH)OF ⋅ 0.66 H2 O into TiO2 (B), and upon prolonged reaction time finally also into anatase TiO2 . Rietveld analysis suggests that when using ILs with longer alkyl chains, the conversion of Ti(OH)OF ⋅ 0.66 H2 O is slower compared to syntheses performed with smaller alkyl chains. Hence, Ti(OH)OF ⋅ 0.66 H2 O appears to be metastable and is stabilized by long-chain ILs serving as surfactant attached to the crystallites' surface. In this view, the ILs shield the nanoparticles and thus slow down the conversion into the more stable compounds. This confirms previous findings that ILs act as both, solvent and reaction medium in this reaction, thus enabling the synthesis of peculiar Ti-oxides.

Comprehensive Characterization of a Mesoporous Cerium Oxide Nanomaterial with High Surface Area and High Thermal Stability.

In the present study, the pore space of a mesoporous cerium oxide material is investigated, which forms by the self-assembly of primary particles into a spherical secondary structure possessing a disordered mesopore space. The material under study exhibits quite stable mesoporosity upon aging at high temperatures (800 °C) and is, thus, of potential interest in high-temperature catalysis. Here, different characterization techniques were applied to elucidate the structural evolution taking place between heat treatment at 400 °C and aging at 800 °C, i.e., in a water-containing atmosphere, which is usually detrimental to nanoscaled porosity. The changes in the mesoporosity were monitored by advanced physisorption experiments, including hysteresis scanning, and electron tomography analysis coupled with a 3D reconstruction of the mesopore space. These methods indicate that the 3D spatial arrangement of the primary particles during the synthesis under hydrothermal conditions via thermal hydrolysis is related to the thermal stability of the hierarchical mesopore structure. The assembly of the primary CeO2 particles (∼4 nm in size) results in an interparticulate space constituting an open 3D mesopore network, as revealed by skeleton analysis of tomography data, being in conformity with hysteresis scanning. At elevated temperatures (800 °C), sinter processes occur resulting in the growth of the primary particles, but the 3D mesopore network and the spherical secondary structure are preserved.

Amine-Functionalized Nanoporous Silica Monoliths for Heterogeneous Catalysis of the Knoevenagel Condensation in Flow.

Porous carrier materials functionalized with organocatalysts offer substantial advantages compared to homogeneous catalysts, e.g., easy separation of the catalyst, scalability, and an improved implementation in continuous operations. Here, we report the immobilization of (3-aminopropyl)trimethoxysilane (APTMS) onto self-prepared silica monoliths and its application as a heterogeneous catalyst in the Knoevenagel condensation between cyano ethylacetate and various aromatic aldehydes under continuous-flow conditions. The meso-macroporous silica monoliths (6-7 cm in length) were optimized to be used in flow taking advantage of their hierarchical meso- and macroporosity. The monoliths were cladded with a poly(ether ether ketone) (PEEK) tube by a refined procedure to guarantee tight connection between the carrier material and PEEK. Functionalization of the bare silica monoliths consisting of APTMS can be efficiently performed in flow in ethanol and toluene. While a large grafting gradient is obtained for toluene, the grafting in ethanol proceeds homogenously throughout the monolith, as evidenced by elemental analysis and time-of-flight secondary ion mass spectrometry (ToF-SIMS). The silica monoliths exhibit high conversion up to 95% with concurrent low back pressures, which is of importance in flow catalysis. By connecting two monoliths, high conversions can be maintained for several flow rates. Two types of monoliths were synthesized, possessing different mesopore sizes. The monolith bearing the larger mesopore size showed an enhanced turnover frequency (TOF), while the monolith with the smaller mesopores allowed for larger quantities of the product to be synthesized, due to the higher surface area. A long-term stability test showed that the functionalized monoliths were still active after 66 h of continuous usage, while the overall yield decreased over time.

Pore Size Gradient Effect in Monolithic Silica Mesopore Networks Revealed by In-Situ SAXS Physisorption.

In disordered mesopore networks, the size distribution and connection between adjacent pores control desorption. How network characteristics can be extracted from corresponding physisorption isotherms is still a matter of research. To elucidate this, we study krypton physisorption (117.8 K) in the mesopore networks of "Nakanishi"-type monolithic silica. Combining physisorption in scanning acquisition mode with synchrotron-based in-situ SAXS provides complementary information on pore-filling states. These data reveal a mean pore size gradient in which pores grow smaller towards the material's network center. This structural motif cannot be derived through conventional isotherm analysis, but it is clearly exposed through scanning desorption curves which do not quite converge but merge individually with the main desorption isotherm before the lower hysteresis closing point. Hence, our findings provide the basis to build advanced models for analyzing scanning isotherms and extracting network characteristics through new descriptors, such as pore size and connectivity distributions as a function of the distance from the network center.

Peering into the Formation of Cerium Oxide Colloidal Particles in Solution by In Situ Small-Angle X-ray Scattering.

The formation of CeO2 colloidal particles upon heating an aqueous solution of (NH4)2Ce(NO3)6 to 100 °C was investigated by time-resolved in situ SAXS analysis using synchrotron radiation, providing absolute intensity data. In particular, the experiments were performed by applying different temperatures between room temperature and 100 °C as well as under variation of the ionic strength and concentration. Using validated SAXS evaluation tools (SASfit and McSAS software), the analyses revealed the presence of two types of particle populations possessing average dimensions of ca. 2 nm and 5-15 nm, with the latter being agglomerates of the 2 nm particles rather than single crystallites. The analysis revealed not only the changes in the size, but also the relative volume fractions of these two CeO2 particle populations as a function of the aforementioned parameters. Increasing the temperature increases the number of the 5-15 nm agglomerates on one hand by the enhanced nucleation rate of the primary particles. On the other hand, especially at high temperatures (90 and 100 °C) the larger agglomerate particles precipitate, resulting in interesting trends in the fractions of the two populations as a function of time, temperature, ionic strength, and precursor concentration. The experimental studies are complemented by calculating colloidal interaction energies based on classical DLVO theory. Thereby, this study provides detailed insight into the nucleation, growth, and agglomeration of CeO2 nanoparticles. The primary objective of this study is to provide a better understanding of the nucleation and growth of particles by the hydrolysis of the tetravalent cerium ion in aqueous solutions.

Correction: An advanced structural characterization of templated meso-macroporous carbon monoliths by small- and wide-angle scattering techniques.

[This corrects the article DOI: 10.3762/bjnano.11.23.].

An advanced structural characterization of templated meso-macroporous carbon monoliths by small- and wide-angle scattering techniques.

This study is dedicated to link the nanoscale pore space of carbon materials, prepared by hard-templating of meso-macroporous SiO2 monoliths, to the corresponding nanoscale polyaromatic microstructure using two different carbon precursors wthat generally exhibit markedly different carbonization properties, i.e., a graphitizable pitch and a non-graphitizable resin. The micro- and mesoporosity of these monolithic carbon materials was studied by the sorption behavior of a relatively large organic molecule (p-xylene) in comparison to typical gas adsorbates (Ar). In addition, to obtain a detailed view on the nanopore space small-angle neutron scattering (SANS) combined with in situ physisorption was applied, using deuterated p-xylene (DPX) as a contrast-matching agent in the neutron scattering process. The impact of the carbon precursor on the structural order on an atomic scale in terms of size and disorder of the carbon microstructure, on the nanopore structure, and on the template process is analyzed by special evaluation approaches for SANS and wide-angle X-ray scattering (WAXS). The WAXS analysis shows that the pitch-based monolithic material exhibits a more ordered microstructure consisting of larger graphene stacks and similar graphene layer sizes compared to the monolithic resin. Another major finding is the discrepancy in the accessible micro/mesoporosity between Ar and deuterated p-xylene that found for the two different carbon precursors, pitch and resin, which can be regarded as representative carbon precursors in general. These differences essentially indicate that physisorption using probe gases such as Ar or N2 can provide misleading parameters if to be used to appraise the accessibility of the nanoscale pore space.

Catalytic Stability Studies Employing Dedicated Model Catalysts.

Long-term stability of heterogeneous catalysts is an omnipresent and pressing concern in industrial processes. Catalysts with high activity and selectivity can be searched for by high-throughput screening methods based maybe on educated guesses provided by ab initio thermodynamics or scaling relations. However, high-throughput screening is not feasible and is hardly able to identify long-term stable catalyst so that a rational and knowledge-driven approach is called for to identify potentially stable and active catalysts. Unfortunately, our current microscopic understanding on stability issues is quite poor. We propose that this gap in knowledge can be at least partly closed by investigating dedicated model catalyst materials with well-defined morphology that allow for a tight link to theory and the application of standard characterization methods. This topic is highly interdisciplinary, combining sophisticated inorganic synthesis with catalysis research, surface chemistry, and powerful theoretical modeling. In this Account, we focus on the stability issues of Deacon catalysts (RuO2 and CeO2-based materials) for recovering Cl2 from HCl by aerobic oxidation and how to deepen our microscopic insight into the underlying processes. The main stability problems under harsh Deacon reaction conditions concomitant with a substantial loss in activity arise from deep chlorination of the catalyst, leaching of volatile chlorides and oxychlorides, and decrease in active surface area by particle sintering. In general, powder materials with undefined particle shape are not well suited for examining catalyst stability, because changes in the morphology are difficult to recognize, for instance, by electron microscopy. Rather, we focus here on model materials with well-defined starting morphologies, including electrospun nanofibers, shape-controlled nanoparticles, and well-defined ultrathin crystalline layers. CeO2 is able to stabilize shape-controlled particles, exposing a single facet orientation so that comparing activity and stability studies can reveal structure sensitive properties. We develop a quasi-steady-state kinetic approach that allows us to model the catalyst chlorination as a function of temperature and gas feed composition. For the case of pure CeO2 nanocubes, this simple approach predicts chlorination to be efficiently suppressed by addition of little amounts of water in the reaction feed or by keeping the catalyst at higher temperature. Both process parameters have great impact on the actual reactor design. Thermal stabilization of CeO2 by intermixing Zr has been known in automotive exhaust catalysis for decades, but this does not necessarily imply also chemical stabilization of CeO2 against bulk-chlorination since Zr can readily form volatile ZrCl4 and may quickly lose its stabilizing effect. Nevertheless, with model experiments the stabilizing effect of Zr in the Deacon process over mixed CexZr1-xO2 nanorods is clearly evidenced. Even higher stability can be accomplished with ultrathin CeO2 coatings on preformed ZrO2 particles, demonstrating the great promise of atomic layer deposition (ALD) in catalysis synthesis.

Comparison of In-Plane Stress Development in Sol-Gel- and Nanoparticle-Derived Mesoporous Metal Oxide Thin Films.

By using an evaporation-induced self-assembly (EISA) process, mesoporous metal oxide thin films are prepared via molecular precursors undergoing a sol-gel transition or by using nanoparticle dispersions as the starting materials. Both methods are employed together with PIB50-b-PEO45 as the structure-directing agent to produce porous TiO2 and ZrO2 thin films with spherical mesopores of around 14 nm in diameter. These nanoparticle- and sol-gel-derived films were investigated in terms of the intrinsic in-plane stress development during the heat treatment up to 500 °C to evaluate the impact of solvent evaporation, template decomposition and crystallization on the mechanical state of the film. The investigation revealed the lowest intrinsic stress for the nanoparticle-derived mesoporous film, which is assigned to the combination of the relaxing effects of the utilized diblock copolymer and the interparticular gaps between the precrystalline nanoparticles. Furthermore, the residual in-plane stress was studied after annealing steps ranging from 300 to 1000 °C and cooling down to room temperature. Here, TiO2 nanoparticle-derived mesoporous films possess a lower residual stress than the sol-gel-derived mesoporous films, while in the case of ZrO2 films, sol-gel-derived coatings reveal the smallest residual stress. The latter is based on the lower thermal expansion coefficient of the dominant monoclinic crystal phase compared to that of the silicon substrate. Hence, the present crystal structure has a strong influence on the mechanical state. The observation in this study helps to further understand the stress-related mechanical properties and the formation of mesoporous metal oxides.

Independent Tailoring of Macropore and Mesopore Space in TiO2 Monoliths.

TiO2 monoliths were synthesized by a partially hindered sol-gel process. Various synthesis parameters like precursor concentrations and gelation temperature were varied to investigate changes in the macroporosity (being in the range of micrometers) and to determine influences on the macropore formation mechanism. Ionic liquids (ILs) were used as templates to vary the mesopore size independently from the macropore size. Depending on the synthesis parameters, TiO2 monoliths with exclusive mesoporosity or with hierarchical meso-/macropore structure were received, and the range of macropores can be shifted between 100 nm and 10 µm without influencing the mesopore diameter. Pore volumes up to 880 mm3/g were achieved, as determined by mercury intrusion porosimetry. The mesopores' diameter can be adjusted between 6 and 25 nm by adding different amounts of IL, and surface areas up to 260 m2/g and mesopore volumes of 0.5 cm3/g were obtained, based on N2-physisorption measurements. The monoliths were cladded by polymer, allowing for studying the flow-through properties depending on the macropore size. This precise control for tailored macropores enables the design of optimized TiO2 monoliths with respect to the desired application requirements.

Synthesis of rare-earth metal and rare-earth metal-fluoride nanoparticles in ionic liquids and propylene carbonate.

Decomposition of rare-earth tris(N,N'-diisopropyl-2-methylamidinato)metal(III) complexes [RE{MeC(N(iPr)2)}3] (RE(amd)3; RE = Pr(III), Gd(III), Er(III)) and tris(2,2,6,6-tetramethyl-3,5-heptanedionato)europium(III) (Eu(dpm)3) induced by microwave heating in the ionic liquids (ILs) 1-butyl-3-methylimidazolium tetrafluoroborate ([BMIm][BF4]), 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([BMIm][NTf2]) and in propylene carbonate (PC) yield oxide-free rare-earth metal nanoparticles (RE-NPs) in [BMIm][NTf2] and PC for RE = Pr, Gd and Er or rare-earth metal-fluoride nanoparticles (REF3-NPs) in the fluoride-donating IL [BMIm][BF4] for RE = Pr, Eu, Gd and Er. The crystalline phases and the absence of significant oxide impurities in RE-NPs and REF3-NPs were verified by powder X-ray diffraction (PXRD), selected area electron diffraction (SAED) and high-resolution X-ray photoelectron spectroscopy (XPS). The size distributions of the nanoparticles were determined by transmission electron microscopy (TEM) and high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) to an average diameter of (11 ± 6) to (38 ± 17) nm for the REF3-NPs from [BMIm][BF4]. The RE-NPs from [BMIm][NTf2] or PC showed diameters of (1.5 ± 0.5) to (5 ± 1) nm. The characterization was completed by energy-dispersive X-ray spectroscopy (EDX).

Critical Role of the Crystallite Size in Nanostructured Li4Ti5O12 Anodes for Lithium-Ion Batteries.

Lithium titanate Li4Ti5O12 (LTO) is regarded as a promising alternative to carbon-based anodes in lithium-ion batteries. Despite its stable structural framework, LTO exhibits disadvantages, such as the sluggish lithium-ion diffusion and poor electronic conductivity. To modify the performance of LTO as an anode material, nanosizing constitutes a promising approach and the impact is studied here by a systematical experimental approach. Phase-pure polycrystalline LTO nanoparticles (NPs) with high crystallinity and crystallite sizes ranging from 4 to 12 nm are prepared by an optimized solvothermal protocol and characterized by several state-of-the-art technologies, including high-resolution transmission electron microscopy, X-ray diffraction (XRD), pair distribution function (PDF) analysis, Raman spectroscopy, and X-ray photoelectron spectroscopy. Through a wide array of electrochemical analyses, including charge/discharge profiles, cyclic voltammetry, and electrochemical impedance spectroscopy, a crystallite size of approx. 7 nm is identified as the optimum particle size. Such NPs exhibit as good reversible capacity as the ones with larger crystallite sizes but with a more pronounced interfacial charge storage. By decreasing the crystallite size to about 4 nm, the interfacial charge storage increases remarkably, however resulting in a loss of reversible capacity. An in-depth structural characterization using the PDF obtained from synchrotron XRD data indicates an enrichment in Ti for NPs with the small crystallite sizes, and this Ti-rich structure enables a higher Li storage. The electrochemical characterization confirms this result and furthermore points to a plausible reason as to why a higher Li storage in very small nanoparticles (4 nm) results in a loss in the reversible capacity.