Titanium is a very attractive candidate for MOFs due to its low toxicity, redox activity, and photocatalytic properties. We present here MIL-125, the first example of a highly porous and crystalline titanium(IV) dicarboxylate (MIL stands for Materials of Institut Lavoisier) with a high thermal stability and photochemical properties. Its structure is built up from a pseudo cubic arrangement of octameric wheels, built up from edge- or corner-sharing titanium octahedra, and terephthalate dianions leading to a three-dimensional periodic array of two types of hybrid cages with accessible pore diameters of 6.13 and 12.55 A. X-ray thermodiffractometry and thermal analysis show that MIL-125 is stable up to 360 degrees C under air atmosphere while nitrogen sorption analysis indicates a surface area (BET) of 1550 m(2) x g(-1). Moreover, under nitrogen and alcohol adsorption, MIL-125 exhibits a photochromic behavior associated with the formation of stable mixed valence titanium-oxo compounds. The titanium oxo cluster are back oxidized in the presence of oxygen. This photochemical phenomenon is analyzed through the combined use of Electron Spin Resonance (ESR) and UV-visible absorption spectroscopies. The photogenerated electrons are trapped as Ti(III) centers, while a concomitant oxidation of the adsorbed alcohol molecules occurs. This new microporous hybrid is a very promising candidate for applications in smart photonic devices, sensors, and catalysis.
We explore the application of a high-temperature precursor delivery system for depositing high boiling point organosilicate precursors on plastics using atmospheric plasma. Dense silica coatings were deposited on stretched poly(methyl methacrylate), polycarbonate and silicon substrates from the high boiling temperature precursor, 1, 2-bis(triethoxysilyl)ethane, and from two widely used low boiling temperature precursors, tetraethoxysilane and tetramethylcyclotetrasiloxane. The coating deposition rate, molecular network structure, density, Young's modulus and adhesion to plastics exhibited a strong dependence on the precursor delivery temperature and rate, and the functionality and number of silicon atoms in the precursor molecules. The Young's modulus of the coatings ranged from 6 to 34 GPa, depending strongly on the coating density. The adhesion of the coatings to plastics was affected by both the chemical structure of the precursor and the extent of exposure of the plastic substrate to the plasma during the initial stage of deposition. The optimum combinations of Young's modulus and adhesion were achieved with the high boiling point precursor which produced coatings with high Young's modulus and good adhesion compared to commercial polysiloxane hard coatings on plastics.
Hyperconnected network architectures can endow nanomaterials with remarkable mechanical properties that are fundamentally controlled by designing connectivity into the intrinsic molecular structure. For hybrid organic–inorganic nanomaterials, here we show that by using 1,3,5 silyl benzene precursors, the connectivity of a silicon atom within the network extends beyond its chemical coordination number, resulting in a hyperconnected network with exceptional elastic stiffness, higher than that of fully dense silica. The exceptional intrinsic stiffness of these hyperconnected glass networks is demonstrated with molecular dynamics models and these model predictions are calibrated through the synthesis and characterization of an intrinsically porous hybrid glass processed from 1,3,5(triethoxysilyl)benzene. The proposed molecular design strategy applies to any materials system wherein the mechanical properties are controlled by the underlying network connectivity.
The reactions of titanium alkoxides with a large excess of different carboxylic acids under nonhydrolytic conditions leads to the reproducible formation of well‐defined nano‐building units (NBUs) with the formula [Ti8O8(OOCR)16] [R = C6H5, C(CH3)3, CH3]. The structures of these titanium–oxo–carboxylate clusters have been determined by crossingdifferent characterization techniques and methodologies (single‐crystal X‐ray diffraction, 13C and 1H NMR spectroscopy, and FTIR spectroscopy). These NBUs are obtained in high yields and, since all the alkoxo ligands have been removed by using solvothermal‐synthesis conditions, they present better stability upon hydrolysis than the often reported alkoxo–carboxylate–titanium–oxo clusters [TinO2n–x/2–y/2(OR′)x(OOCR)y] (n ≥ 2; x ≥ 1; y ≥ 1). In addition, the solubility and transferability of these clusters in common solvents can be tuned by selecting the nature of the organic ligand. Moreover, we also report for the first time, a robust post‐modification of the carboxylate ligands by transesterification reactions on the titanium–oxo clusters. These reactions keep the integrity of the octameric titanium–oxo core intact, while completely exchanging the organic shell of the cluster. This family of [Ti8O8(OOCR)16] clusters, which present 16 points of extension, a symmetric shape, and the ability to be post‐modified with conservation of the core structure, can therefore be considered as interesting NBUs to form new metal–organic frameworks.
Selective protection of the porosity can be implemented in porous materials processing by using an organic polymer fill. This strategy is employed to protect ultralow‐k (ULK) materials during patterning of 250‐nm lines and spaces. Structures with significantly less sidewall and trench bottom damage are obtained, proving the potential of this novel approach in materials science.
Increasing the porosity of oxycarbosilane dielectrics is a key approach to lower the interconnect signal delay and thus enable manufacturing of lower power consumption and higher performance microprocessors. However, this path leads to excessive dielectric process damage as the industry adapts procedures developed for dense and microporous insulators to mesoporous materials. Currently ultralow dielectric constant (k) materials cannot be integrated at the most aggressive pitch. Here, it is reported that the post porosity plasma protection enables the mitigation of process damage across a wide range of porosity regimes. The exponential increase in plasma damage with porosity when going from microporous k = 2.4 to mesoporous k = 1.8 is shown. Using the same range of materials, the strategy allows a reduction in process damage to a constant minimal level on both blanket wafers and patterned structures. The results demonstrate how the strategy can enable the extendibility of current materials and processes to future technology nodes.
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Entanglements between polymer chains are responsible for the strength and toughness of polymeric materials. When the chains are too short to form entanglements, the polymer becomes weak and brittle. Here we show that molecular bridging of oligomers in molecular-scale confinement can dramatically toughen materials even when intermolecular entanglements are completely absent. We describe the fabrication of nanocomposite materials that confine oligomer chains to molecular-scale dimensions and demonstrate that partially confined unentangled oligomers can toughen materials far beyond rule-of-mixtures estimates. We also characterize how partially confined oligomers affect the kinetics of nanocomposite cracking in moist environments and show that the presence of a backfilled oligomeric phase within a nanoporous organosilicate matrix leads to atomistic crack path meandering in which the failure path is preferentially located within the matrix phase.
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