Dielectric Properties of Zeolitic Imidazolate Frameworks in the Broad-Band Infrared Regime.

The field of metal-organic framework (MOF) materials is rapidly advancing toward practical applications; consequently, it is urgent to achieve a better understanding and precise control of their physical properties. Yet, research on the dielectric properties of MOFs is at its infancy, where studies are confined to the static dielectric behavior or lower-frequency response (kHz-MHz) only. Herein, we present the pioneering use of synchrotron-based infrared reflectivity experiments combined with density functional theory (DFT) calculations to accurately determine the dynamic dielectric properties of zeolitic imidazolate frameworks (ZIFs, a topical family of MOFs). We show, for the first time, the frequency-dependent dielectric response of representative ZIF compounds, bridging the near-, mid-, and far-infrared (terahertz, THz) broad-band frequencies. We establish the structure-property relations as a function of framework porosity and structural change. Our comprehensive results will pave the way for novel ZIF-based terahertz applications, such as infrared optical sensors and high-speed wireless communications.

Metamorphic records of multiple seismic cycles during subduction.

Large earthquakes occur in rocks undergoing high-pressure/low-temperature metamorphism during subduction. Rhythmic major-element zoning in garnet is a common product of such metamorphism, and one that must record a fundamental subduction process. We argue that rhythmic major-element zoning in subduction zone garnets from the Franciscan Complex, California, developed in response to growth-dissolution cycles driven by pressure pulses. Using electron probe microanalysis and novel techniques in Raman and synchrotron Fourier transform infrared microspectroscopy, we demonstrate that at least four such pressure pulses, of magnitude 100-350 MPa, occurred over less than 300,000 years. These pressure magnitude and time scale constraints are most consistent with the garnet zoning having resulted from periodic overpressure development-dissipation cycles, related to pore-fluid pressure fluctuations linked to earthquake cycles. This study demonstrates that some metamorphic reactions can track individual earthquake cycles and thereby opens new avenues to the study of seismicity.

Probing Dielectric Properties of Metal-Organic Frameworks: MIL-53(Al) as a Model System for Theoretical Predictions and Experimental Measurements via Synchrotron Far- and Mid-Infrared Spectroscopy.

Emerging nanoporous materials, such as metal-organic frameworks (MOFs), are promising low-k dielectrics central to next-generation electronics and high-speed communication. Hitherto, the dielectric characterization of MOFs is scarce, with very limited experimental data for guiding new materials design and synthesis. Herein we demonstrate the efficacy of high-resolution synchrotron infrared (IR) specular reflectance experiments to study the dynamic dielectric properties of a flexible MOF structure: bistable MIL-53(Al) that exhibits switching between a large pore (LP) and a narrow pore (NP) architecture. We show that the ratio of LP:NP content of a polycrystalline sample can be changed via increased mechanical stress applied for pelletizing the MIL-53(Al) powder. We quantify the frequency-dependent dielectric constants over ∼1 to 120 THz, identifying all dielectric transitions as a function of stress and phase mixtures, showing how porosity modifies MOF's dielectric properties.

Tracking thermal-induced amorphization of a zeolitic imidazolate framework via synchrotron in situ far-infrared spectroscopy.

We present the first use of in situ far-infrared spectroscopy to analyze the thermal amorphization of a zeolitic imidazolate framework material. We explain the nature of vibrational motion changes during the amorphization process and reveal new insights into the effect that temperature has on the Zn-N tetrahedra.

Synchrotron-Based Infrared Microanalysis of Biological Redox Processes under Electrochemical Control.

We describe a method for addressing redox enzymes adsorbed on a carbon electrode using synchrotron infrared microspectroscopy combined with protein film electrochemistry. Redox enzymes have high turnover frequencies, typically 10-1000 s(-1), and therefore, fast experimental triggers are needed in order to study subturnover kinetics and identify the involvement of transient species important to their catalytic mechanism. In an electrochemical experiment, this equates to the use of microelectrodes to lower the electrochemical cell constant and enable changes in potential to be applied very rapidly. We use a biological cofactor, flavin mononucleotide, to demonstrate the power of synchrotron infrared microspectroscopy relative to conventional infrared methods and show that vibrational spectra with good signal-to-noise ratios can be collected for adsorbed species with low surface coverages on microelectrodes with a geometric area of 25 × 25 µm(2). We then demonstrate the applicability of synchrotron infrared microspectroscopy to adsorbed proteins by reporting potential-induced changes in the flavin mononucleotide active site of a flavoenzyme. The method we describe will allow time-resolved spectroscopic studies of chemical and structural changes at redox sites within a variety of proteins under precise electrochemical control.

Broadband near-field infrared spectromicroscopy using photothermal probes and synchrotron radiation.

In this paper, we experimentally demonstrate the use of infrared synchrotron radiation (IR-SR) as a broadband source for photothermal near-field infrared spectroscopy. We assess two methods of signal transduction; cantilever resonant thermal expansion and scanning thermal microscopy. By means of rapid mechanical chopping (50-150 kHz), we modulate the IR-SR at rates matching the contact resonance frequencies of atomic force microscope (AFM) cantilevers, allowing us to record interferograms yielding Fourier transform infrared (FT-IR) photothermal absorption spectra of polystyrene and cyanoacrylate films. Complementary offline measurements using a mechanically chopped CW IR laser confirmed that the resonant thermal expansion IR-SR measurements were below the diffraction limit, with a spatial resolution better than 500 nm achieved at a wavelength of 6 µm, i.e. λ/12 for the samples studied. Despite achieving the highest signal to noise so far for a scanning thermal microscopy measurement under conditions approaching near-field (dictated by thermal diffusion), the IR-SR resonant photothermal expansion FT-IR spectra measured were significantly higher in signal to noise in comparison with the scanning thermal data.

Investigating the magnetic field-dependent conductivity in magnetite thin films by modelling the magnetorefractive effect.

A model of the magnetorefractive effect is developed for metallic oxides which allows the MRE to be used to study the magnetic dependence of their transport and phononic properties. This model is successfully applied to Fe3O4 and compared to experiments on a series of magnetite thin films of varying thickness (10, 18, 37, 64 and 110 nm) deposited on MgO(111) substrates. Reflection spectra were modelled as a function of film thickness, calculated from the Fresnel equations using an Fe3O4 dielectric function consisting of Drude, hopping, phononic and d-s transition conductivity processes. The reflectivity spectra of the different thickness films are reasonably reproduced by the model and reveal that the Fe3O4 18.5 µm phonon peak is shifted to a shorter wavelength in the thin films, approaching the bulk value for t > 110 nm. The MRE spectra are modelled by introducing a magnetic field dependence to the hopping and phononic terms, where previous models have considered the magnetic dependence to be on the Drude term only. In addition, the position of the Fe3O4 18.5 µm phonon peak was also found to shift in energy in the applied magnetic field by 0.05 µm. These results demonstrate the potential for using the MRE technique for probing the underlying magnetoelectronic properties of thin film oxides in a quick and non-destructive way.

A rare cause of abdominal pain.

Pacemaker migration is a rare, but important, complication of pacemaker insertion mainly documented in children. We report the case of a 60-year-old woman who was admitted with right iliac fossa pain thought to be caused by appendicitis. She was noted to have both an epicardial and endocardial pacemaker in situ. Imaging and laparoscopy revealed migration of the epicardial pacemaker to the right iliac fossa. We describe the possible mechanisms of pacemaker migration.