Lifting up to Himself: John Calvin's Doctrine of the Trinity and Its Implications for the Lord's Supper and Worship

This study probes the eucharistic implications of the doctrine of the Trinity in the theology of John Calvin (1509-1564). Calvin scholarship has established that the doctrine of the Trinity is the key paradigm of divine-human relationship in Calvin’s theology. Drawing upon this, this study explores how the doctrine affects Calvin’s concept of divine-human interplay in worship and the Lord’s Supper, and how it has liturgical implications for both disciplines. After a reflection on the connection between the doctrine of the Trinity and worship and the sacraments in Calvin’s thought, this thesis shows that the doctrine of the Trinity is an underpinning paradigm for Calvin’s distinctive understanding of the Lord’s Supper as a heavenly communion, a concept by which a personal, experiential, and dynamic, nature of eucharistic communion is highlighted. It also provides surveys of the meaning of the eucharistic heaven, and of the actual mode of the heavenly communion in the ministry of the church, along with a consideration of how this Trinitarian doctrine of the Lord’s Supper distinguishes Calvin’s liturgical thought and practice from those of other reformers. From these surveys it is concluded that the doctrine of the Trinity is the essence of Calvin’s theology and practice of the eucharist

Nanoscale spectroscopic studies of two different physical origins of the tip-enhanced force: dipole and thermal

When light illuminates the junction formed between a sharp metal tip and a sample, different mechanisms can con-tribute to the measured photo-induced force simultaneously. Of particular interest are the instantaneous force be-tween the induced dipoles in the tip and in the sample and the force related to thermal heating of the junction. A key difference between these two force mechanisms is their spectral behaviors. The magnitude of the thermal response follows a dissipative Lorentzian lineshape, which measures the heat exchange between light and matter, while the induced dipole response exhibits a dispersive spectrum and relates to the real part of the material polarizability. Be-cause the two interactions are sometimes comparable in magnitude, the origin of the nanoscale chemical selectivity in the recently developed photo-induced force microscopy (PiFM) is often unclear. Here, we demonstrate theoretically and experimentally how light absorption followed by nanoscale thermal expansion generates a photo-induced force in PiFM. Furthermore, we explain how this thermal force can be distinguished from the induced dipole force by tuning the relaxation time of samples. Our analysis presented here helps the interpretation of nanoscale chemical measure-ments of heterogeneous materials and sheds light on the nature of light-matter coupling in van der Waals materials.Comment: 17 pages, 10 figure

Quantification of titanium dioxide (TiO2) anatase and rutile polymorphs in binary mixtures by Raman spectroscopy: an interlaboratory comparison

This article presents an interlaboratory comparison (ILC) on Raman spectroscopy as a technique for relative quantification of the two most common polymorphs of titanium dioxide (TiO2)-anatase and rutile-in binary mixtures. Some standard methods are currently employed internationally for the determination of TiO2 content in samples (ISO 591-1, ASTM D3720-90), but require extensive sample preparation, do not distinguish between the two polymorphs or are accurate only for small fractions of either polymorph. Raman spectroscopy is a well-suited characterization technique for measuring and differentiating TiO2 in a fast, non-invasive way, while requiring no particular reagent or sample preparation. Eleven international participants conducted the study under the framework of Versailles Project on Advanced Materials and Standards. The collected data was analyzed by means of partial least squares regression after spectral preprocessing. The resulting models all show discrepancies of lower than 2% from the nominal values in the quantitative analysis over the concentration range of 5%-95% mixture fractions, with many datasets showing substantial improvement margins on this figure. The results of this ILC provide validation of Raman spectroscopy as a reliable method for quantification of TiO2 phases

Photo-Induced Force Microscopy by Using Quartz Tuning-Fork Sensor

We present the photo-induced force microscopy (PiFM) studies of various nano-materials by implementing a quartz tuning fork (QTF), a self-sensing sensor that does not require complex optics to detect the motion of a force probe and thus helps to compactly configure the nanoscale optical mapping tool. The bimodal atomic force microscopy technique combined with a sideband coupling scheme is exploited for the high-sensitivity imaging of the QTF-PiFM. We measured the photo-induced force images of nano-clusters of Silicon 2,3-naphthalocyanine bis dye and thin graphene film and found that the QTF-PiFM is capable of high-spatial-resolution nano-optical imaging with a good signal-to-noise ratio. Applying the QTF-PiFM to various experimental conditions will open new opportunities for the spectroscopic visualization and substructure characterization of a vast variety of nano-materials from semiconducting devices to polymer thin films to sensitive measurements of single molecules

Fabrication of Al-Ni Alloys for Fast Hydrogen Production from Hydrolysis in Alkaline Water

Hydrogen generation through the hydrolysis of aluminum alloys has attracted significant attention because it generates hydrogen directly from alkaline water without the need for hydrogen storage technology. The hydrogen generation rate from the hydrolysis of aluminum in alkaline water is linearly proportional to its corrosion rate. To accelerate the corrosion rate of the aluminum alloy, we designed Al-Ni alloys by continuously precipitating an electrochemically noble Al3Ni phase along the grain boundaries. The Al-0.5~1 wt.% Ni alloys showed an excellent hydrogen generation rate of 16.6 mL/cm2·min, which is about 6.4 times faster than that of pure Al (2.58 mL/cm2·min). This excellent performance was achieved through the synergistic effects of galvanic and intergranular corrosion on the hydrolysis of Al. By raising the solution temperature to 50 °C, the optimal rate of hydrogen generation of Al-1 wt.% Ni in 10 wt.% NaOH solutions at 30 °C can be further increased to 54.5 mL/cm2·min

Interfacial-Water-Modulated Photoluminescence of Single-Layer WS₂ on Mica

Because of their bandgap tunability and strong light–matter interactions, two-dimensional (2D) semiconductors are considered promising candidates for next-generation optoelectronic devices. However, their photophysical properties are greatly affected by their surrounding environment because of their 2D nature. In this work, we report that the photoluminescence (PL) of single-layer WS2 is substantially affected by interfacial water that is inevitably present between it and the supporting mica substrates. Using PL spectroscopy and wide-field imaging, we show that the emission signals from A excitons and their negative trions decreased at distinctively different rates with increasing excitation power, which could be attributed to the more efficient annihilation between excitons than between trions. By gas-controlled PL imaging, we also prove that the interfacial water converted the trions into excitons by depleting native negative charges through an oxygen reduction reaction, which rendered the excited WS2 more susceptible to nonradiative decay via exciton–exciton annihilation. Understanding the role of nanoscopic water in complex low-dimensional materials will eventually contribute to devising their novel functions and related devices

3D Porous Cobalt–Iron–Phosphorus Bifunctional Electrocatalyst for the Oxygen and Hydrogen Evolution Reactions

A 3D porous Co–Fe–P foam fabricated using electrodeposition is presented as a high-performance and durable catalyst for both oxygen and hydrogen evolution reactions. To establish optimal Fe/Co ratio of the catalyst, Co–Fe–P films were electrodeposited with Fe/Co ratio of 0.2, 0.4, 1.1, and 3.3. Among the prepared samples, the Co–Fe–P film with the Fe/Co ratio of 1.1 (Co–Fe–P-1.1) exhibited the highest activity for the oxygen evolution reaction, which could be attributed to the transfer of the valence electron from Co to Fe and P. To improve performance of the Co–Fe–P-1.1, a 3D porous foam structure was adopted using the electrodeposition. The Co–Fe–P foam had 94 times larger electrochemical active surface area (ECSA) than the Co–Fe–P film with similar Fe/Co ratios of 1.1, resulting in an distinguished activity for the oxygen evolution reaction (294 mV at 10 mA/cm²) and hydrogen evolution reaction (73 mV at 10 mA/cm²) in an alkaline solution. Since the electrodeposited Co–Fe–P foam itself can be directly used as an electrode, it is free from binders, and microstructure of the electrode can be engineered by controlling the electrodeposition condition, leading to the enlarged ECSA and improved performance. Thus, the Co–Fe–P foam presented in this study offers a facile and controllable synthesis of catalyst and electrode through an easy electrodeposition process

Delayed Triplet-State Formation through Hybrid Charge Transfer Exciton at Copper Phthalocyanine/GaAs Heterojunction

Light absorption in organic molecules on an inorganic substrate and subsequent electron transfer to the substrate create so-called hybrid charge transfer exciton (HCTE). The relaxation process of the HCTE states largely determines charge separation efficiency or optoelectronic device performance. Here, the study on energy and time-dispersive behavior of photoelectrons at the hybrid interface of copper phthalocyanine (CuPc)/<i>p</i>-GaAs­(001) upon light excitation of GaAs reveals a clear pathway for HCTE relaxation and delayed triplet-state formation. According to the ground-state energy level alignment at the interface, CuPc/<i>p</i>-GaAs­(001) shows initially fast hole injection from GaAs to CuPc. Thus, the electrons in GaAs and holes in CuPc form an unusual HCTE state manifold. Subsequent electron transfer from GaAs to CuPc generates the formation of the triplet state in CuPc with a few picoseconds delay. Such two-step charge transfer causes delayed triplet-state formation without singlet excitation and subsequent intersystem crossing within the CuPc molecules