科研成果

Koinon assemblies during the Principate were occasions when member communities dispatch delegations to gather at specifically designated cities, where they elect koinon officers and deliberate a range of affairs –– chiefly among which were festivities and sacrifices that honored the Roman emperors and the local cultic and civic traditions, but also revenues and expenditures, administrative tasks delegated by the imperial government, among others (Deininger 1965: 137-147; Edelmann-Singer 2015: 193-248, 309-310). Much has been discussed regarding the institutional aspects of the koinon assemblies; what could benefit from more discussion is the act of traveling to koinon assemblies. This paper assembles a small number of literary and epigraphic references that provide circumstantial references to koinon assembly-related travel anecdotes. Of particular importance among these are Strabo's description of the gathering of delegates from Lycian cities to the koinon meeting each year (Strab. 13.3.3), Aelius Aristides' account of the city of Smyrna's manipulative nomination of him as a candidate for the high priest of Asia (Ael. Arist. Hieroi Logoi 4.99-104), and the inscription honoring Quintus Popilius Python's gift to attendees of the koinon assembly while serving as the high priest of the Macedonian koinon (EKM 117). By assembling these and other evidence, this paper wishes to suggest that koinon assemblies were compulsory events that each member community would have to participate in, often at their own expense. Wealthy koinon-officeholders may opt to offset the burdens that communities (or their designated representatives) would have to shoulder in dispatching delegation, and such benefaction may be viewed from the perspective of a soft mobilization of the provincial elites in order to facilitate the orderly execution of business in the interest of the public weal.

In this article, we present the capacitance–voltage ( C – V ) characteristics of Hfx Zr1−x O2 metal–ferroelectric–metal (MFM) thin-film capacitors with various Zr doping, thicknesses, and annealing temperatures. The influence of doping, electric field cycling, and annealing temperature on tuning characteristics (tunability) was analyzed and an optimized bias region for the maximum tunability was defined. Additional focus was made on an antiferroelectric-like (AFE) behavior, which occurs for > 50% Zr doping. The presence of both the ferroelectric and the AFE phase manifests itself in specific C – V behavior, where a reduced bias range is required for tuning, however, at the cost of a smaller tunability. The suitability of this behavior for varactor applications is also discussed.

Covalent organic frameworks (COFs) have great application potentials in photocatalytic water treatment. By using p-phenylenediamine with different numbers and locations of heterocyclic nitrogen atoms as a precursor, five types of COFs with different nitrogen positions were synthesized. We found that Cr(VI) photoreduction,Escherichia coli inactivation, and paracetamol degradation by COFs were heterocyclic nitrogen location-dependent. Particularly, the photocatalytic performance for all three tested pollutants by five types of COFs followed the order of the best performance for COF-PDZ with two ortho position heterocyclic N atoms, medium for COF-PMD with two meta position heterocyclic N atoms, and COF-PZ with two para position heterocyclic N atoms, and COF-PD with a single heterocyclic N atom, the worst performance for COF-1 without a heterocyclic N atom. Compared to the other COFs, COF-PDZ contained improved quantum efficiency and thus enhanced generation of electrons. The lower energy barriers and larger energy gaps of COF-PDZ contributed to its improved quantum efficiencies. The stronger affinity to Cr(VI) with lower adsorption energy of COF-PDZ also contributed to its excellent Cr(VI) reduction performance. By transferring into a more stable keto form, COF-PDZ showed great stability through five regeneration and reuse cycles. Overall, this study provided an insight into the synthesis of high-performance structure-dependent COF-based photocatalysts.

Covalent organic frameworks (COFs) have great application potentials in photocatalytic water treatment. By using p-phenylenediamine with different numbers and locations of heterocyclic nitrogen atoms as a precursor, five types of COFs with different nitrogen positions were synthesized. We found that Cr(VI) photoreduction,Escherichia coli inactivation, and paracetamol degradation by COFs were heterocyclic nitrogen location-dependent. Particularly, the photocatalytic performance for all three tested pollutants by five types of COFs followed the order of the best performance for COF-PDZ with two ortho position heterocyclic N atoms, medium for COF-PMD with two meta position heterocyclic N atoms, and COF-PZ with two para position heterocyclic N atoms, and COF-PD with a single heterocyclic N atom, the worst performance for COF-1 without a heterocyclic N atom. Compared to the other COFs, COF-PDZ contained improved quantum efficiency and thus enhanced generation of electrons. The lower energy barriers and larger energy gaps of COF-PDZ contributed to its improved quantum efficiencies. The stronger affinity to Cr(VI) with lower adsorption energy of COF-PDZ also contributed to its excellent Cr(VI) reduction performance. By transferring into a more stable keto form, COF-PDZ showed great stability through five regeneration and reuse cycles. Overall, this study provided an insight into the synthesis of high-performance structure-dependent COF-based photocatalysts. © 2021 American Chemical Society.

The gas adsorption hysteresis effects have strong implications for the characterization of the micropore structure, which is one of the most important properties of shales. This study describes one of the first investigations of low-pressure CO2 adsorption hysteresis illustrated on the Antrim Shale samples, Michigan Basin. A total of 23 samples were characterized by using a combination of X-Ray diffraction (XRD), Rock-Eval pyrolysis, scanning electron microscope (SEM) imaging and CO2 adsorption. The partial least linear regression (PLS) was employed to study the influence of rock composition on the micropore structures and hysteresis index (HI). The results showed that the micropore parameters (surface area and volume) are positively correlated to the amount of organic matter and clay minerals, and have a negative correlation to non-clay minerals. In the Antrim Shale samples, the CO2 adsorption hysteresis seen under low pressure appears to be controlled mainly by the pore network effect caused by the presence of ink-bottle shaped pores, rather than by the swelling of clays and organic matter.

Understanding the creep behavior of shale is essential to precisely predict borehole instability issues and model fracturing of unconventional shale reservoirs. In this study, the creep behavior of shale in micron scale is investigated by integrating the nano-dynamic mechanical analysis (nano-DMA) grid nanoindentation (15 × 15 indents) and data clustering techniques. The results showed that the creep displacement, the creep rate, and hardness, both can be related through a logarithmic function with creep time. Furthermore, contact creep modulus increased as the hardness or Young’s modulus increased. The clustering analysis revealed that three separate phases are present in the samples where Phase 1(clay/organic matter) has the smallest contact creep modulus and Phase 3 (quartz) the largest. While creep is in progress, the creep displacement, hardness and contact creep modulus of all three phases obey the logarithmic function. Under the same creep time, reduction in the contact creep modulus of Phase 3 appears to be faster than Phase 1 while the creep rate of Phase 3 is much less than Phase 1. Ultimately, contact creep modulus is better correlated with hardness than Young’s modulus.