科研成果

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.

This chapter assesses the 1926-1927 Uprising in Indonesia across several interconnected geographic and institutional scales: In the Comintern, where exiled leaders of the Partai Komunis Indonesia conferred with Comintern representatives about the situation at home; in the highest levels of the Politburo, where disagreements over revolutionary tactics in China exacerbated the power struggle between Stalin and Trotsky; and in Indonesia itself, where colonial repression inspired the abortive uprising. In so doing, this chapter shows how the Uprising demonstrated the limits of internationalism. As PKI leaders were unable to maintain effective contact with the movement in Indonesia, gaps in information undermined decision-making and led to conflict over the applicability of Russian models to the Indonesian context. Debates over Moscow’s China policy diverted attention from other territories and drew PKI members into the Stalin-Trotsky feud. Comintern support for the Uprising, therefore, did not materialize, further undermining the communist movement in Indonesia.