Publications by authors named "Wan-Yu Tsai"

Introduction: This study examined the training effects of an online game-based cognitive bias modification for interpretation (CBM-I) program in reducing fear during the COVID-19 pandemic in Hong Kong. In addition to investigating the changes in both proximal (i.e.

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Objectives: By studying Mainland Chinese immigrant women who married Hong Kong men, this study examined the association between their perceived discrimination and psychological distress after the 2019-2020 social movement in Hong Kong. Additionally, this study examined the indirect effects of individual coping strategies (tolerance of uncertainty) and couples' coping strategies (common dyadic coping), guided by the cultural and developmental psychopathology framework.

Method: Ninety-nine Mainland Chinese immigrant women who married Hong Kong men participated in this cross-sectional survey.

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Background: Although the "white skin roll" of the lip is often considered a line, it is better defined as the subunit between the vermilion border and the upper lip horizontal groove. In many unilateral cleft lip repair techniques, this structure is approximated between both sides of the cleft without restoration. This study aimed to analyze the white skin roll height in patients with unilateral cleft lip.

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Cobalt-free cation-disordered rocksalt (DRX) cathodes are a promising class of materials for next-generation Li-ion batteries. Although they have high theoretical specific capacities (>300 mA h/g) and moderate operating voltages (∼3.5 V vs Li/Li), DRX cathodes typically require a high carbon content (up to 30 wt %) to fully utilize the active material which has a detrimental impact on cell-level energy density.

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Understanding the deformation of energy storage electrodes at a local scale and its correlation to electrochemical performance is crucial for designing effective electrode architectures. In this work, the effect of electrolyte cation and electrode morphology on birnessite (δ-MnO) deformation during charge storage in aqueous electrolytes was investigated using a mechanical cyclic voltammetry approach via atomic force microscopy (AFM) and molecular dynamics (MD) simulation. In both KSO and LiSO electrolytes, the δ-MnO host electrode underwent expansion during cation intercalation, but with different potential dependencies.

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Article Synopsis
  • * This study focuses on compatibilization, testing three commercial ethylene copolymer compatibilizers (EAA, PTW, and Surlyn) on a blend of PET and HDPE, common packaging materials.
  • * Researchers assess how the location of these compatibilizers within the polymer blend impacts compatibility, which helps in understanding their effectiveness and improving strategies for upcycling waste plastics.
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Reversible electrochemical intercalation of cations into the interlayer space of 2D materials induces tunable physical and chemical properties in them. In MXenes, a large class of recently developed 2D carbides and nitrides, low intercalation energy, high storage capacitance, and reversible intercalation of various cations have led to their improved performance in sensing and energy storage applications. Herein, a coupled nanopore-actuator system where an ultrathin free-standing MXene film serves as a nanopore support membrane and ionically active actuator is reported.

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Identifying and understanding charge storage mechanisms is important for advancing energy storage. Well-separated peaks in cyclic voltammograms (CVs) are considered key indicators of diffusion-controlled electrochemical processes with distinct Faradaic charge transfer. Herein, we report on an electrochemical system with separated CV peaks, accompanied by surface-controlled partial charge transfer, in 2D TiCT MXene in water-in-salt electrolytes.

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Article Synopsis
  • Nanostructured birnessite is a promising electrode material for energy storage due to its high specific capacitance and ideal capacitive behavior in aqueous solutions.
  • The electrochemical capacitance mechanism in birnessite involves both Faradaic (redox reactions) and non-Faradaic (electrostatic) processes, requiring comprehensive analysis through various advanced characterization techniques.
  • Research insights reveal that charge storage is primarily facilitated by interlayer cation intercalation, influenced by nanoconfined water that supports interactions with minimal structural alterations.
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Alkali ion insertion into Prussian blue from aqueous electrolytes is characterized with operando AFM and EQCM, showing coupling of current with deformation and mass change rates. Stable cycling occurs only with K, attributed to its lower hydration energy. The (de)insertion of K results in reversible deformation even in the open framework structure.

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This work focuses on the mechanisms of interfacial processes at the surface of amorphous silicon thin-film electrodes in organic carbonate electrolytes to unveil the origins of the inherent nonpassivating behavior of silicon anodes in Li-ion batteries. Attenuated total reflection Fourier-transform infrared spectroscopy, X-ray absorption spectroscopy, and infrared near-field scanning optical microscopy were used to investigate the formation, evolution, and chemical composition of the surface layer formed on Si upon cycling. We found that the chemical composition and thickness of the solid/electrolyte interphase (SEI) layer continuously change during the charging/discharging cycles.

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The structure of electrical double layers at electrified interfaces is of utmost importance for electrochemical energy storage as well as printable, flexible, and bioelectronic devices, such as ion-gated transistors (IGTs). Here we report a study based on atomic force microscopy force-distance profiling on electrical double layers forming at the interface between the ionic liquid 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide and sol-gel films of mesoporous tungsten oxide. We successfully followed, under conditions, the evolution of the arrangement of the ions at the interface with the tungsten oxide films used as channel materials in IGTs.

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Electrochemical reactions and ionic transport underpin the operation of a broad range of devices and applications, from energy storage and conversion to information technologies, as well as biochemical processes, artificial muscles, and soft actuators. Understanding the mechanisms governing function of these applications requires probing local electrochemical phenomena on the relevant time and length scales. Here, we discuss the challenges and opportunities for extending electrochemical characterization probes to the nanometer and ultimately atomic scales, including challenges in down-scaling classical methods, the emergence of novel probes enabled by nanotechnology and based on emergent physics and chemistry of nanoscale systems, and the integration of local data into macroscopic models.

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The presence of structural water in tungsten oxides leads to a transition in the energy storage mechanism from battery-type intercalation (limited by solid state diffusion) to pseudocapacitance (limited by surface kinetics). Here, we demonstrate that these electrochemical mechanisms are linked to the mechanical response of the materials during intercalation of protons and present a pathway to utilize the mechanical coupling for local studies of electrochemistry. Operando atomic force microscopy dilatometry is used to measure the deformation of redox-active energy storage materials and to link the local nanoscale deformation to the electrochemical redox process.

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During natural evolution, the spindles often scale with cell sizes to orchestrate accurate chromosome segregation. Whether in cancer evolution, when the constraints on genome integrity are relaxed, cancer cells may evolve the spindle to confer other advantages has not been investigated. Using invasion as a selective pressure in vitro, we found that a highly metastatic cancer clone displays a lengthened metaphase spindle, with faster spindle elongation that correlates with transiently elevated speed of cell migration.

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Supercapacitors store charge through the electrosorption of ions on microporous electrodes. Despite major efforts to understand this phenomenon, a molecular-level picture of the electrical double layer in working devices is still lacking as few techniques can selectively observe the ionic species at the electrode/electrolyte interface. Here, we use in situ NMR to directly quantify the populations of anionic and cationic species within a working microporous carbon supercapacitor electrode.

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Article Synopsis
  • Phalaenopsis orchids are a key economic crop within the Orchidaceae family, notable for their beauty but limited aroma among most species.
  • This study investigated the volatile components of P. Nobby's Pacific Sunset using solid-phase microextraction with gas chromatography techniques, successfully identifying 31 volatile compounds.
  • Findings revealed that the highest odor concentration occurred between 09:00 and 13:00 on the eighth day of storage, with the dorsal sepals and petals emitting the strongest scents compared to the column.
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Electrochemical quartz crystal microbalance (EQCM) and cyclic voltammetry (CV) measurements were used to characterize ion adsorption in carbide-derived carbon (CDC) with two different average pore sizes (1 and 0.65 nm), from neat and solvated 1-Ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (EMI-TFSI) electrolytes. From the electrode mass change in neat EMI-TFSI, it was shown that one net charge stored corresponds almost to one single ion at high polarization; in that case, no ion-pairing or charge screening by co-ions were observed.

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