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1.
Sci Rep ; 12(1): 391, 2022 Jan 10.
Article in English | MEDLINE | ID: mdl-35013483

ABSTRACT

High quality FeySe1-xTex epitaxial thin films have been fabricated on TiO2-buffered SrTiO3 substrates by pulsed laser deposition technology. There is a significant composition deviation between the nominal target and the thin film. Te doping can affect the Se/Te ratio and Fe content in chemical composition. The superconducting transition temperature Tc is closely related to the chemical composition. Fe vacancies are beneficial for the FeySe1-xTex films to exhibit the higher Tc. A 3D phase diagram is given that the optimize range is x = 0.13-0.15 and y = 0.73-0.78 for FeySe1-xTex films. The anisotropic, effective pining energy, and critical current density for the Fe0.72Se0.94Te0.06, Fe0.76Se0.87Te0.13 and Fe0.91Se0.77Te0.23 films were studied in detail. The scanning transmission electron microscopy images display a regular atomic arrangement at the interfacial structure.

2.
Adv Mater ; 34(6): e2107799, 2022 Feb.
Article in English | MEDLINE | ID: mdl-34818689

ABSTRACT

The superconducting proximity effect (SPE) induces a superconductivity transition in otherwise non-superconducting thin films in proximity with a superconductor. The SPE usually occurs in real space and decays exponentially with film thickness. Herein, an abnormal SPE in a topological insulator (TI)/superconductor heterostructure is unveiled, which is attributed to the topologically protected surface state. Surprisingly, such abnormal SPE occurs in momentum space regardless of the TI film thickness, as long as the topological surface states are robust and form a continuous conduction loop. Combining transport measurements and scanning tunneling microscopy/spectroscopy techniques, the SPE in Bi2 Se3 /FeSe0.5 Te0.5 heterostructures is explored, where Bi2 Se3 is an ideal 3D topological insulator and FeSe0.5 Te0.5 a typical iron-based superconductor. As the thickness of the Bi2 Se3 thin film exceeds 400 nm, there still exists SPE-induced superconductivity on the surface of Bi2 Se3 thin film with a transition temperature Tc not less than 10 K. Such an extraordinary behavior is induced by the unique properties of topologically protected surface states of Bi2 Se3 . This research deepens the understanding of the important role of topologically protected surface states in the SPE.

3.
Biomed Res Int ; 2018: 8065252, 2018.
Article in English | MEDLINE | ID: mdl-29850568

ABSTRACT

We investigate numerically the microscale blood flow in which red blood cells (RBCs) are partially infected by Plasmodium falciparum, the malaria parasite. The infected RBCs are modeled as more rigid cells with less deformability than healthy ones. Our study illustrates that, in a 10 µm microvessel in low-hematocrit conditions (18% and 27%), the Plasmodium falciparum-infected red blood cells (Pf-IRBCs) and healthy ones first form a train of cells. Because of the slow moving of the Pf-IRBCs, the local hematocrit (Hct) near the Pf-IRBCs is then increased, to approximately 40% or even higher values. This increase of the local hematocrit is temporary and is kept for a longer length of time because of the long RBC train formed in 27%-Hct condition. Similar hematocrit elevation at the downstream region with 45%-Hct in the same 10 µm microvessel is also observed with the cells randomly located. In 20 µm microvessels with 45%-Hct, the Pf-IRBCs slow down the velocity of the healthy red blood cells (HRBCs) around them and then locally elevate the volume fraction and result in the accumulation of the RBCs at the center of the vessels, thus leaving a thicker cell free layer (CFL) near the vessel wall than normal. Variation of wall shear stress (WSS) is caused by the fluctuation of local Hct and the distance between the wall and the RBCs. Moreover, in high-hematocrit condition (45%), malaria-infected cells have a tendency to migrate to the edge of the aggregates which is due to the uninterrupted hydrodynamic interaction between the HRBCs and Pf-IRBC. Our results suggest that the existence of Pf-IRBCs is a nonnegligible factor for the fluctuation of hematocrit and WSS and also contributes to the increase of CFL of pathological blood flow in microvessels. The numerical approach presented has the potential to be utilized to RBC disorders and other hematologic diseases.


Subject(s)
Erythrocyte Membrane/parasitology , Erythrocytes/parasitology , Hematocrit , Malaria, Falciparum , Plasmodium falciparum/physiology , Hemodynamics/physiology , Humans , Malaria, Falciparum/blood , Malaria, Falciparum/physiopathology , Stress, Mechanical
4.
Sci Rep ; 6: 20262, 2016 Feb 02.
Article in English | MEDLINE | ID: mdl-26830454

ABSTRACT

Blood exhibits a heterogeneous nature of hematocrit, velocity, and effective viscosity in microcapillaries. Microvascular bifurcations have a significant influence on the distribution of the blood cells and blood flow behavior. This paper presents a simulation study performed on the two-dimensional motions and deformation of multiple red blood cells in microvessels with diverging and converging bifurcations. Fluid dynamics and membrane mechanics were incorporated. Effects of cell shape, hematocrit, and deformability of the cell membrane on rheological behavior of the red blood cells and the hemodynamics have been investigated. It was shown that the blood entering the daughter branch with a higher flow rate tended to receive disproportionally more cells. The results also demonstrate that red blood cells in microvessels experienced lateral migration in the parent channel and blunted velocity profiles in both straight section and daughter branches, and this effect was influenced by the shape and the initial position of the cells, the hematocrit, and the membrane deformability. In addition, a cell free region around the tip of the confluence was observed. The simulation results are qualitatively consistent with existing experimental findings. This study may provide fundamental knowledge for a better understanding of hemodynamic behavior of micro-scale blood flow.


Subject(s)
Erythrocyte Deformability/physiology , Erythrocytes/physiology , Microvessels/physiology , Models, Biological , Algorithms , Blood Flow Velocity , Computer Simulation , Hemodynamics , Hemorheology , Humans , Viscosity
5.
Biomed Res Int ; 2016: 1801403, 2016.
Article in English | MEDLINE | ID: mdl-28105411

ABSTRACT

The malaria-infected red blood cells experience a significant decrease in cell deformability and increase in cell membrane adhesion. Blood hemodynamics in microvessels is significantly affected by the alteration of the mechanical property as well as the aggregation of parasitized red blood cells. In this study, we aim to numerically study the connection between cell-level mechanobiological properties of human red blood cells and related malaria disease state by investigating the transport of multiple red blood cell aggregates passing through microchannels with symmetric stenosis. Effects of stenosis magnitude, aggregation strength, and cell deformability on cell rheology and flow characteristics were studied by a two-dimensional model using the fictitious domain-immersed boundary method. The results indicated that the motion and dissociation of red blood cell aggregates were influenced by these factors and the flow resistance increases with the increase of aggregating strength and cell stiffness. Further, the roughness of the velocity profile was enhanced by cell aggregation, which considerably affected the blood flow characteristics. The study may assist us in understanding cellular-level mechanisms in disease development.


Subject(s)
Erythrocyte Deformability , Erythrocyte Membrane/metabolism , Malaria/physiopathology , Microvessels/physiopathology , Models, Cardiovascular , Biological Transport, Active , Blood Flow Velocity , Cell Adhesion , Constriction, Pathologic/physiopathology , Erythrocyte Membrane/parasitology , Humans
7.
Sci Rep ; 4: 6433, 2014 Sep 22.
Article in English | MEDLINE | ID: mdl-25242541

ABSTRACT

Transition metal selenide and telluride have recently receive considerable attention due to their possible structural relation to ferropnictide. Pressure is often used as an efficient way to modify the crystal or electronic structure that in many cases lead to new material states of interest. Here we search the structures of IrTe2 up to 150 GPa using crystal structure prediction techniques combining with ab initio calculations. Three new stable phases under high pressures are predicted, and their electronic structure properties, phonon spectra, and electron-phonon couplings are also investigated. Significant reconstructions of band structures and Fermi surfaces are found in these new phases. Calculated results show that while the C2/m-2 phase has bad metal behavior and very weak electron-phonon coupling, the and I4/mmm phases have relatively higher electron-phonon coupling up to ~ 1.5 and 0.7, respectively. The variable-composition searching have been performed, newly compounds with different stoichiometries, such as IrTe3, IrTe, and Ir3Te, are predicted to be thermodynamically and dynamically stable at high pressures. The pressure range investigated here is accessible in the diamond anvil cell experiments, thus our results might stimulate further experimental studies.

8.
Biomed Mater Eng ; 24(6): 2511-7, 2014.
Article in English | MEDLINE | ID: mdl-25226952

ABSTRACT

This paper presents a fluid-particle interaction algorithm using the distributed Lagrange multiplier based fictitious domain method. The application of this method to the numerical investigation of motion and aggregation of red blood cells in two-dimensional microvessels is discussed. The cells are modelled as rigid biconcave-shaped neutrally buoyant particles. The aggregating force between two cells is derived from a Morse type potential function. The cell-cell interaction is coupled with the fluid-cell interaction through a time splitting scheme. Simulation results of multiple red blood cells in Poiseuille flow are presented. Because of its modular nature, this algorithm is applicable to a large class of problems involving the processes of particle aggregation and fluid-particle interaction.


Subject(s)
Blood Flow Velocity/physiology , Cell Communication/physiology , Erythrocyte Aggregation/physiology , Erythrocyte Deformability/physiology , Erythrocytes/physiology , Microvessels/physiology , Models, Cardiovascular , Algorithms , Animals , Blood Pressure/physiology , Computer Simulation , Humans , Shear Strength/physiology
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