30 research outputs found

    Highly Tunable Intrinsic Exchange Bias from Interfacial Reconstruction in Epitaxial NixCoyFe3-x-yO4(111)/{\alpha}-Al2O3(0001) Thin Films

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    Intrinsic exchange bias up to 12.6 kOe is observed in NixCoyFe3-x-yO4(111)/{\alpha}-Al2O3(0001) (0<=x+y<=3) epitaxial thin films where 0.15<=y<=2. An interfacial layer of rock-salt structure emerges between NixCoyFe3-x-yO4 thin films and {\alpha}-Al2O3 substrates and is proposed as the antiferromagnetic layer unidirectionally coupled with ferrimagnetic NixCoyFe3-x-yO4. In NiCo2O4(111)/{\alpha}-Al2O3(0001) films, results of reflection high energy electron diffraction, X-ray photoelectron spectroscopy, X-ray reflectometry, and polarized neutron reflectometry support that the interfacial layer is antiferromagnetic NixCo1-xO (0.32<=x<=0.49) of rock-salt structure; the interfacial layer and exchange bias can be controlled by growth oxygen pressure revealing the key role of oxygen in the mechanism of the interfacial reconstruction. This work establishes a family of intrinsic exchange bias materials with great tunability by stoichiometry and growth parameters and emphasizes the strategy of interface engineering in controlling material functionalities.Comment: Main Text: 14 pages, 5 figures; Supplemental Materials: 12 pages, 11 figure

    Duality of switching mechanisms and transient negative capacitance in improper ferroelectrics

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    The recent discovery of transient negative capacitance has sparked an intense debate on the role of homogeneous and inhomogeneous mechanisms in polarizations switching. In this work, we report observation of transient negative capacitance in improper ferroelectric h-YbFeO3 films in a resistor-capacitor circuit, and a concaved shape of anomaly in the voltage wave form, in the early and late stage of the polarizations switching respectively. Using a phenomenological model, we show that the early-stage negative capacitance is likely due to the inhomogeneous switching involving nucleation and domain wall motion, while the anomaly at the late stage, which appears to be a reminiscent negative capacitance is the manifestation of the thermodynamically unstable part of the free-energy landscape in the homogeneous switching. The complex free-energy landscape in hexagonal ferrites may be the key to cause the abrupt change in polarization switching speed and the corresponding anomaly. These results reconcile the two seemingly conflicting mechanisms in the polarization switching and highlight their different roles at different stages. The unique energy-landscape in hexagonal ferrites that reveals the dual switching mechanism suggests the promising application potential in terms of negative capacitance.Comment: 14 pages,5 figure

    GW501516, a PPARĪ“ Agonist, Ameliorates Tubulointerstitial Inflammation in Proteinuric Kidney Disease via Inhibition of TAK1-NFĪŗB Pathway in Mice

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    Peroxisome proliferator-activated receptors (PPARs) are a nuclear receptor family of ligand-inducible transcription factors, which have three different isoforms: PPARĪ±, Ī“ and Ī³. It has been demonstrated that PPARĪ± and Ī³ agonists have renoprotective effects in proteinuric kidney diseases; however, the role of PPARĪ“ agonists in kidney diseases remains unclear. Thus, we examined the renoprotective effect of GW501516, a PPARĪ“ agonist, in a protein-overload mouse nephropathy model and identified its molecular mechanism. Mice fed with a control diet or GW501516-containing diet were intraperitoneally injected with free fatty acid (FFA)-bound albumin or PBS(āˆ’). In the control group, protein overload caused tubular damages, macrophage infiltration and increased mRNA expression of MCP-1 and TNFĪ±. These effects were prevented by GW501516 treatment. In proteinuric kidney diseases, excess exposure of proximal tubular cells to albumin, FFA bound to albumin or cytokines such as TNFĪ± is detrimental. In vitro studies using cultured proximal tubular cells showed that GW501516 attenuated both TNFĪ±- and FFA (palmitate)-induced, but not albumin-induced, MCP-1 expression via direct inhibition of the TGF-Ī² activated kinase 1 (TAK1)-NFĪŗB pathway, a common downstream signaling pathway to TNFĪ± receptor and toll-like receptor-4. In conclusion, we demonstrate that GW501516 has an anti-inflammatory effect in renal tubular cells and may serve as a therapeutic candidate to attenuate tubulointerstitial lesions in proteinuric kidney diseases

    Colossal intrinsic exchange bias from interfacial reconstruction in epitaxial CoFe\u3csub\u3e2\u3c/sub\u3e O\u3csub\u3e4\u3c/sub\u3e/Al\u3csub\u3e2\u3c/sub\u3e O\u3csub\u3e3\u3c/sub\u3e thin films

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    We have studied the epitaxial CoFe2O4 (111) films grown on Al2O3 (0001) substrates of different thickness at various temperature and discovered colossal intrinsic exchange bias up to 7 Ā± 2 kOe. X-ray and electron diffraction clearly indicate an interfacial layer about 2 nm of different crystal structure from the ā€œbulkā€ part of the CoFe2O4 film. The thickness dependence of the exchange bias suggests a hidden antiferromagnetic composition in the interfacial layer that couples to the ferrimagnetic ā€œbulkā€ part of the CoFe2O4 film as the origin of the exchange bias. Considering the structural, magnetic, and electronic structure, CoO has been identified as the most likely candidate of the antiferromagnetic composition in the interfacial layer. This work suggests a path for enhancing intrinsic exchange bias using combination of film and substrate of large structural differences, highlighting the role of interfacial atomic and electronic reconstructions

    Energy consumption analysis of a ground water-source heat pump for the plant factory based on TRNSYS simulation

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    The ground water-source heat pump system for the plant factory lacks a scientific operation strategy to solve the problem of high energy consumption in winter and summer. It is very difficult and uneconomical to change the operation conditions by experimental means to obtain actual operation data. The current study aims to build a TRNSYS simulation model of the ground water-source heat pump system of Shanghai Chongming Natural Light Plant Factory. For the heating season, the simulation of energy consumption was 2315 GJ. Compared with the actual energy consumption, the relative error is -0.98%, which indicates that the simulation results are accurate and the simulation model developed is appropriate and usable. Numerical simulations for the whole year on this basis yielded that the plant factory energy supply system operates from November to March with a heating energy consumption of 3530.84 GJ and from June to September with a cooling energy consumption of 1126.24 GJ. In most cases, the indoor temperature fluctuates within a reasonable range, but in the summer high-temperature season, the plant factory temperature will reach above 40ā„ƒ, which seriously affects plant growth. After optimization, the plant factory stops production in July and August, and the system stops running, the results are that the optimized system can save 56% of the annual cooling energy consumption, totalling 767.48 GJ, which can reduce the costs by 160,318.05 RMB

    Hepatitis B Virus X Protein Reduces Podocyte Adhesion via Downregulation of Ī±3Ī²1 Integrin

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    Background/Aims: Hepatitis B virus (HBV)-associated glomerulonephritis (HBV-GN) is characterized by a reduced number of podocytes due to apoptosis and shedding from the basement membrane. However, the pathological mechanism of HBV-GN is unclear. We previously showed that hepatitis B virus X protein (HBx) promotes apoptosis in tubular epithelial cells. In this study, we transfected podocytes with HBx and examined the effects on adhesion and apoptosis of these cells. Methods: Podocytes were transfected with pc-DNA3.1 (+)-HBx. One control group was not transfected and another control group was transfected with empty plasmids. Podocyte adhesion was assessed by a fluorescence assay, apoptosis was measured by flow cytometry and fluorescence microscopy, and expression of Ī±3Ī²1 integrin was determined by western blotting and the reverse transcription polymerase chain reaction (RT-PCR). Activity of caspase-8 was measured by a spectrophotometric assay. Results: Relative to controls, podocytes with pc-DNA3.1(+)-HBx had reduced cell adhesion, increased apoptosis, reduced expression of Ī±3Ī²1 integrin, and increased caspase-8 activity. Ī²1 integrin blockage reduced podocyte adhesion, but increased apoptosis and caspase-8 activity. Treatment of transfected podocytes with a caspase-8 inhibitor (Z-IETD-FMK) had no effect on the HBx-mediated integrin downregulation and reduced podocyte adhesion, suggesting that Ī±3Ī²1 integrin downregulaton is sufficient to alter cell adhesion. Conclusions: Our in vitro results indicate that HBx reduced podocyte adhesion and expression of Ī±3Ī²1 integrin, and increased apoptosis. Moreover, HBx-mediated downregulation of Ī±3Ī²1 integrin expression is sufficient to reduce podocyte adhesion. HBx-induced apoptosis of podocytes may contribute to HBV-GN
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