| 1. |
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| 2. |
- Kelly, John J., et al.
(författare)
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Snapshots of actin and tubulin folding inside the TRiC chaperonin
- 2022
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Ingår i: Nature Structural and Molecular Biology. - : Springer Science and Business Media LLC. - 1545-9993 .- 1545-9985. ; 29:5, s. 420-429
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Tidskriftsartikel (refereegranskat)abstract
- The integrity of a cell’s proteome depends on correct folding of polypeptides by chaperonins. The chaperonin TCP-1 ring complex (TRiC) acts as obligate folder for >10% of cytosolic proteins, including he cytoskeletal proteins actin and tubulin. Although its architecture and how it recognizes folding substrates are emerging from structural studies, the subsequent fate of substrates inside the TRiC chamber is not defined. We trapped endogenous human TRiC with substrates (actin, tubulin) and cochaperone (PhLP2A) at different folding stages, for structure determination by cryo-EM. The already-folded regions of client proteins are anchored at the chamber wall, positioning unstructured regions toward the central space to achieve their native fold. Substrates engage with different sections of the chamber during the folding cycle, coupled to TRiC open-and-close transitions. Further, the cochaperone PhLP2A modulates folding, acting as a molecular strut between substrate and TRiC chamber. Our structural snapshots piece together an emerging model of client protein folding within TRiC.
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| 3. |
- Ahmed, Istaq, 1972, et al.
(författare)
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Structural study and proton conductivity of BaZr0.90Ga0.10O2.95
- 2006
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Ingår i: Advances of Solid Oxide Fuel Cells II, Ceramic Engineering and Science Proceedings. - Hoboken, NJ, USA : John Wiley & Sons, Inc.. ; 27:4, s. 105-117
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Tidskriftsartikel (refereegranskat)abstract
- Traditional solid state sintering has been used to prepare the perovskite BaZr0.9Ga0.1O2.95. Analysis of X-ray powder diffraction data shows that a decrease of the unit cell parameter a was observed compared to the undoped BaZrO3, which confirms successful substitution of Ga3+ for Zr4+ at the B site. Rietveld analysis of room temperature neutron powder diffraction data confirmed cubic symmetry (space group Pm-3m) for both as- prepared and deuterated BaZr0.90Ga0.10O2.95 samples. The strong O-H stretch band (2500-3500 cm−1) in the infrared absorbance spectrum clearly manifests the presence of protons in the pre-hydrated material. The bulk and total conductivities of prehydrated BaZr0.9Ga0.1O2.95 are 1.17 × 10−5 and 3.55 × 10−6 Scm−1, respectively at 400°C, which are more than one order of magnitude higher than for dried a sample at the same temperature. In contrast, the total conductivity of pre-hydrated and dried samples is similar at higher temperature, e. g. T > 800 °C. The higher activation energy (e. g. 0.7 eV) for pre-hydrated sample compared to typical value (0.4-0.5 eV) of proton conduction may suggest that the protons are trapped in the material.
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| 4. |
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| 5. |
- Andersson, A. K. E., et al.
(författare)
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Chemical Expansion Due to Hydration of Proton-Conducting Perovskite Oxide Ceramics
- 2014
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Ingår i: Journal of the American Ceramic Society. - : Wiley. - 0002-7820 .- 1551-2916. ; 97:8, s. 2654-2661
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Tidskriftsartikel (refereegranskat)abstract
- The crystal structures of proton-conducting BaZr1-xYxO3-x/2 (BZY05-BZY20) and BaCe0.8Y0.2O2.9 (BCY20) during hydration/dehydration has been studied by in situ high-temperature X-ray diffraction and thermal analysis. A contraction/expansion of the crystal lattice associated with dehydration/hydration was observed for all materials at elevated temperatures and the polymorphic phase transition temperatures of BaCe0.8Y0.2O2.9 were depressed by lowering the vapor pressure of water. A thermodynamic formalism is introduced to describe the chemical expansion associated with the hydration of oxygen vacancies in acceptor-doped oxides. A conventional point defect model was applied to describe the lattice strain associated with the hydration. The chemical expansion is discussed with respect to the available volumetric data on the hydration of proton-conducting oxide materials and its likely impact on ceramic fuel cells/hydrogen separation membranes utilizing a proton-conducting electrolyte.
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| 6. |
- Bandara, T M W J, 1968, et al.
(författare)
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Novel photo-voltaic device based on Bi_{1−x}La_xFeO_3 perovskite films with higher efficiency
- 2019
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Ingår i: Journal of Materials Science: Materials in Electronics. - : Springer Science and Business Media LLC. - 1573-482X .- 0957-4522. ; 30:2, s. 1654-1662
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Tidskriftsartikel (refereegranskat)abstract
- Photovoltaic cells using polycrystalline La substituted bismuth iron oxide, Bi1−xLaxFeO3, (0.1 ≤ x ≤ 0.4), films as the light harvesting component were investigated in this work. A novel cell set-up utilizing a double layered TiO2 film as top contact and a thin layer of quasi-solid polymer electrolyte as back contact was used and a significant enhancement in cell efficiency was observed for assemblies based on x ≥ 0.2 samples, coincident with a structural transition of Bi1−xLaxFeO3 from ferroelectric to non-ferroelectric. The power conversion efficiency of the PV device was 0.13% for the cell with x = 0.2 at 1 sun irradiation. The short circuit current density for this La composition was 0.35 mA cm−2. A hysteretic behaviour was observed for higher La compositions when the scanning is from open-circuit (OP) to short-circuit (SC) which may be attributed to polarization effects. The results at x ≥ 0.2 show an improved performance with respect to BiFeO3 based systems, suggesting the stabilization of the non-ferroelectric crystal structure leads either to a more efficient separation of photo-generated electron–hole pairs and/or enhanced charge transport. The findings represent a step towards the realisation of facile to fabricate, inorganic solid state photovoltaic devices.
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| 7. |
- Eriksson, Annika, 1975, et al.
(författare)
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High temperature phase transition of the magnetoelectric double perovskite Sr2NiMoO6 by neutron diffraction
- 2006
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Ingår i: Materials Research Bulletin. - 0025-5408. ; 41, s. 144-157
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Tidskriftsartikel (refereegranskat)abstract
- The magnetic ferroelectric double perovskite Sr2NiMoO6 has been characterised using neutron powder diffraction (NPD) data and magnetic susceptibility measurements. High temperature NPD data indicate that the material undergoes a continuous structural phase transition from tetragonal (I4/m) to cubic (Fm(3) over barm) at approximately 550 K. The transition is linked to the level of rotation of the NiO6 and MoO6 octahedra, which form perfectly segregated sub-lattices in the material. The reduction in symmetry at 550 K is linked to the onset of a spontaneous dipole in the material allowing the structural perturbation to be described as an improper ferroelectric phase transition. The appearance of low angle reflections in the 20 K dataset indicates the presence of an antiferromagnetic ordered around state. The magnetic moment was refined to 1.88(8) mu(B) confirming that the magnetism originates from the Ni2+ (S = 1) ions. (C) 2005 Elsevier Ltd. All rights reserved.
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| 8. |
- Eriksson Andersson, A.K., et al.
(författare)
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Thermal evolution of the crystal structure of proton conducting BaCe 0.8 Y 0.2 O 3-δ from high-resolution neutron diffraction in dry and humid atmosphere
- 2015
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Ingår i: Dalton Transactions. - : Royal Society of Chemistry (RSC). - 1477-9226 .- 1477-9234. ; 44:23, s. 10834-10846
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Tidskriftsartikel (refereegranskat)abstract
- The crystal structure of the proton conducting perovskite BaCe0.8Y0.2O3-δ (BCY20) has been studied via high-resolution in situ neutron diffraction performed in controlled dry and humid (heavy water) oxygen flow. Two phase transitions, cubic Pm3m→R3c (775 °C)→Imma (250 °C) were observed on cooling from 1000 °C in dry O2. A significant shift of the phase stability fields was observed on cooling in wet oxygen (pD2O ≈ 0.2 atm) with the R3c structure stabilised at 900 °C, and the R3c→Imma transition occurring at 675 °C. On cooling below 400 °C a monoclinic, I2/m, phase started to appear. The structural dependence on hydration level is primarily due to the de-stabilisation of the correlated, octahedra tilts as a consequence of structural relaxation around the oxygen vacancies present in the non-hydrated phase. The tendency of hydrated BaCe0.8Y0.2O3-δ to show octahedral tilting is also found to be enhanced, indicating that the deuteronic (protonic) defects influence the crystal structure, possibly via hydrogen bonding. Stabilisation of the monoclinic I2/m phase is attributed to the structural effect of deuterons that is inferred to increase on cooling as deuterons localise to a greater extent. Changing from wet oxidising (O2 + D2O(g)) to wet reducing (5% H2 in Ar + D2O(g)) atmosphere did not influence the structure or the phase stability, indicating that Ce4+ was not reduced under the present conditions. Based on the observed cell volume expansion protonic defects are present in the material at 900 °C at a D2O partial pressure of ∼0.2 atm. The origin of the chemical expansion is explained by the effective size of the oxygen vacancy being significantly smaller than the [OD] defect. Rietveld analysis has been used to locate possible sites for the deuterons in the high temperature, R3c and Imma, phases that are most relevant for proton transport.
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| 9. |
- Fujita, K., et al.
(författare)
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LiNbO3-Type InFeO3: Room-Temperature Polar Magnet without Second-Order Jahn-Teller Active Ions
- 2016
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Ingår i: Chemistry of Materials. - : American Chemical Society (ACS). - 1520-5002 .- 0897-4756. ; 28:18, s. 6644-6655
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Tidskriftsartikel (refereegranskat)abstract
- Great effort has been devoted to developing single-phase magnetoelectric multiferroics, but room-temperature coexistence of large electric polarization and magnetic ordering still remains elusive. Our recent finding shows that such polar magnets can be synthesized in small-tolerance-factor perovskites AFeO(3) with unusually small cations at the A-sites, which are regarded as having a LiNbO3-type structure (space group R3c). Herein, we experimentally reinforce this finding by preparing a novel room-temperature polar magnet, LiNbO3-type InFeO3. This compound is obtained as a metastable quench product from an orthorhombic perovskite phase stabilized at 15 GPa and an elevated temperature. The structure analyses reveal that the polar structure is characterized by displacements of In3+ (d(10)) and Fe3+ (d(5)) ions along the hexagonal c-axis (pseudocubic [111] axis) from their centrosymmetric positions, in contrast to well-known perovskite ferroelectrics (e.g., BaTiO3, PbTiO3, and BiFeO3) where d(0) transition-metal ions and/or 6s(2) lone-pair cations undergo polar displacements through the so-called second-order Jahn-Teller (SOJT) distortions. Using density functional theory calculations, the electric polarization of LiNbO3-type InFeO3 is estimated to be 96 mu C/cm(2) along the c-axis, comparable to that of an isostructural and SOJT-active perovskite ferroelectric, BiFeO3 (90-100 mu C/cm(2)). Magnetic studies demonstrate weak ferromagnetic behavior at room temperature, as a result of the canted G-type antiferromagnetic ordering of Fe3+ moments below T-N similar to 545 K. The present work shows the functional versatility of small-tolerance-factor perovskites and provides a useful guide for the synthesis and design of room-temperature polar magnets.
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| 10. |
- Galati, R., et al.
(författare)
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Hydration, Structure, and Superconductivity of KOs2O6·nH2O
- 2008
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Ingår i: Chemistry of Materials. - : American Chemical Society (ACS). - 0897-4756 .- 1520-5002. ; 20:4, s. 1652-1659
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Tidskriftsartikel (refereegranskat)abstract
- In moist air or by contact with water during washing, KOs2O6 absorbs water molecules into the structure to produce KOs2O6·nH2O, 0 < n < 0.1. This water is reversibly lost on heating above ∼430 K in flowing or static gas environments. Variable temperature powder neutron and X-ray diffraction show that an increase in lattice parameter occurs when water enters the pyrochlore structure and the water molecules are located in the α cages displacing a portion of the potassium ions to adjacent sites. On removing water the lattice parameter and structure revert to those of the normal β-pyrochlore crystallographic description. Hydration has the effect of reducing the onset of superconducting behavior from a critical temperature of 10.25 K in fully dry KOs2O6 to 9.75 K in KOs2O6·0.1H2O.
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