Manipulating magnetic and magnetoresistive properties by oxygen vacancy complexes in GCMO thin films.

The effect ofin situannealing is investigated in Gd0.1Ca0.9MnO3(GCMO) thin films in oxygen and vacuum atmospheres. We show that the reduction of oxygen content in GCMO lattice by vacuum annealing induced more oxygen complex vacancies in both subsurface and interface regions and larger grain domains when compared with the pristine one. Consequently, the double exchange interaction is suppressed and the metallic-ferromagnetic state below Curie temperature turned into spin-glass insulating state. In contrast, the magnetic and resistivity measurements show that the oxygen treatment increases ferromagnetic phase volume, resulting in greater magnetization (MS) and improved magnetoresistivity properties below Curie temperature by improving the double exchange interaction. The threshold field to observe the training effect is decreased in oxygen treated film. In addition, the positron annihilation spectroscopy analysis exhibits fewer open volume defects in the subsurface region for oxygen treated film when compared with the pristine sample. These results unambiguously demonstrate that the oxygen treated film with significant spin memory and greater magnetoresistance can be a potential candidate for the future memristor applications.

Tuneable exchange-spring stiffness in amorphous magnetic trilayer structures.

We investigate the magnetic properties of amorphous Sm10Co90/Co60(Al70Zr30)40/Co85(Al70Zr30)15exchange-spring magnet trilayers. The magnetically soft Co85(Al70Zr30)15layer is coupled to the magnetically hard Sm10Co90layer through the weakly magnetic low-TcCo60(Al70Zr30)40spacer layer. The strength of the coupling can be controlled with temperature and the coupling persists above the intrinsicTcof the spacer layer due to a long-range magnetic proximity effect. Polarized neutron reflectivity is used to examine the magnetic profile of the trilayers during magnetization reversal. A two-step switching occurs, with the switching angle of the soft layer strongly dependent on the strength of the coupling. In the strong coupling regime a magnetic state can be achieved where the soft layer magnetization is perpendicular to the hard layer whereas in the weak coupling regime the soft layer reverses fully.

Tuned AFM-FM coupling by the formation of vacancy complex in Gd0.6Ca0.4MnO3thin film lattice.

The effect ofin situoxygen and vacuum annealings on the low bandwidth manganite Gd1-xCaxMnO3(GCMO) thin film withx= 0.4 was investigated. Based on the magnetic measurements, the AFM-FM coupling is suppressed by the vacuum annealing treatment via destroying the double exchange interaction and increasing the unit cell volume by converting the Mn4+to the Mn3+. Consequently, resistance increases significantly compared to pristine film. The results are explained by a model obtained from the positron annihilation studies, where the vacuum annealing increased the annihilation lifetime in A and B sites due to the formation of vacancy complexesVA,B-VO, which was not the case in the pristine sample. The positron annihilation analysis indicated that most of the open volume defects have been detected in the interface region rather than on the subsurface layer and this result is confirmed by detailed x-ray reflection analysis. On the other hand, the effect of oxygen annealing on the unit cell volume and magnetization was insignificant. This is in agreement with positron annihilation results which demonstrated that the introduction of oxygen does not change the number of cation vacancies significantly. This work demonstrates that the modification of oxygen vacancies and vacancy complexes can tune magnetic and electronic structure of the epitaxial thin films to provide new functionalities in future applications.

Metastable ferromagnetic flux closure-type domains in strain relaxed Gd0.1Ca0.9MnO3thin films.

We have systematically studied the structural, electrical transport, and magnetic properties of Gd0.1Ca0.9MnO3thin films in function of thickness, which ranged from 22 nm up to 220 nm. We have found that, although no strong substrate-induced strain was detected for any thickness, a sudden change in the electric transport properties was observed when the film thickness increases above 80 nm. While thinner samples are insulating in the whole temperature range, the samples thicker than 80 nm show a clear insulator-to-metal transition (IMT) at around 100 K. The IMT coincides with the appearance of a ferromagnetic phase that is absent in the thinner samples. We associate this change in behavior with a critical film thickness that induces a sudden change in domain configuration, from in-plane domain to a closed flux-type domain with out-of-plane orientations. These out-of-plane oriented domains are meta-stable ferromagnetic in nature and result in an IMT which is accompanied by a hysteretic magnetoresistance behavior.

Dirty limit scattering behind the decreased anisotropy of doped YBa2Cu3O7-δ thin films.

We measured the resistivity of pulsed-laser-deposited BaCeO3 (BCO)-doped YBCO thin films containing spherical BCO particles in fields up to 30 T. The average diameter of the particles depends on the dopant concentration being below 4 nm in all the samples. Raised values of the upper critical field, Bc2, were observed in all the samples. Additionally, the parameter γ, describing the electron mass anisotropy, decreased from 6.2 in the undoped sample to 3.1 in the 8 wt.% BCO-doped sample. These results can be explained by the increased number of defects decreasing the mean free path of electrons and thus lowering the coherence length, which in turn increases Bc2.

The predominance of substrate induced defects in magnetic properties of Sr2FeMoO6 thin films.

A systematic study of epitaxially grown Sr2FeMoO6 thin films on SrTiO3, (LaAlO3)0.3(Sr2AlTaO6)0.7, SrLaAlO4 and MgO single crystal substrates were made. Transmission electron microscopy investigations showed sharp substrate/films interfaces and increased defect concentration with increased lattice mismatch, indicating defect formation such as dislocations, low angle grain boundaries and stacking faults as a strain relaxation mechanism. Large enough compressive mismatch cause the over-relaxation of the lattice parameters through reorganization or interface defects, which was observed as a tensile strain in films with compressive mismatch larger than -1.05%. All the films with compressive mismatch were phase pure and epitaxially textured while signatures of SrMoO4 parasitic particle was found only in the film grown on MgO. No correlation between the antisite disorder and other structural defects or magnetic properties were found. Instead, the saturation magnetization, Curie temperature, magnetic domain rotation etc are higly dependent on the lattice mismatch induced defects, which outshines the possible correlation with B-site ordering.

Giant vortex states in type I superconductors simulated by Ginzburg-Landau equations.

The quantization of magnetic flux in superconductors is usually seen as vortices penetrating the sample. While vortices are unstable in bulk type I superconductors, restricting the superconductor causes a variety of vortex structures to appear. We present a systematic study of giant vortex states in type I superconductors obtained by numerically solving the Ginzburg-Landau equations. The size of the vortices is seen to increase with decreasing film thickness. In type I superconductors, giant vortices appear at intermediate thicknesses but they do not form a well-defined vortex lattice. In the thinnest type I films, singly quantized vortices seem to be stabilized by the geometry of the sample instead of an increase in the effective Ginzburg-Landau parameter.

Dynamic interaction of Trichoderma reesei cellobiohydrolases Cel6A and Cel7A and cellulose at equilibrium and during hydrolysis.

The binding of cellobiohydrolases to cellulose is a crucial initial step in cellulose hydrolysis. In the search for a detailed understanding of the function of cellobiohydrolases, much information concerning how the enzymes and their constituent catalytic and cellulose-binding domains interact with cellulose and with each other and how binding changes during hydrolysis is still needed. In this study we used tritium labeling by reductive methylation to monitor binding of the two Trichoderma reesei cellobiohydrolases, Cel6A and Cel7A (formerly CBHII and CBHI), and their catalytic domains. Measuring hydrolysis by high-performance liquid chromatography and measuring binding by scintillation counting allowed us to correlate activity and binding as a function of the extent of degradation. These experiments showed that the density of bound protein increased with both Cel6A and Cel7A as hydrolysis proceeded, in such a way that the adsorption points moved off the initial binding isotherms. We also compared the affinities of the cellulose-binding domains and the catalytic domains to the affinities of the intact proteins and found that in each case the affinity of the enzyme was determined by the linkage between the catalytic and cellulose-binding domains. Desorption of Cel6A by dilution of the sample showed hysteresis (60 to 70% reversible); in contrast, desorption of Cel7A did not show hysteresis and was more than 90% reversible. These findings showed that the two enzymes differ with respect to the reversibility of binding.