Thin films of β-W are the most interesting for manipulating magnetic moments using spin–orbit torques, and a clear understanding of α to β phase transition in W by doping impurity, especially oxygen, is needed. Here we present a combined experimental and theoretical study using grazing incidence X-ray diffraction, photoelectron spectroscopy, electron microscopy, and ab initio calculations to explore atomic structure, bonding, and oxygen content for understanding the formation of β-W. It is found that the W films on SiO2/Si have 13–22 at.% oxygen in A15 β structure. Ab initio calculations show higher solution energy of oxygen in β-W, and a tendency to transform locally from α to β phase with increasing oxygen concentration. X-ray absorption spectroscopy also revealed local geometry of oxygen in β-W, in agreement with the simulated one. These results offer an opportunity for a fundamental understanding of the structural transition in α-W and further development of β-W phase for device applications.

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Piezoresponse force microscopy (PFM) is a powerful tool for probing nanometer-scale ferroelectric and piezoelectric properties. Hysteretic switching of the phase and amplitude of the PFM response are believed to be the hallmark of ferroelectric and piezoelectric behavior respectively.However, the application of PFM is limited by the fact that similar hysteretic effects may also arise from mechanisms not related to ferroelectricity or piezoelectricity. In this paper we report our studies on regular glass slides that show ferroelectric-like signal without being ferroelectric and frequently used as a substrate in PFM experiments. We demonstrate how the substrates and other environmental factors like relative humidity and experimental conditions may influence the PFM results on novel materials.

The high-mobility 2DEGs formed at the interfaces between certain insulating perovskite oxides have been known to be a novel playground of exotic physical orders like, superconductivity and ferromagnetism and their inter-coupling. There have been efforts to accomplish even more exotic properties at such interfaces of oxide heterostructures through nano-structuring of the surface.In this paper we report writing and erasing charge domains on such an oxide heterostructure LaVO 3 /SrTiO 3 using a conductive AFM cantilever. We have patterned these domains in a periodic fashion in order to create artificial lattices on the surface. Through kelvin probe microscopy, electrostatic force microscopy and conductivity mapping of such artificial lattices we found that the domains not only trap charge carriers but also develop a controllable potential landscape on the surface which coincides with a modulation of local electrical conductivity. The ability to pattern such nanostructures reversibly offers unprecedented opportunities of realizing ultra-high storage density devices in high mobility oxide heterostructures.

Unlike graphene nanostructures, various physical properties of nanostructured MoS have remained unexplored due to the lack of established fabrication routes. Herein, we have reported unique electrostatic properties of MoS nanostructures, fabricated in a controlled manner of different geometries on 2D flake by using focused laser irradiation technique. Electrostatic force microscopy has been carried out on MoS nanostructures by varying tip bias voltage and lift height. The analysis depicts no contrast flip in phase image of the patterned nanostructure due to the absence of free surface charges. However, prominent change in phase shift at the patterned area is observed. Such contrast changes signify the capacitive interaction between tip and nanostructures at varying tip bias voltage and lift height, irrespective of their shape and size. Such unperturbed capacitive behavior of the MoS nanostructures offer modulation of capacitance in periodic array on 2D MoS flake for potential application in capacitive devices.