arXiv subjects

Jay R. Paudel

Publications and source records attributed to Jay R. Paudel.

3 recordsLinked to original sources

arXiv2026

Dual-Sublattice Ferromagnetism Driven by Cooperative Double Exchange and Superexchange at NdNiO$_3$/CaMnO$_3$ Interfaces

Engineering emergent ferromagnetism at correlated-oxide interfaces offers a powerful route to creating collective states that do not exist in the parent materials. Here, we show that interfacial valence reconstruction in NdNiO$_3$/CaMnO$_3$ superlattices generates dual-sublattice ferromagnetism involving both Mn and Ni. Depth-resolved standing-wave X-ray photoelectron spectroscopy reveals enhanced Mn$^{3+}$ character on the CaMnO$_3$ side of the interface and enhanced Ni$^{2+}$ character on the NdNiO$_3$ side, establishing the configurations required for Mn$^{4+}$-O-Mn$^{3+}$ double exchange and Ni$^{2+}$-O-Mn$^{4+}$ superexchange, respectively. At low temperature, element-specific XMCD reveals ferromagnetic responses from both sublattices, with the Ni response concentrated predominantly in the Ni$^{2+}$-derived spectral component that SW-XPS independently shows to be enhanced at the interface. Together, these results show that cooperative double exchange within CaMnO$_3$ and superexchange across the interface couple the Mn and Ni sublattices, providing a general strategy for engineering interfacial ferromagnetism in correlated oxides.

cond-mat.mtrl-sci↗

arXiv2023

Ultra-thin Epitaxial MgB2 on SiC: Substrate Surface Polarity Dependent Properties

High quality, ultrathin, superconducting films are required for advanced devices such as hot-electron bolometers, superconducting nanowire single photon detectors, and quantum applications. Using Hybrid Physical-Chemical Vapor Deposition (HPCVD), we show that MgB2 films as thin as 4 nm can be fabricated on the carbon terminated 6H-SiC (0001) surface with a superconducting transition temperature above 33K and a rms roughness of 0.7 nm. Remarkably, the film quality is a function of the SiC surface termination, with the C-terminated surface preferred to the Si-terminated surface. To understand the MgB2 thin film/ SiC substrate interactions giving rise to this difference, we characterized the interfacial structures using Rutherford backscattering spectroscopy/channeling, electron energy loss spectroscopy, and x-ray photoemission spectroscopy. The MgB2/SiC interface structure is complex and different for the two terminations. Both terminations incorporate substantial unintentional oxide layers influencing MgB2 growth and morphology, but with different extent, intermixing and interface chemistry. In this paper, we report measurements of transport, resistivity, and critical superconducting temperature of MgB2/SiC that are different for the two terminations, and link interfacial structure variations to observed differences. The result shows that the C face of SiC is a preferred substrate for the deposition of ultrathin superconducting MgB2 films.

cond-mat.supr-con↗

arXiv2020

Strain-induced anion ordering in perovskite oxyfluoride films

Anionic ordering is a promising route to engineer physical properties in functional heteroanionic materials. A central challenge in the study of anion-ordered compounds lies in developing robust synthetic strategies to control anion occupation and in understanding the resultant implications for electronic structure. Here, we show that epitaxial strain induces preferential occupation of F and O on the anion sites in perovskite oxyfluoride SrMnO2.5-dFg films grown on different substrates. Under compressive strain, F tends to take the apical-like sites, which was revealed by F and O K-edge linearly polarized x-ray absorption spectroscopy and density functional theory calculations, resulting in an enhanced c-axis expansion. Under tensile strain, F tends to take the equatorial-like sites, enabling the longer Mn-F bonds to lie within the plane. The anion ordered oxyfluoride films exhibit a significant orbital polarization of the 3d electrons, distinct F-site dependence to their valence band density of states, and an enhanced resistivity when F occupies the apical-like anion site compared to the equatorial-like site. By demonstrating a general strategy for inducing anion-site order in oxyfluoride perovskites, this work lays the foundation for future materials design and synthesis efforts that leverage this greater degree of atomic control to realize new polar or quasi-two-dimensional materials.

cond-mat.mtrl-sci↗