arXiv subjects

Taro Hitosugi

Publications and source records attributed to Taro Hitosugi.

8 recordsLinked to original sources

arXiv2026

Born-Qualified: An Autonomous Framework for Deploying Advanced Energy and Electronic Materials

Autonomous science is transforming how we discover materials and chemical systems for advanced energy technologies. However, many initially promising systems never reach deployment. This "valley of death" stems from optimization that prioritizes laboratory metrics over industrial viability. We propose a new strategy: "born-qualified" autonomous development, which embeds manufacturability, cost, and durability constraints from the outset. This approach is enabled by four pillars, including the development of multi-objective metrics, causal models, a modular infrastructure, and embedding manufacturing in the discovery loop. Realizing this vision will require sustained, community-wide commitment, but the potential return on that investment is commensurate with the scale of the challenge.

cond-mat.mtrl-sci↗

arXiv2017

Scanning tunneling spectroscopy of superconductivity on surfaces of LiTi2O4(111) thin films

Unique superconductivity at surfaces/interfaces, as exemplified by LaAlO3/SrTiO3 interfaces, and the high transition temperature in ultrathin FeSe films, have triggered intense debates on how superconductivity is affected in atomic and electronic reconstructions. The surface of superconducting cubic spinel oxide LiTi2O4 is another interesting system because its inherent surface electronic and atomic reconstructions add complexity to superconducting properties. Investigations of such surfaces are hampered by the lack of single crystals or high-quality thin films. Here, using low-temperature scanning tunneling microscopy, we report an unexpected small superconducting energy gap and a long coherence length on the surface of LiTi2O4 (111) epitaxial thin films. Furthermore, we find that a pseudogap opening at the Fermi energy modifies the surface superconductivity. Our results open an avenue, exploring anomalous superconductivity on the surface of cubic transition-metal oxides where the electronic states are spontaneously modulated with involving rich many-body interactions.

cond-mat.supr-con↗

arXiv2016

Quasiparticle interference on cubic perovskite oxide surfaces

We report the first observation of coherent surface states on cubic perovskite oxide SrVO3(001) thin films through spectroscopic imaging scanning tunneling microscopy. A direct link between the observed atomic-scale interference patterns and the formation of a dxy-derived surface state is supported by first-principles calculations. Furthermore, we show that the apical oxygens on the topmost VO2 plane play a critical role in controlling the spectral weight of the observed coherent surface state.

cond-mat.mtrl-sci↗

arXiv2012

STM Studies of Isolated Mn12-Ph Single Molecule Magnets

We study Mn12O12(C6H5COO)16(H2O)4 (Mn12-Ph) single-molecule magnets on highly ordered pyrolytic graphite (HOPG) using low temperature scanning tunneling microscopy (LT-STM) experiments. We report Mn12-Ph in isolation, resembling single molecules with metallic core atoms and organic outer ligands. The local tunneling current observed within the molecular structure shows a strong bias voltage dependency, which is distinct from that of the HOPG surface. Further, evidence of internal inhomogeneity in the local density of states has been observed with high spatial resolution, and this inhomogeneity appears to be due to localized metallic behavior. These results facilitate magneto-metric studies of single molecule magnets in isolation. As compared to bulk crystal studies, our experiments allow the specific investigation of atomic sites in the molecule.

cond-mat.mes-hall↗

arXiv2011

Atomic-scale visualization of initial growth of homoepitaxial SrTiO3 thin film on an atomically ordered substrate

The initial homoepitaxial growth of SrTiO3 on a (\surd13\times\surd13) - R33.7°SrTiO3(001) substrate surface, which can be prepared under oxide growth conditions, is atomically resolved by scanning tunneling microscopy. The identical (\surd13\times\surd13) atomic structure is clearly visualized on the deposited SrTiO3 film surface as well as on the substrate. This result indicates the transfer of the topmost Ti-rich (\surd13\times\surd13) structure to the film surface and atomic-scale coherent epitaxy at the film/substrate interface. Such atomically ordered SrTiO3 substrates can be applied to the fabrication of atom-by-atom controlled oxide epitaxial films and heterostructures.

cond-mat.mtrl-sci↗

arXiv2011

Stripe charge ordering in SrO-terminated SrTiO3(001) surfaces

The local electronic structure of the SrO-terminated SrTiO3(001) surface was explored using scanning tunneling microscopy. At low bias voltages in the empty states, a unidirectional structure with a periodicity of 3 unit cells, superimposed on a c(2 x 2) reconstructed structure, was found to develop along the crystallographic a axis. This structure indicates a charge-ordered stripe induced by carrier doping from oxygen vacancies in the SrO and the subsurface TiO2 planes. In the filled states, localized deep in-gap states were observed in addition to large energy gaps in the tunneling spectra. This result represents inelastic tunneling due to significant electron-lattice interaction associated with unidirectional lattice distortion in the SrO-terminated surface.

cond-mat.str-el↗

arXiv2010

Thickness-dependent Local Surface Electronic Structures of Homoepitaxial SrTiO3 Thin Films

We have investigated the atomically-resolved substrate and homoepitaxial thin film surfaces of SrTiO3(001) using low-temperature scanning tunneling microscopy/spectroscopy (STM/STS) combined with pulsed laser deposition (PLD). It was found that annealing at 1000 oC in an oxygen partial pressure of 1*10-6 Torr, which is a typical annealing treatment for the preparation of SrTiO3 substrates, unexpectedly resulted in a disordered surface on an atomic scale. In contrast, homoepitaxial SrTiO3 thin films grown on this disordered substrate exhibited (2*2) surface reconstructions. The differential conductance spectra, dI/dV in STS measurements, revealed a number of surface defects in a 10-unit-cell-thick SrTiO3 film, but much fewer in a 50-unit-cell-thick film. These results indicate that the defect density in the film strongly depends on the film thickness, suggesting non-uniform stoichiometry along the growth direction.

cond-mat.mtrl-sci↗

arXiv2010

Atomically Resolved Surface Structure of SrTiO3(001) Thin Films Grown in Step-Flow Mode by Pulsed Laser Deposition

The surface structure of SrTiO3(001) thin films homoepitaxially grown by PLD in step-flow mode was characterized using low temperature STM. It was found that one-dimensional (1D) TiOx-based nanostructures were formed on the thin film surface and their density increased with increasing thin film thickness. Most of the 1D nanostructures disappeared after a post-deposition annealing, indicating that this structure is metastable due to the nonequilibrium growth mode. The resulting surface after annealing exhibited similar features to that of a thinner film, having a domain structure with (2x1) and (1x2) reconstructions, but with fewer oxygen-vacancy-type defects. These results imply that the step-flow growth is likely to produce TiOx-rich surface and Ti deficiencies in the film. By the post-deposition annealing, the rich TiOx would diffuse from the surface into the film to compensate defects associated with Ti vacancies and oxygen vacancies, resulting in the stable surface structure with fewer oxygen vacancies. Thus, STM measurements can provide us with a microscopic picture of surface stoichiometry of thin films originating in the dynamics of the growth process, and can present a new approach for designing functional oxide films.

cond-mat.mtrl-sci↗