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Tieqiong Zhang

Publications and source records attributed to Tieqiong Zhang.

2 recordsLinked to original sources

Observation of mirror-odd and mirror-even spin texture in ultrathin epitaxially strained RuO2 films

Recently, rutile ruthenium dioxide (RuO$_2$) has attracted renewed interest due to expectations of prominent altermagnetic spin splitting. However, accumulating experimental evidence suggests that, in its bulk and thick-film forms, RuO$_2$ does not display any form of magnetic ordering. Despite this, the spin structure of RuO$_2$ remains largely unexplored in the ultrathin limit, where substrate-imposed epitaxial strain can be substantial. Here, we use spin-resolved angle-resolved photoemission spectroscopy, supported by ab initio calculations, to reveal the electronic structure of 2-nanometer-thick epitaxial RuO$_2$ heterostructures. We observe an unconventional spin texture characterized by the coexistence of mirror-even and mirror-odd momentum-dependent components. A comprehensive symmetry analysis rules out nonmagnetic origins of this spin texture. These findings suggest an emergent nonrelativistic spin structure enabled by epitaxial strain in the ultrathin limit, marking a distinct departure from the behavior of relaxed or bulk RuO$_2$. Our work opens previously unexplored perspectives for exploring symmetry-breaking mechanisms and spin textures in oxide heterostructures.

cond-mat.mtrl-sci↗

Martensitic-like transition between liquid crystalline and crystalline phases of prototypical discotic organic semiconductor

Phase transitions between crystalline solids occur either through the nucleation and growth mechanism, a process that is slow and destructive or through the diffusion-less and order preserving Martensitic route. In both organic and inorganic materials, Martensitic transformations are known to occur only between phases with crystalline symmetry. We demonstrate here that for canonical discotic organic semiconductor HAT6, the transition between the liquid crystalline columnar hexagonal phase (ColH) and the crystalline solid can occur through a mechanism that exhibits the hallmarks of Martensitic transformations: orientational correlations between parent and daughter phases, structural reversibility, and ultrafast kinetics. To access Martensitic-like solidification, the ColH phase of HAT6 is biaxially aligned in lithographically defined microchannels and crystallization is induced on deep supercooling. The transition mechanism is studied using a combination of polarized optical microscopy and X-ray scattering. At the largest accessible supercooling, the ColH - Crystal phase transition occurs at speeds of ~100 micrometer/s, a value that is seven orders of magnitude greater than the theoretical prediction for growth from isotropic melts. Our work suggests that Martensitic-like transformations can occur even between liquid crystals and crystals and are therefore more general than previously believed. Further, our work demonstrates that Martensitic-like transformations of anchored liquid crystals can be used to grow biaxially aligned crystals of organic molecules over arbitrarily long distances. As lattice alignment over large areas is desirable for devices like field-effect transistors and as several high-performance molecular semiconductors exhibit a ColH phase, our results hold general significance for organic electronics.

cond-mat.mtrl-sci↗