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Wenchuan Jing

Publications and source records attributed to Wenchuan Jing.

6 recordsLinked to original sources

Termination-Dependent Surface States and Magnetic Fingerprints of Chiral Helimagnet Cr1/3TaS2

Chiral helimagnets based on intercalated transition-metal dichalcogenides, characterized by nano-scale spin ordering, provide a powerful route to engineer chiral spin textures (e.g. the topologically protected magnetic solitons) and emergent electronic functionality at reduced dimensions, where surface and interface states often dominate device operation. However, despite growing interest, direct experimental studies of termination-dependent surface electronic structures and their temperature-driven magnetic evolution remain largely unexplored, hindering a microscopic understanding of the electronic states that is crucial for the development of low-dimensional spintronic devices. Here, for the first time, taking Cr1/3TaS2 as a representative example, we systematically investigate the termination-dependent surface electronic states of the chiral helimagnets and uncover their distinct temperature evolution across the magnetic transition (TC~142K) by combining high-resolution ARPES with a micro-focused beam and surface-state-resolved first-principles calculations. The TaS2-terminated surface hosts folded monolayer-like TaS2 bands under the $\sqrt3\times\sqrt3$ superlattice potential and a shallow triangular electron pocket at the superlattice $\bar K$ point arising from Cr-Ta orbital hybridization. In contrast, the Cr-terminated surface exhibits reconstructed hole pockets with pronounced magnetic band splitting. This splitting disappears above TC and closely follows the chiral helimagnetic order parameter, providing a direct spectroscopic fingerprint of chiral helimagnetic order. In addition, multiple ultranarrow Cr-d-derived surface flat bands are resolved. These findings establish Cr1/3TaS2 as a model system in which surface electronic states are strongly coupled to chiral magnetism, opening new opportunities for chiral spintronic and valleytronic micro/nanodevices.

cond-mat.mtrl-sci

Altermagnetism, ARPES, symmetry, non-relativistic band splitting

Altermagnetism arises from composite real-space and spin-space symmetries, combining zero net magnetization with pronounced momentum-dependent spin splitting. This review highlights the pivotal role of angle-resolved photoemission spectroscopy (ARPES), along with its spin-resolved (SARPES) and circular-dichroism (CD-ARPES) variants, in directly visualizing nonrelativistic band splitting and spin textures in altermagnets. Within the spin-group framework, we distinguish ferromagnetic, antiferromagnetic, and altermagnetic orders and elucidate the symmetry origin of spin polarization. We then systematically review representative systems: the debated d-wave prototype RuO2, layered d-wave altermagnets KV2Se2O and Rb1-delta V2Te2O, and a series of g-wave compounds including MnTe (domain-tunable) and CrSb (topological), together with the noncoplanar antiferromagnet MnTe2 and other emerging candidate platforms. Overall, ARPES has become a key probe for resolving symmetry-driven spin splitting. Future advances in micro/nano-beam and in-situ spectroscopies, combined with strain and domain engineering, heterostructure design, and exploration of broader unconventional magnetic states, are expected to drive the joint evolution of altermagnetism and photoemission spectroscopy, paving the way for spintronic and correlated quantum research.

cond-mat.mtrl-sci

Direct Observation of Unidirectional Density Wave and Band splitting in a Single-Domain Trilayer Nickelate Pr$_4$Ni$_3$O$_{10}$

Unraveling the interplay between density-wave (DW) instabilities and multi-orbital physics is critical for understanding superconductivity in Ruddlesden-Popper nickelates, yet intrinsic electronic features have been persistently obscured by material inhomogeneity and thus the multi-domain averaging effect. Here, we employ micro-focused angle-resolved photoemission spectroscopy ($\mu$-ARPES) on single-domain Pr$_4$Ni$_3$O$_{10}$ to disentangle the complex hierarchy of intrinsic and back-folded bands, explicitly identifying the electronic states driving the DW phase transition. We provide decisive spectroscopic evidence that the low-energy reconstruction is governed by inter-orbital nesting between the $\alpha$ and $\beta$ bands. Specifically, we resolve a orbital-dependent gap of $\sim44$ meV on the $\alpha$ pocket, a value quantitatively consistent with prior measurements, unifying previously conflicting experimental reports regarding the locus and magnitude of the DW gap. Furthermore, we reveal strong orbital-selective mass renormalization in the $d_{z^2}$ states and successfully resolve the long-sought intrinsic trilayer $\beta$-band splitting, establishing a critical lower bound for the outer-layer hopping. These results define a coherent microscopic fingerprint for the trilayer nickelates, identifying the specific nesting channels and correlation effects that underpin the phase diagram.

cond-mat.supr-con

Many-body electronic structure in pyrochlore superconductor CsBi2 and spin liquid Pr2Ir2O7

The pyrochlore lattice materials can exhibit geometrical frustration, while the related many-body electronic states remain elusive. In this work, we performed scanning tunneling microscopy measurements on the pyrochlore superconductor CsBi2 and spin liquid Pr2Ir2O7 at 0.3 K. For the first time, we obtained atomically resolved images of their (111) surfaces, revealing a hexagonal lattice or a kagome lattice. Tunneling spectroscopy in CsBi2 reveals a nearly fully opened superconductivity gap. The ratio of 2{\Delta}/kBTC = 4.7 suggests relatively strong coupling superconductivity, as compared with that in kagome superconductors AV3Sb5 (A = K, Rb, Cs). In contrast to the previous study categorizing CsBi2 as a type-I superconductor, the applied magnetic field induces a hexagonal vortex lattice in which each vortex core exhibits an intriguing three-fold symmetry state. In Pr2Ir2O7, we observed a spatially homogeneous Kondo-lattice resonance, which is compared with that in the kagome Kondo-lattice material CsCr6Sb6. We further discover that the Kondo resonance exhibits a spatial modulation with three-fold symmetry, and the applied magnetic field induces a Zeeman splitting of the Kondo resonance with intriguing atomic site dependence. We discuss the relations of these many-body electronic phenomena with the pyrochlore lattice geometry and its charge or spin frustration. Our systematic observations offer atomic-scale insights into the many-body electronic structures of the geometrically frustrated pyrochlore superconductors and spin liquids.

cond-mat.str-el

Large band-splitting in $g$-wave type altermagnet CrSb

Altermagnetism (AM), a newly discovered magnetic state, ingeniously integrates the properties of ferromagnetism and antiferromagnetism, representing a significant breakthrough in the field of magnetic materials. Despite experimental verification of some typical AM materials, such as MnTe and MnTe$_2$, the pursuit of AM materials that feature larger spin splitting and higher transition temperature is still essential. Here, our research focuses on CrSb, which possesses N{é}el temperature of up to 700K and giant spin splitting near the Fermi level ($E_F$). Utilizing high-resolution angle-resolved photoemission spectroscopy and density functional theory calculations, we meticulously map the three-dimensional electronic structure of CrSb. Our photoemission spectroscopic results on both (0001) and (10$\overline{1}$0) cleavages of CrSb collaboratively reveal unprecedented details on AM-induced band splitting, and subsequently pin down its unique bulk $g$-wave symmetry through quantitative analysis of the angular and photon-energy dependence of spin splitting. Moreover, the observed spin splitting reaches the magnitude of 0.93~eV near $E_F$, the most substantial among all confirmed AM materials. This study not only validates the nature of CrSb as a prototype $g$-wave like AM material but also underscores its pivotal role in pioneering applications in spintronics.

cond-mat.mtrl-sci

Flat bands, non-trivial band topology and electronic nematicity in layered kagome-lattice RbTi$_3$Bi$_5$

Layered kagome-lattice materials with 3$d$ transition metals provide a fertile playground for studies on geometry frustration, band topology and other novel ordered states. A representative class of materials AV$_3$Sb$_5$ (A=K, Rb, Cs) have been proved to possess various unconventional phases such as superconductivity, non-trivial $\mathbb{Z}_2$ band topology, and electronic nematicity, which are intertwined with multiple interlaced charge density waves (CDW). However, the interplay among these novel states and their mechanisms are still elusive. Recently, the discovery of isostructural titanium-based single-crystals ATi$_3$Bi$_5$ (A=K, Rb, Cs), which demonstrate similar multiple exotic states but in the absence of the concomitant intertwined CDW, has been offering an ideal opportunity to disentangle these complex novel states in kagome-lattice. Here, we combine the high-resolution angle-resolved photoemission spectroscopy and first-principles calculations to systematically investigate the low-lying electronic structure of RbTi$_3$Bi$_5$. For the first time, we experimentally demonstrate the coexistence of flat bands and multiple non-trivial topological states, including type-II Dirac nodal lines and non-trivial $\mathbb{Z}_2$ topological surface states therein. Furthermore, our findings as well provide the hint of rotation symmetry breaking in RbTi$_3$Bi$_5$, suggesting the directionality of the electronic structure and possibility of emerging pure electronic nematicity in this new family of kagome compounds, which may provide important insights into the electronic nematic phase in correlated kagome metals.

cond-mat.str-el