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Xinfeng Chen

Publications and source records attributed to Xinfeng Chen.

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Anomalous Transverse Response and Multi-Field Ferrialtermagnetic-Ferroelectric Valve with CrSb Flakes

Altermagnets combine the zero-stray-field of antiferromagnets with the spin polarization of ferromagnets, showing great potential for spintronic applications. Here, we propose ferrialtermagnetism as a distinct subclass of altermagnetic family, where symmetry-inequivalent altermagnetic sublattices possess nonidentical Neel vectors, preventing mutual cancellation of alternating spin splitting and conferring intrinsic robustness against perturbations. This concept is realized in the three-atomic-layer CrSb (110) flakes, which exhibits spin splitting of 344 meV, moderate uniaxial magnetic anisotropy, and high Neel temperature of 657 K. The magneto-optical Kerr and the anomalous Hall effects are observed. Integrating this ferrialtermagnetic CrSb with ferroelectric Sc2CO2 and Cu spacer, we design an ferrialtermagnetic-ferroelectric valve. This device displays equilibrium tunneling magnetoresistance and electroresistance of ~10^3%, and non-equilibrium magnitudes under bias, thermal, or light field reaches ~10^4% with high spin filtering of 90%. The negative differential resistance and photogalvanic effects, and photocurrent extinction ratio of 283.8 are achieved. These findings establish ferrialtermagnetism as a fertile platform for multi-field-controlled, ultracompact, and self-powered spintronics and electronics.

cond-mat.mtrl-sci

Two-dimensional vertically polarized Hg3AsSe4I monolayer for efficient photocatalytic water-splitting: promoting carrier separation by intrinsic electric field and Rashba effect

Efficient separation of photo-excited electron-hole pairs is essential for developing the high performance photocatalysts towards light-driven water-splitting applications. To this end, pho tocatalytic performances of two-dimensional (2D) semiconducting ferroelectric (FE) materials with out-of-plane polarizations have been extensively explored. However, out-of-plane polarizations in 2D FE materials are susceptible to the critical thickness limitation and can be easily compensated by surface adsorbates. On the other hand, 2D vertically polarized materials with stable and ir reversible out-of-plane polarizations may overcome the critical thickness limitation, enabling the practical advantage for spatial separation of photo-excited electron-hole pairs during the photo catalytic reactions. In the current work, 2D vertically polarized Hg3AsSe4I, an experimentally synthesized van der Waals (vdW) layered material, has been systematically investigated as a high performance 2D photocatalyst. Owing to its semiconducting band gap suitable for visible-light absorption, high carrier mobility, and desirable band edge alignment ideally matching water reduc tion and oxidation potentials, Hg3AsSe4I monolayer fulfills both optical and electronic prerequisites for photocatalytic water-splitting reactions. Besides the stable vertical polarization able to persist in Hg3AsSe4I monolayer, the dual mechanism for efficient separation of photo-excited carriers has also been demonstrated. Rashba spin-orbit coupling (SOC) of large strength emerges within 2D Hg3AsSe4I, splitting the band edges into spin-resolved band branches with unique spin-momentum locking characters.........

cond-mat.mtrl-sci

Nonmagnetic-magnetic Transitions in Rutile RuO2

Rutile RuO$_2$ has recently attracted great interest, as its magnetic ground state remains controversial. Experimental studies have reported either nonmagnetic (NM) or altermagnetic (AM) ground states in different crystalline samples of RuO$_2$, highlighting the need for a reasonable explanation to resolve this contradiction. In this study, density functional theory calculations are performed to reveal the correlation-sensitive and strain-dependent magnetism of bulk RuO$_2$. On one hand, multiple AM phases with different magnitudes of the spin magnetic moment are identified in the Hubbard parameter space for RuO$_2$. On the other hand, when appropriate strains that significantly change the crystal cell volume are applied, the ground state of RuO$_2$ can undergo transitions between the NM state (with no spin splitting) and the magnetic states (with spin splitting in the band structure). These findings not only demonstrate intriguing physics in 4\textit{\textit{d}}-electron-correlated RuO$_2$, but also retain its potential for spintronic applications.

cond-mat.mtrl-sci

Distinguish the Orientation of Sliding Ferroelectricity by Second-Harmonic Generation

As the emerging ferroelectric (FE) materials, the ultrathin two-dimensional (2D) sliding ferroelectrics without phase-matching bottleneck, usually exhibit the pronounced second harmonic generation (SHG) responses. Despite the structural polarity of sliding ferroelectrics can be precisely detected via SHG characterizations, distinguishing the orientations of sliding ferroelectricity based on SHG responses has rarely been realized, as SHG intensities for upward and downward polarization states are supposed to be same. In current work, combining computational simulations and experimental characterizations, the orientation of sliding ferroelectricity is demonstrated to be readily distinguishable via SHG responses in 2D SnP2S6 (SnP2Se6), a new sliding FE material. Specifically, owing to the unique symmetry operation within FE-SnP2S6 (SnP2Se6), the intersection between \c{hi}xxx and \c{hi}yyy SHG susceptibility coefficients with opposite signs leads to the effective rotation of SHG polar directions upon switching of sliding ferroelectricity. Moreover, the remarkable dependence of SHG polar directions on the orientation of sliding ferroelectricity is further validated by experimental characterizations performed on SnP2S6 crystal in a single FE domain structural form. This work opens up the avenue for in-situ detecting the ferroelectricity orientation of 2D sliding ferroelectrics based on SHG nonlinear optical responses, and also demonstrates the controllable optical nonlinearly for new "slidetronics" applications.

cond-mat.mtrl-sci

Simultaneous Motion Monitoring and Truth-In-Delivery Analysis Imaging Framework for MR-guided Radiotherapy

Intrafraction motion can play a pivotal role in the success of abdominal and thoracic radiation therapy. Hybrid magnetic resonance-guided radiotherapy systems have the potential to control for intrafraction motion. Recently, we introduced an MRI sequence capable of acquiring real-time cine imaging in two orthogonal planes (SOPI). We extend SOPI here to permit dynamic updating of slice positions in one plane while keeping the other plane position fixed. In this implementation, cine images from the static plane are used for motion monitoring and as image navigators to sort stepped images in the other plane, producing dynamic 4D image volumes for use in dose reconstruction. A custom 3D-printed target filled with radiochromic FXG gel was interfaced to a dynamic motion phantom. 4D-SOPI was acquired in a dynamic motion phantom driven by an actual patient respiratory waveform displaying amplitude/frequency variations and drifting and in a healthy volunteer. Unique 4D-MRI epochs were reconstructed from a time series of phantom motion. Dose from a static 4cmx15cm field was calculated on each 4D respiratory phase bin and epoch image, scaled by the time spent in each bin, and then rigidly accumulated. The phantom was then positioned on an Elekta MR Linac and irradiated while moving. Following irradiation, actual dose deposited to the FXG gel was determined by applying a R1 versus dose calibration curve to R1 maps of the phantom. The 4D-SOPI cine images produced a respiratory motion navigator that was highly correlated with the actual phantom motion (CC=0.9981). The mean difference between the accumulated and measured dose inside the target was 4.4% of the maximum prescribed dose. These results provide early validation that 4D-SOPI simultaneously enables real-time motion monitoring and truth-in-delivery analysis for integrated MR-guided radiation therapy (MR-gRT) systems.

physics.med-ph