Xiaoye Chen
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Xiaoye Chen has a total of 60 co-authors. Here are the top co-authors by number of shared publications:
- Anjan Soumyanarayanan
Institute of Materials Research & Engineering, Agency for Science, Technology & Research (A*STAR), Singapore, Singapore
5 shared publications - Hang Khume Tan
Institute of Materials Research and Engineering (IMRE)
4 shared publications - Jian Feng Kong
Institute of High Performance Computing
2 shared publications - T. S. Suraj
National University of Singapore
2 shared publications A. S. Padgett
Department of Physics, University of Florida, Gainesville, Florida 32611, USA
1 shared publicationAbhijit Ghosh
Institute of Materials Research and Engineering, Agency for Science, Technology and Research Singapore Singapore
1 shared publication
Latest Publications
- Open Access
- 4 March 2026
- Published by Wiley in Advanced Materials
- Vol. 38 (18) , e21980
Analog Control of Reconfigurable GHz Resonances from Chiral Spin Texture Ensembles
Gigahertz excitations of magnetic films are widely explored for energy‐efficient, high‐frequency microelectronics. The advent of nanoscale chiral spin textures (CSTs) with topological dynamics promises novel resonance characteristics. However, prior works on technologically relevant chiral multilayers encountered key material constraints, precluding the realization of functional CST resonances. We address this by engineering a minimally damped, strongly chiral multilayer with a robust broadband resonance spectrum. Microwave spectroscopy, Lorentz microscopy, and simulations elucidate contrasting resonance features on either side of zero magnetic field arising from distinct irreversible CST transitions. A simple analytical model can quantitatively describe these robust inter‐textural resonances over the entire field‐frequency range. Crucially, in situ CST reconfigurability enables analog tunability of the resonant dispersion ‐ with wide‐band, deterministic, non‐linear (or linear) modulation via the input knob. Our work unlocks the microwave potential of multilayer CSTs by leveraging their unique thermodynamics. It opens the door to fabrication‐free reconfigurable magnonics, toward broadband transmission and unconventional computing.
- 4 March 2026
- Published by Wiley in Advanced Materials
- Vol. 38 (18) , e21980
Open AccessAnalog Control of Reconfigurable GHz Resonances from Chiral Spin Texture Ensembles
Gigahertz excitations of magnetic films are widely explored for energy‐efficient, high‐frequency microelectronics. The advent of nanoscale chiral spin textures (CSTs) with topological dynamics promises novel resonance characteristics. However, prior works on technologically relevant chiral multilayers encountered key material constraints, precluding the realization of functional CST resonances. We address this by engineering a minimally damped, strongly chiral multilayer with a robust broadband resonance spectrum. Microwave spectroscopy, Lorentz microscopy, and simulations elucidate contrasting resonance features on either side of zero magnetic field arising from distinct irreversible CST transitions. A simple analytical model can quantitatively describe these robust inter‐textural resonances over the entire field‐frequency range. Crucially, in situ CST reconfigurability enables analog tunability of the resonant dispersion ‐ with wide‐band, deterministic, non‐linear (or linear) modulation via the input knob. Our work unlocks the microwave potential of multilayer CSTs by leveraging their unique thermodynamics. It opens the door to fabrication‐free reconfigurable magnonics, toward broadband transmission and unconventional computing.
- 29 December 2023
- Published by American Chemical Society (ACS) in ACS Applied Materials & Interfaces
- Vol. 16 (1) , 1025-1032
Quantifying the Magnetic Interactions Governing Chiral Spin Textures Using Deep Neural Networks
The interplay of magnetic interactions in chiral multilayer films gives rise to nanoscale topological spin textures that form attractive elements for next-generation computing. Quantifying these interactions requires several specialized, time-consuming, and resource-intensive experimental techniques. Imaging of ambient domain configurations presents a promising avenue for high-throughput extraction of parent magnetic interactions. Here, we present a machine learning (ML)-based approach to simultaneously determine the key magnetic interactions-symmetric exchange, chiral exchange, and anisotropy-governing the chiral domain phenomenology in multilayers, using a single binarized image of domain configurations. Our convolutional neural network model, trained and validated on over 10,000 domain images, achieved R-2 > 0.85 in predicting the parameters and independently learned the physical interdependencies between magnetic parameters. When applied to microscopy data acquired across samples, our model-predicted parameter trends are consistent with those of independent experimental measurements. These results establish ML-driven techniques as valuable, high-throughput complements to conventional determination of magnetic interactions and serve to accelerate materials and device development for nanoscale electronics.
- 29 December 2023
- Published by American Chemical Society (ACS) in ACS Applied Materials & Interfaces
- Vol. 16 (1) , 1025-1032
Quantifying the Magnetic Interactions Governing Chiral Spin Textures Using Deep Neural Networks
The interplay of magnetic interactions in chiral multilayer films gives rise to nanoscale topological spin textures that form attractive elements for next-generation computing. Quantifying these interactions requires several specialized, time-consuming, and resource-intensive experimental techniques. Imaging of ambient domain configurations presents a promising avenue for high-throughput extraction of parent magnetic interactions. Here, we present a machine learning (ML)-based approach to simultaneously determine the key magnetic interactions-symmetric exchange, chiral exchange, and anisotropy-governing the chiral domain phenomenology in multilayers, using a single binarized image of domain configurations. Our convolutional neural network model, trained and validated on over 10,000 domain images, achieved R-2 > 0.85 in predicting the parameters and independently learned the physical interdependencies between magnetic parameters. When applied to microscopy data acquired across samples, our model-predicted parameter trends are consistent with those of independent experimental measurements. These results establish ML-driven techniques as valuable, high-throughput complements to conventional determination of magnetic interactions and serve to accelerate materials and device development for nanoscale electronics.
- 8 March 2023
- Published by American Physical Society (APS) in Physical Review B
- Vol. 107 (9) , 094405
Quantifying symmetric exchange in ultrathin ferromagnetic films with chirality
The symmetric (Heisenberg) exchange interaction is fundamental to magnetism and assumes critical importance in designing magnetic materials for novel emergent phenomena and device applications. However, quantifying exchange is extremely challenging for ultrathin magnetic films, as techniques and approximations reliably used for bulk materials are largely inapplicable in the two-dimensional limit. Here we present and contrast the measurement of exchange stiffness by several methods on a series of five Co/Pt-based ultrathin ( nm) films. We compare results from (a) spin-wave spectroscopy by Brillouin light scattering, (b) three analytical models describing the temperature dependence of magnetization obtained by magnetometry, (c) microscopic domain periodicity measurements and simulations, and (d) ab initio density functional theory calculations. While different methods present some qualitatively consistent trends across samples, we note, for any given sample, considerable differences (up to in the absolute values of across the techniques, consistent with discrepancies of reported in literature for nominally similar samples. We analyze possible sources of the discrepancies across various methods, notably including their relationship to the spin-wave dispersion, and the wave-vector ranges probed. We compare the strengths and limitations of the techniques, and outline directions for their future use in characterizing exchange interactions in ultrathin films.- 8 March 2023
- Published by American Physical Society (APS) in Physical Review B
- Vol. 107 (9) , 094405
Quantifying symmetric exchange in ultrathin ferromagnetic films with chirality
The symmetric (Heisenberg) exchange interaction is fundamental to magnetism and assumes critical importance in designing magnetic materials for novel emergent phenomena and device applications. However, quantifying exchange is extremely challenging for ultrathin magnetic films, as techniques and approximations reliably used for bulk materials are largely inapplicable in the two-dimensional limit. Here we present and contrast the measurement of exchange stiffness by several methods on a series of five Co/Pt-based ultrathin ( nm) films. We compare results from (a) spin-wave spectroscopy by Brillouin light scattering, (b) three analytical models describing the temperature dependence of magnetization obtained by magnetometry, (c) microscopic domain periodicity measurements and simulations, and (d) ab initio density functional theory calculations. While different methods present some qualitatively consistent trends across samples, we note, for any given sample, considerable differences (up to in the absolute values of across the techniques, consistent with discrepancies of reported in literature for nominally similar samples. We analyze possible sources of the discrepancies across various methods, notably including their relationship to the spin-wave dispersion, and the wave-vector ranges probed. We compare the strengths and limitations of the techniques, and outline directions for their future use in characterizing exchange interactions in ultrathin films.- 20 April 2022
- Published by American Physical Society (APS) in Physical Review Applied
- Vol. 17 (4) , 044039
Thermal Evolution of Skyrmion Formation Mechanism in Chiral Multilayer Films
Magnetic skyrmions form in chiral multilayers from the shrinking or fission of elongated stripe textures. Here we report an experimental and theoretical study of the temperature dependence of this stripe-to-skyrmion transition in /-based multilayers. Field-reversal magnetometry and Lorentz microscopy experiments over 100–350 K establish the increased efficacy of stripe-to-skyrmion fission at higher temperatures—driven primarily by the thermal evolution of key magnetic interactions—which enhances the resulting skyrmion density. Atomistic calculations elucidate that the energy barrier to fission governs the thermodynamics of skyrmion formation. Our results establish a mechanistic picture of the stripe-to-skyrmion transition and advance the use of thermal knobs for efficient skyrmion generation.- 20 April 2022
- Published by American Physical Society (APS) in Physical Review Applied
- Vol. 17 (4) , 044039
Thermal Evolution of Skyrmion Formation Mechanism in Chiral Multilayer Films
Magnetic skyrmions form in chiral multilayers from the shrinking or fission of elongated stripe textures. Here we report an experimental and theoretical study of the temperature dependence of this stripe-to-skyrmion transition in /-based multilayers. Field-reversal magnetometry and Lorentz microscopy experiments over 100–350 K establish the increased efficacy of stripe-to-skyrmion fission at higher temperatures—driven primarily by the thermal evolution of key magnetic interactions—which enhances the resulting skyrmion density. Atomistic calculations elucidate that the energy barrier to fission governs the thermodynamics of skyrmion formation. Our results establish a mechanistic picture of the stripe-to-skyrmion transition and advance the use of thermal knobs for efficient skyrmion generation.- 30 November 2020
- Published by American Physical Society (APS) in Physical Review Materials
- Vol. 4 (11) , 114419
Skyrmion generation from irreversible fission of stripes in chiral multilayer films
Competing interactions produce finite-size textures in myriad condensed matter systems, typically forming elongated stripe or round bubble domains. Transitions between stripe and bubble phases, driven by field or temperature, are expected to be reversible in nature. Here we report on the distinct character of the analogous transition for nanoscale spin textures in chiral Co/Pt-based multilayer films, known to host Néel skyrmions, using microscopy, magnetometry, and micromagnetic simulations. Upon increasing field, individual stripes fission into multiple skyrmions, and this transition exhibits a macroscopic signature of irreversibility. Crucially, upon field reversal, the skyrmions do not fuse back into stripes, with many skyrmions retaining their morphology down to zero field. Both the macroscopic irreversibility and the microscopic zero-field skyrmion density are governed by the thermodynamic material parameter determining chiral domain stability. These results establish the thermodynamic and microscopic framework underlying ambient skyrmion generation and stability in chiral multilayer films and provide immediate directions for their functionalization in devices.
- 30 November 2020
- Published by American Physical Society (APS) in Physical Review Materials
- Vol. 4 (11) , 114419
Skyrmion generation from irreversible fission of stripes in chiral multilayer films
Competing interactions produce finite-size textures in myriad condensed matter systems, typically forming elongated stripe or round bubble domains. Transitions between stripe and bubble phases, driven by field or temperature, are expected to be reversible in nature. Here we report on the distinct character of the analogous transition for nanoscale spin textures in chiral Co/Pt-based multilayer films, known to host Néel skyrmions, using microscopy, magnetometry, and micromagnetic simulations. Upon increasing field, individual stripes fission into multiple skyrmions, and this transition exhibits a macroscopic signature of irreversibility. Crucially, upon field reversal, the skyrmions do not fuse back into stripes, with many skyrmions retaining their morphology down to zero field. Both the macroscopic irreversibility and the microscopic zero-field skyrmion density are governed by the thermodynamic material parameter determining chiral domain stability. These results establish the thermodynamic and microscopic framework underlying ambient skyrmion generation and stability in chiral multilayer films and provide immediate directions for their functionalization in devices.
- 3 August 2020
- Published by American Physical Society (APS) in Physical Review B
- Vol. 102 (8) , 081102
Strong in-plane anisotropy in the electronic structure of fixed-valenceThe origin of intrinsic quantum criticality in the heavy-fermion superconductor has been attributed to strong Yb valence fluctuations and its peculiar crystal structure. Here, we assess these contributions individually by studying the isostructural but fixed-valence compound . Quantum oscillation measurements and density functional theory calculations reveal a Fermi surface in markedly different from that of , consistent with a “large” Fermi surface in the latter. We also find an unexpected in-plane anisotropy of the electronic structure, in contrast to the isotropic Kondo hybridization in .- 3 August 2020
- Published by American Physical Society (APS) in Physical Review B
- Vol. 102 (8) , 081102
Strong in-plane anisotropy in the electronic structure of fixed-valenceThe origin of intrinsic quantum criticality in the heavy-fermion superconductor has been attributed to strong Yb valence fluctuations and its peculiar crystal structure. Here, we assess these contributions individually by studying the isostructural but fixed-valence compound . Quantum oscillation measurements and density functional theory calculations reveal a Fermi surface in markedly different from that of , consistent with a “large” Fermi surface in the latter. We also find an unexpected in-plane anisotropy of the electronic structure, in contrast to the isotropic Kondo hybridization in .- 23 October 2017
- Published by Springer Nature in Nature Physics
- Vol. 14 (2) , 166-172
Fermi surface in the absence of a Fermi liquid in the Kondo insulator SmB6
- 23 October 2017
- Published by Springer Nature in Nature Physics
- Vol. 14 (2) , 166-172
Fermi surface in the absence of a Fermi liquid in the Kondo insulator SmB6