电磁辐射
密度泛函理论
消散
熵(时间箭头)
非线性系统
材料科学
物理
自旋工程
凝聚态物理
自旋极化
量子力学
电子
作者
N. L. Wang,Xin Kou,Lihua Zhong,Gui-Jun Zeng,Amjad Farid,Xue Zhou,Qianfeng Wang,Ding Xi,Gehong Su,Hui Huang,Yongpeng Zhao
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2025-10-10
卷期号:11 (41)
标识
DOI:10.1126/sciadv.adz2218
摘要
Chiral electromagnetic materials, with their unique spatial configurations, can regulate the propagation and polarization of electromagnetic waves, serving as powerful tools for tailoring electromagnetic behavior. However, their functional potential is often limited by the intrinsic constraints of conventional host materials, which typically lack sufficient flexibility in defect engineering, magnetic modulation, and spin-orbit coupling (SOC) enhancement. To address this challenge, we introduce high-entropy metal oxides (HEMOs) into carbon-based chiral frameworks, constructing HEMO and carbon nanocoil (HEMO@CNC) composites. By combining advanced microscopy, electromagnetic measurements, and density functional theory (DFT) calculations, it is revealed that increasing entropy and helical strain jointly induce nonlinear changes in SOC strength and defect-related localized states. Benefiting from these effects, the HEMO@CNC system achieves an ultrawide bandwidth, outperforming linear structures and low-entropy systems. This work provides a potential paradigm for integrating topological defect engineering and high-entropy quantum modulation, offering deeper insights into advancing electromagnetic functional materials from macroscopic design toward geometry-defect-spin synergistic regulation.
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