多铁性
自旋电子学
铁电性
材料科学
异质结
凝聚态物理
磁化
插层(化学)
铁磁性
各向异性
磁各向异性
联轴节(管道)
光电子学
磁电效应
极化(电化学)
纳米技术
自发磁化
分子束外延
电荷(物理)
各向异性能量
磁场
静电学
作者
Zhongxuan Wang,Yong Hu,Zhenyao Fang,Yixiao Wang,Peng Yan,Jiayue Sun,Mario Lopez,Ryan Stadel,Yuchen Niu,Joshua M. Little,Qimin Yan,Po-Yen Chen,Cheng Gong,Joseph W. Bennett,G D Gu,Qiang Li,Zhijie Chen,Taylor J. Woehl,Efrain E. Rodriguez,Kai Liu
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-05-18
卷期号:26 (21): 6883-6890
被引量:1
标识
DOI:10.1021/acs.nanolett.6c00485
摘要
. Molecular insertion reshapes the interfacial electrostatic environment, induces charge redistribution, and expands the interlayer spacing, resulting in enhanced ferroic order, including a 5-fold increase in magnetic anisotropy energy (0.35→1.6 meV/Fe) and strengthened ferroelectric polarization. The resulting chiral CIPS-FGT heterostructures exhibit robust room-temperature magnetoelectric coupling (∼4.8% magnetization modulation) and enable helicity-dependent control of ferroic states under circularly polarized light, producing a 54.4% resistance modulation. This work establishes molecular intercalation as a general strategy for engineering light-responsive 2D multiferroics for optically tunable magnetoelectric and spintronic devices.
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