单层
各向异性
材料科学
光电子学
扫描隧道显微镜
半导体
极化(电化学)
微晶
石墨烯
Crystal(编程语言)
分子物理学
结晶学
光学
化学物理
化学
纳米技术
物理
物理化学
冶金
程序设计语言
计算机科学
作者
Tomojit Chowdhury,Fauzia Mujid,Zehra Naqvi,Ariana Ray,Ce Liang,David A. Muller,Nathan P. Guisinger,Jiwoong Park
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-03-25
卷期号:25 (14): 5852-5859
被引量:3
标识
DOI:10.1021/acs.nanolett.5c00731
摘要
Controlling the spectral and polarization response of two-dimensional (2D) crystals is vital for developing ultrathin platforms for compact optoelectronic devices. However, independently tuning optical anisotropy and spectral response remains challenging in conventional semiconductors due to the intertwined nature of their lattice and electronic structures. Here, we report spectra-orthogonal optical anisotropy─where polarization anisotropy is tuned independently of spectral response─in wafer-scale, one-atom-thick 2D molecular crystal (2DMC) monolayers synthesized on monolayer transition-metal dichalcogenide (TMD) crystals. Utilizing the concomitant spectral consistency and structural tunability of perylene derivatives, we demonstrate tunable optical polarization anisotropy in 2DMCs with similar spectral profiles, as confirmed by room-temperature scanning tunneling microscopy and cross-polarized reflectance microscopy. Additional angle-dependent analysis of the single-crystal and polycrystalline molecular domains reveals an epitaxial relationship between the 2DMC and TMD. Our results establish a scalable, molecule-based 2D crystalline platform for unique and tunable functionalities unattainable in covalent 2D solids.
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