TY - JOUR
T1 - Atomically Precise Bottom-Up Fabrication of Ultra-Narrow Semiconducting Zigzag BiP Nanoribbons
AU - Zhou, Dechun
AU - Feng, Yisui
AU - Zhang, Lei
AU - Gao, Wenjin
AU - Li, Heping
AU - Li, Hui
AU - Zhou, Miao
AU - Niu, Tianchao
N1 - Publisher Copyright:
© 2024 Wiley-VCH GmbH.
PY - 2024/9/4
Y1 - 2024/9/4
N2 - 1D semiconductors with atomically precise edge and well-controlled width hold significant promise as channel materials for next-generation electronics. Here a method to fabricate the narrowest zigzag-edged bismuth phosphide (BiP) nanoribbons (NRs) is presented, achieving widths of three atoms (≈0.7 nm), through molecular beam epitaxy on bismuthene in a wide P coverage range. Using scanning tunneling microscopy and first-principles calculations, it is revealed that these BiP NRs exhibit a blue-phosphorene-like structure, with a theoretical bandgap of 0.38 eV. Notably, first-principles calculations reveal spin-polarized states located on the zigzag edges, presenting an option for spintronics applications. Formation of these uniform BiP NRs is attributed to tensile strain from lattice-registry confinement. During epitaxial growth, P clusters act dually as feedstock and catalysts, suggesting a self-catalyzed growth mechanism. The bottom-up strategy offers an effective approach for the atomically precise fabrication of 1D BiP NRs, paving the way for the creation of diverse low-dimensional binary materials with tailored chemical and electronic properties, facilitated by selecting suitable elemental 2D materials as substrates.
AB - 1D semiconductors with atomically precise edge and well-controlled width hold significant promise as channel materials for next-generation electronics. Here a method to fabricate the narrowest zigzag-edged bismuth phosphide (BiP) nanoribbons (NRs) is presented, achieving widths of three atoms (≈0.7 nm), through molecular beam epitaxy on bismuthene in a wide P coverage range. Using scanning tunneling microscopy and first-principles calculations, it is revealed that these BiP NRs exhibit a blue-phosphorene-like structure, with a theoretical bandgap of 0.38 eV. Notably, first-principles calculations reveal spin-polarized states located on the zigzag edges, presenting an option for spintronics applications. Formation of these uniform BiP NRs is attributed to tensile strain from lattice-registry confinement. During epitaxial growth, P clusters act dually as feedstock and catalysts, suggesting a self-catalyzed growth mechanism. The bottom-up strategy offers an effective approach for the atomically precise fabrication of 1D BiP NRs, paving the way for the creation of diverse low-dimensional binary materials with tailored chemical and electronic properties, facilitated by selecting suitable elemental 2D materials as substrates.
KW - density functional theory
KW - molecular beam epitaxy
KW - scanning tunneling microscopy
KW - spin-polarization
KW - zigzag edge
UR - https://www.scopus.com/pages/publications/85189912558
U2 - 10.1002/adfm.202401347
DO - 10.1002/adfm.202401347
M3 - 文章
AN - SCOPUS:85189912558
SN - 1616-301X
VL - 34
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 36
M1 - 2401347
ER -