TY - JOUR
T1 - Nontrivial Raman Characteristics in 2D Non-Van der Waals Mo5N6
AU - Yao, Ching Hsiang
AU - Gao, Hongze
AU - Ping, Lu
AU - Gulo, Desman Perdamaian
AU - Liu, Hsiang Lin
AU - Tuan Hung, Nguyen
AU - Saito, Riichiro
AU - Ling, Xi
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/11/26
Y1 - 2024/11/26
N2 - Resonant Raman spectra of a two-dimensional (2D) non-van der Waals (vdW) material, molybdenum nitride (Mo5N6), are measured across varying thicknesses, ranging from a few to tens of nanometers. Fifteen distinct Raman peaks are observed experimentally, and their assignments are made using first-principles calculations for the most stable AABB-stacking structure of Mo5N6. The assignments are further supported by angular-dependent Raman measurements for all peaks, except the most intense one at 215 cm-1. Calculations reveal that the 215 cm-1 peak does not appear for three-dimensional molybdenum nitrides and is not a first-order Raman-active mode. We further investigated the origin of the 215 cm-1 peak and assigned it as a defect-induced double-resonance peak. Moreover, thickness-dependent Raman measurements reveal that both the 215 and 540 cm-1 peaks─assigned to out-of-plane and in-plane modes, respectively─blue shift as thickness increases, reaching a plateau around 20 nm. This thickness-dependent Raman shift over a wide thickness range is nontrivial compared to other common vdW 2D materials and is attributed to the much stronger stacking interaction between the constituent layers in non-vdW materials. This finding highlights Raman spectroscopy as a valuable tool for characterizing the thickness of 2D non-vdW materials.
AB - Resonant Raman spectra of a two-dimensional (2D) non-van der Waals (vdW) material, molybdenum nitride (Mo5N6), are measured across varying thicknesses, ranging from a few to tens of nanometers. Fifteen distinct Raman peaks are observed experimentally, and their assignments are made using first-principles calculations for the most stable AABB-stacking structure of Mo5N6. The assignments are further supported by angular-dependent Raman measurements for all peaks, except the most intense one at 215 cm-1. Calculations reveal that the 215 cm-1 peak does not appear for three-dimensional molybdenum nitrides and is not a first-order Raman-active mode. We further investigated the origin of the 215 cm-1 peak and assigned it as a defect-induced double-resonance peak. Moreover, thickness-dependent Raman measurements reveal that both the 215 and 540 cm-1 peaks─assigned to out-of-plane and in-plane modes, respectively─blue shift as thickness increases, reaching a plateau around 20 nm. This thickness-dependent Raman shift over a wide thickness range is nontrivial compared to other common vdW 2D materials and is attributed to the much stronger stacking interaction between the constituent layers in non-vdW materials. This finding highlights Raman spectroscopy as a valuable tool for characterizing the thickness of 2D non-vdW materials.
KW - Brite-Wigner-Fano (BWF)
KW - defect-induced peak
KW - metal nitrides
KW - resonant Raman
KW - thickness dependence
KW - two-dimensional materials
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U2 - 10.1021/acsnano.4c06250
DO - 10.1021/acsnano.4c06250
M3 - Article
C2 - 39531421
AN - SCOPUS:85209077929
SN - 1936-0851
VL - 18
SP - 32458
EP - 32467
JO - ACS Nano
JF - ACS Nano
IS - 47
ER -