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Evaluation of ultrananocrystalline diamond size by UV Raman spectroscopy and a phonon confinement model. / Kumar, N; Panda, Kalpataru; Kozakov, A T и др.

в: Physical chemistry chemical physics : PCCP, Том 27, № 42, 29.10.2025, стр. 22746-22754.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Kumar, N, Panda, K, Kozakov, AT, Nikolskii, AV, Volodin, VA & Goryainov, SV 2025, 'Evaluation of ultrananocrystalline diamond size by UV Raman spectroscopy and a phonon confinement model', Physical chemistry chemical physics : PCCP, Том. 27, № 42, стр. 22746-22754. https://doi.org/10.1039/d5cp02967h

APA

Kumar, N., Panda, K., Kozakov, A. T., Nikolskii, A. V., Volodin, V. A., & Goryainov, S. V. (2025). Evaluation of ultrananocrystalline diamond size by UV Raman spectroscopy and a phonon confinement model. Physical chemistry chemical physics : PCCP, 27(42), 22746-22754. https://doi.org/10.1039/d5cp02967h

Vancouver

Kumar N, Panda K, Kozakov AT, Nikolskii AV, Volodin VA, Goryainov SV. Evaluation of ultrananocrystalline diamond size by UV Raman spectroscopy and a phonon confinement model. Physical chemistry chemical physics : PCCP. 2025 окт. 29;27(42):22746-22754. doi: 10.1039/d5cp02967h

Author

Kumar, N ; Panda, Kalpataru ; Kozakov, A T и др. / Evaluation of ultrananocrystalline diamond size by UV Raman spectroscopy and a phonon confinement model. в: Physical chemistry chemical physics : PCCP. 2025 ; Том 27, № 42. стр. 22746-22754.

BibTeX

@article{936bdfd116fc4ef3b2327c9b35e156da,
title = "Evaluation of ultrananocrystalline diamond size by UV Raman spectroscopy and a phonon confinement model",
abstract = "This study applied ultraviolet (UV) Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) to investigate phonon modes and chemical bonding in ultrananocrystalline diamond films. XPS analysis revealed distinct carbon hybridization states, with the ultrananocrystalline diamond film exhibiting dominant sp3 bonding and the diamond nanowire film showing reduced sp3 content alongside sp2 hybridization. The sp3-bonded T2g phonon mode, selectively probed by UV Raman spectroscopy via near-resonance enhancement, demonstrated crystallite sizes of 5.6 nm for ultrananocrystalline diamond and 2.1 nm for nanowires through characteristic phonon confinement effects. The measured dimensions showed quantitative agreement with theoretical confinement models, confirming phonon localization within nanodiamond domains. The combined results demonstrated that nanoscale carbon hybridization governs the material properties, with the XPS-derived sp3/sp2 ratios directly correlating with the Raman-measured phonon confinement effects.",
author = "N Kumar and Kalpataru Panda and Kozakov, {A T} and Nikolskii, {A V} and Volodin, {V A} and Goryainov, {S V}",
year = "2025",
month = oct,
day = "29",
doi = "10.1039/d5cp02967h",
language = "English",
volume = "27",
pages = "22746--22754",
journal = "Physical Chemistry Chemical Physics",
issn = "1463-9076",
publisher = "Royal Society of Chemistry",
number = "42",

}

RIS

TY - JOUR

T1 - Evaluation of ultrananocrystalline diamond size by UV Raman spectroscopy and a phonon confinement model

AU - Kumar, N

AU - Panda, Kalpataru

AU - Kozakov, A T

AU - Nikolskii, A V

AU - Volodin, V A

AU - Goryainov, S V

PY - 2025/10/29

Y1 - 2025/10/29

N2 - This study applied ultraviolet (UV) Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) to investigate phonon modes and chemical bonding in ultrananocrystalline diamond films. XPS analysis revealed distinct carbon hybridization states, with the ultrananocrystalline diamond film exhibiting dominant sp3 bonding and the diamond nanowire film showing reduced sp3 content alongside sp2 hybridization. The sp3-bonded T2g phonon mode, selectively probed by UV Raman spectroscopy via near-resonance enhancement, demonstrated crystallite sizes of 5.6 nm for ultrananocrystalline diamond and 2.1 nm for nanowires through characteristic phonon confinement effects. The measured dimensions showed quantitative agreement with theoretical confinement models, confirming phonon localization within nanodiamond domains. The combined results demonstrated that nanoscale carbon hybridization governs the material properties, with the XPS-derived sp3/sp2 ratios directly correlating with the Raman-measured phonon confinement effects.

AB - This study applied ultraviolet (UV) Raman spectroscopy and X-ray photoelectron spectroscopy (XPS) to investigate phonon modes and chemical bonding in ultrananocrystalline diamond films. XPS analysis revealed distinct carbon hybridization states, with the ultrananocrystalline diamond film exhibiting dominant sp3 bonding and the diamond nanowire film showing reduced sp3 content alongside sp2 hybridization. The sp3-bonded T2g phonon mode, selectively probed by UV Raman spectroscopy via near-resonance enhancement, demonstrated crystallite sizes of 5.6 nm for ultrananocrystalline diamond and 2.1 nm for nanowires through characteristic phonon confinement effects. The measured dimensions showed quantitative agreement with theoretical confinement models, confirming phonon localization within nanodiamond domains. The combined results demonstrated that nanoscale carbon hybridization governs the material properties, with the XPS-derived sp3/sp2 ratios directly correlating with the Raman-measured phonon confinement effects.

UR - https://pubmed.ncbi.nlm.nih.gov/41089059/

U2 - 10.1039/d5cp02967h

DO - 10.1039/d5cp02967h

M3 - Article

C2 - 41089059

VL - 27

SP - 22746

EP - 22754

JO - Physical Chemistry Chemical Physics

JF - Physical Chemistry Chemical Physics

SN - 1463-9076

IS - 42

ER -

ID: 71470954