Near- and Deep-Ultraviolet Resonance Raman Spectroscopy of Pyrazine-Al-4 Complex and Al-3-Pyrazine-Al-3 Junction
(2009) In Journal of Physical Chemistry C 113(44). p.19328-19334- Abstract
- Near- and deep-ultraviolet (UV) resonance Raman spectroscopy of pyrazine-Al-4 complex and Al-3-pyrazine-Al-3 junction was investigated theoretically with a quantum chemical method. Here, 325 and 244 nm were employed as near- and deep-UV sources in our theoretical study The intensities of static normal Raman spectra of pyrazine-Al-4 complex and Al-3-pyrazine-Al-3 junction were enhanced oil the orders of 10 and 10(3) by a static chemical mechanism, respectively The calculated absorption spectra reveal strong B-6(2) and B-13(2u) electronic transitions near 325 nm for pyrazine-Al-4 complex and 244 nm for Al-3-pyrazine-Al-3 junction, respectively. The analyses of orbital transitions in electronic transitions reveal they are the mixture of... (More)
- Near- and deep-ultraviolet (UV) resonance Raman spectroscopy of pyrazine-Al-4 complex and Al-3-pyrazine-Al-3 junction was investigated theoretically with a quantum chemical method. Here, 325 and 244 nm were employed as near- and deep-UV sources in our theoretical study The intensities of static normal Raman spectra of pyrazine-Al-4 complex and Al-3-pyrazine-Al-3 junction were enhanced oil the orders of 10 and 10(3) by a static chemical mechanism, respectively The calculated absorption spectra reveal strong B-6(2) and B-13(2u) electronic transitions near 325 nm for pyrazine-Al-4 complex and 244 nm for Al-3-pyrazine-Al-3 junction, respectively. The analyses of orbital transitions in electronic transitions reveal they are the mixture of (metal to molecule) charge transfer excitation and intracluster excitation. The intensity of near-UV resonance Raman spectroscopy of pyrazine-Al-4 complex and the intensity of deep-UV resonance Raman spectroscopy of Al-3-pyrazine-Al-3 junction are strongly enhanced on the order of 10(5) and 10(4), respectively, compared to the Raman intensity of isolated pyrazine excited at 325 and 244 nm. The calculations of Mic theory and the three-dimensional finite-difference time domain method reveal strong surface plasmon resonance and strong electromagnetic enhancements at 325 and 244 nm for single and dimer nanoparticles at suitable sizes and gap distance, respectively. The strongest SERS enhancement in the system of junction is on the order of 10(8) at the incident lights of 325 and 244 nm. The total enhancements, including the chemical and electromagnetic enhancements, can reach Lip to 10(13). So, Al is a suitable material for near- and deep-UV surface-enhanced resonance Raman scattering (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/1505379
- author
- Sun, Mengtao ; Zhang, Shunping ; Fang, Yurui ; Yang, Zhilin ; Wu, Deyin ; Dong, Bin and Xu, Hongxing LU
- organization
- publishing date
- 2009
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Journal of Physical Chemistry C
- volume
- 113
- issue
- 44
- pages
- 19328 - 19334
- publisher
- The American Chemical Society (ACS)
- external identifiers
-
- wos:000271105500051
- scopus:70449558796
- ISSN
- 1932-7447
- DOI
- 10.1021/jp908107u
- language
- English
- LU publication?
- yes
- id
- bbad7736-a82c-4fa1-8bfe-9b534cbbfb3a (old id 1505379)
- date added to LUP
- 2016-04-01 12:21:46
- date last changed
- 2022-01-27 02:43:07
@article{bbad7736-a82c-4fa1-8bfe-9b534cbbfb3a,
abstract = {{Near- and deep-ultraviolet (UV) resonance Raman spectroscopy of pyrazine-Al-4 complex and Al-3-pyrazine-Al-3 junction was investigated theoretically with a quantum chemical method. Here, 325 and 244 nm were employed as near- and deep-UV sources in our theoretical study The intensities of static normal Raman spectra of pyrazine-Al-4 complex and Al-3-pyrazine-Al-3 junction were enhanced oil the orders of 10 and 10(3) by a static chemical mechanism, respectively The calculated absorption spectra reveal strong B-6(2) and B-13(2u) electronic transitions near 325 nm for pyrazine-Al-4 complex and 244 nm for Al-3-pyrazine-Al-3 junction, respectively. The analyses of orbital transitions in electronic transitions reveal they are the mixture of (metal to molecule) charge transfer excitation and intracluster excitation. The intensity of near-UV resonance Raman spectroscopy of pyrazine-Al-4 complex and the intensity of deep-UV resonance Raman spectroscopy of Al-3-pyrazine-Al-3 junction are strongly enhanced on the order of 10(5) and 10(4), respectively, compared to the Raman intensity of isolated pyrazine excited at 325 and 244 nm. The calculations of Mic theory and the three-dimensional finite-difference time domain method reveal strong surface plasmon resonance and strong electromagnetic enhancements at 325 and 244 nm for single and dimer nanoparticles at suitable sizes and gap distance, respectively. The strongest SERS enhancement in the system of junction is on the order of 10(8) at the incident lights of 325 and 244 nm. The total enhancements, including the chemical and electromagnetic enhancements, can reach Lip to 10(13). So, Al is a suitable material for near- and deep-UV surface-enhanced resonance Raman scattering}},
author = {{Sun, Mengtao and Zhang, Shunping and Fang, Yurui and Yang, Zhilin and Wu, Deyin and Dong, Bin and Xu, Hongxing}},
issn = {{1932-7447}},
language = {{eng}},
number = {{44}},
pages = {{19328--19334}},
publisher = {{The American Chemical Society (ACS)}},
series = {{Journal of Physical Chemistry C}},
title = {{Near- and Deep-Ultraviolet Resonance Raman Spectroscopy of Pyrazine-Al-4 Complex and Al-3-Pyrazine-Al-3 Junction}},
url = {{http://dx.doi.org/10.1021/jp908107u}},
doi = {{10.1021/jp908107u}},
volume = {{113}},
year = {{2009}},
}