Temperature dependence of vibrational modes of CH3-C≡C(ads) and I(ads) coadsorbed on Ag(111): Ab initio molecular dynamics approach

doi:10.1002/jcc.22958

淡江大學機構典藏 > 理學院 > 化學學系暨研究所 > 期刊論文 > Item 987654321/76986

請使用永久網址來引用或連結此文件: https://tkuir.lib.tku.edu.tw/dspace/handle/987654321/76986

題名:	Temperature dependence of vibrational modes of CH3-C≡C(ads) and I(ads) coadsorbed on Ag(111): Ab initio molecular dynamics approach
作者:	Lin, Jyh Shing;Lu, Shao-Yu;Tseng, Po-Jung;Chou, Wen-Chi
貢獻者:	淡江大學化學學系
關鍵詞:	ab initio molecular dynamics;autocorrelation function;Ag(111) surface;vibrational modes;Fourier transform;Alkyne coupling
日期:	2012-05
上傳時間:	2012-05-23 14:33:43 (UTC+8)
出版者:	Hoboken: John Wiley & Sons, Inc.
摘要:	Ab initio molecular dynamics (AIMD) simulations accompanied by a Fourier transform of the dipole moment (aligned perpendicular to the surface) autocorrelation function (FT-DMAF) are implemented to investigate the temperature-dependent infrared (IR) active vibrational modes of CH3-C(β)≡C(α)(ads) and I(ads) when coadsorbed on an Ag(111) surface at 200 K and 400 K, respectively. The analytic scheme of the Fourier transform of a structural coordinate autocorrelation function (FT-SCAF) is used to identify two distinguishable IR active peaks of C(β)≡C(α) stretching, which are characterised by two types of dynamic motion of adsorbed CH3-C(β)≡C(α)(ads) at 200K, namely, the motion of the tilted -C-C(β)≡C(α)- axis and the motion of the stand-up -C-C(β)≡C(α)- axis. These two recognisable IR active peaks of C(β)≡C(α) stretching are gradually merged into one peak as a result of the dominant motion of the stand-up -C-C(β)≡C(α)- axis as the temperature increases from 200 K to 400 K. The calculated intensities of the IR active peaks of the asymmetrical deformation mode of CH3 and the asymmetrical stretching mode of CH3, with their dynamic dipole moments nearly perpendicular to the -C-C(β)≡C(α)- axis, become relatively weak; however, the symmetrical deformation mode of CH3 and the symmetrical stretching mode of CH3, with their dynamic dipole moments randomly directed away from the -C-C(β)≡C(α)- axis, will not have direct correspondence between the intensities of their IR active peaks and the angle between the Ag(111) surface and the -C-C(β)≡C(α)- axis as the temperature increases from 200 K to 400 K. Finally, the increased flipping from the motion of the tilted -C-C(β)≡C(α)- axis to the motion of the stand-up -C-C(β)≡C(α)- axis followed by its diffusion, resulting from the increasing temperature from 200 K to 400 K or even higher, seems to be the initial event that initiates the alkyne self-coupling reaction that leads to the final production of H3C-C≡C-C≡C-CH3.
關聯:	Journal of Computational Chemistry 33(13), pp.1274–1283
DOI:	10.1002/jcc.22958
顯示於類別:	[化學學系暨研究所] 期刊論文

文件中的檔案:

檔案	描述	大小	格式	瀏覽次數
index.html		0Kb	HTML	63	檢視/開啟

在機構典藏中所有的資料項目都受到原著作權保護.

TAIR相關文章

資料載入中.....