Quantitative analysis of surface amine groups on plasma-polymerized ethylenediamine films using UV-visible spectroscopy compared to chemical derivatization with FT-IR spectroscopy, XPS and TOF-SIMS

被引:81
作者
Kim, Jinmo
Jung, Donggeun
Park, Yongsup
Kim, Yongki
Moon, Dae Won
Lee, Tae Geol [1 ]
机构
[1] Korea Res Inst Stand & Sci, Div Adv Technol, Taejon 305600, South Korea
[2] Sungkyunkwan Univ, Brain Korea Phys Res Div 21, Dept Phys, Suwon 440746, South Korea
[3] Sungkyunkwan Univ, Inst Basic Sci, Suwon 440746, South Korea
关键词
plasma polymerization; ethylenediamine; inductively coupled plasma chemical vapor deposition (ICP-CVD); Fourier transform infrared (FT-IR) spectroscopy; X-ray photoemission spectroscopy (XPS); time-of-flight secondary ion mass spectrum (TOF-SIMS); quantitative analysis;
D O I
10.1016/j.apsusc.2006.09.011
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A quantitative analysis of the surface density of amine groups on a plasma-polymerized ethylenediamine thin film deposited on a platinum surface using inductively coupled plasma chemical vapor deposition method is described. UV-visible spectroscopy together with a chemical derivatization technique using Fourier transform infrared (FT-IR) spectroscopy was used to obtain the quantitative information. Chemical tags of pentafluorobenzaldehyde were hybridized with the surface amine groups and were easily detected due to the characteristic absorption bands of C-F stretching, aromatic ring and C=N stretching vibrations in the reflection-absorption FT-IR spectra. The surface amine density was reproducibly controlled as a function of deposition plasma power and quantified using UV-visible spectroscopy. A good linear correlation was observed between the FT-IR intensities of the characteristic absorption bands and the surface amine densities, suggesting the possibility of using this chemical derivatization technique to quantify the surface densities of specific functional groups on an organic surface. Chemical derivatization was also used with X-ray photoelectron spectroscopy on the same samples, and the results were compared with those obtained from FT-IR and time-of-flight secondary ion mass spectrometry. Although each analysis technique has different probing depths from the surface, the three different data sets obtained from the chemical tags correlated well with each other since each analysis technique measured the chemical tags on the sample surface. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:4112 / 4118
页数:7
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