Kim Joonyeong, Seidler Paul, Wan Lai Sze, Fill Catherine
Department of Chemistry, Buffalo State, State University of New York, 1300 Elmwood Avenue, Buffalo, NY 14222, USA.
J Colloid Interface Sci. 2009 Jan 1;329(1):114-9. doi: 10.1016/j.jcis.2008.09.031. Epub 2008 Oct 18.
Amino-functionalized organic films were prepared by self-assembling 3-aminopropyltriethoxysilane (APTES) on silicon wafers in either anhydrous toluene or phosphate-buffered saline (PBS) for varied deposition times. Fourier transform infrared spectroscopy (FTIR) and ellipsometry have shown that the structure and thickness of APTES films are governed by the deposition time and reaction solution. Deposition from an anhydrous toluene solution produces APTES films ranging from 10 to 144 A in thickness, depending on the reaction time. FTIR spectra indicate that film growth initially proceeds by adsorption of APTES to the silicon surface followed by siloxane condensation, and after an extended period of time APTES molecules accumulate on the underlying APTES film by either covalent or noncovalent interactions. In contrast, spectroscopically indistinguishable APTES films in thickness ranging from 8 to 13 A were formed when deposition was conducted in aqueous solutions. Measured water contact angles indicate that APTES films deposited in aqueous solutions are more hydrophilic compared to those prepared in toluene solutions. Fluorescence measurements revealed that APTES films prepared in toluene solutions contain more reactive surface amino groups by ca. 3 to 10 times than those prepared in aqueous solutions for the identical reaction time.
通过在硅片上于无水甲苯或磷酸盐缓冲盐水(PBS)中自组装3-氨丙基三乙氧基硅烷(APTES),制备了氨基功能化有机薄膜,沉积时间各不相同。傅里叶变换红外光谱(FTIR)和椭偏仪表明,APTES薄膜的结构和厚度受沉积时间和反应溶液的影响。从无水甲苯溶液中沉积会产生厚度在10至144埃之间的APTES薄膜,这取决于反应时间。FTIR光谱表明,薄膜生长最初是通过APTES吸附到硅表面,随后是硅氧烷缩合,经过较长时间后,APTES分子通过共价或非共价相互作用在下层APTES薄膜上积累。相比之下,当在水溶液中进行沉积时,会形成厚度在8至13埃之间、光谱上无法区分的APTES薄膜。测量的水接触角表明,与在甲苯溶液中制备的APTES薄膜相比,在水溶液中沉积的APTES薄膜更亲水。荧光测量显示,在相同反应时间下,在甲苯溶液中制备的APTES薄膜所含的活性表面氨基比在水溶液中制备的APTES薄膜多约3至10倍。