Rijal Kishan, Mutharasan Raj
Department of Chemical Engineering, Drexel University, 32nd and Chestnut Streets, Philadelphia, Pennsylvania 19104, USA.
Langmuir. 2007 Jun 5;23(12):6856-63. doi: 10.1021/la063768r. Epub 2007 May 5.
We describe a cantilever-based method for measuring the self-assembly of alkanethiols on a gold surface in a flow system that permits easy step changes in concentration and acquire a continuous in situ measure of the resulting chemisorption through the change in resonance frequency. A gold-coated (2.2 mm2), piezoelectric-excited, millimeter-sized cantilever (PEMC) sensor was exposed to 1-hexadecanethiol (HDT) in ethanol at concentrations ranging from 1 fM to 1 mM, sequentially and separately. A high-order flexural mode at approximately 850 kHz was monitored during the self-assembly. The resonance frequency decreases as a result of increased mass as chemisorption occurs on the surface. We show for the first time that the chemisorption of HDT at 1 fM is readily measurable and gave a response of 220 +/- 13 Hz (n = 4). At higher concentrations (10 and 100 fM; 1, 10, and 100 pM; 1, 10, and 100 nM; 1 microM; and 1 mM), the responses were proportionately, but nonlinearly, higher. At high concentrations (1 mM), the responses to C4, C8, C11, C16, and C18 alkanethiols were linearly proportional and were complete in approximately 25 min. We report for the first time that, once the Au surface is equilibrated at 1 pM, further chemisorption at a lower HDT concentration does not take place, even though over 99% of surface adsorption sites are available. At 1 fM, the overall chemisorption rate did not increase with a 2-fold increase in the HDT flow rate, suggesting that chemisorption at 1 fM is not transport-limited. The measured overall chemisorption rate constant at 1 fM was more rapid than 0.1 min-1.
我们描述了一种基于悬臂梁的方法,用于在流动系统中测量金表面上链烷硫醇的自组装,该流动系统允许浓度轻松进行阶跃变化,并通过共振频率的变化获得对所得化学吸附的连续原位测量。一个镀金(2.2平方毫米)、压电激发的毫米级悬臂梁(PEMC)传感器依次单独暴露于乙醇中浓度范围为1飞摩尔至1毫摩尔的1-十六烷硫醇(HDT)。在自组装过程中监测了约850千赫兹的高阶弯曲模式。由于表面发生化学吸附导致质量增加,共振频率降低。我们首次表明,1飞摩尔的HDT化学吸附易于测量,响应为220±13赫兹(n = 4)。在较高浓度(10和100飞摩尔;1、10和100皮摩尔;1、10和100纳摩尔;1微摩尔;以及1毫摩尔)下,响应成比例但非线性地更高。在高浓度(1毫摩尔)下,对C4、C8、C11、C16和C18链烷硫醇的响应呈线性比例,并且在约25分钟内完成。我们首次报告,一旦金表面在1皮摩尔下达到平衡,即使超过99%的表面吸附位点可用,在较低HDT浓度下也不会发生进一步的化学吸附。在1飞摩尔时,HDT流速增加2倍,总体化学吸附速率并未增加,这表明1飞摩尔的化学吸附不受传输限制。在1飞摩尔下测得的总体化学吸附速率常数快于0.1分钟-1。