Shanmugham Saravanarajan, Jeong Jonghwa, Alkhateeb Abdullah, Aston D Eric
Department of Chemical Engineering, P.O. Box 441021, University of Idaho, Moscow, Idaho 83844-1021, USA.
Langmuir. 2005 Oct 25;21(22):10214-8. doi: 10.1021/la050538o.
The mechanical bending behavior of polymer nanowires-polypyrrole and poly(3,4-ethylene dioxythiophene-co-styrene sulfonate)-produced by template molding were measured using a new innovation in atomic force microscopy (AFM). Digital pulsed force mode (DPFM) was used to image and simultaneously perform three-point bend tests along nanowires spanning microchannels in silicon. The bending profiles were analyzed for apparent elastic moduli variations along the suspended length of individually isolated nanowires and compared to classic beam deflection models for various geometric and boundary conditions. The elastic moduli calculated from these AFM data are 2-7 times that expected for bulk polymer values (approximately 1-3 GPa), demonstrating an apparent strengthening of nanostructured polymer even for diameters greater than 100 nm--the accepted boundary for nanoscience. Furthermore, detailed analysis of deflection data versus loading location demonstrates the experimental dependence on test geometry and inherent errors in relying solely on midpoint bending measurements or any single loading configuration for nanomechanical testing as well as the significant contribution of nanoindentation effects.
利用原子力显微镜(AFM)的一项新创新技术,对通过模板成型制备的聚合物纳米线(聚吡咯和聚(3,4-乙撑二氧噻吩-共-苯乙烯磺酸盐))的机械弯曲行为进行了测量。数字脉冲力模式(DPFM)用于成像,并同时沿着跨越硅微通道的纳米线进行三点弯曲测试。分析了弯曲轮廓,以研究沿着单独分离的纳米线的悬浮长度的表观弹性模量变化,并与各种几何和边界条件下的经典梁挠度模型进行了比较。从这些AFM数据计算出的弹性模量是本体聚合物值(约1-3 GPa)预期值的2-7倍,这表明即使对于直径大于100 nm(纳米科学公认的界限)的纳米结构聚合物,也有明显的强化作用。此外,对挠度数据与加载位置的详细分析表明,实验依赖于测试几何形状,以及仅依靠中点弯曲测量或任何单一加载配置进行纳米力学测试时存在的固有误差,以及纳米压痕效应的显著贡献。