Qi Baohua, Lu Wen, Mattes Benjamin R
Santa Fe Science and Technology, Inc., 3216 Richards Lane, Santa Fe, New Mexico 87507.
J Phys Chem B. 2004 May 20;108(20):6222-7. doi: 10.1021/jp031092s.
The electrochemical linear actuation of polyaniline fiber actuators has been studied in a variety of acidic aqueous electrolytes. Experimental results show that the linear strain changes significantly but nonlinearly with the anion volume. For anions smaller than Br-, a larger strain was obtained for a larger anion, that is, Br- > Cl- > F-, while once the anion was larger than Br-, a larger anion produced a smaller strain, that is, BF4- > ClO4- > CF3SO3-. On the basis of the definition of the ECR (elongation/charge ratio), that is, the contribution of a unit charge to fiber elongation, the maximum linear strain can be estimated by assuming the electrochemical efficiency is 100%. Furthermore, under isotonic conditions and the application of a constant voltage, the energy efficiency without energy recovery was shown to be proportional to the ECR and applied force and inversely proportional to the applied voltage. Under the same conditions, the highest energy efficiency is obtained in HBr. By assuming that ion and solvent insertion contributes mostly to the fiber expansion, a simple mathematical description is developed for the linear strain to show how it is determined by the volume and carried charge of the insert complex and the anisotropicity of the fiber. The difference between the theoretical and experimental results suggests that due to the crystallite structure, not all exchanged charge contributes to the fiber expansion. As the anion becomes larger, it may become more difficult for the anions to be inserted into the polymer fiber.
聚苯胺纤维致动器的电化学线性驱动已在多种酸性水性电解质中进行了研究。实验结果表明,线性应变随阴离子体积显著但非线性地变化。对于小于Br-的阴离子,阴离子越大,应变越大,即Br->Cl->F-,而一旦阴离子大于Br-,阴离子越大,应变越小,即BF4->ClO4->CF3SO3-。根据伸长率/电荷比(ECR)的定义,即单位电荷对纤维伸长的贡献,假设电化学效率为100%,则可估算出最大线性应变。此外,在等渗条件和恒定电压施加下,无能量回收时的能量效率与ECR和施加力成正比,与施加电压成反比。在相同条件下,HBr中的能量效率最高。通过假设离子和溶剂插入主要导致纤维膨胀,对线性应变进行了简单的数学描述,以说明它是如何由插入配合物的体积和携带电荷以及纤维的各向异性决定的。理论结果与实验结果的差异表明,由于微晶结构,并非所有交换电荷都对纤维膨胀有贡献。随着阴离子变大,阴离子插入聚合物纤维可能变得更加困难。