Nanotechnology and Functional Materials, Department of Engineering Sciences, The Angström Laboratory, Uppsala University, Box 534, 751 21 Uppsala, Sweden.
J Phys Chem B. 2010 Apr 1;114(12):4178-82. doi: 10.1021/jp911272m.
It is demonstrated that it is possible to coat the individual fibers of wood-based nanocellulose with polypyrrole using in situ chemical polymerization to obtain an electrically conducting continuous high-surface-area composite. The experimental results indicate that the high surface area of the water dispersed material, to a large extent, is maintained upon normal drying without the use of any solvent exchange. Thus, the employed chemical polymerization of polypyrrole on the microfibrillated cellulose (MFC) nanofibers in the hydrogel gives rise to a composite, the structure of which-unlike that of uncoated MFC paper-does not collapse upon drying. The dry composite has a surface area of approximately 90 m(2)/g and a conductivity of approximately 1.5 S/cm, is electrochemically active, and exhibits an ion-exchange capacity for chloride ions of 289 C/g corresponding to a specific capacity of 80 mAh/g. The straightforwardness of the fabrication of the present nanocellulose composites should significantly facilitate industrial manufacturing of highly porous, electroactive conductive paper materials for applications including ion-exchange and paper-based energy storage devices.
研究表明,通过原位化学聚合,可以将木基纳米纤维素的各个纤维用聚吡咯进行涂层,从而获得具有导电性的连续高表面积复合材料。实验结果表明,水分散材料的高表面积在很大程度上得以保留,而无需使用任何溶剂交换进行正常干燥。因此,在水凝胶中对微原纤纤维素(MFC)纳米纤维进行的聚吡咯的化学聚合导致了一种复合材料,其结构与未涂层的 MFC 纸不同,在干燥过程中不会坍塌。干燥的复合材料的比表面积约为 90 m²/g,电导率约为 1.5 S/cm,具有电化学活性,并且对氯离子的离子交换容量为 289 C/g,对应的比容量为 80 mAh/g。这种纳米纤维素复合材料的制备方法简单易行,将极大地促进高多孔、电活性导电纸材料的工业化制造,用于包括离子交换和基于纸张的储能装置在内的应用。