Self-assembly of silveragraphene hybrid on electrospun polyurethane nanofibers as flexible transparent conductive thin films

A method of integrating hybrid thin films of graphene nanosheets (GNSs) and silver nanoparticles (AgNps) by in situ chemical reduction to prepare transparent conductive films (TCFs) is studied. The surface functional groups of graphite oxide (GO) serve as nucleation sites of silver ions for adsorpti...

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Veröffentlicht in:Carbon (New York) 2012-08, Vol.50 (10), p.3473-3481
Hauptverfasser: Huang, Yuan-Li, Baji, Avinash, Tien, Hsi-Wen, Yang, Ying-Kui, Yang, Shin-Yi, Wu, Sheng-Yen, Ma, Chen-Chi M, Liu, Hong-Yuan, Mai, Yiu-Wing, Wang, Nian-Hau
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Sprache:eng
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Zusammenfassung:A method of integrating hybrid thin films of graphene nanosheets (GNSs) and silver nanoparticles (AgNps) by in situ chemical reduction to prepare transparent conductive films (TCFs) is studied. The surface functional groups of graphite oxide (GO) serve as nucleation sites of silver ions for adsorption of AgNps. To fabricate conductive films with high transmittance, polyurethane (PU) nanofibers are introduced to help construct two-dimensional conductive networks consisting of AgNps and GNSs (AgNpsaGNSs). This method requires only a low percentage of conducting AgNpsaGNSs covering the transparent substrate, thereby improving the transmittance. The flexible GNSs serve as nanoscale bridges between conductive AgNps and PU nanofibers, resulting in a highly flexible TCF. The optical transmittance can be further increased after melting the PU nanofibers at 100 [deg]C. A fused film obtained after electrospinning (ES) a PU solution for 120 s and immersion in 0.05 wt.% AgNpaGNS (5: 1) solution has a surface resistance of 150 ICO/sq and 85% light transmittance. Mechanical testing shows that AgNpsaGNSs on flexible substrates yield excellent robustness. Thus, TCFs with a 3: 1 ratio of AgNps: GNSs have high conductivity, good mechanical durability, and barely one order of magnitude increase of surface resistance when bent to an angle of 90[deg].
ISSN:0008-6223
DOI:10.1016/j.carbon.2012.03.013