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Solution-processed transparent electrodes

Published online by Cambridge University Press:  20 October 2011

David S. Hecht
Affiliation:
TE Connectivity, 301 Constitution Dr., USA; dhecht@gmail.com
Richard B. Kaner
Affiliation:
University of California, Los Angeles, CA, USA; kaner@chem.ucla.edu

Abstract

Typically, materials with high electrical conductivity such as metals are opaque, and materials with high optical transparency such as glass are insulating. Finding materials that are both transparent to visible light and electrically conductive has proven to be a challenge. The need for such materials continues to grow, as many of today’s popular devices such as liquid-crystal displays and organic light-emitting diodes in televisions, touch screens in phones or tablet computers, electrophoretic displays in e-readers, or solar cells on a roof require one or more layers to transmit visible light, while simultaneously applying a voltage or conducting a current. Today, the industry’s need for such a material is serviced by various metal oxides, of which indium tin oxide (ITO) is by far the most common. The opto-electronic properties of ITO satisfy industry need for most devices; however, ITO has several drawbacks (e.g., brittle, expensive, and typically applied via costly sputtering techniques). To address these issues, recent advances in solution-processed nanomaterials have enabled several printable alternatives to sputtered ITO. These nanomaterials include conducting polymers, metallic nanostructures, ITO nanostructures, carbon nanotubes, and graphene. The ability to apply nanomaterials from the liquid phase opens the possibility to print these electronic materials roll-to-roll, greatly reducing cost and increasing yield and throughput, while the nanomaterial topology enables truly flexible devices.

Information

Type
Introduction
Copyright
Copyright © Materials Research Society 2011
Figure 0

Figure 1. Atomic force microscopy/scanning electron microscopy images of transparent conducting films of (a) carbon nanotubes. Reprinted with permission from Reference 48. ©2010, American Chemical Society. (b) Silver nanowires. Reprinted with permission from Reference 12. ©2010, American Chemical Society. (c) Graphene flakes. Reprinted with permission from Reference 36. ©2008, Nature Publishing Group. (d) Indium tin oxide nanoparticles. Reprinted with permission from Reference 5. ©2010, Elsevier.

Figure 1

Figure 2. (a) Vials of carbon nanotube (CNT) inks; (b) a CNT conductive film being coated by a slot-die; and (c) a roll of printed transparent conducting film of CNT on poly(ethylene terephthalate).

Figure 2

Figure 3. (a) Transmittance versus wavelength for graphene films of one to four layers. Each layer of graphene absorbs about 2.5% of light at 550 nm. The inset shows little change in transmission after doping with nitric acid. (b) Visible light transmission (%) versus sheet resistance for graphene films made via various techniques (RGO, reduced graphene oxide; CMG, chemically modified graphene), compared to what is required by the industry and what is theoretically possible for perfect, highly doped graphene. Black square at 30 OPS and 90% T was added by the authors of this article to reflect the data of Bae et al. (Reprinted with permission from Reference 18. ©2010, American Chemical Society). (c) An image of large area graphene film on poly(ethylene terephthalate) grown roll-to-roll by chemical vapor deposition. Reprinted with permission from Reference 19. ©2010, Nature Publishing Group. (d) A schematic showing solution processing of graphene/carbon nanotube hybrid film using hydrazine.

Figure 3

Figure 4. (a) An organic light-emitting diode with a solution processed graphene electrode shows similar performance to that with an indium tin oxide electrode in terms of current density (filled symbols) and luminance (open symbols). Reprinted with permission from Reference 20. ©2009, American Chemical Society. (b) Operation of a four-wire resistive touch screen using graphene electrodes. Reprinted with permission from Reference 19. ©2010, Nature Publishing Group. (c) A solution processed solar cell using a laminated silver nanowire electrode. Reprinted with permission from Reference 47. ©2010, American Chemical Society.