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High energy electron beam stimulated nanowelding of silver nanowire networks encapsulated with graphene for flexible and transparent electrodes.

ABSTRACT: Low-dimensional nanostructures and their complementary hybridization techniques are in the vanguard of technological advances for applications in transparent and flexible nanoelectronics due to the intriguing electrical properties related to their atomic structure. In this study, we demonstrated that welding of Ag nanowires (NWs) encapsulated in graphene was stimulated by flux-optimized, high-energy electron beam irradiation (HEBI) under ambient conditions. This methodology can inhibit the oxidation of Ag NWs which is induced by the inevitably generated reactive ozone as well as improve of their electrical conductivity. We have systematically explored the effects of HEBI on Ag NWs and graphene. The optimized flux for HEBI welding of the Ag NWs with graphene was 150 kGy, which decreased the sheet resistance of the graphene/Ag NWs to 12 Ohm/sq. Following encapsulation with graphene, the initial chemical states of the Ag NWs were well-preserved after flux-tuned HEBI, whereas graphene underwent local HEBI-induced defect generation near the junction area. We further employed resonant Raman spectroscopy to follow the structural evolution of the sacrificial graphene in the hybrid film after HEBI. Notably, the sheet resistance of the welded Ag NWs encapsulated with graphene after HEBI was well-maintained even after 85 days.

SUBMITTER: Lee SJ

PROVIDER: S-EPMC6598987 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Flexible, transparent patterned electrodes based on graphene oxide/silver nanowire nanocomposites fabricated utilizing an accelerated ultraviolet/ozone process to control silver nanowire degradation.

Project description:We developed flexible, transparent patterned electrodes, which were fabricated utilizing accelerated ultraviolet/ozone (UV/O3)-treated graphene oxide (GO)/silver nanowire (Ag-NW) nanocomposites via a simple, low-cost pattern process to investigate the feasibility of promising applications in flexible/wearable electronic and optoelectronic devices. The UV/O3 process of the GO/Ag-NW electrode was accelerated by the pre-heat treatment, and the degradation interruption of Ag NWs was removed by the GO treatment. After the deposition of the GO-treated Ag NW electrodes, the sheet resistance of the thermally annealed GO-treated Ag-NW electrodes was significantly increased by using the UV/O3 treatment, resulting in a deterioration of the GO-treated Ag NWs in areas exposed to the UV/O3 treatment. The degradation of the Ag NWs caused by the UV/O3 treatment was confirmed by using the sheet resistances, scanning electron microscopy images, X-ray photoelectron microscopy spectra, and transmittance spectra. While the sheet resistance of the low-density Ag-NW electrode was considerably increased due to the pre-thermal treatment at 90 °C for 10 min, that of the high-density Ag-NW electrode did not vary significantly even after a UV/O3 treatment for a long time. The degradation interference phenomenon caused by the UV/O3 treatment in the high-density Ag NWs could be removed by using a GO treatment, which resulted in the formation of a Ag-NW electrode pattern suitable for promising applications in flexible organic light-emitting devices. The GO treatment decreased the sheet resistance of the Ag-NW electrode and enabled the pattern to be formed by using the UV/O3 treatment. The selective degradation of Ag NWs due to UV/O3 treatment decreased the transparency of the Ag-NW electrode by about 8% and significantly increased its sheet resistance more than 100 times.

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