Search

With the increasing importance of power storage devices, demand for the development of supercapacitors possessing both rapid reversible chargeability and high energy density is accelerating. Here we propose a simple process for the room temperature fabrication of pseudocapacitor electrodes consisting of a faradaic redox reaction layer on a metallic electrode with an enhanced surface area. As a model metallic electrode, an Au foil was irradiated with Ar

Herein, we present a direct observation of the formation of graphene from a single copper–carbon nanoneedle (Cu–CNN) during the measurement of current–voltage (I–V) and direct heating via in situ transmission electron microscopy (TEM). Significant structural transformation of Cu–CNN was observed with an applied potential in a two probe system. Under a high current flow between 4.9 μA to 49.0 μA, the Cu nanoparticles melted and evaporated due to Joule heating. The amorphous carbon began crystallizing and transformed into sp2 hybridized hollow graphitic carbon, which was catalyzed by the dispersed Cu nanoparticles. The temperature generated during the current flow was estimated to be 1073 K, as revealed by an in situ TEM heating experiment. The graphene nanoneedle formed exhibited a high current density of 106 A cm−2, which is comparable to Cu in normal interconnect applications. Thus, the graphene nanoneedle formed will be promising for future alternative interconnect materials.

We have studied graphene formation from a single Ag-incorporated carbon nanofiber (CNF) during electron emission using in situ transmission electron microscopy. The formation of graphene from the Ag-incorporated CNF structure was observed under a high current of between 900 nA to 2.03 μA during field and thermal electron emission. Joule heating during the process generated an increased temperature, estimated at approximately 440 K to 1030 K, leading to the transformation of a significant amount of the amorphous carbon surrounding Ag particles to a graphene structure, and to the nearly simultaneous evaporation of Ag particles. This evaporation interrupted the thermal electron emission process, thus leading to a decrease of the emission current to ∼300 nA. Also, graphene stopped forming after the Ag particles had evaporated. In this paper, the effect of Ag particle size on its ability to catalyze the fabrication of high-quality graphene are discussed.