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2025 (English)In: Carbon, ISSN 0008-6223, E-ISSN 1873-3891, Vol. 237, article id 120108Article in journal (Refereed) Published
Abstract [en]
The high current-carrying capacity of graphene is essential for its use as an interconnect in electronic and spintronic circuits. At the same time, knowing the breakdown limits and mechanism under high fields can enable new device design strategies. In this work, we push the current carrying capacity of the scalable form of chemical vapor deposited (CVD) graphene employing a high-thermal conducting single crystalline diamond substrate. Our experiments on CVD graphene reveal extremely high current densities > 109 A/cm2 in graphene on the diamond with both ohmic (low-resistive) and tunneling tunnel (high-resistive) contacts. Measurements on ferromagnetic (TiOx/Co) and metallic (Ti/Au) contacts demonstrate current densities of ∼1.16×109 A/cm2 and ∼1.7×109 A/cm2, respectively. The tunnel (high-resistive) contacts exhibit a shunting of graphene under high currents via the bottom graphitized diamond, resulting in dielectric breakdown and via alternative conducting paths. Electrical measurements show a distinct threshold for conducting paths of graphitized diamond, in tune accordance with Middleton-Wingreen's theory. Our results of high current densities achieved in CVD graphene, with distinct dependence on ohmic and tunneling, contact resistance, and the observed breakdown mechanism, provide new insights for enabling high-current all carbon circuits.
Place, publisher, year, edition, pages
Elsevier, 2025
Keywords
CVD Graphene, diamond, high current carrying capacity, fractal pattern
National Category
Condensed Matter Physics
Identifiers
urn:nbn:se:uu:diva-550657 (URN)10.1016/j.carbon.2025.120108 (DOI)001460969300001 ()2-s2.0-85218100128 (Scopus ID)
Funder
EU, European Research Council, 101002772Olle Engkvists stiftelse, 200–0602Swedish Energy Agency, 48698-1Swedish Energy Agency, 48591-1Swedish Research Council, 2021-05932Swedish Research Council, 22-04186-5Swedish Research Council Formas, 2019-01326Swedish Research Council Formas, 2023-01607Knut and Alice Wallenberg Foundation, 2022.0079
2025-02-172025-02-172025-11-20Bibliographically approved