Reversible Transition of Semiconducting PtSe2 and Metallic PtTe2 for Scalable All-2D Edge-Contacted FETsShow others and affiliations
2024 (English)In: Nano Letters, ISSN 1530-6984, E-ISSN 1530-6992, Vol. 24, no 6, p. 1891-1900Article in journal, Letter (Refereed) Published
Abstract [en]
Two-dimensional (2D) transition metal dichalcogenide (TMD) layers are highly promising as field-effect transistor (FET) channels in the atomic-scale limit. However, accomplishing this superiority in scaled-up FETs remains challenging due to their van der Waals (vdW) bonding nature with respect to conventional metal electrodes. Herein, we report a scalable approach to fabricate centimeter-scale all-2D FET arrays of platinum diselenide (PtSe2) with in-plane platinum ditelluride (PtTe2) edge contacts, mitigating the aforementioned challenges. We realized a reversible transition between semiconducting PtSe2 and metallic PtTe2 via a low-temperature anion exchange reaction compatible with the back-end-of-line (BEOL) processes. All-2D PtSe2 FETs seamlessly edge-contacted with transited metallic PtTe2 exhibited significant performance improvements compared to those with surface-contacted gold electrodes, e.g., an increase of carrier mobility and on/off ratio by over an order of magnitude, achieving a maximum hole mobility of similar to 50.30 cm(2) V-1 s(-1) at room temperature. This study opens up new opportunities toward atomically thin 2D-TMD-based circuitries with extraordinary functionalities.
Place, publisher, year, edition, pages
American Chemical Society (ACS), 2024. Vol. 24, no 6, p. 1891-1900
Keywords [en]
2D PtTe2 layer, 2D PtSe2 layer, anion exchange, chemical transition, edge contact, 2D TMD heterostructure
National Category
Electrical Engineering, Electronic Engineering, Information Engineering
Research subject
Physics, Electrotechnology
Identifiers
URN: urn:nbn:se:lnu:diva-127898DOI: 10.1021/acs.nanolett.3c03666ISI: 001158890700001PubMedID: 38150559Scopus ID: 2-s2.0-85183091025OAI: oai:DiVA.org:lnu-127898DiVA, id: diva2:1839263
2024-02-202024-02-202025-02-12Bibliographically approved