Controlled Fabrication of Native Ultra-Thin Amorphous Gallium Oxide from 2D Gallium Sulfide for Emerging Electronic Applications

Fuente: arXiv
Saved in:
Bibliographic Details
Main Authors: AlMutairi, AbdulAziz, Xhameni, Aferdita, Guo, Xuyun, Chircă, Irina, Nicolosi, Valeria, Hofmann, Stephan, Lombardo, Antonio
Format: Preprint
Published: 2024
Subjects:
Online Access:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1866910440152367104
author AlMutairi, AbdulAziz
Xhameni, Aferdita
Guo, Xuyun
Chircă, Irina
Nicolosi, Valeria
Hofmann, Stephan
Lombardo, Antonio
author_facet AlMutairi, AbdulAziz
Xhameni, Aferdita
Guo, Xuyun
Chircă, Irina
Nicolosi, Valeria
Hofmann, Stephan
Lombardo, Antonio
contents Oxidation of two-dimensional (2D) layered materials has proven advantageous in creating oxide/2D material heterostructures, opening the door for a new paradigm of low-power electronic devices. Gallium (II) sulfide ($β$-GaS), a hexagonal phase group III monochalcogenide, is a wide bandgap semiconductor with a bandgap exceeding 3 eV in single and few layer form. Its oxide, gallium oxide (Ga$_2$O$_3$), combines large bandgap (4.4-5.3 eV) with high dielectric constant (~10). Despite the technological potential of both materials, controlled oxidation of atomically-thin $β$-GaS remains under-explored. This study focuses into the controlled oxidation of $β$-GaS using oxygen plasma treatment, achieving ultrathin native oxide (GaS$_x$O$_y$, ~4 nm) and GaS$_x$O$_y$/GaS heterostructures where the GaS layer beneath remains intact. By integrating such structures between metal electrodes and applying electric stresses as voltage ramps or pulses, we investigate their use for resistive random-access memory (ReRAM). The ultrathin nature of the produced oxide enables low operation power with energy use as low as 0.22 nJ per operation while maintaining endurance and retention of 350 cycles and 10$^4$ s, respectively. These results show the significant potential of the oxidation-based GaS$_x$O$_y$/GaS heterostructure for electronic applications and, in particular, low-power memory devices.
format Preprint
id arxiv_https___arxiv_org_abs_2405_05632
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle Controlled Fabrication of Native Ultra-Thin Amorphous Gallium Oxide from 2D Gallium Sulfide for Emerging Electronic Applications
AlMutairi, AbdulAziz
Xhameni, Aferdita
Guo, Xuyun
Chircă, Irina
Nicolosi, Valeria
Hofmann, Stephan
Lombardo, Antonio
Applied Physics
Mesoscale and Nanoscale Physics
Oxidation of two-dimensional (2D) layered materials has proven advantageous in creating oxide/2D material heterostructures, opening the door for a new paradigm of low-power electronic devices. Gallium (II) sulfide ($β$-GaS), a hexagonal phase group III monochalcogenide, is a wide bandgap semiconductor with a bandgap exceeding 3 eV in single and few layer form. Its oxide, gallium oxide (Ga$_2$O$_3$), combines large bandgap (4.4-5.3 eV) with high dielectric constant (~10). Despite the technological potential of both materials, controlled oxidation of atomically-thin $β$-GaS remains under-explored. This study focuses into the controlled oxidation of $β$-GaS using oxygen plasma treatment, achieving ultrathin native oxide (GaS$_x$O$_y$, ~4 nm) and GaS$_x$O$_y$/GaS heterostructures where the GaS layer beneath remains intact. By integrating such structures between metal electrodes and applying electric stresses as voltage ramps or pulses, we investigate their use for resistive random-access memory (ReRAM). The ultrathin nature of the produced oxide enables low operation power with energy use as low as 0.22 nJ per operation while maintaining endurance and retention of 350 cycles and 10$^4$ s, respectively. These results show the significant potential of the oxidation-based GaS$_x$O$_y$/GaS heterostructure for electronic applications and, in particular, low-power memory devices.
title Controlled Fabrication of Native Ultra-Thin Amorphous Gallium Oxide from 2D Gallium Sulfide for Emerging Electronic Applications
topic Applied Physics
Mesoscale and Nanoscale Physics
url https://arxiv.org/abs/2405.05632