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Title: Direct Synthesis of Layer-Tunable and Transfer-Free Graphene on Device-Compatible Substrates Using Ion Implantation Toward Versatile Applications

Journal Article · · Energy & Environmental Materials
DOI: https://doi.org/10.1002/eem2.12730 · OSTI ID:2448400
 [1];  [2];  [3];  [1];  [4];  [5];  [6]; ORCiD logo [7]; ORCiD logo [5];  [8]
  1. Ningbo University (China)
  2. Nanjing Univ. of Information Science and Technology (China)
  3. Los Alamos National Laboratory (LANL), Los Alamos, NM (United States). Center for Integrated Nanotechnologies (CINT)
  4. Chinese Academy of Sciences (CAS), Shanghai (China)
  5. Southern University of Science and Technology (SUSTech), Shenzhen (China)
  6. Nanjing Univ. of Information Science and Technology (China); Southern University of Science and Technology (SUSTech), Shenzhen (China)
  7. Ningbo University (China); Chinese Academy of Sciences (CAS), Shanghai (China)
  8. Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)

Direct synthesis of layer-tunable and transfer-free graphene on technologically important substrates is highly valued for various electronics and device applications. State of the art in the field is currently a two-step process: a high-quality graphene layer synthesis on metal substrate through chemical vapor deposition (CVD) followed by delicate layer transfer onto device-relevant substrates. Here, we report a novel synthesis approach combining ion implantation for a precise graphene layer control and dual-metal smart Janus substrate for a diffusion-limiting graphene formation to directly synthesize large area, high quality, and layer-tunable graphene films on arbitrary substrates without the post-synthesis layer transfer process. Carbon (C) ion implantation was performed on Cu–Ni film deposited on a variety of device-relevant substrates. A well-controlled number of layers of graphene, primarily monolayer and bilayer, is precisely controlled by the equivalent fluence of the implanted C-atoms (1 monolayer ~4 × 1015 C-atoms/cm2). Upon thermal annealing to promote Cu-Ni alloying, the pre-implanted C-atoms in the Ni layer are pushed toward the Ni/substrate interface by the top Cu layer due to the poor C-solubility in Cu. As a result, the expelled C-atoms precipitate into a graphene structure at the interface facilitated by the Cu-like alloy catalysis. After removing the alloyed Cu-like surface layer, the layer-tunable graphene on the desired substrate is directly realized. The layer-selectivity, high quality, and uniformity of the graphene films are not only confirmed with detailed characterizations using a suite of surface analysis techniques but more importantly are successfully demonstrated by the excellent properties and performance of several devices directly fabricated from these graphene films. Molecular dynamics (MD) simulations using the reactive force field (ReaxFF) were performed to elucidate the graphene formation mechanisms in this novel synthesis approach. With the wide use of ion implantation technology in the microelectronics industry, this novel graphene synthesis approach with precise layer-tunability and transfer-free processing has the promise to advance efficient graphene-device manufacturing and expedite their versatile applications in many fields.

Research Organization:
Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)
Sponsoring Organization:
National Natural Science Foundation of China (NSFC); USDOE National Nuclear Security Administration (NNSA); USDOE Office of Science (SC), Basic Energy Sciences (BES). Scientific User Facilities (SUF)
Grant/Contract Number:
89233218CNA000001
OSTI ID:
2448400
Report Number(s):
LA-UR--24-20865
Journal Information:
Energy & Environmental Materials, Journal Name: Energy & Environmental Materials Journal Issue: 5 Vol. 7; ISSN 2575-0356
Publisher:
Wiley - Zhengzhou UniversityCopyright Statement
Country of Publication:
United States
Language:
English

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