Loading…

Catalyst-Free Growth of Networked Nanographite on Si and SiO2 Substrates by Photoemission-Assisted Plasma-Enhanced Chemical Vapor Deposition

We have developed a photoemission-assisted plasma-enhanced chemical vapor deposition (CVD) process, where DC discharge plasma is assisted by photoelectrons emitted from the substrate under ultraviolet (UV) light irradiation. Under Ar gas atmosphere and in vacuum, plasma current was measured as a fun...

Full description

Saved in:
Bibliographic Details
Published in:E-journal of surface science and nanotechnology 2009/12/12, Vol.7, pp.882-890
Main Authors: Takami, Tomohide, Ogawa, Shuichi, Sumi, Haruki, Kaga, Toshiteru, Saikubo, Akihiko, Ikenaga, Eiji, Sato, Motonobu, Nihei, Mizuhisa, Takakuwa, Yuji
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:We have developed a photoemission-assisted plasma-enhanced chemical vapor deposition (CVD) process, where DC discharge plasma is assisted by photoelectrons emitted from the substrate under ultraviolet (UV) light irradiation. Under Ar gas atmosphere and in vacuum, plasma current was measured as a function of sample bias voltage to clarify the mechanism, by which photoemission-assisted plasma is generated. Owing to the advantages of the photoemission-assisted plasma-enhanced CVD, where the plasma is generated close to the substrate and in a controllable volume, we have succeeded in growing shiny black films of networked nanographite, without any catalyst, on Si(001) and SiO2(350 nm)/Si(001) substrates at a deposition rate of ∼2 μm/min despite of low electric power consumption of plasma, ∼4 W. Cross-sectional transmission electron microscopy (TEM) and diffraction (TED) observations revealed that samples grown at ∼700°C with Ar-diluted CH4 were composed of multilayer graphene particles (diameter of ∼10 nm) that were closely connected to each other and shared some graphene sheets between them, although their crystallographic configurations were randomly oriented. In bulk-sensitive C 1s photoelectron spectra using synchrotron radiation at 7933 eV, a chemically-shifted component of sp2-bonded carbon atom was dominant and the π—π* transition loss peak was clearly observed for the samples grown on both substrates, indicating that the multilayer graphene particles substantially contain high-quality graphene sheets in agreement with evaluations by microscopic Raman spectroscopy. We named the layered carbon structure “carbon mille-feuille.” [DOI: 10.1380/ejssnt.2009.882]
ISSN:1348-0391
1348-0391
DOI:10.1380/ejssnt.2009.882