Liquid‐source growth of graphene on Ag(001) (Phys. Status Solidi B 8/2015). Issue 8 (August 2015)
- Record Type:
- Journal Article
- Title:
- Liquid‐source growth of graphene on Ag(001) (Phys. Status Solidi B 8/2015). Issue 8 (August 2015)
- Main Title:
- Liquid‐source growth of graphene on Ag(001) (Phys. Status Solidi B 8/2015)
- Authors:
- Grandthyll, Samuel
Jacobs, Karin
Müller, Frank - Abstract:
- <abstract abstract-type="graphical"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Graphene formation on weakly interacting surfaces is of particular interest especially for transfer processes since the lack of strong covalent bonding may reduce the risk of inducing defects when separating the graphene layer from the metal support. The study by Grandthyll, Jacobs, and Müller (pp. <ext-link ext-link-type="uri" xlink:href="http://doi.wiley.com/10.1002/pssb.201552048" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">1695–1699</ext-link>) compares the performance of graphene formation via liquid precursor deposition (LPD) with that one via chemical vapor deposition (CVD) for a weakly interacting surface such as Ag(001).</p> <p>The figures on the front cover show the Fermi surfaces of the clean Ag(001) substrate and after the formation of about one monolayer graphene via LPD. In the latter case, the ring‐like structure exhibits a radius of about 1.7 Å–1 which is exactly the ΓK‐distance of the Dirac points in k‐space. Due to the arbitrary orientation of the graphene domains with respect to the lattice of the Ag(001) surface, the Dirac hexagons add to this Dirac 'ring'. The XPS data demonstrate that there is no uptake of carbon via the standard CVD technique (using propene) while the LPD synthesis (using acetone) provides a distinct C‐1s signal. <graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pgj2c6j3g64" orientation="portrait"<abstract abstract-type="graphical"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Graphene formation on weakly interacting surfaces is of particular interest especially for transfer processes since the lack of strong covalent bonding may reduce the risk of inducing defects when separating the graphene layer from the metal support. The study by Grandthyll, Jacobs, and Müller (pp. <ext-link ext-link-type="uri" xlink:href="http://doi.wiley.com/10.1002/pssb.201552048" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink">1695–1699</ext-link>) compares the performance of graphene formation via liquid precursor deposition (LPD) with that one via chemical vapor deposition (CVD) for a weakly interacting surface such as Ag(001).</p> <p>The figures on the front cover show the Fermi surfaces of the clean Ag(001) substrate and after the formation of about one monolayer graphene via LPD. In the latter case, the ring‐like structure exhibits a radius of about 1.7 Å–1 which is exactly the ΓK‐distance of the Dirac points in k‐space. Due to the arbitrary orientation of the graphene domains with respect to the lattice of the Ag(001) surface, the Dirac hexagons add to this Dirac 'ring'. The XPS data demonstrate that there is no uptake of carbon via the standard CVD technique (using propene) while the LPD synthesis (using acetone) provides a distinct C‐1s signal. <graphic position="anchor" mimetype="image" xlink:href="ark:/27927/pgj2c6j3g64" orientation="portrait" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" /></p> </abstract> … (more)
- Is Part Of:
- Physica status solidi. Volume 252:Issue 8(2015:Aug.)
- Journal:
- Physica status solidi
- Issue:
- Volume 252:Issue 8(2015:Aug.)
- Issue Display:
- Volume 252, Issue 8 (2015)
- Year:
- 2015
- Volume:
- 252
- Issue:
- 8
- Issue Sort Value:
- 2015-0252-0008-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2015-08
- Subjects:
- Solid state physics -- Periodicals
Solids -- Periodicals
Atomic structure -- Periodicals
530.41 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3951 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pssb.201570350 ↗
- Languages:
- English
- ISSNs:
- 0370-1972
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.230000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3568.xml