Jan Ingo Flege

Dr. Jan Ingo Flege


Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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6 April 2008 in Nature Materials
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PSPeter W. Sutter
Peter W. Sutter
JFJan Ingo Flege
Jan Ingo Flege
ESEli A. Sutter
Eli A. Sutter

31 October 2019 in Small
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NMNeeraj Mishra
Neeraj Mishra
SFStiven Forti
Stiven Forti
Filippo FabbriFilippo Fabbri
Filippo Fabbri
LMLeonardo Martini
Leonardo Martini
CMClifford McAleese
Clifford McAleese
CCCamilla Coletti
Camilla Coletti
The adoption of graphene in electronics, optoelectronics, and photonics is hindered by the difficulty in obtaining high‐quality material on technologically relevant substrates, over wafer‐scale sizes, and with metal contamination levels compatible with industrial requirements. To date, the direct growth of graphene on insulating substrates has proved to be challenging, usually requiring metal‐catalysts or yielding defective graphene. In this work, a metal‐free approach implemented in commercially available reactors to obtain high‐quality monolayer graphene on c‐plane sapphire substrates via chemical vapor deposition is demonstrated. Low energy electron diffraction, low energy electron microscopy, and scanning tunneling microscopy measurements identify the Al‐rich reconstruction ° of sapphire to be crucial for obtaining epitaxial graphene. Raman spectroscopy and electrical transport measurements reveal high‐quality graphene with mobilities consistently above 2000 cm2 V−1 s−1. The process is scaled up to 4 and 6 in. wafers sizes and metal contamination levels are retrieved to be within the limits for back‐end‐of‐line integration. The growth process introduced here establishes a method for the synthesis of wafer‐scale graphene films on a technologically viable basis.

14 January 2020 in Journal of Vacuum Science & Technology A
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AMAli Mahmoodinezhad
Ali Mahmoodinezhad
Christoph JanowitzChristoph Janowitz
Christoph Janowitz
FNFranziska Naumann
Franziska Naumann
PPPaul Plate
Paul Plate
HGHassan Gargouri
Hassan Gargouri
JFJan Ingo Flege
Jan Ingo Flege
Gallium oxide (Ga2O3) thin films were deposited by plasma-enhanced atomic layer deposition (PEALD) applying a capacitively coupled plasma source where trimethylgallium (TMGa) as the gallium precursor and oxygen (O2) plasma were used in a substrate temperature (Ts) in range of 80–200 °C. TMGa exhibits high vapor pressure and therefore facilitates deposition at lower substrate temperatures. The Ga2O3 films were characterized by spectroscopic ellipsometry (SE), x-ray photoelectron spectroscopy (XPS), and capacitance-voltage (C-V) measurements. The SE data show linear thickness evolution with a growth rate of ∼0.66 Å per cycle and inhomogeneity of ≤2% for all samples. The refractive index of the Ga2O3 thin films is 1.86 ± 0.01 (at 632.8 nm) and independent of temperature, whereas the bandgap slightly decreases from 4.68 eV at Ts of 80 °C to 4.57 eV at 200 °C. XPS analysis revealed ideal stoichiometric gallium to oxygen ratios of 2:3 for the Ga2O3 layers with the lowest carbon contribution of ∼10% for the sample prepared at 150 °C. The permittivity of the layers is 9.7 ± 0.2 (at 10 kHz). In addition, fixed and mobile oxide charge densities of 2–4 × 1012 and 1–2 × 1012 cm−2, respectively, were observed in the C-V characteristics. Moreover, the Ga2O3 films show breakdown fields in the range of 2.2–2.7 MV/cm. Excellent optical and electrical material properties are maintained even at low substrate temperatures as low as 80 °C. Hence, the TMGa/O2 PEALD process is suitable for electronic and optoelectronic applications where low-temperature growth is required.

15 May 2014 in Physica Status Solidi (RRL) – Rapid Research Letters
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JFJan Ingo Flege
Jan Ingo Flege
Eugene KrasovskiiEugene Krasovskii
Eugene Krasovskii

19 August 2008 in Advanced Functional Materials
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BGBernhard Gehl
Bernhard Gehl
AFAndreas Frömsdorf
Andreas Frömsdorf
VAVesna Aleksandrovic
Vesna Aleksandrovic
TSThomas Schmidt
Thomas Schmidt
APAngelika Pretorius
Angelika Pretorius
MBMarcus Baumer
Marcus Baumer

4 December 2012 in The Journal of Physical Chemistry C
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Journal Article
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BKB. Kaemena
B. Kaemena
SSSanjaya D. Senanayake
Sanjaya D. Senanayake
AMA. Meyer
A. Meyer
Jerzy T. SadowskiJerzy T. Sadowski
Jerzy T. Sadowski
JFJ. Falta
J. Falta
JFJan Ingo Flege
Jan Ingo Flege