JangWon-Ho1
ChoiJune-Heang1
HanChang-Yeol2
YangHeesun2
ChaHo-Young1
-
(School of Electrical and Electronic Engineering, Hongik University, Mapo-gu, Seoul,
04066, Korea)
-
(Department of Materials Science and Engineering, Hongik University, Seoul 04066, Korea)
Copyright © The Institute of Electronics and Information Engineers(IEIE)
Index Terms
Phototransistor, gallium nitride, ultraviolet detectors, ZnO nanodot
I. INTRODUCTION
Ultraviolet (UV) detectors are widely used in various fields including industry, military,
space research, and medical application (1). Wide energy bandgap semiconductors are suitable materials for UV detection due to
their solar blind property. Gallium nitride (GaN) is direct bandgap materials with
a wide energy bandgap (>~3.4 eV) suitable for UV detection below ~ 360 nm wavelength
region and allows stable operation at high voltage and temperature than Silicon based
UV detector (2). Bandgap engineering in aluminum gallium nitride (Al$_{\mathrm{x}}$Ga$_{\mathrm{1-x}}$N)
mole fraction can adjust cut-off wavelength 200 nm to 360 nm wavelength (3).
An AlGaN/GaN heterojunction has the unique properties of high interface channel carrier
density, resulting from spontaneous and piezoelectric polarizations, and high channel
mobility (4). Since the channel carrier density depends strongly on the surface potential, the
phototransistor output signal is highly sensitive to changes in the surface potential,
and this feature can be utilized for sensor implementation. AlGaN/GaN heterojunction-based
phototransistors with high photoresponsivity and fast response characteristics have
been reported (5).
In this study, we fabricated AlGaN/GaN heterojunction phototransistors and investigated
the effect of ZnO nanodot coating layer on the photoresponsivity characteristics.
ZnO thin film and related nanostructures have been widely studied for UV detection
applications because of wide energy bandgap and high UV absorption characteristics
(6). It was also reported that ZnO nanostructures have improved photoresponsivity owing
to the high surface-to-volume ratio of the sensing area (6,7). However, to the best of our knowledge, there has been no study on a ZnO nanodot
layer on AlGaN/GaN phototransistors.
II. DEVICE STRUCTURE AND FABRICATION
The epitaxial structure of the phototransistors consisted of a 4 nm GaN cap layer,
a 20 nm Al$_{\mathrm{0.23}}$Ga$_{\mathrm{0.77}}$N layer, a 1 nm AlN layer, a 2.1 ${μ}$m
unintentionally doped GaN layer, and a 3900 nm GaN buffer layer on a Si (111) substrate.
The fabrication started with a solvent-cleaning process, and subsequently, an ohmic
metal stack (Ti/Al/Ni/Au) was deposited and annealed by rapid thermal annealing at
820 $^{\circ}$C for 30 s in N$_{2}$ ambient. Device isolation was achieved through
Cl$_{2}$/BCl$_{3 }$based plasma etching with an etch depth of 400 nm. A Ti/Au metal
stack was evaporated for forming the pad electrodes. ZnO nanodots were prepared by
a simple solution process with 5 mmol of zinc acetate dihydrate and 30 mL of dimethyl
sulfoxide. To this solution, a solution obtained by dissolving 5 mmol of tetramethylammonium
hydroxide in 10 mL of ethanol was added. The ZnO nanodots were precipitated by the
acetone and dispersed using ethanol (8,9). The ZnO nanodots are spherical shapes with an average diameter of 3.5 nm. Finally,
the synthesized ZnO solution was spin coated on the surface of the phototransistor.
Cross-sectional schematics of phototransistors with and without ZnO nanodot layer
are shown in Fig. 1(a) and (b), respectively. The TEM image of synthesized ZnO nanodots are shown in the
inset of Fig. 1(c). The distance between two ohmic electrodes was 6 ${μ}$m with a channel width of 50
${μ}$m. (i.e., detection area = 6 ${\times}$ 50 ${μ}$m$^{2}$).
Fig. 1. Cross-sectional schematics of AlGaN/GaN hetero-junction phototransistors (a)
without a ZnO nanodot layer, (b) with a ZnO nanodot layer, (c) TEM image of synthesized
ZnO nanodots.
Fig. 2. Dark current and photocurrent at the wavelength of 300~nm versus the bias
voltage.
III. RESULT AND DISCUSSION
Plots of the dark current and photocurrent versus the bias voltage for two phototransistors
are presented in Fig. 2 for comparison; the wavelength of the incident light was 300 nm. Notably, the phototransistor
with a ZnO nanodot layer exhibited significantly lower dark current, which was because
of the absorption of free oxygen at the ZnO surface with negatively ionized states
(6). The negatively charged oxygen ions partially depleted the channel charges, resulting
in a lower current density. Under UV illumination, electron-hole pairs were generated.
The electrons moved to the AlGaN/GaN interface channel, while the holes migrated to
the surface. The holes recombined with electrons trapped in the negatively ionized
oxygen (10), resulting in an increase in the surface potential, which in turn enhanced the photocurrent.
The difference between the dark current and photocurrent was more significant in the
phototransistor with a ZnO nanodot layer, and therefore, the photoresponsivity of
the phototransistor was higher. For example, the photoresponsivity increased by about
75% from 1.0 ${\times}$10$^{6}$ A/W to 1.75 ${\times}$10$^{6}$ A/W at the wavelength
of 300 nm.
As shown in Fig. 3, the photoresponsivity was enhanced in the entire wavelength range investigated in
the experiments where the bias voltage was fixed to be 0.3~V. It should be noted that
the cut-off photoresponsivity characteristics were not observed for the phototransistor
with a ZnO nanodot layer due to the many defect sites in the ZnO nanodot layer (11).
Fig. 3. Photoresponsivity at 0.3 V versus the wavelength for the AlGaN/GaN heterojunction
phototransistors with and without a ZnO nanodot layer.
Fig. 4. TEM EDS analysis results for samples (a) without a ZnO nanodot layer, (b)
with a ZnO nanodot layer.
Fig. 4(a) and (b) show the transmission electron microscopy-energy dispersive X-ray spectroscopy
(TEM-EDS) analysis results for the phototransistor without and with a ZnO nanodot
layer, respectively. The thickness of the ZnO nanodot coating layer was 25 nm. The
phototransistor with a ZnO nanodot layer exhibited a relatively higher oxygen cps
value than that without a ZnO layer. This can explain the dark current reduction through
free oxygen absorption at the ZnO surface.
IV. CONCLUSIONS
We introduced a ZnO nanodot layer on the surface of AlGaN/GaN heterojunction phototransistors
by using a spin-coating process. The layer not only reduced the dark current but also
significantly increased the photocurrent, which enhanced the photoresponsivity. Therefore,
it is concluded that a ZnO nanodot layer is very effective in enhancing the photoresponsivity
of AlGaN/GaN heterojunction phototransistor.
ACKNOWLEDGMENTS
This work was supported by Korea Electric Power Corporation (Grant R18XA02) and Basic
Science Research Program (2015R1A6A1A03031833 and 2019R1A2C1008894)
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Author
Won-Ho Jang received the B.S. and M.S. degrees in Electronic and Electrical Engineering
from Hongik University, Seoul, Korea, in 2016 and 2018, respectively.
He is currently pursuing the Ph.D. degree at Hongik University.
His research interests include the analysis of gallium nitride devices.
June-Heang Choi received B.S. degree in Materials Science & Engineering from Hongik
University in Seoul, Korea, in 2015 and received M.S. degree in Electronic and Electrical
Engineering in 2018, respectively.
He is currently pursuing the Ph.D. degree at Hongik University.
His research interest is wide-bandgap semiconductor devices.
Chang-Yeol Han received the B.S. and M.S. degrees in Materials Science and Engineering
from Hongik University in 2014 and 2016, respectively.
He is currently pursuing a Ph.D. degree at the same institute.
His main interests are the synthesis of non-Cd quantum dots and fabrication of quantum
dot-light-emitting diodes.
Heesun Yang is a professor in the Department of Materials Science and Engineering
at Hongik University.
Yang received his Ph.D. degree in Materials Science and Engineering from University
of Florida, and his Mater’s/bachelor degrees in Ceramic Engineering from Yonsei University
in South Korea.
After obtaining his Ph.D. degree, he conducted two-year postdoctoral research at University
of Florida and then joined Hongik University in 2006.
For over 19 years, he dedicated all his efforts to the synthesis of fluorescent quantum
dots with various the semiconductor compositions of the II-VI, III-V, and I-III-VI
families and their applications to optoelectronic devices.
Ho-Young Cha received the B.S. and M.S. degrees in Electrical Engineering from the
Seoul National University, Seoul, Korea, in 1996 and 1999, respectively, and the Ph.D.
degree in Electrical and Computer Engineering from Cornell University, Ithaca, NY,
in 2004.
He was a Postdoctoral Research Associate with Cornell University until 2005, where
he focused on the design and fabrication of wide bandgap semiconductor devices.
He was with the General Electric Global Research Center, Niskayuna, NY, from 2005
to 2007, developing wide-bandgap semiconductor sensors and high-power devices.
Since 2007, he has been with Hongik University, Seoul, where he is currently Professor
in the School of Electronic and Electrical Engineering.
His research interests include wide-bandgap semiconductor devices.
He has authored over 130 publications in his research area.