Subscriber access provided by Nottingham Trent University
Organic Electronic Devices
Low-Voltage, High Performance Flexible Organic Field Effect Transistors Based on Ultrathin Single Crystal Microribbons Hongming Chen, Xing Xing, Miao Zhu, Jupeng Cao, Muhammad Umair Ali, Aiyuan Li, Yaowu He, and Hong Meng ACS Appl. Mater. Interfaces, Just Accepted Manuscript • DOI: 10.1021/acsami.9b13871 • Publication Date (Web): 28 Aug 2019 Downloaded from pubs.acs.org on August 28, 2019
Just Accepted “Just Accepted” manuscripts have been peer-reviewed and accepted for publication. They are posted online prior to technical editing, formatting for publication and author proofing. The American Chemical Society provides “Just Accepted” as a service to the research community to expedite the dissemination of scientific material as soon as possible after acceptance. “Just Accepted” manuscripts appear in full in PDF format accompanied by an HTML abstract. “Just Accepted” manuscripts have been fully peer reviewed, but should not be considered the official version of record. They are citable by the Digital Object Identifier (DOI®). “Just Accepted” is an optional service offered to authors. Therefore, the “Just Accepted” Web site may not include all articles that will be published in the journal. After a manuscript is technically edited and formatted, it will be removed from the “Just Accepted” Web site and published as an ASAP article. Note that technical editing may introduce minor changes to the manuscript text and/or graphics which could affect content, and all legal disclaimers and ethical guidelines that apply to the journal pertain. ACS cannot be held responsible for errors or consequences arising from the use of information contained in these “Just Accepted” manuscripts.
is published by the American Chemical Society. 1155 Sixteenth Street N.W., Washington, DC 20036 Published by American Chemical Society. Copyright © American Chemical Society. However, no copyright claim is made to original U.S. Government works, or works produced by employees of any Commonwealth realm Crown government in the course of their duties.
Page 1 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
Low-Voltage, High Performance Flexible Organic Field Effect Transistors Based on Ultrathin Single Crystal Microribbons Hongming Chena, Xing Xingb, Miao Zhuc, Jupeng Caoa, Muhammad Umair Alid, Aiyuan Lia, Yaowu Hea, Hong Menga*
aSchool
of Advanced Materials, Peking University Shenzhen Graduate School, Peking
University, Shenzhen 518055, P.R. China
bResearch
& Development Institute of Northwest Polytechnical University (Shenzhen),
Northwestern Polytechnical University, Shenzhen 518057, P. R. China
cCollege
of Physics Science and Technology, Lingnan Normal University, Zhanjiang
524048, P. R. China
1 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
dDepartment
Page 2 of 40
of Materials Science and Engineering, College of Engineering, Peking
University,
Beijing, 100871, P.R. China
ABSTRACT: Organic field effect transistors (OFETs) have acquired increasing attention
owing of their wide range of potential applications in electronics, nevertheless, high
operating voltage and low carrier mobility are considered as major bottlenecks in their
commercialization. In this work, we demonstrate low-voltage, flexible OFETs based on
ultrathin
single
crystal
microribbons.
Flexible
OFETs
fabricated
with
2,7-
dioctylbenzothieno[3,2-b]benzothiophene (C8-BTBT) based solution processed ultrathin single crystal microribbon as the semiconductor layer and high-k polymer, polysiloxane-
poly(vinyl alcohol) composite (HPCPS), as an insulator layer manifest a significantly low operating voltage of -4 V and several devices showed a high mobility of > 30 cm2 V-1 s-1.
Besides, the carrier mobility of the fabricated devices exhibits a slight degradation in static
bending condition, which can be retained by 83.3% compared with its original value under
a bending radius of 9 mm. As compared to the bulk C8-BTBT single crystal based OFET
2 ACS Paragon Plus Environment
Page 3 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
which showed a large crack only after 50 times dynamic bending, our ultrathin single
crystal based counterpart demonstrates much better dynamic force stability. Moreover,
under a 20 mm bending radius, the mobility of the device decreased by only 11.7% even
after 500 bending cycles and no further decrease was observed until 1,000 times bending.
Our findings reveal that ultrathin C8-BTBT single crystal based flexible OFETs are
promising candidates for various high performance flexible electronic devices.
KEYWORDS: Single Crystal, Microribbons, OFETs, High-k, Polymer Insulator, Flexible
1. INTRODUCTION
Organic semiconductors, owing to their versatile chemical structures, high flexibility and
low-cost processing, are considered as promising materials for flexible electronics. In
recent years, flexible organic field effect transistors (OFETs) have attracted great
attention due to their extensive applications in various flexible electronic devices, such as flexible organic light-emitting diode (OLED) displays1, wearable electronics2-4 and printable radiofrequency identification tags (RFID) etc.5 However, the reported flexible OFETs usually suffer from high operating voltage (|Vd| >20 V)6-7 or low carrier mobility83 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
10,
Page 4 of 40
which limits their real applications. Therefore, it is necessary to realize flexible OFTEs
with low operating voltage and high carrier mobility for their potential applications in
flexible electronics.
The operating voltage is mainly related to the dielectric constant of the gate insulator and high dielectric constant (high-k) materials are preferred to achieve satisfactory operating
voltage in flexible OFETs. In previous reports, various approaches have been adopted to realize low-voltage flexible OFETs by employing high-k gate insulators. The operating
voltage of flexible OFETs is reported to be decreased to below 5 V via employing AlOx modified with ultrathin self-assembled monolayer (SAM) as the gate insulator.2,
9, 11-12
Incorporation of various high-k polymer or inorganic films, such as PVDF-TrFE7,
13,
BST,14-15 and sol-gel silica16 etc. as the gate insulators is also observed to yield flexible OFETs with < 5 V operating voltage. We recently reported a novel high-k polymer,
polysiloxane-poly(vinyl alcohol) composite (HPCPS), and demonstrated HPCPS/Si based OFETs with a low driving voltage (|Vd| 30 cm2 V-1 s-1 under a low operating voltage of -4 V only, which is the best performance
among low-voltage, flexible OFETs reported to date. Moreover, the carrier mobility of our
flexible SCFETs demonstrated a good stability in static and dynamic bending conditions.
Interestingly, no noticeable damage on the ultrathin single crystal microribbons was
observed even after 1,000 times of dynamic bending tests, while bulk C8-BTBT single
crystal (with a thickness of about 135 nm) showed a large crack after only 50 times of
dynamic bending. Our results demonstrate that OFETs with a rational combination of ultrathin single crystal microribbon as the active layer and HPCPS as the high-k gate
insulator could be promising candidates for applications in high performance flexible
electronic devices.
2. EXPERIMENTAL SECTION
C8-BTBT
single
crystal
microribbons
growth.
The
2,7-dioctylbenzothieno[3,2-
b]benzothiophene (C8-BTBT) powder was synthesized by a previously reported method24
and purified three times before use. The C8-BTBT based ultrathin single crystals were 7 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Page 8 of 40
grown by previously reported ‘space-confirmed strategy’.23 C8-BTBT powder was
dissolved in chlorobenzene and dichloromethane mixed solvent in a concentration of 2
mg/mL (the solvent ratio of chlorobenzene and dichloromethane was set to be 4:1 in
volume). Then, 15 µL of the solution was dropped onto the surface of sodium dodecyl sulfate (SDS) aqueous solution (1×10-3 mg/mL). After the complete evaporation of the
solvent, C8-BTBT single crystal microribbons were obtained on the water surface.
Device fabrication. We fabricated flexible organic SCFETs in a bottom-gate, top-contact (BG-TC) configuration. The ITO/PET (230 nm/160 U 3 substrates were pre-treated by
oxygen plasma (80 W) for 120 seconds. Then, the HPCPS sol-gel was spin-coated onto
the substrates at 4000 rpm for 50 seconds with a typical thickness of ~130 nm. The synthesis method for HPCPS sol-gel has been reported elsewhere.17 In next step, the HPCPS film was thermal annealed at 80 oC for 30 min in air. After that, the C8-BTBT single crystal microribbon was transferred onto the HPCPS layer.22 Finally, gold
electrodes were evaporated onto the single crystal microribbon through a copper grid (45 nm) mask.25
8 ACS Paragon Plus Environment
Page 9 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
Characterization. The polarized optical microscopy (POM) was used to capture the POM images of single crystal microribbons and flexible SCFETs. X-ray diffraction (XRD)
patterns were obtained using a Bruker D8 with an X-ray wavelength of 1.541 Å 2
?HW
source). Transmission electron microscopy (TEM) and selected-area electron diffraction
(SAED) characterizations were conducted with a FEI Tecnai G2F30. Atomic force
microscopy (AFM) on SPA400HV instrument with SPI 3800 controller (Seiko Instruments)
was used to investigate the surface morphology of the microribbons and substrates.
All the electrical characterizations were performed by an Agilent B1500A semiconductor
parameter analyzer at room temperature (25 oC) in ambient atmosphere. The hole mobility (U) of flexible SCFETs at the saturation region is estimated from the transfer curve
based on the following equation (1):
I ds
WCi (Vg Vth ) 2 2L
(1)
where Ids, W, L, Vg and Vth refer to the drain-source current, channel width, channel length, gate voltage and threshold voltage, respectively. Ci represents the capacitance per unit
9 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Page 10 of 40
area of the gate dielectric layer, which is obtained by capacitance-frequency
measurement with Agilent E4980A in MIM (metal-insulator-metal) structure. The value of
Ci measured at a frequency of 20 Hz is 88.6 nF/cm2, as shown in Figure S1 (a) (Supporting Information). The dielectric constant of HPCPS can be calculated using
equation (2), as given below:
ci d
k
(2)
0
where d is the thickness of the film and
0
is the vacuum permittivity. The dielectric
constant for HPCPS is found to be ~13.0, which is much higher than our previous report where the Ci was measured at 10 kHz.17 It is to be noticed that the Ci value at a frequency of 20 Hz is widely used to calculate the carrier mobility in several previous reports [26-28].
Also, 20 Hz is the lowest possible frequency of our capacitance measurement equipment. Therefore, we calculated the carrier mobility based on the Ci value of 88.6 nF/cm2. We further performed a theoretical calculation for capacitance vs frequency curve in the
frequency range of 0.1 - 20 Hz (Figure S1(c)-(d)) and predicted the carrier mobility at a
frequency of 0.1 Hz. The detailed procedure adopted herein for the projection of carrier
10 ACS Paragon Plus Environment
Page 11 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
mobility can be found in Supporting Information. The current on/off ratio is defined as the
Ids, max/ Ids, min.
3. RESULTS AND DISCUSSION
Characterization of C8-BTBT single crystal microribbons. After complete evaporation of the solvent, the C8-BTBT microribbon was transferred on a pre-treated n-doped SiO2 (300 nm)/Si wafer. Figure 1(a) shows C8-BTBT microribbon film image obtained by a
bright-field optical microscope which revealed no obvious cracks or grain boundaries,
indicating the excellent quality of our single crystal. The length of the prepared
microribbons was more than one millimeter (Figure S2). The color of the sample changed
from brown to complete dark when it was rotated from 0 degree to 45 degrees under a
cross polarized optical microscope (Figure 1(b)-(c)). This birefringence phenomenon in
C8-BTBT microribbon film under the cross polarized mode verifies that the prepared
microribbon films possess single crystalline nature. As demonstrated in Figure 1 (d), a
typical TEM image revealed uniform morphology of the fabricated film while SAED pattern
(Figure 1 (e)) also confirmed the single crystalline nature of C8-BTBT microribbon film.
11 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Page 12 of 40
Besides, the morphology of the single crystal microribbon is also investigated using AFM
(Figure S3 (a)), which showed the surface roughness of an ultrathin C8-BTBT single
crystal to be 0.255 nm in the frame selected area, indicating that the single crystal formed
a very flat surface on SiO2 /Si wafer.
As compared to the XRD pattern of C8-BTBT powder in Figure 1(f), the XRD pattern of
the C8-BTBT single crystal microribbons only exhibited (001), (002) and (003) peaks, indicating that the single crystal microribbons are arranged along the c-axis.23, 29-30 The
thickness of C8-BTBT microribbon is 21.69 nm, i.e. about 7-8 molecular layers (Figure
S3 (c)). The thickness difference of 2.96 nm in the crystal (red axis in Figure S3 (a)) fits-
well with the thickness of a single molecular layer of C8-BTBT (2.918 nm), which confirms
the layer by layer crystal growth.
12 ACS Paragon Plus Environment
Page 13 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
(a)
(b)
(c)
150 m
150 m (d)
(f)
(e) b
150 m (001) S
(020)
C8H17 C8H17 S
a (200) (002)(003)
single crystal powder
1 m
5 1/nm
Figure 1. (a)-(c) Bright-field and cross POM images of C8-BTBT single crystal microribbon; (d)-(e)
TEM image and the corresponding SAED pattern of C8-BTBT microribbon; (f) Powder and single
crystal XRD patterns of C8-BTBT on SiO2/Si substrate, the inset shows the chemical structure of C8BTBT.
Electrical properties of C8-BTBT SCFETs. To evaluate the performance of C8-BTBT based SCFETs, C8-BTBT single crystal microribbon was transferred onto the
HPCPS/ITO/PET substrate followed by thermal evaporation of Au electrodes. Figure 2(a)
shows the device structure (in BG-TC configuration). The optical microscope image of the
13 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Page 14 of 40
device with a single crystal microribbon is shown in Figure 2(b). Furthermore, all the
devices fabricated in this work contain only one single crystal microribbon aligned along
its long axis. The operating voltage, threshold voltage and on/off ratio for this device were measured to be -4 V, -1.1 V and 9.18×104, respectively as presented in Figure 2 (c). This fabricated SCFETs exhibited a high saturated mobility of 33.4 cm2 V-1 s-1 with a leakage current of < 10 nA. Furthermore, the trap density (Ntrap) of the device is 2.48×1012 cm-2 (calculated by Equation S2, Supporting Information), which is much smaller than a C8-
BTBT SCFET device based on an OTS modified SiO2/Si substrate (Ntrap =1.21×1014 cm-2, Figure S4(d)). It indicates low trap states at the interface between C8-BTBT single crystal
and HPCPS dielectric, which means HPCPS dielectric film can effectively suppress the
interfacial traps as compared to the OTS modified SiO2/Si substrate. It is well-proved by previous reports that high quality single crystals can obtain a very high carrier mobility
because of their single crystalline nature and low trapping effect between the singlecrystal surface and the dielectric layer.31-32 Therefore, such a high mobility in our SCFETs
could be attributed to the low charge traps in our high quality C8-BTBT single crystals
14 ACS Paragon Plus Environment
Page 15 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
and further reduction in the interfacial traps by the polar chloropropyl chain in HPCPS dielectric layer. 17, 32
To critically evaluate the extracted mobility in our devices, the reliability factor “r” and the effective mobility “Ueff” of SCFETs were calculated by the equation (3) and (4) 26:
| I ds |max | I ds |0 2 WCi r ( ) /( ) | Vg |max 2L
eff
r
(3)
(4)
where |Ids|max, |Ids|0, Vg, W, L, Ci, and U refer to the experimental maximum source-drain current at the maximum gate voltage |Vg|max, source-drain current at Vg = 0, gate voltage, channel width, channel length, capacitance per unit area of the gate dielectric layer and
the calculated carrier mobility based on equation (1), respectively. By substituting the equation (1) into equation (3), the reliability factor, r could be expressed as:
| I ds |max | I ds |0 2 r ( ) (Vg Vth ) 2 / I ds max | Vg | (5)
15 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Page 16 of 40
The reliability factor, r of our SCFET was measured to be 39.6%, which indicates the effective mobility, Ueff of 13.3 cm2 V-1 s-1. According to the equation (5), we found that the reliability factor is strongly related with the threshold voltage Vth: the lower the threshold voltage in an OFET device, the larger would be the reliability factor. Therefore, the high effective mobility in our devices is mainly due to the low threshold voltage Vth and high output current Ids, indicating the high intrinsic carrier transport in C8-BTBT single crystal microribbons.
A nonlinear behavior at low Vd is observed (Figure 2(d)), which is usually considered as an effect of the contact resistance between the electrodes and semiconductors.33-34 The
contact resistance effect can also be inferred from transfer curve (Figure 2(c)), i.e. the transfer curve demonstrates downward curvature at the highest Vg, indicating that the Ids may become more contact-limited as the interface of accumulation layer becomes more conducting at high Vg.
35-36
The mobility and threshold voltage against counts of 30
devices (fabricated in this work) can be seen in Figure 2(e) and (f), respectively, which
16 ACS Paragon Plus Environment
Page 17 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Page 18 of 40
Figure 3(a), the AFM image of the channel in SCFET shows a roughness difference
between the single crystal and HPCPS surfaces. The roughness of HPCPS film surface
is 1.71 nm (Figure 3(a)), while that of single crystal surface is 1.48 nm (Figure 3(b)). Considering the surface of the microribbon to be very flat (Figure S3 (a), Ra=0.255 nm) on SiO2 substrate, the flexible substrate should not change the molecular packing and surface morphology during the transfer process as it would result in roughness mismatch
between the flat C8-BTBT single crystal and relatively rough flexible substrate, as
illustrated by the schematic diagram in Figure 3(d). Based on the calculation in Support
information, it is evident that the roughness mismatch between the two materials has little
influence on the capacitance. The trap density of C8-BTBT SCFET in Figure 2(c) is 2.48×1012 cm-2, while it is smaller for the device fabricated on HPCPS/Si substrate17. In fact, there are fewer defects in C8-BTBT single crystal due to high quality single crystalline nature and no grainboundaries effect as compared to the bulk C8-BTBT based OFET. Therefore, the roughness mismatch between the two materials introduces more interfacial traps in the device, which hinder efficient carrier transport thereby deteriorating the device performance.[37-38] The
roughness mismatch between the microribbon and insulator surface appears randomly,
i.e. some flexible organic SCFETs could have higher mismatch density while the others
18 ACS Paragon Plus Environment
Page 19 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
may have relatively less. For the devices with smaller mismatch, the charge carriers can
transport efficiently with a mobility much closer to the intrinsic mobility of the single crystal.
While, for the devices with higher mismatch between the semiconductor and insulator
interface, the effect of mismatch defects will decrease the carrier mobility. Therefore, the carrier mobility for our 30 devices ranges from 9 cm2V-1s-1 to 33.4 cm2V-1s-1. This suggests
that the distribution of carrier mobility can be further reduced by decreasing the roughness mismatch. The highest mobility among recent reports on low operating voltage (|Vd| < 10 V) flexible OFETs based on various semiconductors and insulators is 6.3 cm2V-1s-1 (with a carrier mobility of >2 cm2V-1s-1) as evident in Table 1,16 whereas, we attained about 5.5 times higher mobility (33.4 cm2 V-1 s-1) as compared to the best reported low-voltage
flexible OFET devices so far.
19 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Paragon Plus Environment
Page 20 of 40
Page 21 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
Semiconducto
Dielectric
Umax
r
(nF/cm2)
(cm2V-1s-1)
Vd
YearRef
200739 200840 200941 200942 200916 200943 201144 201212 20132 201345 201828
This
Pentacene
Pentacene
Pentacene
Pentacene
Pentacene
C60
Polyvinyl alcohol(400) Sol-gel silica (260) BaTiO2 nanoparticles (106) BaSrTiO2 nanoparticles (216) Sol-gel silica (160) AlOx/polystyrene (300)
Substrate
(V)
2.6
-5
2×103
PET
3.5
-3
105
PET
3.5
-3
2 ×104
PET
3.4
-5
103
PET
6.3
-3
2 ×105
PET
2.2 (8e)
9.5
105
PEN
DNTT
AlOx/SAM (100)
2.1
-1.5
108
PEN
C10-DNTT
AlOx/SAM (68)
4.3
-2
108
PEN
DNTT
SAM+Al2O3 (280)
3
-5
107
PEN
PDVT-8
AlOx/SAM (-)
2.41
-1
106
PI
5.6
-3
33.4
-4
Pentacene
PAA+PI copolymer (20)
1.4 × 106
PET
C8-BTBT HPCPS (88.6)
Work
Ion/Ioff
105
PET
single crystal
Flexibility of C8-BTBT SCFETs. A C8-BTBT based SCFET with tensile strain loading and the bending test diagram can be seen in Figure 4(a). The device was attached on the
21 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Page 22 of 40
surface of a glass bottle in ambient atmosphere for 5 minutes, and then its electrical
properties in the bending state were tested. The carrier mobility for this device before bending was measured to be 18.9 cm2 V-1 s-1 (Figure S5). This device was tested at
bending radii (R) of 20 mm, 15 mm and 9 mm with tensile strains of 0.40%, 0.53% and
0.88%, respectively. Figure 4(b) shows the transfer curves for the device during bending
test, which indicate that the carrier mobility of the device decreased as a function of an
increase in tensile strain. A noticeable phenomenon in these transfer curves is the downward curvature at the highest Vg caused by the contact resistance effect, as discussed above. With a bending radius of 20 mm and 15 mm, the carrier mobility of the
device decreased very slightly, (1.1% and 3.8%, respectively). The mobility of the device
can still be retained by 83.3% compared with its original value under a bending radius of
9 mm. The variation in saturation mobility and the threshold voltage of the organic SCFET
at different tensile strains is shown in Figure 4(d). AFM image of the device channel
(Figure 4(c)) revealed no noticeable damage on the microribbon after bending tests. The
bending test induces an interfacial strain on the single crystal and the dielectric layer,
which may change the intermolecular spacing inside the single crystal leading to the 22 ACS Paragon Plus Environment
Page 23 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
degradation of the carrier mobility.46-47 It is worth noticing that the negative shifts in
threshold voltage of the device after 0.88% tensile strain loading were reduced by 13.3%
(-1.3 V to -1.5 V) compared with the initial state (Figure 4(d)). It may have caused by the
cracking or buckling of the gold electrodes with increased resistance of the electrodes, resulting in the need of a higher bias for transistor operation.48
(b)
(a)
Device L R Bottle
(d) (e)
(c)
Crystal
Substrate Substrate 4 m
Figure 4. (a) A C8-BTBT based flexible SCFET attached on the surface of a glass bottle and the
bending test schematic diagram. The radii of the bottles were 20 mm, 15 mm and 9 mm. Bending test
23 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Page 24 of 40
with bottles of different radii for 5 min: (b) Transfer curves for an organic SCFET and (c) the AFM image after bending test. (d) The change in the relative mobility and the threshold voltage of the device under different tensile strains.
Furthermore, a flexible organic SCFET was tested after various bending cycles with a
radius of 20 mm, as shown in Fig. 5(a)-(b). The carrier mobility for this device before bending was measured to be 18.3 cm2 V-1 s-1 (Figure S6). The device was bent every one
second for one time and the electrical performance was measured on a flat plate after bending, the schematic diagram for this bending test can be seen in a previous report13.
The saturated mobility of the device bent on the bottle surface can be retained by 88.3%
compared with its original value after 500 bending cycles, which was maintained until
1,000 bending cycles, as evident in Figure 5(b). For this device, the threshold voltage
also showed a negative shift from -1.2 V to -1.4 V. The AFM image of the device channel
shows no noticeable crack after bending test (Figure 5(c)). However, a bulk single crystal
bent under the same radius shows a large crack, as can be observed in Figure 5(d) and
5(e). The thickness of this bulk C8-BTBT single crystal microribbon was about 135 nm
(Figure 5(f)), which indicates that the bulk C8-BTBT single crystal cannot stand dynamic
24 ACS Paragon Plus Environment
Page 25 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
bending test even for 50 times. These results suggest that ultrathin C8-BTBT single
crystal is a more suitable option for flexible OFETs as compared to the bulk counterpart.
(a)
(b)
(c) 21.2 nm
2 m
(d)
(e)
(f) 135 nm
25 m
25 m
2 m
Figure 5. (a) Transfer curves, (b) the relative mobility and the threshold voltage with different bending times
and (c) the AFM image of a flexible SCFET bent on a 20 mm radius bottle for different bending times.
(d) The POM image in original state; (e) the POM image after 50 times bending and (f) the
corresponding AFM image for the frame selected area in (e) of a bulk C8-BTBT single crystal bent on
a 20 mm bottle with different bending times.
4. CONCLUSION 25 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Page 26 of 40
In conclusion, we fabricated low-voltage, ultrathin single crystal microribbons based
flexible OFETs with ultra-high carrier mobility and decent flexible stability. The solution
processed C8-BTBT single crystal microribbons used in our OFETs are as thin as ~21 nm. Our flexible devices exhibit an average saturated mobility of 18.5 cm2V-1s-1 and several devices showed a high mobility of > 30 cm2 V-1 s-1 under a low operating voltage
of -4 V only, which is the best performance for low-voltage, flexible OFETs reported to
date. We ascribe this high mobility observed in our flexible OFETs to the low charge traps
in C8-BTBT single crystal, and possibility of further reduction in the interfacial traps by the
polar chloropropyl chain in novel HPCPS dielectric layer. Besides, the carrier mobility of
the fabricated devices exhibited a small degradation without noticeable damage on the
single crystal microribbon after static bending test. With the bending radius of 20 mm and
15 mm, the carrier mobility of our devices showed only a slight decrease (1.1% and 3.8%,
respectively). Furthermore, it can still be retained by 83.3% compared with its original
value under a bending radius of 9 mm. As compared to the bulk C8-BTBT single crystal
based OFET which exhibited a large crack after 50 times dynamic bending test, our
ultrathin single crystal based counterpart demonstrates a much better dynamic force 26 ACS Paragon Plus Environment
Page 27 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
stability. Under a 20 mm bending radius, the mobility of the device decreased by only
11.7% after 500 bending times and without further decrease until 1,000 times bending
cycles. Our results reveal that OFETs with a rational combination of ultrathin single crystal microribbon as the active layer and HPCPS as the high-k gate insulator could be potential
candidates for applications in high performance flexible electronic devices.
ASSOCIATED CONTENT
Supporting Information.
The Supporting Information is available free of charge on the ACS Publications website
(http://pubs.acs.org).
Capacitance vs. voltage plots; optical image of C8-BTBT single crystal microribbon; POM
image of a SCFET and corresponding transfer curve with a reverse sweep; AFM image
of C8-BTBT single crystal on SiO2 substrate.
AUTHOR INFORMATION
27 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Page 28 of 40
Corresponding Author
*E-mail:
[email protected] (Hong Meng)
ORCID
Muhammad Umair Ali: 0000-0003-4115-0702
Yaowu He: 0000-0003-2887-735X
Hong Meng: 0000-0001-5877-359X
Notes
All authors have given approval to the final version of the manuscript and declare no
competing financial interest. ACKNOWLEDGMENTS
This work was financially supported by the China (Shenzhen)-Japan Technology
Collaboration Project (GJHZ20170313145614463). H. M. thanks the support from the
Guangdong Key Research Project (No. 2019B010924003), Shenzhen Engineering
Laboratory SFG (2016)1592. H.C. is supported by the Shenzhen Science and
28 ACS Paragon Plus Environment
Page 29 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
Technology Research Grant (JCYJ20180302153514509). M.Z. is supported by the
Shenzhen Science and Technology Research Grant (JCYJ20170412150946440). A.L.
and Y.H. acknowledge funding from the Shenzhen Science and Technology Research
Grant (JCYJ20160510144254604 and JCYJ20170412151139619).
REFERENCES
1. Mizukami, M.; Cho, S.-I.; Watanabe, K.; Abiko, M.; Suzuri, Y.; Tokito, S.; Kido, J.,
Flexible Organic Light-Emitting Diode Displays Driven by Inkjet-Printed High-Mobility Organic Thin-Film Transistors. IEEE Electron Device Lett. 2018, 39 (1), 39-42.
2. Kaltenbrunner, M.; Sekitani, T.; Reeder, J.; Yokota, T.; Kuribara, K.; Tokuhara, T.;
Drack, M.; Schwodiauer, R.; Graz, I.; Bauer-Gogonea, S.; Bauer, S.; Someya, T., An Ultra-Lightweight Design for Imperceptible Plastic Electronics. Nature 2013, 499 (7459),
458-463.
3. Fukuda, K.; Takeda, Y.; Yoshimura, Y.; Shiwaku, R.; Tran, L. T.; Sekine, T.; Mizukami,
M.; Kumaki, D.; Tokito, S., Fully-Printed High-Performance Organic Thin-Film Transistors and Circuitry on One-Micron-Thick Polymer Films. Nat. Commun. 2014, 5, 4147.
29 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Page 30 of 40
4. Oh, J. Y.; Rondeau-Gagne, S.; Chiu, Y. C.; Chortos, A.; Lissel, F.; Wang, G. N.;
Schroeder, B. C.; Kurosawa, T.; Lopez, J.; Katsumata, T.; Xu, J.; Zhu, C.; Gu, X.; Bae,
W. G.; Kim, Y.; Jin, L.; Chung, J. W.; Tok, J. B.; Bao, Z., Intrinsically Stretchable and Healable Semiconducting Polymer for Organic Transistors. Nature 2016, 539 (7629),
411-415.
5. Wang, B.; Huang, W.; Chi, L.; Al-Hashimi, M.; Marks, T. J.; Facchetti, A., High-k Gate Dielectrics for Emerging Flexible and Stretchable Electronics. Chem. Rev. 2018, 118 (11),
5690-5754.
6. Ren, H.; Cui, N.; Tang, Q.; Tong, Y.; Zhao, X.; Liu, Y., High-Performance, Ultrathin, Ultraflexible Organic Thin-Film Transistor Array Via Solution Process. Small 2018, 14
(33), 1801020.
7. Khim, D.; Xu, Y.; Baeg, K. J.; Kang, M.; Park, W. T.; Lee, S. H.; Kim, I. B.; Kim, J.; Kim,
D. Y.; Liu, C.; Noh, Y. Y., Large Enhancement of Carrier Transport in Solution-Processed Field-Effect Transistors by Fluorinated Dielectric Engineering. Adv. Mater. 2016, 28 (3),
518-526.
30 ACS Paragon Plus Environment
Page 31 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
8. Zhang, L.; Wang, H.; Zhao, Y.; Guo, Y.; Hu, W.; Yu, G.; Liu, Y., Substrate-Free UltraFlexible Organic Field-Effect Transistors and Five-Stage Ring Oscillators. Adv. Mater. 2013, 25 (38), 5455-5460.
9. Sekitani, T.; Zschieschang, U.; Klauk, H.; Someya, T., Flexible Organic Transistors and Circuits with Extreme Bending Stability. Nat. Mater. 2010, 9 (12), 1015-1022.
10. Xu, J.; Wang, S.; Wang, G.-J. N.; Zhu, C.; Luo, S.; Jin, L.; Gu, X.; Chen, S.; Feig, V.
R.; To, J. W. F.; Rondeau-Gagné, S.; Park, J.; Schroeder, B. C.; Lu, C.; Oh, J. Y.; Wang,
Y.; Kim, Y.-H.; Yan, H.; Sinclair, R.; Zhou, D.; Xue, G.; Murmann, B.; Linder, C.; Cai, W.;
Tok, J. B.-H.; Chung, J. W.; Bao, Z., Highly Stretchable Polymer Semiconductor Films Through the Nanoconfinement Effect. Science 2017, 355 (6320), 59-64.
11. Klauk, H.; Zschieschang, U.; Pflaum, J.; Halik, M., Ultralow-Power Organic Complementary Circuits. Nature 2007, 445 (7129), 745-748.
12. Zschieschang, U.; Kang, M. J.; Takimiya, K.; Sekitani, T.; Someya, T.; Canzler, T. W.;
Werner, A.; Blochwitz-Nimoth, J.; Klauk, H., Flexible Low-Voltage Organic Thin-Film Transistors and Circuits Based on C10-DNTT. J. Mater. Chem. 2012, 22 (10), 4273-4277.
31 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Page 32 of 40
13. Li, J.; Liu, D.; Miao, Q.; Yan, F., The Application of a High-k Polymer in Flexible LowVoltage Organic Thin-Film Transistors. J. Mater. Chem. 2012, 22 (31), 15998-16004.
14. Wang, Z.; Ren, X.; Leung, C. W.; Shi, S.; Chan, P. K. L., A UV-Ozone Treated
Amorphous Barium–Strontium Titanate Dielectric Thin Film for Low Driving Voltage Flexible Organic Transistors. J. Mater. Chem. C 2013, 1 (24), 3825-3832.
15. Wang, Z. R.; Xin, J. Z.; Ren, X.; Wang, X. L.; Leung, C. W.; Shi, S.; Ruotolo, A.; Chan,
P. K. L., Low Power Flexible Organic Thin Film Transistors with Amorphous
Ba0.7Sr0.3TiO3 Gate Dielectric Grown by Pulsed Laser Deposition at Low Temperature.
Org. Electron. 2012, 13 (7), 1223-1228. 16. Tan, H. S.; Mathews, N.; Cahyadi, T.; Zhu, F. R.; Mhaisalkar, S. G., The Effect of
Dielectric Constant on Device Mobilities of High-Performance, Flexible Organic Field Effect Transistors. Appl. Phys. Lett. 2009, 94 (26), 263303.
17. Cao, J.; Wei, X.; Che, Y.; Li, A.; He, Y.; He, C.; Zhu, Y.; Chen, X.; Li, T.; Murtaza, I.;
Yan, L.; Perepichka, D. F.; Meng, H., Polysiloxane–Poly(vinyl alcohol) Composite Dielectrics for High-Efficiency Low Voltage Organic Thin Film Transistors. J. Mater.
Chem. C 2019, 7 (16), 4879-4886. 32 ACS Paragon Plus Environment
Page 33 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
18. Ding, R.; Feng, J.; Dong, F. X.; Zhou, W.; Liu, Y.; Zhang, X. L.; Wang, X. P.; Fang, H.
H.; Xu, B.; Li, X. B.; Wang, H. Y.; Hotta, S.; Sun, H. B., Highly Efficient Three Primary
Color Organic Single-Crystal Light-Emitting Devices with Balanced Carrier Injection and Transport. Adv. Funct. Mater. 2017, 27 (13), 1604659.
19. Takeya, J.; Yamagishi, M.; Tominari, Y.; Hirahara, R.; Nakazawa, Y.; Nishikawa, T.;
Kawase, T.; Shimoda, T.; Ogawa, S., Very High-Mobility Organic Single-Crystal Transistors with In-Crystal Conduction Channels. Appl. Phys. Lett. 2007, 90 (10), 102120.
20. Zaumseil, J.; Friend, R. H.; Sirringhaus, H., Spatial Control of the Recombination Zone in an Ambipolar Light-Emitting Organic Transistor. Nat. Mater. 2005, 5 (1), 69-74.
21. Yang, F.; Cheng, S.; Zhang, X.; Ren, X.; Li, R.; Dong, H.; Hu, W., 2D Organic Materials for Optoelectronic Applications. Adv. Mater. 2018, 30 (2), 1702415.
22. Xu, C.; He, P.; Liu, J.; Cui, A.; Dong, H.; Zhen, Y.; Chen, W.; Hu, W., A General
Method for Growing Two-Dimensional Crystals of Organic Semiconductors by "Solution Epitaxy". Angew. Chem. Int. Ed. 2016, 55 (33), 9519-9523.
33 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Page 34 of 40
23. Wang, Q.; Yang, F.; Zhang, Y.; Chen, M.; Zhang, X.; Lei, S.; Li, R.; Hu, W., Space-
Confined Strategy toward Large-Area Two-Dimensional Single Crystals of Molecular Materials. J. Am. Chem. Soc. 2018, 140 (16), 5339-5342.
24. H $` #
B. i.; Kozmik, V.; Svoboda, J. í.; Novotná, V.; D
`& P. e.; Glogarová, M.,
Novel Liquid Crystals Based on [1]Benzothieno[3,2- b][1]benzothiophene. Liq. Cryst. 2003, 30 (5), 603-610. 25. Wang, C.; Dong, H.; Jiang, L.; Hu, W., Organic Semiconductor Crystals. Chem. Soc.
Rev. 2018, 47 (2), 422-500. 26. Choi, H. H.; Cho, K.; Frisbie, C. D.; Sirringhaus, H.; Podzorov, V., Critical Assessment of Charge Mobility Extraction in FETs. Nat. Mater. 2017, 17 (1), 2-7.
27. Pfattner, R.; Foudeh, A. M.; Chen, S.; Niu, W.; Matthews, J. R.; He, M.; Bao, Z., DualGate Organic Field-Effect Transistor for pH Sensors with Tunable Sensitivity. Adv.
Electron. Mater. 2019, 5 (1), 1800381. 28. Ji, D.; Li, T.; Zou, Y.; Chu, M.; Zhou, K.; Liu, J.; Tian, G.; Zhang, Z.; Zhang, X.; Li, L.;
Wu, D.; Dong, H.; Miao, Q.; Fuchs, H.; Hu, W., Copolymer Dielectrics with Balanced
34 ACS Paragon Plus Environment
Page 35 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
Chain-Packing Density and Surface Polarity for High-Performance Flexible Organic Electronics. Nat. Commun. 2018, 9 (1), 2339.
29. Liu, C.; Minari, T.; Lu, X.; Kumatani, A.; Takimiya, K.; Tsukagoshi, K., Solution-
Processable Organic Single Crystals with bandlike Transport in Field-Effect Transistors.
Adv. Mater. 2011, 23 (4), 523-526. 30. Ebata, H.; Izawa, T.; Miyazaki, E.; Takimiya, K.; Ikeda, M.; Kuwabara, H.; Yui, T.,
Highly Soluble [1]Benzothieno[3,2-b]benzothiophene (BTBT) Derivatives for HighPerformance, Solution-Processed Organic Field-Effect Transistors. J. Am. Chem. Soc. 2007, 129 (51), 15732-15733.
31. Jurchescu, O. D.; Popinciuc, M.; "
cI
$ B. J.; Palstra, T. T. M., Interface-
Controlled, High-Mobility Organic Transistors. Adv. Mater. 2007, 19 (5), 688-692.
32. Minemawari, H.; Yamada, T.; Matsui, H.; Tsutsumi, J.; Haas, S.; Chiba, R.; Kumai, R.; Hasegawa, T., Inkjet Printing of Single-Crystal Films. Nature 2011, 475 (7356), 364-
367.
33. Liu, C.; Xu, Y.; Noh, Y.-Y., Contact Engineering in Organic Field-Effect Transistors.
Mater. Today 2015, 18 (2), 79-96. 35 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Page 36 of 40
34. Liu, J.; Dong, H.; Wang, Z.; Ji, D.; Cheng, C.; Geng, H.; Zhang, H.; Zhen, Y.; Jiang,
L.; Fu, H.; Bo, Z.; Chen, W.; Shuai, Z.; Hu, W., Thin Film Field-Effect Transistors of 2,6diphenyl Anthracene (DPA). Chem. Commun. 2015, 51 (59), 11777-11779.
35. Sirringhaus, H., 25th Anniversary Article: Organic Field-Effect Transistors: the Path Beyond Amorphous Silicon. Adv. Mater. 2014, 26 (9), 1319-1335. 36. Braga, D.; Horowitz, G., High-Performance Organic Field-Effect Transistors. Adv.
Mater. 2009, 21 (14-15), 1473-1486. 37. Bolognesi, A.; Berliocchi, M.; Manenti, M.; Di Carlo, A.; Lugli, P.; Lmimouni, K.; Dufour,
C., Effects of Grain Boundaries, Field-Dependent Mobility, and Interface Trap States on the Electrical Characteristics of Pentacene TFT. IEEE Trans. Electron Devices 2004, 51
(12), 1997-2003.
38. Erlen, C.; Lugli, P., Analytical Model of Trapping Effects in Organic Thin-Film Transistors. IEEE Trans. Electron Devices 2009, 56 (4), 546-552.
39. Oyama, T.; Ye, R.; Baba, M.; Ohta, K., High Performance Pentacene Thin Film Transistors with a PVA Gate Dielectric. Mol. Cryst. Liq. Cryst. 2007, 471 (1), 205-211.
36 ACS Paragon Plus Environment
Page 37 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
40. Tan, H. S.; Kulkarni, S. R.; Cahyadi, T.; Lee, P. S.; Mhaisalkar, S. G.; Kasim, J.; Shen,
Z. X.; Zhu, F. R., Solution-Processed Trilayer Inorganic Dielectric for High Performance Flexible Organic Field Effect Transistors. Appl. Phys. Lett. 2008, 93 (18), 183503.
41. Cai, Q. J.; Gan, Y.; Chanpark, M. B.; Yang, H.; Lu, Z.; Li, C. M.; Guo, J.; Dong, Z.,
Solution-Processable Barium Titanate and Strontium Titanate Nanoparticle Dielectrics for Low-Voltage Organic Thin-Film Transistors. Chem. Mater. 2009, 21 (14), 3153-3161.
42. Gan, Y.; Cai, Q. J.; Li, C. M.; Yang, H.; Lu, Z.; Gong, C.; Chanpark, M. B., Solution-
Prepared Hybrid-Nanoparticle Dielectrics for High-Performance Low-Voltage Organic Thin-Film Transistors. ACS Appl. Mater. Interfaces 2009, 1 (10), 2230-2236.
43. Zhang, X.-H.; Potscavage, W. J.; Choi, S.; Kippelen, B., Low-Voltage Flexible Organic Complementary Inverters with High Noise Margin and High dc Gain. Appl. Phys. Lett. 2009, 94 (4), 043312.
44. Zschieschang, U.; Ante, F.; Kälblein, D.; Yamamoto, T.; Takimiya, K.; Kuwabara, H.;
Ikeda, M.; Sekitani, T.; Someya, T.; Nimoth, J. B.; Klauk, H., Dinaphtho[2,3-b:2
,3
-
f]thieno[3,2-b]thiophene (DNTT) Thin-Film Transistors with improved Performance and Stability. Org. Electron. 2011, 12 (8), 1370-1375. 37 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
Page 38 of 40
45. Kim, S. H.; Kang, I.; Kim, Y. G.; Hwang, H. R.; Kim, Y.-H.; Kwon, S.-K.; Jang, J., High
Performance
Ink-Jet
Printed
Diketopyrrolopyrrole-Based
Copolymer
Thin-Film
Transistors using a Solution-Processed Aluminium Oxide Dielectric on a Flexible Substrate. J. Mater. Chem. C 2013, 1 (13), 2408-2411.
46. Briseno, A. L.; Tseng, R. J.; Ling, M. M.; Falcao, E. H. L.; Yang, Y.; Wudl, F.; Bao, Z., High-Performance Organic Single-Crystal Transistors on Flexible Substrates. Adv. Mater. 2006, 18 (17), 2320-2324.
47. Ho, M. T.; Tao, Y. T., Effect of Bending on the Electrical Characteristics of Flexible Organic Single Crystal-Based Field-Effect Transistors. J. Vis. Exp. 2016, (117), e54651.
48. Sokolov, A. N.; Cao, Y.; Johnson, O. B.; Bao, Z., Mechanistic Considerations of Bending-Strain Effects within Organic Semiconductors on Polymer Dielectrics. Adv.
Funct. Mater. 2012, 22 (1), 175-183.
38 ACS Paragon Plus Environment
Page 39 of 40 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Applied Materials & Interfaces
TOC graphics
39 ACS Paragon Plus Environment
ACS Applied Materials & Interfaces 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60
ACS Paragon Plus Environment
Page 40 of 40