A low magnification SEM image of the fabricated 2 2 ZnO based triode array is

Similar documents
ZnO nanostructures epitaxially grown on ZnO seeded Si (100) substrates by chemical vapor deposition

Structural, Optical & Surface Morphology of Zinc Oxide (ZnO) Nanorods in Molten Solution

Fabrication of Zinc Oxide Thin Films for Acoustic Resonators

Piezoelectric Nanogenerator Using p-type ZnO Nanowire Arrays

NANOSTRUCTURAL ZnO FABRICATION BY VAPOR-PHASE TRANSPORT IN AIR

GaN/ZnO and AlGaN/ZnO heterostructure LEDs: growth, fabrication, optical and electrical characterization

Structural and Optical Properties of Single- and Few-Layer Magnetic

Epitaxial Growth of ZnO Nanowires on Graphene-Au

Nanostructured ZnO as a solution-processable transparent electrode material for low-cost photovoltaics

Photoelectrochemical Water Splitting

Synthesis and Characterization of Mn 2+ Doped Zn 2. Phosphor Films by Combustion CVD Method

Outline of the talk. FIB fabrication of ZnO nanodevices. Properties of ZnO 4/19/2011. Crystal structure of ZnO. Collaborators. Wurtzite structure

Supplementary Fig. 1.

Highly active oxide photocathode for. photoelectrochemical water reduction

A Solution Processed ZnO Thin Film

Reagent-Free Electrophoretic Synthesis of Few-Atom- Thick Metal Oxide Nanosheets

Large-Scale Synthesis of Six-Nanometer-Wide ZnO Nanobelts

Fabrication of ZnO nanotubes using AAO template and sol-gel method

Journal of Crystal Growth

Structural Properties of ZnO Nanowires Grown by Chemical Vapor Deposition on GaN/sapphire (0001)

Supplementary Figures

CHAPTER 6. BLUE GREEN AND UV EMITTING ZnO NANOPARTICLES SYNTHESIZED THROUGH A NON AQUEOUS ROUTE

Supporting Information. Observing Solid-state Formation of Oriented Porous. Functional Oxide Nanowire Heterostructures by in situ

Supplementary Figure 1. Sample preparation schematic. First (Stage I), square islands of MoO 3 are prepared by either photolithography followed by

Chapter VI Development of ISFET model. simulation

Strain-Gated Field Effect Transistor of a MoS 2 -ZnO 2D-1D Hybrid-Structure

ULTRA THIN INDIUM TIN OXIDE FILMS ON VARIOUS SUBSTRATES BY PULSED LASER DEPOSITION

Investigation of Structure, Morphology, Optical And Luminescent Properties of Hydrothermally Grown Zno Nanorods for Photocatalytic Applications

Supporting Information

Complex ZnO Nanotree Arrays with Tunable Top, Stem and Branch Structures

Characterization of Zinc Oxide Nanolaminate Films. B. J. Oleson, L. M. Bilke, J. S. Krueger, S. T. King

Path to High-Quality Films on Continuous Substrates

LIQUID JUNCTION PHOTOCELLS SYNTHESIZED WITH DYE COATED ZINC OXIDE FILMS. Department of Physics, University of Peradeniya, Peradeniya, Sri Lanka

Keywords: Thin films, Zinc Oxide, Sol-gel, XRD, Optical properties

Supplementary Information

Hydrogen-Sensing Characteristics of Palladium-Doped Zinc-Oxide Nanostructures

Supporting Information. Solar Cells and the Improvement on Open-Circuit. Voltage

Supporting Information

Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, , P. R.

THE EFFECTS OF DOPING CONCENTRATION ON THE ELECTRICAL PERFORMANCE OF DC-SPUTTERED p-zno/n-si HETEROJUNCTION

The electrical properties of ZnO MSM Photodetector with Pt Contact Electrodes on PPC Plastic

Supporting Information

Supplementary Figures

Abstract. Keywords: Zinc Oxide, Eu doped ZnO, Dy doped ZnO, Thin film INTERNATIONAL JOURNAL OF INFORMATION AND COMPUTING SCIENCE ISSN NO:

SPONTANEOUS AND STIMULATED EMISSION OF ZnO NANORODS OF DIFFERENT SHAPE

CHAPTER 3. EFFECT OF PRASEODYMIUM DOPING ON THE STRUCTURAL AND OPTICAL PROPERTIES OF ZnO NANORODS

Department of Electrical & Computer Engineering, The Ohio State University, 205 Dreese Lab, 2015

Preparation of ZnO Nanowire Arrays Growth on Sol-Gel ZnO-Seed-Coated Substrates and Studying Its Structure and Optical Properties

Supporting Information

CHAPTER 8 SUMMARY AND FUTURE SCOPE

Influence of Indium doping on Zinc oxide thin film prepared by. Sol-gel Dip coating technique.

Thin-film barriers using transparent conducting oxides for organic light-emitting diodes

Theerapong Santhaveesuk, * Duangmanee Wongratanaphisan and Supab Choopun

Low-temperature growth and Raman scattering study of. vertically aligned ZnO nanowires on Si substrate

The Effect of Stabiliser s Molarity to the Growth of ZnO Nanorods

Structural and luminescent properties of ZnO flower-like microstructures synthesized using the chemical bath deposition method

Engineering of efficiency limiting free carriers and interfacial energy. barrier for an enhancing piezoelectric generation

ABSTRACT. DLC Thin Film Assisted ZnO Nanowires Growth. Sheng-Yu Young, Master of Science, 2008

ABSTRACT 1. INTRODUCTION

Growth and Characterizations of Electrochemically Deposited ZnO Thin Films

SUPPLEMENTARY INFORMATION

Analysis of Li-related defects in ZnO thin films influenced by annealing ambient

Evidence of intrinsic ferromagnetism in individual dilute magnetic semiconducting nanostructures O-K. (a) Zn-L Zn-L 2,3

ZnO Thin Films Synthesized by Chemical Vapor Deposition

PREPARATION AND CHARACTERIZATION OF METAL OXIDE NANOPOWDERS BY MICROWAVE- ASSISTED COMBUSTION METHOD FOR GAS SENSING DEVICES

Chapter CHAPTER 7. ELECTRICAL PROPERTIES OF ZnO DOPED MAGESIUM ALUMIUM SILICATE GLASS-CERAMICS

Influence of Growth Time on Zinc Oxide Nano Rods Prepared By Dip Coating Method

Supplementary Figures

CHAPTER 4. CHARACTERIZATION OF ZINC DOPED TIN OXIDE (Zn:SnO 2 ) THIN FILMS

Solution-processed ZnO films as an alternative to sputtered buffer layers for inorganic photovoltaics

Polychiral Semiconducting Carbon Nanotube-Fullerene Solar Cells. Supporting Information

GCEP award #40654: High-Efficiency, Low-Cost Thin Film Solar Cells

Electric field induced reversible control of visible. photoluminescence from ZnO nanoparticles

Technology and TEM characterization of Al doped ZnO nanomaterials

Ceramic Processing Research

Method to Convert a Horizontal Furnace to Grow ZnO Nanowires for Gas Sensing by the VLS Method.

CHAPTER 8 SYNTHESIS, STRUCTURAL, OPTICAL AND ELECTRICAL PROPERTIES OF. TRANSITION METAL (TM) DOPED ZnO NANORODS. (TM=Mn, Co, Ni AND Fe).

Deposition of aluminum-doped zinc oxide films by RF magnetron sputtering and study of their surface characteristics

ABSTRACT. GROWTH AND TRANSPORT PROPERTIES OF Sb-DOPED ZnO NANO/MICROWIRES. by Nada Ali Masmali

A Facile Method for Enhancing the Sensing Performance of Zinc Oxide. Nanofibers Gas Sensors

Growth of ZnO nanoneedles on silicon substrate by cyclic feeding chemical vapor deposition: Structural and optical properties

Interface and defect structures of Zn ZnO core shell heteronanobelts

Fe-doped ZnO synthesized by parallel flow precipitation process for improving photocatalytic activity

Tungston Doped ZnO Thin film Prepared by Spray Pyrolysis for enhanced Hydrogen Sensing

Exploring Physical And Optical Behavior Of Co:Zno Nanostructures

Electronic Supplementary Information

Selective MOCVD Growth of ZnO Nanotips

Supplementary Information

Transparent ALD-grown Ta2O5 protective layer for highly stable ZnO photoelectrode in solar water splitting

A Correlation between Optical and Structural Property of. ZnO Nanocrystalline Films

List of Figure. Figure 1.1. Selective pathways for the metabolism of arachidonic acid

ALD and CVD Ni using Ni Amidinate Precursor

REACTIVE HIGH POWER IMPULSE MAGNETRON SPUTTERING OF ZINC OXIDE FOR THIN FILM TRANSISTOR APPLICATIONS. Dissertation. Submitted to

Evolution of Zinc Oxide Nanostructures through Kinetics Control

Metal-Semiconductor Zn-ZnO Core-Shell Nanobelts and Nanotubes

Supporting Information

ZnO Thin Films Generated by Ex-Situ Thermal Oxidation of Metallic Zn for Photovoltaic Applications

Direct and Large-Area Growth of One-Dimensional ZnO Nanostructures from and on a Brass Substrate

Transparent p-n Heterojunction Thin Film Diodes

Direct Growth of Feather-Like ZnO Structures by a Facile Solution Technique for Photo-Detecting Application

Transcription:

Chapter 6 Characteristics of Field Emission Triode 6.1 Planar Gated Field Emission Triode 6.1.1 Structural and Electrical Analysis A low magnification SEM image of the fabricated 2 2 ZnO based triode array is shown in the inset of Fig. 6.1, indicating that the cathode active region is a square opening of 100 100 µm 2, and the distance between the two active regions is 500 µm. The ZnO NWs are successfully and selectively grown inside the gate hole with ZnO seeding areas, but no NWs and other impurities are grown on the gate regions. Figure 6.1 is the enlarged image of the triode device, in which well-aligned ZnO NWs with an average diameter of 50 nm and a number density of 3.4 10 10 cm -2. These ZnO NWs are randomly oriented, uniformly and selectively grown on ZnO seeding layers inside the cathode active regions. The cross sectional SEM image of ZnO NWs on the substrate is shown in Fig. 6.1(b), indicating that the ZnO NWs were directly grown on the substrate with average length of 500 nm. The polycrystalline ZnO seeding film with the distinct orientation results in the nonvertical random distribution of ZnO NWs. Figure 6.2 (a) shows the XRD pattern of the ZnO NWs of the field emission triode. The peaks at 33.08 o and 38.5 o in the XRD patterns are caused by the Si substrate and Al metal gate, respectively. The crystal structure of these ZnO NWs is wurtzite and no other phases appear. The lattice constants calculated from the XRD patterns of hydrothermally grown ZnO NWs are a = b = 3.25 Å and c = 5.21Å, which are consistent with that recorded in ICDD No. 80-0074. The HR-TEM image and the corresponding selected area electron diffraction (SAED) pattern of hydrothermally grown ZnO NWs are shown in Fig. 6.2 (b), illustrating the growth orientation and 94

crystal structure of the NWs. As shown in the figure, the ZnO NWs grew uniformly along [002] direction and the distance between parallel [002] lattice fringes of the ZnO NW is 5.21 Å. The SAED pattern indexed in Fig. 6.2(b) shows that the ZnO nanowire is a single crystalline structure. The lattice constants calculated from the indexed pattern are a = b = 3.25 Å and c = 5.21 Å, which are consistent with those calculated from the XRD result. The emission current density (J) versus gate bias (V g ) characteristic plots at various applied electric fields (E a ) are shown in Fig. 6.3(a), indicating that a controllable behavior could be divided into three parts: gate leakage region, linear region and saturation region. After the E a becomes larger than the threshold electric field, the electrons can emit from ZnO NW emitters without applying V g. Then, the J decreases with an increase in V g in the gate leakage region. With an increase of V g from 0 V, the electric field gradient near the ZnO NW emitters will increase due to the short emitter-gate spacing, and consequently some emitted electrons might be trapped by the gate under the gate leakage region which results in the lowering of J., The emission current density in the gate leakage region is decreasing as the gate bias increases since there are more electrons trapped by the gate. As the V g is continuously increased up to 14 V, the J abruptly increases at linear region. The linear intercept on V g axis is defined as threshold gate voltage of the linear region, V gth. It is believed that, the induced electric field gradient in the linear region is large enough to accelerate the electrons; consequently, the emitting electrons gain the momentum while passing through the gate to the anode without being trapped. Finally, the field emission current density is saturated as the V g is larger than 18 V. The high emission current of the triode operated in saturating region may be due to the short gate-tip spacing, small gate aperture and high aspect ratio of the ZnO NWs. The J saturates in the saturating region is owing to the space charge effect of the semiconductor emitters. 189 Here, the 95

gate leakage region is defined as the field emission off region and the saturation region is the on region. Then, the on/off current density ratio of this field emission triode is about 10 2 under the anode electric field of 2.2 V/µm. The field emission characteristics can also be observed in the variation of small single transconductance (g m ). Figure 6.3 (b) depicts the relationships between g m and V g of the ZnO NW-based field emission triode. The g m is expressed as the following: g m di e = [6.1] dv g V a It is to be noted that the g m is nearly zero below V gth because the I e is very small at the gate leakage region. The g m increases in the linear region, goes through a maximum at the point of inflection of linear region to saturation region in the J-V g curve, and then decreases in the saturating region. The ZnO NW based triode exhibits a high g m of 2.2 µs under the applied electric field of 2.2 V/µm and a low operating gate bias of 17 V which is the optimized operation voltage of the field emission triode. The µ is an another parameter to evaluate the ability of gate voltage on the emission current density, according to the anode voltage (V a ) and the gate voltage (V g ), which is expressed as, dv µ = a [6.2] dv g I From Fig. 6.3 (a), µ is about 100 under the current density of 2 ma/cm 2. Although this µ value is smaller than that (µ=250) of a triode based on plasma-enhanced chemical vapor deposition diamond film, but the low temperature (75 o C) synthesized ZnO NWs is the first time to be used in the fabrication of the field emission triode device with the controllable ability. The relationship between J and E a of the ZnO NW-based triode for different V g is shown in Fig. 6.3 (c). The turn on electric field (E on, current density of 1.0 µa/cm 2 ) 96

and threshold electric field (E th, current density of 1.0 ma/cm 2 ) are 1.6 and 2.1 V/µm under the zero gate bias, respectively. As the V g increases to 10 V, the J is depressed to 36 µa/cm 2 under the E a of 2.2 V/µm. While the V g increases to 18 V, the E th slightly decreases to 2.0 V/µm but the J abruptly increases to 12 ma/cm 2 under the E a of 2.2 V/µm. The corresponding F N plots [ln(j/e 2 ) vs. E -1 ] of the ZnO NW-based triode are depicted in the inset of Fig. 6.3(c), indicating that the measured field emission characteristics fit the F N relationship. The F N relationship is as the following: J = 2 Aβ E φ 2 3/ 2 Bφ exp [6.3] βe Where J is the current density, E the applied field, Φ the work function of the ZnO (5.37 ev), β the field enhancement factor, A= 1.56 10 10-2 (AV ev) and 3-3/2 B = 6.83 10 (VeV µm -1 ). 136 Thus, the value of β can be calculated from the slope of the F-N plot. As shown in the figure, the F-N plot under a V g of 10 V is deviated from the F-N fitting, and that under V g of 0 and 18 V are obeying the relationship with the same slope. The calculated β value of ZnO NW-based triode under a V g of 0 V is 3340. It is well known that the β value depends only on the geometry, structure, tip size and number of the emitters on the substrate, thus, the β value should be constant under various gate voltages. It is suggested that the observed large deviation from F-N fitting under a V g of 10 V is attributed to that the gate trapping is the main mechanism at the gate leakage region. The measurement of field emission properties of field emission triode based on low temperature synthesized ZnO NWs under a 30 W incandescent lamp irradiation with V g of 20 V (operating in the gate controlled saturation region) was carried out to realize the influence of the illumination on the triode. As shown in Fig. 6.4 (a), the triode operating in the saturation region exhibits the typical field emission characteristics under the illumination. This J-E curve can also be divided into three 97

parts: zero emission (region 1 of Fig. 6.4 (a)), F N field emission (region 2) and current saturation regions (region 3). The E on and E th decrease to 0.9 and 1.3 V/µm, respectively and the maximum current density increases to 2.5 A/cm 2 under the V g of 20 V and E a of 2.2 V/µm. The β value (3050) of illuminated ZnO NWs based field emission triode calculated from the slopes of the F N plot (inset in the Fig. 6.4 (a)) is close to that of dark one. Therefore, it is demonstrated that the carriers in the ZnO NWs are excited during the illumination leading to increase the emission current density. The J-V g plots with various E a of triode under a 30 W incandescent lamp irradiation are shown in Fig. 6.4(b). It is indicated that triode under such an illumination keeps the controllable behavior that could be separated into gate leakage region, linear region and saturation region. There is a large increase in the field emission current density under the optical illumination and the threshold gate bias of the triode operated under illumination is about 20 V. The average current density in the off region under the E a of 2.2 V/µm is about 0.1 ma/cm 2, while that in the on region is about 0.5 A/cm 2. Thus, the triode performs the controllable field emission characteristics under the illumination, and the on/off current density ratio of this triode is about 5000 under the anode electric field of 2.2 V/µm. The inset in Fig. 6.4 (b) shows the relationships between g m and V g of the with E a of 1.6 V/µm under the illumination, which exhibits a high g m of 10 µs under the anode field of 1.6 V/µm and a gate bias of 20 V which is the optimized operation voltage of such a triode. Moreover, the µ value is about 200 under 2 ma/cm 2. Obviously, not only the emission current density was photoenhanced but the controllable ability is also enhanced under the optical illumination. Figure 6.5 shows the field emission characteristics of the triode measured under the various pressures to realize the influence of measuring pressure on the 98

characteristics. This ZnO NWs based triode was swept from 0 to 2.2 V/µm with V g of 0 V (avoiding the effects from the gate) under 1 10-6 Torr in the first 29 operations. In the first 29 tests, the field emission current densities are similar with the average current density of 2 ma/cm 2. Then, the following 2 sweeps were carried out under 1 10-3 Torr with Ar gas flowing in, and the current density is abruptly increased to 27 ma/cm 2. Finally, the pressure was decreased to 1 10-6 Torr again for the last 19 operations and the field emission current density remains in the average value of 27 ma/cm 2, which shows significant increase in comparison with that in the first 29 tests under the same measuring pressure. The field emission characteristics of the 1 st and 50 th sweeps of the triode are depicted in Fig. 6.5 (b), indicating that the E th of 1 st sweep is 2.1 V/µm while that of 50 th sweep 1.6 V/µm. The calculated β value of 50 th sweep of this triode device is 5203. Thus, such a triode exhibits the better emission properties, including the low turn-on and threshold electric fields, high emission current density and high β value after the measurement at high pressure of 1 10-3 Torr The field emission ability and β value strongly depend upon the morphology of ZnO NWs. Figure 6.6 shows the FE-SEM image of the ZnO NWs after measuring in the high pressure and 50 times sweep, indicating that these ZnO NWs have smaller tips than the origin ones (Fig. 6.1(a)). It is suggested that these ZnO NWs measured in the high pressure were bombarded by argon ions leading to the formation of the smaller tips at the front of the NWs. Therefore, the observed improved emission properties of the triode are mainly due to such smaller tips of ZnO NWs. This result also provides a possible simple method to enhance the field emission properties of ZnO NWs based triode. Based on the previous studies of our group 136, the vapor-liquid-solid (VLS) synthesized ZnO NWs with the higher aspect ratio and smaller tip diameter performed the better field emission characteristics (low threshold electric field, high current 99

density and high β value). However, those ZnO NWs applied in field emission devices are restricted to the high reaction temperature. In this article, the hydrothermal method provides a low temperature process to fabricate the ZnO NWs, which would be not only compatible with the Si-based microelectrics fabrication process but also possibly used in the polymer-based flexible electrooptical applications. 6.1.2 Conclusions In this work, a field emission triode based on low temperature hydrothermally grown ZnO NWs was fabricated and characterized. The ZnO NWs based triode emitter was designed with a 100 100µm 2 cathode active region, which exhibits the gate controllable behavior and emits electrons at a threshold gate bias of 14 V with saturation current density of 12 ma/cm 2, g m of 2.2 µs at a low operating E a of 2.2 V/µm, and on-off ratio of up to 10 2. These controllable field emission properties of the triode can be enhanced under illumination. Moreover, the ZnO NWs based triode performs the better field emission properties after it was measured under high pressure leading to the formation of smaller tips of ZnO NWs. Our field emission triode with controllable transistor characteristics is expected to be appropriate for field emission display applications. 100

6.2 Under Gated Field Emission Triode 6.2.1 Structural and Electrical Analysis The FE-SEM images of the fabricated ZnO based under gate structure are shown in the Figs. 6.7 (a), (b) and (c), indicating that the cathode active line is 10 µm in width, and the distance between the two active lines is 10 µm, respectively. The ZnO NWs are successfully and selectively grown on the ZnO seeding areas on the cathode metal regions, but no NWs and other impurities are grown on the gate metal regions. Figs. 6.7. (b) and (c) are the enlarged images of the under gate field emission device, the surface morphology of ZnO NWs on Al cathode metal can be classified into two morphology types: one type is the ZnO NWs that aggregate to form the flower-like secondary particles region and another is the few randomly distributed NWs grown on part of the cathode metal. Such a morphology variation is caused by the high lattice mismatch between Al (a = b = c = 4.05 Å) and ZnO (a = b = 3.25 Å, c= 5.21 Å). The lattice mismatch leads to be difficulty for the direct deposition of ZnO NWs on the Al cathode metal. Once ZnO grains are deposited on the substrate, the subsequent deposition of ZnO would be directed to the existing crystals. The type of nucleation results in forming the flower-like secondary particles. Thus, the ZnO NWs based under gate field emission device with the surface morphology of nonuniformity, random distribution and low number density. Based on the previous studies of our group 194, this flower-like ZnO NWs perform the better field emission characteristics (low threshold electric field, high current density and high β value) is suitable for field emission applications. The relationship between emission current density (J) and applied anode electric field (E a ) of the ZnO NWs based under gate field emission triode for different gate bias (V g ) is shown in Fig. 6.8. As shown in the figure, the emission current density is 101

as small as the level of 10-7 A/cm 2 under the zero gate bias. While the V g increases to 7.5 V, the electric threshold field (under current density of 1 ma/cm 2, E th ) is 1.5 V/µm but the J abruptly increases to 27 ma/cm 2 under E a of 2.2 V/µm. Thus, the on/off current density ratio is up to 50000 under the anode electric field of 2.2 V/µm. The corresponding Fowler-Norheim (F N) plots [ln(j/e 2 a ) vs. E -1 a ] are depicted in the inset of Fig. 6.8, and the field enhancement factor, β, can be calculated from the slope of F N plot by adopting the work function of ZnO (5.37 ev). As shown in the figure, the F-N plot under V g of 7.5 V is obeying F-N relationship, and the calculated β value of ZnO NWs based under gate field emission device under a V g of 7.5 V is 4551. Therefore, the field emission characteristics can be easily modulated by gate bias. Figure 6.9 (a) shows the V g dependence of J under various E a of a under low temperature synthesis ZnO NW based gate field emission triode with 10 µm cathode width. As shown in the figure, the electron can t be emitted from ZnO NW emitters under the V g of 0 V. The emission current started at a gate voltage of 6.0 V, and the anode current density abruptly increases to 27 ma/cm 2 under the anode electric field of 2.2 V/µm as the gate voltage was increased to 7.5 V. The linear intercept on V g axis is the linear region threshold gate voltage, V gth, and the threshold gate voltage of this under-gate field emission device is 6.5 V. The corresponding F N plots (ln(i/v 2 g ) vs. V -1 g ) are shown in the inset of Fig. 6.9, indicating that the field emission ability is obeying F-N relationship under the various anode bais. Like the gate bias increases, the anode electric field increases induce the change in the current density. Thus, the field emission under gate triode is not only the gate controllable but an anode controllable device. The field emission characteristics also could be observed in the variation of small single transconductance (g m ) and amplification factor (µ). The inset in Fig. 6.9 (b) depicts the relationships between g m and V g of the ZnO NW-based under-gate field 102

emission triode. It is to be noted that the g m is nearly zero below V gth because the I e is small at zero emission region. It goes through a maximum at the point of inflection of linear region in the I a -V g curve. The ZnO NW based under-gate field emission device exhibits a high g m of 0.38 ms under the applied electric field of 2.2 V/µm and a low operating gate bias of 7.5 V which is the optimized operation of the field emission triode. From Fig. 6.9(a) µ 400 under the current density of 15 ma/cm 2 which is larger than that of planer triode based on low temperature ZnO NWs fabricated by our group 195 ( µ 100). As the point of view, under gate field emission triode with the controllable ability is suitable for the FED applications. 6.2.2 Conclusions In this study, an under-gate field emission device based on low temperature hydrothermally grown ZnO NWs was successfully fabricated. The ZnO NW based under-gate emitter was design with a 10 µm cathode active region in width. This device exhibits the gate controllable behavior and emits electrons with the V gth of 7 V and the J up to 27 ma/cm 2 under the V g of 7.5 V and E a of 2.2 V/µm. The triode also displays a high g m of 0.38 ms at a low operating E a of 2.2 V/µm and V g of 7.5 V. Thus, this insulator patterning under gate field emission triode with controllable characteristics is appropriate for field emission displays applications. 103

Figure 6.1 (a) FE SEM micrographs of the triode near the gate edge. The inset is the 4 5 array triode with ZnO NWs islands grown inside gate holes. (b) Cross sectional FE SEM image of ZnO NWs on the substrate. 104

Figure 6.2 (a) XRD pattern of ZnO NWs triode. (b) HRTEM micrograph of ZnO NWs, and the inset is the corresponding SAED of the NWs. 105

Figure 6.3 (a) Field emission current density versus gate voltage (J V g ) curves under the various applied electric field. (b) Relation of transconductance versus gate voltage of the field emission triode. (c) Field emission current density versus applied electric field curves under the gate voltage of 0, 10 and 18V, respectively. The inset is the corresponding Fowler Nordheim plots. 106

Figure 6.4 (a) Photoenhanced field emission characteristics of ZnO NWs triode device operating at 20 V of V g. The insert is the corresponding F N plots. (b) Photoenhanced field emission current density versus gate voltage (J V g ) curves under the various applied electric field, and the insert is the gm vs. V g under E a of 2.2 V/µm. 107

Figure 6.5 (a) The emission current density of ZnO NWs based field emission triode under various pressures. (b) The 1 st and 50 th sweep of J-E a curves and the corresponding F-N plots. Figure 6.6 FE-SEM images of ZnO NWs after 50 th J-E a sweeps. 108

Figure 6.7 FE SEM micrographs of the under-gate field emission triode. 109

Figure 6.8 Field emission current density versus applied electric field curves under the gate voltage of 0 and 7.5V, respectively. The inset is the corresponding Fowler Nordheim plot under gate voltage of 7.5V. 110

Figure 6.9 (a) Field emission current density versus gate voltage curves under the various anode electric fields. The inset is the corresponding F-N plot under anode electric field of 2.2 V/µm. (b) The relation of transconductance versus gate voltage of the under-gate field emission device. 111