Evaluation of interface state density in three … 2012 Master thesis Evaluation of interface state...

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1 2012 Master thesis Evaluation of interface state density in three-dimensional SiO 2 gated MOS capacitors Supervisor Professor Hiroshi Iwai Department of Electronics and Applied Physics Interdisciplinary Graduate School of Science and Engineering Tokyo Institute of Technology 10M53567 Wei Li

Transcript of Evaluation of interface state density in three … 2012 Master thesis Evaluation of interface state...

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2012 Master thesis

Evaluation of interface state density in

three-dimensional SiO2 gated MOS capacitors

Supervisor

Professor Hiroshi Iwai

Department of Electronics and Applied Physics

Interdisciplinary Graduate School of Science and

Engineering

Tokyo Institute of Technology

10M53567

Wei Li

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CONTENTS

Chapter 1 Introduction 1.1 CMOS Scaling 5 1.2 Planar Device Scaling Limit 6 1.3 Introduction of Three-Dimensional Structure 9 1.4 Purpose of This Thesis 13 References 14

Chapter 2 Fabrication and Characterization Method 2.1 Substrate Cleaning 17 2.2 Thermal Oxidation Process 17 2.3 Photolithograph 19 2.4 RF Magnetron Sputtering 22 2.5 Thermal Evaporation for Al Back Contact 23 2.6 Rapid Thermal Annealing Process 24 2.7 Capacitance-Voltage (C-V) Curves 25 2.8 Conductance Method 29 2.9 Quasi-static Method 32 2.10 Scanning Electron Microscopy (SEM) Method 34 2.11 Conclusion of This Chapter 36 References 37

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Chapter 3 Interface State Density Extraction of Three-Dimensional Channel Structure 3.1 Device Fabrication Process 39 3.2 Analysis of Fin Structure with SEM Images 41 3.3 Analysis of C-V Curves 43 3.4 Extraction of Interface State Density of planar and Fin devices by Quasi-static C-V Method 44 3.5 Extraction of Interface State Density of planar devices by Conductance Method 47 3.6 Conclusion of This Chapter 50 References 51

Chapter 4 Modeling of Conductance Spectra by Deconvolution 4.1 Numerical simulation of surface potential of 3D channel 53 4.2 Deconvolution of Conductance Spectra of Fin Devices 54 4.3 Conclusion of This Chapter 55 References 56

Chapter 5 Conclusion of This Study 5.1 Conclusion 57 Acknowledgments

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Chapter1 Introduction

1.1 CMOS Scaling

1.2 Planar Device Scaling Limit

1.3 Introduction of Three-Dimensional Structure

1.4 Issues of Three-Dimensional Structure

1.5 Purpose of This Thesis

References

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1.1 CMOS Scaling The semiconductor industry has been sustained over the past four decades by the step

change in functionality and performance from one technology generation to another. As

device dimensions are shrinking, the speed increases and the energy consumption

reduces. A hierarchy of reasons related to fabrication and device operation impose

fundamental physical limits on how small a transistor can be made and still operate as a

transistor. Moore’s Law describes a long-term trend in the history of computing

hardware: the number of transistors that can be placed inexpensively on an integrated

circuit doubles approximately every two years.

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This can be explained using the constant-field scaling theory which was proposed by Dennard et al. in 1974. Tab. 1.1.1 shows the detail of this constant-field scaling theory.

Scaling Factor Device dimension tox, L, W 1/κ Doping concentration Na κ Voltage V 1/κ Current I 1/κ Capacitance 1/κ Delay time per circuit 1/κ Power dissipation per circuit 1/κ2 Power density 1

Table 1.1.1 Scaling factors of the constant-field scaling theory proposed by Dennard et al. in 1974[1.1.1].

1.2 Planar Device Scaling Limit

Moore’s Law scaling has continued for more than half a century and is expected to

continue until at least 2015 or 2020. However, the 2010 update to the International

Technology Roadmap for Semiconductors has growth slowing at the end of 2013, after

which time transistor counts and densities are to double only every three years. On 13

April 2005, Gordon Moore stated in an interview that the law cannot be sustained

indefinitely: “It can’t continue forever. The nature of exponentials is that you push them

out and eventually disaster happens.” He also noted that transistors would eventually

reach the limits of miniaturization at atomic levels.

There are four main reasons that explains why CMOS will reach its scaling limit in the

near future: 1) the increment of tunneling and leakage currents, 2) lithography-based

technique limit, and 3) economic limitation [1.2.1].

1) Increment of tunneling and leakage currents

The gate electrode together with gate dielectric controls the switching operation of

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CMOS transistors. The voltage of the gate electrode controls the flow of electric

current across the transistor. The gate dielectric should be made as thin as possible to

increase the performance of the transistor. In additional, it is critical to keep short

channel effects under control when a transistor is turned on and reduce sub-threshold

leakage when a transistor is off. In order to maintain the electric field as CMOS

transistors are scaled, the gate dielectric thickness should also be shrunk proportionally.

An oxide thickness of 3 nm is needed for CMOS transistors with channel lengths of

100 nm or less [1.2.2]. This thickness comprises only a few layers of atoms and is

approaching fundamental limits which is around 1 to 1.5 nm[1.2.3]. The thin oxide

layer is subject to quantum-mechanical tunneling, giving rise to a gate leakage current

that increases exponentially as the oxide thickness is scaled down. This tunneling

current can initiate a damage leading to the fallible of the dielectric.

2) Lithography-based technique limit

CMOS transistors are basically patterned on wafer by means of lithography and

masks. It means that the lithography technology is one of the main drives behind the

transistor scaling. Ironically, the lithography processes cannot cope with the shrinking

feature of CMOS transistors' layout. Lithography techniques such as proximity X-ray

steppers and ion beam are limited by difficulties in controlling mask-wafer gap and

uniform exposure of photoresists on wafer respectively. Another problem is the

inability of polishing process to maintain the uniform thickness of wafer and reliable

mask. According to [1.2.4], patterning smaller feature than wavelength of light

requires trade-off between complex, costly masks and possible design constraint. So

the current optical-based fabrication technology may be not able to support the

resolution that is needed to pattern feature smaller CMOS sizes.

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3) Economic limitation

Another biggest drive behind the downscaling is the economic consideration. The

rising cost in semiconductor sector is basically contributed by the cost of production,

and testing that escalating exponentially with time as the CMOS size is scaling down.

As predicted by the National Institute of Standards and Technology (NIST), a new

wafer foundry could cost approximately 25 billion dollar today, and will increase by

one-fold in 2010 as depicted in Figure 1.2.1 [1.2.5].

Figure 1.2.1 Wafer foundry cost.

The cost explosion is also primarily contributed by the equipment cost, clean room

facilities, and lithography process complexity [1.2.5]. Traditional top down silicon

based fabrication requires over 35 masks, and 700 steps for a 90nm process [1.2.6].

The same trend is also stated in [1.2.7] for DRAM process fabrication. Moreover,

design revisions cause a hike in mask cost, and reduction in the number of wafer that

can be produced in single mask set. The mask contribution is becoming the dominant

factor in lithography costs, particularly as minimum feature sizes fall below the

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exposure wavelength. These problems lead to the combination of wafer production to

the best equipped foundries [1.2.8]. The alliances between companies and

participation from universities and government that inject funding are also the strategy

used to reduce the cost. Smaller size circuit is vulnerable to hard and soft defects.

These defective-prone circuits needs to be tested thoroughly in order to guarantee the

required quality. However, more sophisticated test method will incur additional testing

steps and time thus increasing test cost [1.2.9].

1.3 Introduction of Three-Dimensional Structure The end of Moore’s Law scaling, however, does not necessarily spell an end to the era

of a big jump every so often, due to a new structure, three-dimensional structure devices.

The three-dimensional transistors were first imagined and built by three researchers at

the University of California, Berkeley, in the late 1990s, in response to a call from the

United States Defense Advanced Research Projects Agency for designs that would allow

transistors to scale below 25 nanometers, an order of magnitude smaller than the ones in

production at the time. Chenming Hu wrote out the technical specs for the new transistor

on a plane ride to Japan in 1996. A Berkeley group made up of Hu, Jeffrey Bokor, and

Tsu-Jae King Liu first made these transistors, which they called FinFETs, in 1999.

Conventional transistors are made up of a metal structure called a gate that's mounted

on top of a flat channel of silicon. The gate controls the flow of current through the

channel from a source electrode to a drain electrode. With every generation of chips, the

channel has become smaller and smaller, enabling companies to fabricate faster chips by

packing in more transistors. But as scaling of CMOS transistors reaches the 22/20 nm

node and beyond, even the most optimized planar MOSFETs suffer degraded electrostatic

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behavior. As transistor scaling gets smaller and smaller, conventional transistors are

subject to a problem called leakage. This means that when the transistor is in the "off"

state, a small amount of current still flows through. This leads to errors and drains power.

However, the three-dimensional structure has shown a different performance. Intel's

three-dimensional structure channel is a raised "fin" of silicon surrounded on three sides

by the gate. This allows for a more intimate connection between the gate and the channel,

and that in turn enables better control, greatly reducing leakage.

Since last year, Intel has shown off the design of its next generation of chips. The new

transistor design, which uses a three-dimensional gate rather than a flat one, will go into

production at the company's fabs this year. The company says the three-dimensional

structure will allow the company to double the density of its chips while also providing

performance gains and lower power consumption. It is the first large-volume production of

three-dimensional transistors. The new chips are 37 percent faster than the company's

current ones when operating at low voltages to keep power consumption low. And they

require half the power to perform at a given switching speed. Power consumption is

important in handheld devices because it determines how long the battery lasts. It's also

crucial in the power-hungry server farms that make up the cloud.

With the announcement of FinFETs going into high-volume manufacturing by the end

of this year, the post-planar era has truly begun. Multiple post-planar transistor options in

the research phase are double-gate, tri-gate, or gate-all-around structures as shown

schematically in Figure 1.3.1.

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G G

Double-gate

G G

Tri-gate

G

All -around

A. B. C.

Figure 1.3.1 Multiple post-planar transistor options[1.3.3]

Double-gate MOSFET consists of a vertical Si fin controlled by self-aligned

double-gate which is schematically shown in Figure 1.3.1(A). Double-gate MOSFET is

close to the conventional MOSFET in layout and fabrication. The features of

Double-gate MOSFET structure include (1) an ultra-thin Si fin for suppression of

short-channel effects; (2) two gates which are self-aligned to each other; (3) raised the

source/drain to reduce parasitic resistance; (4) a short Si fin for quasi-planar topography;

and (5) gate-last process compatible with low-T, high-k gate dielectrics[1.3.5]

Though double-gate transistors offer excellent short channel effect control, the vertical

nature of the device and the difficulties in fabricating such a device suggest that the

Tri-Gate might be the next transistor design. Tri-Gate structure is shown in Figure

1.3.1(B). It has been reported that the tri-gate devices demonstrated that full depletion at

silicon body dimensions approximately 1.5-2 times greater than either single gate SOI or

double-gate SOI for similar gate lengths, indicating that tri-gate devices are easier to

fabricate using the conventional fabrication tools [1.3.6].

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Gate all- around (GAA) MOSFETs have attracted much attention. GAA structure is

shown in Figure 1.3.1(C). As the name suggests, the GAA FET features the gate fully

surrounding the channel body and thus providing the best possible electrostatic control.

The reduction in channel width and thickness can further increase the effectiveness of

the gate control. Therefore, an ultrathin and narrow body (nanowire) MOSFET, when

combined with the GAA structure, is considered to be a major candidate for extreme

CMOS scaling provided the process complexities such as fabrication of short wires and

the gate definition under the body are solved. Besides theoretical studies, there have

been several experimental attempts that demonstrated the advantages of GAA.

These structures have been suggested to the scientific community to overcome the

limitation of the conventional single gate MOSFET, namely, the short channel effects

(SCE). Since the superior electrostatic control on the channel can be achieved by

introducing more than one gate, MuGFET is a strong candidate to replace the

conventional MOSFET.

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1.4 Purpose of this thesis Silicon metal-oxide-semiconductor (MOS) field-effect-transistors (FETs) with

three-dimensional (3D) channels, such as Fin FETs, Tri-gates and Si nanowire FETs,

have attracted a strong interest owing to their excellent properties [1.5.1]. Performance

and reliability of 3D-channel devices are largely dependent on the electrical properties of

insulator and silicon interfaces. Crystallographic orientation of silicon surface is one of

the main determinants of the interface quality, and commonly (100) surfaces are used to

meet the device performance. As 3D channels consist of several crystallographic

orientations, the interface state density (Dit) of 3D surfaces may become an issue for

device performance.

Two methods have been adopted in this study to obtain characteristics of interface

state density of three-dimensional MOS devices. One is quasi-static capacitance-voltage

method and the other is conductance method. By comparison of the results obtained by

these two methods, an evaluation of interface state density in three-dimensional devices

has been proposed.

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Refernces

[1.1.1] R. H. Dennard, F. H. Gaensslen, H. N. Yu, V. L. Rideout, E. Bassous, and A.

R.LeBlanc. Design of ion-implanted MOSFETs with very small physical dimensions.

IEEE. J. Solid-State Circuits.

[1.2.1] Harson, N.Z; Hamdioui, S; Design and Test Workshop, 2008.IDT 2008. 3rd

International,pp: 98-103.

[1.2.2] Y. Taur, "CMOS design near the limit of scaling", IBM Journal ofR&D, vol. 46,

iss. 2, pp. 213-222, 2002.

[1.2.3] R. D. Isaac, "The Future of CMOS Technology", IBM Journal ofR&D, vol. 44,

iss. 3, pp. 369-378, 2000.

[1.2.4] T. Skotnicki, et. aI, "The End of CMOS Scaling: Towards the Introduction of

New Materials and Structural Changes to Improve MOSFET Performance", IEEE

Circuits and Devices Magazine, vol. 21, issues 1, pp. 16-26, 2005.

[1.2.5] A. W. Wieder and F. Neppi, "CMOS Technology Trends and Economics", IEEE

Micro, vol. 12 , iss. 4, pp. 10-19, 1992.

[1.2.6] W. Trybula, "Technology acceleration and the economics of lithography (cost

containment and roi)", Future Fab IntI., vol. 14, no. 19, 2003.

[1.2.7] H. Stork, "Economies of CMOS Scaling", http://www.eeel.nist.gov/- Stork.pdf.

[9] International Technology Roadmap for Semiconductor (ITRS), 2008 up data

[1.2.8] S. Hillenius, "The Future of Silicon Microelectronics", Proc. IEEE Workshop on

Microelectronics and Electron Devices, pp. 3-4, 2004.

[1.2.9] B. R. Benware, "Achieving sub 100 DPPM Defect Levels on VDSM and

Nanometer ASICS", Proc. IEEE Intl. Test Conference, p. 1418,2004.

[1.3.1] A. Tilke, Physik Journal, 6 (2007) 35.

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[1.3.2] K. Okano, Int. Elec. Dev. Meeting Tech. Dig. (2005), 721. [1.3.3] H. Iwai, 2011 Tsukuba Nanotechnology Symposium (TNS’11), Tsukuba

University, 2011 " Si Nano Electronics " C.-Y. Chang, Int. Elec. Dev. Meeting Tech. Dig. (2009) 293.

[1.3.5] X. Huang, W.C. Lee, C. Kuo, D. Hisamoto, L. Chang, J. Kedzierski et al., Sub

50-nm FinFET: PFET, in Technical Digest of IEDM (1999), 67-70.

[1.3.6] B. S. Doyle et al.,IEEE Electron Device Letters, VOL. 24, 2003,pp 263.

[1.5.1] Iwai.H, et al., Science China, Volume 54, p. 1004-1011 (2011).

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Chapter2 Fabrication and Characterization Method

2.1 Substrate Cleaning 2.2 Thermal Oxidation Process 2.3 Photolithograph 2.4 RF Magnetron Sputtering 2.5 Thermal Evaporation for Al Back Contact 2.6 Rapid Thermal Annealing Process 2.7 Capacitance-Voltage (C-V) Method 2.8 Conductance Method 2.9 Quasi-static Method 2.10 Scanning Electron Microscopy (SEM) Method 2.11 Conclusion References

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2.1 Substrate Cleaning Si substrate cleaning is of great importance in the manufacture of semiconductor. Lots

of contamination, such as particle contamination, metal contamination, organic

contamination, ionic contamination, water absorption, native oxide and atomic scale

roughness are introduced into wafers[2.1.1]. Chemical liquid and de-ionized water are

mainly used to prepare clean wafers. DI water is highly purified and filtered to remove

all traces of ionic, particulate, and bacterial contamination. The theoretical resistivity of

pure water is 18.25 MΩ・cm at 25oC. Ultra-pure water (UPW) system used in this study

provided UPW of more than 18.2 MΩ・cm at resistivity, fewer than 1 colony of bacteria

per milliliter and fewer than 1 particle per milliliter. The silicon wafers were immersed

into the mixed solution of H2O2 and H2SO4 (H2O2 : H2SO4 = 1:4) and heated at 1500C

for 5 minutes. This process helps remove organic material and metallic impurities. After

that, samples were rinsed with running DI (de-ionized) water to remove the chemical

liquid. H2SO4 can remove carbon and metal and H2O2 can remove particles. But at the

same time, H2O2 oxidized Si into SiO2 which contains particles. Then wafers were

immersed into 1% HF at room temperature for 3 minutes to remove silicon oxide. At last,

the samples were cleaned again by DI water.

2.2 Thermal Oxidation Process Thermal oxidation is a method of producing a thin layer of silicon dioxide on silicon

wafer surface. It is usually performed at a temperature between 800 and 12000C. There

are two types of thermal oxidation: wet oxidation ( Si + 2H2O → SiO2 + 2H2 ) and dry

oxidation ( Si + O2 → SiO2 ). Dry oxidation has a lower growth rate than wet oxidation

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but the oxide film quality is better. In wet oxidation, the chemical reaction process is

that the water molecule dissociates at high temperature to form hydroxide OH which

can diffuse in the silicon faster than oxygen. Therefore dry oxidation is normally used to

produce gate oxide and wet oxidation is usually adopted to grow thick oxides. In this

work, the oxidation furnace was used, which is shown in Figure2.2.1 and Figure 2.2.2,

and dry oxidation was performed. A furnace typically consists of: 1) a cabinet; 2) a

heating system; 3) a temperature measurement and control system; 4) fused quartz

process tubes where the wafers undergo oxidation; 5) a system which transfers process

gases in and out of the process tubes; and 6) a loading stick used for loading (or

unloading) wafers into (or from) the process tubes. In order to grow uniform and

high-quality oxide film, the samples were taken on a quartz boat and sent into the center

of the 3-zone furnace at 8000C temperature at a uniform slow speed in the nitrogen

atmosphere by a quartz stick. The mass flow of oxygen was controlled in 1L/min and

last for 30 minutes at 10000C temperature.

Gas inlet

Gas outlet

Quartz Cap

3-zone furnace

Quartz boat Samples

Quartz tube

Figure 2.2.1. the schematic structure of oxidation furnace

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Figure 2.2.2 Oxidation furnace which was used in this work.

2.3 Photolithograph Photolithography is a process used in microfabrication to selectively remove parts of a

thin film or the bulk of a substrate. It uses light to transfer a geometric pattern from a

photomask to a light-sensitive chemical "photoresist", or simply "resist," on the substrate.

A series of chemical treatments then either engraves the exposure pattern into, or enables

deposition of a new material in the desired pattern upon, the material underneath the

photo resist. Figure 2.3.1 shows the schematic photolithograph process flow.

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mask

resist

light

developer solution

wet etching

remove resist

Figure 2.3.1 the schematic photolithograph process flow.

In the process of the sample fabrication, positive photoresist layer of S1805 was used.

At first, a uniform thin positive photoresist layer was set on the surface of the sample by

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high speed spin coating. Then the sample was pre-baked at 1150C for 5 minutes to

remove off moisture. Next, the photoresist-coated sample was aligned under the

microscope and exposed through e-beam patterned hard-mask with high-intensity

ultraviolet (UV) light at 405 nm wavelength. MJB4 of Karl Süss contact-type mask

aligner was used in this experiment[2.3.1]. The exposure duration was controlled in 1.2

seconds. After that, developing process was performed with a specified developer called

NMD-3 (Tokyo Ohka Co. Ltd) for 40 seconds. At last, the sample was post-baked at

1300C for 10 minutes to solidify the remaining photoresist for the following wet

chemical etching. The wet etching was performed with H2O2 solution for 2 minutes. The

fabrication process flow and a photo of the photolithography apparatus used throughout

this study are shown in Figure 2.3.2.

Coating photoresist (S1805)

Pre-baking at 1150C for 5 minutes

Alignment

UV exposure for 1.2 s

Development in NMD-3 for 40 seconds

Post-baking at 1300C for 10 minutes

Figure 2.3.2 The process flow and the photo of photolithography apparatus.

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2.4 RF Magnetron Sputtering After thermal oxidation to form silicon dioxide, a 50 nm W film was deposited

by RF magnetron sputtering to form gate electrode. Sputtering is one of the vacuum

processes used to deposit ultra thin films of various materials on substrates and

extensively used in the semiconductor industry. A high voltage across a

low-pressure gas (usually argon at about 5 mTorr) is applied to create a “plasma”

which consists of electrons and gas ions in a high-energy state. Then the energized

plasma ions strike the “target” composed of the desired coating material, and cause

atoms of the target to be ejected with enough energy to travel to the substrate

surface. The sputtering process is schematically shown in Figure 2.4.1. The base

pressure of the sputtering chamber was controlled at 10-6 Pa during the substrate

transfer. Argon gas flow was set to 7sccm while holding the deposition chamber

pressure at of which was set to be 1.33Pa. The 150W RF current power was used to

produce plasma. Figure 2.4.2 shows the sputtering system used in this work.

Ar+

Sputtering Gas

Sample

Sputtering Target

Figure 2.4.1 the schematic of RF magnetron sputtering

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Figure 2.4.2 a photo of sputtering system used in this work.

2.5 Thermal Evaporation for Al Back Contact Aluminium (Al) electrode was deposited on the back side of the samples. In this

experiment, a bell-jar type vacuum thermal evaporation method was adopted to

form back side Al electrode at a background pressure up to 1.0x10-3 Pa. The

schematic illustration of bell jar is shown in Figure. Filament made of tungsten (W)

was used to hold highly pure Al wires. Current flowed in the circuit connected with

tungsten boat and about 50A current was large enough for Al to melt. Then melting

Al was vaporized and deposited on the back side of samples. Chamber pressure

during evaporation was controlled under 4x10-3 Pa.

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D.P.FORE

ROUGHCLOSE

R.P.

R.P. VENT

shutter

AlTungsten boat

VENT VALVE

MAIN VALVE

BELL JAR

samples

(Diffusion Pump)(Rotary Pump)

Figure 2.5.1 the schematic illustration of Bell jar

2.6 Rapid Thermal Annealing Process Rapid thermal annealing is a semiconductor fabrication process which heats

silicon wafers to a high temperature in a short time of several seconds. Then during

the cooling, sample temperatures must be brought down slowly in order not to

break samples due to thermal shock. In this experiment, a thermal annealing process

was performed to improve the quality of the interface of silicon and silicon dioxide.

The sample was heated in the forming gas (97% N2 + 3% H2) ambient (1L/min) at

4200C for 30 minutes. Samples were taken out of the chamber under 1000C. In this

process, H2 molecules heated in high temperature were broke down into hydrogen

atoms which recombined with the silicon dangling bonds in the interface of silicon

and silicon dioxide. Figure 2.6.1 shows the schematic of thermal annealing process

and Figure 2.6.2 shows the apparatus used in this work.

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Si-substrate

SiO2

Si Si Si Si Si Si

Dangling bonds

H+H+ H+

H+

H+

Si-substrate

SiO2

Si Si Si Si Si SiH H H H

Figure 2.6.1 the schematic illustration of thermal annealing

Figure 2.6.2 the photo of thermal annealing apparatus used in this work.

2.7 Capacitance-Voltage (C-V) Method C-V characteristic measurements were performed with various frequencies

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(1KHz~1MHz) by precision LCR Meter (HP 4284A, Agilent). The energy band

diagram of an MOS capacitor on a p-type substrate is shown in figure 2.7.1. The

intrinsic energy level Ei or potential φin the neutral part of device is taken as the

zero reference potential. The surface potential φs is measured from this reference

level. The capacitance is defined as

dVdQC = (2.7.1)

It is the change of charge due to a change of voltage and is most commonly given in

units of farad/unit area. During capacitance measurements, a small-signal ac voltage

is applied to the device. The resulting charge variation gives rise to the capacitance.

Looking at an MOS-C from the gate, GG dVdQC /= , where GQ and GV are the

gate charge and the gate voltage. Since the total charge in the device must be zero,

)( itsG QQQ +−= assuming no oxide charge. The gate voltage is partially dropped

across the oxide and partially across the semiconductor. This gives

soxFBG VVV φ++= , where FBV is the flatband voltage, oxV the oxide voltage, and

sφ the surface potential, allowing Eq.(2.7.1) to be rewritten as

sox

its

ddVdQdQC

φ++

−= (2.7.2)

The semiconductor charge density sQ , consists of hole charge density pQ ,

space-charge region bulk charge density bQ , and electron charge density nQ . With

nbps QQQQ ++= , Eq.(2.7.2) becomes

itnbp

s

its

ox

dQdQdQdQd

dQdQdVC

++++

+

−= φ1 (2.7.3)

Utilizing the general capacitance definition of Eq.(2.7.1), Eq.(2.7.3) becomes

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itnbpox

itnbpox

itnbpox

CCCCCCCCCC

CCCCC

C++++

+++=

++++

=)(

111 (2.7.4)

The positive accumulation charge pQ dominates for negative gate voltages for

p-substrate devices. For positive GV , the semiconductor charge are negative. The

minus sign in Eq.(2.7.3) cancels in either case.

Equation (2.7.4) is represented by the equivalent circuit in Figure 2.7.2(a). For

negative gate voltages, the surface is heavily accumulated and pQ dominates. pC

is very high approaching a short circuit. Hence, the four capacitances are shorted as

shown by the heavy line in Figure 2.7.2(b) and the overall capacitance is oxC . For

small positive gate voltages, the surface is depleted and the space-charge region

charge density, WqNQ Ab −= , dominates. Trapped interface charge capacitance

also contributes. The total capacitance is the combination of oxC in series with bC

in parallel with itC as shown in Figure 2.7.2(c). In weak inversion nC begins to

appear. For strong inversion, nC dominates because nQ is very high. If nQ is

able to follow the applied ac voltage, the low-frequency equivalent circuit (Figure

2.7.2(d)) becomes the oxide capacitance again. When the inversion charge is unable

to follow the ac voltage, the circuit in Figure 2.7.2(e) applies in inversion, with

invsb WKC /0ε= with invW the inversion space-charge region width[2.7.1].

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VG

NA

0 tox tox+W x

Vox

φs

φF

Ec/q

Ei/q, φ

Ev/qEF/q, φF

Figure 2.7.1 Cross-section and potential band diagram of an MOS capacitor.

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Cox

Cp Cb Cn Cit

Cox

Cp Cb Cn Cit

Cox

Accumulation

(b)

Cox

Cp Cb Cn Cit

Cox

CbCit

Depletion

(c)

Cox

Cp Cb Cn Cit

Cox

Inversion- Low Frequency

(d)

Cox

Cp CbCn Cit

Cox

Cb

Inversion- High Frequency

(e)

(a)

Figure 2.7.2 Capacitance of an MOS capacitor for various bias condition.

2.8 Conductance Method The conductance method was proposed by Nicollian and Goetzberger in 1967

and is one of the most sensitive methods to determine Dit. Interface trap densities of

109 cm-2eV-1 and lower can be measured. It can give information about Dit in the

depletion and weak inversion, the capture cross-section of majority carriers and the

surface potential fluctuations. The conductance method is to measure the equivalent

parallel conductance Gp of an MOS-C as a function of bias voltage and frequency.

Conductance Gp represents the loss mechanism caused by interface trap capture and

emission of carriers, which is a measure of interface state density. Figure 2.8.1(a)

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shows the simplified equivalent circuit of an MOS-C. Cox is the oxide capacitance,

CS is the semiconductor capacitance, Cit is the interface trap capacitance and Rit is

the lossy process caused by the capture-emission of carriers due to interface state

density.

Cox

CS

Cit

Rit

Cox

CP GP

Cm Gm

•(a) (b) (c)

Figure 2.8.1 Equivalent circuits for conductance measurement. (a) MOS-C with

interface trap time constant, (b) simplified circuit, (c) measured circuit

The circuit of Figure 2.8.1(a) can be simplified by the circuit of Figure 2.8.1(b).

Cp and Gp are represented by Eq. (2.8.1) and (2.8.2).

2)(1 it

itSp

CCCωτ+

+= (2.8.1)

2)(1 it

ititp DqGωτ

ωτω +

= (2.8.2)

where Cit=q2Dit, ω=2πf (f=measurement frequency) and τit=RitCit, the interface trap

time constant, given by τit=[vthσpNAexp(-qφs/kT]-1. Dividing Gp by ω makes Eq.

(2.8.2) symmetrical in ωτit. Equation (2.8.1) and (2.8.2) are for interface traps with a

single energy level in the band gap. Interface traps at the SiO2-Si interface, however,

are continuously distributed in energy throughout the Si band gap. Capture and

emission occurs primarily by traps located within a few kT/q above and below the

31

Fermi level, leading to a time constant dispersion and giving the normalized

conductance as

])(1ln[2

2it

it

itp qDGωτ

ωτω+= (2.8.3)

Equations (2.8.2) and (2.8.3) show that the conductance is easier to interpret than

the capacitance, because Eq.(2.8.2) does not require CS. The conductance is

measured as a function of frequency and plotted as Gp/ω versus ω. Gp/ω has a

maximum at ω=1/τit and at that maximum Dit =2 Gp/qω. For Eq.(2.8.3) we find

itτω /2≈ and Dit=2.5 Gp/qω at the maximum. Hence we determine Dit from the

maximum Gp/ω and determine τit from ω at the peak conductance location on the

ω-axis.

Experimental Gp/ω versus ω curves are generally broader than predicted by

Eq(2.8.3). attributed to interface trap time constant dispersion caused by surface

potential fluctuations due to non-uniformities in oxide charge and interface traps as

well as doping density. Surface potential fluctuations are more pronounced in p-Si

than in n-Si. Surface potential fluctuations complicate the analysis of the

experimental data. When such fluctuations are taken into account, Eq(2.8.3)

becomes

ssitit

itp dUUPDqG)(])(1ln[

22ωτ

ωτω+= ∫

(2.8.4)

where P(Us) is a probability distribution of the surface potential fluctuation given by

)2

)(exp(2

1)( 2

2

2 σπσss

sUUUP −

−= (2.8.5)

with SU and σthe normalized mean surface potential and standard deviation,

32

respectively. An approximate expression giving the interface trap density in terms

of the measured maxium conductance is

max

5.2⎟⎠⎞

⎜⎝⎛≈

ωP

itG

qD (2.8.6)

Capacitance meters generally assume the device to consist of the parallel Cm-Gm

combination in Figure 2.8.1(c). A circuit comparison of Figure 2.8.1(b) to 2.8.1(c)

gives Gp/ω in terms of the measured capacitance Cm, the oxide capacitance, and the

measured conductance Gm as

222

2

)( moxm

oxmP

CCGCGG

−+=

ωω

ω (2.8.7)

assuming negligible series resistance. The conductance measurement must be carried out

over a wide frequency range. The portion of the band gap probed by conductance

measurements is typically from flatband to weak inversion. The measurement frequency

should be accurately determined and the signal amplitude should be kept at around

50mV or less to prevent harmonics of the signal frequency giving rise to spurious

conductances. The conductance depends only on the device area for a given Dit.

However, a capacitor with thin oxide has a high capacitance relative to the conductance,

especially for low Dit and the resolution of the capacitance meter is dominated by the

out-of-phase capacitive current component. Reducing Cox by increasing the oxide

thickness helps this measurement problem[2.7.1].

2.9 Quasi-static Method The low-frequency or quasi-static method is a common interface trapped charge

measurement method. It provides information only on the interface trapped charge

density, but not on their capture cross-sections. The basic theory of the quasi-static

33

method was developed by Berglund. The method compares a low-frequency C–V curve

with one free of interface traps. The latter can be a theoretical curve, but is usually an hf

C–V curve determined at a frequency where interface traps are assumed not to respond.

“Low frequency” means that interface traps and minority carrier inversion charges must

be able to respond to the measurement ac probe frequency. The interface trap response

has similar limitations. Fortunately, the limitations are usually less severe than for

minority carrier response and frequencies low enough for inversion layer response are

generally low enough for interface trap response.

The lf capacitance is given by Eq. (2.9.1) in depletion-inversion as

1)11( −

++=

itSoxlf CCC

C (2.9.1)

CS is the lf semiconductor capacitance, Cit is related to the interface trap density Dit by

Dit = Cit/q2, giving

)(12 S

lfox

lfoxit C

CCCC

qD −

−= (2.9.2)

Equation (2.9.2) is suitable for interface trap density determination over the entire

band gap.

Clf and CS must be known to determine Dit . Clf is measured as a function of gate

voltage and the calculation of CS is simplified by Castagn´e and Vapaillen who proposed

a method to eliminate the uncertainty associated with the calculation of CS and gave the

Equation (2.9.3):

hfox

hfoxS CC

CCC

−= (2.9.3)

Substituting Eq. (2.9.3) into (2.9.2) gives Dit in terms of the measured lf and hf C–V

curves as

34

)/1

//1

/(2

oxhf

oxhf

oxlf

oxlfoxit CC

CCCC

CCqC

D−

−−

= (2.9.4)

Equation (2.9.4) gives Dit over only a limited range of the band gap, typically from the

onset of inversion, but not strong inversion, to a surface potential towards the majority

carrier band edge where the ac measurement frequency equals the inverse of the

interface trap emission time constant. This corresponds to an energy about 0.2 eV from

the majority carrier band edge. The higher the frequency the closer to the band edge can

be probed[2.7.1].

2.10 Scanning Electron Microscopy (SEM) Method Fin structures were observed by scanning electron microscope (SEM).

An electron microscope uses an electron beam (e-beam) to produce a magnified image

of the sample. The three principal electron microscopes are: scanning, transmission and

emission. In the scanning and transmission electron microscope, an electron beam

incident on the sample produces an image while in the field-emission microscope the

specimen itself is the source of electrons. A scanning electron microscope consists of an

electron gun, a lens system, scanning coils, an electron collector, and a cathode ray

display tube (CRT). The electron energy is typically 10–30 keV for most samples. The

use of electrons has two main advantages over optical microscopes: much larger

magnifications are possible since electron wavelengths are much smaller than photon

wavelengths and the depth of field is much higher. De Broglie proposed in 1923 that

particles can also behave as waves. The electron wavelength λe depends on the electron

velocity v or the accelerating voltage V as

(2.10.1) ][22.12

nmVqmV

hmvh

e ===λ

35

λe = 0.012 nm for V = 10, 000 V—a wavelength significantly below the 400 to 700 nm

wavelengths of visible light—making the resolution of an SEM much better than that of

an optical microscope[2.7.1].

Figure 2.10.1 Photograph of SEM equipment.

36

Virtual Source

First Condenser Lens

Condenser Aperture

Objective Aperture

Second Condenser Lens

Scan Coils

Objective Lens

Sample

Figure 2.10.2 Schematic view of internal configuration of SEM equipment.

2.11 Conclusion In this chapter, the MOS device fabrication methods used in this work including

SPM cleaning, dry oxidation, RF magnetron sputtering, photolithograph, thermal

evaporation for aluminium back electrode formation and rapid thermal annealing were

introduced. Then the measurement methods (C-V method, conductance method, QSCV

method and SEM) were explained in detail.

37

Refernces

[2.1.1] Wemer Kern, The Evolution of Silicon Wafer Cleaning Technology, J.

Electronchem. Soc., Vol. 137, No.6, June 1990

[2.3.1] http://www.suss.com

[2.7.1] D. Schroder, Semiconductor material and device characterization, 3rd edition, p.

347-350, Willey Interscience, NJ (2006).

38

Chapter3 Interface State Density Extraction of

Three-Dimensional Channel Structure

3.1 Device Fabrication Process

3.2 Analysis of Fin Structure with SEM Images

3.3 Analysis of C-V Curves

39

3.4 Extraction of Interface State Density of planar and Fin

devices by Quasi-static C-V Method

3.5 Extraction of Interface State Density of planar devices by

Conductance Method

3.6 Conclusion of This Chapter

References

40

3.1 Device Fabrication Process Line structures (Fins) with heights of 50 nm were formed with lithography and dry

etching process on a (100) oriented p-type silicon bulk wafers with a doping density of 1015 cm-2. As the lines were aligned to <110> direction, the etching side surfaces have the orientation of (110). For references, p-type planar wafers with (100) and (110)-oriented surface were prepared. After chemical cleaning, devices were performed with a dry oxidation process (1000 oC for 30min). After dry oxidation, tungsten films were deposited by RF magnetron sputtering and lithographically etched to form gate electrodes. Al contacts were used as back contacts by thermal evaporation. Finally, the samples were annealed in forming gas (FG) (N2/H2: 97/3%) ambient at 420 oC for 30 minutes. The process flow is shown in figure 3.1.1 and the device structure is shown in figure 3.1.2.

1 SPM+HF cleaning

p-Si (100), (110)Fin50nm substrate

3

4

5

6

2 Dry oxidation for 30 min

W deposition

Gate patterning

Al contact formation on backside

F.G. gas annealing at 420oC for 30min

Measurement

Figures 3.1.1 the device fabrication process flow

41

Al

SiO2

p-Si

W

Al

p-Si

SiO2

W

Al

SiO2

p-Si

W

(110) (100)

50nmW

•••

100

Figures 3.1.2 the schematic device structures

42

3.2 Analysis of Fin Structure with SEM Images Figure 3.2.1 shows the SEM image of bulk silicon fin with the height of 50nm after

MOS device fabrication. The bulk silicon fin consists of two types of orientation surface: the top surface and etching surface are (100)-oriented surfaces and the side surface is (110)-oriented surface.

50nm

Tox=30nmW

(100)-oriented

(110)-oriented

Dry oxidation 30min 1L/min

Figure 3.2.1 the SEM images of bulk silicon fin with the height of 50nm

The studies of oxidation have shown that the oxidation rate also depends on the

crystal orientation of the silicon substrate. Experiments have demonstrated that the oxide growth is faster on (110) oriented surfaces than on (100) oriented at any temperature for dry as well as wet oxidation. Figure3.2.2 shows an oxidation rate comparison plot on different orientation surfaces.

43

0 1 2 3 4 5 6 7 8Oxidation time (hr)

00.10.20.30.40.50.60.70.80.91.01.11.21.31.41.5

Oxi

datio

n th

ickn

ess

(um

)

Figure 3.2.2 the oxidation rate comparison on different orientation surface

According to the oxidation rates on different orientation surfaces, the (110)-oriented

side surface should have thicker silicon oxide than the (100)-oriented top surface and

etching surface. But the SEM image shows that the top surface has about the same

thickness of silicon oxide as the side surface and the etching surface has the thickest

silicon oxide. It can be explained by the reference [3.2.1]. The article demonstrates that

retardation oxidation exits at silicon convex and concave surfaces and convex is more

severe than concave. As the side surface became convex due to oxidation, the oxidation

rate of (110)-oriented side surface was slowed down, which resulted the roughly same

silicon oxide thickness as the (100)-oriented top surface. Besides, the etching surface has

the most fast oxidation rate due to the flat property.

44

3.3 Analysis of C-V Characteristics For characterization of depletion and inversion capacitance, Capacitance-Voltage

curves were measured in the frequencies of 1MHz, 100kHz, 10kHz and 1kHz. Figure

3.3.1 shows the C-V characteristics at the frequency 100kHz of Fin with the height of

50nm and (100)-oriented planar MOS devices.

It is shown that in accumulation the Cox value in planar MOS device is roughly the

same as bulk silicon fin 50nm MOS device, which is supposed to be the rough same

effective thickness of silicon dioxide.

In the inversion condition, a little lower capacitance in Fin 50nm may be explained

by the fully-depletion theory of Fin structure since surrounding-gate MOSFETs’ gate has

a greater control on the channel[3.3.1].

0.00E+00

2.00E-08

4.00E-08

6.00E-08

8.00E-08

1.00E-07

1.20E-07

-2.5 -2 -1.5 -1 -0.5 0 0.5 1 1.5-2 -1 0 1.00

0.04

0.08

0.12

Cap

acita

nce

(μF/

cm2 )

Gate voltage (V)

(100)-oriented planar

Fin 50nm

-2.5 -1.5 -0.5 0.5 1.5

0.02

0.06

0.10

at 100kHz

Figure 3.3.1 a comparison C-V characteristic of Fin and planar

45

3.4 Extraction of Interface State Density of planar and

Fin devices by Quasi-static C-V Method First, a quasi-static C-V method was adopted to extract the interface state density of

(100)-oriented planar and (110)-oriented planar devices. Eq. (2.9.4) is used to calculate

Dit [3.4.1].

)/1

//1

/(2

oxhf

oxhf

oxlf

oxlfoxit CC

CCCC

CCqC

D−

−−

= (2.9.4)

The measurement gate voltage ranges from -2V to 1V and QSCV measurement

voltage is 100mv. The QSCV characteristics of planar and Fin devices are respectively

shown in Figure 3.4.1(a) (b) (c). High frequency (100kHZ) was also measured for

calculation (shown in Figure 3.4.1(a) (b) (c)). Figure 3.4.1(d) shows the interface state

density energy distribution.

0.00E+00

2.00E-08

4.00E-08

6.00E-08

8.00E-08

1.00E-07

1.20E-07

-2.00E+00 -1.50E+00 -1.00E+00 -5.00E-01 0.00E+00 5.00E-01 1.00E+00

Cap

acita

nce

(μF/

cm2 )

0

0.04

0.08

0.12(100)-oriented planar

at 100kHz

qscv

-2.0 -1.0 0.0Gate voltage (V)

1.0

(a)

46

0.00E+00

1.00E-08

2.00E-08

3.00E-08

4.00E-08

5.00E-08

6.00E-08

7.00E-08

8.00E-08

9.00E-08

-2.00E+00 -1.50E+00 -1.00E+00 -5.00E-01 0.00E+00 5.00E-01 1.00E+00

at 100kHz

qscv

(110)-oriented planar

-2.0 -1.0 0.0 1.0Gate voltage (V)

0

0.02

0.06

0.04

0.08

Cap

acita

nce

(μF/

cm2 )

(b)

Cap

acita

nce

(μF/

cm2 )

0.00E+00

2.00E-08

4.00E-08

6.00E-08

8.00E-08

1.00E-07

1.20E-07

-2.00E+00 -1.50E+00 -1.00E+00 -5.00E-01 0.00E+00 5.00E-01 1.00E+00

Gate voltage (V)-2.0 0.0 1.0-1.0

0

0.04

0.08

0.12Fin

qscv

at 100kHz

(c)

47

Dit(c

m-2

eV-1

) (110)

(100)

0.0 0.2 0.4 0.6 0.8 1.0E-Ev (eV)

3D channel

1010

1011

1012

(d)

Figure 3.4.1 measurement result by quasi-static method

According to the Figure 3.4.1, quasi-static method can show the amount of interface

state density in planar and Fin. However, it cannot give any more information about the

interface state characteristic.

48

3.5 Extraction of Interface State Density by

Conductance Method In order to obtain more information about characteristics of interface state density,

conductance method was adopted to extract the interface state density of (100)-oriented

planar and (110)-oriented planar devices. Eq. (2.8.4) and (2.8.5) are used to calculate Dit

[3.4.1].

ssitit

itp dUUPDqG)(])(1ln[

22ωτ

ωτω+= ∫

(2.8.4)

where P(Us) is a probability distribution of the surface potential fluctuation given by

)2

)(exp(2

1)( 2

2

2 σπσss

sUUUP −

−= (2.8.5)

The measurement gate voltage ranges from flatband to the onset of inversion. The

small signal voltage amplitude is 50mv and frequency is from 20Hz to 2MHz. Figure

3.5.1 shows the typical conductance spectra of (100) and (110) oriented planar devices.

The time constants of the two surfaces are also obtained by conductance method. Figure

3.5.2 shows that the two surfaces have different time constants.

49

0.00E+00

1.00E-09

2.00E-09

3.00E-09

4.00E-09

5.00E-09

6.00E-09

7.00E-09

8.00E-09

9.00E-09

1.00E-08

1.00E+01 1.00E+02 1.00E+03 1.00E+04 1.00E+05 1.00E+06 1.00E+07

Frequency (Hz)101 103 105 107

0

5x10-9

1x10-8

Gp/ω

(F/c

m2 )

(100)

0 .00E+00

5 .00E-09

1 .00E-08

1 .50E-08

2 .00E-08

2 .50E-08

3 .00E-08

3 .50E-08

4 .00E-08

4 .50E-08

5 .00E-08

1 .00E+01 1 .00E+02 1 .00E+03 1 .00E+04 1 .00E+05 1 .00E+06 1 .00E+07

101 103 105 107

Frequency (Hz)

0

2x10-8

Gp/

ω(F

/cm

2 )

4x10-8

(110)

Figure 3.5.1 the typical conductance spectra of (100) and (110) oriented surfaces.

50

1 . 0 0E- 0 7

1 . 0 0E- 0 6

1 . 0 0E- 0 5

1 . 0 0E- 0 4

1 . 0 0E- 0 3

1 . 0 0E- 0 2

1 . 0 0E- 0 1

1 . 0 0E+ 0 0

0 .0 0 E+ 0 0 5 . 0 0 E- 0 2 1 . 0 0 E- 0 1 1 . 5 0 E- 0 1 2 . 0 0 E- 0 1 2 . 5 0 E- 0 1 3 . 0 0 E- 0 1 3 . 5 0 E- 0 1 4 . 0 0 E- 0 1 4 . 5 0E- 0 10.0 0.3 0.5

Surface potential (eV)

Tim

e co

nsta

nt (s

)

10-7

10-5

10-3

10-1

(100)

(110)

Figure 3.5.2 different time constants of (100) and (110) oriented surfaces.

0.00E+00

5.00E+10

1.00E+11

1.50E+11

2.00E+11

2.50E+11

3.00E+11

3.50E+11

0.00E+00 1.00E-01 2.00E-01 3.00E-01 4.00E-01 5.00E-01 6.00E-01 7.00E-010.0 0.2 0.4 0.6 0.8

1x10-11

2x10-11

3x10-11

Dit(c

m-2

eV-1

)

Surface potential (eV)

(110)

(100)

conductance QSCV

Figure 3.5.3 a comparison of interface state density of the two surfaces with

quasi-static method and conductance method.

Then a comparison of the energy distributions of the interface state density of the two

planar devices by the two methods is given in Figure 3.5.3. The surface potential

fluctuations of (100) and (110) oriented surfaces are different, which are respectively

about 0.05 and 0.07. From the comparison, it shows that the interface state densities

measured by the two methods are comparable.

51

3.6 Conclusion of This Chapter In this chapter, quasi-static method is adopted to extract interface state density of

planar and Fin. Then conductance method is adopted to extract interface state density of

planar devices. This method also gave time constant information of the two planar

devices. A comparison of interface state density of the two planar devices by the two

methods is conducted and shows comparable Dit value.

52

Reference

[3.2.1] DAH-BIN KAO, et al.,IEEE Transactions on electron devices,VOL. ED-34,

NO.5, MAY 1987.

[3.3.1] Christopher P. Auth, IEEE ELECTRON DEVICE LETTERS, VOL.18, NO.2,

February 1997.

[3.4.1] D. Schroder, Semiconductor material and device characterization, 3rd edition, p.

347-350, Willey Interscience, NJ (2006).

53

Chapter4 Modeling of Conductance Spectra by

Deconvolution

4.1 Numerical simulation of surface potential of 3D channel

4.2 Deconvolution of Conductance Spectra of Fin Devices

4.3 Conclusion of This Chapter

References

54

4.1 Numerical simulation of surface potential of

3D channel Because of different oxidation rates of (100) and (110) oriented planar surfaces,

different surface potentials may co-exist within the channel for 3D channel device. So it

is necessary to conduct a simulation of surface potential of 3D channel to obtain the

surface potential distribution. Figure 4.1.1 shows the simulation results. We choose one

point from top and side surfaces.

Extract surface potentials from these two points

55

-5.00E-02

0.00E+00

5.00E-02

1.00E-01

1.50E-01

2.00E-01

2.50E-01

3.00E-01

3.50E-01

-0.6 -0.5 -0.4 -0.3 -0.2 -0.1 0-0.6 -0.5 -0.4 -0.3 -0.2 -0.1 00

0.1

0.2

0.3

Gate voltage(V)

Sur

face

Pot

entia

l (eV

)

top

side

Figure 4.1.1 the simulation result of surface potential in top and side surfaces.

4.2 Deconvolution of Conductance Spectra of Fin

Devices Due to the higher surface potential of 30meV in top than side surface, a modeling of

conductance spectra by deconvolution has been proposed. We choose the conductance

spectra of (100) oriented surface in ψs = 0.036 and (110) oriented surface in ψs=

0.007. Then a fitting process of Fin is done with the two surfaces. Figure 4.2.1 shows a

rough fitting result. It showed a roughly agreement of conductance spectra between the

experiment data and fitting data of Fin, which demonstrates that the electrical response

of Dit with 3D surface can be roughly modeled with two planar surfaces[4.1.1]. In the

fitting process, 80% component of (100) oriented and 20% component of (110) oriented

surfaces are observed. It coincided the area ratios of top and side surfaces in the total

56

area showed in SEM image. It demonstrated that interface state density of Fin may be

expressed by weighted average of the two surfaces.

0.00E+00

1.00E-09

2.00E-09

3.00E-09

4.00E-09

5.00E-09

6.00E-09

7.00E-09

8.00E-09

9.00E-09

1.00E-08

1.00E+01 1.00E+02 1.00E+03 1.00E+04 1.00E+05 1.00E+06 1.00E+07

101 103 105 107

5x10-9

1x10-8

Gp/ω

(F/c

m2 )

Frequency (Hz)

0

Fin

(100) component

(110) component

Figure 4.2.2 the fitting results of conductance spectra of Fin

4.3 Conclusion of This Chapter A modeling of conductance spectra by deconvolution has been proposed in this study.

Fitting results show that the conductance spectra can be roughly expressed by weighted

average of the two surfaces. Based on the above analysis it is suggested that the

electrical response of interface state with three-dimensional surface can be roughly

modeled with two interface state of planar

57

References [4.1.1] S. Ogata, et al., Applied Physics Letters, Volume 98, Issue 9, p. 092906-092906-3

(2011)

58

Chapter5 5.1 Conclusion of This Study

In this study, we evaluate the interface state density of silicon bulk Fin devices with

different channel orientations. Two methods have been adopted in this study to obtain

characteristics of interface state density of three-dimensional MOS devices. One is

quasi-static capacitance-voltage method and the other is conductance method. By

comparison of the results obtained by these two methods, an evaluation of interface

state density in three-dimensional devices has been proposed.

At first, the interface state density of (100)-oriented and (110)-oriented planar devices

and Fin have been investigated by quasi-static method. Then the extraction of the

interface state density of planar surfaces has been done again by conductance method.

The two methods showed the similar energy distribution of interface state density.

Through comparison of time constant of planar devices, a difference has been found.

Then a modeling of conductance spectra by deconvolution has been proposed in this

study. The fitting results showed that conductance spectra of Fin can be roughly

expressed by weighted average of the two surfaces.

Based on the above analysis it is suggested that the electrical response of interface

state with three-dimensional surface can be roughly modeled with two interface state of

planar surfaces

59

Acknowledgments I would like to thank my supervisor at Tokyo Institute of Technology, Professor Hiroshi

Iwai, for his excellent guidance and continuous encouragement, as well as financial

support of my life in Japan.

I also would like to thank Prof. Takeo Hattori, Prof. Kenji Natori, Prof. Y. Kataoka, Prof.

Kazuo Tsutsui, Prof. Nobuyuki Sugii, Prof. Akira Nishiyama, Prof. P. Ahmet for

valuable advice.

Special thanks to Assistant Prof. Kakushima for kind guidance and discussion at literally

every step of the study.

The author would like to thank all members of Professor Iwai’s Laboratory, for the kind

friendship and help and advice at experimental procedures.

The author would like to express sincere gratitude to laboratory secretaries, Ms. A.

Matsumoto and Ms. Nishizawa.

At last but not the least, I want to thank my parents who are living in China for their

supports.