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6

Materials Science

1984 Kudo

FET 10-5 10-7 cm2/Vs


2

FET

FET 1 cm2/Vs
3

2,3 2,4 2,5 1,2


4 2 1,2

50 cm2/Vs
FET
4

2010 6

1. ............................................................................................................ 2
2. .................................................. 2
2.1 .................................................................. 2
2.2 ................................. 3
2.3 FET MOS-FET ......................................... 3
2.4 ......................................................... 4
3. .......................................................................... 5
3.1 .................................................................................. 5
3.2 ........................................................................ 6
3.3 TFT ............................................... 6
4. .........................................................................13
4.1 Cr/Au .................13
4.2 ......................14
4.3 .......................................................................15
4.4 FET .......................................................................16
5. ...........................................................................................................16
6. ...........................................................................................................17

EL 5

6
RFID 7
8
9

2.
2.1

1.

Organic Thin-Film TransistorOTFT


Organic Field-Effect Transistor

2-1
(A)

OFET

(B)

Gate
Gate

(A)

Gate
Gate

Gate
Gate

Gate
Gate

1950

(C)

(D)

Gate
Gate

Gate

Gate

Gate
Gate

Gate

Gate

AB
C
D 1 , 2
, 3 , 4 , 5 , 6

2-1

1980

2-1 AC

1983

FET 1

Tel:03-5796-7330Fax:03-5796-7335 E-mail:sialjpts@sial.com

2-1

BD

14

2-2

15,16

4
MIS
Metal Insulator Semiconductor

(A)

AB

C
D

Gate

Gate

Gate

Gate

Gate
Gate

Gate
Gate

10

(C)

Emitter
Emitter

(B)

Floating
Metal
FloatingMetal

n
n

11

Base
Base

2-2

Gate
Gate

A - B
C

Gate

Gate

p
p
Collector
Collector

2.3 FET MOS-FET

FET
MOSMetal-Oxide-SemiconductorMOSFET

2-3

Chemical Vapor Deposition

CVD

n-

n-

12,13

2.2
2.1

MIS-FET

OFFn-p-n

pn

OFF

pp

2-3 FET MOS-FET

MOS-FET

FET

/ p n

AsP

FET

OFF n-p-n OFF

FET /

OFF

FET FET

p p

MOS-FET

30 m

SUS

Tel:03-5796-7340Fax:03-5796-7345 E-mail:safcjp@sial.com

2.4

Organic FETOFET

Id
Vg

/ / MIS

MIS

2-5
1Vg 0 V Vd

Ld

Vg 2-5
2Vg VthVd

Vg-VthVg V
ground
s

2-4 FET

Vth

W L

Vg VthVg

FET

Vd
Id

Vd

Vg

2-5
3
Vg VthVd Vg-Vth Vd

Vd Vg-Vth

Vd Vd

Vg-Vth 2-54 Vd
L

2-4 FET

Vd Id

Id-Vd
W2 mmL100 m

-0.7

-250

Drain current (nA)

-0.5
-0.4

-0.3

-0.2

Drain current (A)

-0.6

-0.1
0

-250

-250

-200

-200

-150

-100

-50
0
0

V d

-50
-20 -40 -60 -80 -100 -120
Drain voltage (V)

2VgVthVd Vg -Vth

-150
-100
-50
0
0

-20 -40 -60 -80 -100 -120


Drain voltage (V)

Vg-100 V

Drain current (A)

Drain current (A)

-100

Vg-100 V

VgVs

1Vg0 V

-150

0
0

-20 -40 -60 -80 -100 -120


Drain voltage (V)

Vg0 V

-200

Vd

Id

3VgVthVdVg -Vth

-20 -40 -60 -80 -100 -120


Drain voltage (V)

Vg-100 V

4VgVthVdVg -Vth

2-5

Tel:03-5796-7330Fax:03-5796-7335 E-mail:sialjpts@sial.com

3.

Si n
n-

3.1

C60 1.5 cm2/Vs n

22

10,000

10,000

1980

Processability

p HOMO
Highest

Occupied Molecular Orbital 5.0 eV


LUMOLowest Unoccupied Molecular Orbital 3.2
eV /
-5.1 eV -4.9 eV Au
HOMO p
Ca
-2.9 eVLUMO n

10-2 cm2/Vs FET

poly
9,9-dioctylfluorene-co-bithiophene
F8T223poly3-hexylthiophene
P3HT24,25P3HT

ambipolar 17

0.1 cm2/Vs

1 cm2/Vs

2009

Facchetti

26

3.2

p 50 cm /Vs
2

n 0.85 cm2/

Vs

p n

18,19
n
0.2 cm2/Vs n

3 cm2/Vs n 20,21

1980 OFET

p 27,281990

29,30 1 cm2/Vs

1 cm /Vs

1997

1 cm2/Vs 31

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pn

3-2

1980

15

10-5 cm2/Vs 1 cm2/Vs

5 3-1

103

cm2/Vs

102

EL

10
1

46,47

10-1
10-2

10-3

10-4
10-5
1985

1990

1995

2000

2005

2010

2015

2004216P111

3-1 TFT

48

2000

TIPS-

Pentacene 32
33,34,35

3-2

1 cm2/Vs

36,37,38,39,40,41

3.2

FET

FET 3

/
Au Au

p n

EL

p
42,43,44,45
p

Au Cu49Ag50Ca51 ITO
Indium Tin Oxide52 53 54
PEDOT-PSS 55,56
5758

pn

Au 4.9 eV n
p
HOMO 59

60,61,62,63

3.3 FET

Tel:03-5796-7330Fax:03-5796-7335 E-mail:sialjpts@sial.com

2-1p 2-2n 2-3

SiO2 64,65

Al2O366 Ta2O567OFET

SiO2

1 1

FET

HexamethyldisilazaneHMDS OctadecyltrichlorosilanOTS
OTS
PFOTS

1-1Aldrich 551112 50

-6T
- CYEPL
PVA
PVC

cm2/Vs
1-2Aldrich
698423 Vth

PMMA

OPV 1-3

68 PI

PVP

69,70

DNTT
1-4

FET

FET 12
1

1-1

Rubrene
Aldrich 551112

1-2

Podzorov, V.Sysoev, S.E.Loginova, E.Pudalov, V. M.Gershenson, M.E.,


Appl. Phys. Lett., 2003, 83, 3504.
Podzorov, V.Pudalov, V.M.Gershenson, M.E., Appl. Phys. Lett., 2003, 82,
1739.
Sundar, V.C.Zaumseil, J.Podzorov, V.Menard, E.Willett, R.L.
Someya, T.Gershenson, M.E.Rogers, J.A., Science, 2004, 303, 1644.
Takeya, J.Yamagishi, M.Tominari, Y.Hirahara, R.Nakazawa, Y.
Nishikawa, T.Kawase, T.Shimoda, T.Ogawa, S., Appl. Phys. Lett.,
2007, 90, 102120.
Pernstich, K.P.Haas, S.Oberhoff, D.Goldmann, C.Gundlach, D.J.
Batlogg, B.Rashid, A.N.Schitter, G., J. Appl. Phys., 2004, 96, 6431.

Pentacene

Takeya, J.Goldmann, C.Haas, S.Pernstich, K.P.Ketterer, B.Batlogg, B.,


J. Appl. Phys., 2003, 94, 5800.
Jurchescu, O.D.Popinciuc, M.Wees, B.J.Palstra, T.T.M., Adv. Mater.,
2007, 19. 688.

1-3

Oligo
p-phenylenevinylene
OPV

Nakanotani, H.Saito, M.Nakamura, H.Adachi, C., Appl. Phys. Lett.,


2009, 95, 033308.

1-4

Dinaphtho2,3-b:2',3'-f
thiopheno3,2-bthiophene
DNTT

Uno, M.Tominari, Y.Yamagishi, M.Doi, I.Miyazaki, E.Takimiya, K.


Takeya, J., Appl. Phys. Lett., 2009, 94, 223308.
Haas, S.Takahashi, Y.Takimiya, K.Hasegawa, T., Appl. Phys. Lett., 2009,
95, 022111.

Aldrich 698423

!
Aldrich

DNTT : Dinaphtho2,3-b:2',3'-f thiopheno

DPh-BDT : 2,6-Diphenylbenzo1,2-b:4,5-b
dithiophene

DPh-BTBT: 2,7-Dipheny1benzothieno3,2-b
benzothiophene

DT-BDT: 2,6-Ditolylbenzo1,2-b:4,5-b
dithiophene

3,2-bthiophene

!
WEB
:

Tel:03-5796-7340Fax:03-5796-7345 E-mail:safcjp@sial.com

2-1p 2
2-1PentaceneAldrich P1802,
684848, 698423 p

FET
75

2-4 FET

P3HT

FET

76

71,72

73

741 cm2/Vs

2-5 BDT

2-2

2-6 BTBT

2.0 cm2/VsHOMO

0.3 cm /Vs

BTBT

DNTT 2-7

2-3Copper
IIphthalocyanineCuPcAldrich

DNTT 2.9 cm2/Vs

546674, 702854 EL

p FET
0.02 cm2/Vs FET

7.9 cm2/Vs 77

2p

2-1

Klauk, H.Gundlach, D.J.Nichols, J.A.Jackson, T.N., IEEEE Trans. Electron


Devices, 1999, 46, 1258.,
Laquindanum, J.G.Katz, H.E.Lovinger, A.J.Dodabalapur, A., Chem. Mater.,
1996, 8, 2542.,
Dimitrakopoulos, C.D.Brown, A.R.Pomp, A., J. Apply. Phys., 1996, 80, 2501.,
Dimitrakopoulos, C.D.Mascaro, D.J., IBM J. Res. & Dev., 2001, 45, 11.

Pentacene
Aldrich P1802, 684848,
698423

2-2

Meng, H.Bendikov, M.Mitchell, G.Helgeson, R.Wudl, F.Bao, Z.Siegrist, T.


Kloc, C.Chen, C.-H., Adv. Mater., 2003, 15, 1090

2,3,9,10-Tetramethylpentacene
Me4PENT

2-3

CopperIIphthalocyanine
CuPc
Aldrich 546674, 702854

Bao, Z.Lovinger, A.J.Dodabalapur, A., Appl. Phys. Lett., 1996, 69, 3066.

2-4

Aldrich

Horowitz, G.Fichou, D.Peng, X.Xu, Z.Garnier, F., Solid State Commum.


1989, 72, 381.

2-5

2,6-Diphenylbenzo1,2-b:4,5-b
dichalcogenophene
DPh-BDX

Takimiya, K.Kunugi, Y.Konda, Y.Niihara, N.Otsubo, T., J. Am. Chem. Soc.,


2004, 126, 5084.

2-6

2,7-Diphenyl1benzothieno3,2-b
benzothiophene
DPh-BTBT

Takimiya, K.Kunugi, Y.Konda, Y.Ebata, H.Toyoshima, Y.Otsubo, T., J.


Am. Chem. Soc., 2006, 128, 3044.,
Takimiya, K.Ebata, H.Sakamoto, K.Izawa, T.Otsubo, T.Kunugi, Y., J. Am.
Chem. Soc., 2006, 128, 12604.

2-7

,3
-f thieno
3,2-b
Dinaphtho2,3-b:2
thiophene
DNTT

Yamamoto, T.Takimiya, K., J. Am. Chem. Soc., 2007, 129, 2224.


Uno, M.Doi, I.Takimiya, K.Takeya, J. Appl. Phys. Lett., 2009, 94, 103307.
Zschieschang, U.Ante, F.Yamamoto, T.Takimiya, K.Kuwabara, H.Ikeda,
M.Sekitani, T.Someya, T.Kern, K.Klauk, H. Adv.Mater., 2010, 22, 982.

2-4
Name

Structure

-Sexithiophene(6T)

S
S

5,5-Dihexyl-2,2:5,2:5,2:5,2:5,2-sexithiophene
(DH-6T)

S
S

594687-1G

S
S

S
CH3(CH2)4CH2

Cat. No.

S
S

CH2(CH2)4CH3

633216-500MG

sigma-aldrich.com/organicelectronics-jp

Tel:03-5796-7330Fax:03-5796-7335 E-mail:sialjpts@sial.com

2-2n 3

2-8N,N'-dioctyl-3,4,9,10-perylene tetracarboxylic diimide


Aldrich 663913 n
0.6 cm2/Vs

1.8 cm2/Vs

Vth

2-11

2-12

HOMO

0.2 cm2/Vs

2-9Copper
II

1,2,3,4,8,9,10,11,15,16,17,18,22,23,24,25-hexadecafluoro29H,31H-phthalocyanineAldrich 446653
0.03 cm2/Vs
n
CMOS n
2-10 n
FET
SiO2 OTS 0.1
cm2/Vs
FET n

FET
C60
2-13Fullerene -C60Aldrich

572500, 379646, 483036 n

3
cm2/Vs
PCBM
2-14Aldrich 684457,
684449, 684430
n
0.2 cm2/Vs
78

79

3n

2-8

N,N'-dioctyl-3,4,9,10-perylene
tetracarboxylic diimide
PTCDI-C8HPTCDI-C8
Aldrich 663913

Malenfant, P.R.L.Dimitrakopoulos, C.D.Gelorme, J.D.Kosbar, L.L.


Graham, T.O.Curioni, A.Andreoni, W., Appl. Phys. Lett., 2002, 80, 2517.

2-9

CopperII1,2,3,4,8,9,10,11,15,16,17,
18,22,23,24,25-hexadecafluoro-29H,
31H-phthalocyanine
F16CuPc
Aldrich 446653

Bao, Z.Lovinger, A.J.Brown, L., J. Am. Chem. Soc., 1998, 120, 207.

2-10

Perfluoropentacene

Sakamoto, Y.Suzuki, T.Kobayashi, M.Gao, Y.Fukai, Y.Inoue, Y.


Sato, F.Tokito, S., J. Am. Chem. Soc., 2004, 126, 8138.

2-11

2,2'-Bis4-trifluoromethylphenyl
-5,5'-bithiazole

Ando, S.Murakami, R.Nishida, J.Tada, H.Inoue, Y.Tokito, S.


Yamashita, Y., J. Am. Chem. Soc., 2005, 127, 14996.

2-12

4,7-Bis5-4'-trifluoromethylphenyl
thiophen-2-ylbenzo1,2,5thiadiazole

Kono, T.Kumaki, D.Nishida, J.Sakanoue, T.Kakita, M.Tada, H.


Tokito, S.Yamashita. Y., Chem. Mater., 2007, 19, 1218.

2-13

Fullerene-C60
C60

Haddon, R.C.Perel, A.S.Morris, R.C.Palstra, T.T.M.Hebard, A.F.


Fleming, R.M., Appl. Phys. Lett., 1995, 67, 121.
Anthopoulos, T.D.Singh, B.Marjanov, N.Sariciftci, N.S.Ramil, A.M.
Sitter, H.Clle, M.Leeuw, D.M., Appl. Phys. Lett., 2005, 89, 213504.
Kinoshita, S.Sakanoue, T.Yahiro, M.Takimiya, K.Ebata, H.Ikeda, M.
Kuwabara, H.Adachi, C., Solid State Commum., 2008, 145, 114.
Haddock, J.N.Zhang, X.Domercq, B.Kippelen, B., Org. Electronics,
2005, 6, 182.

Aldrich 572500, 379646,


483036

2-14

6,6-Phenyl C61 butyric acid methyl

ester

PCBM60PCBM
Aldrich 684457, 684449,
684430

Chikamatsu, M.Itakura, A.Yoshida, Y.Azumi, R.Yase, K., Chem.


Mater., 2008, 20, 7366.

Tel:03-5796-7340Fax:03-5796-7345 E-mail:safcjp@sial.com

2-15

6,13-Bistriisopropylsilylethynyl
pentacene
TIPS-pentacene
Aldrich 716006

Anthony, J.E.Brooks, J.S.Eaton, D.L.Parkin, S.R., J. Am. Chem. Soc.,


2001, 123, 9482.
Payne, M.M.Delcamp, J.H.Parkin, S.R.Anthony, J.E., Org. Lett., 2004, 6,
1609.
Payne, M.M.Odom, S.A.Parkin, S.R.Anthony, J.E., Org. Lett., 2004, 6,
3325.

2-16

5,11-Bistriethylsilylethynylanthra
2,3-b:6,7-b' dithiophene
TES anthradithiophene

Payne, M.M.Parkin, S.R.Anthony, J.E.Kuo, C.C.Jackson, T.N., J. Am.


Chem. Soc., 2005, 127, 4986.

2-17

2,7-Dialkyl1benzothieno3,2-b
benzothiophene
alkyl-BTBT

Ebata, H.Izawa, T.Miyazaki, E.Takimiya, K.Ikeda, M.Kuwabara, H.


Yui, T., J. Am. Chem. Soc., 2007, 129, 15732.
Izawa, T.Miyazaki, E.Takimiya, K. Adv. Mater., 2008, 20, 3388.
Kang, M.J.Doi, I.Mori, H.Miyazaki, E.Takimiya, K.Ikeda, M.
Kuwabara, H., Adv. Mater., 2011, 23, 1222.

2-3 4
2-15
TIPS-PentaceneAldrich 716006

cm2/Vs TOFTime of Flight

FET

TIPS
0.17
cm2/Vs
1 cm2/Vs

3-2 6
90 3-4
3-5

80

2-16 1 cm2/Vs

A
SmA 10-4 cm2/

Vs ESmE 10-2 cm2/Vs


3-6
Lcol 10-3
cm2/Vs
3-7

C13 2.8 cm2/Vs

HOMO

SmH

BTBT 2-17
1 cm2/Vs

TOF SmH 0.1 cm2/

Vs

3-1 5

3-1

FET 0.14 cm2/Vs

H0.1 cm2/Vs

3-9 0.5 cm2/Vs

Mllen p

on/off 10715

3-2

PR-TRMC
Pulse-

Radiolysis Time-Resolved Microwave Conductivity


0.1 1 cm2/Vs
3-3 Colr Colh10-1

10

3-8

4 7

FET 90

4-1 3-
P3RT

Tel:03-5796-7330Fax:03-5796-7335 E-mail:sialjpts@sial.com

3-1

2,3,6,7,10,11-Hexahexylthiotriphenylene
HHTT

Adam, D.Schuhmacher, P.Simmerer, J.Hussling, L.


Siemensmeyer, K. Nature 1994, 371, 141.

3-2

Alkyl-hexabenzocoronene
HBC

van de Craats, A.M.Warman, J. M.Fechtenktter, A.Brand, J. D.


Harbison, M. A., Mllen, K. Adv.Mater. 1999, 11, 1469.

3-3

1,4,8,11,15,18,22,
25-Octaoctylphthalocyanine

Iino, H.Hanna, J.Bushby, R. J.Movaghar, B.Whitaker, B. J.Cook, M.


J. Appl.Phys.Lett. 2005, 87, 132102.

3-4

2-4'-heptyloxyphenyl
-6-dodecylthiobenzothiazole

Funahashi, M.Hanna, J. Phys. Rev. Lett. 1997, 78, 2184.

3-5

2-4'-octylphenyl
-6-dodecyloxynaphthalene
8-PNP-O12

Funahashi, M.Hanna, J. Appl. Phys. Lett. 1997, 71, 602.

3-6

1Benzothieno
3,2-b
1

benzothiophene-2,7-dicarboxylate
BTBT

Mry, S.Haristoy, D.Nicoud, J.-F.Guillon, D.Diele, S.Monobe, H.


Shimizu, Y. J. Mater. Chem. 2002, 12, 37.

3-7

5-Propyl-5''''-henynyl-2,2':5',2'':
5'',2'''-quanterthiophene
3-QTP-yne-4

Funahashi, M.Hanna, J. Adv.Mater. 2005, 17, 594.

3-8

5,5'-Bis7-hexyl-9H-fluoren-2-yl
-2,2'-bithiophene
DHFTTF

Meng, H.Zheng, J.Lovinger, A. J.Wang, B.-C.Van Patten, P. G.Bao, Z.


Chem.Mater. 2003, 15, 1778.

3-9

Bis-5'-hexylthiophen-2'-yl
-2,6-anthracene
DHTAnt

Meng, H.Sun, F.Goldfinger, M.B.Jaycox, G. D.Li, Z.Marshall, W. J.


Blackman, G. S. J. Am. Chem. Soc. 2005, 127, 2406.

TM

Vol.4 No.3

TIPS
John E. Anthony
Tobin Marks
Iain McCullochMartin Heeney

Thomas Bjrnholm

www.sigma-aldrich.com/sacatalog-jp

Tel:03-5796-7340Fax:03-5796-7345 E-mail:safcjp@sial.com

11

FET 0.1 cm2/Vs P3RT

PF

PF 4-6 265

MEH-PPV P3RT

4-6

FET-LED

4-2

FET 0.1

0.1 cm /Vs
4-3
FET
5 m
0.15 cm2/Vs
1
4-4
0.6 cm2/Vs
4-5 4-4
FET
0.08 cm2/Vs Tg 150
2

0.2 cm2/Vs
5 8 PF

4-7 TOF FET


0.01 cm2/Vs

PF 4-8PF
0.01 cm2/Vs

0.25 cm2/Vs

4-1

Poly3-alkylthiophene
P3RT

Sirringhaus, H.Tessler, N.Friend, R.H. Science 1998, 280, 1741.


Bao, Z.Dodabalapur, A.Lovinger, A. J. Appl. Phys. Lett. 1996, 69, 4108.

4-2

Poly3,3'''-dialkyl-quaterthiophene
PQT

Ong, B. S.Wu, Y.Liu, P.Gardner, S. J. Am. Chem. Soc. 2004, 126, 3378.

4-3

Poly2,5-bis3-decylthiophen-2-yl
thieno2,3-bthiophene

Heeney, M.Bailey, C.Genevicius, K.Shkunov, M.Sparrowe, D.


Tierney, S.McCulloch, I. J. Am. Chem. Soc. 2005, 127, 1078.

4-4

Poly2,5-bis3-alkylthiophen-2-yl
thieno3,2-bthiophene

McCulloch, I.Heeney, M.Bailey, C.Genevicius, K.MacDonald,


I.Shkunov,M.Sparrowe, D.Tierney, S.Wagner, R.Zhang, W.
Chabinyc, M.L.Kline, R. J.McGehee, M. D.Toney M. F. Nat.Mater.
2006, 5, 328.

4-5

Poly2,5-bis2-thienyl-3,6-dialkylthieno
3,2-bthiophene

Li, Y.Wu, Y.Liu, P.Birau , M.Pan, H.Ong, B. S. Adv. Mater. 2006,


18, 3029.

4-6

Poly-9,9'-dioctyl-uorene-cobithiophene
F8T2
Aldrich 685070
Polytriarylamine
PTAA
Aldrich 702471

Sirringhaus, H.Wilson, R. J.Friend, R. H.Inbasekaran, M.Wu, W.


Woo, E. P.Grell, M.,Bradley, D. D. C. Appl. Phys. Lett. 2000, 77, 406.

4-7

4-8

Veres, J.Ogier, S.D.Leeming, S.W.Cupertino, D.C.Khaffaf, S. M. Adv.


Funct. Mater. 2003, 13, 199.

Poly9,9-dioctylfluorenyl-2,7-diyl
-co-4,4-N-4-sec-butylphenyl
diphenylamine
TFB

Fong, H. H.Papadimitratos, A.Malliaras, G. G. Appl.Phys.Lett. 2006, 89,


172116.

4-13-
Name

S-tructure

Mobility

Average Molecular Weight

Cat. No.

regioregular

445703-1G

104 - 101cm2/Vs

average Mn 25,00035,000
regioregular, electronic grade, Plexcore OS 1100

698989-250MG
698989-1G
698989-5G

104 - 101cm2/Vs

average Mn 45,00065,000
regioregular, electronic grade, Plexcore OS 2100

698997-250MG
698997-1G

Poly(3-hexylthiophene-2,5-diyl) (P3HT)
CH2(CH2)4CH3
S
n

*Plexcore is a registered trademark of Plextronics, Inc.


sigma-aldrich.com/organicelectronics-jp

12

Tel:03-5796-7330Fax:03-5796-7335 E-mail:sialjpts@sial.com

4.

4.1

Cr/Au

TFT

50 ml 10 ml

40 ml

photolithography

14
vol ratio

300 nm

70

n++-Si

10

10

dangling bond

3 2

pH pH

IPAisopropyl alcohol

3 IPA

IPA

50ml

100

HMDS
1,1,1,3,3,3Hexamethyldisilazane LOL1000Lift
off layerTSMR-8900

Orientation Flat

15mm

4-1

HMDS

1,000 rpm
30

110

100

HMDS 5

HMDS
HMDS

4-1

HMDS LOL
HMDS

LOL1000 0.45 m

111

HMDS

45

4,000 rpm 30

150

Tel:03-5796-7340Fax:03-5796-7345 E-mail:safcjp@sial.com

13

5 HMDS
2 LOL1000

Au Cr Au

Cr

TSMR-8900

EB

3,000 rpm 30

110 5

1.0 10-4 Pa

rpm

EB Cr 30 Au 500
y1

4 m

30

Cr Au

IPA

4-3

Cr/Au Micro
Posit Remover 1165
70

20 30

Au

NMD-3

30

2 IPA

4-2

4.2

FET

W
2mm

20
25mm

4mmW

4mm

100mm50mm25mm10mm5mm

UV/ UV/
UV253
1 3.7

mW/cm2 3 12 UV

4-2

(a)

Pt

TSMR-8900 m
100nm
Si
Au

BC
SiO2

LOLBC
SEM

mmol/L 100 ml

(b)

40

Au

Pt

BC
SiO2
LOLBC
SEM

4-3

14

1
110 5

HMDS

HMDS

Tel:03-5796-7330Fax:03-5796-7335 E-mail:sialjpts@sial.com

110
HMDS

4 /

4-4

FET /

HMDS

FET /

110 5

n FET
Au

Cr

50 m
/

Si

HMDS

4-4HMDS

3
FET FET

5
10-4 Pa 2.0 /s 3.0 /s
300 500

4.3
FET

4-5

FET

Agilent

B1500A Keithley 4200-SCS

10-4 Pa 10-6 Pa
0.1 /s
0.5 /s 500

Triaxial

70

cableTXA

Coaxial cable BNC


TXA

L =100mm
L =150mm
L =200mm

L =50mm

TXA-

BNC
4-6
bBNC
(
)

a
TXA
(
)

a
FET

c
TXA-BNC

b
FET

TXABNC

4-6

4-5 FET

TXA

Tel:03-5796-7340Fax:03-5796-7345 E-mail:safcjp@sial.com

15

Ground

Q
xId

4-2

Ground

12

4-3

4-3Id x
Id x Id x 0 L

Id-Vd

4-4

300 nm
100V

4-3 V
0 0V
L Vd

20 V -100 V -10 V

Id-Vd

+20 V -100 V -1 V

4-5

4-7
a
Id-Vd

Id-Vg

4-6

-100 V
+20 V -100 V -1 V 4-7b
Id-Vg

-90V

-150

-80V

-100
-50

Drain current (A)

Drain current ( A)

Vg=-100V
-200

-70V
-60V
~20V

-3

10

-4

10

-5

Drain voltage (V)

0.012

10

-6

0.010

-7

0.008

10

-8

0.006

10

-9

0.004

-10

0.002

10

0.014

10

10

0
-140 -120 -100 -80 -60 -40 -20

Vd =-100 V
=0.7 cm2/Vs
Vth=-37 V

-11

-120 -100-80 -60 -40 -20

0.016

Drain current1/2 (A1/2 )

-250

10

Ci

0
0 20 40

Vg Vth Vg Vth
Vg
Vg-Vth

4-7
Vp dId/dVd 0

Gate voltage (V)

aFET Id -Vd

b
FETId -Vg
Vg =-100V

4-7 FET
W 2 mmL 100 m FET

4-8
4-7 Idsat

4-9

4.4 FET

Id-Vg
4-8 L FET

- 0

4-9

4-10

Q(x)V(x)F(x)
S
G
0

Id1/2-Vd WC/2L1/2

4-8 FET

WSiO2 d
r 3.9
m x

4-7 FET FET


0.7 cm2/VsVth -37 V

5.

- V
x

cm2/Vs n
2010 5 432
240 RGB EL

4-1

16

Tel:03-5796-7330Fax:03-5796-7335 E-mail:sialjpts@sial.com

EL FET
FET
peri-Xanthenoxanthene
PXX
0.4 cm2/Vs FET

FET

2000

6.
1 Ebisawa, F.; Kurokawa, T.; Nara, S. J. Appl. Phys. 1983, 54, 3255.
2 Kudo, K.; Yamashina, M.; Moriizumi, T. Jpn. J. Appl. Phys. 1984, 23, 130.
3 Kelley, T. W.; Boardman, L. D.; Dunbar, T. D.; Muyres, D. V.; Pellerite, M. J., Smith; T. P. J. Phys.
Chem. B, 2003, 107, 5877.
4 Takeya, J.; Yamagishi, M.; Tominari, Y.; Hirahara, R.; Nakazawa, Y.; Nishikawa, T.; Kawase, T.;
Shimoda T.; Ogawa S. Appl. Phys. Lett. 2007, 90, 102120.
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6 Sekitani, T.; Noguchi, Y.; Hata, K.; Fukushima, T,; Aida, T.; Someya, T. Science, 2008, 321, 1468.
7 Myny, K.; Steudela, S.; Viccaa, P.; Beenhakkersd, M. J.; van Aerled, N. A.J.M.; Gelincke, G. H.;
Genoe, J.; Dehaenea, W.; Heremans, P. Solid-State Electronics. 2009, 53, 1220.
8 Hepp, A.; Heil, H.; Weise, W.; Ahles, M.; Schmechel, R.; von Seggern, H. Phys. Rev. Lett. 2003,
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9 Nakanotani, H.; Saito, M.; Nakamura, H.; Adachi, C. Appl. Phys. Lett.,2009, 95, 033308.
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13 Diallo, K.; Erouel, M.; Tardy, J.; Andr, E.; Garden, J.-L. Appl. Phys. Lett., 2007, 91, 183508.
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19 Sakanoue, T.; Yahiro, M.; Adachi, C.; Uchiuzou, H.; Takahashi, T.; Toshimitsu, A. Appl. Phys. Lett.,
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20 Itaka, K.; Yamashiro, M.; Yamaguchi, J.; Haemori, M.; Yaginuma, S.; Matsumoto, Y.; Kondo, M.;
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22 Kato,T.; Origuchi, C.; Shinoda, M; Adachi, C. Jpn. J. Appl. Phys., 2011, 50, 050202.
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25 Sirringhaus, H; Brown P. J.;Friend R. H.; Nielsen M. M.; Bachgaard K.; Langeveld-Voss B. M. W.;
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38 Uemura, T.; Hirose, Y.; Uno, M.; Takimiya, K.; Takeya, J., Appl. Phys. Exp., 2009, 2, 111501.
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41 Nakayama, K.; Hirose, Y.; Soeda, J.; Yoshizumi, M.; Uemura, T.; Uno, M.; Li, W.; Kang, M.J.;
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43 Chua, L. L.; Zaumseil, J.; Chang, J. F.; Ou, E. C.-W.; Ho, P. K.-H.; Sirringhaus, H.; Friend , R. H.
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44 Zaumseil, J.; Friend, R. H.; Sirringhaus, H. Nat. Mater., 2006, 5, 69.
45 Takahashi, T.; Takenobu, T.; Takeya, J.; Iwasa, Y. Adv. Funct. Mater., 2007, 17, 1623.
46 Zaumseil, J.; Groves, C.; Wineld, J. M.; Greenham, N. C.; Sirringhaus, H. Adv. Funct. Mater.,
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47 Nakanotani, H.; Saito, M.; Nakamura, H.; Adachi, C. Adv. Funct. Mater.,2010, 20, 1610.
48 Bisri, S. Z.; Takenobu, T.; Yomogida, Y.; Shimotani, H.; Yamao, T.; Hotta, S.; Iwasa, Y. Adv. Funct.
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49 Wang, S.D.; Minari, T.; Miyadera, T.; Aoyagi, Y.; Tsukagoshi, K. Appl. Phys. Lett. 2008, 92, 063305.
50 Li, Y.; Wu, Y.; Ong, B.S. J. Am. Chem. Soc.,2005, 127, 3266.
51 Zhang, X.H.;Kippelen, B.; Appl. Phys. Lett., 2008, 93, 133305.
52 Kajii, H.; Koiwai, K.; Hirose, Y.; Ohmori, Y., Org. Electr., 2010, 11, 509.
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54 Zhang, Y.Y.; Shi, Y.; Chen, F.; Mhaisalkar, S. G.; Li, L.J.; Ong, B.S.; Wu, Y., Appl. Phys. Lett., 2007, 91,
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55 Kang, H.S.; Lee, J.W.; Kim, M.K.; Joo, J.; Ko, J. M.; Lee, J.Y., J. Appl. Phys., 2006, 100, 064508.,
56 Takahashi, Y.; Hasegawa, T.; Abe, Y.; Tokura, Y.; Nishimura, K.; Saito, G., Appl. Phys. Lett., 2002,
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57 Kato T.; Origuchi, C.; Shinoda, M.; Adachi, C., Jpn. J. Appl. Phys., 2011, 50, 050202. ,
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59 Hamadani, B.H.; Natelson, D., J. Appl. Phys., 2005, 97, 064508.
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64 Kudo,K.; Yamashina, M.; Moriizumi, T., Jan.J.Appl.Phys., 1984, 23, 130.
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66 Lee, J.; Kim, J.H.; Im, S., Appl.Phys.Lett., 2003, 83, 2689.
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17

sigma-aldrich.com/organicelectronics-jp
Name
Thieno[2,3-b]thiophene

Structure
S

Thieno[3,2-b]thiophene

Purity
95%

Catalog No.
702641-1G
702641-5G

95%

702668-1G
702668-5G

97%

710172-500MG

97%

691925-1G
691925-5G

95%

697400-1G
697400-5G

95%

688312-1G

97%

694258-1G

97%

456373-1G
456373-5G
456373-25G
515493-1G
515493-5G

S
S

Dithieno[3,2-b:2',3'-d]thiophene

2-Bromo-3-hexylthiophene

CH2(CH2)4CH3

S
S

Br

3-Hexylthiophene-2-boronic acid pinacol ester

2-Bromo-3-dodecylthiophene

CH2(CH2)10CH3
Br

5-Bromo-2-hexylthiophene
Br

CH2(CH2)4CH3

2,5-Dibromo-3-hexylthiophene

CH2(CH2)4CH3
Br

Br

5,5'-Dibromo-2,2'-bithiophene

99%

2,2'-Bithiophene-5,5'-diboronic acid bis(pinacol) ester

97%

647020-1G
647020-5G

3,3'-Dibromo-2,2'-bithiophene

97%

733725-1G
733725-5G

97%

699098-500MG

97%

701254-1G

97%

704199-1G

2,1,3-Benzothiadiazole-4,7-bis(boronic acid pinacol ester)

95%

702803-1G

4,7-Dibromobenzo[c]-1,2,5-thiadiazole

95%

693847-1G
693847-5G

4,7-Bis(2-bromo-5-thienyl)-2,1,3-benzothiadiazole

99.0% (HPLC)

732435-1G

97%

708283-500MG

95%

708267-500MG

>97%

731757-1G

97%

717274-5G

5,5''-Dibromo-2,2':5',2''-terthiophene

Br

Br

2-Bromo-7-hexyl-9H-fluorene
Br

4,4'-Biphenyldiboronic acid bis(pinacol) ester

CH2(CH2)4CH3

H3C
H3C

H3C

O
CH3

O
B

B
O

5-Fluoro-2,3-thiophenedicarboxaldehyde

CH3
CH3
CH3
CH3

H
H

S
O

2,8-Dibromo-6,12-dihydro-6,6,12,12-tetraoctylindeno[1,2-b]fluorene

CH2(CH2)6CH3

CH3(CH2)6CH2

Br

Br
CH3(CH2)6CH2

CH2(CH2)6CH3

9-Ethyl-9H-carbazole-3-boronic acid pinacol ester

1,3,6,8-Tetrabromopyrene

Br
Br

Br
Br

18

Tel:03-5796-7330Fax:03-5796-7335 E-mail:sialjpts@sial.com

sigma-aldrich.com/organicelectronics-jp
Name
Anthracene

Structure

Purity
sublimed grade 99%

Catalog. No.
694959-5G
694959-25G
max = 277 nm
em = 481, 514 nm in
dichloromethane-d2

698415-1G

Benz[b]anthracene

sublimed grade 99.99%


trace metals basis

Pentacene

triple-sublimed grade
99.995% trace metals basis

698423-500MG

sublimed grade
99.9% trace metals basis

684848-1G

Perylene

sublimed grade 99.5%


99.99 trace metal basis

max = 436 nm
em = 447 nm in
tetrahydrofuran

394475-1G
394475-5G

4,4'-Bis(N-carbazolyl)-1,1'-biphenyl (CBP,
DCBP)

sublimed grade 99.9%


trace metals basis

max = 532 nm

699195-1G
699195-5g

556696-500MG
556696-1G

sublimed grade 99%

N,N'-Di-[(1-naphthyl)-N,N'-diphenyl]-1,1'biphenyl)-4,4'-diamine (NPB, NPD)


N

Rubrene

sublimed grade

max = 299 nm
em = 550 nm in
tetrahydrofuran

551112-100MG
551112-1G
551112-5G

Bathocuproine

sublimed grade 99.99%


trace metals basis

max = 277 nm
em = 386 nm in
tetrahydrofuran

699152-500MG

sublimed grade 96%

max = 282 nm
ex = 305nm
em = 507 nm in
chloroform

694924-250MG

sublimed grade

max = 324 nm
ex = 324nm
em = 615 nm in
tetrahydrofuran

688118-250MG

sublimed grade 99.995%


trace metals basis

max = 259 nm
ex = 390nm
em = 519 nm

697737-1G

triple-sublimed grade
>99.99% trace metals basis

max = 678 nm
em = 404 nm

702854-500MG

sublimed grade Dye


content 99 %

max = 678 nm
em = 404 nm

546674-1G
546674-5G

N
CH3

H3C

Tris[2-phenylpyridinato-C2,N]iridium(III)
(Ir(ppy)3)

Ir
N
3

Tris[1-phenylisoquinoline-C2,N]iridium(III)
(Ir(piq)3)
Ir
N
3

Tris-(8-hydroxyquinoline)aluminum (Alq3)
N

O
N
Al

O
N

Copper(II) phthalocyanine (CuPc)


N
N

N
Cu

N
N

N
N

Fullerene-C60

sublimed 99.9%

572500-250MG
572500-1G
572500-5G

[5,6]-Fullerene-C70

sublimed,99 (HPLC)

709476-250MG

Tel:03-5796-7340Fax:03-5796-7345 E-mail:safcjp@sial.com

19

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SAJ1366 2011.8

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