Organic electronics for electrochromic materials and devices:
Gespeichert in:
| 1. Verfasser: | |
|---|---|
| Format: | Buch |
| Sprache: | English |
| Veröffentlicht: |
Weinheim, Germany
Wiley-VCH
[2021]
|
| Schlagworte: | |
| Online-Zugang: | http://www.wiley-vch.de/publish/dt/books/ISBN978-3-527-34871-8/ Inhaltsverzeichnis |
| Beschreibung: | xiv, 514 Seiten Illustrationen, Diagramme 24.4 cm x 17 cm |
| ISBN: | 3527348719 9783527348718 |
Internformat
MARC
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| 020 | |a 3527348719 |9 3-527-34871-9 | ||
| 020 | |a 9783527348718 |c hardcover |9 978-3-527-34871-8 | ||
| 024 | 3 | |a 9783527348718 | |
| 028 | 5 | 2 | |a Bestellnummer: 1134871 000 |
| 035 | |a (OCoLC)1249681246 | ||
| 035 | |a (DE-599)DNB1217131507 | ||
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| 084 | |a VE 9580 |0 (DE-625)147158:253 |2 rvk | ||
| 084 | |a 540 |2 sdnb | ||
| 100 | 1 | |a Meng, Hong |d 1966- |e Verfasser |0 (DE-588)1235805891 |4 aut | |
| 245 | 1 | 0 | |a Organic electronics for electrochromic materials and devices |c Hong Meng |
| 264 | 1 | |a Weinheim, Germany |b Wiley-VCH |c [2021] | |
| 300 | |a xiv, 514 Seiten |b Illustrationen, Diagramme |c 24.4 cm x 17 cm | ||
| 336 | |b txt |2 rdacontent | ||
| 337 | |b n |2 rdamedia | ||
| 338 | |b nc |2 rdacarrier | ||
| 650 | 0 | 7 | |a Elektrochromes Material |0 (DE-588)4292130-2 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Organischer Halbleiter |0 (DE-588)4172780-0 |2 gnd |9 rswk-swf |
| 653 | |a CH90: Physikalische Chemie | ||
| 653 | |a Chemie | ||
| 653 | |a Chemistry | ||
| 653 | |a Components & Devices | ||
| 653 | |a EE60: Komponenten u. Bauelemente | ||
| 653 | |a Electrical & Electronics Engineering | ||
| 653 | |a Elektrotechnik u. Elektronik | ||
| 653 | |a Komponenten u. Bauelemente | ||
| 653 | |a MS50: Optische u. Nichtlineare Optische Materialien | ||
| 653 | |a Materials Science | ||
| 653 | |a Materialwissenschaften | ||
| 653 | |a Optical and Non-Linear Optical Materials | ||
| 653 | |a Optische u. Nichtlineare Optische Materialien | ||
| 653 | |a Physical Chemistry | ||
| 653 | |a Physikalische Chemie | ||
| 689 | 0 | 0 | |a Elektrochromes Material |0 (DE-588)4292130-2 |D s |
| 689 | 0 | 1 | |a Organischer Halbleiter |0 (DE-588)4172780-0 |D s |
| 689 | 0 | |5 DE-604 | |
| 710 | 2 | |a Wiley-VCH |0 (DE-588)16179388-5 |4 pbl | |
| 776 | 0 | 8 | |i Erscheint auch als |n Online-Ausgabe, PDF |z 978-3-527-83061-9 |
| 776 | 0 | 8 | |i Erscheint auch als |n Online-Ausgabe, EPUB |z 978-3-527-83062-6 |
| 776 | 0 | 8 | |i Erscheint auch als |n Online-Ausgabe |z 978-3-527-83063-3 |
| 856 | 4 | 2 | |m X:MVB |u http://www.wiley-vch.de/publish/dt/books/ISBN978-3-527-34871-8/ |
| 856 | 4 | 2 | |m DNB Datenaustausch |q application/pdf |u http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=032633659&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |3 Inhaltsverzeichnis |
| 999 | |a oai:aleph.bib-bvb.de:BVB01-032633659 | ||
Datensatz im Suchindex
| _version_ | 1804182359003627520 |
|---|---|
| adam_text | CONTENTS
PREFACE
XIII
ABOUT
THE
AUTHOR
XIV
1
INTRODUCTION
1
1.1
GENERAL
INTRODUCTION
1
1.2
THE
HISTORY
OF
ELECTROCHROMIC
MATERIALS
3
1.3
THE
KEY
PARAMETERS
OF
ELECTROCHROMISM
5
1.3.1
ELECTROCHROMIC
CONTRAST
5
1.3.2
SWITCHING
TIME
8
1.3.3
COLORATION
EFFICIENCY
9
1.3.4
OPTICAL
MEMORY
11
1.3.5
STABILITY
12
1.4
CONCLUSION
14
REFERENCES
14
2
ADVANCES
IN
POLYMER
ELECTROLYTES
FOR
ELECTROCHROMIC
APPLICATIONS
17
2.1
INTRODUCTION
17
2.2
REQUIREMENTS
OF
POLYMER
ELECTROLYTES
IN
ELECTROCHROMIC
APPLICATIONS
18
2.3
TYPES
OF
POLYMER
ELECTROLYTES
20
2.3.1
GEL
POLYMER
ELECTROLYTES
(GPES)
20
2.3.1.1
PEO-/PEG-BASED
ELECTROLYTES
21
23.1.2
PMMA-BASED
POLYMER
ELECTROLYTES
21
2.3.1.3
PVDF-BASED
POLYMER
ELECTROLYTES
22
2.3.2
SELF-HEALING
POLYMER
ELECTROLYTES
24
2.3.3
CROSS-LINKING
POLYMER
ELECTROLYTES
(CPES)
26
2.3.4
CERAMIC
POLYMER
ELECTROLYTES
27
2.3.5
IONIC
LIQUID
POLYMER
ELECTROLYTES
30
2.3.6
GELATIN-BASED
POLYMER
ELECTROLYTES
32
2.4
CONCLUSION
AND
FUTURE
OUTLOOK
33
REFERENCES
40
VI
CONTENTS
3
ELECTROCHROMIC
SMALL
MOLECULES
49
3.1
BACKGROUND
OF
SMALL
MOLECULE
ELECTROCHROMIC
49
3.2
TECHNOLOGY
DEVELOPMENT
OF
SMALL
MOLECULE
ELECTROCHROMIC
MATERIALS
50
3.3
VIOLENE-CYANINE
HYBRIDS
(AIE
PL
OEC)
50
3.4
TEREPHTHALATE
DERIVATIVES
(MULTICOLOR
OEC)
56
3.4.1
CONCLUSION
63
3.5
ISOPHTHALATE
DERIVATIVES
64
3.5.1
CONCLUSION
79
3.6
METHYL
KETONE
DERIVATIVES
79
3.6.1
CONCLUSION
84
3.7
DIPHENYLACETYLENES
84
3.8
FLUORAN
DYE
DERIVATIVES
85
3.9
PH-RESPONSIVE
MOLECULE
DERIVATIVES
92
3.10
TPA
DYE
DERIVATIVES
95
3.11
HYDROCARBON
DERIVATIVES-NIR-OEC
99
3.12
CONCLUSIONS
AND
PERSPECTIVE
101
REFERENCES
101
4
VIOLOGEN
OEC
105
4.1
THE
INTRODUCTION
OF
OEC
AND
VIOLOGEN
105
4.1.1
GENERAL
INTRODUCTION
105
4.1.2
RESEARCH
HISTORY
OF
VIOLOGEN
105
4.1.2.1
FIRST
STAGE
(1930S-1970S)
107
4.1.2.2
SECOND
STAGE
(1970S-2000S)
107
4.1.2.3
THIRD
STAGE
(2000S-2010S)
107
4.1.2.4
FOURTH
STAGE
(201
OS-PRESENT)
108
4.1.3
ELECTROCHROMISM
AND
ELECTROCHEMISTRY
OF
VIOLOGENS
AND
THEIR
DEVICE
109
4.2
DIFFERENT
STRUCTURES
OF
VIOLOGEN-BASED
ELECTROCHROMIC
MATERIALS
110
4.2.1
SYNTHESIS
OF
VIOLOGENS
110
4.2.1.1
DIRECT
SUBSTITUTION
REACTION
110
4.2.1.2
ZINCKE
REACTION
110
4.2.1.3
METHODS
FOR
SYNTHESIZING
BIPYRIDINE
110
4.2.2
THE
L,L -SUBSTITUTED
VIOLOGEN
111
4.2.2.1
SIMPLE
ALKYL
111
4.2.2.2
ACID
GROUP
111
4.2.23
ESTER
AND
NITROGEN
HETEROCYCLE
112
4.2.2.4
ASYMMETRIC
SUBSTITUTION
113
4.2.3
CONJUGATE
RING
SYSTEM
EXPANSION
113
4.2.3.1
THIAZOLOTHIAZOLE
(TTZ)
UNIT
113
4.23.2
PERYLENEDIIMIDE
(PDI)
UNIT
115
4.233
PBEDOTPH
115
4.23.4
HETEROATOMS
BRIDGED
115
4.23.5
BITHIOPHENE
BRIDGED
118
CONTENTS
VII
4.2.4
4.2.4.1
4.2.4.2
4.3
4.3.1
4.3.1.1
4.3.1.2
4.3.1.3
4.3.1.4
4.3.2
4.3.3
4.3.4
4.3.5
4.3.5.1
4.3.5.2
4.3.5.3
4.3.5.4
4.3.5.5
4.3.6
4.4
4.4.1
4.4.2
4.4.3
4.5
VIOLOGEN-BASED
POLYMER
119
VIOLOGEN
IN
THE
SIDE
CHAIN
120
VIOLOGEN
IN
THE
MAIN
CHAIN
122
VIOLOGEN
ELECTROCHROMIC
DEVICE
124
DEVICE
STRUCTURE
124
FIVE-LAYER
CLASSIC
STRUCTURE
124
SIMPLE
SANDWICH
STRUCTURE
125
CATHODIC
ANODE
SEPARATION
STRUCTURE
125
REFLECTIVE
DEVICE
STRUCTURE
126
ELECTROLYTE
126
REDOX
MEDIATOR
126
CONDUCTIVE
MEDIUM
128
PROBLEMS
WITH
VIOLOGEN
COMPOUND
128
DIMERIZATION
128
AGGREGATION
AND
SOLUBILITY
131
RESPONSE
TIME
131
DRIVING
VOLTAGE
131
CONCLUSION
131
EXAMPLES
OF
VIOLOGEN-BASED
ECD
132
COMPANIES
OPERATING
IN
THE
FIELD
OF
VIOLOGEN
ELECTROCHROMISM
132
GENTEX
132
ESSILOR
134
HAORUO
134
CONCLUSION
134
REFERENCES
135
5
5.1
5.2
5.3
5.4
5.5
5.6
5.7
5.8
5.9
METALLOHEXACYANATES
143
BACKGROUND
143
TECHNOLOGY
DEVELOPMENT
OF
PB
144
CRYSTAL
STRUCTURE
144
ELECTROCHROMIC
MECHANISM
145
SYNTHESIS
147
ELECTROCHROMIC
DEVICES
(ECDS)
150
NANOCOMPOSITES
154
PB
ANALOGS
160
MULTIFUNCTIONAL
APPLICATIONS
170
REFERENCES
175
6
6.1
6.1.1
6.1.2
6.2
6.2.1
6.2.2
ELECTROCHROMIC
CONJUGATED
POLYMERS
(ECPS)
183
INTRODUCTION
183
COMMON
CATEGORIES
AND
OPERATION MECHANISM
183
SYNTHETIC
METHODS
186
THIOPHENE-BASED
CONJUGATED
ELECTROCHROMIC
POLYMERS
190
INTRODUCTION
190
COLOR-TUNING
STRATEGIES
FOR
THIOPHENE-BASED
POLYMERS
191
VIII
CONTENTS
6.2.2.1
STERIC
EFFECTS
192
6.2.2.2
SUBSTITUENT
AND
ELECTRONIC
EFFECTS
193
6.2.3
TYPICAL
COLORED
POLYMERS
195
6.2.3.1
YELLOW
AND
ORANGE
196
6.2.3.2
RED
198
6.233
MAGENTA
AND
PURPLE
199
6.2.3.4
BLACK
202
6.23.5
MULTICOLORED
203
6.23.6
ANODICALLY
COLORING
POLYMERS
205
6.2.4
WATER
OR
GREEN
SOLVENTS
-SOLUBLE
ECPS
208
6.3
POLYPYRROLES-BASED
CONJUGATED
ELECTROCHROMIC
POLYMERS
216
6.3.1
INTRODUCTION
216
6.3.2
ELECTROCHROMIC
PROPERTIES
OF
POLYPYRROLES
(PPY)
218
6.3.3
TUNING
OF
ELECTROCHROMIC
PROPERTIES
OF
POLYPYRROLE
(PPY)
218
6.3.3.1
STRUCTURAL
MODIFICATION
218
633.2
3
AND
3,4-SUBSTITUTED
POLYPYRROLES
235
6333
DONOR-ACCEPTOR
APPROACH
236
6.3.3.4
TERARYLENE
SYSTEMS
237
6.4
POLYCARBAZOLE-BASED
CONJUGATED
ELECTROCHROMIC
POLYMERS
237
6.4.1
INTRODUCTION
237
6.4.2
ELECTROCHROMIC
PROPERTIES
OF
POLYCARBAZOLES
(PCARB)
238
6.4.3
ELECTROCHROMIC
PROPERTIES
OF
POLYCARBAZOLES
DERIVATIVES
238
6.4.3.1
LINEAR
POLYCARBAZOLE
DERIVATIVES
241
6.4.3.2
CROSS-LINKED
POLYCARBAZOLES
DERIVATIVES
249
REFERENCES
260
7
TA-BASED
ELECTROCHROMIC
POLYIMIDES
AND
POLYAMIDES
269
7.1
INTRODUCTION
269
7.1.1
AROMATIC
POLYIMIDES
AND
POLYAMIDES
269
7.1.2
TRIARYLAMINE-BASED
AROMATIC
POLYMERS
270
7.1.3
ELECTROCHEMICAL
AND
ELECTROCHROMIC
BEHAVIORS
OF
MV
TRIARYLAMINE
SYSTEMS
272
7.2
DEVELOPMENT
OF
TA-BASED
ELECTROCHROMIC
POLYIMIDES
AND
POLYAMIDES
272
7.2.1
SIDE
GROUP
ENGINEERING
276
7.2.1.1
INTRODUCTION
OF
PROTECTING
GROUPS
276
7.2.
1.2
INTRODUCTION
OF
ELECTROACTIVE
GROUPS
TO
ACHIEVE
COLOR
TUNING
OF
EC
MATERIAL
277
7.2.1.3
INTRODUCTION
OF
SIDE
GROUPS
TO
ACHIEVE
ELECTROFLUOROCHROMIC
MATERIALS
278
7.2.1.4
INTRODUCTION
OF
OTHER
FUNCTIONAL
SIDE
GROUPS
TO
ACHIEVE
MULTIPLE
FUNCTIONS
EC
MATERIAL
281
7.2.2
BACKBONE
MODULATION
283
7.2.2.1
EXTENDING
THE
POLYMER
BACKBONE
BY
INTRODUCING
MORE
ELECTROACTIVE
GROUPS
283
CONTENTS
IX
7.2.2.2
INTRODUCTION
OF
AMIDE
LINKAGE
INTO
POLYIMIDE
BACKBONE
285
7.2.23
INTRODUCTION
OF
ETHER
LINKAGE
INTO
PIS/PAS
BACKBONE
285
7.2.2.4
INTRODUCTION
OF
ALICYCLIC
STRUCTURES
INTO
PIS/PAS
BACKBONE
288
7.3
CONCLUSIONS
290
REFERENCES
290
8
METALLO-SUPERMOLECULAR
POLYMERS
295
8.1
INTRODUCTION
295
8.2
SINGLE
METALLIC
SYSTEM
296
8.2.1
FE(II)
AND
RU(II)-BASED
METALLO-SUPRAMOLECULAR
POLYMERS
296
8.2.2
CO
11
-BASED
METALLO-SUPRAMOLECULAR
POLYMERS
299
8.2.3
ZN
N
-BASED
METALLO-SUPRAMOLECULAR
POLYMERS
301
8.2.4
CU-BASED
METALLO-SUPRAMOLECULAR
POLYMERS
305
8.2.5
EU
111
-BASED
METALLO-SUPRAMOLECULAR
POLYMERS
308
8.3
HETERO-METALLIC
SYSTEM
311
8.4
THE
FABRICATION
METHOD
OF
METALLOPOLYMER
FILM
314
8.4.1
LAYER-BY-LAYER
SELF-ASSEMBLY
AND
DIP-COATING
METHODS
314
8.4.2
ELECTROPOLYMERIZED
CONDUCTING
METALLOPOLYMERS
315
8.5
CONCLUSION
323
REFERENCES
323
9
METAL-ORGANIC
FRAMEWORK
(MOF)
AND
COVALENT
ORGANIC
FRAMEWORK
(COF)-BASED
ELECTROCHROMISM
(EC)
327
9.1
INTRODUCTION
327
9.2
CURRENT
STUDIES
IN
EC
MOFS
327
9.2.1
THE
ORGANIC
LINKERS
IN
EC
MOFS
328
9.2.1.1
NDI-BASED
ORGANIC
LINKERS
328
9.2.1.2
OTHER
ORGANIC
LINKERS
332
9.2.2
THE
TRANSPORT
OF
ELECTROLYTE
IONS
IN
EC
MOFS
335
9.2.3
SPECIAL
EC
MOFS
338
9.2.3.1
PHOTOCHROMIC
AND
ELECTROCHROMIC
MULTI-RESPONSIVE
MOF
338
9.23.2
MOF-BASED
DOUBLE-SIDED
EC
DEVICE
AND
OTHER
COLOR-SWITCHING
MECHANISMS
339
9.233
EC
BASE
ON
GUEST@MOF
COMPOSITE
SYSTEM
340
9.3
CURRENT
STUDIES
IN
EC
COFS
341
9.4
CONCLUSION
AND
PROSPECT
348
REFERENCES
348
10
NANOSTRUCTURE-BASED
ELECTROCHROMISM
353
10.1
INTRODUCTION
353
10.2
CURRENT
STUDIES
OF
NANOSTRUCTURE
IN
ELECTROCHROMISM
354
10.2.1
NON-ELECTROCHROMIC
ACTIVE
MATERIALS
AS
A
TEMPLATE
FOR
ECS
354
10.2.1.1
PHOTONIC
CRYSTALS
AS
TEMPLATES
FOR
ECS
354
10.2.1.2
PLASMONIC
STRUCTURES
AS
TEMPLATES
FOR
ECS
359
X
CONTENTS
10.2.2
10.3
NANOSTRUCTURED
ELECTROCHROMIC
MATERIALS
IN
ECS
365
CONCLUSION
AND
PROSPECT
369
REFERENCES
369
11
11.1
11.2
11.2.1
11.2.2
11.2.3
11.3
11.3.1
11.3.2
11.3.3
11.4
11.4.1
11.4.1.1
11.4.1.2
11.4.1.3
11.4.2
11.4.3
11.4.3.1
11.4.3.2
11.4.4
11.5
ORGANIC
ELECTROLUMINOCHROMIC
MATERIALS
373
INTRODUCTION
373
CONVENTIONAL
MECHANISMS
OF
ELECTROLUMINOCHROMISM
375
INTRINSIC
MECHANISM
375
ELECTRON
TRANSFER
(ET)
MECHANISM
376
ENERGY
TRANSFER
(ENT)
MECHANISM
376
ELECTROLUMINOCHROMIC
PERFORMANCE
PARAMETERS
376
EMISSION
CONTRAST
376
SWITCHING
TIME
377
LONG-TERM
STABILITY/CYCLE
LIFE
377
CLASSICAL
MATERIALS
378
SMALL
MOLECULES
378
SMALL
MOLECULAR
DYADS
378
REDOX-ACTIVE
MOIETY
AND
LUMINOPHORES
SYSTEM
380
ELECTROACTIVE
LUMINOPHORES
382
TRANSITION
METAL
COMPLEXES
386
POLYMERS
387
NON-CONJUGATED
POLYMERS
387
CONJUGATED
POLYMERS
396
NANOCOMPOSITE
FILMS
407
FUTURE
PERSPECTIVES
AND
CONCLUSION
408
REFERENCES
408
12
12.1
12.2
12.2.1
12.2.1.1
12.2.1.2
12.2.1.3
12.2.2
12.2.2.1
12.2.2.2
12.2.2.3
12.2.3
12.2.4
12.3
ORGANIC
PHOTOELECTROCHROMIC
DEVICES
415
INTRODUCTION
415
STRUCTURE
DESIGN
OF
PECDS
417
POWER
SUPPLY
FOR
PECD
417
DSSC-BASED
PECD
418
PSC-BASED
PECD
423
OPV-BASED
PECD
423
ELECTROCHROMIC
MATERIALS
IN
PECD
425
SMALL
MOLECULE
425
CONDUCTING
POLYMERS
427
NEAR-INFRARED
(NIR)
ELECTROCHROMIC
MATERIALS
433
ELECTROLYTES
IN
PECD
435
SUBSTRATES
IN
PECD
435
FUTURE
PERSPECTIVES
AND
CONCLUSION
436
REFERENCES
436
13
13.1
APPLICATION
OF
OEC
DEVICES
445
SMART
WINDOW
445
CONTENTS
XI
13.1.1
THE
STRUCTURE
AND
WORKING
MECHANISM
OF
SMART
WINDOWS
445
13.1.2
THE
MATERIALS
FOR
ELECTROCHROMIC
WINDOWS
446
13.1.3
PROSPECTS
450
13.2
DIMMABLE
REARVIEW
MIRROR
450
13.3
SENSORS
451
13.3.1
APPLICATION OF
ELECTROCHROMIC
SENSORS
ON
FOOD
PRESERVATION
451
13.3.2
APPLICATION
IN
BIO-SENSING
454
13.4
THE
APPLICATION
OF
ELECTROCHROMIC
DEVICE
IN
DISPLAY
460
13.5
OTHER
APPLICATIONS
OF
OEC
462
REFERENCES
469
14
COMMERCIALIZED
OEC
MATERIALS
AND
RELATED
ANALYSIS
OF
COMPANY
PATENTS
471
14.1
GENERAL
INTRODUCTION
471
14.2
GENTEX
CORPORATION
471
14.3
RICOH
COMPANY,
LTD.
475
14.4
CANON
INC.
476
14.5
BOE
TECHNOLOGY
GROUP
CO.,
LTD.
AND
OPPO
GUANGDONG
MOBILE
COMMUNICATIONS
CO.,
LTD.
477
14.6
OTHER
IMPORTANT
ENTERPRISES
481
14.6.1
NINBO
NINUO
ELECTRONIC
TECHNOLOGY
CO.,
LTD.
481
14.6.2
AMBILIGHT
INC.
483
14.6.3
FURCIFER
INC.
483
14.6.4
CHANGZHOU
SPECTRUM
NEW
MATERIAL
CO.
LTD.
484
14.7
CONCLUSION
485
REFERENCES
485
15
MAIN
CHALLENGES
FOR
THE
COMMERCIALIZATION
OF
OEC
491
15.1
INTRODUCTION
491
15.2
THE
LONG-TERM
STABILITY
OF
OEC
MATERIALS
491
15.3
THE
MECHANICAL
STABILITY
OF
OEC
DEVICES
(ENCAPSULATION
TECHNOLOGY)
495
15.4
LARGE-AREA
PROCESS
TECHNOLOGY:
SPRAY
COATING
AND
ROLL-TO-ROLL
PROCESSES
498
15.4.1
INKJET
PRINTING
498
15.4.2
SPRAY
COATING
500
15.4.3
SLOT-DIE
COATING
500
15.4.4
SCREEN
PRINTING
501
15.5
CONCLUSIONS
AND
PERSPECTIVE
501
REFERENCES
502
INDEX
505
|
| adam_txt |
CONTENTS
PREFACE
XIII
ABOUT
THE
AUTHOR
XIV
1
INTRODUCTION
1
1.1
GENERAL
INTRODUCTION
1
1.2
THE
HISTORY
OF
ELECTROCHROMIC
MATERIALS
3
1.3
THE
KEY
PARAMETERS
OF
ELECTROCHROMISM
5
1.3.1
ELECTROCHROMIC
CONTRAST
5
1.3.2
SWITCHING
TIME
8
1.3.3
COLORATION
EFFICIENCY
9
1.3.4
OPTICAL
MEMORY
11
1.3.5
STABILITY
12
1.4
CONCLUSION
14
REFERENCES
14
2
ADVANCES
IN
POLYMER
ELECTROLYTES
FOR
ELECTROCHROMIC
APPLICATIONS
17
2.1
INTRODUCTION
17
2.2
REQUIREMENTS
OF
POLYMER
ELECTROLYTES
IN
ELECTROCHROMIC
APPLICATIONS
18
2.3
TYPES
OF
POLYMER
ELECTROLYTES
20
2.3.1
GEL
POLYMER
ELECTROLYTES
(GPES)
20
2.3.1.1
PEO-/PEG-BASED
ELECTROLYTES
21
23.1.2
PMMA-BASED
POLYMER
ELECTROLYTES
21
2.3.1.3
PVDF-BASED
POLYMER
ELECTROLYTES
22
2.3.2
SELF-HEALING
POLYMER
ELECTROLYTES
24
2.3.3
CROSS-LINKING
POLYMER
ELECTROLYTES
(CPES)
26
2.3.4
CERAMIC
POLYMER
ELECTROLYTES
27
2.3.5
IONIC
LIQUID
POLYMER
ELECTROLYTES
30
2.3.6
GELATIN-BASED
POLYMER
ELECTROLYTES
32
2.4
CONCLUSION
AND
FUTURE
OUTLOOK
33
REFERENCES
40
VI
CONTENTS
3
ELECTROCHROMIC
SMALL
MOLECULES
49
3.1
BACKGROUND
OF
SMALL
MOLECULE
ELECTROCHROMIC
49
3.2
TECHNOLOGY
DEVELOPMENT
OF
SMALL
MOLECULE
ELECTROCHROMIC
MATERIALS
50
3.3
VIOLENE-CYANINE
HYBRIDS
(AIE
PL
OEC)
50
3.4
TEREPHTHALATE
DERIVATIVES
(MULTICOLOR
OEC)
56
3.4.1
CONCLUSION
63
3.5
ISOPHTHALATE
DERIVATIVES
64
3.5.1
CONCLUSION
79
3.6
METHYL
KETONE
DERIVATIVES
79
3.6.1
CONCLUSION
84
3.7
DIPHENYLACETYLENES
84
3.8
FLUORAN
DYE
DERIVATIVES
85
3.9
PH-RESPONSIVE
MOLECULE
DERIVATIVES
92
3.10
TPA
DYE
DERIVATIVES
95
3.11
HYDROCARBON
DERIVATIVES-NIR-OEC
99
3.12
CONCLUSIONS
AND
PERSPECTIVE
101
REFERENCES
101
4
VIOLOGEN
OEC
105
4.1
THE
INTRODUCTION
OF
OEC
AND
VIOLOGEN
105
4.1.1
GENERAL
INTRODUCTION
105
4.1.2
RESEARCH
HISTORY
OF
VIOLOGEN
105
4.1.2.1
FIRST
STAGE
(1930S-1970S)
107
4.1.2.2
SECOND
STAGE
(1970S-2000S)
107
4.1.2.3
THIRD
STAGE
(2000S-2010S)
107
4.1.2.4
FOURTH
STAGE
(201
OS-PRESENT)
108
4.1.3
ELECTROCHROMISM
AND
ELECTROCHEMISTRY
OF
VIOLOGENS
AND
THEIR
DEVICE
109
4.2
DIFFERENT
STRUCTURES
OF
VIOLOGEN-BASED
ELECTROCHROMIC
MATERIALS
110
4.2.1
SYNTHESIS
OF
VIOLOGENS
110
4.2.1.1
DIRECT
SUBSTITUTION
REACTION
110
4.2.1.2
ZINCKE
REACTION
110
4.2.1.3
METHODS
FOR
SYNTHESIZING
BIPYRIDINE
110
4.2.2
THE
L,L'-SUBSTITUTED
VIOLOGEN
111
4.2.2.1
SIMPLE
ALKYL
111
4.2.2.2
ACID
GROUP
111
4.2.23
ESTER
AND
NITROGEN
HETEROCYCLE
112
4.2.2.4
ASYMMETRIC
SUBSTITUTION
113
4.2.3
CONJUGATE
RING
SYSTEM
EXPANSION
113
4.2.3.1
THIAZOLOTHIAZOLE
(TTZ)
UNIT
113
4.23.2
PERYLENEDIIMIDE
(PDI)
UNIT
115
4.233
PBEDOTPH
115
4.23.4
HETEROATOMS
BRIDGED
115
4.23.5
BITHIOPHENE
BRIDGED
118
CONTENTS
VII
4.2.4
4.2.4.1
4.2.4.2
4.3
4.3.1
4.3.1.1
4.3.1.2
4.3.1.3
4.3.1.4
4.3.2
4.3.3
4.3.4
4.3.5
4.3.5.1
4.3.5.2
4.3.5.3
4.3.5.4
4.3.5.5
4.3.6
4.4
4.4.1
4.4.2
4.4.3
4.5
VIOLOGEN-BASED
POLYMER
119
VIOLOGEN
IN
THE
SIDE
CHAIN
120
VIOLOGEN
IN
THE
MAIN
CHAIN
122
VIOLOGEN
ELECTROCHROMIC
DEVICE
124
DEVICE
STRUCTURE
124
FIVE-LAYER
CLASSIC
STRUCTURE
124
SIMPLE
SANDWICH
STRUCTURE
125
CATHODIC
ANODE
SEPARATION
STRUCTURE
125
REFLECTIVE
DEVICE
STRUCTURE
126
ELECTROLYTE
126
REDOX
MEDIATOR
126
CONDUCTIVE
MEDIUM
128
PROBLEMS
WITH
VIOLOGEN
COMPOUND
128
DIMERIZATION
128
AGGREGATION
AND
SOLUBILITY
131
RESPONSE
TIME
131
DRIVING
VOLTAGE
131
CONCLUSION
131
EXAMPLES
OF
VIOLOGEN-BASED
ECD
132
COMPANIES
OPERATING
IN
THE
FIELD
OF
VIOLOGEN
ELECTROCHROMISM
132
GENTEX
132
ESSILOR
134
HAORUO
134
CONCLUSION
134
REFERENCES
135
5
5.1
5.2
5.3
5.4
5.5
5.6
5.7
5.8
5.9
METALLOHEXACYANATES
143
BACKGROUND
143
TECHNOLOGY
DEVELOPMENT
OF
PB
144
CRYSTAL
STRUCTURE
144
ELECTROCHROMIC
MECHANISM
145
SYNTHESIS
147
ELECTROCHROMIC
DEVICES
(ECDS)
150
NANOCOMPOSITES
154
PB
ANALOGS
160
MULTIFUNCTIONAL
APPLICATIONS
170
REFERENCES
175
6
6.1
6.1.1
6.1.2
6.2
6.2.1
6.2.2
ELECTROCHROMIC
CONJUGATED
POLYMERS
(ECPS)
183
INTRODUCTION
183
COMMON
CATEGORIES
AND
OPERATION MECHANISM
183
SYNTHETIC
METHODS
186
THIOPHENE-BASED
CONJUGATED
ELECTROCHROMIC
POLYMERS
190
INTRODUCTION
190
COLOR-TUNING
STRATEGIES
FOR
THIOPHENE-BASED
POLYMERS
191
VIII
CONTENTS
6.2.2.1
STERIC
EFFECTS
192
6.2.2.2
SUBSTITUENT
AND
ELECTRONIC
EFFECTS
193
6.2.3
TYPICAL
COLORED
POLYMERS
195
6.2.3.1
YELLOW
AND
ORANGE
196
6.2.3.2
RED
198
6.233
MAGENTA
AND
PURPLE
199
6.2.3.4
BLACK
202
6.23.5
MULTICOLORED
203
6.23.6
ANODICALLY
COLORING
POLYMERS
205
6.2.4
WATER
OR
"
GREEN
SOLVENTS
"
-SOLUBLE
ECPS
208
6.3
POLYPYRROLES-BASED
CONJUGATED
ELECTROCHROMIC
POLYMERS
216
6.3.1
INTRODUCTION
216
6.3.2
ELECTROCHROMIC
PROPERTIES
OF
POLYPYRROLES
(PPY)
218
6.3.3
TUNING
OF
ELECTROCHROMIC
PROPERTIES
OF
POLYPYRROLE
(PPY)
218
6.3.3.1
STRUCTURAL
MODIFICATION
218
633.2
3
AND
3,4-SUBSTITUTED
POLYPYRROLES
235
6333
DONOR-ACCEPTOR
APPROACH
236
6.3.3.4
TERARYLENE
SYSTEMS
237
6.4
POLYCARBAZOLE-BASED
CONJUGATED
ELECTROCHROMIC
POLYMERS
237
6.4.1
INTRODUCTION
237
6.4.2
ELECTROCHROMIC
PROPERTIES
OF
POLYCARBAZOLES
(PCARB)
238
6.4.3
ELECTROCHROMIC
PROPERTIES
OF
POLYCARBAZOLES
DERIVATIVES
238
6.4.3.1
LINEAR
POLYCARBAZOLE
DERIVATIVES
241
6.4.3.2
CROSS-LINKED
POLYCARBAZOLES
DERIVATIVES
249
REFERENCES
260
7
TA-BASED
ELECTROCHROMIC
POLYIMIDES
AND
POLYAMIDES
269
7.1
INTRODUCTION
269
7.1.1
AROMATIC
POLYIMIDES
AND
POLYAMIDES
269
7.1.2
TRIARYLAMINE-BASED
AROMATIC
POLYMERS
270
7.1.3
ELECTROCHEMICAL
AND
ELECTROCHROMIC
BEHAVIORS
OF
MV
TRIARYLAMINE
SYSTEMS
272
7.2
DEVELOPMENT
OF
TA-BASED
ELECTROCHROMIC
POLYIMIDES
AND
POLYAMIDES
272
7.2.1
SIDE
GROUP
ENGINEERING
276
7.2.1.1
INTRODUCTION
OF
PROTECTING
GROUPS
276
7.2.
1.2
INTRODUCTION
OF
ELECTROACTIVE
GROUPS
TO
ACHIEVE
COLOR
TUNING
OF
EC
MATERIAL
277
7.2.1.3
INTRODUCTION
OF
SIDE
GROUPS
TO
ACHIEVE
ELECTROFLUOROCHROMIC
MATERIALS
278
7.2.1.4
INTRODUCTION
OF
OTHER
FUNCTIONAL
SIDE
GROUPS
TO
ACHIEVE
MULTIPLE
FUNCTIONS
EC
MATERIAL
281
7.2.2
BACKBONE
MODULATION
283
7.2.2.1
EXTENDING
THE
POLYMER
BACKBONE
BY
INTRODUCING
MORE
ELECTROACTIVE
GROUPS
283
CONTENTS
IX
7.2.2.2
INTRODUCTION
OF
AMIDE
LINKAGE
INTO
POLYIMIDE
BACKBONE
285
7.2.23
INTRODUCTION
OF
ETHER
LINKAGE
INTO
PIS/PAS
BACKBONE
285
7.2.2.4
INTRODUCTION
OF
ALICYCLIC
STRUCTURES
INTO
PIS/PAS
BACKBONE
288
7.3
CONCLUSIONS
290
REFERENCES
290
8
METALLO-SUPERMOLECULAR
POLYMERS
295
8.1
INTRODUCTION
295
8.2
SINGLE
METALLIC
SYSTEM
296
8.2.1
FE(II)
AND
RU(II)-BASED
METALLO-SUPRAMOLECULAR
POLYMERS
296
8.2.2
CO
11
-BASED
METALLO-SUPRAMOLECULAR
POLYMERS
299
8.2.3
ZN
N
-BASED
METALLO-SUPRAMOLECULAR
POLYMERS
301
8.2.4
CU-BASED
METALLO-SUPRAMOLECULAR
POLYMERS
305
8.2.5
EU
111
-BASED
METALLO-SUPRAMOLECULAR
POLYMERS
308
8.3
HETERO-METALLIC
SYSTEM
311
8.4
THE
FABRICATION
METHOD
OF
METALLOPOLYMER
FILM
314
8.4.1
LAYER-BY-LAYER
SELF-ASSEMBLY
AND
DIP-COATING
METHODS
314
8.4.2
ELECTROPOLYMERIZED
CONDUCTING
METALLOPOLYMERS
315
8.5
CONCLUSION
323
REFERENCES
323
9
METAL-ORGANIC
FRAMEWORK
(MOF)
AND
COVALENT
ORGANIC
FRAMEWORK
(COF)-BASED
ELECTROCHROMISM
(EC)
327
9.1
INTRODUCTION
327
9.2
CURRENT
STUDIES
IN
EC
MOFS
327
9.2.1
THE
ORGANIC
LINKERS
IN
EC
MOFS
328
9.2.1.1
NDI-BASED
ORGANIC
LINKERS
328
9.2.1.2
OTHER
ORGANIC
LINKERS
332
9.2.2
THE
TRANSPORT
OF
ELECTROLYTE
IONS
IN
EC
MOFS
335
9.2.3
SPECIAL
EC
MOFS
338
9.2.3.1
PHOTOCHROMIC
AND
ELECTROCHROMIC
MULTI-RESPONSIVE
MOF
338
9.23.2
MOF-BASED
DOUBLE-SIDED
EC
DEVICE
AND
OTHER
COLOR-SWITCHING
MECHANISMS
339
9.233
EC
BASE
ON
"
GUEST@MOF
"
COMPOSITE
SYSTEM
340
9.3
CURRENT
STUDIES
IN
EC
COFS
341
9.4
CONCLUSION
AND
PROSPECT
348
REFERENCES
348
10
NANOSTRUCTURE-BASED
ELECTROCHROMISM
353
10.1
INTRODUCTION
353
10.2
CURRENT
STUDIES
OF
NANOSTRUCTURE
IN
ELECTROCHROMISM
354
10.2.1
NON-ELECTROCHROMIC
ACTIVE
MATERIALS
AS
A
TEMPLATE
FOR
ECS
354
10.2.1.1
PHOTONIC
CRYSTALS
AS
TEMPLATES
FOR
ECS
354
10.2.1.2
PLASMONIC
STRUCTURES
AS
TEMPLATES
FOR
ECS
359
X
CONTENTS
10.2.2
10.3
NANOSTRUCTURED
ELECTROCHROMIC
MATERIALS
IN
ECS
365
CONCLUSION
AND
PROSPECT
369
REFERENCES
369
11
11.1
11.2
11.2.1
11.2.2
11.2.3
11.3
11.3.1
11.3.2
11.3.3
11.4
11.4.1
11.4.1.1
11.4.1.2
11.4.1.3
11.4.2
11.4.3
11.4.3.1
11.4.3.2
11.4.4
11.5
ORGANIC
ELECTROLUMINOCHROMIC
MATERIALS
373
INTRODUCTION
373
CONVENTIONAL
MECHANISMS
OF
ELECTROLUMINOCHROMISM
375
INTRINSIC
MECHANISM
375
ELECTRON
TRANSFER
(ET)
MECHANISM
376
ENERGY
TRANSFER
(ENT)
MECHANISM
376
ELECTROLUMINOCHROMIC
PERFORMANCE
PARAMETERS
376
EMISSION
CONTRAST
376
SWITCHING
TIME
377
LONG-TERM
STABILITY/CYCLE
LIFE
377
CLASSICAL
MATERIALS
378
SMALL
MOLECULES
378
SMALL
MOLECULAR
DYADS
378
REDOX-ACTIVE
MOIETY
AND
LUMINOPHORES
SYSTEM
380
ELECTROACTIVE
LUMINOPHORES
382
TRANSITION
METAL
COMPLEXES
386
POLYMERS
387
NON-CONJUGATED
POLYMERS
387
CONJUGATED
POLYMERS
396
NANOCOMPOSITE
FILMS
407
FUTURE
PERSPECTIVES
AND
CONCLUSION
408
REFERENCES
408
12
12.1
12.2
12.2.1
12.2.1.1
12.2.1.2
12.2.1.3
12.2.2
12.2.2.1
12.2.2.2
12.2.2.3
12.2.3
12.2.4
12.3
ORGANIC
PHOTOELECTROCHROMIC
DEVICES
415
INTRODUCTION
415
STRUCTURE
DESIGN
OF
PECDS
417
POWER
SUPPLY
FOR
PECD
417
DSSC-BASED
PECD
418
PSC-BASED
PECD
423
OPV-BASED
PECD
423
ELECTROCHROMIC
MATERIALS
IN
PECD
425
SMALL
MOLECULE
425
CONDUCTING
POLYMERS
427
NEAR-INFRARED
(NIR)
ELECTROCHROMIC
MATERIALS
433
ELECTROLYTES
IN
PECD
435
SUBSTRATES
IN
PECD
435
FUTURE
PERSPECTIVES
AND
CONCLUSION
436
REFERENCES
436
13
13.1
APPLICATION
OF
OEC
DEVICES
445
SMART
WINDOW
445
CONTENTS
XI
13.1.1
THE
STRUCTURE
AND
WORKING
MECHANISM
OF
SMART
WINDOWS
445
13.1.2
THE
MATERIALS
FOR
ELECTROCHROMIC
WINDOWS
446
13.1.3
PROSPECTS
450
13.2
DIMMABLE
REARVIEW
MIRROR
450
13.3
SENSORS
451
13.3.1
APPLICATION OF
ELECTROCHROMIC
SENSORS
ON
FOOD
PRESERVATION
451
13.3.2
APPLICATION
IN
BIO-SENSING
454
13.4
THE
APPLICATION
OF
ELECTROCHROMIC
DEVICE
IN
DISPLAY
460
13.5
OTHER
APPLICATIONS
OF
OEC
462
REFERENCES
469
14
COMMERCIALIZED
OEC
MATERIALS
AND
RELATED
ANALYSIS
OF
COMPANY
PATENTS
471
14.1
GENERAL
INTRODUCTION
471
14.2
GENTEX
CORPORATION
471
14.3
RICOH
COMPANY,
LTD.
475
14.4
CANON
INC.
476
14.5
BOE
TECHNOLOGY
GROUP
CO.,
LTD.
AND
OPPO
GUANGDONG
MOBILE
COMMUNICATIONS
CO.,
LTD.
477
14.6
OTHER
IMPORTANT
ENTERPRISES
481
14.6.1
NINBO
NINUO
ELECTRONIC
TECHNOLOGY
CO.,
LTD.
481
14.6.2
AMBILIGHT
INC.
483
14.6.3
FURCIFER
INC.
483
14.6.4
CHANGZHOU
SPECTRUM
NEW
MATERIAL
CO.
LTD.
484
14.7
CONCLUSION
485
REFERENCES
485
15
MAIN
CHALLENGES
FOR
THE
COMMERCIALIZATION
OF
OEC
491
15.1
INTRODUCTION
491
15.2
THE
LONG-TERM
STABILITY
OF
OEC
MATERIALS
491
15.3
THE
MECHANICAL
STABILITY
OF
OEC
DEVICES
(ENCAPSULATION
TECHNOLOGY)
495
15.4
LARGE-AREA
PROCESS
TECHNOLOGY:
SPRAY
COATING
AND
ROLL-TO-ROLL
PROCESSES
498
15.4.1
INKJET
PRINTING
498
15.4.2
SPRAY
COATING
500
15.4.3
SLOT-DIE
COATING
500
15.4.4
SCREEN
PRINTING
501
15.5
CONCLUSIONS
AND
PERSPECTIVE
501
REFERENCES
502
INDEX
505 |
| any_adam_object | 1 |
| any_adam_object_boolean | 1 |
| author | Meng, Hong 1966- |
| author_GND | (DE-588)1235805891 |
| author_facet | Meng, Hong 1966- |
| author_role | aut |
| author_sort | Meng, Hong 1966- |
| author_variant | h m hm |
| building | Verbundindex |
| bvnumber | BV047229143 |
| classification_rvk | ZN 3499 VE 9580 |
| ctrlnum | (OCoLC)1249681246 (DE-599)DNB1217131507 |
| discipline | Chemie / Pharmazie Elektrotechnik / Elektronik / Nachrichtentechnik |
| discipline_str_mv | Chemie / Pharmazie Elektrotechnik / Elektronik / Nachrichtentechnik |
| format | Book |
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| id | DE-604.BV047229143 |
| illustrated | Illustrated |
| index_date | 2024-07-03T16:59:53Z |
| indexdate | 2024-07-10T09:06:17Z |
| institution | BVB |
| institution_GND | (DE-588)16179388-5 |
| isbn | 3527348719 9783527348718 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-032633659 |
| oclc_num | 1249681246 |
| open_access_boolean | |
| owner | DE-29T DE-634 DE-83 DE-19 DE-BY-UBM DE-703 |
| owner_facet | DE-29T DE-634 DE-83 DE-19 DE-BY-UBM DE-703 |
| physical | xiv, 514 Seiten Illustrationen, Diagramme 24.4 cm x 17 cm |
| publishDate | 2021 |
| publishDateSearch | 2021 |
| publishDateSort | 2021 |
| publisher | Wiley-VCH |
| record_format | marc |
| spelling | Meng, Hong 1966- Verfasser (DE-588)1235805891 aut Organic electronics for electrochromic materials and devices Hong Meng Weinheim, Germany Wiley-VCH [2021] xiv, 514 Seiten Illustrationen, Diagramme 24.4 cm x 17 cm txt rdacontent n rdamedia nc rdacarrier Elektrochromes Material (DE-588)4292130-2 gnd rswk-swf Organischer Halbleiter (DE-588)4172780-0 gnd rswk-swf CH90: Physikalische Chemie Chemie Chemistry Components & Devices EE60: Komponenten u. Bauelemente Electrical & Electronics Engineering Elektrotechnik u. Elektronik Komponenten u. Bauelemente MS50: Optische u. Nichtlineare Optische Materialien Materials Science Materialwissenschaften Optical and Non-Linear Optical Materials Optische u. Nichtlineare Optische Materialien Physical Chemistry Physikalische Chemie Elektrochromes Material (DE-588)4292130-2 s Organischer Halbleiter (DE-588)4172780-0 s DE-604 Wiley-VCH (DE-588)16179388-5 pbl Erscheint auch als Online-Ausgabe, PDF 978-3-527-83061-9 Erscheint auch als Online-Ausgabe, EPUB 978-3-527-83062-6 Erscheint auch als Online-Ausgabe 978-3-527-83063-3 X:MVB http://www.wiley-vch.de/publish/dt/books/ISBN978-3-527-34871-8/ DNB Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=032633659&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | Meng, Hong 1966- Organic electronics for electrochromic materials and devices Elektrochromes Material (DE-588)4292130-2 gnd Organischer Halbleiter (DE-588)4172780-0 gnd |
| subject_GND | (DE-588)4292130-2 (DE-588)4172780-0 |
| title | Organic electronics for electrochromic materials and devices |
| title_auth | Organic electronics for electrochromic materials and devices |
| title_exact_search | Organic electronics for electrochromic materials and devices |
| title_exact_search_txtP | Organic electronics for electrochromic materials and devices |
| title_full | Organic electronics for electrochromic materials and devices Hong Meng |
| title_fullStr | Organic electronics for electrochromic materials and devices Hong Meng |
| title_full_unstemmed | Organic electronics for electrochromic materials and devices Hong Meng |
| title_short | Organic electronics for electrochromic materials and devices |
| title_sort | organic electronics for electrochromic materials and devices |
| topic | Elektrochromes Material (DE-588)4292130-2 gnd Organischer Halbleiter (DE-588)4172780-0 gnd |
| topic_facet | Elektrochromes Material Organischer Halbleiter |
| url | http://www.wiley-vch.de/publish/dt/books/ISBN978-3-527-34871-8/ http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=032633659&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
| work_keys_str_mv | AT menghong organicelectronicsforelectrochromicmaterialsanddevices AT wileyvch organicelectronicsforelectrochromicmaterialsanddevices |