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Book Details
Abstract
Interest in and attention on electrochromic technology has been growing since the 1970s, with the advent of numerous electrochromic devices in commercial and industrial settings. Many laboratory-based colour-changing electrochromic device prototypes have surfaced following research breakthroughs in recent years, and the consumer market has been expanding continuously. Electrochromic devices have a wide range of applications, such as displays, self-dimming mirrors for automobiles, electrochromic e-skins, textiles, and smart windows for energy-efficient buildings. Electrochromic Smart Materials covers major topics related to the phenomenon of electrochromism, including fundamental principles, different classes and subclasses of electrochromic materials, and device processing and manufacturing. It also highlights a broad range of existing and potential applications of electrochromic devices, with an analysis of the current market needs and future trends. Providing a comprehensive overview of the field, this book will serve as introductory reading to those new to this area, as well as a resource providing detailed, in-depth knowledge and insights to the seasoned audience. Featuring contributions from researchers across the globe, it will be of interest to postgraduate students and researchers in both academia and industry interested in smart design, materials science and engineering.
Table of Contents
Section Title | Page | Action | Price |
---|---|---|---|
Cover | Cover | ||
Preface | vii | ||
Contents | ix | ||
Chapter 1 Introduction to Electrochromism | 1 | ||
1.1 General Introduction | 1 | ||
1.2 History of Electrochromism | 2 | ||
1.3 Mechanism of Electrochromism and EC Devices | 3 | ||
1.4 Applications of EC Materials | 4 | ||
1.4.1 Smart Glass/Windows | 4 | ||
1.4.2 Car Rear-view Mirrors | 7 | ||
1.4.3 EC Displays | 7 | ||
1.4.4 Wearable Apparel and Devices | 8 | ||
1.4.5 Modulation of Microwave and Near-Infrared Radiation | 13 | ||
1.5 Conclusion | 14 | ||
References | 15 | ||
Chapter 2 Fundamentals of Electrochromic Materials and Devices | 22 | ||
2.1 Introduction | 22 | ||
2.1.1 Types of Electrochromes | 22 | ||
2.2 Classes of Electrochromic Materials | 23 | ||
2.2.1 Metal Oxides | 24 | ||
2.2.2 Metal Hexacyanometallates | 25 | ||
2.2.3 Metal Phthalocyanines | 25 | ||
2.2.4 Viologens | 28 | ||
2.2.5 Conjugated Polymers | 29 | ||
2.2.6 Other Organic Electrochromes | 32 | ||
2.3 Architecture and Components of Electrochromic Devices | 33 | ||
2.3.1 Electrode | 34 | ||
2.3.1.1 Optically Transparent Electrode | 34 | ||
2.3.1.2 Reflective Electrode | 35 | ||
2.3.2 Electrolyte | 35 | ||
2.3.2.1 Liquid Electrolytes | 35 | ||
2.3.2.2 Semi-solid/Solid Electrolytes | 35 | ||
2.3.2.3 Room Temperature Ionic Liquids | 37 | ||
2.3.2.4 Green and Biodegradable Electrolytes | 37 | ||
2.3.3 Electrochromic Layer | 37 | ||
2.3.3.1 Film Deposition and Patterning | 37 | ||
2.3.3.2 Film Morphology | 40 | ||
2.3.4 Charge-storing/Counter Layer | 40 | ||
2.3.5 Sealant | 41 | ||
2.4 Electrochromic Performance Parameters | 41 | ||
2.4.1 Colour Quantification | 42 | ||
2.4.2 Optical Contrast/Photopic Contrast | 42 | ||
2.4.3 Switching Time | 44 | ||
2.4.4 Colouration Efficiency | 44 | ||
2.4.5 Optical Memory | 44 | ||
2.4.6 Stability/Cycle Life | 45 | ||
2.5 Concluding Remarks | 45 | ||
References | 46 | ||
Chapter 3 Conjugated Polymers for Electrochromic Applications | 51 | ||
3.1 Introduction | 52 | ||
3.2 RGB (Red, Green, Blue) Based Electrochromics | 53 | ||
3.3 CMYK (Cyan, Magenta, Yellow, Key) Based Electrochromics | 62 | ||
3.4 Water Processable Electrochromic Polymers | 68 | ||
3.5 PEDOT and Its Derivatives: Attractive Electrochromic Polymers | 71 | ||
3.6 Fluorescent Polymers | 78 | ||
3.7 Triphenylamine (TPA) Bearing Polymers | 89 | ||
3.8 Concluding Remarks | 97 | ||
References | 98 | ||
Chapter 4 Donor-Acceptor Type Conjugated Electrochromic Polymers | 103 | ||
4.1 Introduction | 103 | ||
4.2 Color Engineering of D-A Polymers | 107 | ||
4.2.1 D-A Polymers with Neutral Primary Red-Green-Blue Colors | 107 | ||
4.2.2 D-A Polymers with Secondary or Tertiary Colors | 111 | ||
4.2.3 D-A Polymers with Multi-color Switching | 113 | ||
4.2.4 D-A Polymers with NIR Switching Ability | 116 | ||
4.3 D-A Polymers Showing High Performance in Electrochromic Devices | 117 | ||
4.3.1 High Optical Contrast and Fast Switching Speed | 117 | ||
4.3.2 High Coloration Efficiency | 119 | ||
4.3.3 High Cycling Stability | 122 | ||
4.4 Conclusion | 123 | ||
Acknowledgments | 124 | ||
References | 124 | ||
Chapter 5 Electrochromic, Electrofluorescent and Light-induced Coloration Effects | 129 | ||
5.1 Introduction | 129 | ||
5.2 Multifunctional Device and Material Films | 130 | ||
5.2.1 AIEE-active and Electrochromic Bifunctional Polymer and Device | 130 | ||
5.2.2 Trifunctional CdSe Quantum Dots-Polymer Composite Film | 133 | ||
5.2.3 Bi-functional Europium Ion Doped WO3 Film | 142 | ||
5.3 Conclusion | 149 | ||
Acknowledgments | 149 | ||
References | 149 | ||
Chapter 6 Bistable Electrochromic Windows from Conjugated Polymers | 151 | ||
6.1 Introduction | 151 | ||
6.1.1 Optical Memory | 152 | ||
6.1.2 Key Parameters for OM and Bistability | 152 | ||
6.1.3 OM of Molecular Level EC Materials | 153 | ||
6.2 Optical Memory of π-conjugated Polymers | 155 | ||
6.2.1 Optical Memory in Electrochromic PEDOTs | 155 | ||
6.2.2 Optical Memory in Thiophenyl Copolymers | 155 | ||
6.2.3 Optical Memory in Indole-containing Copolymers with PEDOT Layer | 158 | ||
6.2.4 Optical Memory in Polyselenophenes | 161 | ||
6.2.5 Donor-Acceptor Type ECPs | 165 | ||
6.3 Electrochromic Bistability of Conjugated Polymers | 168 | ||
6.3.1 Optical Memory of Poly (2,2-dimethyl-3,4-propylenedioxythiophene) (PProDOT-Me2) | 168 | ||
6.3.2 IET and IDT Mechanism to Reach Bistability | 171 | ||
6.3.3 Bistability of Side Chain Engineered ProDOTs | 174 | ||
6.3.4 Charge Balanced Bistable ECDs | 182 | ||
6.4 Conclusion | 188 | ||
Acknowledgments | 189 | ||
References | 189 | ||
Chapter 7 Electroluminochromism: Classical Materials and New Developments | 192 | ||
7.1 Introduction | 192 | ||
7.2 Conventional Mechanism of Electroluminochromism | 193 | ||
7.3 Electroluminochromism Based on Small Organic Molecules | 194 | ||
7.4 Electroluminochromism Based on Emissive Polymeric Films | 200 | ||
7.5 Electroluminochromism Based on Photofunctional Transition-metal Complexes | 204 | ||
7.6 Electroluminochromism Based on Emissive Nanocomposite Films | 210 | ||
7.7 Summary and Outlook | 213 | ||
Acknowledgments | 215 | ||
References | 215 | ||
Chapter 8 Donor-Acceptor Electrochromic Conjugated Polymers with Different Structures | 218 | ||
8.1 Introduction and Background | 218 | ||
8.1.1 Electrochromism in Conjugated Polymer | 218 | ||
8.1.2 Donor-Accepter Approach | 219 | ||
8.2 Representative Donor Units | 220 | ||
8.2.1 Thiophene and Its Derivatives | 220 | ||
8.2.2 EDOT and Its Derivatives | 222 | ||
8.2.3 Pyrrole and Its Derivatives | 224 | ||
8.2.4 Carbazole and Its Derivatives | 226 | ||
8.2.5 Triphenylamine and Its Derivatives | 226 | ||
8.3 Electrochromic Polymers with Different D-A Structures | 228 | ||
8.3.1 EC Polymers with D and A Units in the Backbone | 230 | ||
8.3.1.1 Thiophene and Its Derivatives as D Units | 230 | ||
8.3.1.2 EDOT and Its Derivatives as D Units | 234 | ||
8.3.1.3 Other D Systems | 241 | ||
8.3.2 D-A Polymers with Pendent A Units | 242 | ||
8.3.3 D-A Polymers Based on Cruciform Monomers | 245 | ||
8.3.4 D-A polymers Based on Star-shaped Monomers | 246 | ||
8.3.5 D-A Polymers Based on Dendritic Monomers | 250 | ||
8.4 Conclusion and Outlook | 251 | ||
Acknowledgments | 252 | ||
References | 252 | ||
Chapter 9 Electrochromic and Electrofluorescence Liquid Crystals | 261 | ||
9.1 Introduction | 261 | ||
9.1.1 Electrochromic/Electrofluorochromic Devices | 262 | ||
9.2 Smart Electrochromic Liquid Crystalline Materials | 266 | ||
9.2.1 Electrochromic Ionic Liquid Crystals with p-Type Character | 267 | ||
9.2.2 Electrochromic Liquid Crystals Incorporating the Classic Viologen as Redox Active Unit (n-Type) | 269 | ||
9.2.3 Viologen-based Liquid Crystalline Rotaxanes | 274 | ||
9.3 Extended Viologens as Multifunctional Smart Liquid Crystals | 277 | ||
9.3.1 Thienoviologens Liquid Crystals | 280 | ||
9.4 Electrofluorochromic Liquid Crystals | 284 | ||
9.5 Conclusions | 287 | ||
Acknowledgments | 288 | ||
References | 288 | ||
Chapter 10 Electrochemical Properties and Electrochromic Device Applications of Polycarbazole Derivatives | 293 | ||
10.1 Fundamental Chemistry of Carbazole | 293 | ||
10.2 Electrochemistry and Electropolymerization of Carbazole Derivatives | 294 | ||
10.3 Electrochromic Properties of Polycarbazoles | 298 | ||
10.3.1 Polymers from Monomers Containing One Carbazole Unit | 301 | ||
10.3.2 Polymers from Monomers Containing Two Carbazole Units | 304 | ||
10.3.3 Polymers from Monomers Containing Multiple Carbazole Units | 308 | ||
10.4 Smart Windows Application of Polycarbazole Derivatives | 313 | ||
10.5 Conclusion | 318 | ||
References | 319 | ||
Chapter 11 Arylamine-based High Performance Polymers for Electrochromic Applications | 323 | ||
11.1 Introduction | 323 | ||
11.1.1 High-performance Polymers | 323 | ||
11.1.2 Electrochromic Arylamine-based Molecules | 328 | ||
11.2 Typical Arylamine-based Electrochromic HPPs | 328 | ||
11.2.1 Polyimides | 328 | ||
11.2.2 Polyamides | 329 | ||
11.2.3 Poly(amide-imide)s | 329 | ||
11.2.4 Poly(ether-imide)s and Poly(ether-amide)s | 330 | ||
11.2.4.1 Organosoluble Poly(ether-imide)s | 333 | ||
11.2.4.2 Fluorinated Poly(ether-imide)s | 333 | ||
11.2.4.3 TPA-based Poly(ether-imide)s and Poly(ether-amide)s | 337 | ||
11.2.5 Poly(hydrazide)s and Poly(oxadiazole)s | 337 | ||
11.2.6 Poly(arylamine)s | 339 | ||
11.3 Development of Triarylamine-based Electrochromic Polymers | 339 | ||
11.3.1 Introduction of Protection Groups | 339 | ||
11.3.2 Strategies for Increasing Electrochromic-coloring Stages | 342 | ||
11.3.3 Facile Electropolymerization for Poly(arylamine)s | 347 | ||
11.4 Electrochromic Devices | 350 | ||
11.4.1 Single Layer Electrochromic Devices | 353 | ||
11.4.2 Complementary Electrochromic Devices | 356 | ||
11.4.3 Flexible Electrochromic Devices | 359 | ||
11.5 Conclusion and Perspectives | 363 | ||
Acknowledgments | 364 | ||
References | 364 | ||
Chapter 12 Viologens-based Electrochromic Materials and Devices | 372 | ||
12.1 Introduction | 372 | ||
12.2 Electrochemistry and Electrochromism of Viologens | 373 | ||
12.2.1 Influence of Anions on Direduced Viologens | 374 | ||
12.2.2 Electrochromism of Viologen Radical Cations | 374 | ||
12.2.2.1 Viologen Radical Cations in Organic Solvents | 374 | ||
12.2.2.2 Dimerized Viologen Radical Cations | 374 | ||
12.2.2.3 Insoluble Viologen Radical Cations | 376 | ||
12.2.2.4 Aging of Insoluble Viologen Radical Cations | 377 | ||
12.2.2.5 Influence of Substitution Groups on Viologen Radical Cations | 379 | ||
12.3 Viologens in Electrochromic Devices | 381 | ||
12.3.1 Mechanism of Viologen-based Electrochromic Devices | 381 | ||
12.3.2 Type-1 Electrochromes-viologens in Non-aqueous Solvents | 384 | ||
12.3.3 Type-2 Electrochromes-insoluble Viologen Radical Cations | 387 | ||
12.3.4 Type-3 Electrochromes-immobilized Viologens | 388 | ||
12.3.4.1 Anchored Viologens | 389 | ||
12.3.4.2 Polyviologens | 390 | ||
12.3.4.3 Viologens in Gel or Solid-state Electrolytes | 394 | ||
Acknowledgments | 400 | ||
References | 400 | ||
Chapter 13 Metallo-supramolecular Polymers with Electrochromic Properties | 406 | ||
13.1 Metallo-supramolecular Polymers: A Comparison with Organic Polymers | 406 | ||
13.1.1 Organic Polymers | 406 | ||
13.1.2 Linear Structures | 407 | ||
13.1.3 Branched Structures | 409 | ||
13.1.4 π-Conjugated Structures | 409 | ||
13.1.5 Metallo-supramolecular Polymers | 410 | ||
13.1.6 Color of Metallo-supramolecular Polymers | 412 | ||
13.2 Linear Metallo-supramolecular Polymers | 413 | ||
13.2.1 Synthesis | 413 | ||
13.2.2 Optical and Electrochemical Properties | 414 | ||
13.2.3 Electrochromic Properties | 416 | ||
13.3 Hyperbranched Metallo-supramolecular Polymers | 417 | ||
13.3.1 Synthesis | 417 | ||
13.3.2 Electrochromic Properties | 418 | ||
13.4 Heterometallo-supramolecular Polymers | 421 | ||
13.4.1 Synthesis | 421 | ||
13.4.2 Electrochemical Properties | 423 | ||
13.4.3 Multicolor Electrochromism | 424 | ||
13.5 Electrochromic Devices with Metallo-supramolecular Polymers | 425 | ||
13.5.1 Device Fabrication | 425 | ||
13.5.2 Flexible Electrochromic Devices | 426 | ||
13.6 Conclusion | 428 | ||
Acknowledgments | 428 | ||
References | 428 | ||
Chapter 14 Nanostructured Electrochromic Materials | 430 | ||
14.1 Introduction | 430 | ||
14.2 One-dimensional Nanomaterials for Enhanced Electrochromism | 431 | ||
14.2.1 The Advantages of One-dimensional Nanostructures for Electrochromism | 431 | ||
14.2.2 Synthesis of One-dimensional Nanostructures | 432 | ||
14.2.2.1 Template-free Approaches | 433 | ||
14.2.2.1.1 Solution-based Process | 433 | ||
14.2.2.1.1.1 Hydrothermal Synthesis | 433 | ||
14.2.2.1.1.2 Ambient Pressure Solution Process | 435 | ||
14.2.2.1.2 Vapor-based Process | 436 | ||
14.2.2.1.3 Electrospinning Process | 438 | ||
14.2.2.1.4 Chemical Oxidative and Electrochemical Polymerization Processes | 439 | ||
14.2.2.2 Template-derived Approaches | 441 | ||
14.2.2.2.1 AAO and PC Templating | 441 | ||
14.2.2.2.2 Surfactant-assistant Templating | 443 | ||
14.2.3 Electrochromism of One-dimensional Nanostructures | 445 | ||
14.2.3.1 WO3 and TiO2 1D Nanostructures | 445 | ||
14.2.3.2 NiO and Co3O4 1D Nanostructures | 448 | ||
14.2.3.3 V2O5 and MoO3 1D Nanostructures | 449 | ||
14.2.3.4 Conductive Polymer 1D Nanostructures | 452 | ||
14.2.4 Outlook of One-dimensional Nanostructures for Electrochromsim | 454 | ||
14.3 3D Nanostructured Electrochromic Materials | 454 | ||
14.3.1 3D nanostructured Inorganic Electrochromic Materials | 455 | ||
14.3.1.1 The Role of 3D Nanostructures in Inorganic Electrochromic Materials | 455 | ||
14.3.1.2 Preparation and Performance of Inorganic Electrochromic Thin Films | 456 | ||
14.3.1.2.1 Physical Vapor Deposition | 456 | ||
14.3.1.2.2 Hydrothermal Synthesis | 458 | ||
14.3.1.2.3 CBD | 458 | ||
14.3.1.2.4 Electrochemical Anodization | 460 | ||
14.3.1.2.5 Electrodeposition | 460 | ||
14.3.1.2.6 Templating | 461 | ||
14.3.2 3D Nanostructured Organic Electrochromic Materials | 466 | ||
14.3.3 Outlook of 3D Nanostructured Electrochromic Materials | 467 | ||
References | 469 | ||
Chapter 15 Electrodeposition Based Electrochromic System | 475 | ||
15.1 Metal Electrodeposition as an Electrochromic Process | 475 | ||
15.2 Metal Deposition Mechanism and Electrochemical Kinetics | 481 | ||
15.2.1 Current for Ag Deposition Under Electrode Reaction Control or Diffusion Control | 481 | ||
15.2.2 Size-selective Electrodeposition of Metal Particles and the Kinetics | 482 | ||
15.3 Localized Surface Plasmon Resonance (LSPR) in Metal Nanoparticles for Full Color EC Devices | 484 | ||
15.3.1 Absorption and Diffusion of Light by LSPR | 485 | ||
15.3.2 Color of Silver Nanostructures with LSPR | 486 | ||
15.3.2.1 Silver Nanospheres | 487 | ||
15.3.2.2 Silver Nanoplates | 487 | ||
15.3.2.3 Silver Thin Films | 489 | ||
15.4 Multicolor EC Device with Reversible Metal Electrodeposition | 489 | ||
Acknowledgments | 491 | ||
References | 492 | ||
Chapter 16 Electrochromic Smart Windows for Green Building Applications | 494 | ||
16.1 Introduction to Electrochromic Smart Windows | 494 | ||
16.2 Electrochromic Materials for Smart Windows | 498 | ||
16.3 Evaluation of Electrochromic Smart Windows | 499 | ||
16.3.1 Energy Savings | 499 | ||
16.3.2 Lighting Performance | 502 | ||
16.3.3 Operation and Control | 505 | ||
16.3.4 Durability | 507 | ||
16.4 Challenge and Future of Electrochromic Smart Windows in Green Building Applications | 509 | ||
16.4.1 Main Challenges | 510 | ||
16.4.2 Future Development | 510 | ||
16.4.2.1 Modification of EC Materials: Solar Absorptive to Solar Reflective | 510 | ||
16.4.2.2 Connection of EC Smart Windows and the Internet of Things (IoT) | 512 | ||
16.4.2.3 Integration of EC Smart Windows and Passive Technologies | 513 | ||
16.5 Market Potential of Electrochromic Smart Windows for Green Building Applications | 514 | ||
16.6 Summary | 515 | ||
Acknowledgments | 516 | ||
References | 516 | ||
Subject Index | 521 |