- About this Journal
- Abstracting and Indexing
- Aims and Scope
- Annual Issues
- Article Processing Charges
- Articles in Press
- Author Guidelines
- Bibliographic Information
- Citations to this Journal
- Contact Information
- Editorial Board
- Editorial Workflow
- Free eTOC Alerts
- Publication Ethics
- Reviewers Acknowledgment
- Submit a Manuscript
- Subscription Information
- Table of Contents
The Scientific World Journal
Volume 2013 (2013), Article ID 713640, 17 pages
A Review on the Fabrication of Polymer-Based Thermoelectric Materials and Fabrication Methods
1Department of Electrical Engineering, Faculty of Engineering, University of Malaya, 50603 Kuala Lumpur, Malaysia
2Department of Mechanical Engineering, Faculty of Engineering, University of Malaya, 50603 Kuala Lumpur, Malaysia
Received 30 August 2013; Accepted 23 September 2013
Academic Editors: O. Gullu and P. Shao
Copyright © 2013 Muhammad Akmal Kamarudin et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Thermoelectricity, by converting heat energy directly into useable electricity, offers a promising technology to convert heat from solar energy and to recover waste heat from industrial sectors and automobile exhausts. In recent years, most of the efforts have been done on improving the thermoelectric efficiency using different approaches, that is, nanostructuring, doping, molecular rattling, and nanocomposite formation. The applications of thermoelectric polymers at low temperatures, especially conducting polymers, have shown various advantages such as easy and low cost of fabrication, light weight, and flexibility. In this review, we will focus on exploring new types of polymers and the effects of different structures, concentrations, and molecular weight on thermoelectric properties. Various strategies to improve the performance of thermoelectric materials will be discussed. In addition, a discussion on the fabrication of thermoelectric devices, especially suited to polymers, will also be given. Finally, we provide the challenge and the future of thermoelectric polymers, especially thermoelectric hybrid model.
Global energy uncertainty and the limited resources coupled with increased energy demands provide the impetus for improving the efficiency of energy conversion technologies . Therefore, the requirements of materials and technologies had been focused on those that contribute to energy conservation, safety, and environmental protection which lower the emission of CO2 . Thermoelectricity, by converting heat energy directly into useable electricity, offers a promising technology to convert heat from the sun and to recover waste heat from industrial sectors and automobile exhausts [1–3]. The thermoelectric effect was first discovered by Thomas Seebeck in 1821  when he discovered that twisting two wires together and twisting one end induced a voltage. The converse effect, that is, application of voltage to induce a temperature gradient across the thermoelectric material, was discovered by Jean Peltier  in 1834, and is thus called the Peltier effect.
The performance of the thermoelectric material is evaluated by the dimensionless figure of merit , , where is the electrical conductivity, is the thermal conductivity, is the absolute temperature, and is the Seebeck coefficient (, that is, the ratio of the induced voltage over the temperature gradient across the thermoelectric device) . Thus, a high performance thermoelectric material requires high electrical conductivity, Seebeck coefficient, and low thermal conductivity. It is really challenging to find a material which has a high Seebeck coefficient in combination with high electrical conductivity and low thermal conductivity . In most materials, the electrical conductivity is directly proportional to the thermal conductivity. An ideal TE material would possess a high Seebeck coefficient as in the crystalline semiconductor, high electrical conductivity as in the crystalline metal, and low absolute temperature as in glass . For practical applications, such as thermal generators (TEGs), a of more than 3 is required, whilst the best efforts currently only produce a of 3 .
Early thermoelectrical devices developed in the early 1960s earned some popularity given the solid state nature of the devices, that is, no moving parts compared to generators and motors. These devices were mainly based on Bi2Te3 [6, 7]. However, these devices have low efficiency (, and a system efficiency of <10%) and are therefore not cost-effective in most applications. In the mid-1990s, a research on thermoelectric started to gain interest again after theoretical predictions suggested that the thermoelectric efficiency could be enhanced through nanostructuring . The introduction of nanostructures in thermoelectric materials served either to increase the electrical conductivity (through quantum dots), or to decrease the thermal conductivity (through nanowires and amorphous structures) [9–11]. Currently, the TE communication has paid the most attention on skutterudites , half-Heusler alloys , clathrates , and pentafluoriade . The common characteristic of these materials is their complex structure, which serves to reduce the thermal conductivity and hence increase the ZT. These materials are usually targeted for high temperature operation, such as electricity generation from waste heat of industrial sources, such as steel furnaces and aluminum melting. This is due to their optimal in a temperature range of 600 K or higher. One of the semiconductor compounds from the chalcogenide family, Bi2Te3, has already been commercially used in Peltier cooler. In terms of efficiency, Bi2Te3 alloys are the best TE materials known , which are able to optimally operate close to room temperature. However, the use of these materials is limited due to their toxic nature and also Te, which is a rare earth metal, makes the production cost uneconomical .
Numerous research works have been carried out to address these issues by replacing the metal- and alloy-based TE materials with organic and polymer materials [18, 19]. However, these materials have poor heat resistance which is unsuitable to be operated at high temperature. These polymer materials also have inferior thermoelectric properties than those of inorganic materials. To realistically apply these polymer materials for thermoelectric applications, applications which operate in the low temperature range (<100°C) need to be targeted. There are numerous polymer-based candidates for thermoelectric applications, which are easy to synthesize and fabricate low cost and low thermal conductivity.
In this paper, a review on the use of polymers in thermoelectric materials and devices will be given. The effect of different polymer structures, molecular concentration, and weight on thermoelectric properties will also be highlighted. Next, useful fabrication methods for solution-process-based fabrication, such as spin coating, inkjet printing, and electrospinning, shall be provided.
2. Polymer-Based Thermoelectric Materials
2.1. Advantages of Polymers in Thermoelectrics
Polymers as TE materials have attracted a lot of attention recently due to its easy fabrication processes and low material cost [20, 21]. Their physical and chemical properties can be tuned to the desired properties through simple molecular modifications, which allows for a large range of flexibility in polymer properties [22, 23]. In addition, carbon, which is the main element in polymers, is abundant in nature and thus the use of polymers in electronic devices is more economical and desirable. Polymers have a low thermal conductivity which proves to be desirable for TE applications. Examples of polymers that have been researched for TE applications are polyacetylene [24, 25], polypyrroles [26, 27], polyanilines [26, 28], polythiophenes [29, 30], and poly(2,7-carbazole)s [31, 32].
2.2. Factors Affecting the Thermoelectric Properties
2.2.1. Various Polymer structures
Different types of polymers have been used in thermoelectric devices, such as polyaniline (PANI) [41, 42], poly(p-phenylene vinylene) (PPV) [43, 44], polyacetylene (PA) [33, 34], poly(2,7-carbazolenevinylene) [32, 45], and poly(2,5-dimethoxy phenylenevinylene) (PMeOPV) . These polymers are chosen due to their conductive nature. Different types of polymers (Figure 1 and Table 1) show different electrical conductivities, thermal conductivities, and figure of merits and exhibit various TE performances. In general, linear backbone polymers such as polyacetylene, polypyrrole, and polyaniline form the main class of conductive polymers. Poly(3-alkylthiophenes) form the basis for organic solar cells and transistors. The molecular basis of conductive properties lies in the conjugation of their bonds. Conductive polymers have continuous backbones of sp2 hybridised electrons, compared to the sp3 hybridised covalent bonds of nonconducting polymers. The valence electron of each sp2 hybridised carbon center combines a molecule wide delocalized orbital. These intrinsic organic semiconductors are typically doped oxidatively to form p-type organic semiconductors through dopants. Analogous to doping of inorganic intrinsic semiconductors, a small amount of doping (of around 0.1 wt%) causes the conductivity of the polymer to surge by 7–9 orders of magnitude. For example, undoped conjugated polymers such as polyacetylene may increase from 10−10 to 10−8 S/cm to around 0.1 S/cm upon doping. The frontrunner in the conductivity performance of conducting polymers is poly(3,4-ethylenedioxythiophene) (PEDOT), which, when doped with polystyrene sulfonate (PSS) or tosylate (Tos), may achieve conductivities of up to 3000 S/cm .
2.2.2. Polymer Concentration
Hiroshige et al.  showed that the electrical conductivity of poly (2,5-dimethoxy phenylenevinylene) (PMeOPV) increases with increasing monomer content of (methoxy phenylene vinylene) MeOPV whilst the Seebeck coefficient remains the same regardless of the monomer concentration. In their research, a relatively high Seebeck coefficient PMeOPV was observed at 39.1 μV/K. To date, the thermal conductivity data and of this material are not available. As the (methoxy phenylene vinylene) MeOPV content in the monomer feed is increased from 0 to 100 mol%, the conductivity increases from about 10−3 to 101 S/cm. Figure 2 shows the relationship of conductivity and monomer content. In the case of PEDOT : PSS blend , the trend is the same as the one described earlier. At high PSS content, PSS is the dominating factor and it is responsible for limiting the carrier transport within itself. But as the PSS content reduces, the distance between PEDOT : PSS cores effectively reduces as well and this affects the charge carrier mobility instead of affecting the charge carrier density. This is confirmed by the constant Seebeck coefficient even after reducing the PSS content. Similar observation has also been observed elsewhere .
2.2.3. Polymer Molecular Weight and Chain Length
It is found that the molecular weights of the polymers have a substantial effect on the electron mobility and consequently affect the electrical conductivity. Kline et al.  found that an increase in chain length/molecular weight leads to the increase in electron mobility due to the fundamental mechanism of electrical conductivity in polymers, through electron hopping along the polymer backbone. A high molecular weight polymer will promote the charge carriers to move longer distances before hopping to another chain, and because longer chains give carriers more opportunities for hopping to neighboring chains. The decrease in the hopping could result in an increased mobility. Figure 3 shows the polymer samples and their molecular weights which can be correlated with the electron mobility. Also, the thermal conductivity of polymer increases with the increase of polymer chain length as has been shown by Zhao et al. [51, 52].
As a semiconducting polymers, the electrical conductivity increases with increasing temperature [19, 53, 54]. This is because when the temperature increases, the electrons that are charge carriers in the conductor will gain energy and jump up into higher energy levels. However, these energy levels are all still in the valence band. So the number of charge carriers will not change for a conductor with an increase in the temperature. On the other hand, the charge on each carrier and the electric field strength are not dependent on the temperature. Figure 4 shows the temperature dependence of electrical conductivities of different types of polymers.
Thermoelectric properties of conductive polymers tend to change with humidity. When humidity is high, the polymer forms carriers from the chemical dopants to result in high electrical conductivity. However, this also causes a corresponding decrease in the Seebeck coefficient. Thus, the improvement of the overall is not significant. This demonstrates the difficulty in optimization of the ; that is, an increase in one parameter may actually cause a corresponding decrease in another parameter. Figure 5 shows the effect of humidity (60%) on the conductivity and Seebeck coefficient .
2.2.6. Alignment of Polymer Chains
Alignment of the polymer chains is also known to increase the electrical conductivity of conductive polymers and thus increasing the value [56, 57]. Toshima  found that the value increased with increasing drawing ratio. Formation of a cast polymer is achieved through extrusion of a molten polymer through a flat die, onto a chill roll. Drawing ratio is defined as the velocity of the chill roll to the velocity of the polymer exiting the die onto an X-ray diffraction patterns and UV-Vis near IR spectra of a (±)-10-camphorsulfonic acid (CSA)-doped stretched polyaniline films suggested that the increase in value can be attributed to the extended coil-like conformation that induced the alignment of polyaniline chains which increases the carrier mobility. It is also found that the stretching can increase the electrical conductivity parallel to the stretched direction twice that of the perpendicular . Similarly, the Seebeck coefficient of the parallel stretched sample is also higher than that of the perpendicularly stretched sample, as shown in Figure 6.
3. Strategies for Improvement of the Thermoelectric Performance
The electric conductivity can be improved by doping the polymers with a sufficient amount of suitable dopants. However, an increase in dopants leads to the decrease in the Seebeck coefficient. As the number of charge carriers increases, the Fermi energy is forced deep inside the conduction band . Some examples of doping agents are iodine () , Fe(III) Chloride (FeCl3) , molybdenum(V) chloride (MoCl5) , and so forth. It is found that an increase in the conductivity decreases the Seebeck coefficient [31, 62, 63]. Figure 7 shows the effect of doping on the Seebeck coefficient and resistivity.
In 2011, Bubnova et al.  optimized a PEDOT : Tos mixture to achieve a maximum of 0.25 at room temperature. PEDOT : PSS is one of the most investigated organic semiconductor, having been extensively investigated for organic photovoltaic (OPV) and organic light emitting diode (OLED) applications, given its stability in air and high electrical conductivity. However, the performance of the PEDOT : PSS is somewhat hindered by the unionised portion of the dopants—typically the PSS dopant has a small ionization fraction, and the unionised portion reduces the carrier mobility and hence the overall thermoelectric power. Kim et al.  recently have optimized the of the PEDOT : PSS mixture by removing the portion of unionized PSS dopant using a choice of solvents, thus achieving a record value of for an organic thermoelectric polymer.
3.2. Addition of Carbon Nanotubes (CNTs)
CNTs are known to have a stable one-dimensional nanostructure and excellent electrical and mechanical properties. When it is incorporated into a polymer matrix, the thermoelectric properties of the materials are affected. Kim et al.  found that PEDOT : PSS particles are spread on the surface of CNTs bridging tube-tube junction and allowing electrons to travel through the composite and thus increasing the electrical conductivity. On the other hand, heat transport in this system is suppressed due to differences in vibrational spectra between CNT and PEDOT : PSS. The highest achieved was 0.02 when 35 wt% CNT was added to the polymer matrix. The addition of CNT as a dopant beyond a certain threshold also resulted in the decrease of both electrical and the Seebeck coefficient [67, 68]. This is due to the fact that CNTs act as impurities within the material and thus preventing the connection of adjacent particles which in turn greatly reduces the mean free path of the charge carriers. Also, an increase in CNT concentration will lead to the increase in the thermal conductivity . Figure 8 shows the effect of CNT doping on the electrical conductivity and Seebeck coefficient.
3.3. Polymer Composite
Unlike CNTs, the addition of inorganic materials such as Te nanorods , Bi2Te3 , and Ca3Co4O9  powders shows different effects. These materials basically have high Seebeck coefficient values. A research by See et al.  showed that by adding Te nanorods into a polymer matrix, the electrical conductivity increased, whereas the thermal conductivity decreased. Due to the Seebeck coefficient being positive and significantly higher than pristine polymer, it is thought that the holes were solely responsible for charge transport and that the transport did not occur exclusively through the polymer. The highest achieved was ~0.1 at room temperature.
3.4. Addition of Semiconducting Stabilizer
CNT is hydrophobic and tends to entangle in water which hinders complete dispersion and/or exfoliation in water [73, 74]. Stabilizing agents have been added to water-based composites containing CNT to make the composites more stable. Various types of stabilizers have been used to disperse CNT in water such as surfactants [75, 76], polymers [77, 78], and inorganic particles [79, 80]. The use of conductive polymer stabilizers especially can greatly improve the electrical conductivity  and hence increase thermopower.
According to Moriarty et al. , the addition of stabilizers such as sodium deoxycholate (DOC) or meso-tetra(4-carboxyphenyl) porphine (TCPP) to CNT-polymer suspension suppresses the thermal conductivity by blocking tube-to-tube junctions which hinders phonon transport. The stabilizer also acts as phonon scattering centers since it is embedded in the composite alongside the CNT. The diameter and length of the tube, morphology of the CNTs, gaps between adjacent tubes, and defects introduced by the CNTs also contributed to the low thermal conductivity. Figures 9 and 10 show the effect of the addition of stabilizing agents on the interaction and thermal conductivity of the polymers.
3.5. Nanostructured Thermoelectric Materials
The use of nanofibers in thermoelectric devices can be potentially useful in achievement of a higher thermoelectric . The reduced dimensionality of the nanofibers will mitigate thermal conductivity without any reduction in the electrical conductivity. This method is better than the use of bulk materials in terms of and cost .
There is an extensive body of theoretical work concerned with efforts to improve , through increase of electrical conductivity or decrease in thermal conductivity. Electrical conductivity may be improved through the use of quantum confinement effects, such as quantum dots, to enhance high electron density of states near the Fermi energy (). Conversely, thermal conductivity may be decreased through phonon blocking/scattering effects through the use of superlattices and nanowires. The ideal superlattice structure triggers phonon scattering and thereby reduces the thermal conductivity, whilst encouraging the motion of charge carriers through the superlattice .
The use of nanostructures also allows selective blocking of phonons whilst allowing transportation of charge carriers. This allows decoupling of thermal and electrical conductivity, which usually increase in tandem in normal conducting materials. This is attributed to the fact that if one increases the concentration of charge carriers in a thermoelectric medium, then this presents a higher possibility of collision of charge carriers with the crystal lattice, and hence thermal conductivity correspondingly increases. On the other hand, if the effective wavelengths of phonon and electrons are recognized and their effects separated, then the effects of thermal and electrical conductivity may be decoupled. The motion of phonons that carries most of the heat has mean free paths of hundreds of nanometers, whereas electrons have 10 nm or less. Hence, it is feasible to confine the movement of phonons without obstructing the electron transportation . Furthermore, there are possibilities to amplify the boundary scattering of phonons without increasing the electron scattering and thus the of the thermoelectric devices can be improved.
In the previous section, it is anticipated that conductive polymers can be potential as thermoelectric materials, given their low thermal conductivity and improved electrical transport through doping with different nanoparticles . This potential can be further exploited by fabrication of these polymer thermoelectrics in the form of nanoscale , through the electrospinning method, chemical vapor deposition method, electrodeposition method, and inkjet printing method.
4. Fabrication Methods for Thermoelectric Polymer Devices
The electrospinning technique is a simple and elegant method to produce nanofibers. In 1934, Formhals patented a process to produce polymer filaments using electrostatic force. Later on, the process evolved and was named as electrospinning [79–81]. This method is able to produce continuous nanofibers from polymer solutions or melts in the presence of high electric fields, in the region of 10–30 kV. So far, hundreds of polymers have been successfully fabricated by electrospinning process . Thermoelectric polymers like carbon nanotube (CNT)/polyaniline (PANI) composite, polyaniline/(polystyrene and polyethylene Oxide) blends, polyaniline, polypyrrole, and polycarbonate nanofibers have been successfully fabricated through electrospinning process . The basic schematic setup for the electrospinning process is shown in Figure 11.
In the electrospinning process a charged liquid polymer solution is introduced into an electric field. A high voltage (HV) direct current (DC) power supply is used to generate the potential differences in the range between 10 and 30 KV. A needle attached to a syringe is used to dispense the liquid polymer solution at a desired voltage between 10 and 30 kV. After that it is deposited on a collector which is grounded. The cathode of the HV power supply is attached to a wire and inserted into the syringe containing the polymer solution and the anode is attached to the ground. A rotating drum, usually wrapped with aluminum foil can be used as a collector. The tip to collector distance is maintained between the ranges of 10–30 cm. The inner diameter of a needle can be between 0.5–1.5 mm. The ejected polymer solution forms a continuous nanofiber when the high voltage overcomes the surface tension. Once the ejection starts, at the tip of the needle, the pendant droplet of the polymer solution forms a conical shape, typically referred to as Taylor cone. Whilst the fluid is charged, the surface charge and the surface tension operate in opposite relation. Therefore, the fluid changes shape and the formed structure is known as the Taylor cone . The images of the formation of a Taylor cone are shown in Figure 12.
The key parameters which affect the formation of nanofibers are (1) solution parameters such as viscosity, conductivity, surface tension, and vapor pressure; (2) process parameters such as shape of collector, needle diameter, solution flow rate, tip to collector distance, and applied voltage; (3) ambient parameters such as solution temperature, humidity, and air velocity in the electrospinning chamber. By varying these parameters the thickness and smoothness of the fibers can be controlled . A typical SEM micrograph of an electrospun nanofiber (Polypyrrole) is shown in Figure 13.
4.2. Inkjet Printing
Recently the inkjet printing approach has been adopted for fabrication of electronics devices, where the colored ink cartridge is replaced with a functional electronic ink, for example, semiconducting ink and conductive ink. Today, inkjet printing is used in electronic industries and research for fabrication of printed circuit boards (PCB), light-emitting diodes (LED), thin film transistors (TFT), solar cells, thermoelectric devices, and many others [91–96].
With that being said, inkjet printing is an attractive method to be used in the fabrication of the whole or part of the structure of thermoelectric devices. Traditionally, thermoelectric devices structure is produced by conventional printing such as lithography and roll-to-roll printing . Conventional methods require series of processes flow such as etching, cleaning, and dicing, which is time consuming and produces a lot of waste material . With the ability to accurately deposit minute amounts of materials onto substrate, inkjet printing provides the alternative for fabrication of thermoelectric devices. A schematic of the operation of the inkjet printer is shown in Figure 14. Ink is deposited onto substrate to fabricate multiple layers structure.
The field of printable electronics is becoming more significant. This technology requires the active electronic materials, such as metals, organometallics, nanoparticles, and biopolymers in solution form, and thus soluble organic or polymeric materials are attractive candidates for this processing method. The inkjet printing method is also tuned for room temperature processing, and only a small amount (in the region of picoliters for a cartridge) is required to produce a device, thus resulting in substantial cost reductions . Ink is directly and accurately deposited onto various types of substrates, and multilayer and planar multicomponent systems are able to be fabricated with this technique . High resolution, in the region of 20–50 micrometers is possible, and no masks are required to form the required device design [91, 96, 100]. As such, on-demand production is possible.
Printing quality is strongly influenced by the ink properties. Printing resolution depends on the ink viscosity and surface tension . The viscosity must be low enough to allow the channel to be refilled in about 100 μs of the droplet dispensed time lapse (deposition and dispensing rate). Figure 15 shows the droplet formation by inkjet printing. To hold the ink without dripping, the ink must possess high surface tension and low pressure. Dispensed droplet energy goes into viscous flow, surface tension, and kinetic energy of the drop [91, 100].
Inkjet printing inks including sol-gel, conducting polymers, ceramics, metals, nanoparticles, and biopolymers ink have been used widely for various inkjet-printed devices [91, 100]. The physical properties of ink play important role in inkjet printing technology. For example, a low ink viscosity of about 20 cP is favorable in order to have the appropriate amount and velocity of ink ejected from the nozzle. Surface tension of the ink will determine the spheroid shape of the ink after ejection, and is typically between 28 mNm−1 and 350 mNm−1. Molten metals typically have very high surface tension; meanwhile, structural polymers possess very low surface tension [91, 100]. Polymeric additives are used to improve dye bonding to the substrate and improve the ink viscosity. Humectants such as ethylene glycol are added at 10%–20% to prevent clogging and drying of the nozzle. The surface tension of the ink is advised to be at a minimum of 35 mNm−1.
Examples of conducting polymers commonly used in inkjet printing are polyaniline (PANI) and PEDOT : PSS . Figure 16 shows the inkjet profile of poly(ethylenedioxythiophene) (PEDOT) and poly(9,9-dioctylfluorene) (F8) aqueous solution being deposited onto a prepatterned substrate. Figure 15 illustrates the impact of the ink’s physical properties on the droplet profile. The formation of F8 long tail is seen from the stroboscopic image. The difference in profile is caused by the difference in viscosity, surface tension, and the polymer molecular weight of the respective solutions.
Printing quality is also controlled by substrates surfaces and ink interaction [91, 101]. Chemical modifications of substrates are a common practice in improving printing quality. The hydrophilic character of substrates surfaces is controlled to prevent excessive absorption of liquids and inks. Surface porosity and roughness influence ink spreading onto the substrate. Synthetic polymer is produced to form a thin film on the substrates surfaces which promote better inkjet printing quality. Substrate treatments are found to be important in keeping excellent printing quality. It must be performed such that hydrophilic character of substrate is kept to allow surface wetting whenever necessary .
As is the case with polymeric thermoelectric materials in general, the inkjet printing process is best suited for low temperature thermoelectric materials, for applications in ambient temperature such as hybrid solar cells, and body heat electricity generation. Even higher resolutions may be attained using electrohydrodynamic jet printing, which allows for high resolution, precision, and speed printing . Jet printing generates small scale droplets targeted on nano- and microscales researche. The use of ultrafine inkjet printer allows a minimum size of dots of less than one micron, thus allowing fabrication of materials and devices using inkjet printing, which enter the realm of nanotechnology .
Thus, given the attractiveness of the inkjet printing method, that is, solution processability, low amounts of ink, direct patterning of device structure onto substrate, the possibility of flexible substrates, and on-demand fabrication, there is much potential for fabrication of thermoelectric devices using inkjet printing.
4.3. Chemical Vapor Deposition
In 1890, Mond, Langer, and Quincke developed the Chemical Vapor Deposition (CVD) technique for large scale applications as a carbonyl process to refine nickel. Numerous earliest applications were implicated in refining or purification of metals and a limited number of nonmetals by carbonyl or halide processes. In recent times, CVD, research, and development efforts have been more concentrated towards the thin-film deposition. It is actually widely used in materials-processing technology. Mostly, it is involved in solid thin-film coatings to surfaces. However, this technique is recurrently used in producing carbon nanotubes (CNTs) high-purity bulk materials and powders, as well as fabricating composite materials via infiltration techniques. So far, the majority of the elements in the periodic table have been deposited by CVD techniques, with some being in the form of the pure elements, but mostly in combinations to form compounds .
In CVD process, precursor gases are brought into a reaction chamber in an activated (light, plasma, and heat) environment and directed towards a heated substrate. Thus, a controlled chemical reaction is induced. The chemical reactions result in the deposition of a solid thin film material onto the substrate surface. It is a very useful processing method for the deposition of polycrystalline, amorphous, and single-crystalline thin films and coatings for a wide range of applications . Figure 17 shows the basic schematic diagram of a CVD setup.
A high-temperature tube furnace with a quartz tube can be used to fabricate nanofibers at temperatures ranging from 300°C to 1200°C. The reaction duration can be varied in the range of 15 min to 8 h according to the desired length of nanowires and thickness of the thin films. The synthesis can be regulated through several parameters such as hydrocarbon’s concentration, catalyst, temperature, pressure, gas-flow rate, deposition time, and reactor’s geometry. Recently, CVD has attracted a lot of attention in producing CNTs through thermal CVD or catalytic CVD (to distinguish it from many other kinds of CVD used for various purposes) . Carbon nanotubes show high electron mobility and high electrical and thermal conductivity and are able to sustain a huge amount of current before structural failure. These properties along with their high Seebeck coefficients make them superlative candidates for thermoelectric applications . SEM images of vertically aligned CNTs fabricated through thermal CVD are given in Figure 18.
4.4. Electrochemical Deposition
Electrochemical deposition or in short electrodeposition has been used in producing thin films and has been intensively used for the last 35 years . It is a nonvacuum, easily scalable, cost-effective, and room temperature technique which made it a more convenient option. Moreover, differently shaped and sized substrates can be used in this method and in contrast to the other gas phase techniques, toxic gaseous precursors are not needed . So far, several thermoelectric thin films have been fabricated through this method. This technique has been used in fabricating both organic and inorganic thin films .
This technique is used as an electrochemical liquid phase thin film preparation method. Usually, the design of an electrochemical cell depends on the specific needs of the experiment. In general, 25–50 mL cell can be used for the laboratory experiments for the sake of handiness. In this process, the reactions are either reduction or oxidation, completed by using an external current source. To carry out the deposition process, an electrochemical cell consists of a reaction vessel and two or three electrodes. In the three-electrode cell, a reference electrode is used to control or measure the potential of the working electrode. However, the current passes between the working electrode and a separate auxiliary or counter electrode. Depositions are controlled by regulating either current or potential. All the compartments of the cell can be separated by using glass frit to reduce the interference of electrochemical reactions. This setup is used when the cell resistivity is relatively higher. The working electrodes work as cathode. Gold, platinum, carbons, mercury, and some semiconductors can be used as working electrodes. Most commonly, reference electrode is “Saturated Calomel Electrode (SCE)” or the Ag/AgCl electrode. Platinum wires or mesh can be used as counter electrodes or anodes. The reactions can occur in room temperature .
Recently, thermoelectric material composed of conductive polymer polyaniline (PANI) and Bi2Te3 nanocomposites was prepared using a simultaneous electrochemical reaction and deposition method. The three-electrode system was used in the fabrication process (Figure 19). After deposition, smaller molecules of Bi2Te3 were found to be dispersed in the macromolecules of PANI . SEM images of samples are prepared by the electrochemical deposition system (Figure 20).
5. Future and Challenges of Thermoelectric Polymers
The developments of polymer thermoelectric materials have seen dramatic increase over the last half decade. Despite that, there is reasonable development to be carried out before real commercialization of polymer-based thermoelectric devices can be realized. Low renders the material suitable for small device applications as these materials consume less energy. Normally, the efficiency of a real device will be much lower than that fabricated in the lab. This can be attributed to the fact that the synthesis is usually not reproducible and sometimes only a small amount could be synthesized and there will always be a problem of large variations in performance between different batches of materials. Second, during manufacturing process, a lot of starting materials are wasted as the most effective fabrication method is still being developed. This contributes to the high cost of manufacturing and thus not favorable to the manufacturer. In order to address this problem, researchers have started to use the inkjet printing technique where only a small amount of thermoelectric sample, in the range of picolitres, is needed to fabricate a device. The resolution of the inkjet printer is suited to those within the range of a few micrometers if only, the inkjet printer is able to print with a resolution as small as nanoscale .
There have been a few drawbacks in polymers to be potential TE materials thus far. Lower Seebeck coefficients and lower electrical conductivity are yet to address to employ the polymer TE material as efficient TE device. Low Seebeck coefficient is improved by the introduction of nanostructures. In addition, the effect of humidity on electrical conductivity is also a constraint to increase the of polymer TE materials as additional treatment in fabrication and encapsulation of the TE device is required in order to mitigate the humidity effects. Summarily, conductive polymers such as PEDOT : PSS and PEDOT : TOS  mixtures have been responsible for the fast trajectory in TE performance in the class of organic electronics, where the has increased from to within the space of 15 years and is a promising indicator that the performance of polymer TE may be close to bridging the gap in performance compared to inorganic TE materials and it will be viable for commercial equations .
5.1. Next Generation Dye-Sensitized Solar Cells (DSSCs)
For the past few decades, research on dye-sensitized solar cells (DSSCs) has attracted the attention of many academics due to the simple fabrication process, low cost, and potentially high efficiency of converting sunlight energy to electric energy [116–119]. The DSSC architecture was first reported by the Grätzel group who successfully developed a DSSC with power conversion efficiency (PCE) of 11% using a liquid electrolyte . The DSSC consists of four major components: (i) a working electrode, (ii) a layer of titanium dioxide (TiO2) coated with dye, (iii) electrolyte, and (iv) a counter electrode. Photons from sunlight are absorbed by the dye. Once the dye is excited, electrons escape from the dye and are accumulated in the nanocrystal TiO2 layer. Due to the large amount of energy lost in the form of heat, the power produced is usually lower than the energy absorbed by the system. The electrons are then diffused into the electrode and eventually return back again into the dye through electrolyte. These processes not only generate electricity but also create a temperature difference where the working electrode is the cool side and the counter electrode is the hot side. In addition, photons with lower energy may be absorbed by glass substrate, electrolyte, and electrodes and convert to heat. Thus, the working temperature of DSSC may be as high as 60°C or higher.
There have been many efforts have been applied to TE materials to harvest electricity from solar energy [121, 122]. For the past few years, there have been efforts to combine thermoelectricity with DSSC and utilizing the waste heat produced by DSSC to generate electricity . This device is expected to have an improved the overall efficiency. In 2010, Guo et al.  fabricated a TE cell-DSSC hybrid system by placing the back of the DSCC to the hot side of the TE cell. They achieved an improvement of 10% of the overall PCE by using the hybrid system compared with a single DSSC. In the hybrid system, DSSC absorbs photon and generates electricity and heat, whilst the TE cell utilizes this waste heat to convert to electric power. One of the interesting parts of this device is that the two subcells can either work at the same time or one at a time as shown in Figure 21.
Wang et al.  found that by adding a solar selective absorber (SSA) to the TE cell-DSSC hybrid system, the conversion efficiency can be further enhanced. SSA can be a material or coating that can maximize solar absorption and minimize thermal emission. Examples of SSA material are PbS, NiCr, NiS-ZnS, and Cr-Cr2O3. The solar energy transmitted through the DSSC is absorbed by the SSA which will convert the energy into heat. This heat is then converted into electricity using the Seebeck effect. The maximum PCE achieved was larger than 13% which shows a promising configuration for realizing very high conversion efficiencies.
The developments of polymer thermoelectric materials have seen dramatic increase over the last half decade. The applications of thermoelectric polymers at low temperatures, especially conductive polymers, have shown various advantages compared to inorganic materials such as easy and low cost of fabrication, light weight, flexibility, and low thermal conductivity. However, thermoelectric polymers have shown some drawbacks such as low electrical conductivity and Seebeck coefficient. Nanostructuring, polymer composites, nanotubes, and addition of semiconducting stabilizers have been shown as important approaches to improve the performance of thermoelectric polymers. By taking advantage of different fabrication techniques, the morphology and structure of the thermoelectric materials and devices can be fine-tuned to suit the intended application. Not only that, but also the control of the morphology will allow for an improvement in the performance of the thermoelectric materials. The use of thermoelectricity with on dye-sensitized solar cells and utilizing the waste heat produced by on dye-sensitized solar cells will be a promising technology to generate electricity from solar energy and low temperature heat sources.
The authors would like to thank the University of Malaya (UM.C/1/625/HIR/MOHE/ENG/29) and Malaysia Toray Science Foundation (55-02-03-1061) for supporting this work.
- D. K. C. M. Donald, Thermoelectricity: An Introduction to the Principles, John Wiley & Sons, 1962.
- D. M. Rowe, Thermoelectrics Handbook: Macro to Nano, CRC Press, 2006.
- W. Liu, X. Yan, G. Chen, and Z. Ren, “Recent advances in thermoelectric nanocomposites,” Nano Energy, vol. 1, no. 1, pp. 42–56, 2012.
- G. J. Snyder and E. S. Toberer, “Complex thermoelectric materials,” Nature Materials, vol. 7, no. 2, pp. 105–114, 2008.
- H. Hosono, Y. Mishima, H. Takezoe, and K. J. D. MacKenzie, Nanomaterials: Research towards Applications, Elsevier Science, 2006.
- M. Tan, Y. Wang, Y. Deng et al., “Oriented growth of A2Te3 (A = Sb, Bi) films and their devices with enhanced thermoelectric performance,” Sensors and Actuators A, vol. 171, no. 2, pp. 252–259, 2011.
- H.-S. Choi, S. Yun, and K.-I. Whang, “Development of a temperature-controlled car-seat system utilizing thermoelectric device,” Applied Thermal Engineering, vol. 27, no. 17-18, pp. 2841–2849, 2007.
- L. D. Hicks and M. S. Dresselhaus, “Effect of quantum-well structures on the thermoelectric figure of merit,” Physical Review B, vol. 47, no. 19, pp. 12727–12731, 1993.
- J.-F. Li, W.-S. Liu, L.-D. Zhao, and M. Zhou, “High-performance nanostructured thermoelectric materials,” NPG Asia Materials, vol. 2, no. 4, pp. 152–158, 2010.
- S. N. Girard, J. He, C. Li et al., “In situ nanostructure generation and evolution within a bulk thermoelectric material to reduce lattice thermal conductivity,” Nano Letters, vol. 10, no. 8, pp. 2825–2831, 2010.
- H. Zhao, M. Pokharel, G. Zhu et al., “Dramatic thermal conductivity reduction by nanostructures for large increase in thermoelectric figure-of-merit of FeSb2,” Applied Physics Letters, vol. 99, pp. 163101–163103, 2012.
- B. Chen, J.-H. Xu, C. Uher et al., “Low-temperature transport properties of the filled skutterudites ,” Physical Review B, vol. 55, no. 3, pp. 1476–1480, 1997.
- C. Uher, J. Yang, S. Hu, D. T. Morelli, and G. P. Meisner, “Transport properties of pure and doped MNiSn (M=Zr, Hf),” Physical Review B, vol. 59, no. 13, pp. 8615–8621, 1999.
- G. S. Nolas, J. L. Cohn, G. A. Slack, and S. B. Schujman, “Semiconducting Ge clathrates: promising candidates for thermoelectric applications,” Applied Physics Letters, vol. 73, no. 2, pp. 178–180, 1998.
- R. T. Littleton, T. M. Tritt, C. R. Feger et al., “Effect of Ti substitution on the thermoelectric properties of the pentatelluride materials (M=Hf, Zr),” Applied Physics Letters, vol. 72, no. 16, pp. 2056–2058, 1998.
- A. Majumdar, “Thermoelectricity in semiconductor nanostructures,” Science, vol. 303, no. 5659, pp. 777–778, 2004.
- (IEEE Cat. No.03TH8726), Proceedings of the 22nd International Conference on Thermoelectrics (ICT '03).
- Y. Sun, P. Sheng, C. Di et al., “Organic thermoelectric materials and devices based on p- and n-type Poly(metal 1,1,2,2-ethenetetrathiolate)s,” Advanced Materials, vol. 24, pp. 932–937, 2012.
- R. Yue, S. Chen, C. Liu et al., “Synthesis, characterization, and thermoelectric properties of a conducting copolymer of 1,12-bis(carbazolyl)dodecane and thieno[3,2-b]thiophene,” Journal of Solid State Electrochemistry, vol. 16, no. 1, pp. 117–126, 2012.
- R. R. Søndergaard, M. Hösel, N. Espinosa, M. Jørgensen, and F. C. Krebs, “Practical evaluation of organic polymer thermoelectrics by large-area R2R processing on flexible substrates,” Energy Science & Engineering, vol. 1, no. 2, pp. 81–88, 2013.
- A. Shakouri, “Recent developments in semiconductor thermoelectric physics and materials,” Annual Review of Materials Research, vol. 41, pp. 399–431, 2011.
- R. Buchner, K. Froehner, C. Sosna, W. Benecke, and W. Lang, “Toward flexible thermoelectric flow sensors: a new technological approach,” Journal of Microelectromechanical Systems, vol. 17, no. 5, pp. 1114–1119, 2008.
- S. Hasebe, J. Ogawa, M. Shiozaki et al., “Polymer based smart flexible thermopile for power generation,” in Proceedings of the 17th IEEE International Conference on Micro Electro Mechanical Systems (MEMS '04), pp. 689–692, January 2004.
- R. Zuzok, A. B. Kaiser, W. Pukacki, and S. Roth, “Thermoelectric power and conductivity of iodine-doped “new” polyacetylene,” The Journal of Chemical Physics, vol. 95, no. 2, pp. 1270–1275, 1991.
- Y. W. Park, “Structure and morphology: relation to thermopower properties of conductive polymers,” Synthetic Metals, vol. 45, no. 2, pp. 173–182, 1991.
- N. Mateeva, H. Niculescu, J. Schlenoff, and L. R. Testardi, “Correlation of Seebeck coefficient and electric conductivity in polyaniline and polypyrrole,” Journal of Applied Physics, vol. 83, no. 6, pp. 3111–3117, 1998.
- N. T. Kemp, A. B. Kaiser, C. J. Liu, et al., “Thermoelectric power and conductivity of different types of polypyrrole,” Journal of Polymer Science Part B, vol. 37, pp. 953–960, 1999.
- H. Yan, N. Sada, and N. Toshima, “Thermal transporting properties of electrically conductive polyaniline films as organic thermoelectric materials,” Journal of Thermal Analysis and Calorimetry, vol. 69, no. 3, pp. 881–887, 2002.
- S. Masubuchi, S. Kazama, K. Mizoguchi et al., “Metallic transport properties in electrochemically as-grown and heavily doped polythiophene and poly(3-methylthiophene),” Synthetic Metals, vol. 57, no. 2, pp. 4962–4967, 1993.
- J.-E. Österholm, P. Passiniemi, H. Isotalo, and H. Stubb, “Synthesis and properties of FeCl4-doped polythiophene,” Synthetic Metals, vol. 18, no. 1–3, pp. 213–218, 1987.
- R. B. Aïch, N. Blouin, A. Bouchard, and M. Leclerc, “Electrical and thermoelectric properties of poly(2,7-carbazole) derivatives,” Chemistry of Materials, vol. 21, no. 4, pp. 751–757, 2009.
- I. Lévesque, P.-O. Bertrand, N. Blouin et al., “Synthesis and thermoelectric properties of polycarbazole, polyindolocarbazole, and polydiindolocarbazole derivatives,” Chemistry of Materials, vol. 19, no. 8, pp. 2128–2138, 2007.
- Y. W. Park, C. O. Yoon, C. H. Lee, H. Shirakawa, Y. Suezaki, and K. Akagi, “Conductivity and thermoelectric power of the newly processed polyacetylene,” Synthetic Metals, vol. 28, no. 3, pp. D27–D34, 1989.
- H. Kaneko, T. Ishiguro, A. Takahashi, and J. Tsukamoto, “Magnetoresistance and thermoelectric power studies of metal-nonmetal transition in iodine-doped polyacetylene,” Synthetic Metals, vol. 57, no. 2, pp. 4900–4905, 1993.
- W. Pukacki, J. Płocharski, and S. Roth, “Anisotropy of thermoelectric power of stretch-oriented new polyacetylene,” Synthetic Metals, vol. 62, no. 3, pp. 253–256, 1994.
- E. B. Park, J. S. Yoo, H. J. Choi, et al., “Positive-thermoelectric power of alkali-metal-doped polyacetylene,” in Proceedings of the International Conference on Science and Technology of Synthetic Metals (ICSM '94), pp. 439–439, 1994.
- A. B. Kaiser, “Systematic conductivity behavior in conducting polymers: effects of heterogeneous disorder,” Advanced Materials, vol. 13, pp. 927–941, 2001.
- A. B. Kaiser, “Thermoelectric power and conductivity of heterogeneous conducting polymers,” Physical Review B, vol. 40, no. 5, pp. 2806–2813, 1989.
- D. M. E. Rowe, CRC Handbook of Thermoelectrics: Macro to Nano, CRC, Boca Raton, Fla, USA, 2005.
- Y. Hiroshige, M. Ookawa, and N. Toshima, “High thermoelectric performance of poly(2,5-dimethoxyphenylenevinylene) and its derivatives,” Synthetic Metals, vol. 156, no. 21–24, pp. 1341–1347, 2006.
- J. Li, X. Tang, H. Li, Y. Yan, and Q. Zhang, “Synthesis and thermoelectric properties of hydrochloric acid-doped polyaniline,” Synthetic Metals, vol. 160, no. 11-12, pp. 1153–1158, 2010.
- C. O. Yoon, M. Reghu, D. Moses, Y. Cao, and A. J. Heeger, “Thermoelectric power of doped polyaniline near the metal-insulator transition,” Synthetic Metals, vol. 69, no. 1–3, pp. 273–274, 1995.
- D. S. Maddison, J. Unsworth, and R. B. Roberts, “Electrical conductivity and thermoelectric power of polypyrrole with different doping levels,” Synthetic Metals, vol. 26, no. 1, pp. 99–108, 1988.
- K. Sato, M. Yamaura, T. Hagiwara, K. Murata, and M. Tokumoto, “Study on the electrical conduction mechanism of polypyrrole films,” Synthetic Metals, vol. 40, no. 1, pp. 35–48, 1991.
- I. Lévesque, X. Gao, D. D. Klug, J. S. Tse, C. I. Ratcliffe, and M. Leclerc, “Highly soluble poly(2,7-carbazolenevinylene) for thermoelectrical applications: from theory to experiment,” Reactive and Functional Polymers, vol. 65, no. 1-2, pp. 23–36, 2005.
- Y. Xia, K. Sun, and J. Ouyang, “Solution-processed metallic conducting polymer films as transparent electrode of optoelectronic devices,” Advanced Materials, vol. 24, no. 18, pp. 2436–2440, 2012.
- M. Leclerc and J.-F. Morin, “Monomers oligomers and polymers of 2-functionalized and 2,7-difunctionalized carbazoles”.
- T. Stöcker, A. Köhler, and R. Moos, “Why does the electrical conductivity in PEDOT:PSS decrease with PSS content? A study combining thermoelectric measurements with impedance spectroscopy,” Journal of Polymer Science Part B, vol. 50, pp. 976–983, 2012.
- R. H. Cruz-Estrada and M. J. Folkes, “Structure formation and modelling of the electrical conductivity in SBS-polyaniline blends—part II. Generalized effective media theories approach,” Journal of Materials Science Letters, vol. 21, no. 18, pp. 1431–1434, 2002.
- R. J. Kline, M. D. McGehee, E. N. Kadnikova, J. Liu, and J. M. J. Fréchet, “Controlling the field-effect mobility of regioregular polythiophene by changing the molecular weight,” Advanced Materials, vol. 15, no. 18, pp. 1519–1522, 2003.
- J. Zhao, J. W. Jiang, N. Wei, et al., “Thermal conductivity dependence on chain length in amorphous polymers,” Journal of Applied Physics, vol. 113, Article ID 184304, 2013.
- J. Zhao, S. Nagao, and Z. Zhang, “Thermomechanical properties dependence on chain length In bulk polyethylene: coarse-grained molecular dynamics simulations,” Journal of Materials Research, vol. 25, no. 3, pp. 537–544, 2010.
- C. A. Hewitt, A. B. Kaiser, M. Craps, R. Czerw, S. Roth, and D. L. Carroll, “Temperature dependent thermoelectric properties of freestanding few layer graphene/polyvinylidene fluoride composite thin films,” Synthetic Metals, vol. 165, pp. 56–59, 2013.
- O. Bubnova, Z. U. Khan, A. Malti et al., “Optimization of the thermoelectric figure of merit in the conducting polymer poly(3,4-ethylenedioxythiophene),” Nature Materials, vol. 10, no. 6, pp. 429–433, 2011.
- Q. Zhang, Y. Sun, W. Xu, and D. Zhu, “Thermoelectric energy from flexible P3HT films doped with a ferric salt of triflimide anions,” Energy & Environmental Science, vol. 5, pp. 9639–9644, 2012.
- J. Luo, D. Billep, T. Waechtler, et al., “Enhancement of the thermoelectric properties of PEDOT: PSS thin films by post-treatment,” Journal of Materials Chemistry A, vol. 1, pp. 7576–7583, 2013.
- Q. Wang, Q. Yao, J. Chang, and L. Chen, “Enhanced thermoelectric properties of CNT/PANI composite nanofibers by highly orienting the arrangement of polymer chains,” Journal of Materials Chemistry, vol. 22, pp. 17612–17618, 2012.
- N. Toshima, “Conductive polymers as a new type of thermoelectric material,” Macromolecular Symposia, vol. 186, pp. 81–86, 2002.
- H. Yan, T. Ohta, and N. Toshima, “Stretched polyaniline films doped by (±)-10-camphorsulfonic acid: anisotropy and improvement of thermoelectric properties,” Macromolecular Materials and Engineering, vol. 286, pp. 139–142, 2001.
- A. Shakouri and S. Li, “Thermoelectric power factor for electrically conductive polymers,” in Proceedings of the 18th International Conference on Thermoelectrics (ICT '99), pp. 402–406, September 1999.
- Y. Nogami, H. Kaneko, T. Ishiguro, A. Takahashi, J. Tsukamoto, and N. Hosoito, “On the metallic states in highly conducting iodine-doped polyacetylene,” Solid State Communications, vol. 76, no. 5, pp. 583–586, 1990.
- Q. Zhang, H. Wang, Q. Zhang, et al., “Effect of silicon and sodium on thermoelectric properties of thallium-doped lead telluride-based materials,” Nano Letters, vol. 12, pp. 2324–2330, 2012.
- L. Fang, K. Zhou, F. Wu, Q. L. Huang, X. F. Yang, and C. Y. Kong, “Effect of doping concentration on the thermolectric properties of nano Ga-doped ZnO films,” in Proceedings of the 3rd International Nanoelectronics Conference (INEC '10), pp. 1175–1176, January 2010.
- G. H. Kim, L. Shao, K. Zhang, and K. P. Pipe, “Engineered doping of organic semiconductors for enhanced thermoelectric efficiency,” Nature Materials, vol. 12, pp. 719–723, 2013.
- Y. Isoda, T. Nagai, H. Fujiu, Y. Imai, and Y. Shinohara, “The effect of Bi doping on thermoelectric properties of Mg2Si0.5Sn0.5,” in Proceedings of the 26th International Conference on Thermoelectrics (ICT '07), pp. 251–255, June 2007.
- D. Kim, Y. Kim, K. Choi, J. C. Grunlan, and C. Yu, “Improved thermoelectric behavior of nanotube-filled polymer composites with poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate),” ACS Nano, vol. 4, no. 1, pp. 513–523, 2010.
- H. Bark, J. S. Kim, and H. Kim, “Effect of multiwalled carbon nanotubes on the thermoelectric properties of a bismuth telluride matrix,” Current Applied Physics, vol. 13, supplement 2, pp. S111–S114, 2013.
- Y. Choi, Y. Kim, S.-G. Park et al., “Effect of the carbon nanotube type on the thermoelectric properties of CNT/Nafion nanocomposites,” Organic Electronics, vol. 12, no. 12, pp. 2120–2125, 2011.
- C. Yu, Y. S. Kim, D. Kim, and J. C. Grunlan, “Thermoelectric behavior of segregated-network polymer nanocomposites,” Nano Letters, vol. 8, no. 12, pp. 4428–4432, 2008.
- K. C. See, J. P. Feser, C. E. Chen, A. Majumdar, J. J. Urban, and R. A. Segalman, “Water-processable polymer-nanocrystal hybrids for thermoelectrics,” Nano Letters, vol. 10, no. 11, pp. 4664–4667, 2010.
- B. Zhang, J. Sun, H. E. Katz, F. Fang, and R. L. Opila, “Promising thermoelectric properties of commercial PEDOT: PSS materials and their Bi2Te3 powder composites,” ACS Applied Materials and Interfaces, vol. 2, no. 11, pp. 3170–3178, 2010.
- C. Liu, F. Jiang, M. Huang, B. Lu, R. Yue, and J. Xu, “Free-standing PEDOT-PSS/Ca3Co4O9 composite films as novel thermoelectric materials,” Journal of Electronic Materials, vol. 40, no. 5, pp. 948–952, 2011.
- L. Vaisman, H. D. Wagner, and G. Marom, “The role of surfactants in dispersion of carbon nanotubes,” Advances in Colloid and Interface Science, vol. 128–130, pp. 37–46, 2006.
- R. Bandyopadhyaya, E. Nativ-Roth, O. Regev, and R. Yerushalmi-Rozen, “Stabilization of individual carbon nanotubes in aqueous solutions,” Nano Letters, vol. 2, no. 1, pp. 25–28, 2002.
- N. R. Tummala and A. Striolo, “SDS Surfactants on carbon nanotubes: aggregate morphology,” ACS Nano, vol. 3, no. 3, pp. 595–602, 2009.
- N. Grossiord, J. Loos, O. Regev, and C. E. Koning, “Toolbox for dispersing carbon nanotubes into polymers to get conductive nanocomposites,” Chemistry of Materials, vol. 18, no. 5, pp. 1089–1099, 2006.
- J. C. Grunlan, L. Liu, and O. Regev, “Weak polyelectrolyte control of carbon nanotube dispersion in water,” Journal of Colloid and Interface Science, vol. 317, no. 1, pp. 346–349, 2008.
- Y. Dror, W. Pyckhout-Hintzen, and Y. Cohen, “Conformation of polymers dispersing single-walled carbon nanotubes in water: a small-angle neutron scattering study,” Macromolecules, vol. 38, no. 18, pp. 7828–7836, 2005.
- Y.-C. Tsai, C.-C. Chiu, M.-C. Tsai et al., “Dispersion of carbon nanotubes in low pH aqueous solutions by means of alumina-coated silica nanoparticles,” Carbon, vol. 45, no. 14, pp. 2823–2827, 2007.
- L. Liu and J. C. Grunlan, “Clay assisted dispersion of carbon nanotubes in conductive epoxy nanocomposites,” Advanced Functional Materials, vol. 17, no. 14, pp. 2343–2348, 2007.
- G. P. Moriarty, J. N. Wheeler, C. Yu, and J. C. Grunlan, “Increasing the thermoelectric power factor of polymer composites using a semiconducting stabilizer for carbon nanotubes,” Carbon, vol. 50, no. 3, pp. 885–895, 2012.
- B. Yang, H. Ahuja, and T. N. Tran, “Thermoelectric technology assessment: application to air conditioning and refrigeration,” HVAC and R Research, vol. 14, no. 5, pp. 635–653, 2008.
- M. S.. Dresselhaus, S. B. Cronin, M. R. Black, and O. Rabin, “Investigation of low-dimensional thermoelectrics,” in Proceedings of the Nonlithographic and Lithographic Methods for Nanofabrication Symposium, S. Smith, Ed., Technomic Publishing Co, Lancaster, Pa, USA, 2001.
- J. Tervo, A. M. Risto Ilola, and H. Hänninen, “State-of-the-art of thermoelectric materials processing, properties and applications,” VTT Technical Research Centre of Finland.
- Y. Shinohara, K. Ohara, Y. Imai, Y. Isoda, and H. Nakanishi, “Problems of conductive polymers as thermoelectric materials,” in Proceedings of the 22nd International Conference on Thermoelectrics (ICT '03), pp. 298–300, 2003.
- D. K. Taggart, Y. Yang, S.-C. Kung, T. M. McIntire, and R. M. Penner, “Enhanced thermoelectric metrics in ultra-long electrodeposited PEDOT nanowires,” Nano Letters, vol. 11, pp. 2192–2193, 2011.
- G. S. Mohammad Chowdhury, “Effect of experimental parameters on the morphology of electrospun Nylon 6 fibres,” International Journal of Basic & Applied Sciences, vol. 10, no. 6, 2010.
- S. R. Dhakate, B. Singla, M. Uppal, and R. B. Mathur, “Effect of processing parameters on morphology and thermal properties of electrospun polycarbonate nanofibers,” Advanced Materials Letters, vol. 1, no. 3, pp. 200–204, 2010.
- B. P. Sautter, Continuous Polymer Nanofibers Using Electrospinning, University of Illinois, Chicago, Ill, USA, 2005.
- Z.-M. Huang, Y.-Z. Zhang, M. Kotaki, and S. Ramakrishna, “A review on polymer nanofibers by electrospinning and their applications in nanocomposites,” Composites Science and Technology, vol. 63, no. 15, pp. 2223–2253, 2003.
- B.-J. de Gans, P. C. Duineveld, and U. S. Schubert, “Inkjet printing of polymers: state of the art and future developments,” Advanced Materials, vol. 16, no. 3, pp. 203–213, 2004.
- S. H. Eom, S. Senthilarasu, P. Uthirakumar et al., “Polymer solar cells based on inkjet-printed PEDOT:PSS layer,” Organic Electronics, vol. 10, no. 3, pp. 536–542, 2009.
- H. M. Haverinen, R. A. Myllylä, and G. E. Jabbour, “Inkjet printing of light emitting quantum dots,” Applied Physics Letters, vol. 94, no. 7, Article ID 073108, 2009.
- T. Kawase, T. Shimoda, C. Newsome, H. Sirringhaus, and R. H. Friend, “Inkjet printing of polymer thin film transistors,” Thin Solid Films, vol. 438-439, pp. 279–287, 2003.
- D. Madan, A. Chen, P. K. Wright, and J. W. Evans, “Dispenser printed composite thermoelectric thick films for thermoelectric generator applications,” Journal of Applied Physics, vol. 109, no. 3, Article ID 034904, 2011.
- H. Sirringhaus, T. Kawase, R. H. Friend et al., “High-resolution inkjet printing of all-polymer transistor circuits,” Science, vol. 290, no. 5499, pp. 2123–2126, 2000.
- Z. Wang, A. Chen, and R. Winslow, “Integration of dispenser-printed ultra-low-voltage thermoelectric and energy storage devices,” Journal of Micromechanics and Microengineering, vol. 22, Article ID 094001, 2012.
- H.-Y. Tseng and V. Subramanian, “All inkjet-printed, fully self-aligned transistors for low-cost circuit applications,” Organic Electronics, vol. 12, no. 2, pp. 249–256, 2011.
- Y. Xia and R. H. Friend, “Polymer bilayer structure via inkjet printing,” Applied Physics Letters, vol. 88, Article ID 163508, 2006.
- P. Calvert, “Inkjet printing for materials and devices,” Chemistry of Materials, vol. 13, no. 10, pp. 3299–3305, 2001.
- I. M. T. Moutinho, P. J. T. Ferreira, and M. L. Figueiredo, “Impact of surface sizing on inkjet printing quality,” Industrial and Engineering Chemistry Research, vol. 46, no. 19, pp. 6183–6188, 2007.
- E. Sutanto, K. Shigeta, Y. K. Kim et al., “A multimaterial electrohydrodynamic jet (E-jet) printing system,” Journal of Micromechanics and Microengineering, vol. 22, no. 4, Article ID 045008, 2012.
- K. Murata, “Super-fine ink-jet printing for nanotechnology,” in Proceedings of the International Conference on MEMS, NANO and Smart Systems, pp. 346–349, 2003.
- J. -H. Park, Chemical Vapor Deposition, 2001.
- K. L. Choy, “Chemical vapour deposition of coatings,” Progress in Materials Science, vol. 48, no. 2, pp. 57–170, 2003.
- M. Kumar and Y. Ando, “Chemical vapor deposition of carbon nanotubes: a review on growth mechanism and mass production,” Journal of Nanoscience and Nanotechnology, vol. 10, no. 6, pp. 3739–3758, 2010.
- Y. Du, S. Z. Shen, W. D. Yang et al., “Facile preparation and characterization of poly (3-hexylthiophene)/multiwalled carbon nanotube thermoelectric composite films,” Journal of Electronic Materials, vol. 41, pp. 1436–1441, 2012.
- S. Wei, W. P. Kang, J. L. Davidson, and J. H. Huang, “Aligned carbon nanotubes fabricated by thermal CVD at atmospheric pressure using Co as catalyst with NH3 as reactive gas,” Diamond and Related Materials, vol. 15, no. 11-12, pp. 1828–1833, 2006.
- H. Saloniemi, Electrodeposition of PbS, PbSe and PbTe Thin Films, Department of Chemistry, University of Helsinki, 2000.
- W. Schwarzacher, “Electrodeposition: a technology for the future,” Electrochemical Society Interface, vol. 15, no. 1, pp. 32–33, 2006.
- B. Y. Yoo, C.-K. Huang, J. R. Lim et al., “Electrochemically deposited thermoelectric n-type Bi2Te3 thin films,” Electrochimica Acta, vol. 50, no. 22, pp. 4371–4377, 2005.
- S. Chen, “Practical electrochemical cells,” in Handbook of Electrochemistry, G. Z. Cynthia, Ed., pp. 33–56, Elsevier, Amsterdam, The Netherlands, 2007.
- K. Chatterjee, A. Suresh, S. Ganguly, K. Kargupta, and D. Banerjee, “Synthesis and characterization of an electro-deposited polyaniline-bismuth telluride nanocomposite—a novel thermoelectric material,” Materials Characterization, vol. 60, no. 12, pp. 1597–1601, 2009.
- J.-U. Park, M. Hardy, S. J. Kang et al., “High-resolution electrohydrodynamic jet printing,” Nature Materials, vol. 6, no. 10, pp. 782–789, 2007.
- Y. Du, S. Z. Shen, K. Cai, and P. S. Casey, “Research progress on polymer-inorganic thermoelectric nanocomposite materials,” Progress in Polymer Science, vol. 37, pp. 820–841, 2011.
- B. O'Regan and M. Grätzel, “A low-cost, high-efficiency solar cell based on dye-sensitized colloidal TiO2 films,” Nature, vol. 353, no. 6346, pp. 737–740, 1991.
- M. K. Nazeeruddin, A. Kay, I. Rodicio et al., “Conversion of light to electricity by cis-X2bis(2,2′-bipyridyl-4,4′-dicarboxylate)ruthenium(II) charge-transfer sensitizers (X = Cl-, Br-, I-, CN-, and SCN-) on nanocrystalline TiO2 electrodes,” Journal of the American Chemical Society, vol. 115, no. 14, pp. 6382–6390, 1993.
- A. Hagfeld and M. Grätzel, “Light-induced redox reactions in nanocrystalline systems,” Chemical Reviews, vol. 95, no. 1, pp. 49–68, 1995.
- M. Grätzel, “Mesoporous oxide junctions and nanostructured solar cells,” Current Opinion in Colloid and Interface Science, vol. 4, no. 4, pp. 314–321, 1999.
- M. Grätzel, “Conversion of sunlight to electric power by nanocrystalline dye-sensitized solar cells,” Journal of Photochemistry and Photobiology A, vol. 164, no. 1–3, pp. 3–14, 2004.
- M. Telkes, “Solar thermoelectric generators,” Journal of Applied Physics, vol. 25, no. 6, pp. 765–777, 1954.
- H. Scherrer, L. Vikhor, B. Lenoir, A. Dauscher, and P. Poinas, “Solar thermolectric generator based on skutterudites,” Journal of Power Sources, vol. 115, no. 1, pp. 141–148, 2003.
- H. Chang, M.-J. Kao, K. D. Huang, S.-L. Chen, and Z.-R. Yu, “A novel photo-thermoelectric generator integrating dye-sensitized solar cells with thermoelectric modules,” Japanese Journal of Applied Physics, vol. 49, no. 6, Article ID 06GG08, 4 pages, 2010.
- X.-Z. Guo, Y.-D. Zhang, D. Qin et al., “Hybrid tandem solar cell for concurrently converting light and heat energy with utilization of full solar spectrum,” Journal of Power Sources, vol. 195, no. 22, pp. 7684–7690, 2010.
- N. Wang, L. Han, H. He, N.-H. Park, and K. Koumoto, “A novel high-performance photovoltaic-thermoelectric hybrid device,” Energy and Environmental Science, vol. 4, no. 9, pp. 3676–3679, 2011.