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A review of electrohydrodynamic casting energy conversion polymer composites

  • This paper provides a brief review on manufacturing polymer composite materials through the nontraditional electrohydrodynamic (EHD) casting approach. First, the EHD technology will be introduced. Then, typical functional polymer composite materials including thermoelectric and photoelectric energy conversion polymers and their composites will be presented. Specifically, how to make composite materials containing functional nanoparticles will be discussed. Converting polymeric fibers into partially carbonized fiber composites will also be shown. The latest research results of polymeric composite materials with energy conversion and sensing functions will be given.

    Citation: Yong X. Gan. A review of electrohydrodynamic casting energy conversion polymer composites[J]. AIMS Materials Science, 2018, 5(2): 206-225. doi: 10.3934/matersci.2018.2.206

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  • This paper provides a brief review on manufacturing polymer composite materials through the nontraditional electrohydrodynamic (EHD) casting approach. First, the EHD technology will be introduced. Then, typical functional polymer composite materials including thermoelectric and photoelectric energy conversion polymers and their composites will be presented. Specifically, how to make composite materials containing functional nanoparticles will be discussed. Converting polymeric fibers into partially carbonized fiber composites will also be shown. The latest research results of polymeric composite materials with energy conversion and sensing functions will be given.


    1. Introduction

    Oxidants are generated as a result of normal intracellular metabolism in mitochondria and peroxisomes, as well as from a variety of cytosolic enzyme systems, in addition, a number of external agents trigger reactive oxygen species ROS production. ROS can be produced endo- or exogenously. The level of ROS is regulated by antioxidants defense mechanisms. In this way, the cell encases an antioxidant/pro-oxidant balance [1]. Organisms have developed an overall antioxidative defense system to mitigate the damaging effects of ROS. To protect against oxidative stress, eukaryotes possess sophisticated defense systems that cope with elevated ROS levels and promote homeostasis [2]. Proteins that protect against high ROS levels include catalases, superoxide dismutases (SODs), and glutathione peroxidases (GSH-Pxs), and these signaling pathways are known to be strongly evolutionarily conserved. Lowering ROS levels below the homeostatic set point may interrupt the physiological role of oxidants in cellular proliferation and host defense. Similarly, increased ROS may also be detrimental and lead to cell death or to an acceleration in ageing and age-related diseases. Many environmental stimuli including produced inflammatory cytokines, ultraviolet radiation, smoking, chemotherapeutic agents and even growth factors generate high levels of ROS that can perturb the normal redox balance and shift cells into a state of oxidative stress. Traditionally, the impairment caused by increased ROS is thought to result from random damage to proteins, lipids and DNA. In addition to these effects, a rise in ROS levels may also induce a stress signal that activates specific redox-sensitive signaling pathways. Once activated, these diverse signaling pathways may have either damaging or potentially protective functions [2]. These defence systems are not effective enough to totally prevent the damage, and therefore, food supplements containing antioxidants may be used to help the human body to reduce oxidative damage [3,4,5] . In several decades, many studies have focused on food sources, nutrients, and components that exert an inhibitory effects on the antioxidative activity in humans and other animals. It has been shown that some lactobacilli possess antioxidant activity, and are able to decrease the risk of accumulation of ROS during ingestion of food [6].

    Lactic acid bacteria (LAB) is well known as "Probiotics". Probiotics have been defined as "live microorganisms, which when administered in adequate amounts, confer a beneficial health effect on the host [7]." LAB are Gram-positive bacteria, widely distributed in nature, and industrially important as they are used in a variety of industrial food fermentations. The potential benefits of LAB for human and animal health include stimulation of the immune system, balancing intestinal flora, and reducing serum cholesterol. Lately, some LAB strains have been found with other important biological functions, such as anti-ageing and antioxidant activities. We review that the effects of LAB to respond to oxidative stress, is connected to oxidative-stress related disease and aging.


    2. The Effects of LAB on the Prevention of Diseases Related to Oxidative Stress

    Lactobacillus rhamnosus GG was found to inhibit lipid peroxidation in vitro due to iron chelation and superoxide anion scavenging ability [8]. In systems mimicking colon fermentation, Lactobacillus paracasei Fn032, Lactobacillus rhamnosus GG and Lactobacillus spp Fn 001 have been shown to prevent hydroxyl radical production [9]. Moreover, it has been shown that orally-administered live recombinant LAB producing bacterial SOD can improve TNBS-induced colitis in rats [10,11]. And Grompone et al . reported that L. rhamnosus CNCM I-3690 has a strong anti-inflammatory profile in co-culture with intestinal epithelial cell-lines, in vitro and this was confirmed in a TNBS-induced colitis model in mice [12]. Guo et al . showed that expolysaccharide of Lactococcus lactis subsp. exhibited antioxidant activity, as shown by evaluation of CAT, SOD and GSH-Px activity, as well as MDA levels in blood serum and the livers of mice [13]. Increasing oxidative stress in accumulated fat is an important pathogenic mechanism of obesity-associated metabolic syndrome. The role of oxidative stress in the pathophysiologic interactions among the constituent factors of the metabolic syndrome has been remarked. Epidemiological, clinical, and animal studies have shown that obesity is coupled with altered redox state and increased metabolic risk. Lactobacillus fermentum ME-3 possessed Mn-superoxide dismutase activity and both its lysates and intact cells were capable of increasing the glutathione redox ratio in blood sera, and improving the composition of the low-density lipids and post-prandial lipids [14]. Lactobacillus casei Zhang was shown to alleviate oxidative stress by reducing lipid peroxidation and improving lipid metabolism both in blood and liver [15]. Lactobacillus plantarum 7FM10 exhibited DPPH and superoxide radical scavenging capacities [16]. Amaretti et al. groups [17] reported that the strains Bifidobacterium animalis subsp. lactis DSMZ 23032, Lactobacillus acidophilus DSMZ 23033, and Lactobacillus brevis DSMZ 23034 exhibited among the highest antioxidants activity within the lactobacilli and bifidobacteria. Park et al . indicated the possibility that probiotic treatment reduce diet-induced obesity and modulate genes associated with metabolism and inflammation in the liver and adipose tissue [18]. Therefore, the effects of antioxidative LAB crosstalk between metabolism and inflammatory signaling pathways.


    3. Free Radical Theory for the Process of Aging

    Aging induced by the accumulation of molecular damage, cellular dysfunction, and reduced functioning of organs for the entire lifetime, often leads to frailty, malfunction and lifestyle-related diseases. Dr. Harman articulated a "free-radical theory" of ageing, speculating that endogenous oxygen radicals were generated in cells and resulted in a pattern of cumulative damage [19]. To protect against oxidative stress, eukaryotes possess sophisticated defense systems that cope with elevated ROS levels and promote homeostasis. Hallmarks of aging include genomic instability, telomere attrition, epigenetic alteration, loss of proteostasis, deregulated nutrient sensing, mitochondrial dysfunction, and cellular senescence [20]. To date, many studies have focused on food sources, nutrients, and components that exert inhibitory effects on the hallmarks of aging in worms, flies, mice, and humans. In 1907, Dr. Metchnikoff first proposed the concept of probiotic bacteria, hypothesizing that lactobacilli were important for promoting human health and longevity [21] and that consumption of lactic-acid-producing bacteria [22], such as the lactobacilli found in yogurt, could be useful for prevention of aging and extension of lifespan. The mechanisms behind the probiotic effects of bacteria, however, are not entirely understood.

    Recently, some groups reported the action mechanism by LAB for longevity by using Caenorhabditis elegans (C.elegans). C.elegans is possibly the most suitable model organism for research on the mechanism of the process for aging. The reason is that it has an evolutionarily conserved metabolism and host defense mechanisms, including insulin/insulin-like growth factor (IGF-1) signaling pathway [23], p38 mitogen-activated protein kinase (p38 MAPK) pathway [24], and the transforming growth factor (TGF-) signaling pathway [25]. Moreover, dietary resources, such as bacteria, play an important role in the control of the lifespan of C. elegans [26]. Aging in C.elegans is a complex process driven by diverse molecular signaling pathways.

    Many genes that are differentially regulated in young versus old animals are known or postulated to be regulated by DAF-16 [forkhead box O (FOXO) transcription factor] [23,27] and SKN-1 [ortholog of mammalian NF-E2-related factor 2 (NRF2)] [28,29]. DAF-16 and SKN-1 play highly conserved roles in regulating stress resistance and longevity genes. Grompone et al . showed that Latobacillus rhamnosus CNCM I-3690 exerted a strong antioxidant effect and extended nematode lifespan through the insulin-like pathway DAF-2/DAF-16 [12]. On the other hand, we recently, found that feeding with Lactobacillus gasseri SBT2055 (LG2055) prolonged the lifespan of C. elegans compared with that with the control E. coli. We also observed that the feeding for C. elegans mutants, daf-2 (e1368) and daf-16 (mgDf50) with LG2055 extended their lifespan similarly to that for the wild-type worms. In contrast, the feeding with LG2055 did not extend the lifespan of skn-1 mutant worms [30]. Therefore, LG2055 was demonstrated to prolong the worm lifespan through the regulation of SKN-1. SKN-1 plays physiological regulatory roles in multiple processes, including detoxification, metabolism, the immune response, and the oxidative-stress defense.

    The maintenance of low ROS levels is critical for function of normal cell function. Thus, we also investigated whether LG2055 stimulated the host defense system and ROS production. Hoeven et al. have shown that ROS released from Ce-Duox1/BLI-3 can activate SKN-1 activity via p38 MAPK signaling [31], with NSY-1 and SEK-1 both able to regulate the p38 MAPK ortholog PMK-1. In response to oxidative stress, PMK-1 phosphorylates SKN-1, which then translocates to the nuclei of intestinal cells and induces the transcription of phase 2 detoxification genes [32]. The p38 MAPK pathway is also known to be crucial for stress response and regulation of immunity. Papp et al. showed that SKN-1 and PMK-1 were central elements in immunosenescence [33]. Immunosenescence, or the age-dependent decline in immune responsivity, is a critical condition that impedes healthy aging [34]. We found that feeding with LG2055 effectively stimulated NSY-1-SEK-1-PMK-1-SKN-1 signaling pathway. Ikeda et al. [35] have also studied the effects of different probiotic strains in C. elegans, including bifidobacterium, Lactobacillus helveticus, and Lactobacillus plantarum. Immune-stimulating molecules, such as peptidoglycan [36], S-layer protein [37], and expolysaccharide [38,39,40] exist on the cell surfaces of these bacteria. Therefore, the beneficial efficacy of LAB may be influenced by differences in the structures of immune-stimulating molecules. In addition, the antioxidants LAB continue to be isolated from traditional fermented food and the intestine of marine organism [41,42]. In the future, some other as yet unknown factors could be shown to be critical for the regulation of immunity.

    In conclusion, the significant antioxidative activity is the basis for the increased resistance of LAB to toxic oxidative compounds and helps some isolates of Lactobacillus spp. to serve as defensive components in intestinal microbial ecosystem. Such antioxidative bacteria strains, with desirable properties, should be a promising material for both applied microbiology and scientific food industry, considering the fact that human microbiota have to be tolerant to endogenous and exogenous oxidative stress to prevent or treat many human diseases.


    Conflict of Interest

    All authors declare no conflicts of interest in this study.


    [1] Ho WJ, Hsiao KY, Hu CH, et al. (2017) Characterized plasmonic effects of various metallic nanoparticles on silicon solar cells using the same anodic aluminum oxide mask for film deposition. Thin Solid Films 631: 64–71. doi: 10.1016/j.tsf.2017.04.016
    [2] Starowicz Z, Kędra A, Berent K, et al. (2017) Influence of Ag nanoparticles microstructure on their optical and plasmonic properties for photovoltaic applications. Sol Energy 158: 610–616. doi: 10.1016/j.solener.2017.10.020
    [3] Taylor G (1969) Electrically Driven Jets. Proc R Soc Lond A 313: 453–475.
    [4] Melcher JR (1963) Field-Couple Surface Waves: A Comparative Study of Surface Coupled Electrohydrodynamic and Magnetohydrodynamic Systems, Cambridge, Massachusetts: The MIT Press, 1–63.
    [5] VillaVelázquez-Mendoza CI, Mendoza-Barraza SS, Rodriguez JL, et al. (2016) Simultaneous synthesis of β-Si3N4 nanofibers and pea-pods and hand-fan like Si2N2O nanostructures by the CVD method. Mater Lett 175: 139–142. doi: 10.1016/j.matlet.2016.04.028
    [6] Maldonado JR, Peckerar M (2016) X-Ray lithography: Some history, current status and future prospects. Microelectron Eng 161: 87–93. doi: 10.1016/j.mee.2016.03.052
    [7] Stoychev GV, Okhrimenko DV, Appelhans D, et al. (2016) Electron beam-induced formation of crystalline nanoparticle chains from amorphous cadmium hydroxide nanofibers. J Colloid Interf Sci 461: 122–127. doi: 10.1016/j.jcis.2015.09.023
    [8] Subbiah T, Bhat GS, Tock RW, et al. (2005) Electrospinning of nanofibers. J Appl Polym Sci 96: 557–559. doi: 10.1002/app.21481
    [9] Gan YX, Chen AD, Gan RN, et al. (2017) Energy conversion behaviors of antimony telluride particle loaded partially carbonized nanofiber composite mat manufactured by electrohydrodynamic casting. Microelectron Eng 181: 16–21. doi: 10.1016/j.mee.2017.06.009
    [10] Gan YX, Draper CW, Gan JB (2017) Carbon nanofiber network made by electrohydrodynamic casting immiscible fluids. Mater Today Commun 13: 248–254. doi: 10.1016/j.mtcomm.2017.10.008
    [11] Han Y, Wei C, Dong J (2015) Droplet formation and settlement of phase-change ink in high resolution electrohydrodynamic (EHD) 3D printing. J Manuf Process 20: 485–491. doi: 10.1016/j.jmapro.2015.06.019
    [12] Han Y, Dong J (2017) High-resolution electrohydrodynamic (EHD) direct printing of molten metal. Procedia Manuf 10: 845–850. doi: 10.1016/j.promfg.2017.07.070
    [13] Zhang Y, Huang ZM, Xu X, et al. (2004) Preparation of core-shell structured PCL-r-gelatin bi-component nanofibers by coaxial electrospinning. Chem Mater 16: 3406–3409. doi: 10.1021/cm049580f
    [14] Loscertales IG, Barrero A, Guerrero I, et al. (2002) Micro/nano encapsulation via electrified coaxial liquid jets. Science 295: 1695–1698. doi: 10.1126/science.1067595
    [15] Kurban Z, Lovell A, Bennington SM, et al. (2010) A solution selection model for coaxial electrospinning and its application to nanostructured hydrogen storage materials. J Phys Chem C 114: 21201–21213. doi: 10.1021/jp107871v
    [16] Wang C, Yan KW, Lin YD, et al. (2010) Biodegradable core/shell fibers by coaxial electrospinning: Processing, fiber characterization, and its application in sustained drug release. Macromolecules 43: 6389–6397. doi: 10.1021/ma100423x
    [17] Zhang YZ, Wang X, Feng Y, et al. (2006) Coaxial electrospinning of (fluorescein isothiocyanate-conjugated bovine serum albumin)-encapsulated poly(ɛ-caprolactone) nanofibers for sustained release. Biomacromolecules 7: 1049–1057. doi: 10.1021/bm050743i
    [18] Zhang H, Zhao CG, Zhao YH, et al. (2010) Electrospinning of ultrafine core/shell fibers for biomedical applications. Sci China Chem 53: 1246–1254. doi: 10.1007/s11426-010-3180-3
    [19] Li F, Zhao Y, Song Y (2010) Core-shell nanofibers: Nano channel and capsule by coaxial electrospinning, In: Kumar A, Nanofibers, Croatia: InTech, 419–438.
    [20] Chan KHK, Kotaki M (2009) Fabrication and morphology control of poly(methyl methacrylate) hollow structures via coaxial electrospinning. J Appl Polym Sci 111: 408–416. doi: 10.1002/app.28994
    [21] Chen H, Wang N, Di J, et al. (2010) Nanowire-in-microtube structured core/shell fibers via multifluidic coaxial electrospinning. Langmuir 26: 11291–11296. doi: 10.1021/la100611f
    [22] Yu JH, Fridrikh SV, Rutledge GC (2004) Production of submicron diameter fibers by two-fluids electrospinning. Adv Mater 16: 1562–1566. doi: 10.1002/adma.200306644
    [23] Gan YX, Chen AD, Gan JB, et al. (2018) Electrohydrodynamic casting bismuth telluride micro particle loaded carbon nanofiber composite material with multiple sensing functions. J Micro Nano-Manuf 6: 011005.
    [24] Sun B, Long YZ, Zhang HD, et al. (2014) Advances in three-dimensional nanofibrous macrostructures via electrospinning. Prog Polym Sci 39: 862–890. doi: 10.1016/j.progpolymsci.2013.06.002
    [25] Zhang Y, Tse C, Rouholamin D, et al. (2012) Scaffolds for tissue engineering produced by inkjet printing. Cent Eur J Eng 2: 325–335.
    [26] Park TH, Shuler ML (2003) Integration of cell culture and microfabrication technology. Biotechnol Progr 19: 243–253. doi: 10.1021/bp020143k
    [27] Lee M, Kim HY (2014) Toward nanoscale three-dimensional printing: Nanowalls built of electrospun nanofibers. Langmuir 30: 1210–1214. doi: 10.1021/la404704z
    [28] Mandrycky C, Wang Z, Kim K, et al. (2016) 3D bioprinting for engineering complex tissues. Biotechnol Adv 34: 422–434. doi: 10.1016/j.biotechadv.2015.12.011
    [29] Huang C, Jian G, DeLisio JB, et al. (2015) Electrospray deposition of energetic polymer nanocomposites with high mass particle loadings: A prelude to 3D printing of rocket motors. Adv Eng Mater 17: 95–101. doi: 10.1002/adem.201400151
    [30] Liu Y, Pollaor S, Wu Y (2015) Electrohydrodynamic processing of p-type transparent conducting oxides. J Nanomater 2015: 423157.
    [31] Sun J, Zhou W, Huang D, et al. (2015) An overview of 3D printing technologies for food fabrication. Food Bioprocess Tech 8: 1605–1615. doi: 10.1007/s11947-015-1528-6
    [32] Mironov V, Trusk T, Kasyanov V, et al. (2009) Biofabrication: A 21st century manufacturing paradigm. Biofabrication 1: 022001. doi: 10.1088/1758-5082/1/2/022001
    [33] Visser J, Peters B, Burger TJ, et al. (2013) Biofabrication of multi-material anatomically shaped tissue constructs. Biofabrication 5: 035007. doi: 10.1088/1758-5082/5/3/035007
    [34] Mittal A, Negi P, Garkhal K, et al. (2010) Integration of porosity and bio-functionalization to form a 3D scaffold: Cell culture studies and in Vitro degradation. Biomed Mater 5: 045001. doi: 10.1088/1748-6041/5/4/045001
    [35] Ozbolat I, Yu Y (2013) Bioprinting towards organ fabrication: Challenges and future trends. IEEE T Biomed Eng 60: 691–699. doi: 10.1109/TBME.2013.2243912
    [36] Mironov V, Rels N, Derby B (2006) Bioprinting: A beginning. Tissue Eng 12: 631–634. doi: 10.1089/ten.2006.12.631
    [37] Catros S, Guillemot F, Nandakumar A, et al. (2011) Layer-by-layer tissue microfabrication supports cell proliferation in vitro and in vivo. Tissue Eng 18: 1–9.
    [38] Vozzi G, Tirella A, Ahluwalia A (2012) Rapid prototyping composite and complex scaffolds with PAM2, In: Liebschner M, Computer-Aided Tissue Engineering. Methods in Molecular Biology (Methods and Protocols), Totowa, NJ: Humana Press, 868: 59–70.
    [39] Shim JH, Yoon MC, Jeong CM, et al. (2014) Efficacy of rhBMP-2 loaded PCL/PLGA/β-TCP guided bone regeneration membrane fabricated by 3D printing technology for reconstruction of calvaria defects in rabbit. Biomed Mater 9: 065006. doi: 10.1088/1748-6041/9/6/065006
    [40] Laudenslager MJ, Sigmund WM (2011) Developments in electrohydrodynamic forming: Fabricating nanomaterials from charged liquids via electrospinning and electrospraying. Am Ceram Soc Bull 90: 23–27.
    [41] Martins A, Chung S, Pedro AJ, et al. (2009) Hierarchical starch-based fibrous scaffold for bone tissue engineering applications. J Tissue Eng Regen M 3: 37–42. doi: 10.1002/term.132
    [42] Zhu W, Masood F, O'Brien J, et al. (2015) Highly aligned nanocomposite scaffolds by electrospinning and electrospraying for neural tissue regeneration. Nanomed-Nanotechnol 11: 693–704. doi: 10.1016/j.nano.2014.12.001
    [43] Erisken C, Kalyon DM, Wang H (2008) Functionally graded electrospun polycaprolactone and b-tricalcium phosphate nanocomposites for tissue engineering applications. Biomaterials 29: 4065–4073. doi: 10.1016/j.biomaterials.2008.06.022
    [44] Giannitelli SM, Mozetic P, Trombetta M, et al. (2015) Combined additive manufacturing approaches in tissue engineering. Acta Biomater 24: 1–11. doi: 10.1016/j.actbio.2015.06.032
    [45] Xu T, Binder KW, Albanna MZ, et al. (2013) Hybrid printing of mechanically and biologically improved constructs for cartilage tissue engineering applications. Biofabrication 5: 015001.
    [46] Nam J, Huang Y, Agarwal S, et al. (2007) Improved cellular infiltration in electrospun fiber via engineered porosity. Tissue Eng 13: 2249–2257. doi: 10.1089/ten.2006.0306
    [47] Abdelaal OAM, Darwish SMH (2013) Review of rapid prototyping techniques for tissue engineering scaffolds fabrication, In: Öchsner A, da Silva L, Altenbach H, Characterization and Development of Biosystems and Biomaterials. Advanced Structured Materials, Berlin, Heidelberg: Springer, 29: 33–54. doi: 10.1007/978-3-642-31470-4_3
    [48] Zhu W, O'Brien C, O'Brien JR, et al. (2014) 3D nano/microfabrication techniques and nanobiomaterials for neural tissue regeneration. Nanomedicine 9: 859–875. doi: 10.2217/nnm.14.36
    [49] Karande TS, Ong JL, Agrawal CM (2004) Diffusion in musculoskeletal tissue engineering scaffolds: Design issues related to porosity, permeability, architecture, and nutrient mixing. Ann Biomed Eng 32: 1728–1743. doi: 10.1007/s10439-004-7825-2
    [50] Jung JW, Lee H, Hong JM, et al. (2015) A new method of fabricating a blend scaffold using an indirect three dimensional printing technique. Biofabrication 7: 045003. doi: 10.1088/1758-5090/7/4/045003
    [51] Kim JT, Seol SK, Pyo J, et al. (2011) Three-dimensional writing of conducting polymer nanowire arrays by meniscus-guided polymerization. Adv Mater 23: 1968–1970. doi: 10.1002/adma.201004528
    [52] Pham QP, Sharma U, Mikos AG (2006) Electrospinning of polymeric nanofibers for tissue engineering applications: A review. Tissue Eng 12: 2249–2257.
    [53] Rosenthal T, Welzmiller S, Neudert L, et al. (2014) Novel superstructure of the rock salt type and element distribution in germanium tin antimony tellurides. J Solid State Chem 219: 108–117. doi: 10.1016/j.jssc.2014.07.014
    [54] Kitagawa H, Takimura K, Ido S, et al. (2017) Thermoelectric properties of crystal-aligned bismuth antimony tellurides prepared by pulse-current sintering under cyclic uniaxial pressure. J Alloy Compd 692: 388–394. doi: 10.1016/j.jallcom.2016.09.054
    [55] Hatsuta N, Takemori D, Takashiri M (2016) Effect of thermal annealing on the structural and thermoelectric properties of electrodeposited antimony telluride thin films. J Alloy Compd 685: 147–152. doi: 10.1016/j.jallcom.2016.05.268
    [56] Sasaki Y, Takashiri M (2016) Effects of Cr interlayer thickness on adhesive, structural, and thermoelectric properties of antimony telluride thin films deposited by radio-frequency magnetron sputtering. Thin Solid Films 619: 195–201. doi: 10.1016/j.tsf.2016.10.069
    [57] Takashiri M, Hamada J (2016) Bismuth antimony telluride thin films with unique crystal orientation by two-step method. J Alloy Compd 683: 276–281. doi: 10.1016/j.jallcom.2016.05.058
    [58] Catrangiu AS, Sin I, Prioteasa P, et al. (2016) Studies of antimony telluride and copper telluride films electrodeposition from choline chloride containing ionic liquids. Thin Solid Films 611: 88–100. doi: 10.1016/j.tsf.2016.04.030
    [59] Masayuki K, Takashiri M (2015) Investigation of the effects of compressive and tensile strain on n-type bismuth telluride and p-type antimony telluride nanocrystalline thin films for use in flexible thermoelectric generators. J Alloy Compd 653: 480–485. doi: 10.1016/j.jallcom.2015.09.039
    [60] Catlin GC, Tripathi R, Nunes G, et al. (2017) An additive approach to low temperature zero pressure sintering of bismuth antimony telluride thermoelectric materials. J Power Sources 343: 316–321. doi: 10.1016/j.jpowsour.2016.12.092
    [61] Urban P, Schneider MN, Oeckler O (2015) Temperature dependent ordering phenomena in single crystals of germanium antimony tellurides. J Solid State Chem 227: 223–231. doi: 10.1016/j.jssc.2015.04.007
    [62] Hu LP, Zhu TJ, Yue XQ, et al. (2015) Enhanced figure of merit in antimony telluride thermoelectric materials by In–Ag Co-alloying for mid-temperature power generation. Acta Mater 85: 270–278. doi: 10.1016/j.actamat.2014.11.023
    [63] Lee WY, Park NW, Hong JE, et al. (2015) Effect of electronic contribution on temperature-dependent thermal transport of antimony telluride thin film. J Alloy Compd 620: 120–124. doi: 10.1016/j.jallcom.2014.09.053
    [64] Rosalbino F, Carlini R, Zanicchi G, et al. (2013) Microstructural characterization and corrosion behavior of lead, bismuth and antimony tellurides prepared by melting. J Alloy Compd 567: 26–32. doi: 10.1016/j.jallcom.2013.03.071
    [65] Kim DH, Kwon IH, Kim C, et al. (2013) Tellurium-evaporation-annealing for p-type bismuth-antimony-telluride thermoelectric materials. J Alloy Compd 548: 126–132. doi: 10.1016/j.jallcom.2012.08.130
    [66] Bochentyn B, Miruszewski T, Karczewski J, et al. (2016) Thermoelectric properties of bismuth-antimony-telluride alloys obtained by reduction of oxide reagents. Mater Chem Phys 177: 353–359. doi: 10.1016/j.matchemphys.2016.04.039
    [67] Qiu W, Yang S, Zhao X (2011) Effect of hot-press treatment on electrochemically deposited antimony telluride film. Thin Solid Films 519: 6399–6402. doi: 10.1016/j.tsf.2011.04.106
    [68] Takashiri M, Tanaka S, Miyazaki K (2010) Improved thermoelectric performance of highly-oriented nanocrystalline bismuth antimony telluride thin films. Thin Solid Films 519: 619–624. doi: 10.1016/j.tsf.2010.08.013
    [69] Takashiri M, Tanaka S, Hagino H, et al. (2014) Strain and grain size effects on thermal transport in highly-oriented nanocrystalline bismuth antimony telluride thin films. Int J Heat Mass Tran 76: 376–384. doi: 10.1016/j.ijheatmasstransfer.2014.04.048
    [70] Lim SK, Kim MY, Oh TS (2009) Thermoelectric properties of the bismuth-antimony-telluride and the antimony-telluride films processed by electrodeposition for micro-device applications. Thin Solid Films 517: 4199–4203. doi: 10.1016/j.tsf.2009.02.005
    [71] Jung H, Myung NV (2011) Electrodeposition of antimony telluride thin films from acidic nitrate-tartrate baths. Electrochim Acta 56: 5611–5615. doi: 10.1016/j.electacta.2011.04.010
    [72] Fan P, Chen T, Zheng Z, et al. (2013) The influence of Bi doping in the thermoelectric properties of Co-sputtering deposited bismuth antimony telluride thin films. Mater Res Bull 48: 333–336. doi: 10.1016/j.materresbull.2012.10.026
    [73] Lensch-Falk JL, Banga D, Hopkins PE, et al. (2012) Electrodeposition and characterization of nano-crystalline antimony telluride thin films. Thin Solid Films 520: 6109–6117. doi: 10.1016/j.tsf.2012.05.078
    [74] Takashiri M, Tanaka S, Miyazaki K (2013) Growth of single-crystalline bismuth antimony telluride nanoplates on the surface of nanoparticle thin films. J Cryst Growth 372: 199–204. doi: 10.1016/j.jcrysgro.2013.03.028
    [75] Kim BG, Choi SM, Lee MH, et al. (2015) Facile fabrication of silicon and aluminum oxide nanotubes using antimony telluride nanowires as templates. Ceram Int 41: 12246–12252. doi: 10.1016/j.ceramint.2015.06.047
    [76] Ganguly S, Zhou C, Morelli D, et al. (2011) Synthesis and evaluation of lead telluride/bismuth antimony telluride nanocomposites for thermoelectric applications. J Solid State Chem 184: 3195–3201. doi: 10.1016/j.jssc.2011.09.031
    [77] Li J, Chen Z, Wang X, et al. (1997) A novel two-dimensional mercury antimony telluride: Low temperature synthesis and characterization of RbHgSbTe3. J Alloy Compd 262–263: 28–33.
    [78] Baba S, Sato H, Huang L, et al. (2014) Formation and characterization of polyethylene terephthalate-based (Bi0.15Sb0.85)2Te3 thermoelectric modules with CoSb3 adhesion layer by aerosol deposition. J Alloy Compd 589: 56–60.
    [79] Bark H, Kim JS, Kim H, et al. (2013) Effect of multiwalled carbon nanotubes on the thermoelectric properties of a bismuth telluride matrix. Curr Appl Phys 13: S111–S114. doi: 10.1016/j.cap.2013.01.019
    [80] Zhang HT, Luo XG, Wang CH, et al. (2004) Characterization of nanocrystalline bismuth telluride (Bi2Te3) synthesized by a hydrothermal method. J Cryst Growth 265: 558–562. doi: 10.1016/j.jcrysgro.2004.02.097
    [81] Sun Y, Cheng H, Gao S, et al. (2012) Atomically thick bismuth selenide freestanding single layers achieving enhanced thermoelectric energy harvesting. J Am Chem Soc 134: 20294–20297. doi: 10.1021/ja3102049
    [82] Prieto AL, Sander MS, Martin-Gonzalez MS, et al. (2001) Electrodeposition of ordered Bi2Te3 nanowire arrays. J Am Chem Soc 123: 7160–7161. doi: 10.1021/ja015989j
    [83] Borca-Tasciuc DA, Chen G, Prieto A, et al. (2004) Thermal properties of electrodeposited bismuth telluride nanowires embedded in amorphous alumina. Appl Phys Lett 85: 6001–6003. doi: 10.1063/1.1834991
    [84] Pang H, Piao YY, Tan YQ, et al. (2013) Thermoelectric behavior of segregated conductive polymer composites with hybrid fillers of carbon nanotube and bismuth telluride. Mater Lett 107: 150–153. doi: 10.1016/j.matlet.2013.06.008
    [85] Chatterjee K, Suresh A, Ganguly S, et al. (2009) Synthesis and characterization of an electro-deposited polyaniline-bismuth telluride nanocomposite-A novel thermoelectric material. Mater Charact 60: 1597–1601. doi: 10.1016/j.matchar.2009.09.012
    [86] Li JF, Liu J (2006) Effect of nano-SiC dispersion on thermoelectric properties of Bi2Te3 polycrystals. Phys Status Solidi A 203: 3768–3773. doi: 10.1002/pssa.200622011
    [87] Kim KT, Choi SY, Shin EH, et al. (2013) The influence of CNTs on the thermoelectric properties of a CNT/Bi2Te3 composite. Carbon 52: 541–549. doi: 10.1016/j.carbon.2012.10.008
    [88] Lu W, Ding Y, Chen Y, et al. (2005) Bismuth telluride hexagonal nanoplatelets and their two-step epitaxial growth. J Am Chem Soc 127: 10112–10116. doi: 10.1021/ja052286j
    [89] Sumithra S, Takas NJ, Misra DK, et al. (2011) Enhancement in thermoelectric figure of merit in nanostructured Bi2Te3 with semimetal nanoinclusions. Adv Energy Mater 1: 1–7.
    [90] Zhao XB, Ji XH, Zhang YH, et al. (2005) Bismuth telluride nanotubes and the effects on the thermoelectric properties of nanotube-containing nanocomposites. Appl Phys Lett 86: 062111. doi: 10.1063/1.1863440
    [91] Chen CL, Chen YY, Lin SJ, et al. (2010) Fabrication and characterization of electrodeposited bismuth telluride films and nanowires. J Phys Chem C 114: 3385–3389. doi: 10.1021/jp909926z
    [92] Toprak M, Zhang Y, Muhammed M (2003) Chemical alloying and characterization of nanocrystalline bismuth telluride. Mater Lett 57: 3976–3982. doi: 10.1016/S0167-577X(03)00250-7
    [93] Kim KT, Koo HY, Lee GG, et al. (2012) Synthesis of alumina nanoparticle-embedded-bismuth telluride matrix thermoelectric composite powders. Mater Lett 82: 141–144. doi: 10.1016/j.matlet.2012.05.053
    [94] Chávez-Ángel E, Reparaz JS, Gomis-Bresco J, et al. (2014) Reduction of the thermal conductivity in free-standing silicon nano-membranes investigated by non-invasive Raman thermometry. APL Mater 2: 012113. doi: 10.1063/1.4861796
    [95] Liang B, Song Z, Wang M, et al. (2013) Fabrication and thermoelectric properties of graphene/Bi2Te3 composite materials. J Nanomater 2013: 210767.
    [96] Goldsmid HJ (2014) Bismuth telluride and its alloys as materials for thermoelectric generation. Materials 2014: 2577–2592.
    [97] Keshavarz MK, Vasilevskiy D, Masut RA, et al. (2013) p-Type bismuth telluride-based composite thermoelectric materials produced by mechanical alloying and hot extrusion. J Electron Mater 42: 1429–1435. doi: 10.1007/s11664-012-2284-2
    [98] Chang HC, Chen CH (2011) Self-assembled bismuth telluride films with well-aligned zero-to three-dimensional nanoblocks for thermoelectric applications. CrystEngComm 13: 5956–5962.
    [99] Deng Y, Nan CW, Wei GD, et al. (2003) Organic-assisted growth of bismuth telluride nanocrystals. Chem Phys Lett 374: 410–415. doi: 10.1016/S0009-2614(03)00783-8
    [100] Liao CN, She TH (2007) Preparation of bismuth telluride thin films through interfacial reaction. Thin Solid Films 515: 8059–8064. doi: 10.1016/j.tsf.2007.03.086
    [101] Sokolova OB, Skipidarova SY, Duvankova NI, et al. (2004) Chemical reactions on the Bi2Te3-Bi2Se3 section in the process of crystal growth. J Cryst Growth 262: 442–448. doi: 10.1016/j.jcrysgro.2003.10.073
    [102] Kim KT, Ha GH (2013) Fabrication and enhanced thermoelectric properties of alumina nanoparticle-dispersed Bi0.5Sb1.5Te3 matrix composites. J Nanomater 2013: 821657.
    [103] Gothard N, Wilks G, Tritt TM, et al. (2010) Effect of processing route on the microstructure and thermoelectric properties of bismuth telluride-based alloys. J Electron Mater 39: 1909–1913. doi: 10.1007/s11664-009-1051-5
    [104] Thiebaud L, Legeai S, Ghanbaja J, et al. (2018) Synthesis of Te-Bi core-shell nanowires by two-step electrodeposition in ionic liquids. Electrochem Commun 86: 30–33. doi: 10.1016/j.elecom.2017.11.010
    [105] Kim J, Lee JY, Lim JH, et al. (2016) Optimization of thermoelectric properties of p-type AgSbTe2 thin films via electrochemical synthesis. Electrochim Acta 196: 579–586. doi: 10.1016/j.electacta.2016.02.206
    [106] Suzuki M, Tsuchiya T, Akedo J (2017) Effect of starting powder morphology on film texture for bismuth layer-structured ferroelectrics prepared by aerosol deposition method. Jpn J Appl Phys 56: 06GH02.
    [107] Chu F, Zhang Q, Zhou Z, et al. (2018) Enhanced thermoelectric and mechanical properties of Na-doped polycrystalline SnSe thermoelectric materials via CNTs dispersion. J Alloy Compd 741: 756–764. doi: 10.1016/j.jallcom.2018.01.178
    [108] Chung DDL (2017) Processing-structure-property relationships of continuous carbon fiber polymer-matrix composites. Mater Sci Eng R 113: 1–29. doi: 10.1016/j.mser.2017.01.002
    [109] Mahmoud L, Alhwarai M, Samad YA, et al. (2015) Characterization of a graphene-based thermoelectric generator using a cost-effective fabrication process. Energy Procedia 75: 615–620. doi: 10.1016/j.egypro.2015.07.466
    [110] Lee S, Kim J, Ku BC, et al. (2012) Structural evolution of polyacrylonitrile fibers in stabilization and carbonization. Adv Chem Eng Sci 2: 275–282. doi: 10.4236/aces.2012.22032
    [111] Saha B, Schatz GC (2012) Carbonization in polyacrylonitrile (PAN) based carbon fibers studied by ReaxFF molecular dynamics simulations. J Phys Chem B 116: 4684–4692. doi: 10.1021/jp300581b
    [112] Ma Q, Gao A, Tong Y, et al. (2016) The densification mechanism of polyacrylonitrile carbon fibers during carbonization. New Carbon Mater 31: 550–554. doi: 10.1016/S1872-5805(16)60031-8
    [113] Hameed N, Sharp J, Nunna S, et al. (2016) Structural transformation of polyacrylonitrile fibers during stabilization and low temperature carbonization. Polym Degrad Stabil 128: 39–45. doi: 10.1016/j.polymdegradstab.2016.02.029
    [114] Liu J, Wang PH, Li RY (1994) Continuous carbonization of polyacrylonitrile-based oxidized fibers: Aspects on mechanical properties and morphological structure. J Appl Polym Sci 52: 945–950. doi: 10.1002/app.1994.070520712
    [115] Wang H, Zhang X, Zhang Y, et al. (2016) Study of carbonization behavior of polyacrylonitrile/tin salt as anode material for lithium-ion batteries. J Appl Polym Sci 2016: 43914.
    [116] Sun J, Wu G, Wang Q (2005) The effects of carbonization temperature on the properties and structure of PAN-based activated carbon hollow fiber. J Appl Polym Sci 97: 2155–2160. doi: 10.1002/app.21955
    [117] Rahaman MSA, Ismail AF, Mustafa A (2007) A review of heat treatment on polyacrylonitrile fiber. Polym Degrad Stabil 92: 1421–1432. doi: 10.1016/j.polymdegradstab.2007.03.023
    [118] Zhao LR, Jang BZ, Zhou JN (1998) Effect of polymeric precursors on properties of semiconducting carbon/carbon composites. J Mater Sci 33: 1809–1817. doi: 10.1023/A:1004392919018
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