scholarly journals Fabrication of PEDOT: PSS-PVP Nanofiber-Embedded Sb2Te3 Thermoelectric Films by Multi-Step Coating and Their Improved Thermoelectric Properties

Materials ◽  
2020 ◽  
Vol 13 (12) ◽  
pp. 2835
Author(s):  
Sang-il Kim ◽  
Kang Yeol Lee ◽  
Jae-Hong Lim
Keyword(s):  
Thermoelectric Properties ◽  
Power Factor ◽  
Photoelectron Spectroscopy ◽  
Hybrid Composites ◽  
Composite Films ◽  
X Ray Diffraction ◽  
Thermoelectric Efficiency ◽  
X Ray ◽  
Seebeck Coefficients ◽  
Electrical Conductivities

Antimony telluride thin films display intrinsic thermoelectric properties at room temperature, although their Seebeck coefficients and electrical conductivities may be unsatisfactory. To address these issues, we designed composite films containing upper and lower Sb2Te3 layers encasing conductive poly(3,4-ethylenedioxythiophene):poly(4-styrenesulfonate) (PEDOT:PSS)- polyvinylpyrrolidone(PVP) nanowires. Thermoelectric Sb2Te3/PEDOT:PSS-PVP/Sb2Te3(ED) (STPPST) hybrid composite films were prepared by a multi-step coating process involving sputtering, electrospinning, and electrodeposition stages. The STPPST hybrid composites were characterized by field-emission scanning electron microscopy, X-ray diffraction, ultraviolet photoelectron spectroscopy, and infrared spectroscopy. The thermoelectric performance of the prepared STPPST hybrid composites, evaluated in terms of the power factor, electrical conductivity and Seebeck coefficient, demonstrated enhanced thermoelectric efficiency over a reference Sb2Te3 film. The performance of the composite Sb2Te3/PEDOT:PSS-PVP/Sb2Te3 film was greatly enhanced, with σ = 365 S/cm, S = 124 μV/K, and a power factor 563 μW/mK.

Study on Phases and Thermoelectric Properties of Bulk Fe4Sb12 and Fe3CoSb12 Prepared by Milling and Sintering

2011 ◽  
Vol 121-126 ◽  
pp. 1526-1529
Author(s):  
Ke Gao Liu ◽  
Jing Li
Keyword(s):  
Thermoelectric Properties ◽  
Impurity Phase ◽  
Semiconductor Materials ◽  
Thermal Constant ◽  
X Ray Diffraction ◽  
X Ray ◽  
Seebeck Coefficients ◽  
Maximum Value ◽  
Type Semiconductor ◽  
P Type

Bulk Fe4Sb12 and Fe3CoSb12 were prepared by sintering at 600 °C. The phases of samples were analyzed by X-ray diffraction and their thermoelectric properties were tested by electric constant instrument and laser thermal constant instrument. Experimental results show that, the major phases of bulk samples are skutterudite with impurity phase FeSb2. The electric resistivities of the samples increase with temperature rising at 100~500 °C. The bulk samples are P-type semiconductor materials. The Seebeck coefficients of the bulk Fe4Sb12 are higher than those of bulk Fe3CoSb12 samples at 100~200 °C but lower at 300~500 °C. The power factor of the bulk Fe4Sb12 samples decreases with temperature rising while that of bulk Fe3CoSb12 samples increases with temperature rising at 100~500 °C. The thermal conductivities of the bulk Fe4Sb12 samples are relatively higher than those of and Fe3CoSb12, which maximum value is up to 0.0974 Wm-1K-1. The ZT value of bulk Fe3CoSb12 increases with temperature rising at 100~500 °C, the maximum value is up to 0.031.The ZT values of the bulk Fe4Sb12 samples are higher than those of bulk Fe3CoSb12 at 100~300 °C while lower at 400~500 °C.

scholarly journals Preparation of N-Doped TiO2-ZrO2Composite Films under Electric Field and Heat Treatment and Assessment of Their Removal of Methylene Blue from Solution

2014 ◽  
Vol 2014 ◽  
pp. 1-4 ◽  
Author(s):  
Lefu Mei ◽  
Ranfang Zuo ◽  
Jing Xie ◽  
Libing Liao ◽  
Hao Ding
Keyword(s):  
Methylene Blue ◽  
Electric Field ◽  
Visible Light ◽  
Composite Film ◽  
Photoelectron Spectroscopy ◽  
Composite Films ◽  
Partial Replacement ◽  
Cutoff Wavelength ◽  
X Ray Diffraction ◽  
X Ray

TiO2-ZrO2composite film with the grain size of 50 nm was synthesized by electric field and heat (EF&H) treatments. Portions of O atoms in the TiO2network structure were replaced by N atoms as revealed by X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) analyses, suggesting formation of a nonstoichiometric compoundTiO2-xNxon the composite film. The UV-Vis spectra of the film suggested that the visible light with wavelength of 550 nm could be absorbed for the N-doped composite film after EF&H treatment in comparison to a cutoff wavelength of 400 nm for the composite film without EF treatment. Photocatalytic experiments showed that the degradation rate of methylene blue by N-doped composite films increased significantly under visible light irradiation. The partial replacement of O by doped N played a very important role in narrowing the band gap and improving the visible light photocatalytic reactivity.

Study on Phases and Thermoelectric Properties of Bulk FexCo4-xSb12 Sintered by MM-SPS

2011 ◽  
Vol 179-180 ◽  
pp. 294-297
Author(s):  
Ke Gao Liu ◽  
Shi Lei
Keyword(s):  
Thermoelectric Properties ◽  
Thermal Constant ◽  
X Ray Diffraction ◽  
Semiconducting Materials ◽  
X Ray ◽  
Seebeck Coefficients ◽  
Plasma Sintering ◽  
Electrical Resistivities ◽  
Spark Plasma ◽  
P Type

Bulk FexCo4-xSb12 with x varies from 0.1 to 2.0 were prepared by mechanical milling (MM) and spark plasma sintering (SPS). The phases of the products were characterized by X-ray diffraction (XRD) and their thermoelectric properties were tested by electric constant instrument and laser thermal constant instrument. Experimental results show that, the major phases of bulk FexCo4-xSb12 are skutterudite. The electrical resistivities of the products increase first and then decrease. The Seebeck coefficients ( ) are negative when x=0.1 at 100 °C and 200 °C while positive at 300~500 °C. The products with x=0.5~2.0 at 100~500 °C are P type semiconducting materials due to their positive values. The thermal conductivities of most samples increase first and then decrease with x increasing and the maximum is up to 0.39 Wm-1K-1 when x=1.0. The ZT values at 200~500 °C increase first and then decrease with x increasing when x=0.1~1.0 and x=1.0~2.0 respectively and the maximum ZT value is 0.196 when x=1.5 at 400 °C.

Phases and Thermoelectric Properties of Bulk CoSb3 Prepared by Wet Milling and Sintering

2011 ◽  
Vol 480-481 ◽  
pp. 402-405
Author(s):  
Ke Gao Liu ◽  
Wei Ping Zhang ◽  
Lei Shi
Keyword(s):  
Thermoelectric Properties ◽  
Milling Time ◽  
Experimental Results ◽  
Thermal Constant ◽  
Wet Milling ◽  
X Ray Diffraction ◽  
Experimental Conditions ◽  
X Ray ◽  
Seebeck Coefficients ◽  
P Type

For investigating the effect of wet milling time on thermoelectric properties, bulk CoSb3 was prepared via wet milling and sintering. The phases of samples were analyzed by X-ray diffraction and their thermoelectric properties were tested by electric constant instrument and laser thermal constant instrument. Experimental results show that, the major phases of the samples sintered from the powders wet-milled 2 and 6 hours are CoSb3 while the samples sintered from powders wet-milled 12 and 20 hours have more impurity phases under the experimental conditions in this work. The electric resistivities of the samples sintered from the powders wet-milled 2 and 6 hours increase with rising temperature, which show the characteristic of typical semiconductor electricity and P-type conducting due to the positive Seebeck coefficients. However, the samples sintered from powders wet-milled 12 and 20 hours show N-type conducting due to their negative Seebeck coefficients. The ZT values of the samples sintered from the powders wet-milled 2 and 6 hours are relatively higher than other samples, which increases with the temperature rising at 100~400 °C, the highest value is 0.078.

Phases and Thermoelectric Properties of Bulk NiSb2 and Composite of NiSb2 and CoSb3 Prepared by Sintering

2012 ◽  
Vol 503-504 ◽  
pp. 507-510 ◽  
Author(s):  
Ke Gao Liu ◽  
Nian Jing Ji ◽  
Zhong Quan Ma
Keyword(s):  
Thermoelectric Properties ◽  
Single Phase ◽  
Semiconductor Materials ◽  
Thermal Constant ◽  
X Ray Diffraction ◽  
X Ray ◽  
Seebeck Coefficients ◽  
Maximum Value ◽  
Type Semiconductor ◽  
Composite Samples

For researching the thermoelectric properties, bulk NiSb2 and the composite of CoSb3 and NiSb2 were prepared by sintering. The phases of samples were analyzed by X-ray diffraction and their thermoelectric properties were tested by electric constant instrument and laser thermal constant instrument. Experimental results show that, Bulk NiSb2 and the composite of NiSb2:CoSb3=2:8 and 4:6 were prepared by sintering at 600°C for 10min and they are N-type semiconductor materials with high densities of 6.998~7.142g/cm3. The bulk NiSb2 sample sintered is nearly single phase NiSb2, while the major phases of the composite of NiSb2:CoSb3=2:8 are major phase CoSb3 with impurity phase NiSb2. The electric resistivity of bulk NiSb2 sample increases with temperature rising while those of the composites (NiSb2:CoSb3=2:8 and 4:6) increase at 400~500 °C. The absolute values of Seebeck coefficients of the composite samples (NiSb2:CoSb3=2:8 and 4:6) increase with temperature rising and are evidently higher than those of bulk NiSb2. The power factors of the composites (NiSb2:CoSb3=2:8 and 4:6) are evidently higher than those of bulk NiSb2 while the power factor of NiSb2 sample varies not obviously with temperature rising, but those of the composites (NiSb2:CoSb3=2:8 and 4:6) increase with temperature rising and reaches the maximum value of 21.3 10-4Wk-2m-1 at 500 °C.

scholarly journals Boosting the Power Factor of Benzodithiophene Based Donor–Acceptor Copolymers/SWCNTs Composites through Doping

Polymers ◽  
2020 ◽  
Vol 12 (7) ◽  
pp. 1447
Author(s):  
Zhongming Chen ◽  
Mengfei Lai ◽  
Lirong Cai ◽  
Wenqiao Zhou ◽  
Dexun Xie ◽  
...  
Keyword(s):  
Electrical Conductivity ◽  
Power Factor ◽  
Room Temperature ◽  
Composite Films ◽  
Side Chain ◽  
Seebeck Coefficients ◽  
Electrical Conductivities ◽  
Before And After ◽  
Donor Acceptor ◽  
Walled Carbon Nanotubes

In this study, a benzodithiophene (BDT)-based donor (D)–acceptor (A) polymer containing carbazole segment in the side-chain was designed and synthesized and the thermoelectric composites with 50 wt % of single walled carbon nanotubes (SWCNTs) were prepared via ultrasonication method. Strong interfacial interactions existed in both of the composites before and after immersing into the 2,3,5,6-Tetrafluoro-7,7,8,8-tetracyanoquinodimethane (F4TCNQ) solution as confirmed by UV-Vis-NIR, Raman, XRD and SEM characterizations. After doping the composites by F4TCNQ, the electrical conductivity of the composites increased from 120.32 S cm−1 to 1044.92 S cm−1 in the room temperature. With increasing the temperature, the electrical conductivities and Seebeck coefficients of the undoped composites both decreased significantly for the composites; the power factor at 475 K was only 6.8 μW m−1 K−2, which was about nine times smaller than the power factor at room temperature (55.9 μW m−1 K−2). In the case of doped composites, although the electrical conductivity was deceased from 1044.9 S cm−1 to 504.17 S cm−1, the Seebeck coefficient increased from 23.76 μV K−1 to 35.69 μW m−1 K−2, therefore, the power factors of the doped composites were almost no change with heating the composite films.

Synthesis of surface-metallized polymeric films by in situ reduction of (4,4,4-trifluoro-1-(2-thienyl)-1,3-butanedionato) silver(I) in a polyimide matrix

1999 ◽  
Vol 14 (7) ◽  
pp. 2897-2904 ◽  
Author(s):  
Robin E. Southward ◽  
Carey K. Bagdassarian ◽  
Christopher J. Sudol ◽  
Jennifer L. Wasyk ◽  
Susanna H. Sproul ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Composite Films ◽  
Mechanical And Thermal Properties ◽  
Gravimetric Analysis ◽  
Face Centered Cubic ◽  
Thermal Curing ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray

Thermal curing of the (4,4,4-trifluoro-1-(2-thienyl)-1,3-butanedionato)silver(I)-containing poly(amic acid) formed from 3,3′,4,4′-benzophenone tetracarboxylic acid dianhydride (BTDA) and 4,4′-oxydianiline (4,4′-ODA) in dimethylacetamide gives both polyimide films via cyclodehydration and reduction of silver(I) to the native metal. Silver(0) migrates to the surface resulting in surface metallized composite films, which can have excellent reflectivity, but do not exhibit surface electrical conductivity. The films retain mechanical and thermal properties similar to those of the parent polyimide. X-ray diffraction shows crystalline face-centered-cubic silver in the films after thermal curing. Microscopy data show that the surface particle sizes are in the range of approximately 50–100 nm. Significant silver remains in the bulk of the polyimide film with varying particles sizes generally less than approximately 15 nm. The interior of the metallized films is not electrically conducting. Films were characterized by x-ray diffraction, differential scanning calorimetry, thermal gravimetric analysis, x-ray photoelectron spectroscopy, transmission electron microscopy, scanning electron microscopy, and mechanical measurements.

Preparation of n-type polyaniline/hexagonal boron nitride composites with a large thermoelectric power factor

2021 ◽  
pp. 096739112110425
Author(s):  
Volkan Ugraskan ◽  
Ebubekir Ceran ◽  
Ozlem Yazici
Keyword(s):  
Boron Nitride ◽  
Power Factor ◽  
Hexagonal Boron Nitride ◽  
Total Reflection ◽  
Attenuated Total Reflection ◽  
X Ray Diffraction ◽  
Thermoelectric Power Factor ◽  
X Ray ◽  
Seebeck Coefficients ◽  
Vis Spectroscopy

In the present study, it was aimed to investigate the thermoelectric (TE) properties of polyaniline/hexagonal boron nitride (PANI/h-BN) composites. First, h-BN was synthesized from boric acid and urea. Then, PANI-HCl was synthesized by oxidative chemical polymerization. Finally, the composites were prepared using different weight ratios of h-BN. The composites were characterized using attenuated total reflection accessory attached Fourier-transform infrared spectroscopy, UV-vis spectroscopy, X-ray diffraction, and scanning electron microscopy/energy dispersive X-ray analyzer. TE investigation of the composites showed that the addition of h-BN significantly contributes to the TE properties of PANI-HCl. The addition of h-BN increased the power factor of PANI-HCl from 0.07 μWm−1K−2 to 143.05 μWm−1K−2. Furthermore, all the composites showed negative Seebeck coefficients which are the characteristics of n-type semiconductors.

Thermoelectric behavior of PEDOT:PSS/CNT/graphene composites

2018 ◽  
Vol 38 (4) ◽  
pp. 381-389 ◽  
Author(s):  
Yan-Xin Liu ◽  
Hai-Hui Liu ◽  
Jian-Ping Wang ◽  
Xing-Xiang Zhang
Keyword(s):  
Power Factor ◽  
Photoelectron Spectroscopy ◽  
Room Temperature ◽  
Hybrid Structure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Styrene Sulfonate ◽  
Transmission Electron ◽  
Multi Walled Carbon Nanotube

AbstractHybrids of poly(3,4-ethylenedioxythiophene) (PEDOT):poly(4-styrene sulfonate) (PSS)/multi-walled carbon nanotube (MWCNT)/graphene (P/M/G), which have high electrical conductivity and low thermal conductivity, were successfully prepared in aqueous solution throughin situpolymerization of 3,4-ethylenedioxythiophene (EDOT) monomers in the presence of poly(sodium 4-styrene sulfonate) (PSSNa). Meanwhile, the composites were characterized by Raman spectroscopy, infrared (IR) spectroscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy. Thermoelectric properties of the samples were measured at room temperature and 50°C. Compared with pristine PEDOT:PSS (P), PEDOT:PSS/MWCNT (P/M) and PEDOT:PSS/graphene (P/G), the power factor of P/M/G composites was significantly improved, whatever the temperature. It increased from 0.061 μW/mK2to 0.105 μW/mK2at room temperature and from 0.070 μW/mK2to 0.142 μW/mK2at 50°C, meaning 72% and 103% enhancement, respectively. The increased power factor is attributed to the synergic effects of MWCNT and graphene, a hybrid structure with excellent electronic coupling and more electric channels.

scholarly journals Solid-Gas Phase Photo-Catalytic Behaviour of Rutile and TiOn (1 < n < 2) Sub-Oxide Phases for Self-Cleaning Applications

Materials ◽  
2019 ◽  
Vol 12 (1) ◽  
pp. 170 ◽  
Author(s):  
Manuel Nuño ◽  
Vaia Adamaki ◽  
David M. Tobaldi ◽  
Maria J. Hortigüela Gallo ◽  
Gonzalo Otero-Irurueta ◽  
...  
Keyword(s):  
Gas Phase ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Catalytic Performance ◽  
Thermal Reduction ◽  
X Ray Diffraction ◽  
X Ray ◽  
Electrical Conductivities ◽  
Oxide Phases ◽  
Self Cleaning

The solid-gas phase photo-catalytic activities of rutile TiO2 and TiOn (1 < n < 2) sub-oxide phases have been evaluated. Varying concentrations of Ti3+ defects were introduced into the rutile polymorph of titanium dioxide through carbo-thermal reduction at temperatures ranging from 350 °C to 1300 °C. The resulting sub-oxides formed were characterized by X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy, impedance spectroscopy and UV-visible diffuse reflectance spectroscopy. The presence of Ti3+ in rutile exposed to high reduction temperatures was confirmed by X-ray diffraction. In addition, a Ti3+-Ti4+ system was demonstrated to enhance the photo-catalytic properties of rutile for the degradation of the air pollutants NO2 and CO2 under UV irradiation of wavelengths (λ) 376–387 nm and 381–392 nm. The optimum reduction temperature for photo-catalytic activity was within the range 350–400 °C and attributed to improved charge-separation. The materials that were subject to carbo-thermal reduction at temperatures of 350 °C and 400 °C exhibited electrical conductivities over one hundred times higher compared to the non-reduced rutile. The results highlight that sub-oxide phases form an important alternative approach to doping with other elements to improve the photo-catalytic performance of TiO2. Such materials are important for applications such as self-cleaning where particles can be incorporated into surface coatings.

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