Thermoelectric measurements of PEDOT:PSS/expanded graphite composites

Poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate)/expanded graphite films were cast as thin films with different expanded graphite contents at room temperature. The thermoelectric properties of the composites were investigated as a function of the graphite concentration. The electrical conductivity and Seebeck coefficient were measured as a function of the graphite concentration. The electrical conductivity and power factor show similar trends with a sharp increase at around 55 wt% of expanded graphite content. The Seebeck coefficient does not show a significant dependence with the graphite content. SEM and TEM images indicate a nearly homogenous distribution of the filler in the matrix. The initial thermal stability is not modified with the filler.     

Promising thermoelectric properties of commercial PEDOT:PSS materials and their bi2Te3 powder composites

Newly commercialized PEDOT:PSS products CLEVIOS PH1000 and FE-T, among the most conducting of polymers, show unexpectedly higher Seebeck coefficients than older CLEVIOS P products that were studied by other groups in the past, leading to promising thermoelectric (TE) power factors around 47 μW/m K(2) and 30 μW/m K(2) respectively. By incorporating both n and p type Bi(2)Te(3) ball milled powders into these PEDOT:PSS products, power factor enhancements for both p and n polymer composite materials are achieved. The contact resistance between Bi(2)Te(3) and PEDOT is identified as the limiting factor for further TE property improvement. These composites can be used for all-solution-processed TE devices on flexible substrates as a new fabrication option.     

电子封装用SiCp/Al复合材料的组织与性能

本文选用粒径为20μm和60μm的SiC混合颗粒,采用挤压铸造方法制备了体积分数为70%的SiCp/LD11(Al-12%Si)复合材料.材料组织致密,颗粒分布均匀.复合材料具有低膨胀、高导热的特性和十分优异的力学性能,并且可以通过退火处理进一步降低其热膨胀系数.采用化学镀方法,在复合材料表面涂覆镍层,以其做为底座的二极管满足器件的可靠性测试要求.     

Influence of ethylene glycol vapor annealing on structure and property of wet-spun PVA/PEDOT:PSS blend fiber

In this study, blend fibers composed of poly(vinyl alcohol) and poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) were prepared via wet-spinning technology. Ethylene glycol (EG) vapor annealing was employed to improve the electrical conductivity and tensile properties of blend fibers. The effects of EG vapor annealing on structures and properties of blend fibers were investigated in detail by analyzing the changes in chemical constituent and structure, molecular structure, surface morphology, surface chemical composition, electrical conductivity, and tensile properties. FTIR spectroscopy indicates that EG vapor annealing does not change the chemical constituent and structure of blend fibers. Raman spectroscopy shows that vapor annealing leads to conformational changes of PEDOT chains from benzoid structure to quinoid structure. AFM and SEM images show that surface morphology of blend fibers become smoother after vapor annealing. XPS measurement shows that EG vapor annealing induces significant phase separation between PEDOT and PSS, forming an enriched PSS layer on the surface of blend fibers, thus leading to a thinner insulating PSS layer between PEDOT grains. This conformational change is beneficial to improve the electrical conductivity of blend fibers. The resultant blend fiber reached conductivity up to 20.4 S cm^?1. The mechanical properties of blend fibers were also improved by EG vapor annealing, with the Young’s modulus and tensile strength increasing from 3.6 GPa and 112 MPa to 4.4 GPa and 132.7 MPa, respectively.     

Microstructure and dielectric properties of BST/MZO ceramic composites for tunable microwave applications

Ba_0.6Sr_0.4TiO₃/Mg_0.9Zn_0.1O (BST/MZO) ceramic composites with different MZO contents were prepared by traditional ceramic process. The crystal structure, fracture surface morphology, and dielectric properties were systematically investigated. The results show that the BST/MZO ceramic composites possess diphase structure, dense, and uniform morphology. The composites have relatively low dielectric loss (in the order of 10⁻³) at microwave frequency. The ceramics all retain substantial tunability (more than 20% at 8 kV/mm DC field) and excellent dielectric strength (more than 19.5 kV/mm). The BST-50 wt% MZO sample has the optimal FOM value (about 256) and should be a better candidate for tunable microwave applications.     

Nanoimprint of dehydrated PEDOT:PSS for organic photovoltaics

We demonstrate the fabrication of poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS) nanogratings by a dehydration-assisted nanoimprint lithographic technique. Dehydration of PEDOT:PSS increases its cohesion to protect the nanostructures formed by nanoimprinting during demolding, resulting in the formation of high quality nanogratings of 60?nm in height, 70?nm in width and 70?nm in spacing (aspect ratio of 0.86). PEDOT:PSS nanogratings are used as hole transport and an electron blocking layer in blended poly(3-hexylthiophene-2,5-diyl) (P3HT):[6,6]-penyl-C61-butyric-acid-methyl-ester (PCBM) organic photovoltaic devices (OPV), showing enhancement of photocurrent and power efficiency in comparison to OPV devices with non-patterned PEDOT:PSS films.     

Composite supercapacitor electrodes made of activated carbon/PEDOT:PSS and activated carbon/doped PEDOT

In this paper, we report on the high electrical storage capacity of composite electrodes made from nanoscale activated carbon combined with either poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) or PEDOT doped with multiple dopants such as ammonium persulfate (APS) and dimethyl sulfoxide (DMSO). The composites were fabricated by electropolymerization of the conducting polymers (PEDOT:PSS, doped PEDOT) onto the nanoscale activated carbon backbone, wherein the nanoscale activated carbon was produced by ball-milling followed by chemical and thermal treatments. Activated carbon/PEDOT:PSS yielded capacitance values of 640 F g^?1 and 26 mF cm^?2, while activated carbon/doped PEDOT yielded capacitances of 1183 F g^?1 and 42 mF cm^?2 at 10 mV s^?1. This is more than five times the storage capacity previously reported for activated carbon–PEDOT composites. Further, use of multiple dopants in PEDOT improved the storage performance of the composite electrode well over that of PEDOT:PSS. The composite electrodes were characterized for their electrochemical behaviour, structural and morphological details and electronic conductivity and showed promise as high-performance energy storage systems.     

PEDOT:PSS as back contact for CdTe solar cells and the effect of PEDOT:PSS conductivity on device performance

Poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) was studied as the back contact of Cadmium telluride (CdTe) solar cells and was compared with conventional Cu-based back contact. A series of PEDOT:PSS aqueous solutions with different conductivities were spin coated onto the glass/SnO2:F/SnO2/CdS/CdTe structures as back contact, and the PEDOT:PSS conductivity dependence of device performance was studied. It was found that PEDOT:PSS back contact with higher conductivity produces devices with lower series resistance and higher shunt resistance, leading to higher fill factor and higher device efficiencies. As the conductivity of PEDOT:PSS increased from 0.03 to 0.24 S/cm, the efficiency of the solar cell increased from 2.7 to 5.1 %. Methanol cleaning also played an important role in increasing the device performance. The efficiency of our best device with PEDOT:PSS back contact has reached 9.1 %, approaching those with conventional Cu/Au back contact (12.5 %).     

环保型电子封装用Sip/Al复合材料性能研究

为研究电子封装用Sip/Al复合材料热物理及力学性能,利用挤压铸造方法制备了体积分数为65%的Sip/LD11(Al-12%Si)可回收环保型复合材料.采用TEM观察、膨胀仪、激光导热综合测试仪以及万能电子拉伸试验机等设备及技术对复合材料进行研究.结果表明:Sip/LD11复合材料组织致密,材料中未观察到孔洞和缺陷;20～50℃时复合材料的热膨胀系数为8.1×10-6/℃,并随着温度的升高而增加,退火处理能够降低复合材料的热膨胀系数;Sip/LD11复合材料铸造状态和热处理状态的热导率分别为132.9、160.1 W/m·℃,复合材料的弯曲强度和比模量较高;可以采用化学镀方法在复合材料表面涂覆Ni层,镀层结合强度良好,是一种优异的电子封装用复合材料.     

PEDOT:PSS/聚(丙烯酰胺-甲基丙烯酸)导电水凝胶的制备与性能

通过原位自由基溶液聚合法制备了聚(3,4-乙撑二氧噻吩):聚苯乙烯磺酸盐(PEDOT:PSS)/聚(丙烯酰胺-甲基丙烯酸)(P(AAM-MAA))导电水凝胶.采用FTIR、Raman、TGA和SEM分别表征了PEDOT:PSS/P(AAM-MAA)的组成与形貌,测定了PEDOT:PSS/P(AAM-MAA)的透光率、电...     

DMSO-treated flexible PEDOT:PSS/PANi fiber electrode for high performance supercapacitors

Wearable energy storage device nowadays gains great interest due to sharply increased demand for highly flexible, stretchable and embedded electronics, where fiber-based supercapacitor (FSC) is a competitive counterpart. The poly(3,4-ethylenedioxythiophene):poly(styrenesulfonic acid)/ polyaniline (PEDOT:PSS/PANi) fiber has been prepared via an accessible technique of one-dimensional (1D) self-assembly. Nevertheless, PSS as the main cross-linking matrix may lead to more hopping sites for charge carriers, lessening the continuous electrically conductive path. Herein, PEDOT:PSS/PANi fiber was treated with dimethyl sulfoxide (DMSO) to remove the insulative PSS chains. Coupling high electroactivity of PANi and high conductivity of PEDOT, the optimized DMSO-PEDOT:PSS/PANi fiber displays enhanced electrochemical properties with a high specific capacitance (C_s) of 367.7 F g^?1 at 0.5 A g^?1 and good rate capability. Moreover, a symmetric FSC based on the DMSO-P₄P₆ fiber exhibits a high energy density of 42.4 Wh kg^?1 at a power density of 302.3 W kg^?1.

Graphical abstract

PEDOT: PSS/PANi fibers are prepared via a simple technique of one-dimensional (1D) self-assembly, and the PEDOT: PSS/PANi fiber exhibits superior flexibility, electrical conductivity, and electrochemical properties.

     

High-performance Ag nanowires/PEDOT:PSS composite electrodes for PVDF-HFP piezoelectric nanogenerators

Journal of Materials Science: Materials in Electronics - The highly transparent and conductive poly(3,4-ethylenedioxythiophene):poly (styrenesulfonate) (PEDOT:PSS)/Ag nanowires (NWs) composite...     

PEDOT:PSS nano-gels for highly electrically conductive silver/epoxy composite adhesives

In this work, we report a methanol-facilitated approach to directly use aqueous Poly(3,4-ethylenedioxythiophene):Poly(styrene sulfonate) (PEDOT:PSS) in the silver/epoxy composites for preparation of highly electrically conductive adhesives (ECAs) and an investigation of the interaction between PEDOT:PSS nano-gels and silver microflakes. PEDOT:PSS nano-gel (18?<?d?<?30 nm) aqueous dispersion is immiscible with epoxy resin and difficult to incorporate into the conventional silver-filled ECAs. To overcome this challenge, we used methanol to facilitate the dispersion of PEDOT:PSS and silver microflake in epoxy resin. The synergetic interactions between PEDOT:PSS and silver and the effect of methanol were investigated using dynamic light scattering (DLS), atomic force microscopy, Kelvin probe force microscopy, and scanning electron microscope. When PEDOT:PSS was exposed to methanol, its morphology changed from coil to coil/linear structure; the contact potential difference between silver microflake and PEDOT:PSS increased from 9.47 to 22.56 mV, showing an increased conductivity between PEDOT:PSS and silver microflake. It was found that the introduction of a small amount of PEDOT:PSS (0.1 wt%) to the conventional ECA with 60 wt% silver microflake remarkably improved the electrical conductivity from 104 to 386 S/cm. A significantly high conductivity of 2526 S/cm was achieved by further increasing the PEDOT:PSS concentration to 1 wt%. The impact of PEDOT:PSS on the adhesive bonding strength towards copper substrate was also examined; the bonding strength slightly decreased when <?1 wt% PEDOT:PSS was used, but abruptly dropped when PEDOT:PSS content was further increased beyond 1 wt%. The incorporation of the optimal 1 wt% PEDOT:PSS into conventional ECAs with 60% silver microflake greatly increased the electrical conductivities by 25 times with limited impact on the shear strength. The results provide insights to the synergetic interplay of conductive polymer and metallic fillers, and might have profound technical implications on the development of advanced conductive composites.     

Nonvolatile write-once-read-many-times memory device with functionalized-nanoshells/PEDOT:PSS nanocomposites

We have investigated the memory effect of the nanocomposites of functionalized carbon nanoshells (f-CNSs) mixed with poly(3,4-ethylenedioxythiophene) doped with polystyrenesulfonate (PEDOT:PSS) polymer. The f-CNSs were synthesized by the spray pyrolysis method and functionalized in situ with functional groups (OH, COOH, C-H, C-OH) with the aim of improving their compatibility in the aqueous dispersion of PEDOT:PSS. The current-voltage (I-V) sweep curves at room temperature for the Al/f-CNSs, for certain concentrations range, embedded in a PEDOT:PSS layer/Al devices showed electrical bistability for write-once-read-many-times (WORM) memory devices. The memory effect observed in the devices can be explained due to the existence of trapped charges in the f-CNSs/PEDOT:PSS layer. The carrier transport mechanisms for the memory devices is studied and discussed.     

Fabrication process and thermal properties of SiCp/Al metal matrix composites for electronic packaging applications

The fabrication process and thermal properties of 50–71 vol% SiC_p/Al metal matrix composites (MMCs) for electronic packaging applications have been investigated. The preforms consisted with 50–71 vol% SiC particles were fabricated by the ball milling and pressing method. The SiC particles were mixed with SiO₂ as an inorganic binder, and cationic starch as a organic binder in distilled water. The mixtures were consolidated in a mold by pressing and dried in two step process, followed by calcination at 1100 °C. The SiC_p/Al composites were fabricated by the infiltration of Al melt into SiC preforms using squeeze casting process. The thermal conductivity ranged 120–177 W/mK and coefficient of thermal expansion ranged 6–10 × 10^–6/K were obtained in 50–71 vol% SiC_p/Al MMCs. The thermal conductivity of SiC_p/Al composite decreased with increasing volume fraction of SiC_p and with increasing the amount of inorganic binder. The coefficient of thermal expansion of SiC_p/Al composite decreased with increasing volume fraction of SiC_p, while thermal conductivity was insensitive to the amount of inorganic binder. The experimental values of the coefficient of thermal expansion and thermal conductivity were in good agreement with the calculated coefficient of thermal expansion based on Turner's model and the calculated thermal conductivity based on Maxwell's model.