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Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

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At least 1,063 records · Page 59
All sourcesNASA NTRSDOE OSTI
DOE OSTI2013

Co-electrospinning fabrication and photocatalytic performance of TiO{sub 2}/SiO{sub 2} core/sheath nanofibers with tunable sheath thickness

Graphical abstract: - Highlights: • The core–sheath TiO{sub 2}/SiO{sub 2} nanofibers were fabricated by co-electrospinning technique. • The catalytic property of nanofibers with different sheath thickness was studied. • The potential methods of improving catalytic efficiency are suggested. - Abstract: In this paper, core/sheath TiO{sub 2}/SiO{sub 2} nanofibers with tunable sheath thickness were directly fabricated via a facile co-electrospinning technique with subsequent calcination at 500 °C. The morphologies and structures of core/sheath TiO{sub 2}/SiO{sub 2} nanofibers were characterized by TGA, FESEM, TEM, FTIR, XPS and BET. It was found that the 1D core/sheath nanofibers are made up of anatase–rutile TiO{sub 2} core and amorphous SiO{sub 2} sheath. The influences of SiO{sub 2} sheath and its thickness on the photoreactivity were evaluated by observing photo-degradation of methylene blue aqueous solution under the irradiation of UV light. Compared with pure TiO{sub 2} nanofibers, the core/sheath TiO{sub 2}/SiO{sub 2} nanofibers performed a better catalytic performance. That was attributed to not only efficient separation of hole–electron pairs resulting from the formation of heterojunction but also larger surface area and surface silanol group which will be useful to provide higher capacity for oxygen adsorption to generate more hydroxyl radicals. And the optimized core/sheath TiO{sub 2}/SiO{sub 2} nanofibers with a sheath thickness of 37 nm exhibited the best photocatalytic performance.

36 MATERIALS SCIENCE↗
DOE OSTI2014

Fabrication and microstructure of cerium doped lutetium aluminum garnet (Ce:LuAG) transparent ceramics by solid-state reaction method

Highlights: • We fabricate Ce doped lutetium aluminum garnet ceramics by solid-state method. • The raw materials include Lu{sub 2}O{sub 3} nanopowders synthesized by co-precipitation method. • The density of the transparent ceramics reach 99.7% of the theoretical value. • The optical transmittance of the bulk ceramic at 550 nm was 57.48%. • Some scattering centers decrease the optical characteristic of the ceramic. - Abstract: Polycrystalline Ce{sup 3+} doped lutetium aluminum garnet (Ce:LuAG) transparent ceramics fabricated by one step solid-state reaction method using synthetic nano-sized Lu{sub 2}O{sub 3}, commercial α-Al{sub 2}O{sub 3} and CeO{sub 2} powders were investigated in this paper. The green compacts shaped by the mixed powders were successfully densified into Ce:LuAG transparent ceramics after vacuum sintering at 1750 °C for 10 h. The in-line optical transmittance of the Ce:LuAG ceramic made by home-made Lu{sub 2}O{sub 3} powders could reach 57.48% at 550 nm, which was higher than that of the ceramic made by commercial Lu{sub 2}O{sub 3} powders (22.96%). The microstructure observation showed that light scattering centers caused by micro-pores, aluminum segregation and refraction index inhomogeneities induced the decrease of optical transparency of the Ce:LuAG ceramics, which should be removed and optimized in the future work.

36 MATERIALS SCIENCE↗
DOE OSTI2014

Effects of thermal treatment on the Mg{sub x}Zn{sub 1−x}O films and fabrication of visible-blind and solar-blind ultraviolet photodetectors

Highlights: • Single-phase wurtzite/cubic Mg{sub x}Zn{sub 1−x}O films were grown by RF magnetron sputtering technique. • We focus on the red-shift caused by annealing the Mg{sub x}Zn{sub 1−x}O films. • MSM-structured visible-blind and solar-blind UV photodetectors were fabricated. - Abstract: A series of single-phase Mg{sub x}Zn{sub 1−x}O films with different Mg contents were prepared on quartz substrates by RF magnetron sputtering technique using different MgZnO targets, and annealed under the atmospheric environment. The absorption edges of Mg{sub x}Zn{sub 1−x}O films can cover the whole near ultraviolet and even the whole solar-blind spectra range, and the solar-blind wurtzite/cubic Mg{sub x}Zn{sub 1−x}O films have been realized successfully by the same method. In addition, the absorption edges of annealed films shift to a long wavelength, which is caused by the diffusion of Zn atoms gathering at the surface during the thermal treatment process. Finally, the truly solar-blind metal-semiconductor-metal structured photodetectors based on wurtzite Mg{sub 0.445}Zn{sub 0.555}O and cubic Mg{sub 0.728}Zn{sub 0.272}O films were fabricated. The corresponding peak responsivities are 17 mA/W at 275 nm and 0.53 mA/W at 250 nm under a 120 V bias, respectively.

36 MATERIALS SCIENCE↗
DOE OSTI2016

Fabrication and characterization of metal–semiconductor–metal ultraviolet photodetector based on rutile TiO{sub 2} nanorod

The fabrication and characterization of a metal–semiconductor–metal ultraviolet photodetector are studied. The photodetector is based on TiO{sub 2} nanorods (NRs) grown on p-type (1 1 1)-oriented silicon substrate seeded with a TiO{sub 2} layer is synthesized by radio frequency reactive magnetron sputtering. A chemical bath deposition is used to grow TiO{sub 2} NRs on Si substrate. The structural and optical properties of the obtained sample are analyzed by using X-ray diffraction and field emission-scanning electron microscopy. Results show a tetragonal rutile structure of the synthesized TiO{sub 2} NRs. Optical properties are further examined using photoluminescence spectroscopy. A sharp and high-intensity UV peak at 367 nm is observed in comparison with visible defect peaks centered at 432 and 718 nm. Upon exposure to 365 nm light (2.3 mW/cm) at 5 V bias, the device displays 76.06 × 10{sup 2} sensitivity, internal photodetector gain of 77.06, photocurrent of the device is 2.62 × 10{sup −5} A and photoresponse peak of 69.7 mA/W. The response and recovery times are calculated as 18.5 and 19.1 ms upon illumination to a pulse UV light (365 nm, 2.3 mW/cm{sup 2}) at 5 V applied bias. These results demonstrate that the fabricated high-quality photodiode is a promising candidate as a low-cost UV photodetector for commercially-integrated photoelectronic applications.

36 MATERIALS SCIENCE↗
DOE OSTI2016

Open porous BiVO{sub 4} nanomaterials: Electronspinning fabrication and enhanced visible light photocatalytic activity

Highlights: • BiVO{sub 4} nanofibers were successfully fabricated by electrospinning method. • PVP was used to adjust the viscosity and increase spinnability of the electrospinning sol. • BiVO{sub 4} nanofibers were used for the degradation of MB. • Compared to the submicron sized BiVO4, BiVO{sub 4} nanofibers show superior photocatalytic activity. - Abstract: Witnessed by X-ray powder diffraction (XRD), Raman, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) studies, BiVO{sub 4} nanofibers and porous nanostructures were successfully fabricated by electrospinning method using NH{sub 4}VO{sub 3} and Bi(NO{sub 3}){sub 3} as starting materials. Polyvinylpyrrolidinone (PVP) was used to tune the viscosity and spinnability of the electrospinning sol. The slow decomposition and combustion of PVP matrix prevented rapid crystal growth of BiVO{sub 4} nanostructures leading to considerably small crystallite size (approximately 19.1–28.3 nm) with less surface defects after two hours calcination at varying temperatures. This paid great tributes to the superior visible light photocatalytic activity when compared to the submicron sized BiVO{sub 4} prepared in the absence of PVP.

36 MATERIALS SCIENCE↗
DOE OSTI2016

A simple method to fabricate an NIR detector by PbTe nanowires in a large scale

Highlights: • PbTe nanowires were grown by tellurization of the Pb sheets for the first time. • It was observed a band gap value for the PbTe nanostructures in the NIR region. • NIR detector was fabricated in a large scale using a simple method. • Effect of Te concentration on morphology of PbTe nanostructures was investigated. - Abstract: A simple method was used to fabricate a near-infrared (NIR) detector using PbTe nanostructures. Samples were synthesized by tellurization of lead sheets in a tube furnace. PbTe nanostructures with wires and flakes shapes were grown on the lead sheets that were placed at 300 and 330 °C, respectively, while, PbTe nanoporous were grown at 360 and 390 °C. X-ray diffraction patterns and X-ray photoelectron spectra results indicated that, the PbTe phase was formed in all samples. UV–vis diffuse reflectance spectra measurements showed a band gap for the PbTe nanostructures in the near-infrared region of the electromagnetic spectrum. Actually, the results indicated that, the band gap values of the PbTe nanowires and nanoporous were 1.54 eV and 1.61 eV, respectively. Finally, the PbTe nanostructures were used as a simple photoresponse device under a red light source. The photoresponse results revealed, PbTe nanowires are promising for photoelectrical applications in the NIR region.

36 MATERIALS SCIENCE↗
DOE OSTI2017

Facile fabrication of micro-floriated AgBr/Bi{sub 2}O{sub 3} as highly efficient visible-light photocatalyst

Highlights: • We successfully fabricate micro-floriated AgBr/Bi{sub 2}O{sub 3} composites by one simple hydrothermal react with precusor BiOBr. This micro-floriated Bi{sub 2}O{sub 3} heterojunction composite is rarely reported by others. • Heterojunction AgBr/Bi{sub 2}O{sub 3} composite exhibits highly efficient photocatalytic activity to decompose pollutant. • The enhanced photocatalytic activity was attributed to the improved visible light harvesting ability and higher separation efficiency of photogenerated electron–hole pairs by the introduction of AgBr. • This composite is beneficial to industrial applications to eliminate the organic pollutants from waste water. - Abstract: Semiconductor with photocatalytic property is the potential solution to solve the problem about water pollution. Novel floriated AgBr/Bi{sub 2}O{sub 3} fabricated through a facile simple two-step hydrothermal method is an efficient photocatalyst. The eminent performance for degradation of methyl orange (MO) was evaluated under visible light irradiation. Many characterization methods, including XPS, XRD, FT-IR, SEM, TEM and UV–vis diffuse reflection spectroscopy, were used to investigate the structure, elemental composition, morphology and catalytic activity. Broad contact between AgBr and Bi{sub 2}O{sub 3} interface enabled hybrid materials possess superior efficiency for the decomposition of MO under visible light irradiation. The optimum photocatalytic activity of samples was approximately 11.7 times higher than pure Bi{sub 2}O{sub 3}. In addition, the photo-generated reactive species were identified based on free radicals trapping experiments, which revealed that superoxide radical is the key factor to the photocatalytic process.

36 MATERIALS SCIENCE↗
DOE OSTI2017

A facile microwave-hydrothermal method to fabricate B doped ZnWO{sub 4} nanorods with high crystalline and highly efficient photocatalytic activity

Highlights: • High-crystallized B/ZnWO{sub 4} nanorods were fabricated via a fast microwave -hydrothermal method. • B doping effectively decreases particle size and increase in specific surface area. • The seperation of photogenerated e{sup −} and h{sup +} was largely promoted by B doping. • B/ZnWO{sub 4} exhibit super photocatalytic activity in degradation organic dyes. - Abstract: A series length of 50∼200 nm B doped ZnWO{sub 4} nanorods with high crystallinity were fabricated via a fast microwave-hydrothermal method. The effects of B doping on the physical properties of ZnWO{sub 4} nanorods were intensively characterized by N{sub 2} physical adsorption, XRD, TEM, FT-IR, XPS, ultraviolet-visible diffuse reflection spectrum (UV–vis DRS), photolunminescence spectrum (PL), transient photocurrent response (TPR). The results indicated that the doped B could replace the lattice tungsten ion in ZnWO{sub 4} crystals, which caused the lattice spacing contraction, particle size decrease, specific surface area increase. More importantly, the separation of the photogenerated electrons and holes in ZnWO{sub 4} was significantly enhanced by B doping. With doped optimum B concentration (2.42 wt%), B/ZnWO{sub 4} displayed super photocatalytic performance in dyes decomposition. The degradation rate constant (0.065 h{sup −1}) of Rhodamine B over B (2.42 wt%)/ZnWO{sub 4} is 4 times of that over ZnWO{sub 4} (0.016 h{sup −1}).

36 MATERIALS SCIENCE↗
DOE OSTI2022

Fabrication and accelerated long-term stability test of asymmetrical hollow fiber-supported thin film oxygen separation membrane

Asymmetrical hollow fiber-supported thin film membrane may provide microstructural advantages for air separation and oxygen production. The fabrication of such a membrane is usually very difficult, particularly the sintering behaviors and thermal expansion coefficient (TEC) mismatch among multiple layers. This directly affects the reliability and long-term stability of the membrane. Here, in this research, the sintering behaviors of a set of simple oxides are systematically studied and ZnO is identified as a material component for composite substrate La 0.6 Sr 0.4 Co 0.2 Fe 0.8 O 3-δ (LSCF)-ZnO. The LSCF-ZnO ratios are further optimized by trading off several factors, e.g., matching the sintering behaviors and TECs of the LSCF-ZnO composite with those of LSCF thin film separation layer while enhancing the substrate strength. With the identified LSCF-ZnO ratio, the LSCF-ZnO composite hollow fiber substrate precursor is formed through slurry spinning process with porous microstructure being formed via phase inversion process. The thin film LSCF dense separation layer is then dip-coated on the substrate followed by co-sintering process. A thin, porous PrBaCo(Fe 0.6 Zr 0.2 Y 0.2 )O 5+δ (PBCFZY) catalyst layer is fabricated on the dense LSCF separation layer with dip-coating and sintering process, forming an asymmetrical membrane device LSCF-ZnO/LSCF/PBCFZY. Oxygen permeation test of the device is systematically conducted, and the fundamental mechanisms are analyzed. An accelerated long-term stability test of the membrane is also conducted (~550h, 46 thermal cycling loads), demonstrating excellent robustness and durability. The device is characterized and analyzed before and after the test. By replacing a considerable amount of high cost LSCF with low cost ZnO in the substrate, it not only enhances the stability but also reduces the capital cost of the membrane for practical applications.

42 ENGINEERING↗
DOE OSTI2022

Polystyrene sulfonate (PSS) stabilized polyethylenimine (PEI) membranes fabricated by spray coating for highly effective CO 2 /N 2 separation

Greenhouse effect, largely caused by CO 2 emission, has become a major concern for global climate change. Post-combustion CO 2 capture is one of the critical strategies to mitigate this issue. Membrane technology for carbon capture has drawn significant attention because of the cost and energy efficiency and scalability. Many membranes for CO 2 capture are limited by the trade-off between CO 2 permeability and CO 2 /N 2 selectivity and the long-term stability under practical operating conditions. Facilitated transport membranes with efficient CO 2 carriers have demonstrated potential to surpass the permeability-selectivity trade-off, but these carriers are often lost under operational conditions. In this work, we designed and fabricated a polystyrene sulfonate (PSS) stabilized polyethylenimine (PEI) membrane by a facile and scalable spray-coating method. The deposited defect-free selective layer, in which the amine carriers in PEI can be stabilized electrostatically by PSS, exhibited superior CO 2 separation performance with good long-term stability under practical operating conditions. The separation performance was optimized by spray-coating cycles, CNT network loading, and PSS loading. Our membrane showed CO 2 permeance ranging from 820 to 1,770 GPU and CO 2 /N 2 selectivity varying from 395 to 460 under vacuum operation mode in the temperature range between 80 and 90 °C. Furthermore, the membrane was successfully scaled up to 200 cm 2 with good uniformity. These results might suggest a novel membrane structure and a scalable approach for fabrication of highly efficient CO 2 separation membranes.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2017

Fabrication and testing of a 4-node micro-pocket fission detector array for the Kansas State University TRIGA Mk. II research nuclear reactor

Advancements in nuclear reactor core modeling and computational capability have encouraged further development of in-core neutron sensors. Micro-Pocket Fission Detectors (MPFDs) have been fabricated and tested previously, but successful testing of these prior detectors was limited to single-node operation with specialized designs. Described in this work is a modular, four-node MPFD array fabricated and tested at Kansas State University (KSU). The four sensor nodes were equally spaced to span the length of the fuel-region of the KSU TRIGA Mk. II research nuclear reactor core. The encapsulated array was filled with argon gas, serving as an ionization medium in the small cavities of the MPFDs. The unified design improved device ruggedness and simplified construction over previous designs. A 0.315-in. (8-mm) penetration in the upper grid plate of the KSU TRIGA Mk. II research nuclear reactor was used to deploy the array between fuel elements in the core. The MPFD array was coupled to an electronic support system which has been developed to support pulse-mode operation. Neutron-induced pulses were observed on all four sensor channels. Stable device operation was confirmed by testing under steady-state reactor conditions. Each of the four sensors in the array responded to changes in reactor power between 10 kWth and full power (750 kWth). Reactor power transients were observed in real-time including positive transients with periods of 5, 15, and 30 s. Manual reactor power oscillations were observed in real-time.

22 GENERAL STUDIES OF NUCLEAR REACTORS↗
DOE OSTI2018

Influence of hot isostatic pressing on the performance of aluminum alloy fabricated by ultrasonic additive manufacturing

Ultrasonic additive manufacturing (UAM) is a solid-state manufacturing technique employing principles of ultrasonic welding coupled with mechanized tape layering to fabricate fully functional parts. However, UAM-fabricated parts often exhibit a reduction in strength when loaded normal to the welding interfaces (Z-direction). Here, the effect of hot isostatic pressing (HIP) on UAM builds of aluminum alloy was explored. Tensile testing and microstructure characterization were conducted; it was established that HIP eliminated the brittle Z-direction fracture and improved the strength and ductility of the Z-direction specimens. HIP eliminated voids and produced recrystallized structure; however, welding interfaces survived the HIP treatment.

36 MATERIALS SCIENCE↗
DOE OSTI2017

Laser Fabrication of Two-Dimensional Rotating-Lattice Single Crystal

A rotating lattice single (RLS) crystal is a unique form of solid, which was fabricated recently as one-dimensional architecture in glass via solid state transformation induced by laser irradiation. In these objects, the lattice rotates gradually and predictably about an axis that lies in the plane of the crystal and is normal to the laser scanning direction. This paper reports on the fabrication of Sb 2 S 3 two-dimensional (2D) RLS crystals on the surface of 16SbI 3 -84Sb 2 S 3 glass, as a model example: individual RLS crystal lines are joined together using "stitching" or "rastering" as two successful protocols. The electron back scattered diffraction mapping and scanning Laue X-ray microdiffraction of the 2D RLS crystals show gradual rotation of lattice comprising of two components, one along the length of each line and another normal to this direction. The former component is determined by the rotation of the first line of the 2D pattern, but the relative contribution of the last component depends on the extent of overlap between two successive lines. By the appropriate choice of initial seed orientation and the direction of scanning, it is possible to control the lattice rotation, and even to reduce it down to 5 for a 50 × 50 μm 2 2D pattern of Sb 2 S 3 crystal.

36 MATERIALS SCIENCE↗
DOE OSTI2021

Fabrication of Ionic Covalent Triazine Framework-Linked Membranes via a Facile Sol–Gel Approach

Covalent triazine framework (CTF)-based membranes have shown unique properties and wide applications in energy-related fields, but there is still no efficient strategy capable of affording CTF membranes functionalized with ionic moieties, which will bring extra merits and application possibilities. In this work, a robust CTF membrane with ionic functionalities was fabricated via a sol–gel approach promoted by a superacid (FSO 3 H). The CTF skeleton was constructed via the trimerization of cyano groups in the monomer, and piperazine moieties were introduced as reactive sites for the formation of ammonium cations coupled with FSO 3 – anions within the backbone. The obtained transparent and red protonated polymeric CTF-based membrane (PP-CTF) exhibited significant absorption at 646 nm in the solid-state ultraviolet–visible diffuse reflectance spectrum. Comparatively, the neutralized deprotonated counterparts turned to yellow color with a significant blueshift absorption to 492 nm. The theoretical calculation demonstrated that PP-CTF and deprotonated polymeric CTF membrane (DP-CTF) were stable with AB-stacking mode, and PP-CTF had a smaller band gap (0.90 eV) than that of DP-CTF (2.17 eV). The significant optical absorption and emission behavior change of PP-CTF and its robust chemical stability endowed it with the capability to act as pH indicators. The synthetic pathway developed in this work and the performance of the resultant ionic membrane opens new opportunities in the aspects of membrane design, fabrication, and application.

36 MATERIALS SCIENCE↗
DOE OSTI2017

Determining the Conduction Band-Edge Potential of Solar-Cell-Relevant Nb{sub 2}O{sub 5} Fabricated by Atomic Layer Deposition

Often key to boosting photovoltages in photo electrochemical and related solar-energy-conversion devices is the preferential slowing of rates of charge recombination especially recombination at semiconductor/solution, semiconductor/polymer, or semiconductor/perovskite interfaces. In devices featuring TiO2 as the semiconducting component, a common approach to slowing recombination is to install an ultrathin metal oxide barrier layer or trap-passivating layer atop the semiconductor, with the needed layer often being formed via atomic layer deposition (ALD). A particularly promising barrier layer material is Nb2O5. Its conduction-band-edge potential Ecg is low enough that charge injection from an adsorbed molecular, polymeric, or solid-state light absorber and into the semiconductor can still occur, but high enough that charge recombination is inhibited. While a few measurements of Ecg have been reported for conventionally synthesized, bulk Nb2O5, none have been described for ALD-fabricated versions. Here, we specifically determine the conduction-band-edge energy of ALD-fabricated Nb2O5 relative to that of TiO2. We find that, while the value for ALD-Nb2O5 is indeed higher than that for TiO2, the difference is less than anticipated based on measurements of conventionally synthesized Nb2O5 and is dependent on the thermal history of the material. The implications of the findings for optimization of competing interfacial rate processes, and therefore photovoltages, are briefly discussed.

Hoffeditz, William L.↗
DOE OSTI2022

Channel Scaling Dependent Photoresponse of Copper-Based Flexible Photodetectors Fabricated Using Laser-Induced Oxidation

Copper (Cu) oxide compounds (Cu x O), which include cupric (CuO) and cuprous (Cu 2 O) oxide, have been recognized as a promising p-channel material with useful photovoltaic properties and superior thermal conductivity. Typically, deposition methods or thermal oxidation can be used to obtain Cu x O. However, these processes are difficult to apply to flexible substrates because plastics have a comparatively low glass transition temperature. Also, additional patterning steps are needed to fabricate applications. In this work, we fabricated a metal–semiconductor–metal photodetector using laser-induced oxidation of thin Cu films under ambient conditions. Raman spectroscopy, scanning electron microscopy–energy-dispersive X-ray spectroscopy, and atomic force microscopy were used to study the composition and morphology of our devices. Moreover, the photoresponse of this device is reported herein. We performed an in-depth analysis of the relationship between the channel size and number of carriers using scanning photocurrent microscopy. The carrier transport behaviors were identified; the photocurrent decreased as the length and width of the channel increased. Furthermore, we verified the suitability of the device as a flexible photodetector using a variety of bending tests. Our in-depth analysis of this Cu-based flexible photodetector could play an important role in understanding the mechanisms of other flexible photovoltaic applications.

36 MATERIALS SCIENCE↗
DOE OSTI2023

Fabrication of Large-Area Metal-on-Carbon Catalytic Condensers for Programmable Catalysis

Catalytic condensers stabilize charge on either side of a high-k dielectric film to modulate the electronic states of a catalytic layer for the electronic control of surface reactions. Here, carbon sputtering provided for fast, large-scale fabrication of metal–carbon catalytic condensers required for industrial application. Carbon films were sputtered on HfO 2 dielectric/p-type Si with different thicknesses (1, 3, 6, and 10 nm), and the enhancement of conductance and capacitance of carbon films was observed upon increasing the carbon thickness following thermal treatment at 400 °C. After Pt deposition on the carbon films, the Pt catalytic condenser exhibited a high capacitance of ∼210 nF/cm 2 that was maintained at a frequency ∼1000 Hz, satisfying the requirement for a dynamic catalyst to implement catalytic resonance. Temperature-programmed desorption of carbon monoxide yielded CO desorption peaks that shifted in temperature with the varying potential applied to the condenser (−6 or +6 V), indicating a shift in the binding energy of carbon monoxide on the Pt condenser surface. A substantial increase in capacitance (∼2000 nF/cm 2 ) of the Pt-on-carbon devices was observed at elevated temperatures of 400 °C that can modulate ∼10% of charge per metal atom when 10 V potential was applied. A large catalytic condenser of 42 cm 2 area Pt/C/HfO 2 /Si exhibited a high capacitance of 9393 nF with a low leakage current/capacitive current ratio (<0.1), demonstrating the practicality and versatility of the facile, large-scale fabrication method for metal–carbon catalytic condensers.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2017

Plasticized Polymer Interlayer for Low-Temperature Fabrication of a High-Quality Silver Nanowire-Based Flexible Transparent and Conductive Film

Silver nanowires (AgNWs) are one of the most promising materials to replace commercially available indium tin oxide in flexible transparent conductive films (TCFs); however, there are still numerous problems originating from poor AgNW junction formation and improper AgNW embedment into transparent substrates. To mitigate these problems, high-temperature processes have been adopted; however, unwanted substrate deformation prevents the use of these processes for the formation of flexible TCFs. In this work, we present a novel poly(methyl methacrylate) interlayer plasticized by dibutyl phthalate for low-temperature fabrication of AgNW-based TCFs, which does not cause any substrate deformation. By exploiting the viscoelastic properties of the plasticized interlayer near the lowered glass-transition temperature, a monolithic junction of AgNWs on the interlayer and embedment of the interconnected AgNWs into the interlayer are achieved in a single-step pressing. The resulting AgNW-TCFs are highly transparent (~92% at a wavelength of 550 nm), highly conductive (<90 Ω/sq), and environmentally and mechanically robust. Therefore, the plasticized interlayer provides a simple and effective route to fabricate high-quality AgNW-based TCFs.

36 MATERIALS SCIENCE↗