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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 19 records
All sourcesNASA NTRSDOE OSTI
DOE OSTI2022

Transparent, High‐Charge Capacity Metal Mesh Electrode for Reversible Metal Electrodeposition Dynamic Windows with Dark‐State Transmission <0.1%

Abstract Dynamic windows allow user control over light and heat flow to save energy and maximize comfort. Reversible metal electrodeposition (RME) dynamic windows can uniquely tint to a color‐neutral privacy state (0.1% visible light transmission). The design parameters of transparent metal mesh counter electrodes for high‐contrast RME dynamic windows: high transparency, charge capacity and surface area with low haze, sheet resistance and cost are discussed, concluding that woven metal meshes meet these design parameters. Electroplated current is measured on an indium tin oxide electrode and two meshes with different wire spacings, showing the meshes’ cylindrical geometry enable them to draw more current per square area. The mesh material composition is analyzed to ensure cycling durability in a CuBi electrolyte by developing a transparent mesh with an inert core (stainless steel, SS), a thin Au coating, and a high charge‐capacity (1.5 C cm −2 ) CuBi outer coating. The study demonstrates that the films maintain a consistent Cu:Bi ratio and optical properties after 250 privacy cycles or 1500 cycles to 10% transmission, showing that the Cu and Bi coating is effective in keeping the films from becoming Cu rich with cycling. Finally, a 100 cm 2 device with excellent uniformity and color neutrality is demonstrated.

Yeang, Andrew L.↗
DOE OSTI2017

Stable Low-Current Electrodeposition of α-MnO 2 on Superaligned Electrospun Carbon Nanofibers for High-Performance Energy Storage

Metal oxide/carbonaceous nanomaterials are promising candidates for energy-storage applications. Yet, inhomogeneous mass and charge transfer across the electrode/electrolyte interface due to unstable metal oxide/carbonaceous nanomaterial synthesis limit their performance in supercapacitors. Here, it is shown that the above problems can be mitigated through stable low-current electrodeposition of MnO 2 on superaligned electrospun carbon nanofibers (ECNFs). The key to this method is coupling a self-designed four steel poles collector for aligned ECNFs and a constant lowcurrent (40 μA) electrodeposition technique to form a uniform Na + -induced α-MnO 2 film which proceeds by a time-dependent growth mechanism involving cluster-“kebab” structures and ending with a compact, uniform MnO 2 film for high-performance energy storage.

36 MATERIALS SCIENCE↗
DOE OSTI2017

Photoelectrochemical Properties and Stability of Nanoporous p-Type LaFeO 3 Photoelectrodes Prepared by Electrodeposition

LaFeO 3 is a p-type oxide that has an ideal bandgap and band edge positions for overall solar water splitting. This study reports an electrochemical synthesis method to produce LaFeO 3 as a high surface area, nanoporous photocathode. The resulting electrode generated a photocurrent density of 0.1 mA/cm 2 at a potential as positive as 0.73 V vs. RHE for photoelectrochemical oxygen reduction with a photocurrent onset potential very close to its flatband potential of 1.45 V vs. RHE. Furthermore, without a protection layer it showed a stable photocurrent generation with no sign of photocorrosion. Due to the poor catalytic nature of the LaFeO 3 surface for water reduction, photocurrent obtained for water reduction was not substantial. Furthermore, its photostability and its ability to achieve a photovoltage for water reduction greater than 1.2 V encourage further studies on doping to enhance electron-hole separation as well as interfacing appropriate hydrogen evolution catalysts.

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

Effect of post-deposition heat treatment on electrodeposited NiCoCrAlY coatings

An electrolytic process was utilised to fabricate NiCoCrAlY coatings, involving deposition of a composite coating consisting of the (Ni,Co) matrix and CrAlY particles, followed by a diffusion heat treatment to convert the composite coating to the desired NiCoCrAlY microstructure. This study focused on the effects of the post-deposition heat-treating conditions (temperature and atmosphere) on the final coating microstructure and composition. The (Ni,Co)–CrAlY composite coatings were heat-treated for 2 h at 1000, 1100 and 1200°C in vacuum and Ar, respectively. Phase constituents and concentrations of the major elements in the coating after heat treatment were examined. Vacuum heat treatment at temperatures ≥1100°C resulted in a significant decrease in Cr content at the coating surface due to Cr evaporation. Heat treatment at 1200°C also caused outward diffusion of Ti from the substrate alloy to the coating layer.

Zhang, L. Z.↗
DOE OSTI2017

Effect of indium concentration on electrochemical properties of electrode-electrolyte interface of CuIn{sub 1-x}Ga{sub x}Se{sub 2} prepared by electrodeposition

Highlights: • CIGS thin film was electrodeposited on a molybdenum (Mo) electrode from a non-pH buffered chloride-based electrolyte. • The electrodeposited time and the concentration of In{sup 3+} control the growth of CIGS thin film prepared in this electrodeposition system. • The kinetic of electrodeposition system was gradually dominated by the diffusion process with the electrodeposition time. - Abstract: In this study, the electrochemical impedance spectroscopy (EIS) technique was used to investigate the electrochemical behavior of the interface between the Mo electrode and the Cu-In-Ga-Se electrolyte. In this electrodeposition system, the main parameters include (1) various deposition times, and (2) the effect of In{sup 3+} concentration on the diffusion processes, electrical double layer, charge transfer resistance, and Warburg impedance. Experimental results revealed that the electrochemical kinetic behavior of CIGS thin film is strongly influenced by (1) the electrical double layer existing between the substrate, and (2) the electrolyte with different concentrations of In{sup 3+}. With an increase in the electrodeposition time, the kinetic behavior of this electrodeposition system was gradually dominated by the diffusion process rather than charge transfer process.

36 MATERIALS SCIENCE↗