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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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11 records
All sourcesNASA NTRSDOE OSTI
DOE OSTI2024

Förster Resonance Energy Transfer and Enhanced Emission in Cs 4 PbBr 6 Nanocrystals Encapsulated in Silicon Nano-Sheets for Perovskite Light Emitting Diode Applications

Encapsulating Cs 4 PbBr 6 quantum dots in silicon nano-sheets not only stabilizes the halide perovskite, but also takes advantage of the nano-sheet for a compatible integration with the traditional silicon semiconductor. Here, we report the preparation of un-passivated Cs 4 PbBr 6 ellipsoidal nanocrystals and pseudo-spherical quantum dots in silicon nano-sheets and their enhanced photoluminescence (PL). For a sample with low concentrations of quantum dots in silicon nano-sheets, the emission from Cs 4 PbBr 6 pseudo-spherical quantum dots is quenched and is dominated with Pb 2+ ion/silicene emission, which is very stable during the whole measurement period. For a high concentration of Cs 4 PbBr 6 ellipsoidal nanocrystals in silicon nano-sheets, we have observed Förster resonance energy transfer with up to 87% efficiency through the oscillation of two PL peaks when UV excitation switches between on and off, using recorded video and PL lifetime measurements. In an area of a non-uniform sample containing both ellipsoidal nanocrystals and pseudo-spherical quantum dots, where Pb 2+ ion/silicene emissions, broadband emissions from quantum dots, and bandgap edge emissions (515 nm) appear, the 515 nm peak intensity increases five times over 30 min of UV excitation, probably due to a photon recycling effect. This irradiated sample has been stable for one year of ambient storage. Cs 4 PbBr 6 quantum dots encapsulated in silicon nano-sheets can lead to applications of halide perovskite light emitting diodes (PeLEDs) and integration with traditional semiconductor materials.

36 MATERIALS SCIENCE↗
DOE OSTI2020

Self-supported MoO 2 /MoS 2 nano-sheets embedded in a carbon cloth as a binder-free substrate for high-energy lithium–sulfur batteries

As one of the most prospective candidates for next-generation rechargeable batteries, lithium-sulfur (Li-S) batteries currently still encounter great challenges associated with the low conductivity, severe shuttle effects, and sluggish redox kinetics. Herein, a self-supported sulfur host is fabricated by an in-situ growth of MoO 2 /MoS 2 nano-sheets on a carbon cloth (CC). First, carbon cloth serves as a good template for the morphology-controlled synthesis of nanostructured materials, which not only alleviates the agglomeration of MoO2/MoS2, but also enhances the flexibility and mechanical strengthen of the hybrid architecture as a free-standing host. Second, the polysulfide-trapping ability can be greatly enhanced by both physical and chemical adsorption from the MoO 2 /MoS 2 -anchored carbon cloth. Moreover, the partially sulfurized MoO 2 /MoS 2 nano-sheets integrate the benefits of conductive MoO 2 and sulfiphilic MoS 2 , thus facilitating fast charge transfer and redox kinetics of polysulfide conversion. As a result, these attributes enable the host to hold a high sulfur loading (up to 7.6 mg cm -2 ), which exceeds most of the reported carbon cloth-related cathode work in the literature. Furthermore, the Li-S cells can achieve a high peak capacity of 1350 mA h g -1 , excellent rate capability (C/20 - 2C rate), impressive areal capacity (up to 6.3 mA h cm -2 ), and a high capacity retention of 85% after 100 cycles.

25 ENERGY STORAGE↗
DOE OSTI2018

Improvement of Li-S battery electrochemical performance with 2D TiS 2 additive

As a multifunctional cathode additive, TiS 2 has been used in Li-S batteries to promote sulfur utilization and improve cell cycle life. The improvement of Li-S cell electrochemical performance in the presence of TiS 2 has been attributed to the ability of TiS 2 in adsorbing polysulfide. To maximize the interaction between polysulfides and TiS 2 , the 2-dimensional (2D) TiS 2 nano-sheets with highly exposed TiS 2 surface area has been successfully synthesized by a two-step sonication synthetic procedure. The 2D TiS 2 particles are micron size in the basal plane direction and are nano-sized along the c-axis direction. 2D TiS 2 nano-sheets may adsorb polysulfides more effectively than the raw TiS 2 powder. Li-S cells with 2D TiS 2 nano-sheets additive exhibit better discharge rate capability and significantly reduced capacity-fading after a long term cell cycling. Here, this improvement can be partially attributed to the uniform distribution of 2D TiS 2 nano-sheets particles within the sulfur cathode matrix, which induces more uniform sulfur and lithium sulfide deposition during the cell charge and discharge.

2D TiS2 nano-sheets↗
DOE OSTI2018

Photocatalytic activity of 3D flower-like MoS2 hemispheres

Highlights: • The ultrathin MoS{sub 2} nano-sheet assembled 3D flower-like MoS{sub 2} hemispheres were prepared via hydrothermal method. • The bandgap of as-synthesized MoS{sub 2} is about 2.05 eV, resulting in a broad absorption in the visible range. • The photocatalyst of MoS{sub 2} present the optimal catalytic property under mild acidity. - Abstract: The novel 3D flower-like MoS{sub 2} hemispheres assembled by ultrathin MoS{sub 2} nano-sheet petals have been successfully prepared via a facile hydrothermal method using CTAB as surfactant. The crystal structure and morphology of the as-synthesized MoS{sub 2} samples were characterized by X-ray diffraction (XRD), Fourier transform infrared spectra (FTIR), Raman spectra and scanning electron microscopy (SEM). Moreover the microstructure and the optical properties of MoS{sub 2} samples were also measured by transmission electron microscopy (TEM) and the UV–vis diffuse reflectance spectra (DRS). The photocatalytic performance of the flower-like MoS{sub 2} hemispheres were evaluated through the degradation of Rhodamine (RhB) and methylene blue (MB) solutions, and the stabilities of photo-catalysts were also studied through the three cycles of experiments. The effects on photo-catalytic performance from the initial pH values (3–9) of RhB and MB solutions were also investigated, indicating the samples present the optimal catalytic property at pH = 5.

36 MATERIALS SCIENCE↗
DOE OSTI2014

Aqueous phase deposition of dense tin oxide films with nano-structured surfaces

Dense tin oxide films were successfully fabricated in an aqueous solution. The pH of the solutions was controlled to pH 1.3 by addition of HCl. Precise control of solution condition and crystal growth allowed us to obtain dense tin oxide films. Concave–convex surface of fluorine-doped tin oxide (FTO) substrates was entirely-covered with the continuous films. The films were about 65 nm in thickness and had nano-structured surfaces. Morphology of the films was strikingly different from our previous reported nano-sheet assembled structures. The films were not removed from the substrates by strong water flow or air blow to show strong adhesion strength. The aqueous solution process can be applied to surface coating of various materials such as nano/micro-structured surfaces, particles, fibers, polymers, metals or biomaterials. - Graphical abstract: Dense tin oxide films of 65 nm were successfully fabricated in an aqueous solution. They had nano-structured surfaces. Concave-convex substrates were entirely-covered with the continuous films. - Highlights: • Dense tin oxide films of 65 nm were successfully fabricated in an aqueous solution. • They had nano-structured surfaces. • Concave–convex substrates were entirely-covered with the continuous films.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2011

Hierarchically Porous Graphene as a Lithium-Air Battery Electrode

Functionalized graphene sheets (FGS) are successfully utilized as a novel air electrode for Li-O2 batteries. An extremely high capacity of 15,000 mAh/g was achieved by using the as-prepared graphene air electrode at a current density of 0.1 mA/cm2 in the pure oxygen environment. Although there is no pore in the two-dimensional FGS the as-prepared graphene air electrode consists of randomly arranged graphene nano-sheets which automatically form tunnels with different sizes. The large tunnels work as highways for the oxygen to quickly flow into the air electrode while the small pore-like tunnels can be considered as the numerous exits where the discharge products are accumulated. Combined with an appropriate electrolyte, the ideal discharge product Li2O2 is obtained without any carbonates byproducts in this system. Even when operated in ambient environment with a relative humidity of ~20% the specific capacity delivered from the pouch type cell achieves more than 5000 mAh/g making the graphene-based air electrode extremely attractive in the energy storage applications.

25 ENERGY STORAGE↗
DOE OSTI2014

NanoSIMS, TEM, and XANES studies of a unique presolar supernova graphite grain

We report on isotopic and microstructural investigations of a unique presolar supernova (SN) graphite grain, referred to as G6, isolated from the Orgueil CI chondrite. G6 contains complex heterogeneities in its isotopic composition and in its microstructure. Nano-scale secondary ion mass spectrometer isotope images of ultramicrotome sections reveal heterogeneities in its C, N, and O isotopic compositions, including anomalous shell-like structures. Transmission electron microscope studies reveal a nanocrystalline core surrounded by a turbostratic graphite mantle, the first reported nanocrystalline core from a low-density SN graphite grain. Electron diffraction analysis shows that the nanocrystalline core consists of randomly oriented 2-4 nm graphene particles, similar to those in cores of high-density (HD) presolar graphite grains from asymptotic giant branch stars. G6's core also exhibits evidence for planar stacking of these graphene nano-sheets with a domain size up to 4.5 nm, which was unobserved in the nanocrystalline cores of HD graphite grains. We also report on X-ray absorption near-edge structure measurements of G6. The complex isotopic- and micro-structure of G6 provides evidence for mixing and/or granular transport in SN ejecta.

79 ASTRONOMY AND ASTROPHYSICS↗
NASA NTRS2017

Graphene Oxide Reduces the Hydrolytic Degradation in Polyamide-11

Graphene oxide (GO) was incorporated into polyamide-11 (PA11) via in-situ polymerization. The GO-PA11 nano-composite had elevated resistance to hydrolytic degradation. At a loading of 1 mg/g, GO to PA11, the accelerated aging equilibrium molecular weight of GO-PA11 was higher (33 and 34 kg/mol at 100 and 120 °C, respectively) compared to neat PA11 (23 and 24 kg/mol at 100 and 120 °C, respectively). Neat PA11 had hydrolysis rate constants (kH) of 2.8 and 12 ( × 10(exp -2) day(exp -1)) when aged at 100 and 120 °C, respectively, and re-polymerization rate constants (kP) of 5.0 and 23 ( × 10(exp -5) day(exp -1)), respectively. The higher equilibrium molecular weight for GO-PA11 loaded at 1 mg/g was the result of a decreased kH, 1.8 and 4.5 ( × 10(exp -2) day(exp -1)), and an increased kP, 10 and 17 ( × 10(exp -5) day(exp -1)) compared with neat PA11 at 100 and 120 °C, respectively. The decreased rate of degradation and resulting 40% increased equilibrium molecular weight of GO-PA11 was attributed to the highly asymmetric planar GO nano-sheets that inhibited the molecular mobility of water and the polymer chain. The crystallinity of the polymer matrix was similarly affected by a reduction in chain mobility during annealing due to the GO nanoparticles' chemistry and highly asymmetric nano-planar sheet structure.

Samuel J A Hocker↗
DOE OSTI2011

Surface Tension

Surface tension in the kitchen sink. At Berkeley Lab's Molecular Foundry, scientists study surface tension to understand how molecules "self-assemble". The coin trick in the video uses the re-arrangement of water molecules to seemingly create order out of disorder. The same principle can be used to create order in otherwise hard-to-handle nano materials. Scientists can then transfer these ordered materials onto surfaces by dipping them through the air-water interface, or (as we've recently shown) squeeze them so that they collapse into the water as two-molecule-thick nano sheets. http://newscenter.lbl.gov/feature-stories/2011/10/17/shaken-not-stirred/

74 ATOMIC AND MOLECULAR PHYSICS↗