Regional assessment of household energy decision-making and technology adoption in the United States
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29 ENERGY PLANNING, POLICY, AND ECONOMY↗
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Will Consumers Really Pay for Green Electricity? Comparing Stated and Revealed Preferences for Residential Programs in the United States
Public support is growing for policy initiatives to spur a transition from a fossil to renewable energy portfolio in the electricity sector. Some utilities in the United States offer programs that allow consumers to voluntarily pay premiums (0.1-7.0 cents/kWh) for electricity from renewable sources. However, it is unclear whether public support translates to paying for green electricity if given the option. Our analysis employs data from two national, longitudinal surveys on energy attitudes and willingness to pay for renewables to investigate whether environmental concerns and stated preferences for renewable energy translate to consumer behavior as measured through ratepayer participation in voluntary utility renewable energy programs known as utility green pricing. We find higher green pricing program participation rates in areas where consumers have stronger feelings about the environmental impacts of energy. Consumers in high-participation areas also have a higher stated willingness to pay for renewable energy, on average, than consumers in low-participation areas. We also find income, homeownership, and home value explain some of the difference between high- and low-participation programs. Further, program participation is lower in areas where utilities charge higher green pricing program premiums. These findings suggest that green power programs - such as utility green pricing - offer a market-based mechanism for consumers to realize their desire to purchase renewable energy. Policymakers may use these results to support further expansion of green power programs in areas where customers currently lack accessible and affordable options to act on their environmental beliefs and concerns.
29 ENERGY PLANNING, POLICY, AND ECONOMY↗
Demonstration of a novel tracer gas method to investigate indoor air mixing and movement
Not Available
Um, Chai Yoon↗
Local ancestry at APOE modifies Alzheimer's disease risk in Caribbean Hispanics
Abstract Introduction Although the relationship between APOE and Alzheimer's disease (AD) is well established in populations of European descent, the effects of APOE and ancestry on AD risk in diverse populations is not well understood. Methods Logistic mixed model regression and survival analyses were performed in a sample of 3067 Caribbean Hispanics and 3028 individuals of European descent to assess the effects of APOE genotype, local ancestry, and genome‐wide ancestry on AD risk and age at onset. Results Among the Caribbean Hispanics, individuals with African‐derived ancestry at APOE had 39% lower odds of AD than individuals with European‐derived APOE , after adjusting for APOE genotype, age, and genome‐wide ancestry. While APOE E2 and E4 effects on AD risk and age at onset were significant in the Caribbean Hispanics, they were substantially attenuated compared with those in European ancestry individuals. Discussion These results suggest that additional genetic variation in the APOE region influences AD risk beyond APOE E2/E3/E4.
Blue, Elizabeth E.↗
Synthesis and characterization of (Bi{sub 0.5}Ba{sub 0.5}) (Fe{sub 0.5}Ti{sub 0.5}) O{sub 3} ceramic
Graphical abstract: Temperature variation of (a) dielectric constant (b) dielectric loss of the sample. - Highlights: • The high values of dielectric permittivity and low value of tangent loss. • It used for microwave applications. • The impedance and dielectric relaxation in the material is non exponential and non Debye-type. • Its ac conductivity obeys Jonscher universal power law. - Abstract: The polycrystalline sample of (Bi{sub 0.5}Ba{sub 0.5}) (Fe{sub 0.5}Ti{sub 0.5}) O{sub 3} (BF–BT) was prepared by a standard mixed oxide method. Analysis of room temperature XRD pattern and Raman/FTIR spectra of the compound does not exhibit any change in its crystal structure of BaTiO{sub 3} on addition of BiFeO{sub 3} in equal ratio. The surface morphology of the gold-plated sintered pellet sample recorded by SEM (scanning electron microscope) exhibits a uniform distribution of grains with less porosity. Detailed studies of nature and quantity of variation of dielectric constant, tangent loss, and polarization with temperature and frequency indicate the existence of ferroelectric phase transition at high-temperature. There is a low-temperature anti-ferromagnetic phase transition below 375 °C in the material. Detailed studies of electrical properties (impedance, modulus, etc.) of the material confirmed a strong correlation between micro-structure and properties.
36 MATERIALS SCIENCE↗
Effect of mechanical alloying synthesis process on the dielectric properties of (Bi{sub 0.5}Na{sub 0.5}){sub 0.94}Ba{sub 0.06}TiO{sub 3} piezoceramics
Highlights: • MA samples show higher dielectric permittivity and Curie temperature. • In MA samples, dielectric loss is almost 27% less than conventional ones. • In MA samples, sintering time and temperature are lower than conventional ones. • In MA samples, particle morphology is more homogeneous conventional ones. • In MA samples, crystallite size is smaller conventional ones. - Abstract: In present work, in order to study the effects of synthesis techniques on dielectric properties, the BNBT lead-free piezoceramics with (Bi{sub 0.5}Na{sub 0.5}){sub 0.94}Ba{sub 0.06}TiO{sub 3} stoichiometry (called as BNBT6) were synthesized by mechanical alloying (MA) and conventional mixed oxides methods. The structural, microstructural, and dielectric properties were carried out by X-ray diffractometer (XRD), scanning electron microscope (SEM), and impedance analyzer LCR meter, respectively. Based on results, the density of MA samples is considerably higher than conventional samples owning to smaller particles size and more uniformity of particle shape of MA samples. Moreover, the dielectric properties of MA samples are comparatively improved in which the dielectric loss of these samples is almost 27% less than conventional ones. Furthermore, MA samples exhibit obviously higher dielectric permittivity and Curie temperature compared to the conventional samples.
36 MATERIALS SCIENCE↗
Ultrathin SnS{sub 2} nanosheets as robust polysulfides immobilizers for high performance lithium-sulfur batteries
Highlights: • Ultrathin SnS{sub 2} nanosheets have large surface area and fast charge transfer properties. • Ultrathin SnS{sub 2} nanosheets can greatly improve the electrochemical properties of S/C composites for Li-S batteries. • Superior electrochemical performance of S/C-SnS{sub 2}-10 composites can be ascribed to the optimized synergistic effects between SnS{sub 2} and porous carbon. - Abstract: Ultrathin SnS{sub 2} nanosheets modified sulfur/carbon (S/C-SnS{sub 2}) composites were synthesized through a facile method by mixing sublimed sulfur, Ketjen Black and ultrathin SnS{sub 2} nanosheets. The ultrathin SnS{sub 2} nanosheets can provide remarkable binding strength, large surface area and fast charge transfer, therefore leading to favorable chemical interaction with polysulfides in Li-S batteries. Accompanied with the synergistic effects between physical confinement of porous carbon and chemical interactions of SnS{sub 2}, S/C-SnS{sub 2} composites with different mass ratio of ultrathin SnS{sub 2} nanosheets and C show much improved electrochemical properties. Among them, S/C-SnS{sub 2} composite with 10 wt% of ultrathin SnS{sub 2} nanosheets and 75 wt% of sulfur maintains superior long term cycling capacities of 800 mAh g{sup −1} at 0.5 C after 300 cycles and 540 mAh g{sup −1} at 2 C after 700 cycles.
36 MATERIALS SCIENCE↗
Enhanced visible-light-driven photocatalytic activities of Bi2Fe4O9/g-C3N4 composite photocatalysts
Highlights: • The novel Bi{sub 2}Fe{sub 4}O{sub 9}/g-C{sub 3}N{sub 4} composite photocatalysts have been designed and prepared. • Combination of Bi{sub 2}Fe{sub 4}O{sub 9} and g-C{sub 3}N{sub 4} could enhance the visible-light-driven photocatalytic degradation for RhB. • The effects of Bi{sub 2}Fe{sub 4}O{sub 9}/g-C{sub 3}N{sub 4} weight ratios on photocatalytic performance in the composite have been discussed. • The Z-scheme photocatalytic mechanism was proposed and discussed in detail. - Abstract: A series of Bi{sub 2}Fe{sub 4}O{sub 9}/g-C{sub 3}N{sub 4} composite photocatalysts are prepared via a facile mixing-calcination method. The crystal structures of composites are investigated by X-ray Diffraction (XRD) and Fourier Transform Infrared Spectroscopy (FT-IR). The Field Emission Scanning Electron Microscope (FE-SEM) in combination with Energy Dispersive X-ray Spectroscopy (EDS) mapping analysis and Transmission Electron Microcopy (TEM) images illustrate the uniform distribution of constituent elements and clear interface between Bi{sub 2}Fe{sub 4}O{sub 9} and g-C{sub 3}N{sub 4} component. The visible-light-driven photocatalytic rates of Rhodamine B over Bi{sub 2}Fe{sub 4}O{sub 9}/g-C{sub 3}N{sub 4} composites increase and then decrease with the increase of g-C{sub 3}N{sub 4} content. The effects of Bi{sub 2}Fe{sub 4}O{sub 9}/g-C{sub 3}N{sub 4} weight ratios on photocatalytic performance are thoroughly discussed. Meanwhile, the active species trapping experiments and the electrochemical impedance spectra as well as the electronic energy-band structure estimation analysis demonstrate that the photocatalytic mechanism for Bi{sub 2}Fe{sub 4}O{sub 9}/g-C{sub 3}N{sub 4} composites is ascribed to the Z-scheme. In addition, the recyclability and stability experiments of the composite are also studied.
36 MATERIALS SCIENCE↗
Impurity-enhanced core valence luminescence via Zn-doping in cesium magnesium chlorides
Scintillators with faster timing capabilities are currently in high demand for use in radiation detection systems in the fields of nuclear and medical physics. The limited number of suitable materials that meet the performance criteria of next generation detection systems presents an opportunity for discovery of new fast scintillator materials. In this work, the effects of doping several ultrafast core-valence luminescent (CVL) scintillators with divalent Zn is explored. Three compounds are investigated – CsMgCl 3 , Cs 2 MgCl 4 , and Cs 3 MgCl 5 – and single crystals of each doped with 5 mol% Zn are grown via the Bridgman method. Additionally, mixing across the full range of concentrations (from 0 % to 100 % Zn) is explored in the Cs 2 Mg 1-x Zn x Cl 4 and Cs 3 Mg 1-x Zn x Cl 5 systems. For low concentrations of Zn, light yields of all three compounds are enhanced (by up to ~60 %) compared to the pure crystals, achieving what we believe to be the brightest known CVL, CsMgCl 3 :Zn 5 % (3400 ± 170 ph/MeV light yield). More importantly, Zn doping does not affect the ultrafast timing properties, with each composition maintaining a single-component decay time around 1–3 ns. A sub-100 ps coincidence time resolution (CTR) is also achieved with CsMgCl 3 :Zn 5 %. The results of this work reveal a new avenue towards obtaining brighter CVL materials, which could open up possibilities for more advanced ultrafast scintillators to be discovered moving forward.
36 MATERIALS SCIENCE↗
A structural and electrochemical study of perfluoropolyether-poly(ethylene oxide) solid polymer electrolytes
Solid polymer electrolytes offer attractive safety, processability, and interfacial adhesion for enabling high–energy solid-state lithium batteries, but they are often limited by narrow oxidative stability windows and low lithium-ion transference numbers. In an attempt to broaden the electrochemical stability window and increase lithium-ion transference number of poly(ethylene oxide) (PEO)-based solid polymer electrolytes, we produce an optically clear, crosslinked membrane of PEO and perfluoropolyether (PFPE) using a mixed solvent method and subsequently infuse the membrane with a lithium salt. Structural and thermal analyses reveal nanoscale phase separation between fluorocarbon and hydrocarbon domains with characteristic spacings of 7–8 nm and an elevated glass transition for the hydrocarbon phase. Consistent with this, PFPE-containing membranes exhibit substantially lower ionic conductivity than PEO analogs (dry and plasticized). The transference number and electrochemical stability are similar to pure PEO. These results demonstrate that fluorination implemented as segregated nanoscale domains does not deliver the anticipated transport or stability benefits; instead, phase separation increases tortuosity and suppresses hydrocarbon-phase dynamics. The work underscores the importance of fluorine placement and morphology control, guiding the design of partially fluorinated solid polymer electrolytes toward architectures that avoid detrimental nanoscale phase separation.
Carden, Peyton [ORNL] (ORCID:0000000162296538)↗
Giant Thermoelectric Power Factor Anisotropy in PtSb 1.4 Sn 0.6
In this work, we report on the giant anisotropy found in the thermoelectric power factor (S 2 σ) of marcasite structure-type PtSb 1.4 Sn 0.6 single crystal. PtSb 1.4 Sn 0.6 , synthesized using an ambient pressure flux growth method upon mixing Sb and Sn on the same atomic site, is a new phase different from both PtSb 2 and PtSn 2 , which crystallize in the cubic Pa$\bar{3}$ pyrite and Fm$\bar{3}$m fluorite unit cell symmetry, respectively. The large difference in S 2 σ for heat flow applied along different principal directions of the orthorhombic unit cell stems mostly from anisotropic Seebeck coefficients.
36 MATERIALS SCIENCE↗
Role of Vibrational Dynamics on Excited-State Electronic Coherence in a Binuclear Platinum Complex
Long-lived quantum coherence between excited electronic states can enable highly efficient energy and charge transport processes in chemical systems. Recent pump-probe experiments on binuclear platinum complexes identified persistent, periodic beating of transient absorption anisotropy signals, indicating long excited-state coherence lifetimes. Our previous simulations of the electronic dynamics of these complexes indicate that coherence lifetimes are sensitive to the balance between competitive electronic couplings. The complexes with shorter Pt-Pt distances underwent no appreciable dephasing in the limit of static nuclei, motivating the inclusion of nuclear motion into our simulations. The tert-butyl-substituted complex is studied in this work using the Ehrenfest method for mixed quantum classical dynamics to investigate the role of vibrational dynamics on a complex shown to support coherence lifetimes. Results indicate that the inclusion of excited-state vibrations drives a rapid collapse of the two-state coherence prior to the experimentally determined intersystem crossing. This further suggests singlet excited-state coherences may not be prerequisites for long-lived triplet coherences.
Radler, Joseph J.↗
Flux crystal growth of uranium(v) containing oxyfluoride perovskites
The novel phases Rb 4 NaU 3 O 12-x F x (1), K 4 NaU 3 O 12-x F x (2), and Rb 2.1 K 1.9 KU 3 O 12-x F x (3) were synthesized by molten flux methods using mixed alkali fluoride melts. The oxyfluorides crystallize in the cubic space group Im[3 with combining macron]m with a lattice parameters of 8.7472(2) Å, 8.6264(2) Å, and 8.8390(3) Å, respectively. All three structures crystallize in a cubic perovskite structure, ABO 3 (A 4 BB' 3 O 12 ), where the A site is fully occupied by an alkali cation, and the B site is shared by the remaining smaller alkali cation and uranium in an ordered fashion such that the alkali cation on the B site is surrounded by square uranyl bipyramids. The structures were characterized by single crystal X-ray diffraction, energy dispersive spectroscopy, X-ray absorption near edge structure spectroscopy, X-ray photoelectron spectroscopy, magnetic susceptibility measurements, DFT calculations, thermogravimetric analysis, and UV-vis spectroscopy, all of which support the presence of U(V) in the three new materials.
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
Effect of composition on electrical properties of lead-free Bi{sub 0.5}(Na{sub 0.80}K{sub 0.20}){sub 0.5}TiO{sub 3}-(Ba{sub 0.98}Nd{sub 0.02})TiO{sub 3} piezoelectric ceramics
Lead-free piezoelectric ceramics with the composition of (1-x)Bi{sub 0.5}(Na{sub 0.80}K{sub 0.20}){sub 0.5}TiO{sub 3}-x(Ba{sub 0.98}Nd{sub 0.02})TiO{sub 3} or (1-x) BNKT-xBNdT (with x = 0-0.20 mol fraction) have been synthesized by a conventional mixed-oxide method. The compositional dependence of phase structure and electrical properties of the ceramics were systemically studied. The optimum sintering temperature of all BNKT-BNdT ceramics was found to be 1125 Degree-Sign C. X-ray diffraction pattern suggested that BNdT effectively diffused into BNKT lattice during sintering to form a solid solution with a perovskite structure. Scanning electron micrographs showed a slight reduction of grain size when BNdT was added. It was found that BNKT-0.10BNdT ceramic exhibited optimum electrical properties ({epsilon}{sub r} = 1716, tan{delta} = 0.0701, T{sub c} = 327 Degree-Sign C, and d{sub 33} = 211 pC/N), suggesting that this composition has a potential to be one of a promising lead-free piezoelectric candidate for dielectric and piezoelectric applications.
36 MATERIALS SCIENCE↗
Structural and dielectric properties of Gd doped bismuth ferrite-lead titanate
0.5BiGd{sub x}Fe{sub 1−x}O{sub 3}−0.5PbTiO{sub 3} with x=0.05, 0.10, 0.15, 0.20 composite was prepared by mixed oxide method. Structural characterization was performed by X-ray diffraction and studied that the materials show tetragonal structure at room temperature for all concentration of Gd. Studies of dielectric properties (ε{sub r} and tanδ) of the above compound at different frequencies in a wide range of temperature (25°-500°C) with an impedance analyser revealed that the dielectric constant increases with increase in Gd concentration as well temperature and the compound do not have any dielectric anomaly in the studied frequency and temperature range.
36 MATERIALS SCIENCE↗
Dynamics in the quantum/classical limit based on selective use of the quantum potential
A classical limit of quantum dynamics can be defined by compensation of the quantum potential in the time-dependent Schrödinger equation. The quantum potential is a non-local quantity, defined in the trajectory-based form of the Schrödinger equation, due to Madelung, de Broglie, and Bohm, which formally generates the quantum-mechanical features in dynamics. Selective inclusion of the quantum potential for the degrees of freedom deemed “quantum,” defines a hybrid quantum/classical dynamics, appropriate for molecular systems comprised of light and heavy nuclei. The wavefunction is associated with all of the nuclei, and the Ehrenfest, or mean-field, averaging of the force acting on the classical degrees of freedom, typical of the mixed quantum/classical methods, is avoided. The hybrid approach is used to examine evolution of light/heavy systems in the harmonic and double-well potentials, using conventional grid-based and approximate quantum-trajectory time propagation. The approximate quantum force is defined on spatial domains, which removes unphysical coupling of the wavefunction fragments corresponding to distinct classical channels or configurations. The quantum potential, associated with the quantum particle, generates forces acting on both quantum and classical particles to describe the backreaction.
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
Reversal of particle flux in collisional-finite beta tokamak discharges
The mixed gradient method [Zhong et al. Phys. Rev. Lett. 111, 265001 (2013)] is adopted and effects of collisions and finite beta are included in the Weiland 9-equation fluid model. The particle flux and particle pinch, obtained using the Weiland anomalous transport fluid model, are compared with Tore Supra experimental results. Particle transport is also studied using predictive simulation data for an experimental advanced superconducting tokamak discharge in which neutral beam heating is utilized. The effects of collisions on particle transport are studied by turning collisions on and off in the Weiland model. It is found that the particle pinch region is related to the mode structure. The particle pinch region coincides with the region where the strong ballooning modes are present due to large gradients. The general properties of the fluid model are examined by finding regions where collisions can enhance the particle pinch.
70 PLASMA PHYSICS AND FUSION TECHNOLOGY↗