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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 361 records · Page 20
All sourcesNASA NTRSDOE OSTI
DOE OSTI2014

Hydrogen Abstraction/Acetylene Addition Revealed

For almost half a century, polycyclic aromatic hydrocarbons (PAHs) have been proposed to play a key role in the astrochemical evolution of the interstellar medium (ISM) and in the chemistry of combustion systems. However, even the most fundamental reaction mechanism assumed to lead to the simplest PAH naphthalene—the hydrogen abstraction–acetylene addition (HACA) mechanism—has eluded experimental observation. Here, by probing the phenylacetylene (C 8 H 6 ) intermediate together with naphthalene (C 10 H 8 ) under combustion-like conditions by photo-ionization mass spectrometry, the very first direct experimental evidence for the validity of the HACA mechanism which so far had only been speculated theoretically is reported.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2019

Inhibition of Polyimide Photodegradation by Incorporation of Titanate Nanotubes into a Composite

The effect of UV light exposure on the properties of hexafluoroisopropylidene-diphthalic anhydride–oxydianiline (6FDA–ODA) polyimide (PI) and polyimide–titanate nanotube (TiNT/PI) composites has been studied using Raman spectroscopy, optical microscopy, nanoidentation and TEM. The degree of polymer photodegradation was estimated by measuring the change in affinity to a positively charged dye (methylene blue, MB). The mechanism of photoassisted transformations in polyimides usually involves scission of polymer chains accompanied by appearance of active radicals, which undergo further rapid transformations to more stable phenol, amine, and carboxylic functional groups. The accumulation of these groups can increase the degree of adsorption of charged dyes in the photodegraded polymer. It was found that neat PI showed a significantly increased capacity to adsorb MB after irradiation with UV, reaching a plateau after 1 h. In contrast, TiNT/PI composite demonstrated a much slower rise in concentration of adsorbed MB even after 4 h of UV exposure. Raman spectra indicated cleavage of C=O and C–F bonds in PI while only the C–F bond was damaged in TiNT/PI. Shorter cracks (≈ 40 µm long) appeared in TiNT/PI composites whereas macro cracks (> 100 µm) were visible in neat PI after 3 h of UV exposure. Brittleness was studied by comparing plasticity index which varied from 0 to 1 (0 corresponding to the most brittle material and 1 the most ductile one). Plasticity index reduced by 51% and 2% for PI and TiNT/PI, respectively after 3 h UV irradiation, indicating that TiNT can protect underlying PI from further damage. The hardness of neat PI decreased whereas, for TiNT/PI, it increased under UV, suggesting crosslinking of broken polymer chains with nanotubes. Graphical Abstract: Photodegradation of a titanate nanotubes/polyimide composite can lead to cross-linking of broken polymer chains by nanostructured material, resulting in increased hardness. .

36 MATERIALS SCIENCE↗
DOE OSTI2013

Crystal structure of the CueO mutants at Glu506, the key amino acid located in the proton transfer pathway for dioxygen reduction

Highlights: •Proton transfer pathway in the four-electron reduction of dioxygen by CueO. •Compensatory hydrogen bond network comprised of only water molecules in the Glu to Ala mutant. •Shutdown of the hydrogen bond network by the Glu to Ile mutation. •X-ray crystal structures of the CueO mutants with the modified proton transport pathway. -- Abstract: Glu506 involved in the hydrogen bond network leading from solvent waters to the trinuclear copper center in a multicopper oxidase, CueO plays a crucial role to transport protons in the four-electron reduction of dioxygen to water. We performed X-ray crystal structure analyses of the Glu506Ala and Glu506Ile mutants, showing the formation of a compensatory proton transport pathway with only water molecules and a disruption of the hydrogen bond network due to the bulky side chain, respectively. We discuss the efficiency of proton transport through the hydrogen bond network based on the present results and our previous modification of the proton transport pathway by the Glu506 to Gln mutation, which have allowed us to trap and characterize the reaction intermediates.

60 APPLIED LIFE SCIENCES↗
DOE OSTI2013

A series of novel gallium and indium borates constructed from [B{sub 5}O{sub 8}(OH){sub 2}]{sup 3-} clusters and metal complex linkers

Four novel gallium and indium borates, [M(en){sub 2}][B{sub 5}O{sub 8}(OH){sub 2}]{center_dot}H{sub 2}O (M=Ga (1), In (2); en=ethylenediamine), [In(dap){sub 2}][B{sub 5}O{sub 8}(OH){sub 2}]{center_dot}H{sub 2}O (3, dap=1,2-diaminopropane), [In(dien)][B{sub 5}O{sub 8}(OH){sub 2}] (4, dien=diethylenetriamine), have been hydrothermally synthesized and characterized by IR spectra, elemental analyses, powder X-ray diffraction, single crystal X-ray diffraction, and thermogravimetric analyses. Compounds 1, 2 and 3 are isostructural and consist of one-dimensional (1-D) chains built up from [B{sub 5}O{sub 8}(OH){sub 2}]{sup 3-} clusters and Ga-/In-complex linkers. The structure of compound 4 features a 1-D chain containing 8-member rings built by [B{sub 5}O{sub 8}(OH){sub 2}]{sup 3-} clusters and {l_brace}In{sub 2}O{sub 4}{r_brace} dimeric cluster linkers which have never observed in the structural chemistry of borates to date. The H-bonding interactions between adjacent chains lead to 3-D supramolecular network structure. - Graphical abstract: Four novel gallium and indium borates with one-dimensional structures built by B{sub 5}O{sub 8}(OH){sub 2}{sup 3+} clusters and metal complex linkers have been successfully synthesized under hydrothermal conditions. Highlights: Black-Right-Pointing-Pointer Four new Ga/In borates have been hydrothermally made. Black-Right-Pointing-Pointer The helical/ribbon-like chains made of B{sub 5}O{sub 8}(OH){sub 2}{sup 3+} clusters and Ga-/In-complex linkers. Black-Right-Pointing-Pointer The chains form novel 3-D supermolecule framework via H-bonds.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2015

A cesium copper vanadyl-diphosphate: Synthesis, crystal structure and physical properties

A non-centrosymmetric orthorhombic diphosphate, Cs{sub 2}Cu{sub 1+x}(VO){sub 2−x}(P{sub 2}O{sub 7}){sub 2} (x=0.1) with a=13.7364(2) Å, b=9.2666(2) Å, c=11.5678(2) Å, Z=4, has been isolated. Its 3D framework is built from Cu atoms in square pyramidal and square planar coordination, VO{sub 5} tetragonal pyramids and P{sub 2}O{sub 7} diphosphate groups, sharing vertices. Large channels are fulfilled by cesium atoms. The ESR study reveals a similarity in behaviour of two paramagnetic (Cu and V) subsystems. The temperature dependences of the ESR linewidth and static magnetic susceptibility data present evidences for a cluster type magnetic ordering in the title compound at T⁎=22 K. The weakness of the relevant anomalies reflects presumably obvious Cu{sup 2+} ions and (VO){sup 2+} units disorder in the system. It is supposed that the charge and geometry of the framework are controlled by the Cu{sup 2+}/(VO){sup 2+} ratio; its variation may lead to a design of new materials. - Graphical abstract: A microporous 3D anionic framework of the first copper vanadium-diphosphate Cs{sub 2}Cu{sub 1.1}(VO){sub 1.9}(P{sub 2}O{sub 7}){sub 2}. The similarity in behaviour of Cu and V paramagnetic subsystems revealed by ESR study. - Highlights: • The first copper vanadium-diphosphate Cs{sub 2}Cu{sub 1.1}(VO){sub 1.9}(P{sub 2}O{sub 7}){sub 2} is reported. • A 3D anionic framework is characterized by disorder in distribution of Cu and V atoms. • Structural relations with topologically similar compounds are discussed. • The similarity in behaviour of Cu and V paramagnetic subsystems has been revealed.

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

Effect of Y/Ti atomic ratio on microstructure of oxide dispersion strengthened alloys

Highlights: • Controlling nano oxide distributions in ODS alloys by tuning Y/Ti ratio. • Advanced characterization techniques have been conducted to comprehensively study the various nano oxides. • A recipe with a Y/Ti ratio of 0.4 was found and the intrinsic oxide formation mechanism was explained. - Abstract: Oxide dispersion strengthened (ODS) alloys are the leading candidate materials for advanced fission and fusion reactor components because of their excellent high temperature creep strength and radiation tolerance. The promising performance of ODS alloys relies on a high-density population of nano oxides. Here, four 9Cr-ODS alloys with varying initial Y/Ti atomic ratio were processed using a combined route of mechanical alloying (MA) and hot isostatic pressing (HIP). Microstructural characterizations of the consolidated alloys were examined by advanced transmission electron microscopy (TEM). Great differences in oxide distribution behavior were observed. 9Cr-ODS alloy with a Y/Ti ratio of 0.4 presented the finest and the highest number density of nano oxides among the four alloys. The effects of Y/Ti ratio on oxide formation were explored, and the precipitated mechanisms of the nano oxides were interpreted.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Development of nano-Y2O3 dispersed Zr alloys synthesized by mechanical alloying and consolidated by pulse plasma sintering

Highlights: • Zr-Fe-Cr-Cu-Ti-1.0wt% nano-Y{sub 2}O{sub 3} dispersed alloys are fabricated by mechanical alloying and pulse plasma sintering. • These alloys record extremely high compressive strength, Young’s modulus, and hardness. • These mechanical properties are superior as compared to other commercially available Zr based alloys. • Dispersion of nanometric FeZr{sub 2}, Y{sub 2}Ti{sub 2}O{sub 7}, Fe{sub 2}Ti, ZrCu, Cr{sub 2}Zr, Y{sub 2}O{sub 3} leads to grain boundary pinning at elevated temperature. - Abstract: In this paper, Zr alloys are synthesized with nominal compositions: 50Zr-30Fe-10Cr-5Cu-5Ti (alloy A), and 49Zr-30Fe-10Cr-5Cu-5Ti-1Y{sub 2}O{sub 3} (alloy B), 45Zr-30Fe-10Cr-10Cu-5Ti (alloy C), 44Zr-30Fe-10Cr-10Cu-5Ti-1Y{sub 2}O{sub 3} (alloy D) (all in wt%) by mechanical alloying and consolidated by pulse plasma sintering at 1173 K (900 °C), 1223 K (950 °C) and 1273 K (1000 °C) using 75 MPa uniaxial pressure applied for 5 min and 70 kA pulsed current at 3 Hz pulse frequency. The microstructure and phase evolution during mechanical alloying and sintering has been characterized by X-ray diffraction (XRD), scanning and transmission electron microscopy (SEM & TEM) and energy dispersive spectroscopy (EDS). Mechanical properties i.e. hardness and compressive strength were determined by using nano-indentation unit and universal testing machine. The produced alloys recorded very high levels of compressive strength (1359–2456 MPa), and hardness (7.05–10.05 GPa) which measures 1.5–2.0 times more than that of other Zr alloys (2 O{sub 3}) particles which can contribute to grain boundary pinning, and improved creep and oxidation resistance at elevated temperature.

77 NANOSCIENCE AND NANOTECHNOLOGY↗
DOE OSTI2018

Generation and healing of porosity in high purity copper by high-pressure torsion

Highlights: • Direct characterization of severe plastic deformation induced and healed porosities. • HPT process of disk with pre-fabricated holes reveals healing of porosity. • Ultrafine grains coexisting with shear bands and pores exhibit high stability. • Excess vacancies and pores cause drag effect on the grain boundary motion. • Accelerated vacancy diffusion leads to the generation and growth of pores. - Abstract: Generation and healing of pores in metals under loading or during processing have long been important research topics, and their mechanisms are still debatable. In recent years, unexpected percolating networks of pores acting as ultra-fast diffusion paths were found in ultrafine-grained metals processed by severe plastic deformation. Herein, we conducted a systematic study of the mechanisms of generation and healing of pores in ultrahigh-purity copper (99.9995 wt%) during high-pressure torsion (HPT). In addition to a solid Cu disk, the disk with holes that were drilled before processing, resulting in nominal initial porosity of 4.48%, was processed by HPT. After HPT, the percolating porosities of 0.07 ± 0.01% and 0.04 ± 0.01% were found in the solid disk, and in the disk with pre-fabricated holes, respectively. Thus, higher initial porosity resulted in lower percolating porosity in the HPT-processed disk. Systemic characterization using scanning electron microscopy revealed that in both cases shear bands and ultra-fine grains are located in the regions with induced and healed pores. We discussed the mechanisms of porosity evolution in both cases. In the end, to verify the possibility of pores nucleation and growth by vacancy agglomeration, vacancy diffusivity during HPT processing was estimated. This work sheds a new light on the mechanisms of pores nucleation and evolution during severe plastic deformation.

36 MATERIALS SCIENCE↗
DOE OSTI2014

PbO networks composed of single crystalline nanosheets synthesized by a facile chemical precipitation method

Graphical abstract: - Highlights: • Synthesis of PbO networks through a simple chemical precipitation route. • The synthesis method is rapid and low-cost. • Each network is composed of single crystalline PbO nanosheets. • A possible growth mechanism is proposed for synthesized PbO networks. - Abstract: For the field of energy storage, nanostructured lead oxide (PbO) shows immense potential for increased specific energy and deep discharge for lead acid battery technologies. In this work, PbO networks composed of single crystalline nanosheets were synthesized utilizing a simple, low cost and rapid chemical precipitation method. The PbO networks were prepared in a single reaction vessel from starting reagents of lead acetate dehydrate, ammonium hydroxide and deionized water. Lead acetate dehydrate was chosen as a reagent, as opposed to lead nitrate, to eliminate the possibility of nitrate contamination of the final product. X-ray diffraction (XRD) analysis, high resolution scanning electron microscopy (HRSEM) and high resolution transmission electron microscopy (HRTEM) analysis were used to characterize the synthesized PbO networks. The reproducible method described herein synthesized pure β-PbO (massicot) powders, with no byproducts. A possible formation mechanism for these PbO networks is proposed. The growth is found to proceed predominately in the 〈1 1 1〉 and 〈2 0 0〉 directions while being limited in the 〈0 1 1〉 direction.

36 MATERIALS SCIENCE↗
DOE OSTI2015

Effects of lithium salt concentration on graphited carbon microbead anodes in the piperidinium-based hybrid electrolytes

Graphical abstract: “Lithium aggregates” usually cause a significant decrease in Li{sup +} mobility and transfer efficiency. Therefore, as important as the problem of SEI, the content of lithium salt and the interaction between Li{sup +} and ILs’ anions should be taken into consideration in the optimization of ILs-based electrolytes for Li-ion batteries. - Highlights: • “Lithium aggregates” in piperidinium-based electrolytes are evidenced by IR and NMR. • High LiPF{sub 6} content could decrease Li{sup +} mobility due to “ionic aggregates”. • Lithium salt concentration is an important factor affecting graphite performances. - Abstract: The variations in LiPF{sub 6} concentration lead to the very different electrochemical performances of carbon microbeads anodes in the piperidinium-based hybrid electrolytes. The “two peaks” behaviors of lithium plating observed in cyclic voltammetry tests, and some detailed changes in infrared spectra and nuclear magnetic resonance indicates that the formation of “ionic aggregates” related to lithium ions”. Therefore, the excessive lithium salts in the piperidinium-based hybrid electrolytes, usually cause a significant decrease in Li{sup +} mobility and transfer efficiency. The main behaviors are that, when LiPF{sub 6} concentrations increased from 0.2 to 1.2 mol kg{sup −1}, the apparent migration energies (E{sub a}) increase largely from 8.83 to 21.16 kJ mol{sup −1}, while the lithium transference numbers (t{sub Li{sup +}}) drop markedly from 0.538 to 0.292.

36 MATERIALS SCIENCE↗
DOE OSTI2022

Reactions of hydrazine with the amidogen radical and atomic hydrogen

The rate coefficient k 1 for NH 2 + N 2 H 4 was measured to be (5.4 ± 0.4) × 10 –14 cm 3 molecule –1 s –1 at 296 K. NH 2 was generated by pulsed laser photolysis of NH 3 at 193 nm, and monitored as a function of time by pulsed laser-induced fluorescence excited at 570.3 nm under pseudo-first order conditions in the presence of excess N 2 H 4 in an Ar bath gas. This reaction was also investigated computationally, with geometries and scaled frequencies obtained with M06-2X/6-311+G(2df,2p) theory, and single-point energies from CCSD(T)-F12b/cc-pVTZ-F12 theory, plus a term to correct approximately for electron correlation through CCSDT(Q). Three connected transition states are involved and rate constants were obtained via Multistructural Improved Canonical Variational Transition State Theory with Small Curvature Tunneling. Combination of experiment and theory leads to a recommended rate coefficient for hydrogen abstraction of k 1 = 6.3 × 10 –23 T 3.44 exp(+289 K/T) cm 3 molecule –1 s –1 . The minor channel for H + N 2 H 4 forming NH 2 + NH 3 was characterized computationally as well, to yield 5.0 × 10 –19 T 2.07 exp(-4032 K/T) cm 3 molecule –1 s –1 . Finally, these results are compared to several discordant prior estimates, and are employed in an overall mechanism to compare with measurements of half-lives of hydrazine in a shock tube.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2015

Effects of sulfur on lead partitioning during sludge incineration based on experiments and thermodynamic calculations

Highlights: • A thermodynamic equilibrium calculation was carried out. • Effects of three types of sulfurs on Pb distribution were investigated. • The mechanism for three types of sulfurs acting on Pb partitioning were proposed. • Lead partitioning and species in bottom ash and fly ash were identified. - Abstract: Experiments in a tubular furnace reactor and thermodynamic equilibrium calculations were conducted to investigate the impact of sulfur compounds on the migration of lead (Pb) during sludge incineration. Representative samples of typical sludge with and without the addition of sulfur compounds were combusted at 850 °C, and the partitioning of Pb in the solid phase (bottom ash) and gas phase (fly ash and flue gas) was quantified. The results indicate that three types of sulfur compounds (S, Na{sub 2}S and Na{sub 2}SO{sub 4}) added to the sludge could facilitate the volatilization of Pb in the gas phase (fly ash and flue gas) into metal sulfates displacing its sulfides and some of its oxides. The effect of promoting Pb volatilization by adding Na{sub 2}SO{sub 4} and Na{sub 2}S was superior to that of the addition of S. In bottom ash, different metallic sulfides were found in the forms of lead sulfide, aluminosilicate minerals, and polymetallic-sulfides, which were minimally volatilized. The chemical equilibrium calculations indicated that sulfur stabilizes Pb in the form of PbSO{sub 4}(s) at low temperatures (<1000 K). The equilibrium calculation prediction also suggested that SiO{sub 2}, CaO, TiO{sub 2}, and Al{sub 2}O{sub 3} containing materials function as condensed phase solids in the temperature range of 800–1100 K as sorbents to stabilize Pb. However, in the presence of sulfur or chlorine or the co-existence of sulfur and chlorine, these sorbents were inactive. The effect of sulfur on Pb partitioning in the sludge incineration process mainly depended on the gas phase reaction, the surface reaction, the volatilization of products, and the concentration of Si, Ca and Al-containing compounds in the sludge. These findings provide useful information for understanding the partitioning behavior of Pb, facilitating the development of strategies to control the volatilization of Pb during sludge incineration.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2021

Layered-rocksalt intergrown cathode for high-capacity zero-strain battery operation

Abstract The dependence on lithium-ion batteries leads to a pressing demand for advanced cathode materials. We demonstrate a new concept of layered-rocksalt intergrown structure that harnesses the combined figures of merit from each phase, including high capacity of layered and rocksalt phases, good kinetics of layered oxide and structural advantage of rocksalt. Based on this concept, lithium nickel ruthenium oxide of a main layered structure ( R $$\bar{3}$$ 3 ¯ m ) with intergrown rocksalt ( Fm $$\bar{3}$$ 3 ¯ m ) is developed, which delivers a high capacity with good rate performance. The interwoven rocksalt structure successfully prevents the anisotropic structural change that is typical for layered oxide, enabling a nearly zero-strain operation upon high-capacity cycling. Furthermore, a design principle is successfully extrapolated and experimentally verified in a series of compositions. Here, we show the success of such layered-rocksalt intergrown structure exemplifies a new battery electrode design concept and opens up a vast space of compositions to develop high-performance intergrown cathode materials.

25 ENERGY STORAGE↗
DOE OSTI2021

Sub-nanometer confinement enables facile condensation of gas electrolyte for low-temperature batteries

Abstract Confining molecules in the nanoscale environment can lead to dramatic changes of their physical and chemical properties, which opens possibilities for new applications. There is a growing interest in liquefied gas electrolytes for electrochemical devices operating at low temperatures due to their low melting point. However, their high vapor pressure still poses potential safety concerns for practical usages. Herein, we report facile capillary condensation of gas electrolyte by strong confinement in sub-nanometer pores of metal-organic framework (MOF). By designing MOF-polymer membranes (MPMs) that present dense and continuous micropore (~0.8 nm) networks, we show significant uptake of hydrofluorocarbon molecules in MOF pores at pressure lower than the bulk counterpart. This unique property enables lithium/fluorinated graphite batteries with MPM-based electrolytes to deliver a significantly higher capacity than those with commercial separator membranes (~500 mAh g −1 vs. <0.03 mAh g −1 ) at −40 °C under reduced pressure of the electrolyte.

25 ENERGY STORAGE↗
DOE OSTI2022

Optimal operation and sizing of pumped thermal energy storage for net benefits maximization

Abstract Current trends in the modern grid are leading to the development and deployment of energy storage to help integrate increasing variable renewable energy sources into the grid. This paper studies a pumped thermal energy storage (PTES) system for multiple grid services including energy arbitrage, frequency regulation, spinning and non‐spinning reserve, and resource adequacy. Optimal dispatch methods are proposed for individual services as well as value stacking from multiple services to maximize the economic benefits. Assessment results demonstrate the superiority of value stacking. Specifically, the study shows the maximum revenue from an individual grid service with a 30‐MWh PTES system was $522,520, while the value stacking could increase the benefits to $678,477. In addition, sensitivity analyses were conducted to explore the cost‐effectiveness of a PTES system with different combinations of power transfer limits and energy capacity. It was found that the power transfer limit had a greater impact than the energy capacity on the benefits. The proposed method could help determine the optimal duration of a future PTES system.

25 ENERGY STORAGE↗
DOE OSTI2022

Effects of short-interval reburns in the boreal forest on soil bacterial communities compared to long-interval reburns

Abstract Increasing fire frequency in some biomes is leading to fires burning in close succession, triggering rapid vegetation change and altering soil properties. We studied the effects of short-interval (SI) reburns on soil bacterial communities of the boreal forest of northwestern Canada using paired sites (n = 44). Both sites in each pair had burned in a recent fire; one site had burned within the previous 20 years before the recent fire (SI reburn) and the other had not. Paired sites were closely matched in prefire ecosite characteristics, prefire tree species composition, and stand structure. We hypothesized that there would be a significant effect of short vs. long fire-free intervals on community composition and that richness would not be consistently different between paired sites. We found that Blastococcus sp. was consistently enriched in SI reburns, indicating its role as a strongly ‘pyrophilous’ bacterium. Caballeronia sordidicola was consistently depleted in SI reburns. The depletion of this endophytic diazotroph raises questions about whether this is contributing to—or merely reflects—poor conifer seedling recolonization post-fire at SI reburns. While SI reburns had no significant effect on richness, dissimilarity between short- and long-interval pairs was significantly correlated with difference in soil pH, and there were small significant changes in overall community composition.

54 ENVIRONMENTAL SCIENCES↗
DOE OSTI2022

Fuzzy dark matter and the Dark Energy Survey Year 1 data

ABSTRACT Gravitational weak lensing by dark matter haloes leads to a measurable imprint in the shear correlation function of galaxies. Fuzzy dark matter (FDM), composed of ultralight axion-like particles of mass m ∼ 10−22 eV, suppresses the matter power spectrum and shear correlation with respect to standard cold dark matter. We model the effect of FDM on cosmic shear using the optimized halo model HMCode, accounting for additional suppression of the mass function and halo concentration in FDM as observed in N-body simulations. We combine Dark Energy Survey Year 1 (DES-Y1) data with the Planck cosmic microwave background anisotropies to search for shear correlation suppression caused by FDM. We find no evidence of suppression compared to the preferred cold dark matter model, and thus set a new lower limit to the FDM particle mass. Using a log-flat prior and marginalizing over uncertainties related to the non-linear model of FDM, we find a new, independent 95 per cent C.L. lower limit log10m > −23 combining Planck and DES-Y1 shear, an improvement of almost two orders of magnitude on the mass bound relative to CMB-only constraints. Our analysis is largely independent of baryonic modelling, and of previous limits to FDM covering this mass range. Our analysis highlights the most important aspects of the FDM non-linear model for future investigation. The limit to FDM from weak lensing could be improved by up to three orders of magnitude with $\mathcal {O}(0.1)$ arcmin cosmic shear angular resolution, if FDM and baryonic feedback can be simultaneously modelled to high precision in the halo model.

79 ASTRONOMY AND ASTROPHYSICS↗