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At least 433 records · Page 24

One-step synthesis of lightly doped porous silicon nanowires in HF/AgNO{sub 3}/H{sub 2}O{sub 2} solution at room temperature

One-step synthesis of lightly doped porous silicon nanowire arrays was achieved by etching the silicon wafer in HF/AgNO{sub 3}/H{sub 2}O{sub 2} solution at room temperature. The lightly doped porous silicon nanowires (pNWs) have circular nanopores on the sidewall, which can emit strong green fluorescence. The surface morphologies of these nanowires could be controlled by simply adjusting the concentration of H{sub 2}O{sub 2}, which influences the distribution of silver nanoparticles (Ag NPs) along the nanowire axis. A mechanism based on Ag NPs-induced lateral etching of nanowires was proposed to explain the formation of pNWs. The controllable and widely applicable synthesis of pNWs will open their potential application to nanoscale photoluminescence devices. - Graphical abstract: The one-step synthesis of porous silicon nanowire arrays is achieved by chemical etching of the lightly doped p-type Si (100) wafer at room temperature. These nanowires exhibit strong green photoluminescence. SEM, TEM, HRTEM and photoluminescence images of pNWs. The scale bars of SEM, TEM HRTEM and photoluminescence are 10 {mu}m, 20 nm, 10 nm, and 1 {mu}m, respectively. Highlights: Black-Right-Pointing-Pointer Simple one-step synthesis of lightly doped porous silicon nanowire arrays is achieved at RT. Black-Right-Pointing-Pointer Etching process and mechanism are illustrated with etching model from a novel standpoint. Black-Right-Pointing-Pointer As-prepared porous silicon nanowire emits strong green fluorescence, proving unique property.

36 MATERIALS SCIENCE↗

Room temperature synthesis of a Zn(II) metal-organic coordination polymer for dye removal

A new one-dimensional (1D) coordination polymer, [Zn(4,4′-bpy)(H{sub 2}O){sub 4}](ADC)·4H{sub 2}O (1) (4,4′-bpy=4,4′-bipyridine and H{sub 2}ADC=acetylenedicarboxylic acid), was synthesized at room temperature. The crystal structure of the coordination polymer was determined by single-crystal X-ray diffraction analysis. Compound 1 was also characterized by FT-IR, powder X-ray diffraction (PXRD) and thermogravimetric analysis (TGA). The catalytic activity of 1 was evaluated in the color removal of Bismarck brown as a representative of dye pollutant in water under mild conditions. Coordination polymer 1 exhibited good catalytic activity and stability in the decolorization of Bismarck brown and could be easily recovered and reused for at least three cycles. - Graphical abstract: A new 1D coordination polymer as catalyst for the degradation of Bismarck brown aqueous solution. - Highlights: • A 1D coordination polymer has been synthesized at room temperature. • The prepared compound was utilized for color removal of Bismarck brown dye. • Good catalytic activity and stability in the dye decolorization has been found.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Room temperature creep behavior of Ti–Nb–Ta–Zr–O alloy

The room temperature creep behavior and deformation mechanisms of a Ti–Nb–Ta–Zr–O alloy, which is also called “gum metal”, were investigated with the nanoindentation creep and conventional creep tests. The microstructure was observed with electron backscattered diffraction analysis (EBSD) and transmission electron microscopy (TEM). The results show that the creep stress exponent of the alloy is sensitive to cold deformation history of the alloy. The alloy which was cold swaged by 85% shows high creep resistance and the stress exponent is approximately equal to 1. Microstructural observation shows that creep process of the alloy without cold deformation is controlled by dislocation mechanism. The stress-induced α' martensitic phase transformation also occurs. The EBSD results show that the grain orientation changes after the creep tests, and thus, the creep of the cold-worked alloy is dominated by the shear deformation of giant faults without direct assistance from dislocations. - Highlights: •Nanoindentation was used to investigate room temperature creep behavior of gum metal. •The creep stress exponent of gum metal is sensitive to the cold deformation history. •The creep stress exponent of cold worked gum metal is approximately equal to 1. •The creep of the cold-worked gum metal is governed by the shear deformation of giant faults.

36 MATERIALS SCIENCE↗

CuSn(OH){sub 6} submicrospheres: Room-temperature synthesis, growth mechanism, and weak antiferromagnetic behavior

Highlights: Black-Right-Pointing-Pointer CuSn(OH){sub 6} spheres have been synthesized via an aqueous solution method at room temperature. Black-Right-Pointing-Pointer The diameters of the CuSn(OH){sub 6} spheres can be tuned by adjusting the molar ratio of SnO{sub 3}{sup 2-} to Cu{sup 2+}. Black-Right-Pointing-Pointer The as-obtained CuSn(OH){sub 6} spheres are antiferromagnetic and have a weak spin-Peierls transition at about 78 K -- Abstract: CuSn(OH){sub 6} submicrospheres with diameters of 400-900 nm have been successfully fabricated using a simple aqueous solution method at room temperature. Influencing factors such as the dosage of reactants and reaction time on the preparation were systematically investigated. The products were characterized with X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TG) and differential thermal analysis (DTA). Results reveal that the CuSn(OH){sub 6} spheres are built from numerous nanoparticles. It is found that the diameter of CuSn(OH){sub 6} spheres can be readily tuned by adjusting the molar ratio of SnO{sub 3}{sup 2-} to Cu{sup 2+}. A possible growth mechanism for the CuSn(OH){sub 6} submicrospheres has been proposed. Amorphous CuSnO{sub 3} submicrospheres were obtained after thermal treatment of the CuSn(OH){sub 6} submicrospheres at 300 Degree-Sign C for 4 h. Standard magnetization measurements demonstrate that the CuSn(OH){sub 6} submicrospheres are antiferromagnetic and have a weak spin-Peierls transition at about 78 K.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Chemical synthesis of Cu{sub 2}Se nanoparticles at room temperature

Graphical abstract: The Cu{sub 2}Se nanoparticles were synthesized by a simple and rapid method at room temperature. The TEM and SEM images show that the Cu{sub 2}Se nanoparticles were spherical. Highlights: Black-Right-Pointing-Pointer Cu{sub 2}Se nanoparticles were synthesized by the reaction of nanoSe{sup 0} sol with Cu{sup +} ions. Black-Right-Pointing-Pointer The Cu{sub 2}Se nanoparticles were spherical with cubic structure and well crystallized. Black-Right-Pointing-Pointer Optical and electrochemical properties of Cu{sub 2}Se nanoparticles were observed. Black-Right-Pointing-Pointer The formation mechanism of Cu{sub 2}Se nanoparticles was proposed. -- Abstract: A simple and rapid method has been developed to synthesize cuprous selenide (Cu{sub 2}Se) nanoparticles by the reaction of selenium nanoparticles sol with copper sulfate solution containing ascorbic acid at room temperature. Cu{sub 2}Se nanoparticles were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), and energy dispersive X-ray analysis (EDX). The results indicated that Cu{sub 2}Se nanoparticles were cubic crystal structure and spherical with the diameter about 75 nm. The ultraviolet-visible absorption spectrum (UV-vis) and cyclic voltammetry of Cu{sub 2}Se nanoparticles were also investigated. The optical band gap energy of Cu{sub 2}Se nanoparticles was 1.94 eV. On the basis of a series of experiments and characterizations, the formation mechanism of Cu{sub 2}Se nanoparticles was discussed.

36 MATERIALS SCIENCE↗

Signature of room temperature ferromagnetism in Mn doped CeO{sub 2} nanoparticles

We report structural and magnetic properties of Mn doped CeO{sub 2} nanoparticles using X-ray diffraction (XRD), field emission transmission electron microscopy (FE-TEM) and dc magnetization measurements. XRD results infer that all the samples have single phase nature and lattice parameters decrease with Mn doping. The particle size calculated using XRD and TEM analysis was found to decrease with Mn doping. Field cooled magnetization measurement shows that the transition temperature is above room temperature. Magnetic hysteresis loop studies indicate that undoped and Mn doped CeO{sub 2} nanoparticles show weak ferromagnetic behavior at room temperature.

36 MATERIALS SCIENCE↗

Effects of air annealing on CdS quantum dots thin film grown at room temperature by CBD technique intended for photosensor applications

Graphical abstract: The effect of different intensities (40, 60 100 and 200 W) of light on CdS quantum dots thin film annealed at 350 °C indicating enhancement in (a) photo-current and (b) photosensitivity. Highlights: ► The preparation of CdS nanodot thin film at room temperature by M-CBD technique. ► Study of air annealing on prepared CdS nanodots thin film. ► The optimized annealing temperature for CdS nanodot thin film is 350 °C. ► Modified CdS thin films can be used in photosensor application. -- Abstract: CdS quantum dots thin-films have been deposited onto the glass substrate at room temperature using modified chemical bath deposition technique. The prepared thin films were further annealed in air atmosphere at 150, 250 and 350 °C for 1 h and subsequently characterized by scanning electron microscopy, ultraviolet–visible spectroscopy, electrical resistivity and I–V system. The modifications observed in morphology and opto-electrical properties of the thin films are presented.

36 MATERIALS SCIENCE↗

Characterization of nanostructured iron selenide thin films grown by chemical route at room temperature

Highlights: ► Nanostructured FeSe thin films were successfully synthesized at room temperature by CBD method. ► The XRD and EDAX characterization confirms nanocrystalline nature of FeSe. ► The SEM and AFM show microporous morphology with nanorods and nanoplates of FeSe. -- Abstract: Iron selenide thin films have been deposited onto glass substrates by using chemical bath deposition technique. Structural characterization of iron selenide thin films was carried out by means of X-ray diffraction and Fourier transforms infrared spectrum. The morphological characterization of FeSe thin film was carried out using scanning electron microscopy and atomic force microscopy, which revealed porous grain morphology of FeSe with some nano rectangular rods and plates grown on it. The as-deposited thin films exhibited optical band gap energy 2.60 eV. The as deposited FeSe thin films are semiconducting in nature with p-type electrical conductivity. The room temperature electrical resistivity is of the order of 1.1 × 10{sup 5} Ω-cm with activation energy 0.26 and 0.95 eV, respectively, in low and high temperature region.

36 MATERIALS SCIENCE↗

Room-temperature ferromagnetism of Fe-doped TiO{sub 2} nanoparticles driven by oxygen vacancy

Graphical abstract: A series of Ti{sub 1−x}Fe{sub x}O{sub 2−δ} (x ≤ 0.03) nanoparticles (NPs) were synthesized by sol–gel route. The room temperature ferromagnetism (RTFM) has been explained in terms of vacancy induced bound magnetic polaron (BMP) model, where the Fe{sup 3+} ions ferromagnetically coupled mediated by oxygen vacancies. Display Omitted Highlights: ► The Fe-doped NPs have been synthesized by sol–gel method. ► Ferromagnetism of Fe-doped TiO{sub 2} NPs are intrinsic property. ► Room temperature ferromagnetism observed in all the Fe-doped samples. ► Variation in M{sub s} is attributed due to oxygen vacancies and defect formation. -- Abstract: A series of Ti{sub 1−x}Fe{sub x}O{sub 2−δ} (0 ≤ x ≤ 0.03) nanoparticles (NPs) were synthesized by sol–gel route. The NPs had a size distribution in the range of 15–40 nm and were identified as the anatase TiO{sub 2} by X-ray diffraction (XRD) and Raman analysis. XRD, selected area electron diffraction, Raman and Mössbauer analysis ruled out the signature of Fe-cluster or any other oxides of Fe. The redshifting of the band edge emission peak observed in UV–vis absorption studies further confirmed the doping of Fe ions in the TiO{sub 2} lattice. Raman studies show the shifting and broadening in E{sub g}(1) and E{sub g}(3) modes with Fe doping. It suggested that the activation of ferromagnetism with increasing Fe doping concentration was related to the oxygen vacancy defects. The presence of such defects was further confirmed from electron paramagnetic resonance (EPR) measurements. The observed ferromagnetism is interpreted in terms of bound magnetic polaron (BMP) model.

36 MATERIALS SCIENCE↗

Room-temperature ferromagnetism properties of monoclinic VO{sub 2} (M1) nanobelts

Highlights: • The unusual room temperature ferromagnetism of the VO{sub 2}(M1) nanobelts is found in magnetic measurement. • The oxygen vacancies induce the change of Bader charge of V atom from +2.34 to +1.84 (V{sup +4} to V{sup +3}). • The ferromagnetic nature is a result of the oxygen vacancies based on the calculations by DFT. - Abstract: The magnetic properties of monoclinic VO{sub 2}(M1) nanobelts synthesized by the hydrothermal method are investigated. The VO{sub 2}(M1) nanobelts exhibit ferromagnetism at room temperature, which disagrees with previous literatures. The excessive oxygen vacancies induce the ferromagnetic nature of VO{sub 2}(B) nanobelts, which is attributed to the fact that the Bader charge of V atom changes from +2.34 to +1.84 (V{sup +4} to V{sup +3}) based on the calculations by using density functional theory (DFT). The calculations indicate that oxygen vacancy may induce the presence of V{sup 3+} atom, in agreement with experimental observations. The observed ferromagnetism should be a result of oxygen vacancies in VO{sub 2}(M1) nanobelts.

36 MATERIALS SCIENCE↗

Room-temperature solid state synthesis of ZnO/Bi{sub 2}O{sub 3} heterojunction and their solar light photocatalytic performance

Highlights: • ZnO/Bi{sub 2}O{sub 3} hierarchical nanostructures were synthesized via a solid-state reaction. • The amount of Bi{sub 2}O{sub 3} plays an important role in controlling the morphology. • The amount of Bi{sub 2}O{sub 3} plays an important role in controlling the photocatalysis. - Abstract: ZnO/Bi{sub 2}O{sub 3} heterojunction was prepared by solid state reaction method at room temperature. The as-prepared nanostructures were characterized as the assembled nanosheets of ZnO on which Bi{sub 2}O{sub 3} nanoparticles were well dispersed. Further studies revealed that the morphology and photocatalytic property could be regulated by tuning the amount of Bi{sub 2}O{sub 3}. The introduction of Bi{sub 2}O{sub 3} can lead to the enhancement of solar light absorption, and the 5% ZnO/Bi{sub 2}O{sub 3} samples exhibited the best photocatalytic activity under the solar light irradiation. The excellent photocatalytic performances could be ascribed to the synergistic effects of the hierarchical nanostructures and the effective separation of photogenerated carriers. Moreover, the hydroxyl radicals (·OH) are found to be the main active species generated in the oxidation reaction of RhB over ZnO/Bi{sub 2}O{sub 3} photocatalyst. Therefore, our work demonstrated a facile way to prepare hierarchical nanostructures with excellent photocatalytic performance using solid state method at room temperature.

36 MATERIALS SCIENCE↗

Dense nanocrystalline yttrium iron garnet films formed at room temperature by aerosol deposition

Highlights: • We deposit yttrium iron garnet films at room temperature using aerosol deposition. • Films are 96% of theoretical density for yttrium iron garnet. • We report magnetic and structural properties post-deposition and post-annealing. • Low-temperature annealing decreases the FMR linewidth. • We discuss features of the FMR spectra at each anneal temperature. - Abstract: We have employed aerosol deposition to form polycrystalline yttrium iron garnet (YIG) films on sapphire at room temperature that are 90–96% dense. We characterize the structural and dynamic magnetic properties of the dense films using scanning electron microscopy, X-ray diffraction, and ferromagnetic resonance techniques. We find that the as-deposited films are pure single-phase YIG formed of compact polycrystallites ∼20 nm in size. The ferromagnetic resonance mode occurs at 2829 G with a linewidth of 308 G. We perform a series of successive anneals up to 1000 °C on a film to explore heat treatment on the ferromagnetic resonance linewidth. We find the narrowest linewidth of 98 G occurs after a 750 °C anneal.

36 MATERIALS SCIENCE↗

Room temperature biosynthesis of greatly stable fluorescent ZnO quantum dots for the selective detection of Cr{sup 3+} ions

Graphical abstract: Biosynthesized fluorescent ZnO quantum dots are extremely stable and are able to sense up to 2 nM of Cr3+ ions in aqueous solution. - Highlights: • ZnO quantum dotes (QDs) are rapidly synthesized from the bio waste at room temperature. • The capping and reducing agent is from natural source hence biodegradable. • The water soluble fluorescent ZnO quantum dots are highly stable. • The QDs are able to sense 2 nM of Cr{sup 3+} ions in aqueous solution. - Abstract: Synthesis of extremely stable and water soluble quantum dots (QDs) would be smart if the method is rapid and eco-friendly. Here in, we have employed a simple strategy for the preparation of well dispersed, luminescent ZnO quantum dots by using pomegranate peel extract at room temperature. This method excludes the use of strong commercial stabilizing agents, different pH conditions, higher temperature and inert atmosphere during the synthesis. The microscopic study has revealed the ZnO QDs to be of a narrow size with an average size distribution of about 4 nm. The water soluble QDs exhibited a strong emission peak at 490 nm and were stable for twelve months. The emission from ZnO QDs are selectively quenched upon addition of Cr{sup 3+} ions. The interaction between the Cr{sup 3+} and the biomolecules on the exterior of ZnO QDs, enables the system to detect up to 2 nM Cr{sup 3+} ions in aqueous solution.

36 MATERIALS SCIENCE↗

Tuning of carrier type, enhancement of Linear magnetoresistance and inducing ferromagnetism at room temperature with Cu doping in Bi2Te3 Topological Insulators

Highlights: • With Cu doping in Bi{sub 2}Te{sub 3}, resistivity increases as Fermi level is shifted into valence band with extra scattering centers. • Cu doping tunes the carrier from n to p type, which is attributed to the presence of Te{sub Bi} and Bi{sub Te} antisites. • The observed Linear Magneto resistance is believed to be associated with gapless linear energy spectrum of surface Dirac Fermions. • Cu doping induces room temperature ferromagnetism. - Abstract: Structural, resistivity, thermoelectric power, magneto-transport and magnetic properties of Cu doped Bi{sub 2}Te{sub 3} topological insulators have been investigated. The tuning of charge carriers from n to p type by Cu doping at Te sites of Bi{sub 2}Te{sub 3} is observed both from Hall effect and thermoelectric power measurements. Carrier mobility decreases with the doping of Cu which provides evidence of the movement of Fermi level from bulk conduction band to the bulk valence band. Thermoelectric power also increases with doping of Cu. Moreover, linear magnetoresistance (LMR) is observed at high magnetic field in pure Bi{sub 2}Te{sub 3} which is associated to the gapless topological surface states protected by time reversal symmetry (TRS). Furthermore, doping of non-magnetic Cu induces ferromagnetism at room temperature and also enhances the magnetoresistance.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Room temperature synthesis of urea based imidazole functionalised ZnO nanorods and their photocatalytic application

Highlights: • Imidazole functionalised ZnO nanorods obtained at room temperature. • Functionalised ZnO nanorods degrade Rh B dye by 84% under Hg lamp illumination. • Rh B dye photocatalysis by functionalised ZnO nanorods follow 1st order kinetics. - Abstract: ZnO, a well known photocatalyst due to its wide band gap, is used for environmental remediation applications. Under present investigation, two urea based imidazole functionalised compounds R and S were synthesised and then used as structure directing agent to further synthesise surface functionalised ZnO nanorods at room temperature (30–40 °C) by simple chemical precipitation route. R: Zn(NO{sub 3}){sub 2}·6H{sub 2}O: NaOH used in two ratios i.e. 1:2:4 and 1:1:1 to synthesise R functionalised ZnO nanorods i.e. R1 and R2 respectively while S: Zn(NO{sub 3}){sub 2}·6H{sub 2}O: NaOH used in 1:2:4 ratio to synthesise S functionalised ZnO nanoparticles i.e. S1. R functionalized ZnO nanorods (R1) have length, breadth, zeta potential and surface area as 330 nm, 19 nm, 34.6 mV and 134 m{sup 2}/g respectively. Rhodamine B dye was degraded as 84% and 63% by R-ZnO (R1) and S-ZnO (S1) respectively under UV lamp for 3 h which is more than twice for R1 in comparison to R.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Room-temperature synthesis and characterization of carbon-encapsulated molybdenum nanoparticles

Highlights: • Carbon-encapsulated molybdenum nanoparticles were synthesized at room temperature. • Different hydrocarbons were used as carbon source for shell formation. • Increase of hydrocarbon mole ratio resulted in decrease of Mo-based nanoparticle cores. • Increase of laser pulses number resulted in increase of Mo content in CEMNPs. • Carbon shells prevented Mo nanoparticles from aggregation. - Abstract: Carbon-encapsulated molybdenum nanoparticles were synthesized by laser-assisted photolysis of gaseous precursors. In the proposed method, gas mixtures containing various hydrocarbons and molybdenum hexacarbonyl vapor diluted in argon were irradiated with a nanosecond pulsed UV laser at room temperature. Particle samples were analyzed by transmission electron microscopy (TEM), electron microdiffraction (EMD), energy-dispersive X-ray spectroscopy (EDS), and high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) techniques to observe the morphology and composition of the Mo/C nanoparticles. The influence of the type of hydrocarbon, its mole fraction, and the number of UV laser pulses on the resulting nanoparticles was investigated. The nanoparticles were heavily aggregated and consisted of Mo-based cores surrounded by carbon. The type of hydrocarbon did not have any visible effects on the nanoparticle structure and the size of the Mo-based cores or aggregates. Increasing the hydrocarbon mole fraction in the precursor mixture led to an increase in the carbon content and decrease of the Mo-based core size. Increasing the number of UV laser pulses led to larger Mo cores.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Microstructural heterogeneities in additively manufactured refractory alloy C103 and their implications for room and elevated temperature mechanical behavior

Considering the vast component design space enabled by fusion-based additive manufacturing (F-BAM) processes, e.g., directed energy deposition (DED), the scale-up manufacturing of Nb-alloys with F-BAM is advantageous for structural applications. However, varying thermokinetic parameters-induced microstructural heterogeneities are prevalent within the F-BAM processed alloys. Such microstructural heterogeneities can have significant implications for the room and elevated temperature mechanical behavior. While a few studies investigating F-BAM processed alloy C103 are available, none of these studies investigate the microstructural heterogeneities – including those associated with solidification growth modes and second phase particles – and the effect thereof on the mechanical behavior. To this end, we investigate the microstructurally heterogeneous regions with varying solidification growth morphologies, segregation behavior, and second phase particle attributes within the laser-DED processed alloy C103. The implications of such heterogeneous regions for room- and elevated-temperature tensile behavior and damage mechanisms are revealed. Particularly, the interface between the cellular and planar region is identified as susceptible to deformation localization. The implications of hot isostatic pressing (HIP) for the consolidation behavior, microstructural evolution, and resulting mechanical behavior are also discussed. Although the recrystallization and grain growth led to a reduced yield strength in the HIPed condition, the homogenization of microstructure alleviated the deformation localization sites, such as the planar/cellular interface within the melt pool. The homogenized microstructure alongside the enhanced consolidation upon HIP led to an enhanced elongation to failure. Findings establish microstructural design considerations in F-BAM processed Nb alloys and also facilitate design of post-processing heat treatments for achieving improved mechanical properties.

36 MATERIALS SCIENCE↗

Room temperature sodium diffusion in sodium iron phosphate investigated with neutron scattering

Sodium iron phosphate, Na x FePO 4 , is currently one of the most promising cathode materials for sodium ion batteries. Here we employ a systematic approach using three neutron scattering techniques to investigate temperature dependent properties with a focus on the charge transfer processes. Two distinct Na + diffusive motions are observed with quasielastic neutron scattering, including room temperature motion. These processes correspond to rapid double jumps through extrinsic vacancy sites of ∼6 Å along with the more fundamental nearest neighbor jumps of 3.1 Å. Experimental observations of room temperature ionic diffusion are highly desirable, as the diffusion pathways are naturally well suited for efficient transport. Inelastic neutron scattering was used to probe the vibrational density of states that assist in the ionic and electronic (polaronic) transport processes, which are further supported with density functional theory. Neutron diffraction examines the disordering of the sodium sublattice upon transition to the solid-solution phase, which is believed to enhance the overall kinetics during sodium insertion/extraction. Finally, 57 Fe Mössbauer spectroscopy measurements probes polaron hopping and the local structural evolution that modifies the electron density surrounding the redox active iron sites. This study sheds light on the temperature induced atomic scale dynamics that occur in olivine Na x FePO 4 .

Novak, Eric [Swarthmore College, Swarthmore, PA (U↗