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At least 91 records · Page 5
All sourcesNASA NTRSDOE OSTI
NASA NTRS1986

Visibility related to backscatter at 1.54 micron

The lidar process was shown to have the necessary potential to fulfill the need for a remote measurement of visibility. Visibility can be inferred from a lidar return optical extinction. The wavelength 1.54 micron was chosen, being near the visible wavelength region and having a high eye safety threshol, 200,000 times higher than 1.06 micron; 1.54 is the erbium laser wavelength. This research utilized 105 measured height profiles of natural droplet size distributions data, taken in clouds, fog, and haze. These profiles were examined to determine the completeness of the droplet counting data. It was found that the particle spectrometer data were incomplete in the very light ford and haze so this portion of the data was eliminated. Utilizing the Mie theory, these droplet size distribution profiles were converted to backscatter at 1.54 micron and extinction in the visible region, 0.55 micron. Using Koschmeider's relationship, the extinction profiles were converted to visibility. The visibility and backscatter profiles were compared to develop a relationship between visibility and backscatter at 1.54 micron.

Barber, T. L.↗
DOE OSTI2011

ESR study on the visible photocatalytic mechanism of nitrogen-doped novel TiO{sub 2}

The visible photocatalytic mechanism of nitrogen-doped novel TiO{sub 2} was studied by means of electron spin resonance spectroscopy (ESR). It was found that, under visible light irradiation, the concentration of single-electron-trapped oxygen vacancy (SETOV, V{sub o}{sup {center_dot}}) of novel TiO{sub 2} remained unchanged, but that of nitrogen-doped novel TiO{sub 2} increased and returned to original state when the light was turned off. This implies that, aside from V{sub o}{sup {center_dot}} in bulk of nitrogen-doped novel TiO{sub 2}, oxygen vacancy without trapped electron (V{sub o}{sup {center_dot}{center_dot}}) was formed on its surface. V{sub o}{sup {center_dot}{center_dot}} as a surface electron trap captured photogenerated electron from the bulk to generate extra V{sub o}{sup {center_dot}}, carrying out photocatalytic reaction on the surface. At the same time, nitrogen doping product NO was chemically adsorbed on the vicinity of V{sub o}{sup {center_dot}{center_dot}} and inhibited the attack of oxygen, allowing V{sub o}{sup {center_dot}{center_dot}} to remain stable in air. The synergistic action of the two kinds of active structures, i.e., bulk V{sub o}{sup {center_dot}}-NO-Ti and surface V{sub o}{sup {center_dot}{center_dot}}-NO-Ti, accounted for the visible photocatalytic activity of N-doped novel TiO{sub 2}. - Graphical abstract: Synergistic action is realized between (V{sub o}{sup {center_dot}}){sub bulk} and (V{sub o}{sup {center_dot}{center_dot}}){sub surf} in the presence of active structures (V{sub o}{sup {center_dot}}){sub bulk}-NO-Ti and (V{sub o}{sup {center_dot}{center_dot}}){sub surf} -NO-Ti. Research Highlights: > The origin of visible photocatalytic activity of the N-TiO{sub 2} was studied by ESR. > (V{sub o}{sup {center_dot}}){sub bulk} and (V{sub o}{sup {center_dot}{center_dot}}){sub surf} formed in N-TiO{sub 2}. > (V{sub o}{sup {center_dot}}){sub bulk} and (V{sub o}{sup {center_dot}{center_dot}}){sub surf} show a synergistic effect in visible photocatalytic. > TiO{sub 2} did not contain (V{sub o}{sup {center_dot}{center_dot}}){sub surf}, so no visible photocatalytic activity.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2012

Synthesis of Mn-intercalated layered titanate by exfoliation-flocculation approach and its efficient photocatalytic activity under visible-light

A novel Mn-intercalated layered titanate as highly active photocatalyst in visible-light region has been synthesized via a convenient and efficient exfoliation-flocculation approach with divalent Mn ions and monolayer titanate nanosheets. The 0.91 nm interlayer spacing of obtained photocatalyst is in accordance with the sum of the thickness of titanate nanosheet and the diameter of Mn ions. The yellow photocatalyst shows a spectral response in visible-light region and the calculated band gap is 2.59 eV. The photocatalytic performance of this material was evaluated by degradation and mineralization of an aqueous dye methylene blue under visible-light irradiation, and an enhanced photocatalytic activity in comparison with protonated titanate as well as the P25 TiO{sub 2} and N-doped TiO{sub 2} was obtained. Additionally, the layered structure is retained, no dye ions intercalating occurs during the photocatalysis process, and a {approx}90% photocatalytic activity can be remained after reusing 3 cycles. - Graphical abstract: Mn-intercalated layered titanate as a novel and efficient visible-light harvesting photocatalyst was synthesized via a convenient and efficient exfoliation-flocculation approach in a mild condition. Highlights: Black-Right-Pointing-Pointer Mn-intercalated titanate has been prepared by exfoliation-flocculation approach. Black-Right-Pointing-Pointer The as-prepared catalyst shows spectral response in the visible-light region. Black-Right-Pointing-Pointer Heat treatment at certain temperature enables formation of Mn-doped TiO{sub 2}. Black-Right-Pointing-Pointer Dye can be degradated effectively by the catalyst under visible light irradiation.

36 MATERIALS SCIENCE↗
DOE OSTI2018

A one-pot, solid-state route for realizing highly visible light active Na-doped gC{sub 3}N{sub 4} photocatalysts

The visible light photocatalytic activity of graphitic carbon nitride (gC{sub 3}N{sub 4}), a promising metal-free photocatalytic material, is rather low, and is not as good as expected. Herein, to realize improved photocatalytic activity, sodium-doped gC{sub 3}N{sub 4} (Na-gC{sub 3}N{sub 4}) is prepared through a novel solid-state process based on the thermal polycondensation of urea in the presence of sodium chloride and ammonium chloride. The proposed solid-state process is simple, requires no solvent, and provides a general route for rapid and large-scale synthesis of metal-doped gC{sub 3}N{sub 4}. The Na species exist in + 1 oxidation state and bind N atoms in the nitride ring of gC{sub 3}N{sub 4}. The photocatalytic activity improvement of gC{sub 3}N{sub 4} for the mineralization of 17α-ethynylestradiol (EE2) under visible light is seen after the Na doping. The improved photocatalytic activity is due to increased absorption of light, increased separation of charge carriers, stronger oxidation ability of valance band holes, and increased specific surface area. The typical photocatalytic activity of 0.6 wt% Na-gC{sub 3}N{sub 4} for the EE2 mineralization with an initial EE2 concentration of 1 mg/L and a catalyst concentration of 1 g/L is 95.7% within 2 h of visible light irradiation. Under identical experimental conditions, the EE2 mineralization by pristine gC{sub 3}N{sub 4} is only 23.5%. - Graphical abstract: Highly visible light active Na-gC{sub 3}N{sub 4} photocatalysts were simply synthesized through a novel one-pot route based on the thermal polycondensation of urea. The doped Na species plays a critical role in improving the photocatalytic activity. Display Omitted - Highlights: • A new solid-state route is introduced to obtain visible light active Na-doped gC{sub 3}N{sub 4}. • The proposed synthesis route is fast, simple, and highly scalable. • Na doping leads to improved light absorption capability. • Na doping leads to improved separation of charge carriers. • Na doping leads to improved photocatalytic activity under visible light.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗
DOE OSTI2014

Supercritical-assistant liquid crystal template approach to synthesize mesoporous titania/multiwalled carbon nanotube composites with high visible-light driven photocatalytic performance

Graphical abstract: We investigate the influence of mesoporous titania content upon the visible-light driven photocatalytic performance of MPT/MWCNTs in phenol degradation. - Highlights: • MPT/MWCNTs were fabricated by liquid-crystal template in supercritical CO{sub 2}. • MPT/MWCNTs show high visible-light driven photoactivity for phenol degradation. • MPT/MWCNTs also show high reusable photoactivity under visible irradiation. • MPT content can control visible-light driven photoactivity of MPT/MWCNTs. • MPT is not easily broken away from from MPT/MWCNT composites. - Abstract: Mesoporous titania (MPT) was deposited onto multiwalled carbon nanotubes (MWCNTs) by deposition of titanium sol containing liquid-crystal template with assistant of supercritical CO{sub 2}. The products were characterized with various analytical techniques to determine their structural, morphological, optical absorption and photocatalytic properties. The results indicate that in photocatalytic degradation of phenol under visible light, the mixtures or composites of MPT and MWCNT show the high efficiency because of synergies between absorbing visible light, releasing electrons and facilitating transfer of charge carriers of MWCNTs and providing activated centers of MPT. Because of the mutual constraint between MPT and MWCNTs on the photocatalytic efficiency, the optimal loading of MPT in MPT/MWCNT-3 for phenol degradation is 48%. Because the intimate contact between MWCNTs and MPT is more beneficial to electron transformation, photoactivity of mixture is lower than that of composites with high reusable performance. The optimum conditions of phenol degradation were obtained.

36 MATERIALS SCIENCE↗
DOE OSTI2015

Photocatalytic activity of attapulgite–BiOCl–TiO{sub 2} toward degradation of methyl orange under UV and visible light irradiation

Highlights: • Excellent photocatalyst was obtained by introducing BiOCl–TiO{sub 2} onto attapulgite. • 100 mg L{sup −1} methyl orange (MO) was totally decomposed under UV light within 70 min. • 92.6% of 10 mg L{sup −1} MO was decomposed within 120 min under visible light. • ATT–BiOCl–TiO{sub 2} show better activity than P{sub 25} especially under visible light. • Mechanism of photocatalytic activity enhancement was identified. - Abstract: An environmental friendly composite photocatalyst with efficient UV and visible light activity has been synthesized by introducing BiOCl–TiO{sub 2} hybrid oxide onto the surface of attapulgite (ATT) (denoted as ATT–BiOCl–TiO{sub 2}), using a simple in situ depositing technique. The obtained products were characterized by XRD, TEM, BET and UV–vis diffuse reflectance spectra measurements. Results showed that BiOCl–TiO{sub 2} composite particles were successfully loaded onto attapulgite fibers' surface without obvious aggregation. The photocatalytic activity of ATT–BiOCl–TiO{sub 2} was investigated by degradation of methyl orange under UV and visible light irradiation. It was found that 100 mg L{sup −1} methyl orange was totally decomposed under UV light within 70 min and 92.57% of 10 mg L{sup −1} methyl orange was decomposed under visible light within 120 min using ATT–BiOCl–TiO{sub 2} as photocatalyst. These results were quite better than that of P{sub 25}, especially under visible light irradiation. Possible mechanism for the enhancement was proposed.

36 MATERIALS SCIENCE↗
DOE OSTI2015

Erbium and nitrogen co-doped SrTiO{sub 3} with highly visible light photocatalytic activity and stability by solvothermal synthesis

Highlights: • Er/N co-doped SrTiO{sub 3} was prepared by a solvothermal process at low temperature. • The co-doping induces the band gap narrowing and prominent absorbance in visible light region. • The samples show excellent catalytic activity and stability under visible light irradiation. - Abstract: Erbium–nitrogen co-doped SrTiO{sub 3} photocatalysts have been synthesized by a facile solvothermal method. The resulting samples were analyzed by FE-SEM, XRD, BET-surface area and UV–vis. The UV–vis absorption spectra of these powders indicated that erbium–nitrogen co-doped SrTiO{sub 3} possessed stronger absorption bands in the visible light region in comparison with that of pure SrTiO{sub 3}. The occurrence of the erbium–nitrogen co-doped cubic SrTiO{sub 3} induced the higher photocatalytic activities for the degradation of methyl orange (MO) under irradiation by ultraviolet light and visible light, respectively, being superior to that of pure SrTiO{sub 3} and commercial TiO{sub 2} (P-25) powders. In addition, the Er–N co-doped SrTiO{sub 3} (initial molar ratios of Sr/Er/N = 1:0.015:0.1, designated as S5) sample showed the best photocatalytic activity with the degradation rate as high as 98% after 30 min under the visible light irradiation. After five cycles, the photocatalytic activity of the S5 catalyst showed no significant decrease, which indicated that the photocatalysts were stable under visible light irradiation.

36 MATERIALS SCIENCE↗
DOE OSTI2015

Visible-light-induced blue MoO{sub 3}–C{sub 3}N{sub 4} composite with enhanced photocatalytic activity

Highlights: • Novel MoO{sub 3}–C{sub 3}N{sub 4} composite was prepared by a mixing-calcination method. • The MoO{sub 3}–C{sub 3}N{sub 4} composite shows remarkably enhanced absorption of visible light. • The MoO{sub 3}–C{sub 3}N{sub 4} composite shows superior visible-light photocatalytic activity. - Abstract: Composite photocatalyst of blue MoO{sub 3}/g-C{sub 3}N{sub 4} (denoted as MoO{sub 3}–C{sub 3}N{sub 4}) was prepared by a simple mixing-calcination method. The obtained MoO{sub 3}–C{sub 3}N{sub 4} composite contains a low amount of molybdenum blue and shows remarkably enhanced absorption of visible light and high efficiency for the degradation of methylene blue dye (MB) under visible light. The enhancement of visible light photocatalytic activity in MoO{sub 3}–C{sub 3}N{sub 4} is attributed to the synergetic effect: (i) the strong and wide absorption of visible light, (ii) the high separation and easy transfer of photogenerated electron–hole pairs at the heterojunction interfaces derived from the match of band position between the g-C{sub 3}N{sub 4} and MoO{sub 3}.

36 MATERIALS SCIENCE↗
DOE OSTI2017

Effective photocatalytic degradation of paracetamol using La-doped ZnO photocatalyst under visible light irradiation

Highlights: • La doping enhanced photocatalytic activity of ZnO under visible light irradiation. • The 1.0 wt% La-doped ZnO was optimal for enhancing photocatalytic activity. • 99% APAP was degraded and 85% TOC was removed under visible light irradiation. • A detail photodegradation pathways were proposed using identified intermediates. - Abstract: Visible light-driven photocatalysts of lanthanum (La) doped ZnO nanoparticles were successfully prepared by a facile precipitation method using various La doping concentrations (0.5, 1.0 and 1.5 wt%). La doping did not modify the crystallinity of ZnO significantly, but enhanced the optical absorption of visible light due to the reduction in particle size and band gap energy. La-doped ZnO photocatalysts were applied to treat 100 mg/L paracetamol in aqueous solution under visible light irradiation after 3 h. 1.0 wt% La-doped ZnO photocatalyst showed the highest photocatalytic activity for the degradation of paracetamol with a degradation efficiency of 99% and TOC removal of 85%. Based on the chemical analysis of photocatalytic products detected, proposed mechanism for paracetamol removal by La-doped ZnO nanoparticles under visible light illumination including radical generation with use of photocatalytic degradation and subsequent reaction pathways was proposed.

36 MATERIALS SCIENCE↗
DOE OSTI2017

Wafer-scale two-dimensional Au-TiO{sub 2} bilayer films for photocatalytic degradation of Palmitic acid under UV and visible light illumination

Highlights: • Successful wafer-scale atomic layer deposition of 2D Au-TiO{sub 2} bilayer photocatalyst films. • The efficient degradation of fatty acid by tailoring 2D TiO{sub 2} films under UV and visible light illumination. • Improved visible light photocatalytic activity and photocurrent density of 2D Au-TiO{sub 2} bilayer films. • Comparable photocatalytic performance of ultra-thin 2D TiO{sub 2} and thick TiO{sub 2} films under UV light illumination. - Abstract: Bilayer Au-TiO{sub 2} configuration with two-dimensional (2D) TiO{sub 2} films enabled sensible improvement in photocatalytic degradation of Palmitic Acid (PA) and also the enhancement of current density under visible light illumination. The improved visible light photocatalytic and photocurrent properties were attained when 35 nm thick 2D TiO{sub 2} film was developed by atomic layer deposition (ALD) on Si/SiO{sub 2}-Au substrate. The Au-TiO{sub 2} bilayer demonstrated the improved photocatalytic and photovoltaic performances compared with those TiO{sub 2} films developed on Si/SiO{sub 2} bare substrate. These improvements can be attributed to the plasmonic effects of Au film acting as antenna for visible light and also serving as hole acceptor during photocatalysis process. The proposed mechanisms for enhanced visible light performance of bilayer films are hot electron injection and the formation of hot spots at Au-TiO{sub 2} interface which contributed to the electron injection to conduction band of TiO{sub 2} or facilitated the separation of generated electron-hole pairs at Au-TiO{sub 2} Schottky junction.

36 MATERIALS SCIENCE↗
DOE OSTI2018

Solvent free solid-state synthesis of Pr6O11/g-C3N4 visible light active photocatalyst for degradation of AV7 dye

Highlights: • A new combination of Pr{sub 6}O{sub 11}/g-C{sub 3}N{sub 4} photocatalyst is synthesized by simple solvent free solid state method. • The photocatalytic activity of Pr{sub 6}O{sub 11}/g-C{sub 3}N{sub 4} is investigated by degradation of AV7 dye under visible light. • Improved performance is attributed to enhanced visible light absorption and efficient charge separation as evidenced by photoelectrochemical study. • Pr{sub 6}O{sub 11}/g-C{sub 3}N{sub 4} also exhibit super capacitance behavior. - Abstract: A new Pr{sub 6}O{sub 11}/g-C{sub 3}N{sub 4} heterostructure material has been prepared by single step solvent free solid state method for photocatalytic environmental cleaning application using visible light. The Pr{sub 6}O{sub 11}/g-C{sub 3}N{sub 4} heterostructure exhibits enhanced visible light absorption, resulting in improved photoelectrochemical properties and photocatalytic performance. The optimized composition of Pr{sub 6}O{sub 11}/g-C{sub 3}N{sub 4} composite shows improved degradation kinetics and completely degrades AV7 dye within 20 min of visible light irradiation. Photoluminescence and electrochemical studies suggest better separation of photogenerated charge carriers in the composite compared to single phase materials. This is further substantiated by the improved photocurrent response of the composite. The notable increase of photocatalytic activity of Pr{sub 6}O{sub 11}/g-C{sub 3}N{sub 4} heterostructure is ascribed to the improved visible light absorption, reduced band gap and better separation of photogenerated electrons and holes. To the best of our knowledge, this new heterostructure photocatalyst is found to be more efficient for the degradation of AV7 dye compared to the systems reported so far.

36 MATERIALS SCIENCE↗
DOE OSTI2013

Quantification of UV-Visible and Laser Spectroscopic Techniques for Materials Accountability and Process Control

Ultraviolet–visible spectroscopy (UV–Visible) and time-resolved laser fluorescence spectroscopy (TRLFS) optical techniques can permit on-line analysis of actinide elements in a solvent extraction process in real time. These techniques have been used for measuring actinide speciation and concentration under laboratory conditions and are easily adaptable to multiple sampling geometries, such as dip probes, fiber-optic sample cells, and flow-through cell geometries. To fully exploit these techniques, researchers must determine the fundamental speciation of target actinides and the resulting influence on spectroscopic properties. Detection limits, process conditions, and speciation of key actinide components can be established and utilized in a range of areas, particularly those related to materials accountability and process control. Through this project, researchers will develop tools and spectroscopic techniques to evaluate solution extraction conditions and concentrations of U, Pu, and Cm in extraction processes, addressing areas of process control and materials accountability. The team will evaluate UV– Visible and TRLFS for use in solvent extraction-based separations. Ongoing research is examining efficacy of UV-Visible spectroscopy to evaluate uranium and plutonium speciation under conditions found in the UREX process and using TRLFS to evaluate Cm speciation and concentration in the TALSPEAK process. A uranyl and plutonium nitrate UV–Visible spectroscopy study met with success, which supports the utility and continued exploration of spectroscopic methods for evaluation of actinide concentrations and solution conditions for other aspects of the UREX+ solvent extraction scheme. This project will examine U and Pu absorbance in TRUEX and TALSPEAK, perform detailed examination of Cm in TRUEX and TALSPEAK, study U laser fluorescence, and apply project data to contactors. The team will also determine peak ratios as a function of solution concentrations for the UV-Visible spectroscopy studies. The use of TRLFS to examine Cm and U will provide data to evaluate lifetime, peak location, and peak ratios (mainly for U). The bases for the spectroscopic techniques have been investigated, providing fundamental evidence for the application’s utility.

11 NUCLEAR FUEL CYCLE AND FUEL MATERIALS↗
DOE OSTI2013

Enhanced performance of dye-sensitized solar cells based on TiO{sub 2} with NIR-absorption and visible upconversion luminescence

TiO{sub 2} with NIR-absorption and visible upconversion luminescence (UC-TiO{sub 2}) is prepared by a sol-gel method and calcined at 700 Degree-Sign C for 6 h. The material broadens the response region of dye sensitized solar cells (DSSCs) from an ultraviolet-visible region to the whole region of the solar spectrum. It shifts NIR sunlight to visible light which matches the strong absorbing region of the dye (N719). DSSCs based on UC-TiO{sub 2} achieved higher conversion efficiency than that on raw TiO{sub 2}. UC-TiO{sub 2} was mixed with commercial raw TiO{sub 2} as additive, and the short-circuit current density, open-circuit voltage and conversion efficiency of the DSSC reached to the optimum values 13.38 mA/cm{sup 2}, 0.78 V and 6.63% (AM1.5 global), comparing with the blank values: 7.99 mA/cm{sup 2}, 0.75 V and 4.07%, respectively. Also the mechanisms of upconversion by multiphoton absorption and energy transfer processes are interpreted in this paper. - Graphical abstract: By introducing TiO{sub 2} with NIR-absorption and visible up-conversion luminescence into DSSC, a signal reflection was explored from ultra-violet region to visible region, and to near-IR region. Highlights: Black-Right-Pointing-Pointer TiO{sub 2} with NIR-absorption and visible up-conversion luminescence (UC-TiO{sub 2}) was prepared by a sol-gel method. Black-Right-Pointing-Pointer A systematic characterization and analysis was carried out to discuss the mechanism. Black-Right-Pointing-Pointer A significantly enhanced performance of DSSC was explored by using UC-TiO{sub 2} as an additive.

36 MATERIALS SCIENCE↗
DOE OSTI2015

Nitrogen-modified nano-titania: True phase composition, microstructure and visible-light induced photocatalytic NO{sub x} abatement

Titanium dioxide (TiO{sub 2}) is a popular photocatalyst used for many environmental and anti-pollution applications, but it normally operates under UV light, exploiting ∼5% of the solar spectrum. Nitrification of titania to form N-doped TiO{sub 2} has been explored as a way to increase its photocatalytic activity under visible light, and anionic doping is a promising method to enable TiO{sub 2} to harvest visible-light by changing its photo-absorption properties. In this paper, we explore the insertion of nitrogen into the TiO{sub 2} lattice using our green sol–gel nanosynthesis method, used to create 10 nm TiO{sub 2} NPs. Two parallel routes were studied to produce nitrogen-modified TiO{sub 2} nanoparticles (NPs), using HNO{sub 3}+NH{sub 3} (acid-precipitated base-peptised) and NH{sub 4}OH (totally base catalysed) as nitrogen sources. These NPs were thermally treated between 450 and 800 °C. Their true phase composition (crystalline and amorphous phases), as well as their micro-/nanostructure (crystalline domain shape, size and size distribution, edge and screw dislocation density) was fully characterised through advanced X-ray methods (Rietveld-reference intensity ratio, RIR, and whole powder pattern modelling, WPPM). As pollutants, nitrogen oxides (NO{sub x}) are of particular concern for human health, so the photocatalytic activity of the NPs was assessed by monitoring NO{sub x} abatement, using both solar and white-light (indoor artificial lighting), simulating outdoor and indoor environments, respectively. Results showed that the onset of the anatase-to-rutile phase transformation (ART) occurred at temperatures above 450 °C, and NPs heated to 450 °C possessed excellent photocatalytic activity (PCA) under visible white-light (indoor artificial lighting), with a PCA double than that of the standard P25 TiO{sub 2} NPs. However, higher thermal treatment temperatures were found to be detrimental for visible-light photocatalytic activity, due to the effects of four simultaneous occurrences: (i) loss of OH groups and water adsorbed on the photocatalyst surface; (ii) growth of crystalline domain sizes with decrease in specific surface area; (iii) onset and progress of the ART; (iv) the increasing instability of the nitrogen in the titania lattice. - Graphical abstract: Nitrogen modified TiO{sub 2} synthesised via a green aqueous sol–gel method showed to degrade nitrogen oxides (NO{sub x}) under visible white-light (indoor artificial lighting), with a photocatalytic activity double than that of the standard P25 TiO{sub 2} NPs. - Highlights: • N–TiO{sub 2} synthesised via a green aqueous sol–gel method. • Advanced X-ray methods used to detect both crystalline and amorphous contents. • Microstructure fully addressed via XRPD and whole powder pattern modelling. • Photocatalytic NO{sub x} removal assessed using both solar and visible-light lamps.

36 MATERIALS SCIENCE↗
DOE OSTI2012

Synthesis and photocatalytic activity of mesoporous cerium doped TiO{sub 2} as visible light sensitive photocatalyst

Graphical abstract: Cerium doped titania having optimum 5 wt% of cerium can decompose methylene blue and reduce selenium (IV) efficiently under visible light. Highlights: Black-Right-Pointing-Pointer Effect of cerium doping on the surface properties and visible light mediated photocatalytic reaction is studied. Black-Right-Pointing-Pointer Cerium doping increases the anatase phase stability, surface area (up to 137 m{sup 2}/g) and visible light absorption. Black-Right-Pointing-Pointer Importance of Ce{sup 3+}/Ce{sup 4+}, oxygen vacancy, surface area and crystallinity is correlated with improved catalytic activity. Black-Right-Pointing-Pointer Material with 5 wt% Ce is found to be most active photocatalyst for methylene blue decomposition and Se (IV) reduction. -- Abstract: Cerium doped titania materials were synthesized varying the cerium concentration from 0 to 10 wt%. Materials are characterised by XRD, TEM, XPS and N{sub 2} adsorption desorption method. Surface area and visible light absorption substantially increases and crystallite size decreases with the increasing cerium content. Cerium doping stabilizes the anatase phase and surface area even at 600 Degree-Sign C calcination. Photocatalytic activity towards methylene blue decomposition and selenium (IV) reduction is found to increase with the cerium content up to 5 wt% and then decreases. Materials calcined at 600 Degree-Sign C shows better activity than that calcined at 400 Degree-Sign C, even though surface area decreases. Anatase crystallinity mostly decides the photocatalytic activity rather than only surface area. It can be concluded that the optimum visible light absorption and oxygen vacancy with 5% cerium doping enhances the photocatalytic activity. In addition photocatalytic performance is found to depend on the presence of Ce{sup 4+}/Ce{sup 3+} rather than only visible light absorption.

36 MATERIALS SCIENCE↗
DOE OSTI2013

Ag{sub 3}PO{sub 4}/ZnO: An efficient visible-light-sensitized composite with its application in photocatalytic degradation of Rhodamine B

Graphical abstract: The free OH radicals generated in the VB of ZnO play the primary role in the visible-light photocatalytic degradation of RhB in Ag{sub 3}PO{sub 4}/ZnO system. The accumulated electrons in the CB of Ag{sub 3}PO{sub 4} can be transferred to O{sub 2} adsorbed on the surface of the composite semiconductors and H{sub 2}O{sub 2} yields. H{sub 2}O{sub 2} reacts with electrons in succession to produce active ·OH to some extent. Display Omitted Highlights: ► Efficient visible-light-sensitized Ag{sub 3}PO{sub 4}/ZnO composites were successfully prepared. ► Effect of Ag{sub 3}PO{sub 4} content on the catalytic activity of Ag{sub 3}PO{sub 4}/ZnO is studied in detail. ► Rate constant of RhB degradation over Ag{sub 3}PO{sub 4}(3.0 wt.%)/ZnO is 3 times that of Ag{sub 3}PO{sub 4}. ► The active species in RhB degradation are examined by adding a series of scavengers. ► Visible light degradation mechanism of RhB over Ag{sub 3}PO{sub 4}/ZnO is systematically studied. -- Abstract: The efficient visible-light-sensitized Ag{sub 3}PO{sub 4}/ZnO composites with various weight percents of Ag{sub 3}PO{sub 4} were prepared by a facile ball milling method. The photocatalysts were characterized by XRD, DRS, SEM, EDS, XPS, and BET specific area. The ·OH radicals produced during the photocatalytic reaction was detected by the TA–PL technique. The photocatalytic property of Ag{sub 3}PO{sub 4}/ZnO was evaluated by photocatalytic degradation of Rhodamine B under visible light irradiation. Significantly, the results revealed that the photocatalytic activity of the composites was much higher than that of pure Ag{sub 3}PO{sub 4} and ZnO. The rate constant of RhB degradation over Ag{sub 3}PO{sub 4}(3.0 wt.%)/ZnO is 3 times that of single-phase Ag{sub 3}PO{sub 4}. The optimal percentage of Ag{sub 3}PO{sub 4} in the composite is 3.0 wt.%. It is proposed that the ·OH radicals produced in the valence band of ZnO play the leading role in the photocatalytic degradation of Rhodamine B by Ag{sub 3}PO{sub 4}/ZnO systems under visible light irradiation.

36 MATERIALS SCIENCE↗
DOE OSTI2013

Ag@AgHPW as a plasmonic catalyst for visible-light photocatalytic degradation of environmentally harmful organic pollutants

Graphical abstract: Ag@Ag{sub x}H{sub 3−x}PW12O40 (Ag@AgHPW) nanoparticles (NPs), a new visible-light driven plasmonic photocatalyst, are prepared by a green photoreduction strategy without the addition of any surfactant, which show a high activity and stability for the degradation of methyl blue (MB) under visible light irradiation. - Highlights: • A new visible-light driven photocatalyst Ag@Ag{sub x}H{sub 3−x}PW{sub 12}O{sub 40} was designed. • The photocatalyst shows a high activity for the degradation of methyl blue. • The high activity can be ascribed to the synergy of photoexcited AgHPW and Ag. - Abstract: Ag@Ag{sub x}H{sub 3−x}PW{sub 12}O{sub 40} (Ag@AgHPW) nanoparticles (NPs), a new visible-light driven plasmonic photocatalyst, are prepared by a green photoreduction strategy without the addition of any surfactant. They show strong absorption in the visible region because of the localized surface plasmon resonance (LSPR) of Ag NPs. This plasmonic photocatalyst shows a high activity and stability for the degradation of methyl blue (MB) under visible light irradiation, which could be attributed to the highly synergy of photoexcited Ag{sub x}H{sub 3−x}PW{sub 12}O{sub 40} (AgHPW) and plasmon-excited Ag NPs and the confinement effects at interfaces between polyoxometalates (POMs) and silver. POM anions have redox ability and high photocatalytic activity, whereas Ag NPs could effectively accelerate the separation of electrons and holes, both of which contribute to their high activity.

36 MATERIALS SCIENCE↗
DOE OSTI2024

A Full Accounting of the Visible Mass in SDSS MaNGA Disk Galaxies

We present a study of the ratio of visible mass to total mass in spiral galaxies to better understand the relative amount of dark matter present in galaxies of different masses and evolutionary stages. Using the velocities of the Hα emission line measured in spectroscopic observations from the Sloan Digital Sky Survey (SDSS) MaNGA Data Release 17 (DR 17), we evaluate the rotational velocity of over 5500 disk galaxies at their 90% elliptical Petrosian radii, R 90 . We compare this to the velocity expected from the total visible mass, which we compute from the stellar, H i, H 2 , and heavy metals and dust masses. H 2 mass measurements are available for only a small subset of galaxies observed in SDSS MaNGA DR17, so we derive a parameterization of the H 2 mass as a function of absolute magnitude in the r band using galaxies observed as part of SDSS DR7. With these parameterizations, we calculate the fraction of visible mass within R 90 that corresponds to the observed velocity. Based on statistically analyzing the likelihood of this fraction, we conclude that the null hypothesis (no dark matter) cannot be excluded at a confidence level better than 95% within the visible extent of the disk galaxies. We also find that when all mass components are included, the ratio of visible to total mass within the visible extent of star-forming disk galaxies increases with galaxy luminosity.

79 ASTRONOMY AND ASTROPHYSICS↗