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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↗

DOE OSTI2017

Biomass burning aerosols and the low-visibility events in Southeast Asia

Abstract. Fires including peatland burning in Southeast Asia have become a major concern to the general public as well as governments in the region. This is because aerosols emitted from such fires can cause persistent haze events under certain weather conditions in downwind locations, degrading visibility and causing human health issues. In order to improve our understanding of the spatiotemporal coverage and influence of biomass burning aerosols in Southeast Asia, we have used surface visibility and particulate matter concentration observations, supplemented by decade-long (2003 to 2014) simulations using the Weather Research and Forecasting (WRF) model with a fire aerosol module, driven by high-resolution biomass burning emission inventories. We find that in the past decade, fire aerosols are responsible for nearly all events with very low visibility (< 7 km). Fire aerosols alone are also responsible for a substantial fraction of low-visibility events (visibility < 10 km) in the major metropolitan areas of Southeast Asia: up to 39 % in Bangkok, 36 % in Kuala Lumpur, and 34 % in Singapore. Biomass burning in mainland Southeast Asia accounts for the largest contribution to total fire-produced PM2.5 in Bangkok (99 %), while biomass burning in Sumatra is a major contributor to fire-produced PM2.5 in Kuala Lumpur (50 %) and Singapore (41 %). To examine the general situation across the region, we have further defined and derived a new integrated metric for 50 cities of the Association of Southeast Asian Nations (ASEAN): the haze exposure day (HED), which measures the annual exposure days of these cities to low visibility (< 10 km) caused by particulate matter pollution. It is shown that HEDs have increased steadily in the past decade across cities with both high and low populations. Fire events alone are found to be responsible for up to about half of the total HEDs. Our results suggest that in order to improve the overall air quality in Southeast Asia, mitigation policies targeting both biomass burning and fossil fuel burning sources need to be implemented.

09 BIOMASS FUELS↗

NASA NTRS1992

Sea surface velocities from visible and infrared multispectral atmospheric mapping sensor imagery

High resolution (100 m), sequential Multispectral Atmospheric Mapping Sensor (MAMS) images were used in a study to calculate advective surface velocities using the Maximum Cross Correlation (MCC) technique. Radiance and brightness temperature gradient magnitude images were formed from visible (0.48 microns) and infrared (11.12 microns) image pairs, respectively, of Chandeleur Sound, which is a shallow body of water northeast of the Mississippi delta, at 145546 GMT and 170701 GMT on 30 Mar. 1989. The gradient magnitude images enhanced the surface water feature boundaries, and a lower cutoff on the gradient magnitudes calculated allowed the undesirable sunglare and backscatter gradients in the visible images, and the water vapor absorption gradients in the infrared images, to be reduced in strength. Requiring high (greater than 0.4) maximum cross correlation coefficients and spatial coherence of the vector field aided in the selection of an optimal template size of 10 x 10 pixels (first image) and search limit of 20 pixels (second image) to use in the MCC technique. Use of these optimum input parameters to the MCC algorithm, and high correlation and spatial coherence filtering of the resulting velocity field from the MCC calculation yielded a clustered velocity distribution over the visible and infrared gradient images. The velocity field calculated from the visible gradient image pair agreed well with a subjective analysis of the motion, but the velocity field from the infrared gradient image pair did not. This was attributed to the changing shapes of the gradient features, their nonuniqueness, and large displacements relative to the mean distance between them. These problems implied a lower repeat time for the imagery was needed in order to improve the velocity field derived from gradient imagery. Suggestions are given for optimizing the repeat time of sequential imagery when using the MCC method for motion studies. Applying the MCC method to the infrared brightness temperature imagery yielded a velocity field which did agree with the subjective analysis of the motion and that derived from the visible gradient imagery. Differences between the visible and infrared derived velocities were 14.9 cm/s in speed and 56.7 degrees in direction. Both of these velocity fields also agreed well with the motion expected from considerations of the ocean bottom topography and wind and tidal forcing in the study area during the 2.175 hour time interval.

Pope, P. A.↗

NASA NTRS2003

Large-Diameter Visible and Buried Impact Basins on Mars: Implications for Age of the Highlands and (Buried) Lowlands and Turn-Off of the Global Magnetic Field

The global populations of visible and buried impact basins greater than 200 km diameter revealed by high resolution gridded MOLA indicate: (a) a small (approximately 10) number of very large basins (D=1300-3000km), most of which have remained visible over martian history; (b) a much larger population of smaller basins (D=200-800 km) with many more buried than visible (on images); (c) a depletion of visible basins at intermediate diameters which may be a signature of some global-scale event (formation of the lowlands? origin of Tharsis?); and (d) a crater retention age for the buried lowlands greater than that of the visible highlands but less than that of the total (visible + buried) highlands. Crustal magnetic anomalies are generally not present in the interiors of the largest basins with two exceptions: these two (which appear to be the oldest) may predate the demise of the global magnetic field.

Frey, H. V.↗

NASA NTRS2003

Large-Diameter Visible and Buried Impact Basins on Mars: Implications for age of the Highlands and (Buried) Lowlands and Turn-off of the Global Magnetic Field

The global populations of visible and buried impact basins less than 200 km diameter revealed by high resolution gridded MOLA indicate: (a) a small (approx. 10) number of very large basins (D=1300-3000km), most of which have remained visible over martian history; (b) a much larger population of smaller basins (D=200-800 km) with many more buried than visible (on images); (c) a depletion of visible basins at intermediate diameters which may be a signature of some global-scale event (formation of the lowlands? origin of Tharsis?); and (d) a crater retention age for the buried lowlands greater than that of the visible highlands but less than that of the total (visible + buried) highlands. Crustal magnetic anomalies are generally not present in the interiors of the largest basins with two exceptions: these two (which appear to be the oldest) may predate the demise of the global magnetic field.

Frey, Herbert V.↗

NASA NTRS2011

Development and Progress in Enabling the Photocatalyst Ti02 Visible-Light-Active

Photocatalytic oxidation (PCO) of organic contaminants is a promising air and water quality management approach which offers energy and cost savings compared to thermal catalytic oxidation (TCO). The most widely used photocatalyst, anatase TiO2, has a wide band gap (3.2 eV) and is activated by UV photons. Since solar radiation consists of less than 4% UV, but contains 45% visible light, catalysts capable of utilizing these visible photons need to be developed to make peo approaches more efficient, economical, and safe. Researchers have attempted various approaches to enable TiO2 to be visible-light-active with varied degrees of success'. Strategies attempted thus far fall into three categories based on their electrochemical' mechanisms: 1) narrowing the band gap of TiO2 by implantation of transition metal elements or nonmetal elements such as N, S, and C, 2) modifying electron-transfer processes during PCO by adsorbing sensitizing dyes, and 3) employing light-induced interfacial electron transfer in the heteronanojunction systems consisting of narrow band gap semiconductors represented by metal sulfides and TiO2. There are diverse technical approaches to implement each of these strategies. This paper presents a review of these approaches and results of the photocatalytic activity and photonic efficiency of the end .products under visible light. Although resulting visible-light-active (VLA) photocatalysts show promise, there is often no comparison with unmodified TiO2 under UV. In a limited number of studies where such comparison was provided, the UV-induced catalytic activity of bare TiO2 is much greater than the visible-light-induced catalytic activity of the VLA catalyst. Furthermore, VLA-catalysts have much lower quantum efficiency compared to the approx.50% quantum efficiency of UV-catalysts. This stresses the need for continuing research in this area.

Levine, Lanfang H.↗

NASA NTRS2022

Secondary Inorganic Aerosol Chemistry and Its Impact on Atmospheric Visibility Over an Ammonia-Rich Urban Area in Central Taiwan

This study investigated the hourly inorganic aerosol chemistry and its impact on atmospheric visibility over an urban area in Central Taiwan, by relying on measurements of aerosol light extinction, inorganic gases, and PM 2.5 water-soluble ions (WSIs), and simulations from a thermodynamic equilibrium model. On average, the sulfate (SO 4 2− ), nitrate (NO 3 − ), and ammonium (NH 4 + ) components (SNA) contributed ∼90% of WSI concentrations, which in turn made up about 50% of the PM 2.5 mass. During the entire observation period, PM 2.5 and SNA concentrations, aerosol pH, aerosol liquid water content (ALWC), and sulfur and nitrogen conversion ratios all increased with decreasing visibility. In particular, the NO 3 − contribution to PM 2.5 increased, whereas the SO 4 2− contribution decreased, with decreasing visibility. The diurnal variations of the above parameters indicate that the interaction and likely mutual promotion between NO 3 − and ALWC enhanced the hygroscopicity and aqueous-phase reactions conducive for NO 3 − formation, thus led to severely impaired visibility. The high relative humidity (RH) at the study area (average 70.7%) was a necessary but not sole factor leading to enhanced NO 3 − formation, which was more directly associated with elevated ALWC and aerosol pH. Simulations from the thermodynamic model depict that the inorganic aerosol system in the study area was characterized by fully neutralized SO 4 2− (i.e. a saturated factor in visibility reduction) and excess NH 4 + amidst a NH 3 -rich environment. As a result, PM 2.5 composition was most sensitive to gas-phase HNO 3 , and hence NOx, and relatively insensitive to NH 3 . Consequently, a reduction of NOx would result in instantaneous cuts of NO 3 − , PM 2.5 , and ALWC, and hence improved visibility. On the other hand, a substantial amount of NH 3 reduction (>70%) would be required to lower the aerosol pH, driving more than 50% of the particulate phase NO 3 − to the gas phase, thereby making NH 3 a limiting factor in shifting PM 2.5 composition.

aerosol chemistry↗

DOE OSTI2012

Sn-doped polyhedral In{sub 2}O{sub 3} particles: Synthesis, characterization, and origins of luminous emission in wide visible range

Sn-doped octahedronal and tetrakaidecahedronal In{sub 2}O{sub 3} particles were successfully synthesized by simple thermal evaporation of indium grains using SnO as dopant. Structural characterization results demonstrated that the Sn-doped tetrakaidecahedronal In{sub 2}O{sub 3} particle had additional six {l_brace}001{r_brace} crystal surfaces compared with the octahedronal one. The luminous properties of both samples were characterized by photoluminescence (PL) and cathodoluminescence (CL) spectroscopy. A broad visible luminous emission around 570 nm was observed. Studies revealed that the emission consisted of three peaks of 511 nm, 564 nm, and 622 nm, which were attributed to radioactive recombination centers such as single ionized oxygen vacancy, indium interstitial, and antisite oxygen, respectively. We believe that the Sn donor level plays an important role in the visible luminous emission. - Graphical abstract: With more oxygen vacancies and tin doping. ITO particles can exhibit a better CL performance. Sn donor level near the conduction band edge plays an important role in luminous emission in wide visible range. Highlights: Black-Right-Pointing-Pointer Polyhedral ITO particles synthesized by thermal evaporation using SnO as dopant. Black-Right-Pointing-Pointer Broad visible luminous emission around 570 nm. Black-Right-Pointing-Pointer Sn donor level plays an important role in the visible emission. Black-Right-Pointing-Pointer ITO particles with more oxygen vacancies have better CL performance in visible range.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

DOE OSTI2015

One-pot synthesis of copper-doped graphitic carbon nitride nanosheet by heating Cu–melamine supramolecular network and its enhanced visible-light-driven photocatalysis

Here we report a novel synthetic pathway for preparation of Cu-doped g-C{sub 3}N{sub 4} (Cu-g-C{sub 3}N{sub 4}) with nanosheet morphology by using a two dimensional Cu–melamine supramolecular network as both sacrificial template and precursor. The specific surface area of Cu-g-C{sub 3}N{sub 4} is 40.86 m{sup 2} g{sup −1}, which is more than 7 times larger than that of pure g-C{sub 3}N{sub 4}. Cu-g-C{sub 3}N{sub 4} showed strong optical absorption in the visible-light region and expanded the absorption to the near-infrared region. The uniform nanosheet morphology, higher surface area and strong visible-light absorption have enabled Cu-g-C{sub 3}N{sub 4} exhibiting enhanced visible light photocatalytic activity for the photo-degradation of methylene blue (MB). The results indicate that metal–melamine supramolecular network can be promising precursors for the one step preparation of efficient metal-doped g-C{sub 3}N{sub 4} photocatalysts. - Graphical abstract: Cu-doped g-C{sub 3}N{sub 4} (Cu-g-C{sub 3}N{sub 4}) with nanosheet morphology was fabricated via a simple one step preparation by using a two dimensional Cu–melamine supra-molecular network as both sacrificial template and precursor. - Highlights: • Cu-doped g-C{sub 3}N{sub 4} (Cu-g-C{sub 3}N{sub 4}) with nanosheet morphology was prepared. • Cu-g-C{sub 3}N{sub 4} showed strong optical absorption in the visible-light region. • Cu-g-C{sub 3}N{sub 4} exhibits enhanced visible light photocatalytic activity.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

DOE OSTI2018

Eco-friendly and effective strategy to synthesize ZnO/Ag{sub 2}O heterostructures and its excellent photocatalytic property under visible light

Highlights: • ZnO/Ag{sub 2}O photocatalysts with heterostructures were synthesized via a facile mechanochemical method. • The synthetic process does not involve any organic solvents and the reaction matrix can be recycled easily. • The synthetic method is gram-scale, and we can easily and routinely scale up this process to produce grams of the heterostructure nanomaterials. • The as-prepared samples without post-calcination show a high degree of crystallinity. - Abstract: ZnO/Ag{sub 2}O photocatalysts with heterostructure were synthesized by a green and effective mechanochemical method. The preparation process was taken in solid state at room temperature with a short grinding time. The as-made products showed a high degree of crystallinity without post-calcination treatment. Such synthetic method does not involve any organic solvents and the reaction matrix can be recycled. The as-prepared ZnO/Ag{sub 2}O samples show excellent photocatalytic activity and photostability for degradation of different organic dyes under visible light. The content of Ag{sub 2}O plays an important role in the photocatalytic activity, which can be tuned by the precursor AgNO{sub 3}. The photodegradation rate constant (k) of the optimal ZnO/Ag{sub 2}O sample under visible light is nearly 0.1004 min{sup −1} for methylene blue (MB), 0.063 min{sup −1} for rhodamine B (RHB) and 0.07 min{sup −1} for methyl orange (MO), which are much better than the pure ZnO (0.0075 min{sup −1}). The enhancement of the visible light photocatalytic activity could be attributed to the heterojunction interfaces induced by the match of crystal lattice and energy band between the Ag{sub 2}O and ZnO. The Ag{sub 2}O generates the excited-state electrons under visible light irradiation. The excited electrons on Ag{sub 2}O could directly transfer to the conduction band (CB) of ZnO, making ZnO/Ag{sub 2}O present remarkable visible light photocatalytic activity.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

DOE OSTI2013

Enhancement of methanol electrocatalytic oxidation on platinized WO{sub 3}–TiO{sub 2} composite electrode under visible light irradiation

Highlights: ► A ternary composite catalyst of Pt–WO{sub 3}–TiO{sub 2} has been synthesized. ► The introduction of WO{sub 3} extends its absorption edge to visible light region. ► The electrode displays high electrocatalytic activity. ► With visible light irradiation, its electrocatalytic activity increases 70%. - Abstract: A ternary composite catalyst of Pt–WO{sub 3}–TiO{sub 2} has been successfully prepared by a chemical method. The prepared composite was systematically characterized by UV–vis diffuse reflectance absorption spectra (DRS), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), and transmission electron microscopy (TEM). The electrocatalytic properties of Pt–WO{sub 3}–TiO{sub 2} for methanol oxidation in an alkaline medium were evaluated by the cyclic voltammetry (CV) and chronoamperometry (CA) with or without visible light irradiation. Compared with the pure TiO{sub 2}, the introduction of WO{sub 3} extends its absorption edge to visible light region. Under visible light illumination, the Pt–WO{sub 3}–TiO{sub 2} composite catalyst exhibits higher electrocatalytic activity toward methanol oxidation in comparison with its counterpart, the pure Pt–TiO{sub 2} catalyst.

36 MATERIALS SCIENCE↗

DOE OSTI2013

Photocatalytic degradation of pentachlorophenol in aqueous solution by visible light sensitive N-F-codoped TiO{sub 2} photocatalyst

Graphical abstract: Schematic representation for the visible light photocatalytic process of N and F codoped TiO{sub 2}. Highlights: ► Visible light sensitive N-F-codoped TiO{sub 2}. ► Photocatalytic degradation of pentachlorophenol. ► Effect of oxidants on photocatalytic degradation of pentachlorophenol. ► PMS is a more efficient oxidant for the photodegradation of PCP. - Abstract: In this present study, N-F-codoped titanium dioxide nanocatalyst (NFTO) has been synthesized by simple sol–gel assisted solvothermal method for the effective utilization of visible light in photocatalytic reactions. Structural characterization of the photocatalyst is analyzed by XRD, UV–vis diffuse reflectance spectra (DRS), SEM and TEM. Moreover the chemical statuses of NFTO are gathered by X-ray photoelectron spectroscopy (XPS). The results show that a high surface area with photoactive anatase phase crystalline is obtained. In addition, nitrogen and fluorine atoms are doped into TiO{sub 2} crystal lattice to extend the visible light absorption and higher photocatalytic activity. The photocatalytic degradation of pentachlorophenol in aqueous solution is examined under visible light irradiation, the addition of oxidants such as PMS, PDS and H{sub 2}O{sub 2} is analyzed in detail. The rate of photocatalytic degradation of pentachlorophenol is obtained in the following order: PMS > PDS > H{sub 2}O{sub 2}.

36 MATERIALS SCIENCE↗

DOE OSTI2014

Synthesis and characterization of g-C{sub 3}N{sub 4}/Cu{sub 2}O composite catalyst with enhanced photocatalytic activity under visible light irradiation

The prepared g-C{sub 3}N{sub 4}/Cu{sub 2}O composite exhibited the enhanced photocatalytic activity under visible-light irradiation due to the stronger ability in separation of electron–hole pairs, which was proven by the transient photocurrent measurement. - Highlights: • The coupled Cu{sub 2}O with g-C{sub 3}N{sub 4} of narrow-band-gap semiconductor has been designed. • g-C{sub 3}N{sub 4}/Cu{sub 2}O is prepared via an alcohol-aqueous based on chemical precipitation method. • g-C{sub 3}N{sub 4}/Cu{sub 2}O exhibits the enhanced photocatalytic activity under visible-light. • The enhanced photocatalytic activity is proven by the transient photocurrent test. • A mechanism for the visible-light-driven photocatalysis of g-C{sub 3}N{sub 4}/Cu{sub 2}O is revealed. - Abstract: To overcome the drawback of low photocatalytic efficiency brought by electron–hole pairs recombination and narrow photo-response range, a novel g-C{sub 3}N{sub 4}/Cu{sub 2}O composite photocatalyst was designed and prepared successfully. Compared with bare Cu{sub 2}O and g-C{sub 3}N{sub 4}, the g-C{sub 3}N{sub 4}/Cu{sub 2}O composite exhibited significantly enhanced photocatalytic activity for acid orange-II (AO-II) degradation under visible light irradiation. Based on energy band positions, the mechanism of enhanced visible-light photocatalytic activity was proposed.

36 MATERIALS SCIENCE↗

DOE OSTI2016

Magnetically separable core–shell ZnFe{sub 2}O{sub 4}@ZnO nanoparticles for visible light photodegradation of methyl orange

Highlights: • Phase pure, magnetic ZnFe{sub 2}O{sub 4}@ZnO nanoparticles synthesized with excellent yield. • ZnFe{sub 2}O{sub 4}@ZnO displayed higher UV photocatalytic efficiency than ZnO nanoparticles. • First report on visible light photodegradation of methyl orange by ZnFe{sub 2}O{sub 4}@ZnO. • Excellent reusability of ZnFe{sub 2}O{sub 4}@ZnO nanoparticles observed for azo dye removal. - Abstract: Visible light photodegradation of aqueous methyl orange using magnetically separable core–shell ZnFe{sub 2}O{sub 4}@ZnO nanoparticles is reported. A combination of low temperature (190 °C) microwave synthesis and hydrothermal method were used to prepare phase pure material with excellent yield (95%). The magnetic separability, surface area of 41 m{sup 2}/g and visible light absorption make ZnFe{sub 2}O{sub 4}@ZnO nanoparticles a good solar photocatalyst. ZnFe{sub 2}O{sub 4}@ZnO displayed greater UV photocatalytic efficiency than ZnO owing to the generation of large number of electron-hole pairs. Visible light photodegradation of MO using ZnFe{sub 2}O{sub 4}@ZnO nanoparticles is reported for the first time. Higher first order rate constants under both UV and visible light for core-shell nanoparticles suggested their superiority over its individual oxides. The ZnFe{sub 2}O{sub 4}@ZnO showed excellent reusability with high photocatalytic efficiencies suggesting its suitability for solar photocatalytic applications.

36 MATERIALS SCIENCE↗

DOE OSTI2017

Remarkable improvement of visible light photocatalytic activity of TiO{sub 2} nanotubes doped sequentially with noble metals for removing of organic and microbial pollutants

Highlights: • Ordered TiO{sub 2} nanotubes (NTs) were synthesized using anodic oxidation. • TiO{sub 2} NTs were modified with Ag and Au NPs that settled separately to widen visible absorption. • TiO{sub 2} NTs modified with Ag and Au NPs is superior visible light photocatalyst. • TiO{sub 2} NTs modified with Ag and Au NPs shows superior antibacterial activity. • Annealing temperature played important role in photocatalytic activity of TiO{sub 2} NTs. - Abstract: The aim of this study was to show that Ag and Au nanoparticles (NPs) can have a synergistic effect on the photocatalytic and antibacterial activity of TiO{sub 2} nanotubes (NTs) under visible irradiation. TiO{sub 2} NTs were grown on Ti substrate by anodic oxidation and modified with Ag and Au NPs by dip coating and sputtering methods, respectively. The spherical 5–20 nm Ag and Au NPs were deposited on TiO{sub 2} NTs with diameter of 50–80 nm. In contrast to obtained results under UV irradiation, visible-light absorption range and visible photocatalytic activity of Ag and Au co-modified TiO{sub 2} NTs were much higher than TiO{sub 2} NTs without modification and TiO{sub 2} NTs modified with monometallic NPs. Photocatalytic activity of modified TiO{sub 2} NTs increased with increasing annealing temperature and appearing rutile phase. Antibacterial activity of Ag and Au-comodified TiO{sub 2} NTs against E. coli was noticeably more than that of TiO{sub 2} NTs modified with monometallic NPs.

36 MATERIALS SCIENCE↗

DOE OSTI2018

Integration of Ag2WO4 and AgBr with TiO2 to fabricate ternary nanocomposites: Novel plasmonic photocatalysts with remarkable activity under visible light

Highlights: • Novel TiO{sub 2}/Ag{sub 2}WO{sub 4}/AgBr nanocomposites as efficient photocatalysts are reported. • The TiO{sub 2}/Ag{sub 2}WO{sub 4}/AgBr (15%) nanocomposite exhibited the highest activity. • Activity was 50.6-folds greater than TiO{sub 2} in RhB degradation under visible light. • The enhanced activity was attributed to n-n heterojunctions and plasmonic effect. - Abstract: Novel and highly efficient visible-light-driven TiO{sub 2}/Ag{sub 2}WO{sub 4}/AgBr plasmonic photocatalysts were fabricated by a simple one-pot strategy and they were characterized using XRD, EDX, FESEM, TEM, HRTEM, UV–vis DRS, FT–IR, and PL instruments. The TiO{sub 2}/Ag{sub 2}WO{sub 4}/AgBr nanocomposites exhibited higher photocatalytic performance under visible light for RhB, fuchsine, and MO degradations compared with the pure TiO{sub 2} and binary TiO{sub 2}/Ag{sub 2}WO{sub 4} and TiO{sub 2}/AgBr nanocomposites. The optimum photocatalytic activity of the TiO{sub 2}/Ag{sub 2}WO{sub 4}/AgBr (15%) nanocomposite is greater than those of the TiO{sub 2}, TiO{sub 2}/Ag{sub 2}WO{sub 4} (10%), and TiO{sub 2}/AgBr (15%) photocatalysts towards the degradation of RhB by a factor of almost 50.6, 22.6, and 5.1, respectively. The degradation reaction was also examined through trapping experiments and a mechanism for generation of the e{sup −}/h{sup +} pairs under visible light and promotion spatial separation of the charges through tandem n-n heterojunctions was proposed. We anticipate that the procedure used in this paper can provide a good protocol to design efficient visible-light-driven photocatalysts using TiO{sub 2} for environmental applications.

77 NANOSCIENCE AND NANOTECHNOLOGY↗