The property-governed activity of silver-modified titania photocatalysts: The influence of titania matrix.

Commercial titania photocatalysts were modified with silver nanoparticles (NPs) by the photodeposition method in the presence/absence of methanol. The obtained photocatalysts were characterized by XRD, XPS, diffuse reflectance spectroscopy, STEM, and time-resolved microwave conductivity (TRMC) methods. The photocatalytic activity was tested under UV/vis irradiation for (i) methanol dehydrogenation (during silver deposition), (ii) oxygen evolution with in situ silver deposition, and (iii) oxidative decomposition of acetic acid, as well as under vis irradiation for 2-propanol oxidation. The action spectra of 2-propanol oxidation were also performed. It has been confirmed that modification of titania with silver causes significant improvement of photocatalytic activity under both UV and vis irradiation as silver works as an electron scavenger (TRMC data) and vis activator (possibly by an energy transfer mechanism). The obtained activities differ between titania samples significantly, suggesting that the type of crystalline phase, particle/crystallite sizes, and electron traps' density are crucial for both the properties of formed silver deposits and resultant photocatalytic activity. It might be concluded that, under UV irradiation, (i) high crystallinity and large specific surface area are recommended for rutile- and anatase-rich samples, respectively, during hydrogen evolution, (ii) mixed crystalline phases cause a high rate of oxygen evolution from water, and (iii) anatase phase with fine silver NPs results in efficient decomposition of acetic acid, whereas under vis irradiation the aggregated silver NPs (broad localized surface plasmon resonance peak) on the rutile phase are promising for oxidation reactions.

Preparation and Chromaticity Control of CoTiO3/NiTiO3 Co-Coated TiO2 Composite Pigments.

In this study, home-made amorphous TiO2 microspheres with good mono-dispersity and large numbers of mesopores on the surface were used as substrates. The intermediate microspheres were obtained by adding Co/Ni sources with different Co/Ni molar ratios in a water bath and making them react by water bath heating. By calcining the intermediate microspheres deposited on the TiO2 ones, a core-shell structured spherical CoTiO3/NiTiO3 inorganic composite pigment was prepared. The synthesized pigments were characterized by X-ray diffraction (XRD), Raman spectroscopy, field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectrometry (EDS), laser particle size (LPS) analysis and colorimetry. The results show that when the calcination temperature is 800 °C and the Co/Ni molar ratio is 0.5:0.5, the pigments consist of a TiO2 core and outer ilmenite CoTiO3/NiTiO3 shell. Moreover, the surface of the product microspheres is smooth, and the particles are of regular sphericity with a uniform particle size of about 1.8 µm. The colorimetric analysis from the samples calcined at 800 °C shows color changes from yellow-green to dark green as the Co/Ni molar ratio increases (0.1:0.9 to 0.9:0.1). A Co/Ni molar ratio that is too high or too low results in the formation of by-products such as Co3O4 or NiO, respectively, which adhere to the product surface and affect the chromaticity of the product. This work has enabled the chromatic modulation of yellow-green inorganic pigments, providing a solution for the preparation of spherical inorganic pigments that are more suitable for industrial inkjet printing.

Octahedral Anatase Titania as Efficient Photocatalyst: Influence of Preparation Conditions.

Octahedral anatase particles (OAPs) belonging to faceted titania photocatalysts exhibit one of the highest photocatalytic activities among various titania photocatalysts, probably due to hindered recombination of charge carriers resulting from low content of defects (recombination centers). In this study, OAPs have been examined for oxidative decomposition of acetic acid, dehydrogenation of methanol and bacteria inactivation. OAPs were prepared from partly protonated potassium nanowires by hydrothermal reaction (HT) at various experimental conditions, i.e., the influences of HT temperature and content of reaction reagents were studied in detail. The morphology, composition and crystal structure of the products were characterized by scanning electron microscopy (SEM), powder X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), diffuse reflectance spectroscopy (DRS) and time-resolved microwave conductivity (TRMC) method. It was found that all parameters during HT influenced simultaneously the morphology of obtained products, and even slight change in one of them could result in significant change in the properties, and thus photocatalytic activities. Moreover, it was shown that titania morphology was a key-factor for photocatalytic activity for decomposition of both organic compounds and microorganisms. Although, an imperfection in octahedral shape (semi-OAPs) did not influence the efficiently for decomposition of organic compounds, it had tremendous negative impact on antimicrobial performance, probably due to hindered adsorption of bacterial cells on the photocatalyst surface (preferential on {101} facets).

Influence of Semiconductor Morphology on Photocatalytic Activity of Plasmonic Photocatalysts: Titanate Nanowires and Octahedral Anatase Nanoparticles.

Octahedral anatase particles (OAP) with eight exposed and thermodynamically most stable (101) facets were prepared by an ultrasonication-hydrothermal (US-HT) reaction from potassium titanate nanowires (TNW). The precursor (TNW) and the product (OAP) of US-HT reaction were modified with nanoparticles of noble metals (Au, Ag or Pt) by photodeposition. Samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), diffuse reflectance spectroscopy (DRS), scanning transmission electron microscopy (STEM) and time-resolved microwave conductivity (TRMC). The photocatalytic activity was investigated in three reaction systems, i.e., anaerobic dehydrogenation of methanol and oxidative decomposition of acetic acid under UV/vis irradiation, and oxidation of 2-propanol under vis irradiation. It was found that hydrogen liberation correlated with work function of metals, and thus the most active were platinum-modified samples. Photocatalytic activities of bare and modified OAP samples were much higher than those of TNW samples, probably due to anatase presence, higher crystallinity and electron mobility in faceted NPs. Interestingly, noble metals showed different influence on the activity depending on the semiconductor support, i.e., gold-modified TNW and platinum-modified OAP exhibited the highest activity for acetic acid decomposition, whereas silver- and gold-modified samples were the most active under vis irradiation, respectively. It is proposed that the form of noble metal (metallic vs. oxidized) as well as the morphology (well-organized vs. uncontrolled) have a critical effect on the overall photocatalytic performance. TRMC analysis confirmed that fast electron transfer to noble metal is a key factor for UV activity. It is proposed that the efficiency of plasmonic photocatalysis (under vis irradiation) depends on the oxidation form of metal (zero-valent preferable), photoabsorption properties (broad localized surface plasmon resonance (LSPR)), kind of metal (silver) and counteraction of "hot" electrons back transfer to noble metal NPs (by controlled morphology and high crystallinity).

Bactericidal Properties of Plasmonic Photocatalysts Composed of Noble Metal Nanoparticles on Faceted Anatase Titania.

Octahedral anatase particles (OAP) with eight equivalent {101} facets and decahedral anatase particles (DAP) with two additional {001} facets were modified with nanoparticles of noble metals (silver, copper, gold and platinum) by photodeposition, and applied for inactivation of Escherichia coli K12. XRD, DRS, XPS and STEM analyses confirmed the presence of noble metals nanoparticles (NPs) on the surface of faceted titania samples. Both OAP and DAP samples modified with silver and copper exhibited high bactericidal activities under visible light irradiation. It was also found that DAP under UV irradiation showed surprisingly high bactericidal activity, which could be attributed to efficient generation of reactive oxygen species, due to intrinsic properties of DAP, i.e., charge carriers' separation (migration of electrons and holes to {101} and {001} facets, respectively). However, an unexpected decrease in activity after DAP modification with gold and platinum NPs (mainly deposited on {101} facets) suggested that bacteria cells were directly decomposed on DAP surface. SEM images revealed that silver-modified samples caused severe damages of cell walls and membranes, due to antibacterial properties of silver (in the dark) and photocatalytic effect under visible and UV irradiation.

Noble metal-modified faceted anatase titania photocatalysts: Octahedron versus decahedron.

Octahedral anatase particles (OAP, with eight equivalent {101} facets) and decahedral anatase particles (DAP, with two additional {001} facets) were modified with nanoparticles of noble metals (Au, Ag, Cu). The titania morphology, expressed by the presence of different arrangements of exposed crystal facets, played a key role in the photocatalytic properties of metal-modified faceted titania. In the UV/vis systems, two-faceted configuration of DAP was more favorable for the reaction efficiency than single-faceted OAP because of an efficient charge separation described by the transfer of electrons to {101} facets and holes to {001} facets. Time-resolved microwave conductivity (TRMC) and reversed double-beam photoacoustic spectroscopy (RDB-PAS) confirmed that distribution of electron traps (ET) and mobility of electrons were key-factors of photocatalytic activity. In contrast, metal-modified OAP samples had higher photocatalytic activity than metal-modified DAP and metal-modified commercial titania samples under visible light irradiation. This indicates that the presence of single type of facets ({101}) is favorable for efficient electron transfer via shallow ET, whereas intrinsic properties of DAP result in fast charge carriers' recombination when gold is deposited on {101} facets (migration of "hot" electrons: Au→{101}→Au).

Preparation of CdS and Bi2S3 quantum dots co-decorated perovskite-type KNbO3 ternary heterostructure with improved visible light photocatalytic activity and stability for phenol degradation.

CdS quantum dot-decorated KNbO3 composite photocatalysts co-modified with Bi2S3 QDs were designed and synthesized by a combination of the hydrothermal method with a linker-assisted adsorption route, using starch and thioglycolic acid as capping agents, which facilitated the attachment of modifiers to the surface of potassium niobate. The quantum dots were successfully deposited onto the surface of the perovskite-type KNbO3 with a good dispersion and a stable heterostructure was formed. The as-prepared photocatalysts were subsequently characterized by UV-Vis diffuse reflectance spectroscopy (DRS), X-ray diffraction (XRD), scanning electron microscopy (SEM), scanning transmission electron microscopy (STEM), Fourier transform infrared spectroscopy (FT-IR), Brunauer-Emmett-Teller (BET) specific surface area, X-ray photoelectron spectroscopy (XPS) and photoluminescence (PL) emission spectroscopy. The obtained KNbO3-based composites showed greatly improved photocatalytic performance for the degradation of phenol in the aqueous phase under visible light irradiation (λ > 420 nm) over pristine KNbO3. The highest photocatalytic performance and enhanced stability were observed for the ternary 30% CdS-5%Bi2S3 quantum dot-decorated KNbO3 composite, which could be related to the enhanced visible-light absorption ability, efficient charge separation in the three-level electron transfer heterojunction, improved stability and appropriate amounts of composite components. The formation of a surface layer of CdO decreased the visible light photoactivity of the CdS QD-decorated KNbO3 photocatalysts. The main phenol oxidation intermediates were benzoquinone, catechol, hydroquinone, and 1,2,4-benzenetriol, which underwent further photooxidation to form non-cyclic organic acids. Action spectral analysis proved the better photocatalytic activity of the ternary CdS/B2S3 QDs co-decorated KNbO3 composite compared to the binary CdS QDs decorated KNbO3 sample and revealed that irradiation ranging from 420 to 520 nm was responsible for the visible light photoactivity.

Noble metal-modified titania with visible-light activity for the decomposition of microorganisms.

Commercial titania photocatalysts were modified with silver and gold by photodeposition, and characterized by diffuse reflectance spectroscopy (DRS), X-ray powder diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and scanning transmission electron microscopy (STEM). It was found that silver co-existed in zero valent (core) and oxidized (shell) forms, whereas gold was mainly zero valent. The obtained noble metal-modified samples were examined with regard to antibacterial (Escherichia coli (E. coli)) and antifungal (Aspergillus niger (A. niger), Aspergillus melleus (A. melleus), Penicillium chrysogenum (P. chrysogenum), Candida albicans (C. albicans)) activity under visible-light irradiation and in the dark using disk diffusion, suspension, colony growth ("poisoned food") and sporulation methods. It was found that silver-modified titania, besides remarkably high antibacterial activity (inhibition of bacterial proliferation), could also decompose bacterial cells under visible-light irradiation, possibly due to an enhanced generation of reactive oxygen species and the intrinsic properties of silver. Gold-modified samples were almost inactive against bacteria in the dark, whereas significant bactericidal effect under visible-light irradiation suggested that the mechanism of bacteria inactivation was initiated by plasmonic excitation of titania by localized surface plasmon resonance of gold. The antifungal activity tests showed efficient suppression of mycelium growth by bare titania, and suppression of mycotoxin generation and sporulation by gold-modified titania. Although, the growth of fungi was hardly inhibited through disc diffusion (inhibition zones around discs), it indicates that gold does not penetrate into the media, and thus, a good stability of plasmonic photocatalysts has been confirmed. In summary, it was found that silver-modified titania showed superior antibacterial activity, whereas gold-modified samples were very active against fungi, suggesting that bimetallic photocatalysts containing both gold and silver should exhibit excellent antimicrobial properties.

Size-controlled gold nanoparticles on octahedral anatase particles as efficient plasmonic photocatalyst.

Octahedral anatase particles (OAPs), prepared by ultrasonication-hydrothermal reaction (US-HT), were modified with 2 wt% of gold by photodeposition. Conditions of US-HT process such as durations of US and durations of HT were varied to obtain OAPs products different by physicochemical and morphological properties. Au/OAPs samples were characterized by X-ray diffraction (XRD), scanning transmission electron microscopy (STEM), X-ray photoelectron spectroscopy (XPS) and diffuse reflectance spectroscopy (DRS). The photocatalytic activity was tested under UV irradiation for decomposition of acetic acid (CO2 system) and dehydrogenation of methanol (H2 system) under aerobic and anaerobic conditions, respectively, and for oxidation of 2-propanol under visible light irradiation. Photodeposition of gold was very fast for all OAPs samples (0.5-10 min) under Ar atmosphere, and the clear correlation between the content of electron traps (ETs) and the induction period, during which nanoparticles (NPs) of gold are formed, indicates that ETs in titania samples are a key-factor for rapidity of gold photodeposition on titania surface. It was found that better morphology of titania (larger content of faceted particles) resulted in formation of larger gold NPs, while small gold NPs were deposited on structural defects. Modification of OAPs with gold NPs resulted in significant enhancement of photocatalytic activity, being e.g., 1.5 (CO2 system), 7.7 (H2 system), and even more than 40 under vis irradiation. It was found that both the properties of titania and gold are crucial for resultant photocatalytic activity, but a direct correlation between one structural/physical property and photocatalytic activity could not be obtained since all structural properties changed simultaneously when conditions of photocatalyst preparation (US-HT) were changed. Therefore, gold NPs of controlled sizes were deposited on OAPs product with the best morphology by modified photodeposition method. Clear correlation between photocatalytic activity under visible light and the size of gold NPs indicates that gold properties are decisive for visible light activity rather than titania properties. 3D-FDTD simulations confirm that an increase in the size of gold NPs results in extended surface areas with field enhancement.

Enhanced photocatalytic, electrochemical and photoelectrochemical properties of TiO2 nanotubes arrays modified with Cu, AgCu and Bi nanoparticles obtained via radiolytic reduction.

TiO2 nanotubes arrays (NTs), obtained via electrochemical anodization of Ti foil, were modified with monometallic (Cu, Bi) and bimetallic (AgCu) nanoparticles. Different amounts of metals' precursors were deposited on the surface of NTs by the spin-coating technique, and the reduction of metals was performed via gamma radiolysis. Surface modification of titania was studied by EDS and XPS analysis. The results show that AgCu nanoparticles exist in a Agcore-Cushell form. Photocatalytic activity was examined under UV irradiation and phenol was used as a model pollutant of water. Over 95% of phenol degradation was achieved after 60 min of irradiation for almost all examined samples, but only slight difference in degradation efficiency (about 3%) between modified and bare NTs was observed. However, the initial phenol degradation rate and TOC removal efficiency was significantly enhanced for the samples modified with 0.31 and 0.63 mol% of Bi as well as for all the samples modified with Cu and AgCu nanoparticles in comparison with bare titania nanotubes. The saturated photocurrent, under the influence of simulated solar light irradiation, for the most active Bi- and AgCu-modified samples, was over two times higher than for pristine NTs. All the examined materials were resistant towards photocorrosion processes that enables their application for long term processes induced by light.

Titania modification with a ruthenium(II) complex and gold nanoparticles for photocatalytic degradation of organic compounds.

Titania of fine anatase nanoparticles (ST01) was modified successively with two components, i.e., a ruthenium(II) complex with phosphonic anchoring groups [Ru(bpy)2(4,4'-(CH2PO3H2)2bpy)](2+) bpy = 2,2'-bipyridine (Ru(II)CP) and gold nanoparticles (Au). Various compositions of two titania modifiers were investigated, i.e., Au, Au + Ru(II)CP, Au + 0.5Ru(II)CP, Ru(II)CP, 0.5Ru(II)CP and 0.25Ru(II)CP, where Au and Ru(II)CP correspond to 0.81 mol% and 0.34 mol% (with respect to titania), respectively. In the case of hybrid photocatalysts, the sequence of modification (ruthenium(II) complex adsorption or gold deposition) was investigated to check its influence on the resultant properties and thus photocatalytic performance. Diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS) and scanning transmission electron microscopy (STEM) were applied to characterize the structural properties of the prepared photocatalysts, which confirmed the successful introduction of modifiers of the ruthenium(II) complex and/or gold NPs. Different distributions of gold particle sizes and chemical compositions were obtained for the hybrid photocatalysts prepared with an opposite sequence. It was found that photocatalytic activities depended on the range of used irradiation (UV/vis or vis) and the kind of modifier in different ways. Gold NPs improved the photocatalytic activities, while Ru(II)CP inhibited the reactions under UV/vis irradiation, i.e., methanol dehydrogenation and acetic acid degradation. Oppositely, Ru(II)CP greatly enhanced the photocatalytic activities for 2-propanol oxidation under visible light irradiation.

The effect of anatase and rutile crystallites isolated from titania P25 photocatalyst on growth of selected mould fungi.

Antifungal properties of anatase and rutile crystallites isolated from commercial titania P25 photocatalyst were investigated by mycelium growth in the dark and under indoor light. Investigated fungi, i.e., Pseudallescheria boydii, Scedosporium apiospermum, Pseudallescheria ellipsoidea, Scedosporium aurantiacum, Aspergillus versicolor, Aspergillus flavus, Stachybotrys chartarum, Penicillium chrysogenum, Aspergillus melleus, were isolated from air and from moisture condensed on walls. Anatase and rutile were isolated from homogenized P25 (homo-P25) by chemical dissolution, and then purified by washing and thermal treatment. For comparison, homo-P25 was also thermally treated at 200 °C and 500 °C. Titania samples were characterized by X-ray diffractometry (XRD), X-ray photoelectron spectroscopy (XPS), diffuse reflectance spectroscopy (DRS) and scanning transmission electron microscopy (STEM). It was found that properties of titania, i.e., band-gap energy, impurities adsorbed on the surface, nanoparticle aggregation, and kind of fungal structure, highly influenced resultant antifungal activities. It is proposed that some fungi could uptake necessary water and nutrient from titania surface. It was also found that even when differences in mycelium growth were not significant, the sporulation and mycotoxin generation were highly inhibited by light and presence of titania.

Morphology-dependent photocatalytic activity of octahedral anatase particles prepared by ultrasonication-hydrothermal reaction of titanates.

Octahedral anatase particles (OAPs) were prepared by an ultrasonication (US)-hydrothermal (HT) reaction of partially proton-exchanged potassium titanate nanowires (TNWs). The structural/physical properties of OAP-containing samples, including specific surface area, crystallinity, crystallite size, particle aspect ratio, composition and total OAP content, were analyzed. Photocatalytic activities of samples were measured under irradiation (>290 nm) for oxidative decomposition of acetic acid (CO2 system) and dehydrogenation of methanol (H2 system) under aerobic and deaerated conditions, respectively. Total density of electron traps (ETs) was measured by double-beam photoacoustic spectroscopy (DB-PAS). Mobility and lifetime of charge carriers (electrons) were investigated by the time-resolved microwave conductivity (TRMC) method. The effects of synthesis parameters, i.e., HT duration, HT temperature and US duration, on properties and photocatalytic activities of final products were examined in detail. The sample prepared with 1 h US duration and 6 h HT duration at 433 K using 267 mg of TNWs in 80 mL of Milli-Q water exhibited the highest photocatalytic activity. It was found that change in HT duration or HT temperature while keeping the other conditions the same resulted in changes in all properties and photocatalytic activity. On the other hand, duration of US treatment, before HT reaction, influenced the morphology of both the reagent (by TNWs breaking) and final products (change in total OAP content); samples prepared with various US durations exhibited almost the same structural/physical properties evaluated in this study but were different in morphology and photocatalytic activity. This enabled clarification of the correlation between morphology and photocatalytic activity, i.e., the higher the total OAP content was, the higher was the level of photocatalytic activity, especially in the CO2 system. Although the decay after maximum TRMC signal intensity (Imax) was almost constant for all samples used in this study, photocatalytic activities were roughly proportional to Imax, which tended to be proportional to total OAP content. Assuming that Imax corresponds to the product of density of electrons in mobile shallow ETs and their mobility, the results suggest that OAP particles have beneficial shallow ETs in higher density and thereby the OAP content governs the photocatalytic activities. Thus, morphology-dependent photocatalytic activity of OAP-containing particles was reasonably interpreted by density of ETs presumably located on the exposed {101} facets.

Influence of post-treatment operations on structural properties and photocatalytic activity of octahedral anatase titania particles prepared by an ultrasonication-hydrothermal reaction.

The influence of changes in structural and physical properties on the photocatalytic activity of octahedral anatase particles (OAPs), exposing eight equivalent {101} facets, caused by calcination (2 h) in air or grinding (1 h) in an agate mortar was studied with samples prepared by ultrasonication (US; 1 h)-hydrothermal reaction (HT; 24 h, 433 K). Calcination in air at temperatures up to 1173 K induced particle shape changes, evaluated by aspect ratio (AR; d001/d101 = depth vertical to anatase {001} and {101} facets estimated by the Scherrer equation with data obtained from X-ray diffraction (XRD) patterns) and content of OAP and semi-OAP particles, without transformation into rutile. AR and OAP content, as well as specific surface area (SSA), were almost unchanged by calcination at temperatures up to 673 K and were then decreased by elevating the calcination temperature, suggesting that calcination at a higher temperature caused dull-edging and particle sintering, the latter also being supported by the analysis of particle size using XRD patterns and scanning electron microscopic (SEM) images. Time-resolved microwave conductivity (TRMC) showed that the maximum signal intensity (Imax), corresponding to a product of charge-carrier density and mobility, and signal-decay rate, presumably corresponding to reactivity of charge carriers, were increased with increase in AR, suggesting higher photocatalytic activity of OAPs than that of dull-edged particles. Grinding also decreased the AR, indicating the formation of dull-edged particles. The original non-treated samples showed activities in the oxidative decomposition of acetic acid (CO2 system) and dehydrogenation of methanol (H2 system) comparable to and lower than those of a commercial anatase titania (Showa Denko Ceramics FP-6), respectively. The activities of calcined and ground samples for the CO2 system and H2 system showed almost linear relations with AR and Imax, respectively, suggesting that those activities may depend on different properties.

A gas-solid reaction growth of dense TiO2 nanowire arrays on Ti foils at ambient atmosphere.

In this paper, a facile method is demonstrated to directly fabricate dense titania nanowire arrays on titanium foils under the atmosphere without extra moist conditions. The influences of temperature, time, different catalysts, and concentrations of the respective catalysts on the growth of titania nanowires are discussed in detail. The morphology, composition and crystal structure of the titania nanostructures are revealed by scanning electron microscopy (SEM), powder-X-ray diffraction (XRD) and transmission electron microscopy (TEM) techniques, by which a gas-solid reaction mechanism is suggested to explain the growth process of TiO2 nanowires on Ti substrate.