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At least 739 records · Page 41

Low temperature grown ZnO@TiO{sub 2} core shell nanorod arrays for dye sensitized solar cell application

High aspect ratio ZnO nanorod arrays were synthesized on fluorine-doped tin oxide glasses via a low temperature solution method. By adjusting the growth condition and adding polyethylenimine, ZnO nanorod arrays with tunable length were successfully achieved. The ZnO@TiO{sub 2} core shells structures were realized by a fast growth method of immersion into a (NH{sub 4}){sub 2}·TiF{sub 6} solution. Transmission electron microscopy, X-ray Diffraction and energy dispersive X-ray measurements all confirmed the existence of a titania shell uniformly covering the ZnO nanorod's surface. Results of solar cell testing showed that addition of a TiO{sub 2} shell to the ZnO nanorod significantly increased short circuit current (from 4.2 to 5.2 mA/cm{sup 2}), open circuit voltage (from 0.6 V to 0.8 V) and fill factor (from 42.8% to 73.02%). The overall cell efficiency jumped from 1.1% for bare ZnO nanorod to 3.03% for a ZnO@TiO{sub 2} core shell structured solar cell with a 18–22 nm shell thickness, a nearly threefold increase. - Graphical abstract: The synthesis process of coating TiO{sub 2} shell onto ZnO nanorod core is shown schematically. A thin, uniform, and conformal shell had been grown on the surface of the ZnO core after immersing in the (NH{sub 4}){sub 2}·TiF{sub 6} solution for 5–15 min. - Highlights: • ZnO@TiO{sub 2} core shell nanorod has been grown on FTO substrate using low temperature solution method. • TEM, XRD, EDX results confirmed the existing of titana shell, uniformly covered rod's surface. • TiO{sub 2} shell suppressed recombination, demonstrated significant enhancement in cell's efficiency. • Core shell DSSC's efficiency achieved as high as 3.03%, 3 times higher than that of ZnO nanorods.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Fabrication of heterostructured BiOBr/Bi{sub 24}O{sub 31}Br{sub 10}/TiO{sub 2} photocatalyst by pyrolysis of MOF composite for dye degradation

The pyrolysis of metal-organic frameworks has emerged as a promising route to synthesize metal oxides with diverse phase compositions, morphologies, sizes and surface areas. The BiOBr/Bi{sub 24}O{sub 31}Br{sub 10}/TiO{sub 2} (BBT) heterostructures have been achieved for the first time by calcining BiOBr/MIL-125(Ti) composite at 500 °C in air. The BBT-2 composite exhibited the highest photocatalytic performance for degradation of RhB under visible light irradiation. The enhanced photocatalytic activity is attributed to narrower band-gaps and synergistic effect originating from the well-aligned straddling band-structures between BiOBr, Bi{sub 24}O{sub 31}Br{sub 10} and TiO{sub 2}, also result in an faster interfacial charge transfer during the photocatalytic reaction. This work could be conductive to the design of heterostructured photocatalysts contained metal oxide by pyrolytic conversion of metal-organic frameworks for significantly improved photocatalytic performance. - Graphical abstract: A novel BiOBr/Bi{sub 24}O{sub 31}Br{sub 10}/TiO{sub 2} heterostructure was achieved by calcining BiOBr/MIL-125(Ti) composite and exhibited the photocatalytic performance for degradation of RhB. Display Omitted - Highlights: • A novel BiOBr/Bi{sub 24}O{sub 31}Br{sub 10}/TiO{sub 2} heterostructure was achieved by calcining BiOBr/MIL-125(Ti) composite. • The heterostructure exhibited the photocatalytic performance for degradation of RhB. • The enhanced photocatalytic activity is attributed to synergistic effect between BiOBr, Bi{sub 24}O{sub 31}Br{sub 10} and TiO{sub 2}. • This work could be conductive to the design of heterostructured photocatalysts by pyrolytic conversion of MOF.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Two Co-zeolite imidazolate frameworks with different topologies for degradation of organic dyes via peroxymonosulfate activation

In this paper, two novel zeolitic imidazole framework (ZIF) materials, ZIF-9 and ZIF-12 were firstly introduced as catalysts to activate PMS for Rhodamine B degradation. ZIF-9 and ZIF-12 have the same composition in metal ions (Co{sup 2+}) and organic linker, but show different structural topologies (SOD and RHO, respectively) and particle size. The two ZIFs were successfully synthesized and characterized via SEM and PXRD. Both ZIF-9 and ZIF-12 as the PMS activation catalysts were evaluated and compared, and the underlying mechanism was proposed. The nanoscale nature enables ZIF-9 a closer contact with PMS, which leading to degradation rate ZIF-9 > ZIF-12 at the time of 5 min (54.8% and 27.7%, respectively). And the degradation of ZIF-12 gradually caught up with ZIF-9 when the reaction time was longer, which can be attributed to the RHO topology and larger cage size of ZIF-12. The efficient degradation of RhB indicates that ZIF-9 and ZIF-12 can be promising heterogeneous catalyst to activate PMS for the degradation of RhB. - Graphical abstract: Two novel zeolitic imidazole framework (ZIF) materials, ZIF-9 and ZIF-12 were firstly introduced as catalysts to activate PMS for Rhodamine B degradation. ZIF-9 and ZIF-12 have the same composition in metal ions (Co{sup 2+}) and organic linker, but show different structural topologies (SOD and RHO, respectively) and particle size. The efficient degradation of RhB indicates that ZIF-9 and ZIF-12 can be promising heterogeneous catalyst to activate PMS for the degradation of RhB. Display Omitted.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Mesoporous ZnO microcube derived from a metal-organic framework as photocatalyst for the degradation of organic dyes

A cube-like porous ZnO architecture was synthesized by direct two-step thermolysis of a zinc-based metal-organic framework [(CH{sub 3}){sub 2}NH{sub 2}][Zn(HCOO){sub 3}]. The obtained ZnO microcube was characterized by powder X-ray diffraction, scanning electron microscopy, transmission electron microscopy and nitrogen adsorption and desorption isotherms. The mesoporous ZnO microcube was comprised by many nanoparticles, and inherited the cube shape from [(CH{sub 3}){sub 2}NH{sub 2}][Zn(HCOO){sub 3}] precursor. With large surface area and mesoporous structure, the ZnO microcube exhibits excellent photocatalytic activities against methyl orange (MO) and rhodamine B (RhB) under UV irradiation, and the degradation rates reached 99.7% and 98.1% within 120 min, respectively. - Graphical abstract: Mesoporous ZnO microcube was synthesized via two-step thermolysis of metal-organic framework [(CH{sub 3}){sub 2}NH{sub 2}][Zn(HCOO){sub 3}], and exhibit excellent photocatalytic activity towards MO and RhB. Display Omitted - Highlights: • Cubic MOF [(CH{sub 3}){sub 2}NH{sub 2}][Zn(HCOO){sub 3}] was prepared by solution-precipitation method. • Mesoporous ZnO microcube was obtained by a two-step calcination of MOF precursor. • ZnO microcube shows photocatalytic activity to MO and RhB under UV irradiation. • The h{sup +} and ∙O{sub 2}{sup -} are main active species during the photodegradation process.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Synthesis, crystal structures, and dye removal properties of a series of discrete and polymeric copper, zinc, cobalt, and cadmium complexes containing bis-pyridyl-bis-amine ligands

Two bis-pyridyl-bis-amine ligands, trans-1,2-bis(m-picolyamino)cyclohexane (rac-m-picchxn) and trans-1,2-bis(p-picolyamino)cyclohexane (rac-p-picchxn), derived from trans-1,2-diaminocyclohexane (rac-chxn), were assembled with CuCl{sub 2}, ZnCl{sub 2}, ZnBr{sub 2}, Co(NO{sub 3}){sub 2}, and CdCl{sub 2} through reactants slow diffusion to afford corresponding metal complexes. Complexes [Cu(R,R-m-picchxn)Cl{sub 2}] (1) and [Zn(rac-m-picchxn)Br{sub 2}] (3) are mononuclear coordination structures, complex [Zn{sub 2}(rac-m-picchxn)Cl{sub 4}]{sub n} (2) adopts a one-dimensional (1D) helical chain, complex {[Co(R,R-p-picchxn)(NO_3)_2]·THF·2/3H_2O}{sub n} (4) has a two-dimensional (2D) kgm layer structure, complex [Cd(rac-p-picchxn)Cl{sub 2}]{sub n} (5) suits a 1D double-stranded zigzag chain structure, and compound [Cu(rac-chxn){sub 2}][CuCl{sub 3}] (6) is a Cu(I)-Cu(II) mixed-valence ionic product generated from the hydrolysis of rac-p-picchxn associated with the reduction of Cu(II) ion. The two bis-pyridyl-bis-amine ligands possess a chelating-bridging mode in forming infinite network and a chelating-only mode in forming discrete complexes. These metal–organic architectures show the influence of metal ion combining with organic ligand and anion on the structure variation. Noteworthy, chain polymers 2 and 5 could be utilized in the removal of methyl orange (MO), acid orange 7 (AO7), and malachite green (MG) from water through adsorptive processes. The adsorption dynamics of MO and AO7 on 2 and MG on both 2 and 5 obeyed a pseudo-second-order kinetics while that of MO and AO7 on 5 followed a pseudo-first-order kinetics.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Mil-100(Fe) nanoparticles supported on urchin like Bi{sub 2}S{sub 3} structure for improving photocatalytic degradation of rhodamine-B dye under visible light irradiation

Highlights: • Facile synthesis a new hybrid photocatalyst MIL-100(Fe)@Bi{sub 2}S{sub 3}. • Investigation enhanced photocatalytic performance of MIL-100(Fe)@Bi{sub 2}S{sub 3} compared to individual components. • Determination the main active species during photocatalytic degradation of RhB over MIL-100(Fe)@Bi{sub 2}S{sub 3}. • Propose photocatalytic mechanism for degradation of RhB over MIL-100(Fe)@Bi{sub 2}S{sub 3}. - Abstract: Metal organic framework (MOFs) have been attracted a great attention as a new type photocatalysts due to their unique properties. In this work, the new hybrid photocatalyst based on fabrication hybrid structures between MIL-100(Fe) and Bi{sub 2}S{sub 3} (MIL-100(Fe)@Bi{sub 2}S{sub 3}) were synthesized via simple hydrothermal method. The photocatalytic degradation of Rhodamine B (RhB) over the as-prepared samples showed that the hybrid photocatalyst samples had higher photocatalytic performance compared to the individual components (MIL-100(Fe) and Bi{sub 2}S{sub 3}). The higher photocatalytic performance of the hybrid photocatalysts was proved by electrochemical and photoelectrochemical analysis such as electrochemical impedance spectroscopy (EIS) and also photocurrent measurement. In addition, the possible photocatalytic mechanism based on the optical, photoelectrochemical and quenching tests was proposed.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Impact of Pt loading methods over mesoporous-assembled TiO{sub 2}–ZrO{sub 2} mixed oxide nanocrystal on photocatalytic dye-sensitized H{sub 2} production activity

Graphical abstract: The Pt loading on the synthesized mesoporous-assembled 0.95TiO{sub 2}–0.05ZrO{sub 2} mixed oxide nanocrystal photocatalyst was comparatively investigated by two methods: single-step sol–gel (SSSG) and photochemical deposition (PCD). The Pt loading by the PCD method was found to be superior to that by the SSSG method in enhancing photocatalytic sensitized hydrogen production under visible light irradiation. The Pt loading amount and PCD conditions, i.e. light irradiation time and light intensity, also had a strong effect on the photocatalytic hydrogen production activity. Highlights: ► Pt-loaded mesoporous-assembled 0.95TiO{sub 2}–0.05ZrO{sub 2} nanocrystals were synthesized. ► Pt loading was performed by single-step sol–gel and photochemical deposition. ► Pt loading by photochemical deposition more enhanced photocatalytic H{sub 2} production. ► Pt loading amount and photochemical deposition conditions were optimized. -- Abstract: In this work, the photocatalytic water splitting under visible light irradiation for hydrogen production was investigated by using Eosin Y-sensitized Pt-loaded mesoporous-assembled TiO{sub 2}–ZrO{sub 2} mixed oxide nanocrystal photocatalysts. The mesoporous-assembled TiO{sub 2}–ZrO{sub 2} mixed oxide with the TiO{sub 2}-to-ZrO{sub 2} molar ratio of 95:5 (i.e. 0.95TiO{sub 2}–0.05ZrO{sub 2}) was synthesized by using a sol–gel process with the aid of a structure-directing surfactant. The Pt loading was comparatively performed via two different effective methods: single-step sol–gel (SSSG) and photochemical deposition (PCD). The synthesized photocatalysts were methodically characterized by N{sub 2} adsorption–desorption, XRD, UV–visible spectroscopy, SEM–EDX, TEM–EDX, TPR, and H{sub 2} chemisorption analyses. The results revealed that the Pt loading by the PCD method greatly enhanced the photocatalytic hydrogen production activity of the synthesized mesoporous-assembled 0.95TiO{sub 2}–0.05ZrO{sub 2} mixed oxide photocatalyst more than that by the SSSG method. The optimum Pt loading by the PCD method was experimentally observed at 0.5 wt.%, which was well associated with the maximum Pt dispersion. In addition, the PCD conditions, i.e. UV light irradiation time and UV light intensity, were investigated and optimized to be 2 h and 44 W, respectively.

36 MATERIALS SCIENCE↗

Converting Y(OH){sub 3} nanofiber bundles to YVO{sub 4} polyhedrons for photodegradation of dye contaminants

Highlights: • YVO{sub 4} polyhedrons were prepared from Y(OH){sub 3} nanofiber bundles through a hydrothermal conversion process. • In contrast to the bulk oxide, the photocatalytic performance of the polyhedrons was much improved. • The main active species involved in photocatalytic oxidative reaction were also investigated. - Abstract: This paper reports a hydrothermal conversion process of rare earth microstructures, Y(OH){sub 3} nanofiber bundles, into YVO{sub 4} polyhedrons, together with the investigation on the related photocatalytic properties. The as-synthesized samples were characterized by a variety of techniques, including XRD, SEM, TEM and UV–vis diffuse reflectance spectroscopy. The photocatalytic activities of YVO{sub 4} polyhedrons were comparatively evaluated by the photodegradation of Rhodamine B and methylene blue. In contrast to the bulk oxide, the photocatalytic performance of the polyhedrons was much improved. The mechanism and the main active species involved in photocatalytic oxidative reaction were also investigated through the carriers trapping experiments.

36 MATERIALS SCIENCE↗

Controlled synthesis of silkworm cocoon-like α-Fe2O3 and its adsorptive properties for organic dyes and Cr(VI)

Highlights: • A hierarchical structured α-Fe{sub 2}O{sub 3} is synthesized by using a simple hydrothermal method. • The as-synthesized α-Fe{sub 2}O{sub 3} shows high adsorption capacities for CR, MO and Cr(VI) ions. The removal efficiency can reach up to 99.2%, 83.9% and 100% under the given conditions. • This kind of material realizes synergistic adsorption of organic and inorganic pollutants. And the adsorption efficiency can reach 94.7% for CR and 97.9% for Cr(VI) ions in a mixed solution. - Abstract: Industrial wastewater containing both organic and inorganic pollutants is being generated all the time. Efficient materials are highly needed to purify the polluted water. Thus, a hierarchical structured α-Fe{sub 2}O{sub 3} with excellent adsorptive property has been synthesized by using a facile hydrothermal method. It can be prepared in macroscopic quantity. The as-synthesized α-Fe{sub 2}O{sub 3} with silkworm cocoon-like morphology shows high efficiency in adsorbing Congo red (CR), Methyl orange (MO) and Cr(VI). The removal efficiency of CR, MO and Cr(VI) can reach 99.2%, 83.9% and 100% under appropriate conditions. Besides, this α-Fe{sub 2}O{sub 3} shows high adsorptive ability for mixed CR and Cr(VI) in aqueous solution and the final removal rates can reach 94.7% and 97.9%, respectively. The adsorption kinetics fits well with the pseudo-second-order kinetic model. The results indicate that the product may find potential application in purification of wastewater containing both organic and inorganic pollutants.

36 MATERIALS SCIENCE↗

Stable and near-infrared absorption enhanced dye-sensitized solar cell based on silver nanoplates@silica nanocrystals

Highlights: • TiO{sub 2}/(Ag NPLs@SiO{sub 2}) photoanodes are successfully fabricated. • TiO{sub 2}/(Ag NPLs@SiO{sub 2}) anode shows enhanced near-infrared light absorbing efficiency. • DSSC based on TiO{sub 2}/(Ag NPLs@SiO{sub 2}) photoanode achieves an enhanced stability. - Abstract: We synthesize the near-infrared light responsive titanium dioxide/(silver nanoplates@silica) (TiO{sub 2}/(Ag NPLs@SiO{sub 2})) photoanode by embellishing the Ag NPLs@SiO{sub 2} on the surface of bare TiO{sub 2} anode. TiO{sub 2}/(Ag NPLs@SiO{sub 2}) photoanode enhances the device performance under simulated sunlight illumination and near-infrared light irradiation, owing to some potential advantages: Ag NPLs can harvest and convert the limited near-infrared light into the plasmonic hot-electron; the surface plasma resonance (SPR) effect of Ag NPLs promotes to produce additional photo-generated carriers; the core-shell structure of Ag NPLs@SiO{sub 2} can accelerate the separation of photo-generated electron-hole pairs and can reduce the recombination; and the SiO{sub 2} shell can protect the Ag NPLs from reuniting in the thermal treatment process, can prevent the Ag NPLs being etched by iodide/triiodide (I{sup −}/I{sub 3}{sup −}) electrolyte, and can improve the stability of devices further.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Photocatalytic enhancement of immobilized TiO2-polyaniline bilayer (TiO2-PBL) system for decolorization of methyl orange dye

Highlights: • TiO{sub 2}-PANI bilayer (TiO{sub 2}-PBL) system was fabricated via dip-coating technique. • MO decolorization by TiO{sub 2}-PBL system was two times better than TiO{sub 2} monolayer. • TiO{sub 2}-PBL showed better optical properties than TiO{sub 2} monolayer. • PANI exhibited a multi-functional role in TiO{sub 2}-PBL system. • Photoetched TiO{sub 2}-PBL system removed MO more effectively than as-prepared system. - Abstract: Immobilized TiO{sub 2}-polyaniline (PANI) bilayer (TiO{sub 2}-PBL) was fabricated on a glass plate for decolorization of methyl orange (MO). The thickness of TiO{sub 2}-PBL was 25.55 μm with the ratio of 0.62:0.38 for TiO{sub 2} to PANI layer. It was observed that the TiO{sub 2}-PBL system emitted less photoluminescence (PL) intensity than the TiO{sub 2} monolayer corresponding to better {sup •} OH radicals production with reduced band gap energy. The removal of MO from the solution after 90 min of treatment was 97% by TiO{sub 2}-PBL and 53% by TiO{sub 2} monolayer which indicates the efficacy of the former system due to the synergistic photocatalytic-adsorption processes. The effect of prewashing (photoetching) of TiO{sub 2}-PBL plate was pronounced as better removal efficiency of MO was observed for ten cycles under UV–vis and visible light irradiations. The results showed that the TiO{sub 2}-PBL system has visible light active properties, reduces the recombination of photogenerated active species and enhances the photocatalytic oxidation of MO.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Synthesis of Fe3O4/Pr-BiOCl/Luffa composites with enhanced visible light photoactivity for organic dyes degradation

Highlights: • Fe{sub 3}O{sub 4}/Pr-BiOCl/Cellulose photocatalysts were synthesized for the first time. • The Fe{sub 3}O{sub 4}/Pr-BiOCl/Cellulose photocatalysts have high photoactivity and stability. • The optimal Pr loading was 0.1%. • The Fe{sub 3}O{sub 4}/Pr-BiOCl/Cellulose photocatalysts are easy to separate from the reaction system. - Abstract: Fe{sub 3}O{sub 4}/Pr-BiOCl/Luffa (FPBL) composites were successfully prepared for the first time via a two-step synthesis method. The composites were characterized by a number of techniques including XRD, FTIR, SEM, DRS, BET, XPS, PL, UV–vis and VSM. The photocatalytic activity of FPBL was further evaluated through the photodegradation efficiency of Rhodamine B (RhB). Almost all RhB was removed after 120 min visible light irradiation in the present of the FPBL. The effects of dose and pH were also studied, and the best performance was achieved at pH 6 while the dose of as-prepared photocatalyst was 1.0 g/L. The as-prepared photocatalyst can be magnetically recycled, and it maintained high photocatalytic activity after six-cycle of photodegradation. The free radical trapping experiments demonstrated that the holes (h{sup +}) and electrons (e{sup −}) were two main active species in the photocatalytic degradation of RhB. This work suggests the Fe{sub 3}O{sub 4}/Pr-BiOCl/Luffa composites are promising photocatalysts for organic pollutant degradation.

36 MATERIALS SCIENCE↗