Engineering Papers⌕ Search

SEARCH · Engineering Papers

Results for “DYES”

Search indexed NASA NTRS and DOE OSTI research on propulsion, heat transfer, battery materials and energy systems. Follow report and document links to the original sources.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 559 records · Page 31

Hydrothermal synthesis of coral-like Au/ZnO catalyst and photocatalytic degradation of Orange II dye

Highlights: ► Coral-like Au/ZnO was successfully prepared using green synthetic method. ► Gold nanoparticles were deposited on the ZnO structure using NaBH{sub 4} and β-D-glucose. ► Coral-like Au/ZnO exhibited superior photocatalytic activity to degrade Orange II. - Abstract: A porous coral-like zinc oxide (c-ZnO) photocatalyst was synthesized by the hydrothermal method. The coral-like structure was obtained by precipitating Zn{sub 4}(CO{sub 3})(OH){sub 6}·H{sub 2}O (ZnCH), which forms nanosheets that aggregate together to form microspheres with the coral-like structure. X-ray diffraction (XRD) studies indicate that after heating at 550 °C the ZnCH microspheres can be converted to ZnO microspheres with a morphology similar to that of ZnCH microspheres. Thermogravimetric analysis (TGA) shows this conversion takes place at approximately 260 °C. A simple electrostatic self-assembly method has been employed to uniformly disperse Au nanoparticles (1 wt.%) on the ZnO surface. In this procedure β-D-glucose was used to stabilize the Au nanoparticles. Scanning electron microscope images indicate that the diameter of coral-like ZnO microspheres (c-ZnO) is about 8 μm. X-ray diffraction reveals that the ZnO is highly crystalline with a wurtzite structure and the Au metallic particles have an average size of about 13 nm. X-ray photoelectron spectroscopic (XPS) studies have confirmed the presence of ZnO and also showed that the Au is present in the metallic state. The photocatalytic degradation of Orange II dye, with either ultraviolet or visible light, is faster on Au/c-ZnO than on c-ZnO.

36 MATERIALS SCIENCE↗

Effects of TiO{sub 2} film thickness on photovoltaic properties of dye-sensitized solar cell and its enhanced performance by graphene combination

Graphical abstract: - Highlights: • DSSC based on TiO{sub 2} film with 8 printing layers showed the highest efficiency. • The photoelectric conversion efficiency of the DSSC increased from 5.52% to 6.49% by graphene combination. • A mechanism for the enhanced performance of the DSSC was proposed. - Abstract: Dye-sensitized solar cells based on TiO{sub 2} films with different printing layers (6-10) were fabricated by screen printing method. The prepared samples were characterized by scanning electron microscopy, X-ray diffraction and UV–vis absorption spectroscopy. The effects of thickness on the photoelectric conversion performance of the as-fabricated DSSCs were investigated. An optimum photoelectric conversion efficiency of 5.52% was obtained in a DSSC with 8 printing layers. Furthermore, after a moderate amount of graphene was combined with TiO{sub 2}, the photoelectric conversion efficiency of the DSSC based on graphene/TiO{sub 2} composite film rose from 5.52% to 6.49%, with an increase of η by 17.6%. The results indicated that graphene not only enhances the transport of electrons from the film to the fluorine doped tin oxide substrates and reduces the charge recombination rate, but also reduces the electrolyte–electrode interfacial resistance, clearly increasing the photoelectric conversion efficiency.

36 MATERIALS SCIENCE↗

Investigation of iodine dopant amount effects on dye-sensitized hierarchically structured ZnO solar cells

Highlights: • The effect of I amount on the photovoltaic performance was investigated. • The enhancement in η of ZnO:I DSSCs was from 38% to 77% compared with ZnO DSSCs. • Appropriate I doping enhanced light harness and inhibited charge recombination. - Abstract: We prepare a series of iodine doped zinc oxide monodisperse aggregates (ZnO:I) with various iodine concentrations as the photoanodes of dye-sensitized solar cells (DSSCs) to study iodine dopant amount-dependent photovoltaic performance. The iodine-doped DSSCs achieve overall conversion efficiency (η) of 3.6–4.6%. The enhancement in η of ZnO:I DSSCs is from 38% to 77% as compared to undoped ZnO DSSCs. The significantly enhanced η of DSSCs is found to be correlated with iodine dopant amount. The optimum iodine dopant amount is determined to be 2.3 wt% by X-ray photoelectron spectroscopy. Furthermore, the incident photon to current conversion efficiency and electrochemical impedance spectroscopy data reveal a systematic correlation between photovoltaic properties and the iodine dopant amount. The enhancement of open-circuit potential of ZnO:I cells is arising from negative shift of their flat-band potential, as demonstrated by Mott–Schottky measurement.

36 MATERIALS SCIENCE↗

Successive ionic layer adsorption and reaction deposited kesterite Cu{sub 2}ZnSnS{sub 4} nanoflakes counter electrodes for efficient dye-sensitized solar cells

Highlights: • Cu{sub 2}ZnSnS{sub 4} nanoflakes by SILAR technique. • Hydrothermal synthesis of TiO{sub 2}. • Counter electrode for DSSC application. • 4.48% conversion efficiency. - Abstract: In this investigation, we have successfully synthesized Cu{sub 2}ZnSnS{sub 4} (CZTS) nanoflakes by successive ionic layer adsorption and reaction (SILAR) method and used as a counter electrode in the hydrothermally grown TiO{sub 2} based dye sensitized solar cells (DSSCs). The prepared CZTS nanoflakes were characterized using X-ray powder diffraction (XRD), field emission scanning electron microscopy (FESEM), micro Raman spectroscopy and energy dispersive analysis. Our DSSCs results revealed that, compared with conventional Pt/FTO counter electrode DSSCs, nanoflakes of p-type CZTS as the photocathode and n-type TiO{sub 2} thin films as the photoanode shows an increased short circuit current (13.35 mA/cm{sup 2}) with 4.84% power conversion efficiency. The detailed interface properties of were analyzed by electrochemical impedance spectroscopy (EIS) measurements.

36 MATERIALS SCIENCE↗

Metal oxide semiconductors for dye degradation

Highlights: • Hydrothermal synthesis of monoclinic and hexagonal WO{sub 3} nanostructures. • Nanocuboid and nanofiber growth using different structure directing agents. • WO{sub 3}–ZnO nanocomposites for dye degradation under UV and visible light. • High photocatalytic efficiency is achieved by 10 wt% monoclinic WO{sub 3}. • WO{sub 3} assists to trap hole in UV and arrests electron in visible light irradiation. - Abstract: Organic contaminants are a growing threat to the environment that widely demands their degradation by high efficient photocatalysts. Thus, the proposed research work primely focuses on the efficient degradation of methyl orange using designed WO{sub 3}–ZnO photocatalysts under both UV and visible light irradiation. Two different sets of WO{sub 3} nanostructures namely, monoclinic WO{sub 3} (m-WO{sub 3}) and hexagonal WO{sub 3} (h-WO{sub 3}) synthesizes in presence of a different structure directing agents. A specific dispersion technique allows the intimate contact of as-synthesized WO{sub 3} and ultra-violet active commercial ZnO photocatalyst in different weight variations. ZnO nanocrystal in presence of an optimum 10 wt% m-WO{sub 3} shows a high degree of photocatalytic activity under both UV and visible light irradiation compared to counterpart h-WO{sub 3}. Symmetrical monoclinic WO{sub 3} assists to trap hole in UV, but electron arresting mechanism predominates in visible irradiation. Coupling of monoclinic nanocuboid WO{sub 3} with ZnO proves to be a promising photocatalyst in both wavelengths.

36 MATERIALS SCIENCE↗

Gadolinium oxide decorated multiwalled carbon nanotube/tridoped titania nanocomposites for improved dye degradation under simulated solar light irradiation

Graphical abstract: Illustration of the collaborative effect between MWCNT-Gd and Gd,N,S-TiO{sub 2} towards degradation of AB 74. - Highlights: • MWCNT-Gd/tridoped titania was successfully prepared via a sol-gel method. • XPS revealed the presence of Ti, C, O, S, N and Gd in MWCNT-Gd/Gd,N,S-TiO{sub 2}. • MWCNT-Gd/Gd,N,S-TiO{sub 2} displayed 100% degradation of acid blue 74 in 150 min. • Over 60% TOC removal by MWCNT-Gd/Gd,N,S-TiO{sub 2}. - Abstract: Neodymium/gadolinium/europium, nitrogen and sulphur tridoped titania (Nd/Gd/Eu, N,S-TiO{sub 2}) was hybridised with pre-synthesised gadolinium oxide decorated multiwalled carbon nanotubes (MWCNT-Gd) using a sol–gel method. Subsequent to drying and calcination, composite photocatalysts: MWCNT-Gd/Nd,N,S-TiO{sub 2}, MWCNT-Gd/Gd,N,S-TiO{sub 2} and MWCNT-Gd/Eu,N,S-TiO{sub 2}, were obtained and characterised using TEM, SEM-EDX, UV–vis, XPS, XRD and FT-IR. Acid blue 74 (AB74) was used as a model dye to investigate the photocatalytic degradation properties of the prepared materials under simulated solar light irradiation. Coupling the different tridoped titania with MWCNT-Gd enhanced their activity compared to MWCNT/TiO{sub 2}, MWCNT-Gd/TiO{sub 2} and MWCNT/Gd,N,S-TiO{sub 2}. MWCNT-Gd/Gd,N,S-TiO{sub 2} showed the highest activity towards AB74 degradation reaching 100% decolourisation after 150 min of irradiation. Total organic carbon analysis revealed that over 50% of the AB74 molecules were completely mineralised after 180 min of irradiation in the presence of MWCNT-Gd/Gd,N,S-TiO{sub 2}.

36 MATERIALS SCIENCE↗

Synthesis of α-MoO{sub 3} nanoplates using organic aliphatic acids and investigation of sunlight enhanced photodegradation of organic dyes

Graphical abstract: Thermodynamically stable α-MoO{sub 3} nanoplates and nanorods were synthesized using organic structure controlling agents and demonstrated sun light enhanced photocatalytic degradation of methylene blue (MB) and rhodamine blue (Rh-B) dyes in aqueous solution. - Highlights: • α-MoO{sub 3} hexagonal nanoplates using organic structure controlling agents. • Tunable optical band gap of MoO{sub 3}. • Demonstrated strong sun light mediated enhanced photodegradation of methylene blue and rhodamine blue. • Photodegradation did not use any other external oxidizing agents. - Abstract: Thermodynamically stable α-MoO{sub 3} nanoplates were synthesized using organic aliphatic acids as structure controlling agents and investigated photocatalytic degradation of methylene blue (MB) and rhodamine blue (Rh-B) in presence of sun light. Three different organic aliphatic acids, citric acid (CA), tartaric acid (TA) and ethylene diamine tetra-acetic acid (EDTA), were employed to control morphologies. CA and TA predominantly produced extended hexagonal plates where EDTA gave nanorods as well as nanoplates. PXRD studies confirmed the formation of α-MoO{sub 3} nanoparticles. HR-TEM and FE-SEM reveal the formation of plate morphologies with 20–40 nm thickness, 50–100 nm diameter and 600 nm lengths. The different morphologies of α-MoO{sub 3} nanoparticles lead to the tunable optical band gap between 2.80 and 2.98 eV which was obtained from diffused reflectance spectra (DRS). Interestingly, the synthesized α-MoO{sub 3} nanoplates exhibited strong photocatalytic degradation of MB and Rh-B up to 99% in presence of sun light without using any oxidizing agents.

36 MATERIALS SCIENCE↗

Hot-compress: A new postdeposition treatment for ZnO-based flexible dye-sensitized solar cells

Highlights: • A new postdeposition treatment named hot-compress is introduced. • Hot-compression gives homogeneous compact layer ZnO photoanode. • I-V and EIS analysis data confirms the efficacy of this method. • Charge transport resistance was reduced by the application of hot-compression. - Abstract: This article introduces a new postdeposition treatment named hot-compress for flexible zinc oxide–base dye-sensitized solar cells. This postdeposition treatment includes the application of compression pressure at an elevated temperature. The optimum compression pressure of 130 Ma at an optimum compression temperature of 70 °C heating gives better photovoltaic performance compared to the conventional cells. The aptness of this method was confirmed by investigating scanning electron microscopy image, X-ray diffraction, current-voltage and electrochemical impedance spectroscopy analysis of the prepared cells. Proper heating during compression lowers the charge transport resistance, longer the electron lifetime of the device. As a result, the overall power conversion efficiency of the device was improved about 45% compared to the conventional room temperature compressed cell.

36 MATERIALS SCIENCE↗

Growth and characterization of ZnO nanostructure on TiO{sub 2}-ZnO films as a light scattering layer for dye sensitized solar cells

Graphical abstract: Pictorial representation of (a,b) electron transport path in nanoparticles and nanorods (red arrow marks), and (c,d) light scattering effect on TiO2-ZnO film without and with light scattering layer (blue, red and green arrow marks are incident, transmit and scattering light, respectively). - Abstract: In the present work, we studied the effect of light scattering layer on the performance of DSSCs. TiO{sub 2}-ZnO thin films were coated onto FTO glass substrate by spin coating technique as a photoanode for DSSCs. ZnO nanorods with flower structures were potentiostatically grown on TiO{sub 2}-ZnO films at various potentials from −1.1 to 1–1.3 V as a light scattering layer. XRD patterns reveal that as the deposition potentials increase the growth of ZnO nanorods increases along with (101) plane orientation. FE-SEM images display agglomerated grains and nanorods with flower structures for TiO{sub 2}-ZnO film, and ZnO has grown on TiO{sub 2}-ZnO film at a deposition potential of −1.3 V. UV–vis spectra confirm the TiO{sub 2}-ZnO with ZnO nanorods having a higher light scattering effect, absorbance and dye loading than that of another film. The efficiency of the DSSCs consisting of without and with scattering layer is estimated to be 0.79 and 1.81%, respectively.

36 MATERIALS SCIENCE↗

Combustion synthesized CeO{sub 2} as an anodic material in dye sensitized solar cells

Highlights: • One-step combustion synthesis of CeO{sub 2}. • Application of synthesized material as an anodic material for DSSC. • DSSC using CeO{sub 2} displayed an efficiency of 1.84%. - Abstract: Cerium oxide (CeO{sub 2}) has received a considerable attention due to its capacity to absorb visible light, low cost, high stability and environmental friendly catalytic applications. Among the various techniques employed to synthesize CeO{sub 2}, solution combustion synthesis is a one-step, economic and effective process. In this work, we report application of combustion synthesized CeO{sub 2} as an anodic material in the dye sensitized solar cell (DSSC). The synthesized material were characterized using standard analytical techniques such as XRD, SEM, BET, UV-DRS, and TEM. DSSC was fabricated using the synthesized material and characterized for incident photon to current conversion efficiency (IPCE), current density-voltage (J-V) measurements and electrochemical impedance spectroscopy. The power conversion efficiency of solar cell was found to be 1.84%. This is the first study to report use of combustion synthesized CeO{sub 2} for DSSC application.

36 MATERIALS SCIENCE↗

Biosynthesis of the palladium/sodium borosilicate nanocomposite using Euphorbia milii extract and evaluation of its catalytic activity in the reduction of chromium(VI), nitro compounds and organic dyes

Highlights: • Green synthesis of Pd/sodium borosilicate nanocomposite using Euphorbia milii aqueous extract. • Characterization of catalyst by FT-IR, XRD, FESEM, EDS, TEM and elemental mapping. • Catalytic reduction of Cr(VI), 2,4-DNPH, 4-NP, CR, MO and MB by Pd/sodium borosilicate nanocomposite. - Abstract: For the first time, a green method is developed to prepare palladium/sodium borosilicate nanocomposite by using aqueous extract of the leaves of Euphorbia milii as bioreducing and stabilizing agent. The immobilization of Pd NPs on the surface of the sodium borosilicate glass was established by several instrumental analysis including X-ray diffraction (XRD), fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), EDS elemental dot maps and transmission electron microscopy (TEM). The green synthesized nanocatalyst exhibited excellent performance in the reduction of the chromium (VI) (Cr(VI)), nitro compounds such as 2,4-dinitrophenylhydrazine (2,4-DNPH) and 4-nitrophenol (4-NP) and some organic dyes containing Congo red (CR), Methyl orange (MO), and Methylene blue (MB). The biosynthesized heterogeneous catalyst was easily recovered and reused at least in 5 consecutive reactions with no losing of its performance.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Effective photocatalytic removal of different dye stuffs using green synthesized zinc oxide nanogranules

Highlights: • Zinc oxide nanoparticles (ZnO-NPs) synthesized by a green strategy using lemon juice and ethylene glycol. • Physicochemical studies confess the formation of hexagonal wurtzite ZnO nanaogranules with some honed faces. • Direct band gap energy obtained for ZnO nano granules was 3.15 eV. • ZnO nano granules act as good catalyst for the photo degradation of methylene blue, congo red, and rhodamine B under UV-light irradiation. - Abstract: Zinc oxide nanoparticles (ZnO-NPs) obtained by a green synthetic strategy using lemon juice and ethylene glycol. The material was characterized using the techniques UV–vis spectroscopy, FTIR spectroscopy, X-ray diffraction analysis, FESEM, EDAX and HRTEM. Diffraction patterns and TEM micrographs confess the formation of hexagonal wurtzite ZnO nanaogranules with some honed faces and having an average size of 49.16 nm. The developed ZnO-NPs was tested for the photocatalytic degradation of Methylene Blue, Congo Red and Rhodamine B target dyes under UV irradiation and found to have remarkable activity.

77 NANOSCIENCE AND NANOTECHNOLOGY↗

Hydrothermal synthesis of bismuth niobates and their application in azo-dyes photo-discoloration

Highlights: • A new method of synthesis for obtaining pure phase bismuth niobates is proposed. • α-BiNbO{sub 4} and β-BiNbO{sub 4} were obtained by the calcination of an amorphous precursor. • Nanosized bismuth niobates have shown high band gap energies (3.2–3.4 eV). • Bismuth niobates are very efficient in the photo-discoloration of methyl orange. - Abstract: Bismuth niobates were obtained by hydrothermal synthesis using bismuth (III) nitrate pentahydrate [Bi(NO{sub 3}){sub 3}·5H{sub 2}O] and a Lindqvist potassium hexaniobate [K{sub 8-x}H{sub x}Nb{sub 6}O{sub 19}.nH{sub 2}O] as soluble precursors. Pure crystalline Bi{sub 5}Nb{sub 3}O{sub 15}, β-BiNbO{sub 4} and α- BiNbO{sub 4} were obtained as pure phases through co-precipitation at pH = 8, followed by hydrothermal treatment and calcination at 600, 700 or 800 °C, respectively, which are milder temperatures than those used in solid state, citrate sol-gel and ball milling methods. Band gap energies of α-BiNbO{sub 4} and β-BiNbO{sub 4} were estimated by UV–vis diffuse reflectance spectroscopy (DRS) as 3.2–3.4 eV, which are higher than experimental values reported in the literature. The materials were evaluated in the methyl orange azo-dye photo-discoloration under UV irradiation and complete bleach was attained. The triclinic phase presented a better efficiency as a photocatalyst than the orthorhombic phase. Unexpectedly, the mixture of both phases resulted in the highest photocatalytic efficiency, similar to that found for Degussa P25 commercial catalyst.

75 CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND↗

Single Component Dye-Sensitized Solar Cells Enabled by Copper Chemistry: Introduction of the Retro Cell

The possibility of utilizing a single molecule to act as both a chromophore and a redox shuttle in a new configuration of a dye-sensitized solar cell (DSSC) is investigated. This design, termed a retro cell, exploits the copper chromophore, [Cu(dsbtmp) 2 ] + (dsbtmp = bis(2,9-di(sec-butyl)-3,4,7,8- tetramethyl-1,10-phenanthroline), which has been shown to have excited state lifetimes in excess of a microsecond, enabling sensitization of TiO 2 while dissolved in solution. The oxidized chromophore can then diffuse to the counter electrode to be regenerated. This concept simplifies the device components and fabrication and eliminates a charge transfer step compared to that of traditional DSSCs. Initial investigations show the concept is viable; however, the performance is suboptimal. We have found the addition of 4-tertbutylpyridine (TBP) to the electrolyte plays a crucial role in enabling solar energy conversion. Evidence of TBP displacing one of the dsbtmp ligands in the oxidized [Cu(dsbtmp) 2 ] 2+ complex has been presented, which likely plays an important role in reducing recombination and enabling charge collection. The performance-limiting steps and routes to improved performance and viability of a retro cell are further discussed.

14 SOLAR ENERGY↗

Inner Layer Control of Performance in a Dye-Sensitized Photoelectrosynthesis Cell

Interfacial charge transfer and core-shell structures play important roles in dye-sensitized photoelectrosynthesis cells (DSPEC) for water splitting into H 2 and O 2 . An important element in the design of the photoanode in these devices is a core/shell structure which controls local electron transfer dynamics. Here, we introduce a new element, an internal layer of Al 2 O 3 lying between the Sb:SnO 2 /TiO 2 layers in a core/shell electrode which can improve photocurrents by up to 300%. In these structures, the results of photocurrent, transient absorption, and linear scan voltammetry measurements point to an important role for the Al 2 O 3 layer in controlling internal electron transfer within the core/shell structure.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Identification of Surface-Exposed Protein Radicals and A Substrate Oxidation Site in A-Class Dye-Decolorizing Peroxidase from Thermomonospora curvata

Dye-decolorizing peroxidases (DyPs) are a family of heme peroxidases in which a catalytic distal aspartate is involved in H 2 O 2 activation to catalyze oxidations under acidic conditions. They have received much attention due to their potential applications in lignin compound degradation and biofuel production from biomass. However, the mode of oxidation in bacterial DyPs remains unknown. We have recently reported that the bacterial TcDyP from Thermomonospora curvata is among the most active DyPs and shows activity toward phenolic lignin model compounds. On the basis of the X-ray crystal structure solved at 1.75 Å, sigmoidal steady-state kinetics with Reactive Blue 19 (RB19), and formation of compound II like product in the absence of reducing substrates observed with stopped-flow spectroscopy and electron paramagnetic resonance (EPR), we hypothesized that the TcDyP catalyzes oxidation of large-size substrates via multiple surface-exposed protein radicals. Among 7 tryptophans and 3 tyrosines in TcDyP consisting of 376 residues for the matured protein, W263, W376, and Y332 were identified as surface-exposed protein radicals. Only the W263 was also characterized as one of the surface-exposed oxidation sites. SDS-PAGE and size-exclusion chromatography demonstrated that W376 represents an off-pathway destination for electron transfer, resulting in the cross-linking of proteins in the absence of substrates. Mutation of W376 improved compound I stability and overall catalytic efficiency toward RB19. While Y332 is highly conserved across all four classes of DyPs, its catalytic function in A-class TcDyP is minimal, possibly due to its extremely small solvent-accessible areas. Identification of surface-exposed protein radicals and substrate oxidation sites is important for understanding the DyP mechanism and modulating its catalytic functions for improved activity on phenolic lignin.

59 BASIC BIOLOGICAL SCIENCES↗

Mechanistic Insights into Dye-Decolorizing Peroxidase Revealed by Solvent Isotope and Viscosity Effects

Dye-decolorizing peroxidases (DyPs) are a family of H 2 O 2 -dependent heme peroxidases that have shown potential applications in lignin degradation and valorization. However, the DyP kinetic mechanism remains underexplored. Using structural biology and solvent isotope (sKIE) and viscosity effects, many mechanistic characteristics have been determined for the B-class ElDyP from Enterobacter lignolyticus. Its structure revealed that a water molecule acts as the sixth axial ligand and two channels at diameters of ~3.0 and 8.0 Å lead to the heme center. A conformational change of ERS* to ERS, which have identical spectral characteristics, was proposed as the final step in DyPs’ bisubstrate Ping-Pong mechanism. This step is also the rate-determining step in ABTS oxidation. The normal KIE of wild-type ElDyP with D 2 O 2 at pD 3.5 suggested that compound 0 deprotonation by the distal aspartate is rate-limiting in the formation of compound I, which is more reactive under acidic pH than under neutral or alkaline pH. The viscosity effects and other biochemical methods implied that the reducing substrate binds with compound I instead of the free enzyme. The significant inverse sKIEs of k cat /K M and k ERS* suggested that the aquo release in ElDyP is mechanistically important and may explain the enzyme’s adoption of two-electron reduction for compound I. The distal aspartate is catalytically more important than the distal arginine and plays key roles in determining ElDyP’s optimum acidic pH. The kinetic mechanism of D143H-ElDyP was also briefly studied. The results obtained will pave the way for future protein engineering to improve DyPs’ lignolytic activity.

37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CH↗

Electric Switching of Fluorescence Decay in Gold–Silica–Dye Nematic Nanocolloids Mediated by Surface Plasmons

Tunable composite materials with interesting physical behavior can be designed through integrating unique optical properties of solid nanostructures with facile responses of soft matter to weak external stimuli, but this approach remains challenged by their poorly controlled coassembly at the mesoscale. Using scalable wet chemical synthesis procedures, we fabricated anisotropic gold–silica-dye colloidal nanostructures and then organized them into the device-scale (demonstrated for square-inch cells) electrically tunable composites by simultaneously invoking molecular and colloidal self-assembly. We show that the ensuing ordered colloidal dispersions of shape-anisotropic nanostructures exhibit tunable fluorescence decay rates and intensity. Here in this paper, we characterize how these properties depend on low-voltage fields and polarization of both the excitation and emission light, demonstrating a great potential for the practical realization of an interesting breed of nanostructured composite materials.

42 ENGINEERING↗