Co3O4 Hollow Polyhedrons as Bifunctional Electrocatalysts for Reduction and Evolution Reactions of Oxygen

It is very important to exploit low‐cost and efficient oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) electrocatalysts for the development of renewable‐energy conversion and storage techniques. Although much attention has been made to develop efficient catalysts for ORR and OER, it is still highly desired to create new bifunctional catalysts. In this study, Co₃O₄ hollow polyhedrons are synthesized as efficient bifunctional electrocatalysts for ORR and OER by simple one‐step annealing Co‐centered metal–organic frameworks (ZIF‐67). Due to the large specific surface areas and high porosity, the as‐prepared Co₃O₄ hollow polyhedrons exhibit excellent electrocatalytic activities for ORR and OER in alkaline media. Co₃O₄ hollow polyhedrons show higher peak current density (0.61 mA cm^?2) with four‐electron pathway than Co₃O₄ particles (0.39 mA cm^?2), better methanol tolerance and superior durability (82.6%) than commercial Pt/C electrocatalyst (58.6%) for ORR after 25 000 s. In addition, Co₃O₄ hollow polyhedrons also display excellent OER performances with smaller overpotential (536 mV) for 10 mA cm^?2 than Co₃O₄ particles (593 mV) and superior stability (86.5%) after 25 000 s. This facile one‐step strategy based on metal–organic frameworks self‐sacrificed templates can be used to develop the promising well‐defined porous hollow metal oxides electrode materials for energy conversion and storage technologies.     

Sonocatalytic degradation of tetracycline hydrochloride with CoFe2O4/g-C3N4 composite

In this work, different mass percent ratios of CoFe₂O₄ coupled g-C₃N₄ (w%-CoFe₂O₄/g-C₃N₄, CFO/CN) nanocomposites were integrated through a hydrothermal process for the sonocatalytic eradication of tetracycline hydrochloride (TCH) from aqueous media. The prepared sonocatalysts were subjected to various techniques to investigate their morphology, crystallinity, ultrasound wave capturing activity and charge conductivity. From the investigated activity of the composite materials, it has been registered that the best sonocatalytic degradation efficiency of 26.71 % in 10 min was delivered when the amount of CoFe₂O₄ was 25% in the nanocomposite. The delivered efficiency was higher than that of bare CoFe₂O₄ and g-C₃N₄. This enriched sonocatalytic efficiency was credited to the accelerated charge transfer and separation of e⁻-h⁺ pair through the S-scheme heterojunctional interface. The trapping experiments confirmed that all the three species i.e. ^•OH, h⁺ and ^•O₂⁻ were involved in the eradication of antibiotics. A strong interaction was shown up between CoFe₂O₄ and g-C₃N₄ in the FTIR study to support charge transfer as confirmed from the photoluminescence and photocurrent analysis of the samples. This work will provide an easy approach for fabricating highly efficient low-cost magnetic sonocatalysts for the eradication of hazardous materials present in our environment.     

Ba2WO3F4, a new fluorotungstate with high luminescence efficiency

Ba₂WO₃F₄ is an efficient luminescent material under UV and X-ray excitation. The luminescence properties show a similarity with those of the tungstates, especially MgWO₄.     

A KTiOAsO4 Raman laser

Efficient nanosecond stimulated Raman scattering is observed in KTiOAsO₄ within an intracavity Raman laser configuration. A diode-end-pumped acousto-optically Q-switched Nd:YAG laser emitting at 1064.2 nm is employed as the pumping source. And efficient generation of the first-Stokes line at 1091.5 nm is observed. With an incident diode power of 8.11 W, a first-Stokes power of 1.38 W is obtained at a pulse repetition rate of 25 kHz, corresponding to a diode-to-Stokes conversion efficiency of 17%. The pulse width is 6.5 ns and the peak power is 8.5 kW. The performance characteristics of the device demonstrate that KTiOAsO₄ is competent and reliable for nanosecond Raman lasers.     

Generation of CO2 pulses by free induction decay in KCI:KReO4

Subnanosecond pulses have been produced by optical free induction decay in KCI:KReO₄. Here the ν₃ vibrational mode of the perrhenate ion (ReO^-₄) acts as a resonant absorber for the 10.6μm, P(26) CO₂ laser line. As the phase relaxation time T₂ of the substitutional molecule ion is very small, efficient picosecond pulses can be produced by this medium if faster shuttering can be devised.     

Spectral-kinetic characteristics of Pr luminescence in LiLuF4 host upon excitation in the UV-VUV range

Spectral-kinetic study of Pr³⁺ luminescence has been performed for LiLuF₄:Pr(0.1 mol%) single crystal upon the excitation within 5-12 eV range at T=8 K. The fine-structure of Pr³⁺ 4f ²→4f 5d excitation spectra is shown for LiLuF₄:Pr(0.1 mol%) to be affected by the efficient absorption transitions of Pr³⁺ ions into 4f 5d involving 4f ¹ core in the ground state. Favourable conditions have been revealed in LiLuF₄:Pr(0.1 mol%) for the transformation of UV-VUV excitation quanta into the visible range. Lightly doped LiLuF₄:Pr crystals are considered as the promising luminescent materials possessing the efficient Pr³⁺³P₀ visible emission upon UV-VUV excitation. The mechanism of energy transfer between Lu³⁺ host ion and Pr³⁺ impurity is discussed.     

Highly efficient double-ended diffusion-bonded Nd:YVO4 1525-nm eye-safe Raman laser under direct 880-nm pumping

A highly efficient 880-nm diode-pumped actively Q-switched eye-safe laser at 1525 nm with a double-ended diffusion-bonded YVO₄–Nd:YVO₄–YVO₄ crystal as the self-Raman medium is demonstrated. As high as 19.2% diode-to-Stokes optical conversion efficiency is obtained with an absorbed pump power of 5.2 W at a pulse repetition rate of 20 kHz.     

Significant Enhancement of Hydrogen Production in MoS2/Cu2ZnSnS4 Nanoparticles

Hydrogen produced from water splitting is a renewable and clean energy source. Great efforts have been paid in searching for inexpensive and highly efficient photocatalysts. Here, significant enhancement of hydrogen production has been achieved by introducing ≈1 mol% of MoS₂ to Cu₂ZnSnS₄ nanoparticles. The MoS₂/Cu₂ZnSnS₄ nanoparticles showed a hydrogen evolution rate of ≈0.47 mmol g⁻¹ h⁻¹ in the presence of sacrificial agents, which is 7.8 times that of Cu₂ZnSnS₄ nanoparticles (0.06 mmol g⁻¹ h⁻¹). In addition, the MoS₂/Cu₂ZnSnS₄ nanoparticles exhibited high stability, and only ≈3% of catalytic activity was lost after a long time irradiation (72 h). Microstructure investigation on the MoS₂/Cu₂ZnSnS₄ nanoparticles reveals that the intimate contact between the nanostructured MoS₂ and Cu₂ZnSnS₄ nanoparticles provides an effective one‐way expressway for photogenerated electrons transferring from the conduction band of Cu₂ZnSnS₄ to MoS₂, thus boosting the lifetime of charge carriers, as well as reducing the recombination rate of electrons and holes.     

Preparation of Ag3PO4/CoWO4 S-scheme heterojunction and study on sonocatalytic degradation of tetracycline

In this study, 0.6Ag₃PO₄/CoWO₄ composites were synthesized by hydrothermal method. The prepared materials were systematically characterized by techniques of scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffractometer (XRD), X-ray photoelectron spectroscopy (XPS), N₂ adsorption/desorption, and UV–vis diffuse reflectance spectrum (DRS). Furthermore, the sonocatalytic degradation performance of 0.6Ag₃PO₄/CoWO₄ composites towards tetracycline (TC) was investigated under ultrasonic radiation. The results showed that, combined with potassium persulfate (K₂S₂O₈), the 0.6Ag₃PO₄/CoWO₄ composites achieved a high sonocatalytic degradation efficiency of 97.89 % within 10 min, which was much better than bare Ag₃PO₄ or CoWO₄. By measuring the electrochemical properties, it was proposed that the degradation mechanism of 0.6Ag₃PO₄/CoWO₄ is the formation of S-scheme heterojunction, which increases the separation efficiency of electron-hole pairs (e^--h⁺) and generates more electrons and holes, thereby enhancing the degradation activity. The scavenger experiments confirmed that hole (h⁺) was the primary active substance in degrading TC, and free radicals (OH) and superoxide anion radical (O₂^–) were auxiliary active substances. The results indicated that 0.6Ag₃PO₄/CoWO₄ nanocomposites could be used as an efficient and reliable sonocatalyst for wastewater treatment.     

CuFe2O4 magnetic heterogeneous nanocatalyst: Low power sonochemical-coprecipitation preparation and applications in synthesis of 4H-chromene-3-carbonitrile scaffolds

The paper presents the synthesis and catalytic activity of CuFe₂O₄ nanoparticles. The CuFe₂O₄ nanoparticles have been prepared by sonochemical route under low power ultrasonic irradiation (UI) and using silent stirring at room temperature only (ST) along with co-precipitation method, without using any additive/capping agent. The synthesized magnetic nanoparticles were successfully used and compared for the synthesis of 4H-chromene-3-carbonitrile derivatives. The CuFe₂O₄ nanoparticles obtained by sonochemical route exhibit higher catalytic activity because of small size (0.5–5 nm), high surface area (214.55 m²/g), high thermal stability up to 700 °C, recyclability and reusability due to its magnetic characteristics than CuFe₂O₄ nanoparticles obtained by room temperature silent stirring. The synthesized CuFe₂O₄ nanoparticles were characterized by FT-IR, SEM–EDX, HR-TEM, XRD, TGA/DTA/DTG, BET, VSM techniques. The present method is of great interest due to its salient features such as environmentally compatible, efficient, short reaction time, chemoselectivity, high yield, cheap, moisture insensitive, green and recyclable catalyst which make it sustainable protocol.     

A comparative study of continuous laser operation on the F3/2-I9/2 transitions of Nd:GdVO4 and Nd:YVO4 crystals

A comparative study of Nd:GdVO₄ and Nd:YVO₄ crystal lasers pumped by a fiber-coupled diode array has been conducted at the ⁴F_3/2-⁴I_9/2 transitions wavelengths of 912 nm and 914 nm, as well as when intracavity frequency-doubled to 456 nm and 457 nm, respectively. At the fundamental wavelength of 912 nm and second harmonic wavelength of 456 nm, maximum output powers from the Nd:GdVO₄ crystal laser were 7.85 W and 4.6 W at a pump power of 29 W. All the results obtained from Nd:GdVO₄ were superior to those of Nd:YVO₄, indicating that Nd:GdVO₄ is a more efficient laser crystal than Nd:YVO₄ for laser operation on the ⁴F_3/2-⁴I_9/2 transitions.     

Self-assembled CaMoO4 and CaMoO4:Eu hierarchical superstructures: Facile sonochemical route synthesis and tunable luminescent properties

Tetragonal CaMoO₄ and CaMoO₄:Eu³⁺ with various novel three-dimensional (3D) hierarchical architectures were successfully synthesized via a facile, efficient sonochemistry process in the absence of any surfactant or template. XRD, EDS, FE-SEM, and photoluminescence (PL) were employed to characterize the as-obtained products. It was found that morphology modulation could be easily realized by changing pH value of the precursor. The pH value of the precursor not only affected the substructures of the hierarchical structures, but also determined the size distributions of the final products. The formation mechanism for different hierarchical architectures was proposed on the basis of time-dependent experiments. The luminescence spectra showed that CaMoO₄:Eu³⁺ phosphors can be effectively excited by the near ultraviolet (UV) (396 nm) and blue (466 nm) light, and exhibited strong red emission around 615 nm, which was attributed to the Eu³⁺⁵D₀→⁷F₂ transition. Compared with Y₂O₃:Eu³⁺ phosphor, CaMoO₄:Eu³⁺ is much more stable, efficient and suitable, therefore, this phosphors could be a promising red component for possible applications in the field of LEDs.     

Enhanced visible-light-driven photocatalytic performance for degradation of organic contaminants using PbWO4 nanostructure fabricated by a new,simple and green sonochemical approach

Water contamination has turned into a critical global concern that menaces the entire biosphere and has a notable effect on the lives of living beings and humans. As a proper and environmentally friendly solution, visible-light photocatalysis technology has been offered for water contamination removal. There is a strong interest in the design of the efficient catalytic materials that are photoactive with the aid of visible light. Herein, to fabricate a highly efficient photocatalyst for removal of organic pollution in water, a facile and swift sonochemical route employed for creation of the spindle shaped PbWO₄ nanostructure with the aid of an environmentally friendly capping agent (maltose) for the first time. To optimize the efficiency, dimension and structure of lead tungstate, various effective factors such as time, dose of precursors, power of ultrasound waves and kind of capping agents were altered. The attributes of PbWO₄ samples were examined with the aid of diverse identification techniques. The produced lead tungstate samples in role of visible-light photocatalyst were applied to remove organic pollution in water. The kinds of pollutants, dose and type of catalyst were examined as notable factors in the capability to eliminate contaminants. Very favorable catalytic yield and durability were demonstrated by spindle-shaped PbWO₄ nanostructure (produced at power of 60 W for 10 min and with usage of maltose). Usage of ultrasonic irradiation could bring to improvement of catalytic yield of PbWO₄ to 93%. Overall, the outcomes could introduce the spindle-shaped PbWO₄ nanostructure as an efficient substance for eliminating water contamination under visible light.     

调控氧空位实现高比表面积Co3O4纳米片上的产氧反应

Electrochemical water splitting requires efficient water oxidation catalysts to accelerate the sluggish kinetics of water oxidation reaction. Here, we designed an efficient Co₃O₄ electrocatalyst using a pyrolysis strategy for oxygen evolution reaction (OER). Morphological characterization confirmed the ultra-thin structure of nanosheet. Further, the existence of oxygen vacancies was obviously evidenced by the X-ray photoelectron spectroscopy and electron spin resonance spectroscopy. The increased surface area of Co₃O₄ ensures more exposed sites, whereas generated oxygen vacancies on Co₃O₄ surface create more active defects. The two scenarios were beneficial for accelerating the OER across the interface between the anode and electrolyte. As expected, the optimized Co₃O₄ nanosheets can catalyze the OER efficiently with a low overpotential of 310 mV at current density of 10 mA/cm² and remarkable long-term stability in 1.0 mol/L KOH.     

Intrinsic and impurity luminescence of rare earth ions doped KYF4 nanophosphors

The KYF₄ nanopowders, non-doped and doped with Ce³⁺ or Tb³⁺, having well-crystallized, unaggregated, monodisperse (±15%) nanoparticles with the cubic (the size in the range from ∼15 to ∼30 nm) or hexagonal (from ∼30 to ∼50 nm) crystal structure have been successfully synthesized by microwave-hydrothermal treatment of as-precipitated gels. In KYF₄ hexagonal nanopowders an intense STE-type luminescence at ∼4.4 eV was observed which is not quenched at room temperature. In contrast to single crystals or cubic nanopowders, in KYF₄ hexagonal nanopowders doped with Ce³⁺ or Tb³⁺, a rather efficient energy transfer is observed from the host to Ce³⁺ or Tb³⁺ ions, respectively, because of overlapping the emission spectrum of STE-type luminescence and the spectrum of efficient absorption on 4f-5d transitions in Ce³⁺ or Tb³⁺.     

Compact and efficient Kerr-lens mode-locked diode-pumped actively Q-switched YVO4-Nd:YVO4 laser

By using a simple linear configuration, a stable and efficient YVO₄-Nd:YVO₄ laser, actively Q-switched by an acousto-optic modulator and passively mode-locked by KLM is realized, from which the great average output power, the high efficiency are obtained and the mode-locked pulse inside the Q-switched pulse has a repetition rate of 470 MHz. The nearly 100% modulation depth of the Q-switched mode-locked pulses can be obtained at any pump power over the threshold. Considering the Kerr-lens effect of laser medium and Q-switching by an acousto-optic modulator, we have analyzed the self-mode-locked YVO₄-Nd:YVO₄ laser by using the nonlinear ABCD propagation matrix and the hyperbolic fluctuation mechanism. The numerical solutions are in good agreement with the experimental results.     

Highly enhanced luminescence of ZnO green phosphors by calcining ZnS with NH4Br as additive

Zinc oxide (ZnO) phosphors with highly efficient green emission have been prepared by calcining ZnS with NH₄Br as additive in air atmosphere. The luminescent properties of as-prepared ZnO phosphors were characterized by X-ray photoelectron spectroscopy and photoluminescence. Our results reveal that the green emission is ascribed to a transition of a photo-generated electron from the localized defect centers (V_o⁺) to a deeply trapped hole (V_Zn⁻) within the band gap. The addition of NH₄Br enhances the luminescent emission of ZnO by promoting the formation of vacancies of both oxygen and zinc.     

Characteristic white light emission via down-conversion SrGdAlO4:Dy3+ nanophosphor

An efficient and cost-effective technique, solution combustion synthesis was used to synthesize Dy³⁺ doped SrGdAlO₄ nanophosphor utilizing urea as a suitable fuel. The tetragonal phase and nano-crystallinity of the synthesized phosphor belonging to I4/mmm space group was confirmed by powder X-ray diffraction (PXRD) and transmission electron microscope (TEM) technique respectively. Various crystal structure parameters and refined atomic positions of host matrix and SrGd_0.95Dy_0.05AlO₄ nanophosphor were determined by Rietveld refinement. The two intense bands i.e. blue and yellow bands were observed in photoluminescence emission spectrum recorded at 352 nm excitation wavelength, associated to transitions ⁴F_9/2 → ⁶H_15/2 (484 nm) and ⁴F_9/2 → ⁶H_13/2 (575 nm) respectively. Photometric characterizations revealed the emission of white color by the synthesized nanophosphor proving its wide applications in WLEDs (white light emitting diodes). Band gap values calculated using diffuse reflectance spectra (DRS) were found to vary in the range of 5.50 eV–5.59 eV for host and doped lattice system. Keeping in mind, the concentration quenching phenomenon, SrGd_0.95Dy_0.05AlO₄ was considered as optimized nanophosphor for WLEDs.     

All solid-state CW Nd:GdVO<Subscript>4</Subscript>-GdCOB laser at 670 nm

We report the efficient compact red laser at 670 nm generation by intracavity frequency doubling of a continuous wave laser operation of a diode pumped Nd:GdVO₄ laser on the ⁴ F _3/2 → ⁴ I _13/2 transition at 1340 nm. An GdCa₄O(BO₃)₃ (GdCOB) crystal, cut for critical type I phase matching at room temperature is used for second harmonic generation of the laser. At an incident pump power of 18.2 W, as high as 1.32 W of continuous wave (CW) output power at 670 nm is achieved with 15-mm-long GdCOB. The optical-to-optical conversion efficiency is up to 7.3%, and the fluctuation of the red output power was better than 3.5% in the given 30 min.     

Synthesis and characterization of Co3O4 nanorods by thermal decomposition of cobalt oxalate

Cobalt oxalate was used as a precursor to prepare Co₃O₄ nanorods by thermal decomposition. The combinations of triphenylphosphine and oleylamine were added as surfactants to control the morphology of the particles. The products were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR) spectroscopy and X-ray photoelectron spectroscopy (XPS). The diameters of Co₃O₄ nanorods are 20 nm and the average lengths are around 500 nm. The hysteresis loops of the obtained samples reveal the ferromagnetic behaviors, the enhanced coercivity (H_c) and decreased saturation magnetization (M_s) in contrast to their respective bulk materials. The study provides a simple and efficient route to synthesize Co₃O₄ nanorods at low temperature.