Biosynthesis of zinc oxide nanoparticles using Euphorbia milii leaf constituents: Characterization and improved photocatalytic degradation of methylene blue dye under natural sunlight

A facile biosynthesis route was followed to prepare zinc oxide nanoparticles (ZnO NPs) using Euphorbia milii (E. milii) leaf constituents. The SEM images exhibited presence of spherical ZnO NPs and the corresponding TEM images disclosed monodisperse nature of the ZnO NPs with diameter ranges between 12 and 20 nm. The Brunauer–Emmett–Teller (BET) analysis revealed that the ZnO NPs have specific surface area of 20.46 m²/g with pore diameter of 2 nm–10 nm and pore volume of 0.908 cm³/g. The EDAX spectrum exemplified the existence of Zn and O elements and non-appearance of impurities that confirmed pristine nature of the ZnO NPs. The XRD pattern indicated crystalline peaks corresponding to hexagonal wurtzite structured ZnO with an average crystallite size of 16.11 nm. The FTIR spectrum displayed strong absorption bands at 512 and 534 cm^?1 related to ZnO. The photocatalytic action of ZnO NPs exhibited noteworthy degradation of methylene blue dye under natural sunlight illumination. The maximum degradation efficiency achieved was 98.17% at an illumination period of 50 min. The reusability study proved considerable photostability of the ZnO NPs during photocatalytic experiments. These findings suggest that the E. milii leaf constituents can be utilized as suitable biological source to synthesis ZnO NPs for photocatalytic applications.     

Gold-Catalyzed Divergent Ring-Opening Rearrangement of Cyclopropenes Enabled by Dichotomous Gold−Carbenes

The gold-catalyzed ring-opening rearrangement of cyclopropenes affords an efficient route to either polysubstituted naphthols or aryl-substituted furans. Owing to the unique dichotomy of gold−carbenes, this protocol provides a switchable reaction selectivity between naphthols and furans enabled by the use of TFP−Au(MeCN)SbF₆ (tri(2-furyl) phosphine) or PNP(AuNTf₂)₂ (bis(diphenylphosphino)(isopropyl) amine) as catalysts respectively. It is proposed that the gold−carbene intermediate might be involved in the cyclopropene→naphthol rearrangement while the gold-carbocation is more likely to be involved in the cyclopropene→furan rearrangement.     

Hybrid cyclotriphosphazene–polysiloxane–nano-SiO2 composites with improved mechanical properties

Starting from the functional cyclotriphosphazene, polysiloxane and nano-SiO₂ precursors, three new hybrid nanocomposites with reinforced mechanical properties were prepared. Young’s modulus values for all the composite samples are similar in the range of 7–11 MPa, stress at fracture increases with the nano-SiO₂ content increase in the material and reaches a maximum value of 36 MPa for the composite with 20% nano-SiO₂. The nanocomposites investigated are elastic and demonstrate the ability to be deformed without failure up to 54% strain.     

Alkaline oxygen evolution: exploring synergy between fcc and hcp cobalt nanoparticles entrapped in N-doped graphene

Herein, we report a Mott-Schottky catalyst by entrapping cobalt nanoparticles inside the N-doped graphene shell (Co@NC). The Co@NC delivered excellent oxygen evolution activity with an overpotential of merely 248 mV at a current density of 10 mA cm^–2 with promising long-term stability. The importance of Co encapsulated in NC has further been demonstrated by synthesizing Co nanoparticles without NC shell. The synergy between the hexagonal close-packed (hcp) and face-centered cubic (fcc) Co plays a major role to improve the OER activity, whereas the NC shell optimizes the electronic structure, improves the electron conductivity, and offers a large number of active sites in Co@NC. The density functional theory calculations have revealed that the hcp Co has a dominant role in the surface reaction of electrocatalytic oxygen evolution, whereas the fcc phase induces the built-in electric field at the interfaces with N-doped graphene to accelerate the H⁺ ion transport.     

Photothermal Oxidation of Cinnamyl Alcohol with Hydrogen Peroxide Catalyzed by Gold Nanoparticle/Antimony-Doped Tin Oxide Nanocrystals

Gold nanoparticles with different mean sizes were formed on antimony-doped tin oxide nanocrystals by the temperature-varied deposition-precipitation method (Au/ATO NCs). Au/ATO NCs possess strong absorption in the near-infrared region due to Drude excitation in addition to the localized surface plasmon resonance (LSPR) of AuNPs around 530 nm. Au/ATO NCs show thermally activated catalytic activity for the oxidation of cinnamyl alcohol to cinnamaldehyde by hydrogen peroxide. The catalytic activity increases with a decrease in the mean Au particle size (d_Au) at 5.3 nm≤d_Au≤8.2 nm. Light irradiation (λ_ex >660 nm, ∼0.5 sun) of Au/ATO NCs increases the rate of reaction by more than twice with ∼95 % selectivity. Kinetic analyses indicated that the striking enhancement of the reaction stems from the rise in the temperature near the catalyst surface of ∼30 K due to the photothermal effect of the ATO NCs.     

Sonocatalytic degradation of EDTA in the presence of Ti and Ti@TiO2 nanoparticles

The sonocatalytic degradation of EDTA (C₀ = 5 10⁻³ M) in aqueous solutions was studied under 345 kHz (P_ac = 0.25 W mL⁻¹) ultrasound at 22–51 °C, Ar/20%O₂, Ar or air, and in the presence of metallic titanium (Ti⁰) or core-shell Ti@TiO₂ nanoparticles (NPs). Ti@TiO₂ NPs have been obtained using simultaneous action of hydrothermal conditions (100–214 °C, autogenic pressure P = 1.0–19.0 bar) and 20 kHz ultrasound, called sonohydrothermal (SHT) treatment, on Ti⁰ NPs in pure water. Ti⁰ is composed of quasi-spherical particles (30–150 nm) of metallic titanium coated with a metastable titanium suboxide Ti₃O. SHT treatment at 150–214 °C leads to the oxidation of Ti₃O and partial oxidation of Ti⁰ and formation of nanocrystalline shell (10–20 nm) composed of TiO₂ anatase. It was found that Ti⁰ NPs do not exhibit catalytic activity in the absence of ultrasound. Moreover, Ti⁰ NPs remain inactive under ultrasound in the absence of oxygen. However, significant acceleration of EDTA degradation was achieved during sonication in the presence of Ti⁰ NPs and Ar/20%O₂ gas mixture. Coating of Ti⁰ with TiO₂ nanocrystalline shell reduces sonocatalytic activity. Pristine TiO₂ anatase nanoparticles do not show a sonocatalytic activity in studied system. Suggested mechanism of EDTA sonocatalytic degradation involves two reaction pathways: (i) sonochemical oxidation of EDTA by OH/HO₂ radicals in solution and (ii) EDTA oxidation at the surface of Ti⁰ NPs in the presence of oxygen activated by cavitation event. Ultrasonic activation most probably occurs due to the local heating of Ti⁰/O₂ species at cavitation bubble/solution interface.     

Nephroprotective properties of chitosan/sodium lignosulfonate/Au nanoparticles in streptozotocin-induced nephropathy in mice: Introducing a novel therapeutic drug for the treatment of nephropathy

In this study, we report the green synthesis of nontoxic, stable, and small size gold nanoparticle by using chitosan/sodium lignosulfonate hydrogel with capping/reducing ability for the synthesis of CS/NaLS/Au NPs. The prepared bio-nanocomposite were characterized by advanced physicochemical techniques like Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), Energy Dispersive X-ray spectroscopy (EDX) and X-ray Diffraction (XRD) study. It has been established that CS/NaLS/Au NPs have a spherical shape with a mean diameter from 20 to 30 nm. Diabetes was induced by administration of 60 mg/kg of streptozotocin (STZ) intraperitoneally in 100 mature male mice and they were randomly divided into 5 groups. The negative control group received normal saline and treatment groups received glibenclamide with dose 0.5 mg/kg and 10 and 40 μg/kg of CS/NaLS/Au NPs through gavage for 50 days. In addition, one group considered as positive control (in treated-diabetic). On the last day, serum levels of samples blood glucose, urea and creatinine were measured. After tissue processing, 5 μm sections of the kidneys were prepared and they were stained by periodic acid Schiff (PAS) and used for stereological analysis. In the antioxidant test, the IC50 of CS/NaLS/Au NPs and BHT against DPPH free radicals were 117 and 86 µg/mL, respectively. In the cellular and molecular part of the recent study, the treated cells with CS/NaLS/Au NPs were assessed by MTT assay for 48 h about the cytotoxicity properties on normal (HUVEC) cell line. The increased levels of blood glucose and urea were decreased (p < 0.05) significantly in CS/NaLS/Au NPs-treated groups as compared to the untreated diabetic. The kidney weight, kidney volume (Volume of cortex, medulla, glomerulus, proximal and distal tubules, collecting ducts, loop of Henle, interstitial tissues, and vessels) and kidney structures length (length of proximal and distal tubules, collecting ducts, loop of Henle, and vessels) decreased significantly (p < 0.05) after treatment with high dose of CS/NaLS/Au NPs (p < 0.05). According to the obtained results, CS/NaLS/Au NPs can regulates the levels of blood glucose and urea and inhibits from kidney damages in STZ-induced diabetic mice. This study suggested CS/NaLS/Au NPs as an antidiabetic and nephroprotective drug in the developing countries.     

Mechanical property and deformation mechanism of gold nanowire with non-uniform distribution of twinned boundaries:A molecular dynamics simulation study

The mechanical property and deformation mechanism of twinned gold nanowire with non-uniform distribution of twinned boundaries(TBs) are studied by the molecular dynamics(MD) method. It is found that the twin boundary spacing(TBS) has a great effect on the strength and plasticity of the nanowires with uniform distribution of TBs. And the strength enhances with the decrease of TBS, while its plasticity declines. For the nanowires with non-uniform distribution of TBs, the differences in distribution among different TBSs have little effect on the Young's modulus or strength, and the compromise in strength appears. But the differences have a remarkable effect on the plasticity of twinned gold nanowire. The twinned gold nanowire with higher local symmetry ratio has better plasticity. The initial dislocations always form in the largest TBS and the fracture always appears at or near the twin boundaries adjacent to the smallest TBS. Some simulation results are consistent with the experimental results.     

钼改性页硅酸镍催化剂催化顺酐加氢性能

通过蒸氨法合成了一系列钼改性的页硅酸镍催化剂, 考察了钼含量对催化剂结构及其催化顺酐液相加氢性能的影响. 采用氮气物理吸附-脱附、 X射线衍射(XRD)、 傅里叶变换红外光谱(FTIR)、 透射电子显微镜(TEM)、 氢气程序升温还原(H₂-TPR)、 氨气程序升温脱附(NH₃-TPD)、 吡啶吸附红外光谱(Py-IR)和原位X射线光子能谱(XPS)等手段对催化剂的结构和形貌等进行了表征. 结果表明, 助剂Mo的引入对催化剂结构形貌及其催化性能影响显著. Mo的引入提高了活性金属Ni的还原度, 增加了催化剂表面金属Ni⁰的数量, 金属Ni在还原过程产生氢溢流, 溢流氢将部分MoO₃还原为具有酸性的MoO_x物种, 由于金属Ni⁰与具有Lewis酸(L酸)特性的MoO_x及Ni^σ+的协同效应, 显著提高了催化剂对顺酐C≡C和C≡O的加氢活性. 当Mo含量(质量分数)为3%时, 其催化活性最高, 在160 ℃和5 MPa H₂气条件下, 反应3 h顺酐的转化率为100%, 产物γ-丁内酯的选择性为27%.     

Electrolyte Effects on the Electrocatalytic Performance of Iridium-Based Nanoparticles for Oxygen Evolution in Rotating Disc Electrodes

Proton exchange membrane water electrolysers are very promising renewable energy conversion devices that produce hydrogen from sustainable feedstocks. These devices are mainly limited by the sluggish kinetics of the oxygen evolution reaction (OER). Ir-based nanoparticles are both reasonably active and stable for the OER in acidic media. The electrolyte composition and the pH may play a crucial role in electrocatalysis, yet they have been widely overlooked for the OER. Herein, we present a study on the effects of the composition and concentration of the electrolyte on commercial Ir black nanoparticles using concentrations of 0.05 M, 0.1 M and 0.5 M of both sulphuric and perchloric acid. The results show an important effect of the electrolyte composition on the catalytic performance of the Ir nanoparticles. The concentration of H₂SO₄ interferes on the oxidation of Ir and decreases the catalytic performance of the catalyst. HClO₄ does not show strong interferences in the electrochemistry of Ir. Higher catalytic performances are observed in HClO₄ electrolytes in comparison to H₂SO₄ with little effect of the concentration of HClO₄.