Ion beam induced evolution of surface morphology and optical properties of SnO2–ZnO nanocomposite thin films

SnO₂–ZnO nanocomposite thin films, prepared by a simple carbothermal reduction based vapor deposition method, were irradiated with 8 MeV Si³⁺ ions for engineering the morphological and optical properties. The surface morphology of the nanocomposites was studied by atomic force microscopy (AFM), while the optical properties were investigated by photoluminescence spectroscopy (PL) and Raman spectroscopy. AFM studies on the irradiated samples revealed growth of nanoparticles at lower fluence and a significant change in surface morphology leading to the formation of nanosheets and their aggregates at higher fluences. A tentative mechanism underlying the observed ion induced evolution of surface morphology of SnO₂–ZnO nanocomposite is proposed. PL studies revealed strong enhancement in the UV emissions from the nanocomposite thin film at lower fluence, while a drastic decrease in the UV emissions along with a significant enhancement in the defect emissions has been observed at higher fluences.     

Three Ln(III)-2,3,5-trichlorobenzoate coordination polymers (Ln = Tb,Ho and Er): Syntheses,structures and magnetic properties

Three novel lanthanide polymers, [Ln(III)(L)₃EtOH]_n (Ln = Tb(1), Ho(2), Er(3), HL = 2,3,5-trichlorobenzoic acid), have been solvothermal synthesized and characterized by single-crystal X-ray diffraction, infrared spectroscopy and element analyses. The three polymers crystallize in triclinic space group P-1. The Ln(III) ions are in turn bridged by double and quadruple carboxylate of L⁻ ligands to form one-dimensional (1D) chains. Magnetic studies reveal that polymer 1 demonstrates dominant ferromagnetic behavior, polymer 2 shows antiferromagnetic behavior, and polymer 3 present spin-canting behavior.     

Nickel foam-supported Fe,Ni-Polyporphyrin microparticles: Efficient bifunctional catalysts for overall water splitting in alkaline media

Developing highly active, stable and sustainable electrocatalysts for overall water splitting is of great importance to generate renewable H₂ for fuel cells. Herein, we report the synthesis of electrocatalytically active, nickel foam-supported, spherical core-shell Fe-poly(tetraphenylporphyrin)/Ni-poly(tetraphenylporphyrin) microparticles (FeTPP@NiTPP/NF). We also show that FeTPP@NiTPP/NF exhibits efficient bifunctional electrocatalytic properties toward both the oxygen evolution reaction (OER) and the hydrogen evolution reaction (HER). Electrochemical tests in KOH solution (1 M) reveal that FeTPP@NiTPP/NF electrocatalyzes the OER with 100 mA cm⁻² at an overpotential of 302 mV and the HER with 10 mA cm⁻² at an overpotential of 170 mV. Notably also, its catalytic performance for OER is better than that of RuO₂, the benchmark OER catalyst. Although its catalytic activity for HER is slightly lower than that of Pt/C (the benchmark HER electrocatalyst), it shows greater stability than the latter during the reaction. The material also exhibits electrocatalytic activity for overall water splitting reaction at a current density of 10 mA cm⁻² with a cell voltage of 1.58 V, along with a good recovery property. Additionally, the work demonstrates a new synthetic strategy to an efficient, noble metal-free-coordinated covalent organic framework (COF)-based, bifunctional electrocatalyst for water splitting.     

Investigation of performance variations due to the amplitude of group-delay ripple in chirped fiber Bragg gratings

We measure the system impacts due to the amplitude of group-delay (GD) ripple in single and cascaded chirped fiber Bragg gratings (CFBGs). Signals with smaller pulse width result in smaller performance variation at the same data rate. A 65-ps peak-to-peak GD ripple induces 0.9, 1.7, and 2.7 dB maximum penalties for 10, 20, and 40-Gb/s, respectively. We also find that cascading gratings with random ripple causes much less degradation than cascading gratings with the same ripple profile.     

Theoretical investigations on the spin Hamiltonian parameters for Er3+ ion in LiYF4

The spin Hamiltonian parameters g_∥, g_⊥, A_∥ and A_⊥ for Er³⁺ ion in LiYF₄ are investigated by using the perturbation formulas of these parameters for a 4f¹¹ ion in tetragonal symmetry. In these formulas, the contributions to the spin Hamiltonian parameters from the second-order perturbation terms and the admixtures of different states are considered. The relevant crystal field parameters are calculated from the superposition model and the local structural parameters of the Y³⁺ site occupied by impurity Er³⁺. The theoretical optical spectra within ⁴I_15/2 and ⁴I_13/2 states and the spin Hamiltonian parameters obtained in this work are consistent with the observed values.     

Time-of-flight secondary ion mass spectrometry as a tool for studying segregation phenomena at nickel–YSZ interfaces

Through a study of Ni–YSZ interfaces it is shown that time-of-flight-secondary ion mass spectrometry (TOF-SIMS) is a powerful and convenient tool for the analysis of ultra thin layers of segregated material at the interfaces and on free surfaces. Two different types of Ni, “pure Ni” (99.995% Ni) and “impure Ni” (99.8% Ni) were investigated. The contact areas on the YSZ and areas outside the contacts were examined with XPS and TOF-SIMS. The impure nickel causes a relatively larger amount of impurities to accumulate at the contact area, e.g. oxides of Mn, Ti, Si and Na. Some impurities migrate to the area outside the contact area. Even though on a larger scale the impurities seem to be homogeneously distributed, detailed analyses in and outside the contact area show the presence of impurity particles, and that the surface species are inhomogeneously distributed amongst the different grains. The extremely low detection limit, the small probe depth, the image capability, and the ease of elemental identification make TOF-SIMS an obvious choice as an analytical tool for studying segregation phenomena at metal–ceramic interfaces such as Ni–YSZ interfaces. XPS, being a quantitative technique, was used as a complementary technique to TOF-SIMS, which is not directly a quantitative technique.     

Upconversion emission of a novel glass ceramic containing Er: BaYF5 nano-crystals

In order to develop highly efficient upconversion (UC) material, Er³⁺-doped oxyfluoride glass ceramics containing BaYF₅ nano-crystals were fabricated for the first time. The randomly distributed BaYF₅ nano-particles with the size of nearly 25 nm precipitated from the glass matrix at about 700 °C, then tended to aggregate slightly with the increase of heating temperature, resulting in the enhancement of Er³⁺ UC emission in the wavelength ranging from 500 nm to 700 nm. The UC process was found very sensitive to Er³⁺ content: with the increase of Er³⁺ content from 0.5% to 1.0%, the UC intensity behaved with drastic exaltation; while further increasing Er³⁺ content to 2.0% resulted in a notable fluorescence quenching. Significantly, the UC efficiency of present glass ceramic preponderates notably over that of the previously reported glass ceramic containing LaF₃, implying its superior UC potentiality.     

Pd/Mg(OH)2 Heterogeneous Nanocatalysts Synthesized by a Facile One-Pot Hydrothermal Method for CO Direct Esterification to Dimethyl Oxalate

Catalysis Letters - Pd-based heterogeneous nanocatalysts have wide application in chemical industry. However, the traditional synthesis process contains multi-steps such as impregnation, dry,...     

Synthesis of NaYF4:20% Yb3+,2% Er3+,2% Ce3+@NaYF4 nanorods and their size dependent uptake efficiency under flow condition

Lanthanide doped fluorescent nanoparticles have gained considerable attention in biomedical applications. However, the low uptake efficiency of nanoparticles by cells has limited their applications. In this work, we demonstrate how the uptake efficiency is affected by the size of nanoparticles under flow conditions. Using the same size NaYF₄:20% Yb³⁺,2% Er³⁺,2% Ce³⁺ (the contents of rare earths elements are in molar fraction) nanoparticles as core, NaYF₄:20% Yb³⁺,2% Er³⁺,2% Ce³⁺@NaYF₄ core–shell structured nanorods (NRs) with different sizes of 60–224 nm were synthesized by thermal decomposition and hot injection method. Under excitation at 980 nm, a strong upconversion green emission (541 nm, ²H_11/2 → ⁴I_15/2 of Er³⁺) is observed for all samples. The emission intensity for each size nanorod was calibrated and is found to depend on the width of NRs. Under flow conditions, the nanorods with 96 nm show a maximum uptake efficiency by endothelial cells. This work demonstrates the importance of optimizing the size for improving the uptake efficiency of lanthanide-doped nanoparticles.