Non-conventional superconductivity in magnetic In and Sn nanoparticles

We report on experimental evidence of non-conversional pairing in In and Sn nanoparticle assemblies. Spontaneous magnetizations are observed, through extremely weak-field magnetization and neutron-diffraction measurements, to develop when the nanoparticles enter the superconducting state. The superconducting transition temperature TC shifts to a noticeably higher temperature when an external magnetic field or magnetic Ni nanoparticles are introduced into the vicinity of the superconducting In or Sn nanoparticles. There is a critical magnetic field and a critical Ni composition that must be reached before the magnetic environment will suppress the superconductivity. The observations may be understood when assuming development of spin-parallel superconducting pairs on the surfaces and spin-antiparallel superconducting pairs in the core of the nanoparticles.

Non-S-Wave Pairing Symmetries in Superconducting in and Sn Nanoparticles

We report on experimental evidence of non-s-wave pairing in In and Sn nanoparticle assemblies. Spontaneous magnetizations are observed, through extremely weak-field magnetization and neutron-diffraction measurements, to develop when the nanoparticles enter the superconducting state. The superconducting transition temperature TC shifts to a noticeably higher temperature when an external magnetic field or magnetic Ni nanoparticles are introduced into the vicinity of the superconducting In or Sn nanoparticles. There is a critical magnetic field and a critical Ni composition that must be reached before the magnetic environment will suppress the superconductivity. Development of spin-parallel superconducting pairs on the surfaces and spin-antiparallel superconducting pairs in the core of the nanoparticles is used to understand the observations.

Reexamining Different Factors of the Resonance-Enhanced High-Order Harmonic Generation in Atomic and Nanoparticle Laser-Induced Tin Plasmas

We reexamine the resonance enhancement of a single harmonic emission during the propagation of ultrafast pulses through atomic and nanoparticle tin-containing laser-induced plasma (LIP). We compare the single atomic Sn and Sn nanoparticle plasmas to demonstrate a distinction in the enhancement factor of the single harmonic in the case of fixed and tunable near-infrared pulses. The analysis of the dynamics of Sn LIP shows the range of optimal delays between heating and driving pulses (130–180 ns), at which the maximal harmonic yield can be achieved. The enhancements of the 17th and 18th harmonics of 806 nm pulses were analyzed in the case of single-color and two-color pumps of LIP, showing up to a 12-fold enhancement of even harmonics in the two-color pump case. We show the enhancement of a single harmonic in the vicinity of the 4d105s25p2P3/2→4d95s25p2 transitions of Sn II ions and demonstrate how this process depends on the constituency of the plasma components at different conditions of target ablation. The application of tunable (1280–1440 nm) radiation allows for demonstrating the variations of single harmonic enhancement using a two-color pump of Sn-containing LIP.

Synthesis and Characterization of Sn/Ag Nanoparticle Composite as Electro-Catalyst for Fuel Cell

In this research, Sn/Ag nanoparticle composite was produced by using chemical reduction method with the aids of sodium borohydride as reducing agent and sodium succinate as protective agent. The XRD, EDX, and TEM analyses showed that the Sn/Ag nanoparticle composite was formed with an average particle size of 4.37 + 0.44 nm. For the application, LSV analysis was done on Sn nanoparticle and Sn/Ag nanoparticle composite samples, and the analysis showed current produced from Sn/Ag nanoparticle composite (4.10 × 10-6 A) is higher than Sn nanoparticle (3.47 × 10-6 A) at the potential of -0.83V.

Carbon supported Pd–Sn nanoparticle eletrocatalysts for efficient borohydride electrooxidation

Carbon supported Pd–Sn (Pd–Sn/C) nanoparticle electrocatalysts are prepared via a facile and environmentally friendly method and successfully applied in BH4− electrooxidation.

Soldering of Passive Components Using Sn Nanoparticle Reinforced Solder Paste: Influence on Microstructure and Joint Strength

In this study, the effects of adding Sn nanopowder (particle size < 150 nm) to three solder pastes SAC3-X(H)F3+, SCAN-Ge071-XF3+, and water washable WW50-SAC3 are evaluated regarding microstructure, morphology, joint strength, and electrical resistance. The nanopowder was added at a rate of 10% by weight and then mechanically mixed until homogenous solder paste was obtained. The results showed that the addition of Sn nanoparticles resulted in homogenous bond formation for SAC-3 and SCAN, while voids and bubbles formation slightly increased within the joint interface for the water washable solder paste. The SCAN + Sn nano reinforced solder paste showed increased variation of joint strength from 12.6 to 39.9 N, while the water washable + Sn nanopowder reinforced solder paste showed less variability in joint strength from 17.3 to 33.9 N. Both sets of solder paste with and without Sn nano reinforced solder paste showed a reliable quality joint under mechanical shock testing after six shocks in six milliseconds with an 87.1 ms pulse duration. The results showed that Sn nanoparticles resulted in a small resistance change, while RDC values (in mΩ) slightly decreased for SAC and increased for SCAN and further increases for water washable solder paste.