Observation of deformation twinning and martensitic transformation during nanoindentation of a transformation-induced plasticity steel

For the first time, deformation twinning and martensitic transformation were observed in retained austenite in a low-Alloyed transformation-induced plasticity steel using nanoindentation in conjunction with electron backscattering diffraction and transmission electron microscopy. Dislocation glide, martensite formation and deformation twinning were correlated to pop-ins and deviation from linearity in the load-displacement curve. Deformation twinning was found to enhance the stability of retained austenite. This observation furthers our understanding of RA stability during straining of low-Alloyed multiphase TRIP steel

CuS2‐Passivated Au-Core, Au3Cu-Shell nanoparticles analyzed by Atomistic-Resolution Cs-Corrected STEM

Au-core, Au3Cu-alloyed shell nanoparticles passivated with CuS2 were fabricated by the polyol method, and characterized by Cs-corrected scanning transmission electron microscopy. The analysis of the high-resolution micrographs reveals that these nanoparticles have decahedral structure with shell periodicity, and that each of the particles is composed by Au core and Au3Cu alloyed shell surrounded by CuS2 surface layer. X-ray diffraction measurements and results from numerical simulations confirm these findings. From the atomic resolution micrographs, we identified edge dislocations at the twin boundaries of the particles, as well as evidence of the diffusion of Cu atoms into the Au region, and the reordering of the lattice on the surface, close to the vertices of the particle. These defects will impact the atomic and electronic structures, thereby changing the physical and chemical properties of the nanoparticles. On the other hand, we show for the first time the formation of an ordered superlattice of Au3Cu and a self-capping layer made using one of the alloy metals. This has significant consequences on the physical mechanism that form multicomponent nanoparticles

Nanodroplets for stretchable superconducting circuits

The prospective utilization of nanoscale superconductors as micro/nanocoils or circuits with superior current density and no electrical resistance loss in next-generation electronics or electromagnetic equipment represents a fascinating opportunity for new microsystem technologies. Here, a family of superconducting liquid metals (Ga-In-Sn alloys) and their nanodroplets toward printable and stretchable superconducting micro/nanoelectronics is developed. By tuning the composition of liquid metals the highest superconducting critical temperature (Tc) in this family can be modulated and achieved as high as 6.6 K. The liquid metal nanodroplets retain their bulk superconducting properties and can be easily dispersed in different solvents as inks. The printable and stretchable superconducting micro/nano coils, circuits and electrodes have been fabricated by inkjet printer or laser etching by using superconducting nanodroplets inks. This novel superconducting system greatly promotes the commercial utilization of superconductors into advanced flexible micro/nanoelectronic devices and offers a new platform for developing more application with superconductors

Nitrogen-Doped Nanoporous Carbon Membranes with Co/CoP Janus-Type Nanocrystals as Hydrogen Evolution Electrode in Both Acidic and Alkaline Environments

Self-supported electrocatalysts being generated and employed directly as electrodes for energy conversion has been intensively pursued in the fields of materials chemistry and energy. Herein, we report a synthetic strategy to prepare freestanding hierarchically structured, nitrogen-doped nanoporous graphitic carbon membranes functionalized with Janus-type Co/CoP nanocrystals (termed as HNDCM-Co/CoP), which were successfully applied as a highly efficient, binder-free electrode in the hydrogen evolution reaction (HER). Benefited from multiple structural merits, such as a high degree of graphitization, three-dimensionally interconnected micro/meso/macropores, uniform nitrogen doping, well-dispersed Co/CoP nanocrystals, as well as the confinement effect of the thin carbon layer on the nanocrystals, HNDCM-Co/CoP exhibited superior electrocatalytic activity and long-term operation stability for HER under both acidic and alkaline conditions. As a proof-of-concept of practical usage, a 5.6 cm x 4 cm x 60 μm macroscopic piece of HNDCM-Co/CoP was prepared in our laboratory. Driven by a solar cell, electroreduction of water in alkaline conditions (pH 14) was performed, and H2 was produced at a rate of 16 mL/min, demonstrating its potential as real-life energy conversion systems

Nitrogen-doped Nanoporous Carbon Membranes Functionalized with Co/CoP Janus-type nanocrystals as Hydrogen Evolution Electrode in Both Acid and Alkaline Environment

Self-supported electrocatalysts being generated and employed directly as electrode for energy conversion has been intensively pursued in the fields of materials chemistry and energy. Herein, we report a synthetic strategy to prepare freestanding hierarchically structured, nitrogen-doped nanoporous graphitic carbon membranes functionalized with Janus-type Co/CoP nanocrystals (termed as HNDCM-Co/CoP), which were successfully applied as a highly-efficient, binder-free electrode in hydrogen evolution reaction (HER). Benefited from multiple structural merits, such as high degree of graphitization, three-dimensionally interconnected micro-/meso-/macropores, uniform nitrogen-doping, well-dispersed Co/CoP nanocrystals as well as the confinement effect of the thin carbon layer on the nanocrystals, HNDCM-Co/CoP exhibited superior electrocatalytic activity and long-term operation stability for HER under both acid and alkaline conditions. As a proof-of-concept of practical usage, a macroscopic piece of HNDCM-Co/CoP of 5.6 cm x 4 cm x 60 um in size was prepared in our laboratory. Driven by a solar cell, electroreduction of water in alkaline condition (pH 14) was performed, and H2 has been produced at a rate of 16 ml/min, demonstrating its potential as real-life energy conversion systems.Comment: 31 pages, 15 page

Influence of capping on the atomistic arrangement in palladium nanoparticles at room temperature

The role that protecting molecules have on the way that palladium atoms arrange themselves in nanoparticles prepared at room temperature was studied by the analysis of aberration-corrected scanning transmission electron microscopy images and atomistic Langevin dynamics simulations. It was found that the arrangement of Pd atoms is less ordered in thiolate-protected nanoparticles than in amine-protected ones. The experimental and theoretical data showed that the disorder in ∼3 nm thiolate-protected particles is promoted by the strong S–Pd bond in the sulfide layer that surrounds the nanoparticles.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicada

New insights into the chemistry of thiolate-protected palladium nanoparticles

This paper establishes the chemical nature of Pd nanoparticles protected by alkanethiolates that were prepared through a ligand place-exchange approach and the two-phase method, first developed for Au nanoparticles by Brust and Schiffrin. After 10 years since the first study on this kind of Pd nanoparticles was published, the surface composition of the particles is a matter of debate in the literature and it has not been unambiguously assessed. The nanoparticles were studied by means of several techniques: UV–visible spectroscopy, scanning transmission electron microscopy, Fourier-transform infrared spectroscopy, extended X-ray absorption fine structure, and X-ray photoelectron spectroscopy. The experimental data, obtained for the 3 nm diameter Pd particles, prepared by both synthetic routes, are consistent with nanoparticles composed by Pd(0) cores surrounded by a submonolayer of sulfide species, which are protected by alkanethiolates. Also, we unambiguously demonstrate that the chemical nature of these particles is very similar to that experimentally found for alkanethiolate-modified bulk Pd. The results from this paper are important not only for handling thiolate-protected Pd nanoparticles in catalysis and sensing, but also for the basic comprehension of metallic nanoparticles and the relation of their surface structure with the synthesis method.Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicada