Synthesis technique for 1D segmented heteronanostructures makes use of stress-induced axial ordering – Uplaza

Above: Schematic illustration of the chemical conversion from Te/M1Te template, exhibiting controllable reactions with the residual Te, the generated M1Te, and each. Beneath: Overview of the ensuing 2nd (highlighted in purple) and third generations (highlighted in indigo) from the preliminary 1st Te template (highlighted in yellow). Credit score: Nature Communications (2024). DOI: 10.1038/s41467-024-47446-7

One-dimensional segmented heteronanostructures (1D-SHs) are promising candidates in fields resembling photoelectrocatalysis (PEC) and thermoelectrics. At present, the synthesis of 1D-SHs primarily focuses on sulfides and selenides, with comparatively much less analysis on telluride supplies, but tellurides have vital software prospects in vitality storage and optoelectronics. Nevertheless, a easy and managed synthesis of telluride 1D-SHs supplies has all the time been difficult.

A analysis crew led by Academician Yu Shuhong from the College of Science and Know-how of China (USTC) of Chinese language Academy of Sciences (CAS) has developed a way for synthesizing 1D-SHs primarily based on stress-induced axial ordering. Additionally they tracked the modifications in stress and pressure vitality in the course of the evolution of periodic ordered buildings utilizing a steady part discipline mannequin.

The examine is printed in Nature Communications.

First, the researchers chosen tellurium nanowires (NWs) with excessive side ratio because the mannequin structural items, and dispersed them in ethylene glycol, with the complexing agent NH4SCN and a stoichiometrically poor quantity of silver ions Ag+ added. Then the Te/Ag2Te 1D-SHs with distinct common segmented buildings appeared rapidly.

To confirm its properties, the researchers used transmission electron microscopy and vitality dispersive X-ray spectrometer to look at its segmented uniformity and decide the fundamental distribution. The researchers additional verified the biphasic nature of the Te/Ag2Te segmented heterostructures utilizing strategies resembling X-ray diffraction spectra, Raman spectroscopy, and X-ray photoelectron spectroscopy.

As well as, via in-situ liquid part transmission electron microscope, researchers summarized that the formation technique of Te/Ag2Te 1D-SHs went via three-stages evolution: island era, stripe penetration and phase ordering.

To discover the vitality change and stress distribution in the course of the formation of Te/Ag2Te 1D-SHs, the researchers reproduced the formation, development, and ordering processes of Ag2Te island buildings.

The outcomes confirmed that the initially generated Ag2Te islands had been affected by radial tensile stress and axial compressive stress, rising alongside the radial path to type poor-ordered stripe buildings. Subsequently, theses stripe buildings regularly evolve into periodic segments.

Researchers additionally synthesized a sequence of 1D-SHs of tellurides, together with supplies like Pd, Cu, Bi, Cd, and many others. Along with this, by combining easy chemical post-transformations, the researchers constructed a library of axial 1D-SHs supplies involving 13 components within the periodic desk.

Researchers additionally proposed a easy solution-phase technique for synthesizing 1D-SHs, and mixed with a easy chemical post-transformation course of, 25 1D-SHs together with 17 NW-NW and eight NW-nanotube nanostructures.

This work not solely enriches the fabric library of 1D-SHs, but in addition gives a brand new strategy for the exact preparation of function-oriented nanomaterials and the exploration of ordered reconstruction of heteronanostructures.

Extra data:
Qing-Xia Chen et al, Stress-induced ordering evolution of 1D segmented heteronanostructures and their chemical post-transformations, Nature Communications (2024). DOI: 10.1038/s41467-024-47446-7

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College of Science and Know-how of China

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Synthesis technique for 1D segmented heteronanostructures makes use of stress-induced axial ordering (2024, July 3)
retrieved 3 July 2024
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