AI Article Synopsis

  • Phase-change materials are crucial for electronics and photonics, switching rapidly between two distinct states that have different electrical, optical, or magnetic properties.
  • Recent advancements have shown promising effects in chalcogenide compounds and specifically in a new composition of Sb-rich equichalcogenides containing equal amounts of S, Se, and Te.
  • The study demonstrates effective resistivity switching below 200 °C, with a nanoscale mechanism linked to the arrangement and bonding of Ge and Sb atoms, allowing integration into multifunctional devices, neuromorphic systems, and sensors.

Article Abstract

Phase-change materials, demonstrating a rapid switching between two distinct states with a sharp contrast in electrical, optical or magnetic properties, are vital for modern photonic and electronic devices. To date, this effect is observed in chalcogenide compounds based on Se, Te or both, and most recently in stoichiometric SbS composition. Yet, to achieve best integrability into modern photonics and electronics, the mixed S/Se/Te phase change medium is needed, which would allow a wide tuning range for such important physical properties as vitreous phase stability, radiation and photo-sensitivity, optical gap, electrical and thermal conductivity, non-linear optical effects, as well as the possibility of structural modification at nanoscale. In this work, a thermally-induced high-to-low resistivity switching below 200 °C is demonstrated in Sb-rich equichalcogenides (containing S, Se and Te in equal proportions). The nanoscale mechanism is associated with interchange between tetrahedral and octahedral coordination of Ge and Sb atoms, substitution of Te in the nearest Ge environment by S or Se, and Sb-Ge/Sb bonds formation upon further annealing. The material can be integrated into chalcogenide-based multifunctional platforms, neuromorphic computational systems, photonic devices and sensors.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9938898PMC
http://dx.doi.org/10.1038/s41598-023-30160-7DOI Listing

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