Tailoring the phase transition pathway of Ag2Te nanowires via surface confinement: an in situ transmission electron microscopy study
Abstract
Controlling the phase transition of Ag2Te is crucial for its application in functional devices since the structural change significantly influences its properties. However, convenient and precise control over this process remains challenging. This study proposes a carbon-encapsulation strategy to tailor the phase transition behavior of Ag2Te nanowires. In situ heating experiments reveal a novel transition from monoclinic Ag2Te to hexagonal Ag5Te3 at 180 °C and to hexagonal Te at 200 °C. Compared to the conventional monoclinic-to-fcc transition at 150 °C, this altered pathway is attributed to the interfacial interaction between the carbon shell and Ag2Te nanowire, which may raise the energy barrier for Ag diffusion and lattice reconstruction. In contrast, partially exposed nanowires exhibit rapid surface diffusion and reconstruction. Using this strategy, an Ag2Te–Te heterojunction is fabricated in situ, exhibiting a transition from ohmic to rectifying characteristics, as supported by DFT calculations. Our findings demonstrate the potential of the carbon-encapsulation strategy for phase modulation of Ag2Te nanostructures, offering valuable insights for structural design of novel Ag2Te-based nanodevices.

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