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March 14, 2026The Journal of Physical Chemistry Letters0 citationsOpen Access

Molecular sp 3 -like Reactivity of Metastable Au 4 Si near Its Deep Eutectic Point Enables Low-Temperature SiC Formation

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JHJhong-Ren HuangYLY. C. LiuSKSatoshi Kameoka

Key Points

  • The research aims to explore the chemical reactivity of metastable Au-Si configurations near their deep eutectic point.
  • High-vacuum coevaporation of Au-Si species and carbon clusters
  • Raman spectroscopy to analyze SiC formation
  • X-ray photoelectron spectroscopy for chemical bonding analysis
  • SiC formation occurs at low temperatures around 636 K
  • Au segregation was observed during reactions
  • Reaction characteristics are inconsistent with traditional catalytic mechanisms

Abstract

Metastable states near deep eutectic points are typically regarded as transient intermediates preceding phase separation, yet their potential chemical reactivity remains largely unexplored. Here, we demonstrate that metastable Au-Si bonding configurations derived from Au4Si near its deep eutectic temperature exhibit molecule-like reactivity associated with an sp3-like local bonding environment, enabling direct Si-C bond formation at temperatures as low as 636 K. Using a high-vacuum coevaporation platform, Au-Si species generated during coevaporation react with carbon clusters to produce SiC accompanied by Au segregation, whereas elemental Si under identical conditions remains chemically inert. Raman spectroscopy and X-ray photoelectron spectroscopy reveal that SiC formation occurs only within a narrow temperature window centered at the eutectic point and displays nonmonotonic temperature dependence inconsistent with conventional catalytic or vapor-liquid-solid mechanisms. These results provide experimental evidence that eutectic metastable bonding configurations can transiently adopt molecule-like characteristics, thereby enabling unconventional low-temperature reaction pathways in metal-semiconductor systems.

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Cite This Study

Huang et al. (2026) studied this question.

synapsesocial.com/papers/69b4fc7fb39f7826a300d669https://doi.org/10.1021/acs.jpclett.6c00179
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