Surface inducing high-temperature superconductivity in layered metal carborides Li2BC3 and LiBC by metallizing σ electrons

Metallizing σ electrons provides a promising route to design high-temperature superconducting materials, such as MgB2 and high-pressure hydrides. Here, we focus on two MgB2-like layered carborides Li2BC3 and LiBC; their bulk does not have superconductivity because the B–C σ states are far away from...

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Veröffentlicht in:Nanoscale 2024-07, Vol.16 (28), p.13534-13542
Hauptverfasser: Wang, Muyao, Liu, Xiaohan, Huang, Xiaowei, Liu, Liangliang
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Sprache:eng
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Zusammenfassung:Metallizing σ electrons provides a promising route to design high-temperature superconducting materials, such as MgB2 and high-pressure hydrides. Here, we focus on two MgB2-like layered carborides Li2BC3 and LiBC; their bulk does not have superconductivity because the B–C σ states are far away from the Fermi level (EF), however, based on first-principles calculations, we found that when their bulk systems are cleaved into surfaces with B–C termination, high Tc of ∼80 K could be observed in the exposed B–C layer on the surfaces. Detailed analysis reveals that surface symmetry reduction, due to lattice periodic breaking, not only introduces hole self-doping into surface B–C layers and shifts the σ-bonding states towards the EF – associated with emergent large electronic occupation, but also makes in-plane stretching modes on the surface layer experience significant softness. The enhanced σ states and softened phonon modes work to produce strong coupling, thus yielding high-Tc surface superconductivity, which distinctly differs from the superconducting features of the MgB2 film, which generates phonon stiffness accompanied by suppressed superconductivity. Our findings undoubtedly provide a novel platform to realize high-Tc surface superconductivity, and also clearly elucidate the microscopic mechanism of surface-enhanced superconductivity in favor of creating more high-Tc surface superconductors among MgB2-like layered materials.
ISSN:2040-3364
2040-3372
2040-3372
DOI:10.1039/d4nr01482k