Strain-Engineered s-C$_3$N$_6$ Monolayer for Efficient Water Splitting: A first-principles study

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Chinese explanation / 中文解读

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Original abstract

Photocatalytic water splitting offers a sustainable route for solar-to-hydrogen energy conversion, yet identifying stable, metal-free semiconductors with suitable electronic, optical, and band-alignment properties remains challenging. Here, we investigate the structural, mechanical, electronic, optical, and photocatalytic properties of the two-dimensional s-C$_3$N$_6$ monolayer using first-principles calculations. Ab initio molecular dynamics and elastic constant analysis confirm its thermal and mechanical stability. Hybrid HSE06 calculations reveal pristine s-C$_3$N$_6$ is a direct-band-gap semiconductor (2.62 eV). However, its conduction-band minimum lies below the hydrogen reduction potential, preventing spontaneous hydrogen evolution. To overcome this limitation, we employ biaxial and uniaxial strains (-10% to +10%) to modulate its electronic structure. We find that compressive biaxial strains of -8% and -10% uniquely tune the band edges to straddle the redox potentials, enabling spontaneous overall water splitting. Crucially, these photocatalytically active states remain mechanically and thermally stable. Optical properties calculations show the fundamental gap in both pristine and strained structures is optically dark, with the primary absorption peak in the UV region. Furthermore, a strain-induced mobility mismatch between electrons and holes facilitates efficient charge separation. However, thermodynamic modeling of surface kinetics reveals that the s-C$_3$N$_6$ surface binds intermediates strongly, necessitating a co-catalyst to overcome kinetic barriers. Our results establish strain engineering as an effective strategy to tailor band-edge alignment, carrier dynamics, and optical transitions in s-C$_3$N$_6$, highlighting its potential for stable 2D photocatalytic water splitting.

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• Official / arXiv page
• PDF from original source

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