Surface modification of atomically thin semiconductors enables their electronic, optical, chemical, and mechanical properties to be tailored and allows these nanosheets to be processed in solutions. Here, we report first-principles density functional theory calculations, through which we show chemical functionalization of black phosphorus using phenyl, phenolate and nitrene species, which were widely investigated for carbon-based materials. We find the formation of dangling bonds is the main cause for defect levels at the Fermi level in black phosphorus when using phenyl and phenolate. We show that covalent functionalization using nitrene-derived species introduces a strong P-N dative bond at the interface without perturbing its intrinsic electronic structure. The Lewis basic and nucleophilic P atom attacks, through a free pair of electrons, the Lewis acidic nitrene species. These results are further compared with other nitrene-derived functional groups on black phosphorus, including N-methylbenzene, N-aminobenzene, and N-nitrobenzene. We find that by tuning the charge redistribution at the interface, the work function of black phosphorus can be tuned by more than 2 eV. These results suggest valuable tunability of the electronic properties of two-dimensional layered black phosphorus by covalent functionalization for future device applications.

Rational surface modification of two-dimensional black phosphorus: Insights from first-principles calculations

256th National Meeting (2018)

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