Covalent functionalization and passivation of exfoliated black phosphorus via aryl diazonium chemistry

Functionalization of atomically thin nanomaterials enables the tailoring of their chemical, optical and electronic properties. Exfoliated black phosphorus (BP)—a layered two-dimensional semiconductor—exhibits favourable charge-carrier mobility, tunable bandgap and highly anisotropic properties, but...

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Veröffentlicht in:Nature chemistry 2016-06, Vol.8 (6), p.597-602
Hauptverfasser: Ryder, Christopher R., Wood, Joshua D., Wells, Spencer A., Yang, Yang, Jariwala, Deep, Marks, Tobin J., Schatz, George C., Hersam, Mark C.
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Sprache:eng
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Zusammenfassung:Functionalization of atomically thin nanomaterials enables the tailoring of their chemical, optical and electronic properties. Exfoliated black phosphorus (BP)—a layered two-dimensional semiconductor—exhibits favourable charge-carrier mobility, tunable bandgap and highly anisotropic properties, but it is chemically reactive and degrades rapidly in ambient conditions. Here we show that covalent aryl diazonium functionalization suppresses the chemical degradation of exfoliated BP even after three weeks of ambient exposure. This chemical modification scheme spontaneously forms phosphorus–carbon bonds, has a reaction rate sensitive to the aryl diazonium substituent and alters the electronic properties of exfoliated BP, ultimately yielding a strong, tunable p-type doping that simultaneously improves the field-effect transistor mobility and on/off current ratio. This chemical functionalization pathway controllably modifies the properties of exfoliated BP, and thus improves its prospects for nanoelectronic applications. Few-layer black phosphorus (BP) is a promising semiconductor, but it is highly reactive and susceptible to ambient degradation. Covalent functionalization with aryl radicals has now been shown to significantly improve the stability of exfoliated BP, as well as the performance of BP-based electronic devices through a controllable p-type doping effect.
ISSN:1755-4330
1755-4349
DOI:10.1038/nchem.2505