Easy and fast in situ functionalization of exfoliated 2D black phosphorus with gold nanoparticles. Issue 33 (6th August 2021)

• Record Type: Journal Article
• Authors: Moschetto, Salvatore; Ienco, Andrea; Manca, Gabriele; Serrano-Ruiz, Manuel; Peruzzini, Maurizio; Mezzi, Alessio; Brucale, Marco; Bolognesi, Margherita; Toffanin, Stefano
• Is Part Of: Dalton transactions. Volume 50:Issue 33(2021)
• Page Start: 11610
• Page End: 11618
• Publication Date: 2021-08-06
• Subjects: Chemistry, Inorganic -- Periodicals; Chemistry, Physical and theoretical -- Periodicals; Chemistry, Inorganic -- Periodicals; 546.05
• DOI: 10.1039/d1dt02123k
• Languages: English
• ISSNs: 1477-9226

Abstract

Abstract : Computational analysis and electronic, structural and morphological properties of a heterostructure of 2D bP with Au nanoparticles formed in situ . Abstract : Heterostructures of single- and few-layer black phosphorus (2D bP) functionalized with gold nanoparticles (Au NPs) have been recently reported in the literature, exploiting their intriguing properties and biocompatibility for catalytic, therapeutical and diagnostic applications. However, a deeper insight on the structural and electronic properties at the interface of the 2D bP/Au NP heterostructure is still lacking. In this work, 2D bP is functionalized with Au nanoparticles (NPs) through in situ deposition–precipitation heterogeneous reaction. The smallest realized Au NPs have a diameter around 10 nm as revealed by atomic-force and scanning electron microscopy, and are partially positively charged as revealed by X-ray Photoelectron Spectroscopy (XPS). XPS, UV-vis and Raman spectroscopy, supported by density functional theory (DFT) calculations, confirmed that while the structural and electronic properties of 2D bP are overall preserved, a soft-pairing between P atoms at the surface of 2D bP and Au atoms at the surface of Au NPs occurs, leading to a partial charge transfer at the 2D bP/Au interface, with a positive charge being localized on the Au atoms directly bonded to 2D bP. DFT calculations also predicted a band gap lowering, by 0.8 eV, for phosphorene functionalized with a tetranuclear Au cluster. Larger effects are expected as the Au cluster nuclearity (and coverage) increases.