"Naked" gold nanoparticles (AuNPs), synthesized in the absence of any capping agents, prepared by pulsed laser ablation in liquid (PLAL) are stabilized by negative charges. Common explanations for this phenomenon involve the presence of gold oxides and/or the anion adsorption. We have found that AuNP ablated in solutions of acids with very different oxidation power, viz. HCl, H2SO4, HNO3 share the same size and ?-potential. Although, gold oxides have pKas ? 4, the ?-potential of AuNPs ablated in solutions with pH ? 4 is always negative. These evidences suggest that the gold oxidation and anion adsorptions have only a minor role on building the negative surface potential and we hypothesize, for the first time, that excess electrons formed within the plasma phase could charge the metallic particles. In our model, a crucial point is that the colloidal size of the NP maintains the energy of the electrons small enough to preclude chemical reactions but with a surface potential yet large enough to stabilize the AuNPs with respect to aggregation. A confirmation of the hypothesis of "electron-stabilized nanoparticles" is that either the addition of macroscopic metallic objects either the contact with a "grounded" copper wire induce the loss of charge and AuNPs aggregation. ? 2016 Elsevier Inc.

On the stability of gold nanoparticles synthesized by laser ablation in liquids

Palazzo G;Dell'Aglio M;De Giacomo;
2017

Abstract

"Naked" gold nanoparticles (AuNPs), synthesized in the absence of any capping agents, prepared by pulsed laser ablation in liquid (PLAL) are stabilized by negative charges. Common explanations for this phenomenon involve the presence of gold oxides and/or the anion adsorption. We have found that AuNP ablated in solutions of acids with very different oxidation power, viz. HCl, H2SO4, HNO3 share the same size and ?-potential. Although, gold oxides have pKas ? 4, the ?-potential of AuNPs ablated in solutions with pH ? 4 is always negative. These evidences suggest that the gold oxidation and anion adsorptions have only a minor role on building the negative surface potential and we hypothesize, for the first time, that excess electrons formed within the plasma phase could charge the metallic particles. In our model, a crucial point is that the colloidal size of the NP maintains the energy of the electrons small enough to preclude chemical reactions but with a surface potential yet large enough to stabilize the AuNPs with respect to aggregation. A confirmation of the hypothesis of "electron-stabilized nanoparticles" is that either the addition of macroscopic metallic objects either the contact with a "grounded" copper wire induce the loss of charge and AuNPs aggregation. ? 2016 Elsevier Inc.
2017
Ablation
Pulsed lasers
electron excess
colloidal stability
agglomeration
pulsed laser ablation in water
gold nanoparticles
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/424155
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 44
  • ???jsp.display-item.citation.isi??? ND
social impact