1 research outputs found
Emergence of Selectivity in Inherently Nonselective Gold Nanoparticles Through Preferential Breaking of Interparticle Interactions
We
demonstrate a fundamentally unique identification strategy to impart
selectivity to a traditionally and inherently nonselective
carboxylate-functionalized gold-nanoparticles ([-] AuNPs), without the aid of
any analyte specific ligands. The
common practice is to use the ability of divalent ions to trigger the
aggregation process in a kinetically trapped dispersed solution of [-] AuNPs.
Aggregation of NPs being a thermodynamically favourable process will result in
a uniform and nonselective turn-off response from most of the strongly binding
divalent ions. Our approach is to use the abilities of various divalent ions to
break a thermodynamically stable inter-nanoparticle precipitates containing [+]
and [-] AuNPs (nanoionic precipitates),
as the means of identification. Importantly both [+] and [-] AuNPs,
independently, were ‘blind’ in terms of selectivity towards divalent ions.
Remarkably, a hybrid-system composed of such nonselective nanoparticles was
able to discriminate between the hard-to-distinguish pair of Pb2+
and Cd2+ ions. The rationale is that only the strongest of strongly
binding ions will be able to break the interactions between the NP precipitates
(thermodynamically stable state) and re-disperse them back in solution
(kinetically trapped state). This is in stark contrast with the conventional
idea of forming an interaction between NPs and divalent ions, with the help of
analyte-specific ligands.</p