<p>Modulating the Reactivity of Liquid Ga Nanoparticle Inks by Modifying Their Surface Chemistry</p>

Micro- and nanosized particles of liquid metals, particularly Ga-based alloys, are attracting increasing attention for applications in several fields. The surface functionalization of Ga-based nanoparticles (NPs) with organic ligands renders easily processable inks. However, little is known about the interaction of these molecules with the native oxide skin, which regulates many properties of liquid metal NPs. Here, we investigate the impact of selected capping ligands on the native oxide thickness of Ga NPs and on their chemical reactivity, choosing the galvanic replacement reaction (Go) as one example. We demonstrate that amines and carboxylic acids promote thicker oxide shells while thiols and phosphines hinder the oxide growth. Upon pondering thermodynamics and kinetics factors, we conclude the affinity of the anchoring group toward the metal core being the major driver in determining the oxide thickness. We go on to prove that thicker shells foster the formation of Cu-Ga nanodimers following the reaction of the Ga NPs with a copper-amine complex. In contrast, thinner oxides lead to formation of isolated Cu NPs. This study reveals the importance of the choice of ligand when studying Ga-based metal NPs for different applications since both their surface chemistry and reactivity are largely affected by this decision.