“…While conductive Ga-LM MNDs possess abundant delocalized electrons/ions at their surface, distinct from dielectric aqueous MNDs, a local electrostatic potential field is also formed at the interface between LM and dielectric surroundings (e.g., aqueous solutions containing ions) during a liquid-phase reaction. , The unique electric microenvironment at the defect-free surface of Ga-LM MNDs is considered as the main factor in modulating the kinetics of chemical reactions, including catalytic processes, between Ga-LM MNDs and dielectric surroundings. , For instance, it has been demonstrated that when Ga-LM MNDs are used as reactants, thermodynamically favorable but kinetically limited reactions between LM and the surrounding aqueous solution can be significantly accelerated, which facilitates the production of diverse functional core–shell nanostructures. − Nevertheless, subjecting to the challenge of experimentally mapping the charge or field distribution with a high spatial resolution, a comprehensive understanding of the effects of the dielectric surface and the electronic state of the interface on the surface reaction of LM MNDs are hindered. Additionally, the diversities of products would be more complicated as both nucleation and diffusion kinetics during the growth procedures should be considered. , Consequently, these challenges in understanding reaction kinetics and product growth at the defect-free surface of Ga-LM MNDs pose obstacles to the application of Ga-LM MNDs in chemistry processes.…”