Electrochemical-Shock Synthesis of Nanoparticles from Sub-femtoliter Nanodroplets

Abstract

ConspectusNanoparticles have witnessed immense development in the past several decades due to their intriguing physicochemical properties. The modern chemist is interested not only in methods of synthesizing nanoparticles with tunable properties but also in the chemistry that nanoparticles can drive. While several methods exist to synthesize nanoparticles, it is often advantageous to put nanoparticles on a variety of conductive substrates for multiple applications (such as energy storage and conversion). Despite enjoying over 200 years of development, electrodeposition of nanoparticles suffers from a lack of control over nanoparticle size and morphology. There have been heroic efforts to address these issues over time. With an understanding that structure-function studies are imperative to understand the chemistry of nanoparticles, new methods are necessary to electrodeposit a variety of nanoparticles with control over macromorphology and also microstructure.This Account details our group's efforts in overcoming challenges of classical nanoparticle electrodeposition by electrodepositing nanoparticles from water nanodroplets. When a nanodroplet full of metal salt precursor is incident on the electrode biased sufficiently negative to drive electroplating, nanoparticles form at a fast rate (on the order of microseconds to milliseconds). We start with the general nuts-and-bolts of the experiment (nanodroplet formation and methods for electrodeposition). The deposition of new nanomaterials often requires one to develop new methods of measurement, and we detail new measurement tools for quantifying nanoparticle porosity and nanopore tortuosity within single nanoparticles. We achieve nanopore characterization by using Focused Ion Beam milling and Scanning Electron Microscopy. Owing to the small size of the nanodroplets and fast mass transfer (the contents of a femtoliter droplet can be electrolyzed in only a few milliseconds), the use of nanodroplets also allows the electrodeposition of high entropy alloy nanoparticles at room temperature.We detail how a deep understanding of ion transfer mechanisms can be used to expand the library of possible metals that can be deposited. Furthermore, simple ion changes in the dispersed droplet phase can decrease the cost per experiment by orders of magnitude. Finally, electrodeposition in aqueous nanodroplets can also be combined with stochastic electrochemistry for a variety of interesting studies. We detail the quantification of the growth kinetics of single nanoparticles in single aqueous nanodroplets. Nanodroplets can also be used as tiny reactors to trap only a few molecules of a metal salt precursor. Upon reduction to the zerovalent metal, electrocatalysis at very small metal clusters can be probed and evaluated with time using steady-state electrochemical measurements. Overall, this burgeoning synthetic tool is providing unexpected avenues of tunability of metal nanoparticles on conductive substrates.