A structural change between amorphous and crystalline phase provides a basis for reliable and modular photonic and electronic devices, such as nonvolatile memory, beam steerers, solid-state reflective displays, or mid-IR antennas. In this paper, we leverage the benefits of liquid-based synthesis to access phase-change memory tellurides in the form of colloidally stable quantum dots. We report a library of ternary M x Ge1–x Te colloids (where M is Sn, Bi, Pb, In, Co, Ag) and then showcase the phase, composition, and size tunability for Sn–Ge–Te quantum dots. Full chemical control of Sn–Ge–Te quantum dots permits a systematic study of structural and optical properties of this phase-change nanomaterial. Specifically, we report composition-dependent crystallization temperature for Sn–Ge–Te quantum dots, which is notably higher compared to bulk thin films. This gives the synergistic benefit of tailoring dopant and material dimension to combine the superior aging properties and ultrafast crystallization kinetics of bulk Sn–Ge–Te, while improving memory data retention due to nanoscale size effects. Furthermore, we discover a large reflectivity contrast between amorphous and crystalline Sn–Ge–Te thin films, exceeding 0.7 in the near-IR spectrum region. We utilize these excellent phase-change optical properties of Sn–Ge–Te quantum dots along with liquid-based processability for nonvolatile multicolor images and electro-optical phase-change devices. Our colloidal approach for phase-change applications offers higher customizability of materials, simpler fabrication, and further miniaturization to the sub-10 nm phase-change devices.

Gold nanoparticles that are partially or fully covered by metal oxide shells provide superior functionality and stability for catalytic and plasmonic applications. Yet, facile methods for controlled fabrication of thin oxide layers on metal nanoparticles are lacking. Here, we report an easy method to reliably engineer thin Ga2O3 shells on Au nanoparticles, based on liquid-phase chemical oxidation of Au–Ga alloy nanoparticles. We demonstrate that, with this technique, laminar and ultrathin Ga2O3 shells can be grown with ranging thickness from sub- to several monolayers. We show how the localized surface plasmon resonance can be used to understand the reaction process and quantitatively monitor the Ga2O3 shell growth. Finally, we demonstrate that the Ga2O3 coating prevents sintering of the Au nanoparticles, providing thermal stability to at least 250 °C. This approach, building on dealloying of bimetallic nanoparticles by the solution-phase oxidation, promises a general technique for achieving controlled metal/oxide core/shell nanoparticles.