Fabrication process independent and robust aggregation of detonation nanodiamonds in aqueous media

Abstract

In the past detonation nanodiamonds (DNDs), sized 3–5 nm, have been praised for their colloidal stability in aqueous media, thereby attracting vast interest in a wide range of applications including nanomedicine. More recent studies have challenged the consensus that DNDs are monodispersed after their fabrication process, with their aggregate formation dynamics poorly understood. Here we reveal that DNDs in aqueous solution, regardless of their post-synthesis de-agglomeration and purification methods, exhibit hierarchical aggregation structures consisting of chain-like and cluster aggregate morphologies. With a novel characterization approach combining machine learning with direct cryo-transmission electron microscopy and with X-ray scattering and vibrational spectroscopy, we show that their aggregate morphologies of chain and cluster ratios and the corresponding size and fractal dimension distributions vary with the post-synthesis treatment methods. In particular DNDs with positive ζ-potential form to a hierarchical structure that assembles aggregates into large networks. DNDs purified with the gas phase annealing and oxidation tend to have more chain-like aggregates. Our findings provide important contribution in understanding the DND interparticle interactions to control the size, polydispersity and aggregation of DNDs for their desired applications.