We follow the history of nanobubbles from the earliest experiments pointing to their existence to recent years. We cover the effect of Laplace pressure on the thermodynamic stability of nanobubbles and why this implies that nanobubbles are thermodynamically never stable. Therefore, understanding bubble stability becomes a consideration of the rate of bubble dissolution, so the dominant approach to understanding this is discussed. Bulk nanobubbles (or fine bubbles) are treated separately from surface nanobubbles as this reflects their separate histories. For each class of nanobubbles, we look at the early evidence for their existence, methods for the production and characterization of nanobubbles, evidence that they are indeed gaseous, or otherwise, and theories for their stability. We also look at applications of both surface and bulk nanobubbles.

Nonclassical crystallization (NCC) summarizes a number of crystallization pathways, which differ from the classical layer-by-layer growth of crystals involving atomic/molecular building units. Common to NCC is that the building units are larger and include nanoparticles, clusters, or liquid droplets, providing multiple handles for their control at each elementary step. Therefore, many different pathways toward the final single crystals are possible and can be influenced by appropriate experimental parameters or additives at each step of crystal growth. NCC allows for a plethora of crystallization strategies toward complex crystalline (hybrid) materials. In this perspective, we summarize the current state of the art with a focus on the new horizons of NCC with respect to mechanistic understanding, high-performance materials, and new applications. This gives a glimpse on what will be possible in the future using these crystallization approaches: Examples are new electrodes and storage materials, (photo)­catalysts, building materials, porous or crystalline materials with complex shape, structural hierarchy, and anisotropic single crystals.

Investigating proteins with techniques such as NMR or neutron scattering frequently requires the partial or complete substitution of D2O for H2O as a solvent, often tacitly assuming that such a solvent substitution does not significantly alter the properties of the protein. Here, we report a systematic investigation of the solvent isotope effect on the phase diagram of the lens protein γB-crystallin in aqueous solution as a model system exhibiting liquid-liquid phase separation. We demonstrate that the observed strong variation of the critical temperature Tc can be described by the extended law of corresponding states for all H2O/D2O ratios, where scaling of the temperature by Tc or the reduced second virial coefficient accurately reproduces the binodal, spinodal, and osmotic compressibility. These findings highlight the impact of H2O/D2O substitution on γB-crystallin properties and warrant further investigations into the universality of this phenomenon and its underlying mechanisms.

The synthesis of cerium oxalate, a reaction intermediate in the preparation of high performance ceramics, is studied in sessile droplets. We compare here the effect of alcoholic solvents with the usage of structured solvents, namely ultra-flexible microemulsions in the water-rich and oil-rich configurations. The nucleation and the growth of cerium oxalate particles are the result of local mixing by the Marangoni flow of droplets loaded with oxalic acid and cerium nitrate. The morphology of the particles is very different depending on the composition of the solvent and on the mixing process. We show that the variation of the particle morphology results from the difference of the structured solvent microphases during the precipitation process. When the precipitation occurs in a water continuous phase, usual needle-like oxalate particles precipitate. When the precipitate is formed in the dispersed phase of the emulsion, structured aggregates, as close-packed aggregates of needles, are compacted by microcapillarity effects