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Aluminum nanocrystals (AlNCs) are of increasing interest as sustainable, earth-abundant nanoparticles for visible wavelength plasmonics and as versatile nanoantennas for energy-efficient plasmonic photocatalysis. Here, we show that annealing AlNCs under various gases and thermal conditions induces substantial, systematic changes in their surface oxide, modifying crystalline phase, surface morphology, density, and defect type and concentration. Tailoring the surface oxide properties enables AlNCs to function as all-aluminum-based antenna-reactor plasmonic photocatalysts, with the modified surface oxides providing varying reactivities and selectivities for several chemical reactions. 

Evaporation-based solar thermal distillation is a promising approach for purifying high-salinity water, but the liquid-vapor phase transition inherent to this process makes it intrinsically energy intensive. Here we show that the exchange of heat between the distilled and input water can fulfill a resonance condition, resulting in dramatic increases in fresh water production. Large gains (500%) in distilled water are accomplished by coupling nanophotonics-enabled solar membrane distillation with dynamic thermal recovery, achieved by controlling input flow rates as a function of incident light intensity. The resonance condition, achieved for the circulating heat flux between the distillate and feed, allows the system to behave in an entirely new way, as a desalination oscillator. The resonant oscillator concept introduced here is universal and can be applied to other systems such as thermal energy storage or solar-powered chemical reactors. 

Matter’s sensitivity to light polarization is characterized by linear and circular polarization effects, corresponding to the system’s anisotropy and handedness, respectively. Recent investigations into the near-field properties of evanescent waves have revealed polarization states with out-of-phase transverse and longitudinal oscillations, resulting in trochoidal, or cartwheeling, field motion. Here, we demonstrate matter’s inherent sensitivity to the direction of the trochoidal field and name this property trochoidal dichroism. We observe trochoidal dichroism in the differential excitation of bonding and antibonding plasmon modes for a system composed of two coupled dipole scatterers. Trochoidal dichroism constitutes the observation of a geometric basis for polarization sensitivity that fundamentally differs from linear and circular dichroism. It could also be used to characterize molecular systems, such as certain light-harvesting antennas, with cartwheeling charge motion upon excitation.