In atom optics a material structure is commonly regarded as an amplitude mask for atom waves. However, atomic diffraction patterns formed using material gratings indicate that material structures also operate as phase masks. In this study a well collimated beam of sodium atoms is used to illuminate a silicon nitride grating with a period of 100 nm. During passage through the grating slots atoms acquire a phase shift due to the van der Waals interaction with the grating walls. As a result the relative intensities of the matter-wave diffraction peaks deviate from those expected for a purely absorbing grating. Thus a complex transmission function is required to explain the observed diffraction envelopes. An optics perspective to the theory of atomic diffraction from material gratings is put forth in the hopes of providing a more intuitive picture concerning the influence of the vdW potential. The van der Waals coefficient C3 = 2.7±0.8 meV nm 3 is determined by fitting a modified Fresnel optical theory to the experimental data. This value of C3 is consistent with a van der Waals interaction between atomic sodium and a silicon nitride surface.

The development of nanotechnology and atom optics relies on understanding how atoms behave and interact with their environment. Isolated atoms can exhibit wave-like (coherent) behaviour with a corresponding de Broglie wavelength and phase which can be affected by nearby surfaces. Here an atom interferometer is used to measure the phase shift of Na atom waves induced by the walls of a 50 nm wide cavity. To our knowledge this is the first direct measurement of the de Broglie wave phase shift caused by atom-surface interactions. The magnitude of the phase shift is in agreement with that predicted by quantum electrodynamics for a non-retarded van der Waals interaction. This experiment also demonstrates that atom-waves can retain their coherence even when atom-surface distances are as small as 10 nm.

Metasurface optics provide an ultrathin alternative to conventional refractive lenses. A present challenge is in realizing metasurfaces that exhibit tunable optical properties and achromatic behavior across the visible spectrum. Here, we report the design, fabrication, and characterization of metasurface lenses (“metalenses”) that use asymmetric titanium dioxide (TiO2) nanostructures to induce a polarization-dependent optical response. By rotating the polarization of linearly polarized input light, the focal length of a 40 μm diameter metalens is tuned from 220 to 550 μm. We show that imparting a wavelength-dependent polarization rotation on incident light enables achromatic focusing over a wide band of the visible spectrum, 483–620 nm. We use this property to demonstrate varifocal color imaging with white light from a halogen source. We also discuss how tunable achromatic metalenses may be useful for display applications.

The strength of an atom-surface interaction is determined by studying atom diffraction from a rotated material grating. A phasor diagram is developed to interpret why diffraction orders are never completely suppressed when a complex transmission function due to the van der Waals interaction is present. We also show that atom-surface interactions can produce asymmetric diffraction patterns. Our conceptual discussion is supported by experimental observations with a sodium atom beam.Comment: 5 pages, 6 figures, submitted to PR

Decoherence due to scattering from background gas particles is observed for the first time in a Mach-Zehnder atom interferometer, and compared with decoherence due to scattering photons. A single theory is shown to describe decoherence due to scattering either atoms or photons. Predictions from this theory are tested by experiments with different species of background gas, and also by experiments with different collimation restrictions on an atom beam interferometer.