We study a method to induce resonant transitions between antihydrogen ($bar{H}$) quantum states above a material surface in the gravitational field of the Earth. The method consists of applying a gradient of magnetic field, which is temporally oscill
ating with the frequency equal to a frequency of transition between gravitational states of antihydrogen. A corresponding resonant change in the spatial density of antihydrogen atoms could be measured as a function of the frequency of applied field. We estimate an accuracy of measuring antihydrogen gravitational states spacing and show how a value of the gravitational mass of the $bar{H}$ atom could be deduced from such a measurement. We also demonstrate that a method of induced transitions could be combined with a free-fall-time measurement in order to further improve the precision.
We study a method to induce resonant transitions between antihydrogen quantum states above a material surface in the gravitational field of the Earth. The method consists in applying a gradient of magnetic field which is temporally oscillating with t
he frequency equal to a frequency of a transition between gravitational states of antihydrogen. Corresponding resonant change in a spatial density of antihydrogen atoms can be measured as a function of the frequency of applied field. We estimate an accuracy of measuring antihydrogen gravitational states spacing and show how a value of the gravitational mass of the antihydrogen atom can be deduced from such a measurement.
Analyzing new experiments with ultracold neutrons (UCNs) we show that physical adsorption of nanoparticles/nano-droplets, levitating in high-excited states in a deep and broad potential well formed by van der Waals/Casimir-Polder (vdW/CP) forces resu
lts in new effects on a cross-road of fundamental interactions, neutron, surface and nanoparticle physics. Accounting for the interaction of UCNs with nanoparticles explains a recently discovered intriguing small heating of UCNs in traps. It might be relevant to the striking conflict of the neutron lifetime experiments with smallest reported uncertainties by adding false effects there.
Physical adsorption of atoms, molecules and clusters on surface is known. It is linked to many phenomena in physics, chemistry, and biology. Usually the studies of adsorption are limited to the particle sizes of up to ~10^2-10^3 atoms. Following a ge
neral formalism, we apply it to even larger objects and discover qualitatively new phenomena. A large particle is bound to surface in a deep and broad potential well formed by van der Waals/ Casimir-Polder forces. The well depth is significantly larger than the characteristic thermal energy. Nanoparticles in high-excited bound states form two-dimensional gas of objects quasi-freely traveling along surface. A particularly interesting prediction is small-energy-transfer scattering of UCN on solid/ liquid surfaces covered by such levitating nanoparticles/ nano-droplets. The change in UCN energy is due to the Doppler shift induced by UCN collisions with nanoparticles; the energy change is about as small as the UCN initial energy. We compare theoretical estimations of our model to all relevant existing data and state that they agree quite well. As our theoretical formalism provides robust predictions and the experimental data are rather precise, we conclude that the recently discovered intriguing phenomenon of small heating of UCN in traps is due to their collisions with such levitating nanoparticles. Moreover, this new phenomenon might be relevant to the striking contradiction between results of the neutron lifetime measurements with smallest reported uncertainties as it might cause major false effects in these experiments; thus it affects fundamental conclusions concerning precision checks of unitarity of the Cabibbo-Kobayashi-Maskawa matrix, cosmology, astrophysics. Dedicated measurements of UCN up-scattering on specially prepared surfaces and nanoparticles levitating above them might provide a unique method to study surface potentials.
