We present results on the determination of the differential Casimir force between an Au-coated sapphire sphere and the top and bottom of Au-coated deep silicon trenches performed by means of the micromechanical torsional oscillator in the range of separations from 0.2 to 8 μm. The random and systematic errors in the measured force signal are determined at the 95% confidence level and combined into the total experimental error. The role of surface roughness and edge effects is investigated and shown to be negligibly small. The distribution of patch potentials is characterized by Kelvin probe microscopy, yielding an estimate of the typical size of patches, the respective r.m.s. voltage and their impact on the measured force. A comparison between the experimental results and theory is performed with no fitting parameters. For this purpose, the Casimir force in the sphere-plate geometry is computed independently on the basis of first principles of quantum electrodynamics using the scattering theory and the gradient expansion. In doing so, the frequency-dependent dielectric permittivity of Au is found from the optical data extrapolated to zero frequency by means of the plasma and Drude models. It is shown that the measurement results exclude the Drude model extrapolation over the region of separations from 0.2 to 4.8 μm, whereas the alternative extrapolation by means of the plasma model is experimentally consistent over the entire measurement range. A discussion of the obtained results is provided.

We report precision measurements of the gradient of the Casimir force between an Au-coated sphere and graphene sheet deposited on a silica plate. The measurement data are compared with exact theory using the polarization tensor found in the framework of the Dirac model including effects of the nonzero chemical potential and energy gap of the graphene sample with no fitting parameters. The very good agreement between experiment and theory demonstrates the unusually big thermal effect at separations below $1\mu \mathrm{m}$ which has never been observed for conventional 3D materials. Thus, it is confirmed experimentally that for graphene the effective temperature is determined by the Fermi velocity rather than by the speed of light.

It is well known that residual electrostatic forces create significant difficulties in precise measurements of the Casimir force and the wide use of Casimir-operated microdevices. We experimentally demonstrate that, with the help of Ar-ion cleaning of the surfaces, it is possible to make electrostatic effects negligibly small compared to the Casimir interaction. Our experimental setup consists of a dynamic atomic force microscope supplemented with an Ar-ion gun and argon reservoir. The residual potential difference between the Au-coated surfaces of a sphere and those of a plate was measured both before and after in situ Ar-ion cleaning. It is shown that this cleaning decreases the magnitude of the residual potential by up to an order of magnitude and makes it almost independent of the separation. The gradient of the Casimir force was measured using ordinary samples subjected to Ar-ion cleaning. The obtained results are shown to be in good agreement both with previous precision measurements using specially selected samples and with theoretical predictions of the Lifshitz theory. The conclusion is made that the suggested method of in situ Ar-ion cleaning is effective in reducing the electrostatic effects and therefore is a great resource for experiments on measuring the Casimir interaction and for Casimir-operated microdevices.

We present the results of an experiment on measuring the gradient of the Casimir force between an Au-coated hollow glass microsphere and graphene-coated fused silica plate by means of a modified atomic force microscope cantilever-based technique operated in the dynamic regime. These measurements were performed in high vacuum at room temperature. The energy gap and the concentration of impurities in the graphene sample used have been measured utilizing scanning tunneling spectroscopy and Raman spectroscopy, respectively. The measurement results for the gradients of the Casimir force are found to be in a very good agreement with theory using the polarization tensor of graphene at nonzero temperature depending on the energy gap and chemical potential with no fitting parameters. The theoretical predictions of the same theory at zero temperature are experimentally excluded over the measurement region from 250 to 517 nm. We have also investigated a dependence of the thermal correction to the Casimir force gradient on the values of the energy gap, chemical potential, and on the presence of a substrate supporting the graphene sheet. It is shown that the observed thermal effect is consistent in size with that arising for pristine graphene sheets if the impact of real conditions such as nonzero values of the energy gap, chemical potential, and the presence of a substrate is included. Implications of the obtained results to the resolution of the long-standing problems in Casimir physics are discussed. In addition to the paper published previously [M. Liu et al., Phys. Rev. Lett. 126, 206802 (2021)], we present measurement results for the energy gap of the graphene sample, double the experimental data for the Casimir force, and perform a more complete theoretical analysis.

Using the recently derived representation for the polarization tensor in (2+1)-dimensional space-time allowing an analytic continuation to the entire plane of complex frequencies, we obtain simple analytic expressions for the reflection coefficients of graphene at nonzero Matsubara frequencies. In the framework of the Lifshitz theory, these coefficients are shown to lead to nearly exact results for the Casimir free energy and pressure between two graphene sheets. The constituent parts of large thermal effect, arising in the Casimir interaction at short separations due to an explicit parametric dependence of the polarization tensor on the temperature and an implicit dependence through a summation over the Matsubara frequencies, are calculated. It is demonstrated that an explicit thermal effect exceeds an implicit one at shorter separations, both effects are similar in magnitudes at moderate separations, and that an implicit effect becomes a larger one with further increase of separation. Possible applications of the developed formalism, other than the Casimir effect, are discussed.

We present a formalism based on first principles of quantum electrodynamics at nonzero temperature which permits us to calculate the Casimir-Polder interaction between an atom and a graphene sheet with arbitrary mass gap and chemical potential, including graphene-coated substrates. The free energy and force of the Casimir-Polder interaction are expressed via the polarization tensor of graphene in $(2+1)$-dimensional space-time in the framework of the Dirac model. The obtained expressions are used to investigate the influence of the chemical potential of graphene on the Casimir-Polder interaction. Computations are performed for an atom of metastable helium interacting with either a freestanding graphene sheet or a graphene-coated substrate made of amorphous silica. It is shown that the impacts of the nonzero chemical potential and the mass gap on the Casimir-Polder interaction are in opposite directions, by increasing and decreasing the magnitudes of the free energy and force, respectively. It turns out, however, that the temperature-dependent part of the Casimir-Polder interaction is decreased by a nonzero chemical potential, whereas the mass gap increases it compared to the case of undoped, gapless graphene. The physical explanation for these effects is provided. Numerical computations of the Casimir-Polder interaction are performed at various temperatures and atom-graphene separations.