Connecting the Dots: Mott for Emulsions,Collapse Models,Colored Noise,Frame Dependence of Measurements,Evasion of the “Free Will Theorem”

We review the argument that latent image formation is a measurement in which the state vector collapses, requiring an enhanced noise parameter in objective reduction models. Tentative observation of a residual noise at this level, plus several experimental bounds, imply that the noise must be colored (i.e., non-white), and hence frame dependent and non-relativistic. Thus a relativistic objective reduction model, even if achievable in principle, would be incompatible with experiment; the best one can do is the non-relativistic CSL model. This negative conclusion has a positive aspect, in that the non-relativistic CSL reduction model evades the argument leading to the Conway–Kochen “Free Will Theorem”.     

Best constants for metric space inversion inequalities

For every metric space (X, d) and origin o ∈ X, we show the inequality I _o (x, y) ≤ 2d _o (x, y), where I _o (x, y) = d(x, y)/d(x, o)d(y, o) is the metric space inversion semimetric, d _o is a metric subordinate to I _o , and x, y ∈ X \ {o} The constant 2 is best possible.     

Spectroscopic fingerprints of valence and spin states in manganese oxides and fluorides

We performed a systematic study of soft X-ray absorption spectroscopy in various manganese oxides and fluorides. Both Mn L-edges and ligand (O and F) K-edges are presented and compared with each other. Despite the distinct crystal structure and covalent/ionic nature in different systems, the Mn-L spectra fingerprint the Mn valence and spin states through spectral lineshape and energy position consistently and evidently. The clear O- and F-K pre-edge features in our high resolution spectra enable a quantitative definition of the molecular orbital diagram with different Mn valence. In addition, while the binding energy difference of the O-1s core electrons leads to a small shift of the O-K leading edges between trivalent and quadrivalent manganese oxides, a significant edge shift, with an order of magnitude larger in energy, was found between divalent and trivalent compounds, which is attributed to the spin exchange stabilization of half-filled 3d system. This shift is much enhanced in the ionic fluoride system. This work provides the spectroscopic foundation for further studies of complicated Mn compounds.