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CsO2 is a member of the family of alkali superoxides (formula AO2 with A= Na, K, Rb and Cs) that exhibit magnetic behavior arising from open $p$-shell electrons residing on O2- molecules. We use neutron diffraction to solve the crystal and magnetic structures of CsO2, and observe a complex series of structures on cooling from room temperature to 1.6 K. These include an incommensurate modulation along the a-axis of the structure at intermediate temperatures, which then locks into a commensurate modulation that doubles the unit cell compared to the previously supposed orthorhombic unit cell. In both incommensurate and commensurate phases our structural solution involves a staggering of the cesium ion positions along the b-axis, in contrast to studies of other alkali superoxides in which staggered tilts of the O2- dimers relative to the c-axis are seen. Below T ~ 10 K we observe magnetic Bragg reflections arising from an antiferromagnetically ordered structure with a wavevector of k = (0,0,0) (relative to the doubled crystallographic unit cell), with moments that point predominantly along the b-axis with a small component along the a-axis that hints at possible anisotropic exchange coupling (consistent with the crystal structure). Measurements of the magnetic Bragg reflections in an applied magnetic field suggest a spin-flop transition takes place between 2 T and 4 T in which moments likely flop to point along the crystallographic a-axis. Our measurements indicate that CsO2 is an interesting example of magnetic properties being inherently linked to the crystal structure, in that the staggered displacement of the cesium ions activates antisymmetric exchange which then permits the observed spin canting., Comment: 13 pages, 11 figures, 6 tables

Isolated impurity states in epitaxially grown semiconductor systems possess important radiative features such as distinct wavelength emission with a very short radiative lifetime and low inhomogeneous broadening which makes them promising for the generation of indistinguishable single photons. In this study, we investigate chlorine-doped ZnSe/ZnMgSe quantum well (QW) nanopillar (NP) structures as a highly efficient solid-state single-photon source operating at cryogenic temperatures. We show that single photons are generated due to the radiative recombination of excitons bound to neutral Cl atoms in ZnSe QW and the energy of the emitted photon can be tuned from about 2.85 down to 2.82 eV with ZnSe well width increase from 2.7 to 4.7 nm. Following the developed advanced technology we fabricate NPs with a diameter of about 250 nm using a combination of dry and wet-chemical etching of epitaxially grown ZnSe/ZnMgSe QW well structures. The remaining resist mask serves as a spherical- or cylindrical-shaped solid immersion lens on top of NPs and leads to the emission intensity enhancement by up to an order of magnitude in comparison to the pillars without any lenses. NPs with spherical-shaped lenses show the highest emission intensity values. The clear photon-antibunching effect is confirmed by the measured value of the second-order correlation function at a zero time delay of 0.14. The developed single-photon sources are suitable for integration into scalable photonic circuits.

The focus of this article is a re-count of Richard Carrington's original sunspot observations from his book drawings (Carrington,1863) by an observer from the World data Center-SILSO network, Thomas H. Teague(UK). This modern recount will enable the use of Carrington's observations in the re-computation of the entire Sunspot Number series in a way Carrington's original counts (Casas and Vaquero,2014) did not. here we present comparison studies of the new recounted series with contemporary observations, new data extracted from the Journals of the Zurich Observatory and other sources of Carrington's own observations and conclude that Carrington's group counting is very close to the modern way of counting while his method for counting individual spots lags significantly behind modern counts. We also test the quality and robustness of the new re-count with methods developed in Mathieu et al.,2019., Comment: 30 pages, 19 figures few of them have subfigures, this article will be submitted to Solar Physics in future

We have investigated the electronic structure of iridates in the double perovskite crystal structure containing either Ir$^{4+}$ or Ir$^{5+}$ using hard x-ray photoelectron spectroscopy. The experimental valence band spectra can be well reproduced using tight binding calculations including only the Ir $5d$, O $2p$ and O $2s$ orbitals with parameters based on the downfolding of the density-functional band structure results. We found that regardless of the A and B cations, the A$_2$BIrO$_6$ iridates have essentially zero O $2p$ to Ir $5d$ charge transfer energies. Hence, double perovskite iridates turn out to be extremely covalent systems with the consequence being that the magnetic exchange interactions become very long-ranged, thereby hampering the materialization of the long-sought Kitaev physics. Nevertheless, it still would be possible to realize a spin-liquid system using the iridates with a proper tuning of the various competing exchange interactions., Comment: 9 pages, 7 figures, submitted to Physical Review B

Recently, a Verwey-type transition in the mixed-valence alkali sesquioxide Cs$_4$O$_6$ was deduced from the charge ordering of molecular peroxide O$_2^{2-}$ and superoxide O$_2^-$ anions accompanied by the structural transformation and a dramatic change in electronic conductivity [Adler et al, Sci. Adv 4, eaap7581 (2018)]. Here, we report that in the sister compound Rb$_4$O$_6$ a similar Verwey-type charge ordering transition is strongly linked to O$_2^-$ orbital and spin dynamics. On cooling, a powder neutron diffraction experiment reveals a charge ordering and a cubic-to-tetragonal transition at $T_{\rm CO}=290$ K, which is followed by a further structural instability at $T_{\rm s}=92$ K that involves an additional reorientation of magnetic O$_2^-$ anions. Magnetic resonance techniques supported by density functional theory computations suggest the emergence of a peculiar type of $\pi^*$-orbital ordering of the magnetically active O$_2^-$ units, which promotes the formation of a quantum spin state composed of weakly coupled spin dimers. These results reveal that similarly as in 3$d$ transition metal compounds, also in in the $\pi^*$ open-shell alkali sesquioxides the interplay between Jahn-Teller-like electron-lattice coupling and Kugel-Khomskii-type superexchange determines the nature of orbital ordering and the magnetic ground state.

Latest measurements suggest that the X(3872) mass lies less than 200 keV away from the D0-Dbar0* threshold, reenforcing its interpretation as a loosely-bound mesonic molecule. This observation implies that in processes like D0-Dbar0-pi0 production, threshold effects could disguise the actual pole position of the X(3872). We propose a new effective field theory with D0, Dbar0 and pi0 degrees of freedom for the X(3872), considering Galilean invariance to be an exact symmetry. The D0* enters as a D0-pi0 p-wave resonance, allowing for a comprehensive study of the influence of pion interactions on the X(3872) width. We calculate relations between the mass of the X(3872), its width, and its line shape in D0-Dbar0-pi0 production up to next-to-leading order. Our results provide a tool for the extraction of the X(3872) pole position from the experimental data near threshold., Comment: 31 pages, 14 figures, published version; added some remarks and four references, edited Figure 12, minor typographic corrections