We report on the high-temperature ferromagnetism in Co-doped ZnO films fabricated by the sol-gel method above 350 K. The lattice constant of c axis of wurtzite Zn 1Ϫx Co x O follows Vergard's law for 0ϽxϽ0.25. For Zn 1Ϫx Co x O with xу0.25, a secondary phase is detected. The Zn 1Ϫx Co x O exhibits ferromagnetic behavior with a Curie temperature higher than 350 K. By the results of x-ray photoelectron spectroscopy measurement, we assume that Co occupied the Zn site without changing the wurtzite structure. In the case of xϭ0.2, the coercive field measured by a magnetizationmagnetic field hysteresis curve at 350 K was nearly 80 Oe. Additionally, we investigated the electric structure through first-principles pseudopotential plane-wave calculation.

Summary Mitochondrial sirtuins, SIRT3-5, are NAD+-dependent deacylases and ADP-ribosyltransferases critical for stress responses. However, a comprehensive understanding of sirtuin targets, regulation of sirtuin activity, and the relationships between sirtuins remains a key challenge in mitochondrial physiology. Here, we employ systematic interaction proteomics to elucidate the mitochondrial sirtuin protein interaction landscape. This work reveals sirtuin interactions with numerous functional modules within mitochondria, identifies candidate sirtuin substrates, and uncovers a fundamental role for sequestration of SIRT3 by ATP synthase in mitochondrial homeostasis. In healthy mitochondria, a pool of SIRT3 binds ATP synthase, but upon matrix pH reduction with concomitant loss of mitochondrial membrane potential, SIRT3 dissociates. This release correlates with rapid deacetylation of matrix proteins and SIRT3 is required for recovery of membrane potential. In vitro reconstitution experiments, as well as Crispr/Cas9 engineered cells, indicate that pH-dependent SIRT3 release requires H135 in ATP5O. Our SIRT3-5 interaction network provides a framework for discovering novel biological functions regulated by mitochondrial sirtuins.

We report on the discovery of a room-temperature ferromagnetism in Cr-doped GaN single crystals with a Tc=280 K. The addition of Cr into GaN single crystals grown by the flux method induces the lattice constant increase due to the larger Cr atomic radius. In x-ray photoelectron spectroscopy measurement, Cr 2p3/2 core-level exhibited spectra near 575.7 eV. This binding energy is similar to the reported value of CrN. The coercive field by magnetization–magnetic field (M–H) hysteresis curve at 250 K was 54 Oe. We verified the presence of ferromagnetic transition in the temperature dependence of the electrical resistance measurements. We discuss the ferromagnetic ordering in Cr-doped GaN bulk single crystals excluding the contribution of the substrate crystal structure.

Solution studies have proposed that crystal nucleation can take more complex pathways than previously expected in classical nucleation theory, such as formation of prenucleation clusters or densified amorphous/liquid phases. These findings show that it is possible to separate fluctuations in the different order parameters governing crystal nucleation, that is, density and structure. However, a direct observation of the multipathways from aqueous solutions remains a great challenge because heterogeneous nucleation sites, such as container walls, can prevent these paths. Here, we demonstrate the existence of multiple pathways of nucleation in highly supersaturated aqueous KH 2 PO 4 (KDP) solution using the combination of a containerless device (electrostatic levitation), and in situ micro-Raman and synchrotron X-ray scattering. Specifically, we find that, at an unprecedentedly deep level of supersaturation, a highconcentration KDP solution first transforms into a metastable crystal before reaching stability at room temperature. However, a low-concentration solution, with different local structures, directly transforms into the stable crystal phase. These apparent multiple pathways of crystallization depend on the degree of supersaturation.multipath nucleation | liquid-droplet levitation | supersaturation | in situ X-ray diffraction | in situ micro-Raman spectroscopy N ucleation is the first step toward crystallization, in which atoms or particles aggregate to form clusters in a metastable liquid, called crystal nuclei. The crystal nuclei in metastable liquid grow continuously if their size exceeds a critical limit, and are subsequently stabilized. Based on the classical nucleation theory (CNT) (1, 2), nucleation is mainly governed by two factors, that is, interfacial free energy and volume Gibbs free energy (or chemical potential) between liquid and crystal phases. Although the volume Gibbs free energy acts to stabilize the crystal nuclei, the interfacial free energy works as an energy barrier preventing the formation of the nuclei. If the crystal-liquid interfacial free energy creates a sufficiently high energy barrier, the liquid can be supercooled, supersaturated, or even supercompressed. In case of liquid metals (3-6), the crystal-liquid interfacial free energy arises from configurational entropy differences between crystal and liquid. That is, the greater difference in local structural orderings between crystal and liquid phases results in higher interfacial free energy, which consequently leads to a higher nucleation barrier and thus deeper supercooling. This concept has been verified in various metallic systems for elements (7) and many alloys (8-12). However, many experimental and theoretical investigations have raised questions that CNT may not be adequate to describe the initial nucleation processes in biomaterials (13-17) and minerals (18)(19)(20)(21)(22)(23)(24)(25)(26).Recently, an alternate nucleation mechanism, called multipathway nucleation (or crystallization) (13-23, 25, 26), has been proposed fo...

We have investigated experimentally the effects of n-type impurities such as Al and H on the magnetic properties of ZnCoO. The carrier density changes slightly upon the introduction of hydrogen but increases significantly in the case of Al. A measurement of magnetic circular dichroism indicates that, of the two impurities, only H induces ferromagnetism in ZnCoO. Our experimental data suggest that, unlike Al, H plays an important role in the enhancement of ferromagnetic spin-spin interactions that goes much beyond a carrier-mediated effect.