Neatly scratching the surface: A facile etching technique assisted by a silver‐nanoparticle network to produce large‐area 1D silicon nanostructure arrays with desired orientation and doping characteristics is demonstrated (see picture). A mechanism for the highly selective etching is proposed on the basis of experimental evidence.

Atomically dispersed catalysts refer to substrate-supported heterogeneous catalysts featuring one or a few active metal atoms that are separated from one another. They represent an important class of materials ranging from single-atom catalysts (SACs) and nanoparticles (NPs). While SACs and NPs have been extensively reported, catalysts featuring a few atoms with well-defined structures are poorly studied. The difficulty in synthesizing such structures has been a critical challenge. Here we report a facile photochemical method that produces catalytic centers consisting of two Ir metal cations, bridged by O and stably bound to a support. Direct evidence unambiguously supporting the dinuclear nature of the catalysts anchored on α-FeO is obtained by aberration-corrected scanning transmission electron microscopy (AC-STEM). Experimental and computational results further reveal that the threefold hollow binding sites on the OH-terminated surface of α-FeO anchor the catalysts to provide outstanding stability against detachment or aggregation. The resulting catalysts exhibit high activities toward HO photooxidation.

Developing catalysts that provide the effective activation of hydrogen and selective absorption of substrate on metal surface is crucial to simultaneously improve activity and selectivity of hydrogenation reaction. Here we present an unique in situ etching and coordination synthetic strategy for exploiting a functionalized metal-organic framework to incorporate the bimetallic platinum–nickel frames, thereby forming a frame within frame nanostructure. The as-grown metal-organic framework serves as a ‘breath shell' to enhance hydrogen enrichment and activation on platinum–nickel surface. More importantly, this framework structure with defined pores can provide the selective accessibility of molecules through its one-dimensional channels. In a mixture containing four olefins, the composite can selectively transport the substrates smaller than its pores to the platinum–nickel surface and catalyse their hydrogenation. This molecular sieve effect can be also applied to selectively produce imines, which are important intermediates in the reductive imination of nitroarene, by restraining further hydrogenation via cascade processes.

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Lysine acetylation is a reversible, dynamic protein modification regulated by lysine acetyltransferases and deacetylases. Recent advances in high-throughput proteomics have greatly contributed to the success of global analysis of lysine acetylation. A large number of proteins of diverse biological functions have been shown to be acetylated in several reports in human cells, E.coli, and dicot plants. However, the extent of lysine acetylation in non-histone proteins remains largely unknown in monocots, particularly in the cereal crops. Here we report the mass spectrometric examination of lysine acetylation in rice (Oryza sativa). We identified 60 lysine acetylated sites on 44 proteins of diverse biological functions. Immunoblot studies further validated the presence of a large number of acetylated non-histone proteins. Examination of the amino acid composition revealed substantial amino acid bias around the acetylation sites and the amino acid preference is conserved among different organisms. Gene ontology analysis demonstrates that lysine acetylation occurs in diverse cytoplasmic, chloroplast and mitochondrial proteins in addition to the histone modifications. Our results suggest that lysine acetylation might constitute a regulatory mechanism for many proteins, including both histones and non-histone proteins of diverse biological functions.

The controlled transformation of materials, both their structure and their physical properties, is key to many devices. Ionic liquid gating can induce the transformation of thin-film materials over long distances from the gated surface. Thus, the mechanism underlying this process is of considerable interest. Here we directly image, using in situ, real-time, high-resolution transmission electron microscopy, the reversible transformation between the oxygen vacancy ordered phase brownmillerite SrCoO2.5 and the oxygen ordered phase perovskite SrCoO3. We show that the phase transformation boundary moves at a velocity that is highly anisotropic, traveling at speeds ~30 times faster laterally than through the thickness of the film. Taking advantage of this anisotropy, we show that three-dimensional metallic structures such as cylinders and rings can be realized. Our results provide a roadmap to the construction of complex meso-structures from their exterior surfaces.

Searching for new materials and phenomena to enable voltage control of magnetism and magnetic properties holds compelling interest for the development of low-power nonvolatile memory devices. In particular, reversible and nonvolatile ON/OFF controls of magnetism above room temperature are highly desirable yet still elusive. Here, we report on a nonvolatile voltage control of magnetism in epitaxial SrCo1–x Fe x O3−δ (SCFO). The substitution of Co with Fe significantly changes the magnetic properties of SCFO. In particular, for the Co/Fe ratio of ∼1:1, a switch between nonmagnetic (OFF) and ferromagnetic (ON) states with a Curie temperature above room temperature is accomplished by ionic liquid gating at ambient conditions with voltages as low as ±2 V, even for films with thickness up to 150 nm. Tuning the oxygen stoichiometry via the polarity and duration of gating enables reversible and continuous control of the magnetization between 0 and 100 emu/cm3 (0.61 μB/f.u.) at room temperature. In addition, SCFO was successfully incorporated into self-assembled two-phase vertically aligned nanocomposites, in which the reversible voltage control of magnetism above room temperature is also attained. The notable structural response of SCFO to ionic liquid gating allows large strain couplings between the two oxides in these nanocomposites, with potential for voltage-controlled and strain-mediated functionality based on couplings between structure, composition, and physical properties.

Topological spin textures as an emerging class of topological matter offer a medium for information storage and processing. The recently discovered topological Hall effect (THE) is considered as a fingerprint for electrically probing non-trivial spin-textures. But the origin of THE in oxides has remained elusive. Here we report an observation of the THE in ultrathin ( 8  unit cells. u.c.) 4d ferromagnetic SrRuO 3 films grown on SrTiO 3 (001) substrates, which can be attributed to the chiral ordering of spin structure (i.e., skyrmion-like) in the single SrRuO 3 layer without contacting 5d oxide SrIrO 3 layer. It is revealed that the RuO 6 octahedral tilting induced by local orthorhombic-to-tetragonal structural phase transition exists across the SrRuO 3 /SrTiO 3 interface, which naturally breaks the inversion symmetry. Our theoretical calculations demonstrate that the Dzyaloshinskii-Moriya (DM) interaction arises owing to the broken inversion symmetry and strong spin-orbit interaction of 4d SrRuO 3 . This DM interaction can stabilize the Né el-type magnetic skyrmions, which in turn accounts for the observed THE in transport. The RuO 6 octahedral tilting-induced DM interaction provides a pathway toward the electrical control of the topological spin textures and resultant THE, which is confirmed both experimentally and theoretically. Besides the fundamental significance, the 3 understanding of THE in oxides and its electrical manipulation presented in this work could advance the low power cost topological electronic and spintronic applications.