Chimera states consisting of domains of coherently and incoherently oscillating identical oscillators with nonlocal coupling are studied. These states usually coexist with the fully synchronized state and have a small basin of attraction. We propose a nonlocal phase-coupled model in which chimera states develop from random initial conditions. Several classes of chimera states have been found: (a) stationary multicluster states with evenly distributed coherent clusters, (b) stationary multicluster states with unevenly distributed clusters, and (c) a single cluster state traveling with a constant speed across the system. Traveling coherent states are also identified. A self-consistent continuum description of these states is provided and their stability properties analyzed through a combination of linear stability analysis and numerical simulation.

Chimera states consisting of domains of coherently and incoherently oscillating oscillators in a two-dimensional periodic array of nonlocally coupled phase oscillators are studied. In addition to the one-dimensional chimera states familiar from one spatial dimension, two-dimensional structures termed twisted chimera states and spiral wave chimera states are identified in simulations. The properties of many of these states, including stability, are determined using an evolution equation for a complex order parameter and are found to be in agreement with the simulations.

Light-driven polymerization, such as photoinduced electron/energy transfer−reversible addition−fragmentation chain transfer (PET-RAFT) polymerization, enables biological benign conditions and versatile functional polymer structure design, which is readily used in protein−polymer bioconjugates. However, conventional metalloporphyrinic homogeneous catalysts for PET-RAFT polymerization suffer from limited aqueous solubility and tedious purification. Here we demonstrate the design of PET-RAFT photocatalyst from the reticular assembled Zr−porphyrinic metal−organic frameworks (MOFs), along with a biomacromolecule-based chain transfer agent, as efficient bioconjugation tools in water. Our methodology offers manufacturing advantages on bioconjugates under mild conditions such that MTT (3-[4,5dimethylthiazol-2-yl]-2,5 diphenyl tetrazolium bromide) and cytotoxicity assays have shown the preservation of the protein integrity, bioactivity, and high cell viability after PET-RAFT polymerization. We find that the fast kinetics are benefiting from the ultrahigh loading of metalloporphyrins in MOF-525-Zn. This heterogeneous catalyst also allows us to maintain living characteristics to incorporate myriads of monomers into block copolymers. Other advantages like easy postreaction purification, reusability, and high oxygen tolerance even in an open system are demonstrated. This study provides a tool of highly efficient heterogeneous photocatalysts for polymer−protein bioconjugation in aqueous media and paves the road for biological applications.

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The corrosion products formed on Sn-Zn solder alloys were systematically studied to elucidate the corrosion mechanism of Sn-Zn alloys in chloridecontaining solution. Sn-Zn alloys were subjected to immersion and polarization treatment in a 0.5 M NaCl solution. Ex situ analysis, including surface and crosssection, of the corrosion products was carried out by scanning electron microscopy (FE-SEM) and energy dispersive X-ray spectroscopy (EDX). The corrosion products presented porous microstructure formed by a fine interlinked network. An increase of zinc content resulted in more pores and cracks of the corrosion products, indicating degradation of corrosion resistance. Intriguing is the finding that a gradient of chlorine concentration from the outer layer inwards the alloys through the Zn-rich precipitates is observed, which demonstrates the migration of chloride ions inwards the alloys. Based on the results, a corrosion mechanism was proposed and discussed that explains the observations. Particular attention was paid to the anodic dissolution of Zn-rich precipitates.