All-magnonic repeater based on bistability.

Bistability, a universal phenomenon found in diverse fields such as biology, chemistry, and physics, describes a scenario in which a system has two stable equilibrium states and resets to one of the two states. The ability to switch between these two states is the basis for a wide range of applications, particularly in memory and logic operations. Here, we present a universal approach to achieve bistable switching in magnonics, the field processing data using spin waves. A pronounced bistable window is observed in a 1 µm wide magnonic conduit under an external rf drive. The system is characterized by two magnonic stable states defined as low and high spin-wave amplitude states. The switching between these two states is realized by another propagating spin wave sent into the rf driven region. This magnonic bistable switching is used to design a magnonic repeater, which receives the original decayed and distorted spin wave and regenerates a new spin wave with amplified amplitude and normalized phase. Our magnonic repeater can be installed at the inputs of each magnonic logic gate to overcome the spin-wave amplitude degradation and phase distortion during previous propagation and achieve integrated magnonic circuits or magnonic neuromorphic networks.

Phase transformation mechanism of MnCO3 as cathode materials for aqueous zinc-ion batteries.

Aqueous rechargeable zinc-ion batteries (ZIBs) have been given more and more attention because of their high specific capacity, high safety, and low cost. The reasonable design of Mn-based cathode materials is an effective way to improve the performance of ZIBs. Herein, a square block MnCO3 electrode material is synthesized on the surface of carbon cloth by a one-step hydrothermal method. The phase transition of MnCO3 was accompanied by the continuous increase of specific capacity, and finally maintained good cycle stability in the charge-discharge process. The maximum specific capacity of MnCO3 electrode material can reach 83.62 mAh g-1 at 1 A g-1. The retention rate of the capacity can reach 85.24% after 1,500 cycles compared with the stable capacity (the capacity is 61.44 mAh g-1 under the 270th cycle). Ex situ characterization indicates that the initial MnCO3 gradually transformed into MnO2 accompanied by the embedding and stripping of H+ and Zn2+ in charge and discharge. When MnCO3 is no longer transformed into MnO2, the cycle tends to be stable. The phase transformation of MnCO3 could provide a new research idea for improving the performance of electrode materials for energy devices.

Direct investigation of the atomic structure and decreased magnetism of antiphase boundaries in garnet.

The ferrimagnetic insulator iron garnets, tailored artificially with specific compositions, have been widely utilized in magneto-optical (MO) devices. The adjustment on synthesis always induces structural variation, which is underestimated due to the limited knowledge of the local structures. Here, by analyzing the structure and magnetic properties, two different antiphase boundaries (APBs) with individual interfacial structure are investigated in substituted iron garnet film. We reveal that magnetic signals decrease in the regions close to APBs, which implies degraded MO performance. In particular, the segregation of oxygen deficiencies across the APBs directly leads to reduced magnetic elements, further decreases the magnetic moment of Fe and results in a higher absorption coefficient close to the APBs. Furthermore, the formation of APBs can be eliminated by optimizing the growth rate, thus contributing to the enhanced MO performance. These analyses at the atomic scale provide important guidance for optimizing MO functional materials.

Atomic-scale insights into quantum-order parameters in bismuth-doped iron garnet.

Bismuth and rare earth elements have been identified as effective substituent elements in the iron garnet structure, allowing an enhancement in magneto-optical response by several orders of magnitude in the visible and near-infrared region. Various mechanisms have been proposed to account for such enhancement, but testing of these ideas is hampered by a lack of suitable experimental data, where information is required not only regarding the lattice sites where substituent atoms are located but also how these atoms affect various order parameters. Here, we show for a Bi-substituted lutetium iron garnet how a suite of advanced electron microscopy techniques, combined with theoretical calculations, can be used to determine the interactions between a range of quantum-order parameters, including lattice, charge, spin, orbital, and crystal field splitting energy. In particular, we determine how the Bi distribution results in lattice distortions that are coupled with changes in electronic structure at certain lattice sites. These results reveal that these lattice distortions result in a decrease in the crystal-field splitting energies at Fe sites and in a lifted orbital degeneracy at octahedral sites, while the antiferromagnetic spin order remains preserved, thereby contributing to enhanced magneto-optical response in bismuth-substituted iron garnet. The combination of subangstrom imaging techniques and atomic-scale spectroscopy opens up possibilities for revealing insights into hidden coupling effects between multiple quantum-order parameters, thereby further guiding research and development for a wide range of complex functional materials.