Janus MXene nanosheets with a strain-induced reversible magnetic state transition for storing information without electricity.

The application of strain induces a transition in the ground-state magnetic configuration of Janus TiVC MXene from A-AFM to FM. A new system and method of solid-state disk information storage without electricity is developed based on the as-discovered reversible magnetic state transition in TiVC, which can achieve efficient storage of information in extremely harsh conditions.

Enhanced Performance of La0.8Sr0.2FeO3-δ-Gd0.2Ce0.8O2-δ Cathode for Solid Oxide Fuel Cells by Surface Modification with BaCO3 Nanoparticles.

Recently, Fe-based perovskite oxides, such as Ln1-xSrxFeO3-δ (Ln = La, Pr, Nd, Sm, Eu) have been proposed as potential alternative electrode materials for solid oxide fuel cells (SOFCs), due to their good phase stability, electrocatalytic activity, and low cost. This work presents the catalytic effect of BaCO3 nanoparticles modified on a cobalt-free La0.8Sr0.2FeO3-δ-Gd0.2Ce0.8O2-δ (LSF-GDC) composite cathode at an intermediate-temperature (IT)-SOFC. An electrochemical conductivity relaxation investigation (ECR) shows that the Kchem value of the modified LSF-GDC improves up to a factor of 17.47, demonstrating that the oxygen reduction process is effectively enhanced after surface impregnation by BaCO3. The area-specific resistance (ASR) of the LSF-GDC cathode, modified with 9.12 wt.% BaCO3, is 0.1 Ω.cm2 at 750 °C, which is about 2.2 times lower than that of the bare cathode (0.22 Ω.cm2). As a result, the anode-supported single cells, with the modified LSF-GDC cathode, deliver a high peak power density of 993 mW/cm2 at 750 °C, about 39.5% higher than that of the bare cell (712 mW/cm2). The single cells based on the modified cathode also displayed good performance stability for about 100 h at 700 °C. This study demonstrates the effectiveness of BaCO3 nanoparticles for improving the performance of IT-SOFC cathode materials.

CrI3/Y2CH2 Heterointerface-Induced Stable Half-Metallicity of Two-Dimensional CrI3 Monolayer Ferromagnets.

Two-dimensional (2D) CrI3 monolayer ferromagnets are key to the development of future miniature spintronic devices and modulating them into a half-metal will greatly expand the application scenarios of CrI3 in nanospintronics. Nevertheless, existing strategies to induce half-metallicity of a CrI3 monolayer remain experimentally challenging and have unstable issues. In this work, the introduction of a 2D electride [Y2C]2+·2e- as an auxiliary layer is shown to be an effective way to achieve the generation of stable half-metallicity in the CrI3 monolayer. When the fully hydrogenated Y2CH2 and ferromagnetic CrI3 monolayer combine to form a heterostructure, surprisingly the appropriate amount of charge injection (0.72 e) turns CrI3 into a half-metal. Hetero-interfacial half-metallicity in CrI3 is an intrinsic one and does not require any chemical functionalization or external physical modification. Therefore, it is advantageous for practical applications of CrI3 in miniature spintronic devices, such as magnetic tunnel junctions, spin valves or spin field-effect transistors. A new strategy of the stable CrI3/Y2CH2 heterostructure was successfully developed to induce the half-metallicity of 2D CrI3 ferromagnets, which is experimentally feasible and half-metallic stable enough. This work paves the way for the application of the CrI3 monolayer in half-metallic-based spintronics.