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.
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.
Proton-conducting solid–oxide fuel cell (H-SOFC) is an alternative promising low-temperature electrochemical cell for renewable energy, but the performance is insufficient because of the low activity of cathode materials at low temperatures. A layered perovskite oxide PrBaFe1.9Zn0.1O5+δ (PBFZ) was synthesized and investigated as a promising cathode material for low-temperature H-SOFC. Here, the partial substitution of Fe by Zn further enhances the electrical conductivity and thermal compatibility of PrBaFe2O5+δ (PBF). The PBFZ exhibits improved conductivity in the air at intermediate temperatures and good chemical compatibility with electrolytes. The oxygen vacancy formed at the PBFZ lattice due to Zn doping enhances proton defects, resulting in an improved performance by extending the catalytic sites to the whole cathode area. A single cell with a Ni-BZCY anode, PBFZ cathode, and BaZr0.7Ce0.2Y0.1O3-δ (BZCY) electrolyte membrane was successfully fabricated and tested at 550–700 °C. The maximum power density and Rp were enhanced to 513 mW·cm−2 and 0.3 Ω·cm2 at 700 °C, respectively, due to Zn doping.
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