We report the synthesis of bimetallic Cu-Au nanotubes (NTs) and Cu@Au core-shell nanowires (NWs) for use as anti-oxidative electrodes. The fabrication involved two key approaches: galvanic replacement to produce Cu-Au NTs and the physical deposition of Au to form Cu@Au core-shell NWs. The galvanic replacement process generated hollow NTs through the Kirkendall effect, driven by the unequal diffusion rates of Cu and Au during the redox reaction. In contrast, the physical deposition of Au, facilitated by fast reduction kinetics using L-ascorbic acid, enabled the formation of a Au shell encapsulating the Cu NWs, preserving their structural integrity. Morphological and structural analyses confirmed the successful formation of both nanostructures. While the Cu-Au NTs exhibited hollow interiors and increased dimensions, the Cu@Au NWs displayed a solid core-shell morphology with minimal diameter increase. Electrical conductivity and thermal stability tests revealed the superior performance of the Cu@Au NWs. The sheet resistance of Cu@Au NWs remained as low as 4 Ω sq-1 and showed exceptional thermal stability, with minimal resistance variation (R/Ro ~1.36) even after 36 h at 120 °C under ambient conditions. In contrast, the Cu-Au NTs suffered rapid oxidation and structural instability. The physical deposition approach holds significant promise for the development of robust, low-resistance electrodes for long-term applications in harsh environments.

We synthesized Fe-doped TiO2/α-Fe2O3 core-shell nanowires(NWs) by means of a co-electrospinning method anddemonstrated their magnetic properties. To investigate the structural, morphological, chemical, and magnetic properties of thesamples, X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and X-ray photoelectronspectroscopy were used, as was a vibrating sample magnetometer. The morphology of the nanostructures obtained aftercalcination at 500oC exhibited core/shell NWs consisting of TiO2 in the core region and α-Fe2O3 in the shell region. In addition,the XPS results confirmed the formation of Fe-doped TiO2 by the doping effect of Fe3+ ions into the TiO2 lattice, which canaffect the ferromagnetic properties in the core region. For comparison, pure α-Fe2O3 NWs were also fabricated using anelectrospinning method. With regard to the magnetic properties, the Fe-doped TiO2/α-Fe2O3 core-shell NWs exhibited improvedsaturation magnetization(Ms) of approximately ~2.96emu/g, which is approximately 6.1 times larger than that of pure α-Fe2O3NWs. The performance enhancement can be explained by three main mechanisms: the doping effect of Fe ions into the TiO2lattice, the size effect of the Fe2O3 nanoparticles, and the structural effect of the core-shell nanostructures.