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Fangfang Ge

Publications and source records attributed to Fangfang Ge.

3 recordsLinked to original sources

Cross-sectional helium irradiation reveals interface-controlled bubble evolution in Cr/CrAlSiN multilayer coatings on zirconium alloys

The irradiation stability of Cr based protective coatings on zirconium alloys is critical for the development of accident-tolerant fuel claddings. However, conventional surface irradiation often produces shallow, nonuniform damage, obscuring interfacial behavior. In this study, we perform cross-sectional He irradiation to directly examine the interfacial response and He bubble evolution across Cr monolayer and Cr and CrAlSiN multilayer coatings on Zr substrates. Irradiation was carried out at 500 C and 750 C to doses of 2 and 3 dpa, enabling a direct comparison of temperature-dependent microstructural evolution. In the Cr monolayer, He implantation produced a homogeneous distribution of nanoscale bubbles throughout the damaged region and large cavities at the Cr and Zr interface, indicating severe Kirkendall-type voiding and interfacial decohesion at elevated temperature. In contrast, the Cr/CrAlSiN multilayer exhibited a periodically modulated bubble distribution, with bubble fragmentation and transformation into nanoscale platelets at CrAlSiN interfaces. A N-enriched Zr(N) interlayer formed spontaneously at the CrAlSiN and Zr interface, effectively suppressing bubble accumulation and interdiffusion. The nanochannel interfaces acted as He sinks and diffusion barriers, enhancing interfacial bonding and mitigating swelling. This work demonstrates that cross-sectional ion irradiation is a powerful approach for probing interfacial stability in multilayer systems, offering new insights into He-defect interactions and radiation tolerance engineering at buried interfaces. The findings highlight the potential of Cr and CrAlSiN multilayers as advanced coating architectures for high-temperature nuclear environments.

cond-mat.mtrl-sci

Organometallic-Inorganic Hybrid MXenes with Tunable Superconductivity

Ti-based two-dimensional transition-metal carbides (MXenes) have attracted attention due to their superior properties and are being explored across various applications1,2. Despite their versatile properties, superconductivity has never been demonstrated, not even predicted, for this important group of 2D materials. In this work, we have introduced an electrochemical intercalation protocol to construct versatile organometallic-inorganic hybrid MXenes and achieved tunable superconductivity in the metallocene-modified layered crystals. Through structural editing of MXene matrix at atomic scale and meticulously modulated intercalation route, Ti3C2Tx intercalated with metallocene species exhibits a superconductive transition temperature (Tc) of 10.2 K. Guest intercalation induced electron filling and strain engineering are responsible for the emerging superconductivity in this intrinsically non-superconducting material. Theoretically, simulated electron-phonon interaction effects further elucidate the nature of the changes in Tc. Furthermore, the Tc of crafted artificial superlattices beyond Ti-based MXenes have been predicted, offering a general strategy for engineering superconductivity and magnetism in layered hybrid materials.

cond-mat.supr-con

High resistance of superconducting TiN thin films against environmental attacks

Superconductors, an essential class of functional materials, hold a vital position in both fundamental science and practical applications. However, most superconductors, including MgB$_2$, Bi$_2$Sr$_2$CaCu$_2$O$_{8+\delta}$, and FeSe, are highly sensitive to environmental attacks (such as water and moist air), hindering their wide applications. More importantly, the surface physical and chemical processes of most superconductors in various environments remain poorly understood. Here, we comprehensively investigate the high resistance of superconducting titanium nitride (TiN) epitaxial films against acid and alkali attacks. Unexpectedly, despite immersion in acid and alkaline solutions for over 7 days, the crystal structure and superconducting properties of TiN films remain stable, as demonstrated by high-resolution X-ray diffraction, electrical transport, atomic force microscopy, and scanning electron microscope. Furthermore, combining scanning transmission electron microscopy analysis with density functional theory calculations revealed the corrosion mechanisms: acid corrosions lead to the creation of numerous defects due to the substitution of Cl ions for N anions, whereas alkaline environments significantly reduce the film thickness through the stabilization of OH$^\ast$ adsorbates. Our results uncover the unexpected stability and durability of superconducting materials against environmental attacks, highlighting their potential for enhanced reliability and longevity in diverse applications.

cond-mat.supr-con