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Prof. YAN Kai

Yangzhou University, Nanjing Institute of Technology, Southeast University

Research Publications & English Decoded Briefs

Showing 2 publications
SCIENCE CHINA Materials2026DOI: 10.1007/s40843-026-4426-y

Advances toward stress-assisted degradation of biomedical Mg alloys

Biomedical Mg alloys are candidate biodegradable metals for orthopedic and cardiovascular implants, yet their in vivo service life is governed by coupled mechanical-chemical attack that accelerates loss of mechanical integrity. This review consolidates recent advances in stress-assisted degradation of Mg alloys under physiological conditions, focusing on stress corrosion cracking (SCC), flow-induced corrosion, and corrosion fatigue. Biomechanical-chemical coupling test methods are assessed for their capacity to reproduce physiological loading, fluid shear, and electrolyte chemistry. Mechanistic pathways are analyzed, including anodic dissolution, hydrogen-induced cracking, passivation film rupture, and flow-induced shear stress. Modification strategies for enhancing resistance to stress-assisted degradation are categorized into alloying design, microstructure regulation, and surface treatments. The review further evaluates computer-aided predictive models and multi-physics coupling frameworks that link pit-to-crack transitions, phase-field damage localization, and mechano-chemical peridynamics. Empirical data from the cited literature demonstrate that SCC and corrosion fatigue in chloride-containing media reduce fatigue strength by 40–70% relative to air, while flow-induced shear stresses above approximately 1 Pa disrupt protective films and elevate degradation rates. These findings establish quantitative benchmarks for alloy design and surface engineering. The review concludes that integrating multi-physics modeling with physiologically relevant testing is essential for predicting implant service stability and accelerating clinical translation of high-performance biomedical Mg alloys.

SCIENCE CHINA Materials2026DOI: 10.1007/s40843-026-4340-0

Mismatching in Meso-/Microscopic Orientation Drives Optical Anisotropy to Unlock Multicolor Nonreciprocal Circularly Polarized Luminescence in Chiral Polymer Elastomeric Films

Thin films with nonreciprocal circularly polarized luminescence (CPL) emit circularly polarized light with opposite handedness from its two opposite sides, holding great promise for advancing optical multiplexing technologies. Herein, we introduce component orientation mismatch into chiral composite films via stretching, which leads to macroscopic optical anisotropy and accordingly drives the films to show nonreciprocal CPL activity. Stretching triggers linear dichroism-linear birefringence (LD-LB) coupling to realize nonreciprocal circular dichroism (CD) in elastomer films consisting of thermoplastic polyurethane (TPU) and chiral polyacetylene (R/S-PSA). Moreover, fluorescence anisotropy-linear birefringence (f-LB) coupling occurs after introducing fluorescent groups into the films to achieve multi-color nonreciprocal CPL. The unstretched films exhibit reciprocal CPL with a luminescence dissymmetry factor (|glum|) of 10⁻¹, with handedness determined by PSA’s intrinsic helical chirality. In the stretched films, the oriented fluorescent groups undergo f-LB coupling with matrix crystallization, resulting in nonreciprocal CPL (|glum|=10⁻²). Based on this distinctive chiroptical feature, we have developed chiral logic gates, multidimensional optical encryption systems, and enantioselective photopolymerization platforms to demonstrate the potential uses of the as-obtained CPL films. This work provides both fundamental insights into and a versatile material platform for developing smart nonreciprocal photonic systems with advanced chiroptical functionality.