生物矿化
材料科学
腐蚀
涂层
生物污染
制作
盐(化学)
成核
化学工程
方解石
多孔性
生物膜
微晶
碳酸钙
纳米技术
电化学
结垢
海水
原位
矿化组织
冶金
胞外聚合物
微生物
摩擦腐蚀
杀生物剂
碳酸盐
生物降解
醋酸
转化膜
作者
Shuangling Yang,Na Guo,Zhangwei Guo,Shiyu Huang,T. Liu
标识
DOI:10.1002/adfm.202529038
摘要
ABSTRACT Biomineralization offers a sustainable strategy for protecting marine infrastructure; however, the lack of standardized criteria for selecting mineralizing microorganisms hinders the transition from laboratory to application. Herein, we report the in situ fabrication of a multifunctional biomineralized coating on steel, driven by a rationally designed marine Pseudoalteromonas consortium (LLA). By elucidating the biofilm‐to‐mineral transformation, we established a definitive screening framework delineating three critical prerequisites: (1) rapid formation of dense biofilms for early‐stage protection; (2) metabolic generation of an alkaline microenvironment; and (3) abundant anionic functional groups in extracellular polymeric substances (EPS) to serve as nucleation templates. Guided by these criteria, the synergistic LLA induced the growth of a dense, polycrystalline calcite coating (∼ 22 µ m thick) with low porosity (< 2%). This coating exhibits integrated multifunctionality: superior corrosion resistance, reducing corrosion rates by > 95% while withstanding 500 h of neutral salt spray and 150 h of acetic acid salt spray exposure; robust anti‐icing performance (freezing delay > 1100 s) attributed to the Gibbs‐Thomson effect within nano‐confined pores; and active self‐healing, where metabolic re‐mineralization autonomously repairs physical and electrochemical defects. This work bridges microbial ecology and materials engineering, offering a scalable, “living” material strategy for next‐generation smart marine coatings.
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